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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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Indexing the ‘dark side of addiction’: substance‐induced affective symptoms and alcohol use disorders

Addiction (Abingdon, England), 2019-01, Vol.114 (1), p.139-149

2019

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SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection

Briefings in bioinformatics, 2021-05, Vol.22 (3)

2021

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Focused ultrasound-mediated blood-brain barrier opening in Alzheimer's disease: long-term safety, imaging, and cognitive outcomes

Journal of neurosurgery, 2023-07, Vol.139 (1), p.275-283

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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Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings

Clinical cancer research, 2016-08, Vol.22 (16), p.4087-4094

2016

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scRNA-seq in medulloblastoma shows cellular heterogeneity and lineage expansion support resistance to SHH inhibitor therapy

Nature communications, 2019-12, Vol.10 (1), p.5829-17, Article 5829

2019

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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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An informatics approach to analyzing the incidentalome

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

2013

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Common genetic substrates of alcohol and substance use disorder severity revealed by pleiotropy detection against GWAS catalog in two populations

Addiction biology, 2021-01, Vol.26 (1), p.e12877-n/a

2021

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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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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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Associations Between Genomic Variants in Alcohol Dehydrogenase Genes and Alcohol Symptomatology in American Indians and European Americans: Distinctions and Convergence

Alcoholism, clinical and experimental research, 2017-10, Vol.41 (10), p.1695-1704

2017

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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 Common and Rare Chromosome 4 GABAergic Gene Variation on Alcohol Use and Antisocial Behavior

Journal of studies on alcohol and drugs, 2019-11, Vol.80 (6), p.585-593

2019

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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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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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Genetic loci for alcohol-related life events and substance-induced affective symptoms: indexing the “dark side” of addiction

Translational psychiatry, 2019-02, Vol.9 (1), p.71, Article 71

2019

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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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Meta‐Analysis of Genetic Influences on Initial Alcohol Sensitivity

Alcoholism, clinical and experimental research, 2018-12, Vol.42 (12), p.2349-2359

2018

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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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Whole genome sequence study of cannabis dependence in two independent cohorts

Addiction biology, 2018-01, Vol.23 (1), p.461-473

2018

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

Indexing the ‘dark side of addiction’: substance‐induced affective symptoms and alcohol use disorders

SMNN: batch effect correction for single-cell RNA-seq data via supervised mutual nearest neighbor detection

Focused ultrasound-mediated blood-brain barrier opening in Alzheimer's disease: long-term safety, imaging, and cognitive outcomes

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

Germline Analysis from Tumor-Germline Sequencing Dyads to Identify Clinically Actionable Secondary Findings

scRNA-seq in medulloblastoma shows cellular heterogeneity and lineage expansion support resistance to SHH inhibitor therapy

The feasibility of genetic dissection of endophenotypes

A greedy regression algorithm with coarse weights offers novel advantages

An informatics approach to analyzing the incidentalome

Common genetic substrates of alcohol and substance use disorder severity revealed by pleiotropy detection against GWAS catalog in two populations

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

Projected t-SNE for batch correction

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

Associations Between Genomic Variants in Alcohol Dehydrogenase Genes and Alcohol Symptomatology in American Indians and European Americans: Distinctions and Convergence

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

Effects of Common and Rare Chromosome 4 GABAergic Gene Variation on Alcohol Use and Antisocial Behavior

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

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

Genetic loci for alcohol-related life events and substance-induced affective symptoms: indexing the “dark side” of addiction

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

Meta‐Analysis of Genetic Influences on Initial Alcohol Sensitivity

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

Whole genome sequence study of cannabis dependence in two independent cohorts

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