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Lista de obras de Tatiana Foroud

18F-florbetapir Positron Emission Tomography-determined Cerebral β-Amyloid Deposition and Neurocognitive Performance after Cardiac Surgery

artículo científico publicado en 2018

A Family-Based Analysis of the Association of the Dopamine D2 Receptor (DRD2) with Alcoholism

scholarly article by Howard J. Edenberg et al published April 1998 in Alcoholism: Clinical and Experimental Research

A Framework for 3D Analysis of Facial Morphology in Fetal Alcohol Syndrome

A GABRA2 polymorphism improves a model for prediction of drinking initiation

artículo científico publicado en 2017

A MULTIVARIATE FINITE MIXTURE LATENT TRAJECTORY MODEL WITH APPLICATION TO DEMENTIA STUDIES

artículo científico publicado en 2016

A Systematic single nucleotide polymorphism screen to fine-map alcohol dependence genes on chromosome 7 identifies association with a novel susceptibility gene ACN9

artículo científico publicado en 2007

A cholinergic receptor gene (CHRM2) affects event-related oscillations

artículo científico publicado en 2006

A commonly carried allele of the obesity-related FTO gene is associated with reduced brain volume in the healthy elderly

artículo científico publicado en 2010

A description of the methods of the Nulliparous Pregnancy Outcomes Study: monitoring mothers-to-be (nuMoM2b).

artículo científico publicado en 2015

A family-based analysis of the association of the dopamine D2 receptor (DRD2) with alcoholism

scientific article published on 01 April 1998

A family-based analysis of whether the functional promoter alleles of the serotonin transporter gene HTT affect the risk for alcohol dependence.

artículo científico publicado en 1998

A genome-wide association study of alcohol dependence

artículo científico publicado en 2010

A genome-wide association study of interhemispheric theta EEG coherence: implications for neural connectivity and alcohol use behavior

artículo científico publicado en 2020

A genome-wide screen for genes influencing conduct disorder

artículo científico publicado en 2004

A genome-wide search for genes that relate to a low level of response to alcohol

artículo científico publicado en 2001

A genomic scan for habitual smoking in families of alcoholics: common and specific genetic factors in substance dependence.

artículo científico publicado en 2004

A large-scale genome-wide association study meta-analysis of cannabis use disorder

artículo científico publicado en 2020

A meta-analysis of two genome-wide association studies to identify novel loci for maximum number of alcoholic drinks

scientific journal article

A multiancestral genome-wide exome array study of Alzheimer disease, frontotemporal dementia, and progressive supranuclear palsy

artículo científico publicado en 2015

A multicenter study of glucocerebrosidase mutations in dementia with Lewy bodies

artículo científico publicado en 2013

A novel non-parametric regression reveals linkage on chromosome 4 for the number of externalizing symptoms in sib-pairs

artículo científico publicado en 2008

A polymorphism in GABRA2 is associated with the medial frontal response to alcohol cues in an fMRI study

artículo científico publicado en 2010

A principal components analysis of the abbreviated Desires for Alcohol Questionnaire (DAQ).

artículo científico publicado en 2010

A quantitative trait locus for alcohol consumption in selectively bred rat lines

artículo científico publicado en 1998

A regulatory variation in OPRK1, the gene encoding the kappa-opioid receptor, is associated with alcohol dependence

artículo científico publicado en 2008

A sex-adjusted and age-adjusted genome screen for nested alcohol dependence diagnoses

artículo científico publicado en 2005

A variant in XPNPEP2 is associated with angioedema induced by angiotensin I-converting enzyme inhibitors

artículo científico publicado en 2005

APOE effect on Alzheimer's disease biomarkers in older adults with significant memory concern

artículo científico publicado en 2015

APOE ε4 and the risk for Alzheimer disease and cognitive decline in African Americans and Yoruba

artículo científico publicado en 2014

Abnormal error-related antisaccade activation in premanifest and early manifest Huntington disease

artículo científico publicado en 2011

Absence of C9ORF72 expanded or intermediate repeats in autopsy-confirmed Parkinson's disease

artículo científico publicado en 2014

Adaptation of Subjective Responses to Alcohol is Affected by an Interaction of GABRA2 Genotype and Recent Drinking

artículo científico publicado en 2015

Affected twins in the familial intracranial aneurysm study

artículo científico publicado en 2015

Age-specific incidence rates for dementia and Alzheimer disease in NIA-LOAD/NCRAD and EFIGA families: National Institute on Aging Genetics Initiative for Late-Onset Alzheimer Disease/National Cell Repository for Alzheimer Disease (NIA-LOAD/NCRAD) an

artículo científico publicado en 2014

Alcohol-preferring rats show decreased corticotropin-releasing hormone-2 receptor expression and differences in HPA activation compared to alcohol-nonpreferring rats

artículo científico publicado en 2014

Alcoholism susceptibility loci: confirmation studies in a replicate sample and further mapping

scientific article published on 01 July 2000

Allele-Specific Expression and High-Throughput Reporter Assay Reveal Functional Variants in Human Brains with Alcohol Use Disorders

Allele-specific expression and high-throughput reporter assay reveal functional genetic variants associated with alcohol use disorders

scientific article published on 02 September 2019

Allelic-based gene-gene interaction associated with quantitative traits

artículo científico publicado en 2009

Alpha-synuclein and familial Parkinson's disease

artículo científico publicado en 2009

Alzheimer's Disease Neuroimaging Initiative biomarkers as quantitative phenotypes: Genetics core aims, progress, and plans

artículo científico publicado en 2010

Alzheimer's Disease Sequencing Project discovery and replication criteria for cases and controls: Data from a community-based prospective cohort study with autopsy follow-up

artículo científico publicado en 2017

Amplitude of visual P3 event-related potential as a phenotypic marker for a predisposition to alcoholism: preliminary results from the COGA Project. Collaborative Study on the Genetics of Alcoholism

artículo científico publicado en 1998

Amyloid pathway-based candidate gene analysis of [(11)C]PiB-PET in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort

artículo científico publicado en 2012

An ADH1B variant and peer drinking in progression to adolescent drinking milestones: evidence of a gene-by-environment interaction

artículo científico publicado en 2014

Analyses of quantitative trait loci contributing to alcohol preference in HAD1/LAD1 and HAD2/LAD2 rats

artículo científico publicado en 2003

Analyses of the National Institute on Aging Late-Onset Alzheimer's Disease Family Study: implication of additional loci

artículo científico publicado en 2008

Analysis of copy number variation in Alzheimer's disease in a cohort of clinically characterized and neuropathologically verified individuals

artículo científico publicado en 2012

Analysis of copy number variation in Alzheimer's disease: the NIALOAD/ NCRAD Family Study

artículo científico publicado en 2012

Analysis of variation in expression of autosomal dominant osteopetrosis type 2: searching for modifier genes

artículo científico publicado en 2005

Analysis of whole genome-transcriptomic organization in brain to identify genes associated with alcoholism

article

Anxiety proneness linked to epistatic loci in genome scan of human personality traits

artículo científico publicado en 1998

Apparent replication of suggestive linkage on chromosome 16 in the NIMH genetics initiative bipolar pedigrees.

