Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes

Rare-Variant Association Analysis: Study Designs and Statistical Tests

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A general framework for estimating the relative pathogenicity of human genetic variants

(2014) Martin Kircher et al.   NATURE GENETICS

Heritability and molecular-genetic basis of the P3 event-related brain potential: A genome-wide association study

(2014) Stephen M. Malone et al.   PSYCHOPHYSIOLOGY

Genome-wide scans of genetic variants for psychophysiological endophenotypes: A methodological overview

(2014) William. G. Iacono et al.   PSYCHOPHYSIOLOGY

In search of rare variants: Preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes

(2014) Scott I. Vrieze et al.   PSYCHOPHYSIOLOGY

Heritability and molecular genetic basis of acoustic startle eye blink and affectively modulated startle response: A genome-wide association study

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Heritability and molecular genetic basis of electrodermal activity: A genome-wide association study

(2014) Uma Vaidyanathan et al.   PSYCHOPHYSIOLOGY

Heritability and molecular genetic basis of antisaccade eye tracking error rate: A genome-wide association study

(2014) Uma Vaidyanathan et al.   PSYCHOPHYSIOLOGY

Neuropathy target esterase (NTE): overview and future

(2012) Rudy J. Richardson et al.   CHEMICO-BIOLOGICAL INTERACTIONS

GENCODE: The reference human genome annotation for The ENCODE Project

(2012) J. Harrow et al.   GENOME RESEARCH

Identification of common variants associated with human hippocampal and intracranial volumes

(2012) Jason L Stein et al.   NATURE GENETICS

Improved linear mixed models for genome-wide association studies

(2012) Jennifer Listgarten et al.   NATURE METHODS

Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes

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The Minnesota Center for Twin and Family Research Genome-Wide Association Study

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Rare-Variant Association Testing for Sequencing Data with the Sequence Kernel Association Test

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Pooled Association Tests for Rare Variants in Exon-Resequencing Studies

(2010) Alkes L. Price et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Rare Variant Association Analysis Methods for Complex Traits

(2010) Jennifer Asimit et al.   Annual Review of Genetics

Deriving the consequences of genomic variants with the Ensembl API and SNP Effect Predictor

(2010) William McLaren et al.   BIOINFORMATICS

Variance component model to account for sample structure in genome-wide association studies

(2010) Hyun Min Kang et al.   NATURE GENETICS

A method and server for predicting damaging missense mutations

(2010) Ivan A Adzhubei et al.   NATURE METHODS

EEG spectral phenotypes: Heritability and association with marijuana and alcohol dependence in an American Indian community study

(2009) Cindy L. Ehlers et al.   DRUG AND ALCOHOL DEPENDENCE

Predicting the effects of coding non-synonymous variants on protein function using the SIFT algorithm

(2009) Prateek Kumar et al.   Nature Protocols

The Enrichment Study of the Minnesota Twin Family Study: Increasing the Yield of Twin Families at High Risk for Externalizing Psychopathology

(2009) Margaret A. Keyes et al.   Twin Research and Human Genetics

Methods for Detecting Associations with Rare Variants for Common Diseases: Application to Analysis of Sequence Data

(2008) Bingshan Li et al.   AMERICAN JOURNAL OF HUMAN GENETICS