(Q30397608)

16 October 2017

In search of rare variants: preliminary results from whole genome sequencing of 1,325 individuals with psychophysiological endophenotypes (English)

1 reference

16 October 2017

whole genome sequencing

1 reference

1 reference

9

1 reference

16 October 2017

10

1 reference

16 October 2017

13

1 reference

16 October 2017

16

Matt McGue

1 reference

16 October 2017

18

William G Iacono

1 reference

16 October 2017

2

Stephen M Malone

1 reference

16 October 2017

17

Goncalo Abecasis

1 reference

16 October 2017

3

Uma Vaidyanathan

1 reference

16 October 2017

1

Scott I Vrieze

1 reference

16 October 2017

15

William Oetting

1 reference

16 October 2017

5

Hyun Min Kang

1 reference

16 October 2017

8

Daniel Irons

1 reference

16 October 2017

11

Giorgio Pistis

1 reference

16 October 2017

Alan Kwong

4

1 reference

16 October 2017

Xiaowei Zhan

series ordinal

6

1 reference

16 October 2017

Matthew Flickinger

series ordinal

7

1 reference

16 October 2017

Richard M Myers

series ordinal

14

1 reference

16 October 2017

1 December 2014

1 reference

16 October 2017

1 reference

16 October 2017

51

1 reference

16 October 2017

12

1 reference

16 October 2017

1309-1320

1 reference

An efficient and scalable analysis framework for variant extraction and refinement from population-scale DNA sequence data

16 October 2017

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Genetic associations of nonsynonymous exonic variants with psychophysiological endophenotypes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Heritability and molecular-genetic basis of resting EEG activity: a genome-wide association study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Joint analysis of functional genomic data and genome-wide association studies of 18 human traits

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

A polygenic burden of rare disruptive mutations in schizophrenia

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

De novo mutations in schizophrenia implicate synaptic networks

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

CNV analysis in a large schizophrenia sample implicates deletions at 16p12.1 and SLC1A1 and duplications at 1p36.33 and CGNL1

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

A genome-wide association study of behavioral disinhibition

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Somatic mutation, genomic variation, and neurological disease

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

The Minnesota Center for Twin and Family Research genome-wide association study

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Analysis of 6,515 exomes reveals the recent origin of most human protein-coding variants

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

An integrated map of genetic variation from 1,092 human genomes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Confluence of genes, environment, development, and behavior in a post Genome-Wide Association Study world

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Systematic localization of common disease-associated variation in regulatory DNA

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

An integrated encyclopedia of DNA elements in the human genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Fast and accurate genotype imputation in genome-wide association studies through pre-phasing

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Patterns and rates of exonic de novo mutations in autism spectrum disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Five years of GWAS discovery

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Exome sequencing in sporadic autism spectrum disorders identifies severe de novo mutations

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Initial impact of the sequencing of the human genome

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

A population-specific HTR2B stop codon predisposes to severe impulsivity

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Research domain criteria (RDoC): toward a new classification framework for research on mental disorders

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Pooled association tests for rare variants in exon-resequencing studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

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

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

A comprehensive review of genetic association studies

20 June 2018

1 reference

https://eutils.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pmc&linkname=pmc_refs_pubmed&retmode=json&id=4231480

A unified approach to genotype imputation and haplotype-phase inference for large data sets of trios and unrelated individuals

20 June 2018

1 reference

https://api.crossref.org/works/10.1111%2FPSYP.12350

The Sanger FASTQ file format for sequences with quality scores, and the Solexa/Illumina FASTQ variants

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPSYP.12350

Improved whole-chromosome phasing for disease and population genetic studies

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPSYP.12350

Detecting and estimating contamination of human DNA samples in sequencing and array-based genotype data

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPSYP.12350

Fast and accurate long-read alignment with Burrows-Wheeler transform

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPSYP.12350

An abundance of rare functional variants in 202 drug target genes sequenced in 14,002 people

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPSYP.12350

Spurious genetic associations.

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPSYP.12350

Rare-variant association testing for sequencing data with the sequence kernel association test

21 January 2018

1 reference

https://api.crossref.org/works/10.1111%2FPSYP.12350

21 January 2018

Identifiers

DOI

10.1111/PSYP.12350

1 reference

16 October 2017

1 reference

16 October 2017

1 reference