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A Strategy for Discovery of Endocrine Interactions with Application to Whole-Body Metabolism

artículo científico publicado en 2018

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

A gene(s) for all-trans-retinoic acid-induced forelimb defects mapped and confirmed to murine chromosome 11

artículo científico publicado en 2005

A genome scan for familial combined hyperlipidemia reveals evidence of linkage with a locus on chromosome 11.

artículo científico publicado en 1999

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

A genomewide scan for attention-deficit/hyperactivity disorder in an extended sample: suggestive linkage on 17p11

artículo científico publicado en 2003

A genomewide screen of 345 families for autism-susceptibility loci

artículo científico publicado en 2003

A large replication study and meta-analysis in European samples provides further support for association of AHI1 markers with schizophrenia

artículo científico publicado en 2010

A non-human primate system for large-scale genetic studies of complex traits

artículo científico publicado en 2012

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

artículo científico publicado en 2011

A quantitative trait locus analysis of social responsiveness in multiplex autism families

artículo científico publicado en 2007

A quantitative trait locus for variation in dopamine metabolism mapped in a primate model using reference sequences from related species

artículo científico publicado en 2007

A susceptibility locus for migraine with aura, on chromosome 4q24.

scientific article published on 08 February 2002

ASD restricted and repetitive behaviors associated at 17q21.33: genes prioritized by expression in fetal brains

artículo científico publicado en 2017

Adipose co-expression networks across Finns and Mexicans identify novel triglyceride-associated genes

artículo científico publicado en 2012

Allowing for sex differences increases power in a GWAS of multiplex Autism families ⬇️

artículo científico publicado el 14 de diciembre de 2010

Amerindian-specific regions under positive selection harbour new lipid variants in Latinos

artículo científico publicado en 2014

Analysis of allele-specific expression in mouse liver by RNA-Seq: a comparison with Cis-eQTL identified using genetic linkage

artículo científico publicado en 2013

Analysis of shared heritability in common disorders of the brain

artículo científico publicado en 2018

Anatomic brain asymmetry in vervet monkeys

artículo científico publicado en 2011

Applications of machine learning and data mining methods to detect associations of rare and common variants with complex traits

artículo científico publicado en 2014

Association analysis of the R620W polymorphism of protein tyrosine phosphatase PTPN22 in systemic lupus erythematosus families: increased T allele frequency in systemic lupus erythematosus patients with autoimmune thyroid disease

artículo científico publicado en 2005

Association between genetic variation in a region on chromosome 11 and schizophrenia in large samples from Europe

artículo científico publicado en 2011

Association between serum amyloid A proteins and coronary artery disease: evidence from two distinct arteriosclerotic processes

artículo científico publicado en 1997

Association of GSK3B with Alzheimer disease and frontotemporal dementia

artículo científico publicado en 2008

Association of IRF5 polymorphisms with activation of the interferon alpha pathway

artículo científico publicado en 2009

Association of a common complement receptor 2 haplotype with increased risk of systemic lupus erythematosus

artículo científico publicado en 2007

Association of common variants in the Joubert syndrome gene (AHI1) with autism

artículo científico publicado en 2008

Association of genetic variants in complement factor H and factor H-related genes with systemic lupus erythematosus susceptibility

artículo científico publicado en 2011

Association of plasma lipids and apolipoproteins with the insulin response element in the apoC-III promoter region in familial combined hyperlipidemia

artículo científico publicado en 1999

Association of stearoyl-CoA desaturase 1 activity with familial combined hyperlipidemia

artículo científico publicado en 2008

Association of the APOLIPOPROTEIN A1/C3/A4/A5 gene cluster with triglyceride levels and LDL particle size in familial combined hyperlipidemia

artículo científico publicado en 2004

Association of the cannabinoid receptor gene (CNR1) with ADHD and post-traumatic stress disorder

scientific article published on December 2008

Association testing in a linked region using large pedigrees

artículo científico publicado en 2005

Attention deficit hyperactivity disorder: fine mapping supports linkage to 5p13, 6q12, 16p13, and 17p11.

artículo científico publicado en 2004

Author Correction: Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS

artículo científico publicado en 2018

Biochemical and Genetic Association of Plasma Apolipoprotein A-II Levels With Familial Combined Hyperlipidemia ⬇️

artículo científico publicado el 8 de mayo de 2003

Brain structure-function associations in multi-generational families genetically enriched for bipolar disorder.

