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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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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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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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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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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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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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Genetic risk for trait aggression and alcohol use predict unique facets of alcohol-related aggression

Psychology of addictive behaviors, 2024-06

2024

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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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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

Volltextzugriff (PDF)

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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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

2019

Volltextzugriff (PDF)

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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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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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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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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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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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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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

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

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

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

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

A greedy regression algorithm with coarse weights offers novel advantages

Genetic risk for trait aggression and alcohol use predict unique facets of alcohol-related aggression

An informatics approach to analyzing the incidentalome

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

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

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

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

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

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

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

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