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Lista de obras de Peter Holmans

A Two-Stage Genome Scan for Schizophrenia Susceptibility Genes in 196 Affected Sibling Pairs

article

A combined analysis of D22S278 marker alleles in affected sib-pairs: support for a susceptibility locus for schizophrenia at chromosome 22q12. Schizophrenia Collaborative Linkage Group (Chromosome 22).

artículo científico publicado en 1996

A comparison of four clustering methods for brain expression microarray data

artículo científico publicado en 2008

A contribution of novel CNVs to schizophrenia from a genome-wide study of 41,321 subjects

A family based association study of T102C polymorphism in 5HT2A and schizophrenia plus identification of new polymorphisms in the promoter.

artículo científico publicado en 1998

A flexible model for association analysis in sibships with missing genotype data

artículo científico publicado en 2011

A full genome scan for late onset Alzheimer's disease.

artículo científico publicado en 1999

A genome-wide screen for linkage in Nordic sib-pairs with multiple sclerosis

article

A genome-wide study shows a limited contribution of rare copy number variants to Alzheimer's disease risk

artículo científico publicado en 2012

A genomewide linkage study of age at onset in schizophrenia

article

A linkage study of chromosome 22q in sib-pairs with schizophrenia

A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia.

artículo científico publicado en 1998

A modifier of Huntington's disease onset at the MLH1 locus

artículo científico publicado en 2017

A novel Alzheimer disease locus located near the gene encoding tau protein.

artículo científico publicado en 2015

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

artículo científico publicado en 2012

A pathway-based analysis provides additional support for an immune-related genetic susceptibility to Parkinson's disease

artículo científico publicado en 2013

A polygenic resilience score moderates the genetic risk for schizophrenia

artículo científico publicado en 2019

A potential endophenotype for Alzheimer's disease: cerebrospinal fluid clusterin

artículo científico publicado en 2015

A scan of chromosome 10 identifies a novel locus showing strong association with late-onset Alzheimer disease

artículo científico publicado en 2005

A simple method for analyzing microsatellite allele image patterns generated from DNA pools and its application to allelic association studies

artículo científico publicado en 1998

A survey of genetic human cortical gene expression

article

A systematic genomewide linkage study in 353 sib pairs with schizophrenia

artículo científico publicado en 2003

A systematic screening to identify de novo mutations causing sporadic early-onset Parkinson's disease

artículo científico publicado en 2015

ACSL6 is associated with the number of cigarettes smoked and its expression is altered by chronic nicotine exposure

artículo científico publicado en 2011

Allowing for genotyping error in analysis of unmatched case-control studies.

artículo científico publicado en 2003

Alpha-2 macroglobulin gene and Alzheimer disease.

artículo científico publicado en 1999

Alpha-T-catenin is expressed in human brain and interacts with the Wnt signaling pathway but is not responsible for linkage to chromosome 10 in Alzheimer's disease

artículo científico publicado en 2004

An examination of single nucleotide polymorphism selection prioritization strategies for tests of gene-gene interaction

artículo científico publicado en 2011

Analysis of 10 independent samples provides evidence for association between schizophrenia and a SNP flanking fibroblast growth factor receptor 2.

artículo científico publicado en 2008

Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.

artículo científico publicado en 2015

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Analysis of shared heritability in common disorders of the brain

Association between a PS-1 intronic polymorphism and late onset Alzheimer's disease

scholarly article by P Kehoe et al published 2 September 1996 in NeuroReport

Association of ABCA1 with late-onset Alzheimer's disease is not observed in a case-control study.

artículo científico publicado en 2004

Association of Elevated Urinary miR-126, miR-155, and miR-29b with Diabetic Kidney Disease

Association of late-onset Alzheimer's disease with genetic variation in multiple members of the GAPD gene family

artículo científico publicado en 2004

Association of slow acetylator genotype for N-acetyltransferase 2 with familial Parkinson's disease

artículo científico publicado en 1997

Association of the angiotensin I converting enzyme gene deletion polymorphism with early onset of ESRF in PKD1 adult polycystic kidney disease

article

Association studies between risk for late-onset Alzheimer's disease and variants in insulin degrading enzyme.

artículo científico publicado en 2005

Association studies in psychiatric genetics

article

Association studies of bipolar disorder at the human serotonin transporter gene (hSERT; 5HTT).