artículo científico publicado en 2015

Characterization of Expression Quantitative Trait Loci in Pedigrees from Colombia and Costa Rica Ascertained for Bipolar Disorder

artículo científico publicado en 2016

Co-regulation and multilocus determinants of gene expression in humans

artículo científico publicado en 2007

Combined analysis of genome scans of dutch and finnish families reveals a susceptibility locus for high-density lipoprotein cholesterol on chromosome 16q

artículo científico publicado en 2003

Common genetic variants on 5p14.1 associate with autism spectrum disorders

artículo científico publicado en 2009

Common variants conferring risk of schizophrenia

artículo científico publicado en 2009

Complex genetic contribution of the Apo AI-CIII-AIV gene cluster to familial combined hyperlipidemia. Identification of different susceptibility haplotypes

artículo científico publicado en 1997

Contribution of common and rare variants to bipolar disorder susceptibility in extended pedigrees from population isolates

artículo científico publicado en 2020

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

artículo científico publicado en 2016

Contribution of the hepatic lipase gene to the atherogenic lipoprotein phenotype in familial combined hyperlipidemia

artículo científico publicado en 2000

Cross-species analyses implicate Lipin 1 involvement in human glucose metabolism

artículo científico publicado en 2005

DMD genotype correlations from the Duchenne Registry: Endogenous exon skipping is a factor in prolonged ambulation for individuals with a defined mutation subtype

artículo científico publicado en 2018

Decreased SMG7 expression associates with lupus-risk variants and elevated antinuclear antibody production

artículo científico publicado en 2016

Detecting rare variant associations: methods for testing haplotypes and multiallelic genotypes ⬇️

artículo científico publicado el 1 de enero de 2011

Detecting responses to treatment with fenofibrate in pedigrees

article

Diet, gonadal sex, and sex chromosome complement influence white adipose tissue miRNA expression

artículo científico publicado en 2017

Diet1, bile acid diarrhea, and FGF15/19: mouse model and human genetic variants

artículo científico publicado en 2018

Effect of arsenite, maternal age, and embryonic sex on spina bifida, exencephaly, and resorption rates in the splotch mouse

artículo científico publicado en 2003

Evidence for Genetic Overlap Between Schizophrenia and Age at First Birth in Women

artículo científico publicado en 2016

Evidence for a Language Quantitative Trait Locus on Chromosome 7q in Multiplex Autism Families ⬇️

artículo científico publicado el 6 de diciembre de 2001

Evidence for linkage of a candidate chromosome 1 region to human systemic lupus erythematosus

scientific article published on February 1997

Evidence for linkage of a tandem duplication polymorphism upstream of the dopamine D4 receptor gene (DRD4) with attention deficit hyperactivity disorder (ADHD).

artículo científico publicado en 2000

Evidence for sex-specific risk alleles in autism spectrum disorder

artículo científico publicado en 2004

Evidence that Smith-McCort dysplasia and Dyggve-Melchior-Clausen dysplasia are allelic disorders that result from mutations in a gene on chromosome 18q12

artículo científico publicado en 2002

Exfoliation syndrome: prevalence and inheritance in a subisolate of the Finnish population

artículo científico publicado en 2007

Expanding the range of ZNF804A variants conferring risk of psychosis

artículo científico publicado en 2010

Familial aggregation of hyperemesis gravidarum

artículo científico publicado en 2010

Familial combined hyperlipidemia in Mexicans: association with upstream transcription factor 1 and linkage on chromosome 16q24.1.

artículo científico publicado en 2005

Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1).

artículo científico publicado en 2004

Familiality and co-occurrence of clinical features of systemic lupus erythematosus

artículo científico publicado en 2002

Families with Familial Combined Hyperlipidemia and Families Enriched for Coronary Artery Disease Share Genetic Determinants for the Atherogenic Lipoprotein Phenotype ⬇️

artículo científico publicado el 1 de agosto de 1998

Family-specific aggregation of lipid GWAS variants confers the susceptibility to familial hypercholesterolemia in a large Austrian family

artículo científico publicado en 2017

Fine mapping of Xq28: both MECP2 and IRAK1 contribute to risk for systemic lupus erythematosus in multiple ancestral groups

artículo científico publicado en 2012

Functional impact of global rare copy number variation in autism spectrum disorders

artículo científico publicado en 2010

GAW20: methods and strategies for the new frontiers of epigenetics and pharmacogenomics