artículo científico publicado en 2002

Are cognitive changes progressive in prediagnostic HD?

artículo científico publicado en 2007

Assessing the genetic risk for alcohol use disorders

artículo científico publicado en 2012

Assessment of executive function declines in presymptomatic and mildly symptomatic familial frontotemporal dementia: NIH-EXAMINER as a potential clinical trial endpoint

scientific article published on 01 January 2020

Assessment of first and second degree relatives of individuals with bipolar disorder shows increased genetic risk scores in both affected relatives and young At-Risk Individuals

artículo científico publicado en 2015

Association analysis of genes encoding the nociceptin receptor (OPRL1) and its endogenous ligand (PNOC) with alcohol or illicit drug dependence

artículo científico publicado en 2007

Association analysis of rare variants near the APOE region with CSF and neuroimaging biomarkers of Alzheimer's disease

artículo científico publicado en 2017

Association between GABRA1 and drinking behaviors in the collaborative study on the genetics of alcoholism sample.

artículo científico publicado en 2006

Association of Alcohol Craving With ?-Synuclein (SNCA)

artículo científico publicado en 2007

Association of Blood Biomarkers With Acute Sport-Related Concussion in Collegiate Athletes: Findings From the NCAA and Department of Defense CARE Consortium

scientific article published on 03 January 2020

Association of GABA(A) receptors and alcohol dependence and the effects of genetic imprinting

artículo científico publicado en 2003

Association of GABRA2 with drug dependence in the collaborative study of the genetics of alcoholism sample

artículo científico publicado en 2006

Association of GABRG3 with alcohol dependence

artículo científico publicado en 2004

Association of Long Runs of Homozygosity With Alzheimer Disease Among African American Individuals

artículo científico publicado en 2015

Association of NFKB1, which encodes a subunit of the transcription factor NF-kappaB, with alcohol dependence

artículo científico publicado en 2007

Association of Polygenic Liability for Alcohol Dependence and EEG Connectivity in Adolescence and Young Adulthood

scientific article published on 17 October 2019

Association of adenylate cyclase 10 (ADCY10) polymorphisms and bone mineral density in healthy adults

artículo científico publicado en 2008

Association of alcohol dehydrogenase genes with alcohol dependence: a comprehensive analysis

article

Association of common genetic variants in GPCPD1 with scaling of visual cortical surface area in humans

artículo científico publicado en 2012

Association of plasma and cortical amyloid beta is modulated by APOE ε4 status

scientific article published on 26 March 2013

Association of single nucleotide polymorphisms in a glutamate receptor gene (GRM8) with theta power of event-related oscillations and alcohol dependence

artículo científico publicado en 2009

Association of substance dependence phenotypes in the COGA sample

artículo científico publicado en 2014

Association of the calcium-sensing receptor gene with blood pressure and urinary calcium in African-Americans

scientific article published on 09 December 2008

Author Correction: Genetic meta-analysis of diagnosed Alzheimer's disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

scientific article published on 01 September 2019

Automatic Prediction of Conversion from Mild Cognitive Impairment to Probable Alzheimer's Disease using Structural Magnetic Resonance Imaging ⬇️

artículo científico publicado el 13 de noviembre de 2010

Bone mineral density variation in men is influenced by sex-specific and non sex-specific quantitative trait loci

artículo científico publicado en 2009

Brain volumetric deficits in MAPT mutation carriers: a multisite study

artículo científico publicado en 2020

Brief report: genetics of alcoholic cirrhosis-GenomALC multinational study

artículo científico publicado en 2015

C9orf72 hexanucleotide repeat expansions in clinical Alzheimer disease

artículo científico publicado en 2013

CLCN7 polymorphisms and bone mineral density in healthy premenopausal white women and in white men.

artículo científico publicado en 2008

Calcium-Sensing Receptor Genotype and Response to Cinacalcet in Patients Undergoing Hemodialysis

artículo científico publicado en 2017

Cancer outcomes among Parkinson's disease patients with leucine rich repeat kinase 2 mutations, idiopathic Parkinson's disease patients, and nonaffected controls

artículo científico publicado en 2019

Candidate genes for alcohol dependence: a review of genetic evidence from human studies

artículo científico publicado en 2003

Characteristics of Bipolar I patients grouped by externalizing disorders

artículo científico publicado en 2015

Charcot-Marie-Tooth gene, SBF2, associated with taxane-induced peripheral neuropathy in African Americans

artículo científico publicado en 2016

Chloride channel 7 (ClCN7) gene mutations and autosomal dominant osteopetrosis, type II

artículo científico publicado en 2003

Chromosome 5 and Parkinson disease

scholarly article by Tatiana Foroud et al published 31 May 2006 in European Journal of Human Genetics

Cis-regulatory variants affect CHRNA5 mRNA expression in populations of African and European ancestry

artículo científico publicado en 2013

Clinical and Dopamine Transporter Imaging Characteristics of Leucine- Rich Repeat Kinase 2 (LRRK2) and Glucosylceramidase Beta (GBA) Parkinson's Disease Participants in the Parkinson's Progression Markers Initiative: A Cross-Sectional Study

scientific article published on 19 February 2020

Clinical and dopamine transporter imaging characteristics of non-manifest LRRK2 and GBA mutation carriers in the Parkinson's Progression Markers Initiative (PPMI): a cross-sectional study

artículo científico publicado en 2019

Clinical and volumetric changes with increasing functional impairment in familial frontotemporal lobar degeneration

artículo científico publicado en 2020

Clinical correlates of depressive symptoms in familial Parkinson's disease

artículo científico publicado en 2008

Clinical features of Parkinson disease patients with homozygous leucine-rich repeat kinase 2 G2019S mutations.

artículo científico publicado en 2006

Clinical implications of gene discovery in Parkinson's disease and parkinsonism

artículo científico

Clinical-Genetic Associations in the Prospective Huntington at Risk Observational Study (PHAROS): Implications for Clinical Trials

artículo científico publicado en 2015

Cognitive scores in carriers of Huntington's disease gene compared to noncarriers

artículo científico publicado en 1995

Collaborative initiative on fetal alcohol spectrum disorders: methodology of clinical projects

artículo científico publicado en 2009

Combined Face-Brain Morphology and Associated Neurocognitive Correlates in Fetal Alcohol Spectrum Disorders

scholarly article by Michael Suttie et al published September 2018 in Alcoholism: Clinical and Experimental Research

Combined analysis from eleven linkage studies of bipolar disorder provides strong evidence of susceptibility loci on chromosomes 6q and 8q

artículo científico publicado en 2005

Combined sequence-based and genetic mapping analysis of complex traits in outbred rats

artículo científico publicado en 2013

Common Genetic Determinants of Vitamin D Insufficiency: A Genome-Wide Association Study