artículo científico publicado en 1997

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

Autosome search for schizophrenia susceptibility genes in multiply affected families

article

Bayesian trio models for association in the presence of genotyping errors.

artículo científico publicado en 2004

Biological overlap of attention-deficit/hyperactivity disorder and autism spectrum disorder: evidence from copy number variants

artículo científico publicado en 2014

Bipolar affective puerperal psychosis: genome-wide significant evidence for linkage to chromosome 16.

artículo científico publicado en 2007

Brain Regions Showing White Matter Loss in Huntington's Disease Are Enriched for Synaptic and Metabolic Genes

artículo científico publicado en 2017

Brain gene expression correlates with changes in behavior in the R6/1 mouse model of Huntington's disease.

artículo científico

Case-Control Genome-Wide Association Study of Attention-Deficit/Hyperactivity Disorder ⬇️

artículo científico publicado el 5 de agosto de 2010

Cis- and trans- loci influence expression of the schizophrenia susceptibility gene DTNBP1.

artículo científico publicado en 2008

Clinical and cognitive characteristics of children with attention-deficit hyperactivity disorder, with and without copy number variants

artículo científico publicado en 2011

Collaborative genome-wide association analysis supports a role for ANK3 and CACNA1C in bipolar disorder

artículo científico publicado en 2008

Common alleles contribute to schizophrenia in CNV carriers.

artículo científico publicado en 2015

Common polygenic variation enhances risk prediction for Alzheimer's disease

artículo científico publicado en 2015

Common schizophrenia alleles are enriched in mutation-intolerant genes and maintained by background selection

article

Common variants at ABCA7, MS4A6A/MS4A4E, EPHA1, CD33 and CD2AP are associated with Alzheimer's disease

artículo científico publicado en 2011

Common variants on chromosome 6p22.1 are associated with schizophrenia

artículo científico publicado en 2009

Comparison of Methods for Combining Case-Control and Family-Based Association Studies

Conservation of regional gene expression in mouse and human brain

artículo científico publicado en 2007

Contribution of copy number variants to schizophrenia from a genome-wide study of 41,321 subjects

artículo científico publicado en 2016

Convergent evidence that oligodendrocyte lineage transcription factor 2 (OLIG2) and interacting genes influence susceptibility to schizophrenia

artículo científico publicado en 2006

Cooperative genome-wide analysis shows increased homozygosity in early onset Parkinson's disease

artículo científico publicado en 2012

Copy number variants in schizophrenia: confirmation of five previous findings and new evidence for 3q29 microdeletions and VIPR2 duplications

artículo científico publicado en 2011

Correction: ACSL6 Is Associated with the Number of Cigarettes Smoked and Its Expression Is Altered by Chronic Nicotine Exposure

artículo científico publicado en 2012

Correction: Genetic Evidence Implicates the Immune System and Cholesterol Metabolism in the Aetiology of Alzheimer's Disease.

artículo científico publicado en 2011

Covariate linkage analysis of GAW14 simulated data incorporating subclinical phenotype, sex, population, parent-of-origin, and interaction

artículo científico publicado en 2005

DNA repair pathways underlie a common genetic mechanism modulating onset in polyglutamine diseases

artículo científico publicado en 2016

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia.

artículo científico publicado en 2011

De novo CNVs in bipolar affective disorder and schizophrenia

artículo científico publicado en 2014

De novo mutations in schizophrenia implicate synaptic networks

artículo científico publicado en 2014

Design of Case-controls Studies with Unscreened Controls

article by V. Moskvina et al published September 2005 in Annals of Human Genetics

Detailed genotyping demonstrates association between the slow acetylator genotype for N-acetyltransferase 2 (NAT2) and familial Parkinson's disease

artículo científico publicado en 2000

Detecting Gene-Gene Interactions Using Affected Sib Pair Analysis with Covariates

article

Does APOE explain the linkage of Alzheimer's disease to chromosome 19q13?