GWA study data mining and independent replication identify cardiomyopathy-associated 5 (CMYA5) as a risk gene for schizophrenia

artículo científico publicado en 2010

Gene expression in large pedigrees: analytic approaches

artículo científico publicado en 2016

Genetic Analysis Workshop 18: Methods and strategies for analyzing human sequence and phenotype data in members of extended pedigrees

artículo científico publicado en 2014

Genetic Analysis Workshop 19: methods and strategies for analyzing human sequence and gene expression data in extended families and unrelated individuals

artículo científico publicado en 2016

Genetic Deficiency of Flavin-Containing Monooxygenase 3 ( Fmo3) Protects Against Thrombosis but Has Only a Minor Effect on Plasma Lipid Levels-Brief Report

scientific article published on 01 June 2019

Genetic analysis of activity, brain and behavioral associations in extended families with heavy genetic loading for bipolar disorder

artículo científico publicado en 2019

Genetic and hormonal control of hepatic steatosis in female and male mice

artículo científico publicado en 2016

Genetic complexity at expression quantitative trait loci

artículo científico publicado en 2016

Genetic contributions to circadian activity rhythm and sleep pattern phenotypes in pedigrees segregating for severe bipolar disorder

artículo científico publicado en 2015

Genetic influences contributing to LDL particle size in familial combined hyperlipidaemia

artículo científico publicado en 2002

Genetic linkage of attention-deficit/hyperactivity disorder on chromosome 16p13, in a region implicated in autism

artículo científico publicado en 2002

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

artículo científico publicado en 2013

Genetic variation and gene expression across multiple tissues and developmental stages in a non-human primate

article

Genetic variation and gene expression across multiple tissues and developmental stages in a nonhuman primate

artículo científico publicado en 2017

Genome Scan for Blood Pressure in Dutch Dyslipidemic Families Reveals Linkage to a Locus on Chromosome 4p ⬇️

artículo científico publicado el 1 de octubre de 2001

Genome scan for adiposity in Dutch dyslipidemic families reveals novel quantitative trait loci for leptin, body mass index and soluble tumor necrosis factor receptor superfamily 1A

artículo científico publicado en 2000

Genome scans provide evidence for low-HDL-C loci on chromosomes 8q23, 16q24.1-24.2, and 20q13.11 in Finnish families

artículo científico publicado en 2002

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

artículo científico publicado en 2009

Genome-wide association analysis identifies 27 novel loci associated with uterine leiomyomata revealing common genetic origins with endometriosis

Genome-wide association and epidemiological analyses reveal common genetic origins between uterine leiomyomata and endometriosis

artículo científico publicado en 2019

Genome-wide association study of NMDA receptor coagonists in human cerebrospinal fluid and plasma

artículo científico publicado en 2015

Genome-wide association study of intelligence: additive effects of novel brain expressed genes

artículo científico publicado en 2012

Genome-wide association study of monoamine metabolite levels in human cerebrospinal fluid.

artículo científico publicado en 2013

Genome-wide burden of deleterious coding variants increased in schizophrenia

artículo científico publicado en 2015

Genome-wide linkage and association analyses implicate FASN in predisposition to Uterine Leiomyomata

artículo científico publicado en 2012

Genome-wide mapping of brain phenotypes in extended pedigrees with strong genetic loading for bipolar disorder

scientific article published on 30 June 2020

Genomic study in Mexicans identifies a new locus for triglycerides and refines European lipid loci

artículo científico publicado en 2013

HLA haplotype sharing and proband genotype in IDDM

scientific article published on 01 January 1986

Haplotype co-segregation with attention deficit-hyperactivity disorder in unrelated german multi-generation families

article

Heritability and genetic loci of fatty liver in familial combined hyperlipidemia

artículo científico publicado en 2006

Heritability of nonalcoholic fatty liver disease

artículo científico publicado en 2009

High density SNP association study of a major autism linkage region on chromosome 17.

artículo científico publicado en 2007

Identification of TNFRSF1B as a novel modifier gene in familial combined hyperlipidemia

scientific article published on 01 September 2000

Identification of common variants associated with human hippocampal and intracranial volumes

artículo científico publicado en 2012

Identification of two common variants contributing to serum apolipoprotein B levels in Mexicans

artículo científico publicado en 2009

Identifying fenofibrate responsive CpG sites

article published in 2018

Identifying heritable brain phenotypes in an extended pedigree of vervet monkeys

artículo científico publicado en 2009

Identifying rare variants from exome scans: the GAW17 experience

artículo científico publicado en 2011

Identifying rare-variant associations in parent-child trios using a Gaussian support vector machine

artículo científico publicado en 2014

Impact of Individual Traits, Saturated Fat, and Protein Source on the Gut Microbiome

scientific article published in 2018

Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal article

Insights into Autism Spectrum Disorder Genomic Architecture and Biology from 71 Risk Loci

artículo científico publicado en 2015

Integration of human adipocyte chromosomal interactions with adipose gene expression prioritizes obesity-related genes from GWAS.