Common genetic determinants of vitamin D insufficiency: a genome-wide association study

artículo científico publicado en 2010

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Common variants at MS4A4/MS4A6E, CD2AP, CD33 and EPHA1 are associated with late-onset Alzheimer's disease

artículo científico publicado en 2011

Comparison of Parent, Peer, Psychiatric, and Cannabis Use Influences Across Stages of Offspring Alcohol Involvement: Evidence from the COGA Prospective Study

artículo científico publicado en 2017

Comparison of vertical and horizontal saccade measures and their relation to gray matter changes in premanifest and manifest Huntington disease

artículo científico publicado en 2011

Comprehensive gene- and pathway-based analysis of depressive symptoms in older adults

artículo científico publicado en 2015

Comprehensive research synopsis and systematic meta-analyses in Parkinson's disease genetics: The PDGene database

artículo científico publicado en 2012

Confirmation of alcohol preference quantitative trait loci in the replicate high alcohol drinking and low alcohol drinking rat lines

artículo científico publicado en 2003

Confirmation of linkage of limb-girdle muscular dystrophy, type 2, to chromosome 15.

artículo científico publicado en 1992

Confirmation of linkage to chromosome 1q for peak vertebral bone mineral density in premenopausal white women

artículo científico publicado en 2004

Contribution of the LRP5 gene to normal variation in peak BMD in women

artículo científico publicado en 2004

Copy number variation accuracy in genome-wide association studies

artículo científico publicado en 2011

Copy number variation in familial Parkinson disease

artículo científico publicado en 2011

Copy-number disorders are a common cause of congenital kidney malformations

artículo científico publicado en 2012

Correction: Rare Variants in APP, PSEN1 and PSEN2 Increase Risk for AD in Late-Onset Alzheimer's Disease Families

artículo científico publicado en 2012

DNM3 and genetic modifiers of age of onset in LRRK2 Gly2019Ser parkinsonism: a genome-wide linkage and association study

artículo científico publicado en 2016

DSM-5 cannabis use disorder: a phenotypic and genomic perspective

artículo científico publicado en 2013

Detecting significant genotype-phenotype association rules in bipolar disorder: market research meets complex genetics

article

Detection of dental fluorosis-associated quantitative trait Loci on mouse chromosomes 2 and 11

artículo científico publicado en 2008

Development of congenic rat strains for alcohol consumption derived from the alcohol-preferring and nonpreferring rats

artículo científico publicado en 2006

Differentially expressed genes strongly correlated with femur strength in rats

artículo científico publicado en 2009

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

artículo científico publicado en 2013

Dopamine transporter imaging predicts clinically-defined α-synucleinopathy in REM sleep behavior disorder

artículo científico publicado en 2020

ERRATUM: Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans

scientific article published on 01 November 2019

Effects of multiple genetic loci on age at onset in late-onset Alzheimer disease: a genome-wide association study

artículo científico publicado en 2014

Efficient region-based test strategy uncovers genetic risk factors for functional outcome in bipolar disorder

scientific article published on 29 November 2018

Endophenotypes successfully lead to gene identification: results from the collaborative study on the genetics of alcoholism

artículo científico publicado en 2005

Epistasis between QTLs for bone density variation in Copenhagen x dark agouti F2 rats

artículo científico publicado en 2009

Epistatic effects contribute to variation in BMD in Fischer 344 x Lewis F2 rats

scientific article published on January 2008

Ethanol treatment of lymphoblastoid cell lines from alcoholics and non-alcoholics causes many subtle changes in gene expression

artículo científico publicado en 2014

Evaluation of laboratory tests for cirrhosis and for alcohol use, in the context of alcoholic cirrhosis

artículo científico publicado en 2017

Evaluation of psychological symptoms among presymptomatic HD gene carriers as measured by selected MMPI scales

artículo científico publicado en 2002

Evaluation of the role of Nurr1 in a large sample of familial Parkinson's disease

artículo científico publicado en 2004

Evidence for a locus on chromosome 1 that influences vulnerability to alcoholism and affective disorder

artículo científico publicado en 2001

Evidence for association between polymorphisms in the cannabinoid receptor 1 (CNR1) gene and cannabis dependence

scientific article published on July 2009

Evidence for association of bipolar disorder to haplotypes in the 22q12.3 region near the genes stargazin, IFT27 and parvalbumin

artículo científico publicado en 2012

Evidence for genes on chromosome 2 contributing to alcohol dependence with conduct disorder and suicide attempts

artículo científico publicado en 2010

Evidence of association between brain-derived neurotrophic factor gene and bipolar disorder

artículo científico publicado en 2008

Evolution of Alzheimer's Disease Cerebrospinal Fluid Biomarkers in Early Parkinson's Disease

artículo científico publicado en 2020

Exceptionally low likelihood of Alzheimer's dementia in APOE2 homozygotes from a 5,000-person neuropathological study

artículo científico publicado en 2020

Exome Sequencing Identifies Candidate Genetic Modifiers of Syndromic and Familial Thoracic Aortic Aneurysm Severity.

artículo científico publicado en 2017

Exome chip meta-analysis fine maps causal variants and elucidates the genetic architecture of rare coding variants in smoking and alcohol use

artículo científico publicado en 2018

Exome-chip association analysis of intracranial aneurysms

scientific article published on 15 November 2019

Expression profiling and QTL analysis: a powerful complementary strategy in drug abuse research

artículo científico publicado en 2005

Facial Curvature Detects and Explicates Ethnic Differences in Effects of Prenatal Alcohol Exposure

artículo científico publicado en 2017

Facial dysmorphism across the fetal alcohol spectrum

artículo científico publicado en 2013

False positive rates in association studies as a function of degree of stratification

artículo científico publicado en 2004

Familial intracranial aneurysms: is anatomic vulnerability heritable?

artículo científico publicado en 2012

Family-based association analysis of alcohol dependence criteria and severity

artículo científico publicado en 2013

Feasibility and Safety of Multicenter Tissue and Biofluid Sampling for α-Synuclein in Parkinson's Disease: The Systemic Synuclein Sampling Study (S4)

scholarly article by Lana M Chahine et al published 2018 in Journal of Parkinson's disease

Feasibility and safety of lumbar puncture in the Parkinson's disease research participants: Parkinson's Progression Marker Initiative (PPMI)

artículo científico publicado en 2019

Finding useful biomarkers for Parkinson's disease

article

Fine mapping and expression of candidate genes within the chromosome 10 QTL region of the high and low alcohol-drinking rats

artículo científico publicado en 2010

Fine mapping of bone structure and strength QTLs in heterogeneous stock rat.