artículo científico publicado en 2008

Dopa-responsive dystonia: A clinical and molecular genetic study

artículo científico publicado en 1998

Effect of Genotyping Error on Type-I Error Rate of Affected Sib Pair Studies with Genotyped Parents

scientific article published on 26 May 2005

Effects of differential genotyping error rate on the type I error probability of case-control studies

artículo científico

Effects of low birth weight, maternal smoking in pregnancy and social class on the phenotypic manifestation of Attention Deficit Hyperactivity Disorder and associated antisocial behaviour: investigation in a clinical sample

artículo científico publicado en 2007

Efficient strategies for genome scanning with affected sib pairs

artículo científico publicado en 1998

Erratum: A meta-analysis and transmission disequilibrium study of association between the dopamine D3 receptor gene and schizophrenia

article

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

scholarly article published in Nature Genetics

Erratum: Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

article

Erratum: Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC

scholarly article published in Molecular Psychiatry

Erratum: Stage 2 of the Wellcome Trust UK–Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16–q21, 4q12–q21, 9p21, 10p14–p12 and 18q22

article

Evaluation of an approximation method for assessment of overall significance of multiple-dependent tests in a genomewide association study

artículo científico publicado en 2011

Evidence for novel susceptibility genes for late-onset Alzheimer's disease from a genome-wide association study of putative functional variants

article

Evidence for rare and common genetic risk variants for schizophrenia at protein kinase C, alpha.

artículo científico publicado en 2009

Evidence that common variation in NEDD9 is associated with susceptibility to late-onset Alzheimer's and Parkinson's disease

artículo científico publicado en 2008

Examining pathways between genetic liability for schizophrenia and patterns of tobacco and cannabis use in adolescence

artículo científico publicado en 2020

Exome arrays capture polygenic rare variant contributions to schizophrenia.

artículo científico publicado en 2016

Expression profiling of Huntington's disease models suggests that brain-derived neurotrophic factor depletion plays a major role in striatal degeneration

artículo científico publicado en 2007

Factor derived sub-syndromes of schizophrenia and familial morbid risks

Factor-derived subsyndromes of schizophrenia and familial morbid risks

artículo científico publicado en 1997

Familial phenotype differences in PKD11.

artículo científico publicado en 1999

Fine mapping of ZNF804A and genome-wide significant evidence for its involvement in schizophrenia and bipolar disorder

artículo científico publicado en 2010

Full genome screen for Alzheimer disease: Stage II analysis

article

Functional gene group analysis identifies synaptic gene groups as risk factor for schizophrenia.

artículo científico publicado en 2011

Gender differences in CNV burden do not confound schizophrenia CNV associations.

artículo científico publicado en 2016

Gene ontology analysis of GWA study data sets provides insights into the biology of bipolar disorder

artículo científico publicado en 2009

Gene-based analysis in HRC imputed genome wide association data identifies three novel genes for Alzheimer's disease

scientific article published on 08 July 2019

Gene-wide analyses of genome-wide association data sets: evidence for multiple common risk alleles for schizophrenia and bipolar disorder and for overlap in genetic risk

artículo científico publicado en 2009

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

artículo científico publicado en 2014

Genetic association of the APP binding protein 2 gene (APBB2) with late onset Alzheimer disease

artículo científico publicado en 2005

Genetic control of human brain transcript expression in Alzheimer disease

artículo científico publicado en 2009

Genetic differences between five European populations

artículo científico

Genetic evidence implicates the immune system and cholesterol metabolism in the aetiology of Alzheimer's disease

artículo científico publicado en 2010

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 predictors of response to serotonergic and noradrenergic antidepressants in major depressive disorder: a genome-wide analysis of individual-level data and a meta-analysis

artículo científico publicado en 2012

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

artículo científico publicado en 2013

Genetic risk sum score comprised of common polygenic variation is associated with body mass index

artículo científico publicado en 2010

Genetic studies on chromosome 12 in late-onset Alzheimer disease.

artículo científico publicado en 1998

Genetic variability at the amyloid-beta precursor protein locus may contribute to the risk of late-onset Alzheimer's disease.

artículo científico publicado en 1999

Genetics of Recurrent Early-Onset Major Depression (GenRED): Final Genome Scan Report

article

Genetics of recurrent early-onset depression (GenRED): design and preliminary clinical characteristics of a repository sample for genetic linkage studies

artículo científico publicado en 2003

Genetics of recurrent early-onset major depression (GenRED): final genome scan report

artículo científico publicado en 2007

Genetics of recurrent early-onset major depression (GenRED): significant linkage on chromosome 15q25-q26 after fine mapping with single nucleotide polymorphism markers.

artículo científico publicado en 2007

Genome scan for association and linkage

Genome screen for loci influencing age at onset and rate of decline in late onset Alzheimer's disease.

artículo científico publicado en 2005

Genome wide significant linkage in schizophrenia conditioning on occurrence of depressive episodes

artículo científico publicado en 2005

Genome-wide analysis of copy number variants in attention deficit hyperactivity disorder: the role of rare variants and duplications at 15q13.3.