artículo científico publicado en 2018

Interaction Testing and Polygenic Risk Scoring to Estimate the Association of Common Genetic Variants With Treatment Resistance in Schizophrenia

artículo científico publicado en 2022

Interactive effects of cadmium and all-trans-retinoic acid on the induction of forelimb ectrodactyly in C57BL/6 mice

artículo científico publicado en 2006

Intracellular adhesion molecule Gly241Arg polymorphism has no impact on ARDS or septic shock in community-acquired pneumonia

artículo científico publicado en 2002

Investigation of variants identified in caucasian genome-wide association studies for plasma high-density lipoprotein cholesterol and triglycerides levels in Mexican dyslipidemic study samples

artículo científico publicado en 2010

Linkage analysis in a Dutch population isolate shows no major gene for left-handedness or atypical language lateralization

artículo científico publicado en 2015

Linkage and interaction of loci on 1q23 and 16q12 may contribute to susceptibility to systemic lupus erythematosus.

artículo científico publicado en 2002

Linkage of a candidate gene locus to familial combined hyperlipidemia: lecithin:cholesterol acyltransferase on 16q.

artículo científico publicado en 1999

Linkage, association, and gene-expression analyses identify CNTNAP2 as an autism-susceptibility gene

artículo científico publicado en 2008

Locus for elevated apolipoprotein B levels on chromosome 1p31 in families with familial combined hyperlipidemia

artículo científico publicado en 2002

Longitudinal differences in familial combined hyperlipidemia quantitative trait loci

artículo científico publicado en 2006

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

artículo científico publicado en 2007

Meta-analysis of genome-wide linkage studies of systemic lupus erythematosus

artículo científico publicado en 2006

MicroRNA-3148 modulates allelic expression of toll-like receptor 7 variant associated with systemic lupus erythematosus

artículo científico publicado en 2013

MicroRNA-3148 modulates differential gene expression of the SLE-associated TLR7 variant.

artículo científico publicado en 2012

Mitochondrial dysfunction, oxidative stress, and apoptosis revealed by proteomic and transcriptomic analyses of the striata in two mouse models of Parkinson's disease

artículo científico publicado en 2008

Model-Based Linkage Analysis of a Binary Trait

artículo científico publicado en 2017

Model-based linkage analysis of a binary trait

artículo científico publicado en 2012

Molecular genetics of autism

scientific article published on April 2009

Multilocus genetic determinants of LDL particle size in coronary artery disease families

artículo científico publicado en 1996

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

artículo científico publicado en 2011

Multisystem component phenotypes of bipolar disorder for genetic investigations of extended pedigrees.

artículo científico publicado en 2014

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

artículo científico publicado en 2015

New genetic variants in the apoA-I and apoC-III genes and familial combined hyperlipidemia

artículo científico publicado en 2001

Obesity and obesogenic growth are both highly heritable and modified by diet in a nonhuman primate model, the African green monkey (Chlorocebus aethiops sabaeus).

artículo científico publicado en 2017

Offering to share: how to put heads together in autism neuroimaging

artículo científico publicado en 2008

Online self-report data for duchenne muscular dystrophy confirms natural history and can be used to assess for therapeutic benefits

scientific article (publication date: 17 October 2014)

PARP alleles within the linked chromosomal region are associated with systemic lupus erythematosus

artículo científico publicado en 1999

Palmar hyperhidrosis: evidence of genetic transmission

artículo científico publicado en 2002

Partial duplication at AZFc on the Y chromosome is a risk factor for impaired spermatogenesis in Han Chinese in Taiwan

artículo científico publicado en 2007

Phenotypic manifestations of MECP2 mutations in classical and atypical Rett syndrome

artículo científico publicado en 2004

Phosphodiesterase genes are associated with susceptibility to major depression and antidepressant treatment response

artículo científico publicado en 2006

Pooled genome-wide linkage data on 424 ADHD ASPs suggests genetic heterogeneity and a common risk locus at 5p13

scientific article published on 01 January 2006

Prediction of serotonin transporter promoter polymorphism genotypes from single nucleotide polymorphism arrays using machine learning methods ⬇️

artículo científico publicado el 1 de agosto de 2012

Preferential binding to Elk-1 by SLE-associated IL10 risk allele upregulates IL10 expression

artículo científico publicado en 2013

Prioritizing GWAS results: A review of statistical methods and recommendations for their application

artículo científico publicado en 2010

Proceedings of the Genetic Analysis Workshop 13: analysis of longitudinal family data for complex diseases and related risk factors. November 11-14, 2002. New Orleans, Louisiana, USA

article

QTL replication and targeted association highlight the nerve growth factor gene for nonverbal communication deficits in autism spectrum disorders ⬇️

artículo científico publicado el 22 de noviembre de 2011

Quantitative trait loci for apolipoprotein B, cholesterol, and triglycerides in familial combined hyperlipidemia pedigrees

artículo científico publicado en 2004

Rare Inherited and De Novo CNVs Reveal Complex Contributions to ASD Risk in Multiplex Families

artículo científico publicado en 2016

Replication of autism linkage: fine-mapping peak at 17q21.

