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Increasing the diagnostic yield of exome sequencing by copy number variant analysis

PloS one, 2018-12, Vol.13 (12), p.e0209185-e0209185

2018

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Pleiotropic loci for cannabis use disorder severity in multi-ancestry high-risk populations

Molecular and cellular neuroscience, 2023-06, Vol.125, p.103852-103852, Article 103852

2023

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Developing, implementing, and evaluating the visiting Neighbors' program in rural Appalachia: A quality improvement protocol

PloS one, 2024-01, Vol.19 (1), p.e0296438-e0296438

2024

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The feasibility of genetic dissection of endophenotypes

Psychophysiology, 2014-12, Vol.51 (12), p.1337-1338

Wilhelmsen, Kirk C.

2014

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A greedy regression algorithm with coarse weights offers novel advantages

Scientific reports, 2022-03, Vol.12 (1), p.5440-14, Article 5440

2022

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Can Genetic Analysis of Putative Blood Alzheimer's Disease Biomarkers Lead to Identification of Susceptibility Loci?

PloS one, 2015-12, Vol.10 (12), p.e0142360-e0142360

2015

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Genetic variation in FAAH is associated with cannabis use disorders in a young adult sample of Mexican Americans

Drug and alcohol dependence, 2016-09, Vol.166, p.249-253

2016

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Projected t-SNE for batch correction

Bioinformatics, 2020-06, Vol.36 (11), p.3522-3527

2020

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Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing

BMC bioinformatics, 2021-07, Vol.22 (1), p.1-374, Article 374

2021

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A blood-based screening tool for Alzheimer's disease that spans serum and plasma: findings from TARC and ADNI

PloS one, 2011-12, Vol.6 (12), p.e28092

2011

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Effects of genetic risk for alcohol dependence and onset of regular drinking on the progression to alcohol dependence: A polygenic risk score approach

Drug and alcohol dependence, 2022-01, Vol.230, p.109117-109117, Article 109117

2022

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Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly

Cell, 2018-02, Vol.172 (5), p.897-909.e21

2018

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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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High Diagnostic Yield of Whole Exome Sequencing in Participants With Retinal Dystrophies in a Clinical Ophthalmology Setting

American journal of ophthalmology, 2015-08, Vol.160 (2), p.354-363.e9

2015

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Polygenic risk scores for cigarettes smoked per day do not generalize to a Native American population

Drug and alcohol dependence, 2016-10, Vol.167, p.95-102

2016

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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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Cannabis dependence in the San Francisco Family Study: Age of onset of use, DSM-IV symptoms, withdrawal, and heritability

Addictive behaviors, 2010-02, Vol.35 (2), p.102-110

2010

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ReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data

BMC bioinformatics, 2012-09, Vol.13 (1), p.221-221, Article 221

2012

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Surface-based correlates of cognition along the Alzheimer's continuum in a memory clinic population

Frontiers in neurology, 2023-09, Vol.14, p.1214083-1214083

2023

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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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DNA methylation in brain tissue and Alzheimer’s disease

Alzheimer's & dementia, 2015-07, Vol.11 (7), p.P485-P485

2015

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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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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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Simulating association studies: a data-based resampling method for candidate regions or whole genome scans

Bioinformatics, 2007-10, Vol.23 (19), p.2581-2588

2007

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Increasing the diagnostic yield of exome sequencing by copy number variant analysis

Pleiotropic loci for cannabis use disorder severity in multi-ancestry high-risk populations

Developing, implementing, and evaluating the visiting Neighbors' program in rural Appalachia: A quality improvement protocol

The feasibility of genetic dissection of endophenotypes

A greedy regression algorithm with coarse weights offers novel advantages

Can Genetic Analysis of Putative Blood Alzheimer's Disease Biomarkers Lead to Identification of Susceptibility Loci?

Genetic variation in FAAH is associated with cannabis use disorders in a young adult sample of Mexican Americans

Projected t-SNE for batch correction

Pre-capture multiplexing provides additional power to detect copy number variation in exome sequencing

A blood-based screening tool for Alzheimer's disease that spans serum and plasma: findings from TARC and ADNI

Effects of genetic risk for alcohol dependence and onset of regular drinking on the progression to alcohol dependence: A polygenic risk score approach

Dissecting the Causal Mechanism of X-Linked Dystonia-Parkinsonism by Integrating Genome and Transcriptome Assembly

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

High Diagnostic Yield of Whole Exome Sequencing in Participants With Retinal Dystrophies in a Clinical Ophthalmology Setting

Polygenic risk scores for cigarettes smoked per day do not generalize to a Native American population

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

Cannabis dependence in the San Francisco Family Study: Age of onset of use, DSM-IV symptoms, withdrawal, and heritability

ReQON: a Bioconductor package for recalibrating quality scores from next-generation sequencing data

Surface-based correlates of cognition along the Alzheimer's continuum in a memory clinic population

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

DNA methylation in brain tissue and Alzheimer’s disease

Protective variant associated with alcohol dependence in a Mexican American cohort

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

Simulating association studies: a data-based resampling method for candidate regions or whole genome scans

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