artículo científico publicado en 2012

Genome-wide analysis of over 106 000 individuals identifies 9 neuroticism-associated loci.

artículo científico publicado en 2016

Genome-wide association analysis identifies 13 new risk loci for schizophrenia

artículo científico publicado en 2013

Genome-wide association of mood-incongruent psychotic bipolar disorder

artículo científico publicado en 2012

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

artículo científico publicado en 2019

Genome-wide association study identifies variants at CLU and PICALM associated with Alzheimer's disease

artículo científico publicado en 2009

Genome-wide association study of 14,000 cases of seven common diseases and 3,000 shared controls

artículo científico publicado en 2007

Genome-wide association study of Alzheimer's disease with psychotic symptoms

artículo científico publicado en 2011

Genome-wide association study of borderline personality disorder reveals genetic overlap with bipolar disorder, major depression and schizophrenia

artículo científico

Genome-wide association study of clinical dimensions of schizophrenia: polygenic effect on disorganized symptoms ⬇️

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 multiplex schizophrenia pedigrees.

artículo científico publicado en 2012

Genome-wide association study of recurrent early-onset major depressive disorder

scientific journal article

Genome-wide linkage and follow-up association study of postpartum mood symptoms

artículo científico publicado en 2009

Genome-wide scan in 124 Indonesian sib-pair families with schizophrenia reveals genome-wide significant linkage to a locus on chromosome 3p26-21.

artículo científico publicado en 2008

Genome-wide scan of bipolar disorder in 65 pedigrees: supportive evidence for linkage at 8q24, 18q22, 4q32, 2p12, and 13q12

article

Genome-wide significant associations in schizophrenia to ITIH3/4, CACNA1C and SDCCAG8, and extensive replication of associations reported by the Schizophrenia PGC.

artículo científico publicado en 2012

Genomewide Linkage Scan in Schizoaffective Disorder

artículo científico publicado en 2005

Genomewide association analysis of symptoms of alcohol dependence in the molecular genetics of schizophrenia (MGS2) control sample

artículo científico publicado en 2011

Genomewide significant linkage to recurrent, early-onset major depressive disorder on chromosome 15q.

artículo científico publicado en 2004

Haplotype-based stratification of Huntington's disease

artículo científico publicado en 2017

High loading of polygenic risk for ADHD in children with comorbid aggression

artículo científico publicado en 2013

Identification of loci associated with schizophrenia by genome-wide association and follow-up

artículo científico publicado en 2008

Identification of risk loci with shared effects on five major psychiatric disorders: a genome-wide analysis

artículo científico publicado en 2013

Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations

artículo científico publicado en 2014

Increased familial risk and genomewide significant linkage for Alzheimer's disease with psychosis.

artículo científico publicado en 2007

Investigating the contribution of common genetic variants to the risk and pathogenesis of ADHD.

artículo científico publicado en 2012

Investigating the genetic architecture of general and specific psychopathology in adolescence

artículo científico publicado en 2018

Investigating the role of p11 (S100A10) sequence variation in susceptibility to major depression

artículo científico publicado en 2007

Likelihood-ratio affected sib-pair tests applied to multiply affected sibships: Issues of power and type I error rate

artículo científico publicado en 2001

Linkage analyses of rheumatoid arthritis and related quantitative phenotypes: the GAW15 experience

artículo científico publicado en 2007

Linkage disequilibrium mapping of a chromosome 15q25-26 major depression linkage region and sequencing of NTRK3.

artículo científico publicado en 2008

Linkage study of chromosome 6p in sib-pairs with schizophrenia.

artículo científico publicado en 1997

Meta-Analysis of Genome-Wide Association Studies of Attention-Deficit/Hyperactivity Disorder ⬇️

artículo científico publicado el 1 de agosto de 2010

Meta-analysis of 32 genome-wide linkage studies of schizophrenia.

artículo científico publicado en 2008

Meta-analysis of 74,046 individuals identifies 11 new susceptibility loci for Alzheimer's disease

artículo científico publicado en 2013

Meta-analysis of genetic association with diagnosed Alzheimer's disease identifies novel risk loci and implicates Abeta, Tau, immunity and lipid processing

Meta-analysis of genome-wide association data of bipolar disorder and major depressive disorder.

artículo científico publicado en 2010

Molecular genetic contribution to the developmental course of attention-deficit hyperactivity disorder.