artículo científico publicado en 2005

Replication of linkage at chromosome 20p13 and identification of suggestive sex-differential risk loci for autism spectrum disorder

scientific article published on 17 February 2014

Repurposing Dantrolene for Long-Term Combination Therapy to Potentiate Antisense-Mediated DMD Exon Skipping in the mdx Mouse.

artículo científico publicado en 2018

Sample-size considerations and strategies for linkage analysis in autosomal recessive disorders.

artículo científico publicado en 1986

Schizophrenia: genome, interrupted

artículo científico publicado en 2008

Search for autism loci by combined analysis of Autism Genetic Resource Exchange and Finnish families

artículo científico publicado en 2006

Seasonal variation of serotonin turnover in human cerebrospinal fluid, depressive symptoms and the role of the 5-HTTLPR

artículo científico publicado en 2013

Sequencing strategies and characterization of 721 vervet monkey genomes for future genetic analyses of medically relevant traits

artículo científico publicado en 2015

Serum C3 but not plasma acylation-stimulating protein is elevated in Finnish patients with familial combined hyperlipidemia

scientific article published on 01 May 2001

Sex-specific association of X-linked Toll-like receptor 7 (TLR7) with male systemic lupus erythematosus

artículo científico publicado en 2010

Social responsiveness, an autism endophenotype: genomewide significant linkage to two regions on chromosome 8

artículo científico publicado en 2014

Stratification based on language-related endophenotypes in autism: attempt to replicate reported linkage

artículo científico publicado en 2006

Support for calcium channel gene defects in autism spectrum disorders

artículo científico publicado en 2012

Systemic lupus erythematosus genome scan: support for linkage at 1q23, 2q33, 16q12-13, and 17q21-23 and novel evidence at 3p24, 10q23-24, 13q32, and 18q22-23.

artículo científico publicado en 2004

Systems biology of the vervet monkey

artículo científico publicado en 2013

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

artículo científico publicado en 2014

The Genetic Architecture of Carbon Tetrachloride-Induced Liver Fibrosis in Mice

scientific article published on 28 August 2020

The SLC6A14 gene shows evidence of association with obesity

artículo científico publicado en 2003

The Tay-Sachs disease gene in North American Jewish populations: geographic variations and origin

artículo científico publicado en 1983

The apoAI-CIII-AIV gene cluster

artículo científico publicado en 2001

The brain-derived neurotrophic factor rs6265 (Val66Met) polymorphism and depression in Mexican-Americans

artículo científico publicado en 2007

The genetic basis of systemic lupus erythematosus.

artículo científico publicado en 1998

Toward localizing genes underlying cerebral asymmetry and mental health

artículo científico publicado en 2005

Transcriptome analysis in whole blood reveals increased microbial diversity in schizophrenia.

artículo científico publicado en 2018

Transcriptomic analysis of autistic brain reveals convergent molecular pathology

artículo científico publicado en 2011

Tumor Necrosis Factor Gene Polymorphisms and the Variable Presentation and Outcome of Community-Acquired Pneumonia

article

Tumor necrosis factor gene polymorphisms and the variable presentation and outcome of community-acquired pneumonia

artículo científico publicado en 2002

Two newly identified SNPs in the APO AI‐CIII intergenic region are strongly associated with familial combined hyperlipidaemia ⬇️

artículo científico publicado el 1 de octubre de 2001

Ulcerative dermatitis in C57BL/6 mice exhibits an oxidative stress response consistent with normal wound healing ⬇️

artículo científico publicado el 1 de junio de 2012

WW-domain-containing oxidoreductase is associated with low plasma HDL-C levels

artículo científico publicado en 2008

Weighted variance FBAT: a powerful method for including covariates in FBAT analyses

artículo científico publicado en 2007

Whole blood transcriptome analysis in bipolar disorder reveals strong lithium effect

Whole blood transcriptome analysis in bipolar disorder reveals strong lithium effect

artículo científico publicado en 2019

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