artículo científico publicado en 2015

Fine mapping quantitative trait loci that influence alcohol preference behavior in the High and Low Alcohol Preferring (HAP and LAP) mice

scientific article published on 24 December 2010

From QTL to candidate gene: a genetic approach to alcoholism research

artículo científico publicado en 2009

Functional microRNAs in Alzheimer's disease and cancer: differential regulation of common mechanisms and pathways

artículo científico publicado en 2012

Functional variant in a bitter-taste receptor (hTAS2R16) influences risk of alcohol dependence

artículo científico publicado en 2005

Functional variants in the LRRK2 gene confer shared effects on risk for Crohn's disease and Parkinson's disease

artículo científico publicado en 2018

G2019S mutation in the leucine-rich repeat kinase 2 gene is not associated with multiple system atrophy

artículo científico publicado en 2007

GABRR1 and GABRR2, encoding the GABA-A receptor subunits rho1 and rho2, are associated with alcohol dependence

artículo científico publicado en 2010

GWAS of longitudinal amyloid accumulation on 18F-florbetapir PET in Alzheimer's disease implicates microglial activation gene IL1RAP.

artículo científico publicado en 2015

Gene expression profiles in Parkinson disease prefrontal cortex implicate FOXO1 and genes under its transcriptional regulation

artículo científico publicado en 2012

Gene-wide analysis detects two new susceptibility genes for Alzheimer's disease

artículo científico publicado en 2014

Genes associated with alcohol outcomes show enrichment of effects with broad externalizing and impulsivity phenotypes in an independent sample

artículo científico publicado en 2015

Genes influencing spinal bone mineral density in inbred F344, LEW, COP, and DA rats

scientific journal article

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Effects for Femoral Biomechanics, Structure, and Density in C57BL/6J and C3H/HeJ Inbred Mouse Strains ⬇️

artículo científico publicado el 1 de octubre de 2003

Genetic Influences on Plasma Homocysteine Levels in African Americans and Yoruba Nigerians

artículo científico publicado en 2015

Genetic Variants Associated with Circulating Fibroblast Growth Factor 23

Genetic analysis of quantitative phenotypes in AD and MCI: imaging, cognition and biomarkers

artículo científico publicado en 2014

Genetic and neurophysiological correlates of the age of onset of alcohol use disorders in adolescents and young adults

artículo científico publicado en 2013

Genetic anticipation and abnormal gender ratio at birth in familial primary pulmonary hypertension ⬇️

artículo científico publicado el 1 de julio de 1995

Genetic architecture of age-related cognitive decline in African Americans

scientific article published on 21 December 2016

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic influences on craving for alcohol

artículo científico publicado en 2012

Genetic loci affecting bone structure and strength in inbred COP and DA rats

artículo científico publicado en 2007

Genetic meta-analysis of diagnosed Alzheimer’s disease identifies new risk loci and implicates Aβ, tau, immunity and lipid processing

artículo científico publicado en 2019

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genetic research: who is at risk for alcoholism

scientific article published on January 2010

Genetic screening for a single common LRRK2 mutation in familial Parkinson's disease

artículo científico publicado en 2005

Genetic screening of a large series of North American sporadic and familial frontotemporal dementia cases

artículo científico publicado en 2020

Genetic strategies to detect genes involved in alcoholism and alcohol-related traits.

artículo científico publicado en 2002

Genetic studies of quantitative MCI and AD phenotypes in ADNI: Progress, opportunities, and plans

artículo científico publicado en 2015

Genetic variants associated with susceptibility to psychosis in late-onset Alzheimer's disease families

artículo científico publicado en 2015

Genetics and alcoholism

artículo científico publicado en 2013

Genetics and genomics of late-onset Alzheimer's disease and its endophenotypes

artículo científico publicado en 2011

Genetics of Parkinson disease

artículo científico publicado en 2004

Genetics of Parkinson disease

artículo científico publicado en 2007

Genetics of alcoholism

artículo científico publicado en 2014

Genetics of osteoporosis

scientific article published on 01 June 2002

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

artículo científico publicado en 2003

Genome scan of a second wave of NIMH genetics initiative bipolar pedigrees: chromosomes 2, 11, 13, 14, and X.

artículo científico publicado en 2003

Genome scan of the fifty-six bipolar pedigrees from the NIMH genetics initiative replication sample: chromosomes 4, 7, 9, 18, 19, 20, and 21.

artículo científico publicado en 2003

Genome screen for QTLs contributing to normal variation in bone mineral density and osteoporosis

artículo científico publicado en 2000

Genome screen for bone mineral density phenotypes in Fisher 344 and Lewis rat strains.

artículo científico publicado en 2005

Genome screen for quantitative trait loci underlying normal variation in femoral structure

artículo científico publicado en 2001

Genome screen in familial intracranial aneurysm

Genome screen to detect linkage to common susceptibility genes for intracranial and aortic aneurysms

artículo científico publicado en 2008

Genome screen to detect linkage to intracranial aneurysm susceptibility genes: the Familial Intracranial Aneurysm (FIA) study

artículo científico publicado en 2008

Genome screen to identify susceptibility genes for Parkinson disease in a sample without parkin mutations

artículo científico publicado en 2002

Genome sequencing analysis identifies new loci associated with Lewy body dementia and provides insights into its genetic architecture

artículo científico publicado en 2021

Genome-Wide Association Studies for Taxane-Induced Peripheral Neuropathy in ECOG-5103 and ECOG-1199.

artículo científico publicado en 2015

Genome-Wide Association Study for Anthracycline-Induced Congestive Heart Failure

artículo científico publicado en 2016

Genome-wide admixture mapping of DSM-IV alcohol dependence, criterion count, and the self-rating of the effects of ethanol in African American populations

scientific article published on 11 July 2020

Genome-wide analysis reveals novel genes influencing temporal lobe structure with relevance to neurodegeneration in Alzheimer's disease

artículo científico publicado en 2010

Genome-wide association analysis identifies new candidate risk loci for familial intracranial aneurysm in the French-Canadian population

artículo científico publicado en 2018

Genome-wide association and genetic functional studies identify autism susceptibility candidate 2 gene (AUTS2) in the regulation of alcohol consumption

scientific journal article

Genome-wide association of bipolar disorder suggests an enrichment of replicable associations in regions near genes

scientific journal article

Genome-wide association of familial late-onset Alzheimer's disease replicates BIN1 and CLU and nominates CUGBP2 in interaction with APOE

artículo científico publicado en 2011

Genome-wide association studies of alcohol dependence, DSM-IV criterion count and individual criteria

artículo científico publicado en 2019

Genome-wide association studies of the self-rating of effects of ethanol (SRE)

scientific article published on 03 July 2019

Genome-wide association study identifies 30 loci associated with bipolar disorder.

artículo científico publicado en 2019

Genome-wide association study identifies loci associated with liability to alcohol and drug dependence that is associated with variability in reward-related ventral striatum activity in African- and European-Americans

artículo científico publicado en 2019

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

artículo científico publicado en 2016

Genome-wide association study of 40,000 individuals identifies two novel loci associated with bipolar disorder

article

Genome-wide association study of alcohol dependence implicates a region on chromosome 11.