artículo científico publicado en 2008

Mood-incongruent psychosis in bipolar disorder: conditional linkage analysis shows genome-wide suggestive linkage at 1q32.3, 7p13 and 20q13.31

article

Most genome-wide significant susceptibility loci for schizophrenia and bipolar disorder reported to date cross-traditional diagnostic boundaries

artículo científico publicado en 2010

Multicenter linkage study of schizophrenia candidate regions on chromosomes 5q, 6q, 10p, and 13q: schizophrenia linkage collaborative group III

artículo científico publicado en 2000

Multicenter linkage study of schizophrenia loci on chromosome 22q.

artículo científico publicado en 2004

Multiple sclerosis and the HLA-D region: linkage and association studies

artículo científico publicado en 1995

Multiple testing in the genomics era: findings from Genetic Analysis Workshop 15, Group 15.

scientific article published on January 2007

New data and an old puzzle: the negative association between schizophrenia and rheumatoid arthritis

artículo científico publicado en 2015

No association between the alpha-2 macroglobulin I1000V polymorphism and Alzheimer's disease.

artículo científico publicado en 1999

No evidence for rare recessive and compound heterozygous disruptive variants in schizophrenia

artículo científico publicado en 2014

No evidence that extended tracts of homozygosity are associated with Alzheimer's disease.

artículo científico publicado en 2011

No evidence that rare coding variants in ZNF804A confer risk of schizophrenia.

artículo científico publicado en 2010

No linkage between multiple sclerosis and the T cell receptor alpha chain locus

artículo científico publicado en 1994

No linkage or association between multiple sclerosis and the myelin basic protein gene in affected sibling pairs

artículo científico publicado en 1994

No major schizophrenia locus detected on chromosome 1q in a large multicenter sample

artículo científico publicado en 2002

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

artículo científico publicado en 2015

Novel loci for major depression identified by genome-wide association study of Sequenced Treatment Alternatives to Relieve Depression and meta-analysis of three studies

artículo científico publicado en 2011

O3-02-06 Linkage analysis of AD SIB pairs indicates evidence of interaction between genes regulating beta-amyloid degradation

article

P4-046 Association of late onset Alzheimer's disease with genetic variation in multiple members of a gene family involved in neuronal apoptosis

article

P4-070 Is APOE exclusively responsible for the AD linkage peak on chromosome 19?

P4-079 Is variation in the gene encoding insulin-degrading enzyme (IDE) a risk factor in late-onset Alzheimer's disease?

article

P4-110 A systematic scan of chromosome 10 single nucleotide polymorphisms identifies novel candidate genes showing strong association to Alzheimer's disease

article

P4-122 Genetic association of an APP binding protein gene with late onset Alzheimer's disease

article

Partial characterization and assignment of the gene for protoporphyrinogen oxidase and variegate porphyria to human chromosome 1q23.

artículo científico publicado en 1995

Pathogenic copy number variants and SCN1A mutations in patients with intellectual disability and childhood-onset epilepsy

artículo científico publicado en 2016

Pathway analyses implicate glial cells in schizophrenia

artículo científico publicado en 2014

Permutation-based approaches do not adequately allow for linkage disequilibrium in gene-wide multi-locus association analysis

artículo científico publicado en 2012

Phenotype evaluation and genomewide linkage study of clinical variables in schizophrenia.

artículo científico publicado en 2011

Phenotypic Manifestation of Genetic Risk for Schizophrenia During Adolescence in the General Population

artículo científico publicado en 2016

Polygenic dissection of diagnosis and clinical dimensions of bipolar disorder and schizophrenia

artículo científico publicado en 2013

Polygenic dissection of the bipolar phenotype

artículo científico publicado en 2011

Population-specific genetic modification of Huntington's disease in Venezuela.

artículo científico publicado en 2018

Promoting Measured Genes and Measured Environments: On the Importance of Careful Statistical Analyses and Biological Relevance—Reply

article

Psychiatric gene discoveries shape evidence on ADHD's biology

artículo científico publicado en 2015

RNA-Seq of Huntington's disease patient myeloid cells reveals innate transcriptional dysregulation associated with proinflammatory pathway activation.

artículo científico publicado en 2016

Rare chromosomal deletions and duplications in attention-deficit hyperactivity disorder: a genome-wide analysis

artículo científico publicado en 2010

Rare chromosomal deletions and duplications increase risk of schizophrenia

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Rare copy number variants: a point of rarity in genetic risk for bipolar disorder and schizophrenia

artículo científico publicado en 2010

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders.

