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An informatics approach to analyzing the incidentalome

Genetics in medicine, 2013-01, Vol.15 (1), p.36-44

2013

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Genome‐wide meta‐analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2017-07, Vol.174 (5), p.557-567

2017

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A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

Genetics in medicine, 2016-05, Vol.18 (5), p.467-475

2016

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Variant calling in low-coverage whole genome sequencing of a Native American population sample

BMC genomics, 2014-01, Vol.15 (1), p.85-85, Article 85

2014

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Whole genome sequence association and ancestry‐informed polygenic profile of EEG alpha in a Native American population

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2017-06, Vol.174 (4), p.435-450

2017

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Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fraction

Prenatal diagnosis, 2022-05, Vol.42 (5), p.567-573

2022

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Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations

Twin research and human genetics, 2017-06, Vol.20 (3), p.197-207

2017

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X-Linked Dominant Scapuloperoneal Myopathy Is Due to a Mutation in the Gene Encoding Four-and-a-Half-LIM Protein 1

American journal of human genetics, 2008-01, Vol.82 (1), p.208-213

2008

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Genetic Influences on Evening Preference Overlap with Those for Bipolar Disorder in a Sample of Mexican Americans and American Indians

Twin research and human genetics, 2017-12, Vol.20 (6), p.499-510

2017

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Integration of expression quantitative trait loci and pleiotropy identifies a novel psoriasis susceptibility gene, PTPN1

The journal of gene medicine, 2017-01, Vol.19 (1-2), p.n/a

2017

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Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease

Circulation. Cardiovascular genetics, 2017-06, Vol.10 (3)

2017

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Association between single nucleotide polymorphisms in the mu opioid receptor gene (OPRM1) and self-reported responses to alcohol in American Indians

BMC medical genetics, 2008-04, Vol.9 (1), p.35-35, Article 35

2008

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The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: Report and review

American journal of medical genetics. Part A, 2015-09, Vol.167A (9), p.2176-2181

2015

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Association and ancestry analysis of sequence variants in ADH and ALDH using alcohol-related phenotypes in a Native American community sample

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2014-12, Vol.165B (8), p.673-683

2014

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Protective variant associated with alcohol dependence in a Mexican American cohort

BMC medical genetics, 2014-12, Vol.15 (1), p.136-136, Article 136

2014

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Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders

Neurology. Genetics, 2018-02, Vol.4 (1), p.e212-e212

2018

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Linkage analyses of stimulant dependence, craving, and heavy use in American Indians

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2011-12, Vol.156B (7), p.772-780

2011

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EEG alpha phenotypes: linkage analyses and relation to alcohol dependence in an American Indian community study

BMC medical genetics, 2010-03, Vol.11 (1), p.43-43, Article 43

2010

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Linkage analyses of cannabis dependence, craving, and withdrawal in the San Francisco family study

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2010-04, Vol.153B (3), p.802-811

2010

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Variants Near CCK Receptors are Associated With Electrophysiological Responses to Pre-pulse Startle Stimuli in a Mexican American Cohort

Twin research and human genetics, 2015-12, Vol.18 (6), p.727-737

2015

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Genomic screen for loci associated with alcohol dependence in Mission Indians

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2004-08, Vol.129B (1), p.110-115

2004

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Genomic screen for loci associated with tobacco usage in Mission Indians

BMC medical genetics, 2006-02, Vol.7 (1), p.9-9, Article 9

2006

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Externalizing disorders in American Indians: Comorbidity and a genome wide linkage analysis

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2008-09, Vol.147B (6), p.690-698

2008

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Genome-wide scan for self-rating of the effects of alcohol in American Indians

Psychiatric genetics, 2010-10, Vol.20 (5), p.221-228

2010

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Localization of a gene for partial epilepsy to chromosome 10q

Nature genetics, 1995-05, Vol.10 (1), p.56-60

1995

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An informatics approach to analyzing the incidentalome

Genome‐wide meta‐analysis identifies a novel susceptibility signal at CACNA2D3 for nicotine dependence

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

Variant calling in low-coverage whole genome sequencing of a Native American population sample

Whole genome sequence association and ancestry‐informed polygenic profile of EEG alpha in a Native American population

Noninvasive prenatal exome sequencing diagnostic utility limited by sequencing depth and fetal fraction

Genome-Wide Association Study of Post-Traumatic Stress Disorder in Two High-Risk Populations

X-Linked Dominant Scapuloperoneal Myopathy Is Due to a Mutation in the Gene Encoding Four-and-a-Half-LIM Protein 1

Genetic Influences on Evening Preference Overlap with Those for Bipolar Disorder in a Sample of Mexican Americans and American Indians

Integration of expression quantitative trait loci and pleiotropy identifies a novel psoriasis susceptibility gene, PTPN1

Whole Exome Sequencing Identifies Truncating Variants in Nuclear Envelope Genes in Patients With Cardiovascular Disease

Association between single nucleotide polymorphisms in the mu opioid receptor gene (OPRM1) and self-reported responses to alcohol in American Indians

The phenotype of multiple congenital anomalies-hypotonia-seizures syndrome 1: Report and review

Association and ancestry analysis of sequence variants in ADH and ALDH using alcohol-related phenotypes in a Native American community sample

Protective variant associated with alcohol dependence in a Mexican American cohort

Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders

Linkage analyses of stimulant dependence, craving, and heavy use in American Indians

EEG alpha phenotypes: linkage analyses and relation to alcohol dependence in an American Indian community study

Linkage analyses of cannabis dependence, craving, and withdrawal in the San Francisco family study

Variants Near CCK Receptors are Associated With Electrophysiological Responses to Pre-pulse Startle Stimuli in a Mexican American Cohort

Genomic screen for loci associated with alcohol dependence in Mission Indians

Genomic screen for loci associated with tobacco usage in Mission Indians

Externalizing disorders in American Indians: Comorbidity and a genome wide linkage analysis

Genome-wide scan for self-rating of the effects of alcohol in American Indians

Localization of a gene for partial epilepsy to chromosome 10q

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