artículo científico publicado en 2010

Genome-wide association study of bone mineral density in premenopausal European-American women and replication in African-American women

artículo científico publicado en 2010

Genome-wide association study of intracranial aneurysms confirms role of Anril and SOX17 in disease risk

artículo científico publicado en 2012

Genome-wide association study of more than 40,000 bipolar disorder cases provides new insights into the underlying biology

artículo científico publicado en 2021

Genome-wide association study of serum iron phenotypes in premenopausal women of European descent

artículo científico publicado en 2015

Genome-wide association study of theta band event-related oscillations identifies serotonin receptor gene HTR7 influencing risk of alcohol dependence

artículo científico publicado en 2010

Genome-wide linkage analyses of non-Hispanic white families identify novel loci for familial late-onset Alzheimer's disease

artículo científico publicado en 2015

Genome-wide parametric linkage analyses of 644 bipolar pedigrees suggest susceptibility loci at chromosomes 16 and 20

artículo científico publicado en 2008

Genome-wide pathway analysis of memory impairment in the Alzheimer's Disease Neuroimaging Initiative (ADNI) cohort implicates gene candidates, canonical pathways, and networks

artículo científico publicado en 2012

Genome-wide scan and conditional analysis in bipolar disorder: evidence for genomic interaction in the National Institute of Mental Health genetics initiative bipolar pedigrees.

artículo científico publicado en 2003

Genome-wide scan for a healthy aging phenotype provides support for a locus near D4S1564 promoting healthy aging

scientific article published on 01 March 2004

Genome-wide search for genes affecting the risk for alcohol dependence

scientific article published on 01 May 1998

Genome-wide significant association between a 'negative mood delusions' dimension in bipolar disorder and genetic variation on chromosome 3q26.1.

artículo científico publicado en 2012

Genome-wide survival analysis of age at onset of alcohol dependence in extended high-risk COGA families

scientific journal article

Genome-wide transcriptome analysis identifies novel dysregulated genes implicated in Alzheimer's pathology

scientific article published on 05 August 2020

Genomewide SNP screen to detect quantitative trait loci for alcohol preference in the high alcohol preferring and low alcohol preferring mice

artículo científico publicado en 2008

Genomewide association study for onset age in Parkinson disease

artículo científico publicado en 2009

Genomewide association study for susceptibility genes contributing to familial Parkinson disease

artículo científico publicado en 2008

Genomewide linkage analyses of bipolar disorder: a new sample of 250 pedigrees from the National Institute of Mental Health Genetics Initiative.

artículo científico publicado en 2003

Genomewide linkage study of modifiers of LRRK2-related Parkinson's disease

artículo científico publicado en 2011

Genomic Copy Number Analysis in Alzheimer's Disease and Mild Cognitive Impairment: An ADNI Study

artículo científico publicado en 2011

Genomic Dissection of Bipolar Disorder and Schizophrenia, Including 28 Subphenotypes

article

Genomic expression analysis of rat chromosome 4 for skeletal traits at femoral neck

artículo científico publicado en 2008

Genomic survey of bipolar illness in the NIMH genetics initiative pedigrees: A preliminary report

article

Global and local ancestry in African-Americans: Implications for Alzheimer's disease risk

artículo científico publicado en 2015

Glutathione S-transferase 8-8 expression is lower in alcohol-preferring than in alcohol-nonpreferring rats

artículo científico publicado en 2004

Greater rupture risk for familial as compared to sporadic unruptured intracranial aneurysms

artículo científico publicado en 2009

Guidelines for the standardization of preanalytic variables for blood-based biomarker studies in Alzheimer's disease research

artículo científico publicado en 2015

Heritability of changes in bone size and bone mass with age in premenopausal white sisters

artículo científico publicado en 2006

Heritability of different forms of memory in the Late Onset Alzheimer's Disease Family Study

artículo científico publicado en 2011

Heterogeneity in hereditary pancreatitis

scientific article published on 01 April 1998

Heterogeneous stock rat: a unique animal model for mapping genes influencing bone fragility

artículo científico publicado en 2011

High-resolution genome screen for bone mineral density in heterogeneous stock rat.

artículo científico publicado en 2014

Human ALOX12, but Not ALOX15, Is Associated With BMD in White Men and Women

article

Identification of QTLs influencing alcohol preference in the High Alcohol Preferring (HAP) and Low Alcohol Preferring (LAP) mouse lines

artículo científico publicado en 2006

Identification of TMEM230 mutations in familial Parkinson's disease

scientific journal article

Identification of a linkage disequilibrium block in chromosome 1q associated with BMD in premenopausal white women

artículo científico publicado en 2008

Identification of a quantitative trait locus on rat chromosome 4 that is strongly linked to femoral neck structure and strength

artículo científico publicado en 2006

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Identification of genes for complex disease using longitudinal phenotypes

artículo científico publicado en 2003

Identification of pathways for bipolar disorder: a meta-analysis

artículo científico publicado en 2014

Immunohistochemical Method and Histopathology Judging for the Systemic Synuclein Sampling Study (S4)

Impact of Genetic Ancestry on Outcomes in ECOG-ACRIN-E5103

artículo científico publicado en 2017

Impact of genotyping errors on the type I error rate and the power of haplotype-based association methods

artículo científico publicado en 2009

Implementation of a shared data repository and common data dictionary for fetal alcohol spectrum disorders research

artículo científico publicado en 2009

In vivo distribution of α-synuclein in multiple tissues and biofluids in Parkinson disease

artículo científico publicado en 2020

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

artículo científico publicado en 2012

Individualized atrophy scores predict dementia onset in familial frontotemporal lobar degeneration

artículo científico publicado en 2020

Inflammatory profile in LRRK2-associated prodromal and clinical PD

artículo científico publicado en 2016

Influence of ADH1B polymorphism on alcohol use and its subjective effects in a Jewish population

artículo científico publicado en 2002

Influence of genetic variation on plasma protein levels in older adults using a multi-analyte panel

artículo científico publicado en 2013

Inheritance of susceptibility to root resorption associated with orthodontic force in mice

artículo científico publicado en 2008

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 1, 6, 8, 10, and 12.

artículo científico publicado en 1997

Initial genome scan of the NIMH genetics initiative bipolar pedigrees: chromosomes 4, 7, 9, 18, 19, 20, and 21q.

artículo científico publicado en 1997

Initial genome screen for bipolar disorder in the NIMH genetics initiative pedigrees: chromosomes 2, 11, 13, 14, and X.

artículo científico publicado en 1997

Initial genomic scan of the NIMH genetics initiative bipolar pedigrees: Chromosomes 3, 5, 15, 16, 17, and 22

article

Integration of bioinformatics and imaging informatics for identifying rare PSEN1 variants in Alzheimer's disease

artículo científico publicado en 2016

Is there a genetic relationship between alcoholism and depression?

artículo científico publicado en 2002

Knowledge gaps and research recommendations for essential tremor

artículo científico publicado en 2016

L1 coupling to ankyrin and the spectrin-actin cytoskeleton modulates ethanol inhibition of L1 adhesion and ethanol teratogenesis

artículo científico publicado en 2017

LRRK2: both a cause and a risk factor for Parkinson disease?