artículo científico publicado en 2016

Regional and cellular gene expression changes in human Huntington's disease brain

artículo científico publicado en 2006

Replication of bipolar disorder susceptibility alleles and identification of two novel genome-wide significant associations in a new bipolar disorder case-control sample

scientific article published on 16 October 2012

Replication of brain function effects of a genome-wide supported psychiatric risk variant in the CACNA1C gene and new multi-locus effects

artículo científico publicado en 2014

Reply to Curtis

S2-01-04 Progress toward the identification of novel genetic risk factors for late onset Alzheimer's disease

scholarly article by Alison M. Goate et al published July 2004 in Neurobiology of Aging

Schizophrenia susceptibility alleles are enriched for alleles that affect gene expression in adult human brain ⬇️

artículo científico publicado el 22 de febrero de 2011

Scientific rigor and the art of motorcycle maintenance

article

Shared polygenic contribution between childhood attention-deficit hyperactivity disorder and adult schizophrenia

artículo científico publicado en 2013

Similar striatal gene expression profiles in the striatum of the YAC128 and HdhQ150 mouse models of Huntington's disease are not reflected in mutant Huntingtin inclusion prevalence

artículo científico publicado en 2015

Stage 2 of the Wellcome Trust UK-Irish bipolar affective disorder sibling-pair genome screen: evidence for linkage on chromosomes 6q16-q21, 4q12-q21, 9p21, 10p14-p12 and 18q22.

artículo científico publicado en 2005

Statistical methods for pathway analysis of genome-wide data for association with complex genetic traits

artículo científico publicado en 2010

Strong evidence that KIAA0319 on chromosome 6p is a susceptibility gene for developmental dyslexia

artículo científico publicado en 2005

Support for the involvement of large copy number variants in the pathogenesis of schizophrenia

artículo científico publicado en 2009

Susceptibility locus for Alzheimer's disease on chromosome 10.

artículo científico publicado en 2000

Susceptibility to multiple sclerosis and the immunoglobulin heavy chain variable region

scientific article published on 01 October 1995

Testing for gene x environment interaction effects in attention deficit hyperactivity disorder and associated antisocial behavior.

artículo científico publicado en 2008

The Genetic Modifiers of Motor OnsetAge (GeM MOA) Website: Genome-wide Association Analysis for Genetic Modifiers of Huntington's Disease

artículo científico publicado en 2015

The HTT CAG-Expansion Mutation Determines Age at Death but Not Disease Duration in Huntington Disease

artículo científico publicado en 2016

The Wellcome trust UK–Irish bipolar affective disorder sibling-pair genome screen: first stage report

article by P Bennett et al published February 2002 in Molecular Psychiatry

The bipolar disorder risk allele at CACNA1C also confers risk of recurrent major depression and of schizophrenia

artículo científico publicado en 2010

The effect of linkage disequilibrium on linkage analysis of incomplete pedigrees

artículo científico publicado en 2005

The role of variation at AβPP, PSEN1, PSEN2, and MAPT in late onset Alzheimer's disease

artículo científico publicado en 2012

Ubiquilin 1 polymorphisms are not associated with late-onset Alzheimer's disease.

artículo científico publicado en 2006

Updated results of the United Kingdom linkage-based genome screen in multiple sclerosis

artículo científico publicado en 2003

Use of phenotypic covariates in association analysis by sequential addition of cases

artículo científico publicado en 2006

Using genome-wide complex trait analysis to quantify 'missing heritability' in Parkinson's disease

artículo científico publicado en 2012

Using genome-wide complex trait analysis to quantify ‘missing heritability’ in Parkinson's disease

artículo científico publicado en 2013

Variation at the GABAA receptor gene, Rho 1 (GABRR1) associated with susceptibility to bipolar schizoaffective disorder

artículo científico publicado en 2010

Variation in DCP1, encoding ACE, is associated with susceptibility to Alzheimer disease

article

Variation in the urokinase-plasminogen activator gene does not explain the chromosome 10 linkage signal for late onset AD.

artículo científico publicado en 2004

Vitreoretinopathy with phalangeal epiphyseal dysplasia, a type II collagenopathy resulting from a novel mutation in the C-propeptide region of the molecule.

artículo científico publicado en 2002

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