Partitioning the Heritability of Tourette Syndrome and Obsessive Compulsive Disorder Reveals Differences in Genetic Architecture

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

(2013) S Hong Lee et al.   NATURE GENETICS

Genetic Risk Factors for Type 2 Diabetes: A Trans-Regulatory Genetic Architecture?

(2012) Steven C. Elbein et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Estimation of pleiotropy between complex diseases using single-nucleotide polymorphism-derived genomic relationships and restricted maximum likelihood

(2012) S.H. Lee et al.   BIOINFORMATICS

Brain Corticostriatal Systems and the Major Clinical Symptom Dimensions of Obsessive-Compulsive Disorder

(2012) Ben J. Harrison et al.   BIOLOGICAL PSYCHIATRY

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

(2012) M. F. Keller et al.   HUMAN MOLECULAR GENETICS

Estimation and partitioning of polygenic variation captured by common SNPs for Alzheimer's disease, multiple sclerosis and endometriosis

(2012) S. H. Lee et al.   HUMAN MOLECULAR GENETICS

Genome-wide association study of obsessive-compulsive disorder

(2012) S E Stewart et al.   MOLECULAR PSYCHIATRY

Genome-wide association study of Tourette's syndrome

(2012) J M Scharf et al.   MOLECULAR PSYCHIATRY

Enrichment of cis-regulatory gene expression SNPs and methylation quantitative trait loci among bipolar disorder susceptibility variants

(2012) E R Gamazon et al.   MOLECULAR PSYCHIATRY

The mystery of missing heritability: Genetic interactions create phantom heritability

(2012) O. Zuk et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Loci nominally associated with autism from genome-wide analysis show enrichment of brain expression quantitative trait loci but not lymphoblastoid cell line expression quantitative trait loci

(2012) Lea K Davis et al.   Molecular Autism

Common genetic variants, acting additively, are a major source of risk for autism

(2012) Lambertus Klei et al.   Molecular Autism

Estimating Missing Heritability for Disease from Genome-wide Association Studies

(2011) Sang Hong Lee et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Homeobox genes in obsessive-compulsive disorder

(2011) G. Nestadt et al.   AMERICAN JOURNAL OF MEDICAL GENETICS PART B-NEUROPSYCHIATRIC GENETICS

Global Gene Expression Profiles of Subcutaneous Adipose and Muscle From Glucose-Tolerant, Insulin-Sensitive, and Insulin-Resistant Individuals Matched for BMI

(2011) Steven C. Elbein et al.   DIABETES

Genomewide linkage analysis in Costa Rican families implicates chromosome 15q14 as a candidate region for OCD

(2011) Jessica Ross et al.   HUMAN GENETICS

Genome partitioning of genetic variation for complex traits using common SNPs

(2011) Jian Yang et al.   NATURE GENETICS

Genome-wide association study identifies five new schizophrenia loci

(2011)   NATURE GENETICS

GCTA: A Tool for Genome-wide Complex Trait Analysis

(2010) Jian Yang et al.   AMERICAN JOURNAL OF HUMAN GENETICS

The Genetics of Autism Spectrum Disorders and Related Neuropsychiatric Disorders in Childhood

(2010) Paul Lichtenstein et al.   AMERICAN JOURNAL OF PSYCHIATRY

Symptom Dimensions in OCD: Item-Level Factor Analysis and Heritability Estimates

(2010) Hilga Katerberg et al.   BEHAVIOR GENETICS

MaCH: using sequence and genotype data to estimate haplotypes and unobserved genotypes

(2010) Yun Li et al.   GENETIC EPIDEMIOLOGY

Missing heritability and strategies for finding the underlying causes of complex disease

(2010) Evan E. Eichler et al.   NATURE REVIEWS GENETICS

ANNOVAR: functional annotation of genetic variants from high-throughput sequencing data

(2010) K. Wang et al.   NUCLEIC ACIDS RESEARCH

Genotype Imputation

(2009) Yun Li et al.   Annual Review of Genomics and Human Genetics

Nine patients with a microdeletion 15q11.2 between breakpoints 1 and 2 of the Prader–Willi critical region, possibly associated with behavioural disturbances

(2009) Marianne Doornbos et al.   European Journal of Medical Genetics

The genetics of Tourette syndrome: A review

(2009) Julia A. O'Rourke et al.   JOURNAL OF PSYCHOSOMATIC RESEARCH

Maternal transmission of a rare GABRB3 signal peptide variant is associated with autism

(2009) R J Delahanty et al.   MOLECULAR PSYCHIATRY

Finding the missing heritability of complex diseases

(2009) Teri A. Manolio et al.   NATURE

Tourette's syndrome, trichotillomania, and obsessive–compulsive disorder: How closely are they related?

(2009) Ygor Arzeno Ferrão et al.   PSYCHIATRY RESEARCH

Genetic Factors Underlie Stability of Obsessive–Compulsive Symptoms

(2009) Daniël S. van Grootheest et al.   Twin Research and Human Genetics

Habits, Rituals, and the Evaluative Brain

(2008) Ann M. Graybiel   Annual Review of Neuroscience

Latent Class Analysis of Gilles de la Tourette Syndrome Using Comorbidities: Clinical and Genetic Implications

(2008) Marco A. Grados et al.   BIOLOGICAL PSYCHIATRY