scientific article published on 01 September 2005

Lack of Association of Alcohol Dependence and Habitual Smoking With Catechol-O-methyltransferase

artículo científico publicado en 2007

Large-scale meta-analysis of genome-wide association data identifies six new risk loci for Parkinson's disease

artículo científico publicado en 2014

Leveraging genome-wide data to investigate differences between opioid use vs. opioid dependence in 41,176 individuals from the Psychiatric Genomics Consortium

artículo científico publicado en 2020

Linkage analyses in Caribbean Hispanic families identify novel loci associated with familial late-onset Alzheimer's disease

artículo científico publicado en 2015

Linkage and linkage disequilibrium of evoked EEG oscillations with CHRM2 receptor gene polymorphisms: implications for human brain dynamics and cognition

artículo científico publicado en 2004

Linkage disequilibrium between the beta frequency of the human EEG and a GABAA receptor gene locus

artículo científico publicado en 2002

Linkage for platelet monoamine oxidase (MAO) activity: results from a replication sample

artículo científico publicado en 2002

Linkage mapping of beta 2 EEG waves via non-parametric regression

artículo científico publicado en 2003

Linkage of a QTL contributing to normal variation in bone mineral density to chromosome 11q12-13.

artículo científico publicado en 1998

Linkage of an Alcoholism-Related Severity Phenotype to Chromosome 16

scholarly article by Tatiana Foroud et al published December 1998 in Alcoholism: Clinical and Experimental Research

Linkage of an alcoholism-related severity phenotype to chromosome 16

scientific article published on 01 December 1998

Linkage of structure at the proximal femur to chromosomes 3, 7, 8, and 19

scientific article published on 01 June 2003

Linkage of the Indiana kindred of Gerstmann-Sträussler-Scheinker disease to the prion protein gene

artículo científico publicado el 1 de abril de 1992

Linkage scan for quantitative traits identifies new regions of interest for substance dependence in the Collaborative Study on the Genetics of Alcoholism (COGA) sample

artículo científico publicado en 2007

Linkage screen for BMD phenotypes in male and female COP and DA rat strains

artículo científico publicado en 2008

Localization of the gene for familial primary pulmonary hypertension to chromosome 2q31–32

article

Loci on chromosomes 6q and 6p interact to increase susceptibility to bipolar affective disorder in the national institute of mental health genetics initiative pedigrees

artículo científico publicado en 2004

Longitudinal Measurements of Glucocerebrosidase activity in Parkinson's patients

artículo científico publicado en 2020

Longitudinal change of clinical and biological measures in early Parkinson's disease: Parkinson's progression markers initiative cohort.

artículo científico publicado en 2018

Longitudinal cognitive and motor changes among presymptomatic Huntington disease gene carriers

artículo científico publicado en 1999

Longitudinal personality changes among presymptomatic Huntington disease gene carriers.

artículo científico publicado en 2002

Marital status, alcohol dependence, and GABRA2: evidence for gene-environment correlation and interaction

artículo científico publicado en 2006

Maternal inheritance and mitochondrial DNA variants in familial Parkinson's disease

artículo científico publicado en 2010

Measurement invariance of DSM-IV alcohol, marijuana and cocaine dependence between community-sampled and clinically overselected studies

artículo científico publicado en 2013

Meta-Analyses of Externalizing Disorders: Genetics or Prenatal Alcohol Exposure?

artículo científico publicado en 2017

Meta-Analysis of Genetic Influences on Initial Alcohol Sensitivity

artículo científico publicado en 2018

Meta-analysis confirms CR1, CLU, and PICALM as alzheimer disease risk loci and reveals interactions with APOE genotypes

artículo científico publicado en 2010

Meta-analysis of Parkinson's disease: identification of a novel locus, RIT2.

artículo científico publicado en 2012

Meta-analysis of genome-wide scans provides evidence for sex- and site-specific regulation of bone mass

artículo científico publicado en 2007

Meta-analysis of genome-wide studies identifies WNT16 and ESR1 SNPs associated with bone mineral density in premenopausal women

artículo científico publicado en 2013

Meta-analysis of up to 622,409 individuals identifies 40 novel smoking behaviour associated genetic loci

artículo científico publicado en 2019

Michael J. Fox Foundation LRRK2 Consortium: geographical differences in returning genetic research data to study participants

artículo científico publicado en 2014

Motor changes in presymptomatic Huntington disease gene carriers

artículo científico publicado en 1996

Multi-omics integration analysis identifies novel genes for alcoholism with potential overlap with neurodegenerative diseases

artículo científico publicado en 2021

Multiple step pattern as a biomarker in Parkinson disease

artículo científico publicado en 2009

Mutations in DJ-1 are rare in familial Parkinson disease

artículo científico publicado en 2006

Mutations in LRRK2 other than G2019S are rare in a north american–based sample of familial Parkinson's disease

article

NIPT and Informed Consent: an Assessment of Patient Understanding of a Negative NIPT Result

artículo científico publicado en 2016

Neurology Individualized Medicine: When to Use Next-Generation Sequencing Panels

artículo científico publicado en 2017

Neuropeptide Y receptor genes are associated with alcohol dependence, alcohol withdrawal phenotypes, and cocaine dependence

artículo científico publicado en 2008

No association of the GABAA receptor genes on chromosome 5 with alcoholism in the collaborative study on the genetics of alcoholism sample.

artículo científico publicado en 2005

Nonlinear Z-score modeling for improved detection of cognitive abnormality

scientific article published on 05 December 2019

Nonparametric linkage and family-based association studies of a simulated complex disorder

scientific article published on 01 January 1999

Novel Alzheimer Disease Risk Loci and Pathways in African American Individuals Using the African Genome Resources Panel: A Meta-analysis ⬇️

artículo científico publicado en 2020

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

Novel late-onset Alzheimer disease loci variants associate with brain gene expression

artículo científico publicado en 2012

Novel recruitment strategy to enrich for LRRK2 mutation carriers

artículo científico publicado en 2015

Obesity, Diabetes, Coffee, Tea, and Cannabis Use Alter Risk for Alcohol-Related Cirrhosis in 2 Large Cohorts of High-Risk Drinkers

artículo científico publicado en 2020

Ondansetron blocks wild-type and p.F503L variant small-conductance Ca2+-activated K+ channels

scientific article published on 20 April 2018

Outcomes of genetic test disclosure and genetic counseling in a large Parkinson's disease research study

artículo científico publicado en 2020

PARK10 is a major locus for sporadic neuropathologically confirmed Parkinson disease

artículo científico publicado en 2015

PLXNA4 is associated with Alzheimer disease and modulates tau phosphorylation

artículo científico publicado en 2014

Parent-of-origin-specific allelic associations among 106 genomic loci for age at menarche

artículo científico publicado en 2014

Parkinson Disease Overview

artículo científico publicado en 2019

Parkinson's disease biomarkers: perspective from the NINDS Parkinson's Disease Biomarkers Program

artículo científico publicado en 2017

Pdgfra protects against ethanol-induced craniofacial defects in a zebrafish model of FASD.

scientific article published on August 2013

Peak bone mineral density at the hip is linked to chromosomes 14q and 15q

scientific article published on 16 March 2004

Penetrance estimate of LRRK2 p.G2019S mutation in individuals of non-Ashkenazi Jewish ancestry.

artículo científico publicado en 2017

Peroxisome proliferator-activated receptors α and γ are linked with alcohol consumption in mice and withdrawal and dependence in humans

artículo científico publicado en 2014

Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment

artículo científico publicado en 2014

Plasma Total-Tau and Neurofilament Light Chain as Diagnostic Biomarkers of Alzheimer's Disease Dementia and Mild Cognitive Impairment in Adults with Down Syndrome

artículo científico publicado en 2020

Polygenic Scores for Major Depressive Disorder and Risk of Alcohol Dependence

artículo científico publicado en 2017

Polygenic contributions to alcohol use and alcohol use disorders across population-based and clinically ascertained samples

scientific article published on 20 January 2020

Polygenic risk for externalizing disorders: Gene-by-development and gene-by-environment effects in adolescents and young adults

artículo científico publicado en 2015

Polygenic risk scores in familial Alzheimer disease

artículo científico publicado en 2017

Polymorphisms in the estrogen receptor beta (ESR2) gene are associated with bone mineral density in Caucasian men and women

artículo científico publicado en 2005

Pooled association genome scanning for alcohol dependence using 104,268 SNPs: validation and use to identify alcoholism vulnerability loci in unrelated individuals from the collaborative study on the genetics of alcoholism

artículo científico publicado en 2006

Possible localization of a major gene for cleft lip and palate to 4q

article

Predicting sensation seeking from dopamine genes. A candidate-system approach

artículo científico publicado en 2010

Predictive Accuracy of Serial Transvaginal Cervical Lengths and Quantitative Vaginal Fetal Fibronectin Levels for Spontaneous Preterm Birth Among Nulliparous Women

artículo científico publicado en 2017

Prenatal alcohol exposure: advancing knowledge through international collaborations

artículo científico publicado en 2003

Presence of an APOE4 allele results in significantly earlier onset of Parkinson's disease and a higher risk with dementia.

artículo científico publicado en 2006

Progression in prediagnostic Huntington disease

artículo científico publicado en 2009

Progression of symptoms in the early and middle stages of Huntington disease

artículo científico publicado en 2001

Protective variant for hippocampal atrophy identified by whole exome sequencing

artículo científico publicado en 2015

Proteomic profiles for Alzheimer's disease and mild cognitive impairment among adults with Down syndrome spanning serum and plasma: An Alzheimer's Biomarker Consortium-Down Syndrome (ABC-DS) study

artículo científico publicado en 2020

Psychosocial moderation of polygenic risk for cannabis involvement: the role of trauma exposure and frequency of religious service attendance

scientific article published on 21 October 2019

Quality of life and caregiver burden in familial frontotemporal lobar degeneration: Analyses of symptomatic and asymptomatic individuals within the LEFFTDS cohort

artículo científico publicado en 2020

Quantitative trait loci analysis of human event-related brain potentials: P3 voltage

artículo científico publicado en 1998

Quantitative trait locus for body weight identified on rat chromosome 4 in inbred alcohol-preferring and -nonpreferring rats: potential implications for neuropeptide Y and corticotrophin releasing hormone 2

artículo científico publicado en 2013

R1514Q substitution in Lrrk2 is not a pathogenic Parkinson's disease mutation

article

Racial Disparities in Adverse Pregnancy Outcomes and Psychosocial Stress

artículo científico publicado en 2018

Rare coding variants in PLCG2, ABI3, and TREM2 implicate microglial-mediated innate immunity in Alzheimer's disease

artículo científico publicado en 2017

Rare variants in APP, PSEN1 and PSEN2 increase risk for AD in late-onset Alzheimer's disease families

artículo científico publicado en 2012

Rarity of the Alzheimer disease-protective APP A673T variant in the United States

artículo científico publicado en 2015

Recent drinking history: association with family history of alcoholism and the acute response to alcohol during a 60 mg% clamp.

artículo científico publicado en 2002

Relation over time between facial measurements and cognitive outcomes in fetal alcohol-exposed children

artículo científico publicado en 2012

Reliability of reported age at onset for Parkinson's disease

artículo científico publicado en 2003

Replication of previous genome-wide association studies of bone mineral density in premenopausal American women

artículo científico publicado en 2010

Root resorption associated with orthodontic force in inbred mice: genetic contributions

artículo científico publicado en 2005

SIBLING family genes and bone mineral density: association and allele-specific expression in humans

artículo científico publicado en 2014

Saccades in presymptomatic and early stages of Huntington disease

artículo científico publicado en 2006

Saccadic eye movements are associated with a family history of alcoholism at baseline and after exposure to alcohol

artículo científico publicado en 2002

Screening for brain aneurysm in the Familial Intracranial Aneurysm study: frequency and predictors of lesion detection

artículo científico publicado en 2008

Serum iron levels and the risk of Parkinson disease: a Mendelian randomization study

artículo científico publicado en 2013

Sex-specific and non-sex-specific quantitative trait loci contribute to normal variation in bone mineral density in men

artículo científico publicado en 2005

Sex-specific genetic loci for femoral neck bone mass and strength identified in inbred COP and DA rats

artículo científico publicado en 2008

Sex-specific quantitative trait loci contribute to normal variation in bone structure at the proximal femur in men

artículo científico publicado en 2005

Shared Genetic Risk Factors of Intracranial, Abdominal, and Thoracic Aneurysms

artículo científico publicado en 2016

Shared genetic risk between eating disorder- and substance-use-related phenotypes: Evidence from genome-wide association studies

artículo científico publicado en 2020

Sibling pair linkage and association studies between bone mineral density and the insulin-like growth factor I gene locus

artículo científico publicado en 1999

Sibling pair linkage and association studies between peak bone mineral density and the gene locus for the osteoclast-specific subunit (OC116) of the vacuolar proton pump on chromosome 11p12-13

artículo científico publicado en 2002

Significant linkage of Parkinson disease to chromosome 2q36-37

artículo científico publicado en 2003

Specific psychiatric manifestations among preclinical Huntington disease mutation carriers

artículo científico publicado en 2007

Spheroid body myopathy revisited ⬇️

artículo científico publicado el 1 de septiembre de 1997

Standard linkage and association methods identify the mechanism of four susceptibility genes for a simulated complex disease

artículo científico publicado en 2005

Steroid Pathway Genes and Neonatal Respiratory Distress After Betamethasone Use in Anticipated Preterm Birth

artículo científico publicado en 2015

Stress-response pathways are altered in the hippocampus of chronic alcoholics

artículo científico publicado en 2013

Structures of α-synuclein filaments from human brains with Lewy pathology

artículo científico publicado en 2022

Subjective perceptions associated with the ascending and descending slopes of breath alcohol exposure vary with recent drinking history

artículo científico publicado en 2011

Suggestive evidence of a locus on chromosome 10p using the NIMH genetics initiative bipolar affective disorder pedigrees

article

Suggestive linkage on chromosome 1 for a quantitative alcohol-related phenotype

artículo científico publicado en 2002

TREM2 is associated with increased risk for Alzheimer's disease in African Americans

artículo científico publicado en 2015

Targeted neurogenesis pathway-based gene analysis identifies ADORA2A associated with hippocampal volume in mild cognitive impairment and Alzheimer's disease

artículo científico publicado en 2017

Telephone assessment of cognitive function in the late-onset Alzheimer's disease family study

artículo científico publicado en 2010

Ten-year rate of longitudinal change in neurocognitive and motor function in prediagnosis Huntington disease

artículo científico publicado en 2008

Test-retest reliability of saccadic measures in subjects at risk for Huntington disease

artículo científico publicado en 2009

Testing influences of APOE and BDNF genes and heart failure on cognitive function

scientific article published on 20 July 2020

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

artículo científico publicado en 2014

The Familial Intracranial Aneurysm (FIA) study protocol

artículo científico publicado en 2005

The Parkinson's progression markers initiative (PPMI) - establishing a PD biomarker cohort

scientific article published on 31 October 2018

The Promise and Pitfalls of Facebook Advertising: a Genetic Counselor's Perspective

artículo científico publicado en 2018

The Role of Cardiovascular Risk Factors and Stroke in Familial Alzheimer Disease

artículo científico publicado en 2016

The Systemic Synuclein Sampling Study: toward a biomarker for Parkinson's disease

artículo científico publicado en 2017

The association of polygenic risk for schizophrenia, bipolar disorder, and depression with neural connectivity in adolescents and young adults: examining developmental and sex differences

The effect of shared genetic and environmental factors on periodontal disease parameters in untreated adult siblings in Guatemala

artículo científico publicado en 2002

The genetics of absorptive hypercalciuria--a note of caution

artículo científico publicado en 2002

The genetics of alcoholism: identifying specific genes through family studies

artículo científico publicado en 2006

The genetics of dementia

artículo científico publicado en 2013

The longitudinal evaluation of familial frontotemporal dementia subjects protocol: Framework and methodology

scientific article published on 06 January 2020

The opioid system in alcohol and drug dependence: family-based association study

artículo científico publicado en 2007

The relationship between smoking and replicated sequence variants on chromosomes 8 and 9 with familial intracranial aneurysm

artículo científico publicado en 2010

The role of GABRA2 in risk for conduct disorder and alcohol and drug dependence across developmental stages

artículo científico publicado en 2006

The role of apolipoprotein E (APOE) genotype in early mild cognitive impairment (E-MCI).

artículo científico publicado en 2013

The search for genetic risk factors associated with suicidal behavior

artículo científico publicado en 2004

The tachykinin receptor 3 is associated with alcohol and cocaine dependence

artículo científico publicado en 2008

Thirty new loci for age at menarche identified by a meta-analysis of genome-wide association studies

artículo científico publicado en 2010

Tracking white matter degeneration in asymptomatic and symptomatic MAPT mutation carriers

artículo científico publicado en 2019

Trans-ancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

scholarly article published 10 March 2018

Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders

artículo científico publicado en 2018

Transethnic genome-wide scan identifies novel Alzheimer's disease loci

artículo científico publicado en 2017

Translation initiator EIF4G1 mutations in familial Parkinson disease

artículo científico publicado en 2011

Translational research on aging: clinical epidemiology as a bridge between the sciences

artículo científico publicado en 2014

Two novel loci, COBL and SLC10A2, for Alzheimer's disease in African Americans

artículo científico publicado en 2016

Two rare AKAP9 variants are associated with Alzheimer's disease in African Americans

artículo científico publicado en 2014

Understanding the effects of prenatal alcohol exposure using three-dimensional facial imaging

artículo científico publicado en 2011

Unique facial features distinguish fetal alcohol syndrome patients and controls in diverse ethnic populations

artículo científico publicado en 2007

Update on chromosomal locations for psychiatric disorders: report of the interim meeting of chromosome workshop chairpersons from the VIIth World Congress of Psychiatric Genetics, Monterey, California, October 14-18, 1999.

artículo científico publicado en 2000

Use of variable marker density, principal components, and neural networks in the dissection of disease etiology.

artículo científico publicado en 2001

Utility of the global CDR® plus NACC FTLD rating and development of scoring rules: Data from the ARTFL/LEFFTDS Consortium

scientific article published on 01 January 2020

Validation of Serum Neurofilament Light Chain as a Biomarker of Parkinson's Disease Progression

scientific article published on 15 August 2020

Variability in skeletal mass, structure, and biomechanical properties among inbred strains of rats

scientific article published on 01 August 2001

Variants associated with Gaucher disease in multiple system atrophy

artículo científico publicado en 2015

Variants in nicotinic receptors and risk for nicotine dependence

artículo científico publicado en 2008

Variants in the ATP-binding cassette transporter (ABCA7), apolipoprotein E ϵ4,and the risk of late-onset Alzheimer disease in African Americans

artículo científico publicado en 2013

Variants located upstream of CHRNB4 on chromosome 15q25.1 are associated with age at onset of daily smoking and habitual smoking

artículo científico publicado en 2012

Variations in GABRA2, encoding the alpha 2 subunit of the GABA(A) receptor, are associated with alcohol dependence and with brain oscillations

artículo científico publicado en 2004

Visual function in Huntington's disease patients and presymptomatic gene carriers

artículo científico publicado en 2003

Visual perception in prediagnostic and early stage Huntington's disease

scientific article published on May 2008

Visual scanning and cognitive performance in prediagnostic and early-stage Huntington's disease

artículo científico publicado en 2009

Voxelwise gene-wide association study (vGeneWAS): multivariate gene-based association testing in 731 elderly subjects

artículo científico publicado en 2011

Voxelwise genome-wide association study (vGWAS)

artículo científico publicado en 2010

Whole exome sequencing of intracranial aneurysm

artículo científico publicado en 2013

Whole genome association study of brain-wide imaging phenotypes for identifying quantitative trait loci in MCI and AD: A study of the ADNI cohort

artículo científico publicado en 2010

Whole-Exome Sequencing in Familial Parkinson Disease

artículo científico publicado en 2015

Whole-genome scan for linkage to bone strength and structure in inbred Fischer 344 and Lewis rats

artículo científico publicado en 2005

alpha-Synuclein maps to a quantitative trait locus for alcohol preference and is differentially expressed in alcohol-preferring and -nonpreferring rats

artículo científico publicado en 2003

regSNPs: a strategy for prioritizing regulatory single nucleotide substitutions

artículo científico publicado en 2012

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