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Analysis of differential gene expression and transcript usage in hippocampus of Apoe null mutant mice: Implications for Alzheimer’s disease

Neuroscience research, 2022-03, Vol.176, p.85-89

2022

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Analysis of single-cell transcriptome data from a mouse model implicates protein synthesis dysfunction in schizophrenia

Genes & Genomics, 2024, 46(9), , pp.1071-1084

2024

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Replication of the pharmacogenetic effect of rs678849 on buprenorphine efficacy in African-Americans with opioid use disorder

The pharmacogenomics journal, 2019-06, Vol.19 (3), p.260-268

2019

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Genetics and prescription opioid use (GaPO): study design for consenting a cohort from an existing biobank to identify clinical and genetic factors influencing prescription opioid use and abuse

BMC medical genomics, 2021-10, Vol.14 (1), p.253-11, Article 253

2021

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Restriction Enzyme Based Enriched L1Hs Sequencing (REBELseq): A Scalable Technique for Detection of Ta Subfamily L1Hs in the Human Genome

G3 : genes - genomes - genetics, 2020-05, Vol.10 (5), p.1647-1655

2020

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Mammary tumor induction in transgenic mice expressing an RNA-binding protein

Cancer research (Chicago, Ill.), 2004, Vol.64 (1), p.209-214

2004

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In vitro and ex vivo analysis of CHRNA3 and CHRNA5 haplotype expression

PloS one, 2011-08, Vol.6 (8), p.e23373

2011

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Analysis of LINE-1 Elements in DNA from Postmortem Brains of Individuals with Schizophrenia

Neuropsychopharmacology (New York, N.Y.), 2017-12, Vol.42 (13), p.2602-2611

2017

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Neonatal Opioid Withdrawal Syndrome (NOWS): A Transgenerational Echo of the Opioid Crisis

Cold Spring Harbor perspectives in medicine, 2021-03, Vol.11 (3), p.a039669

2021

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Failure to Replicate an Association of a LINE-1 Element in ERI1 Exoribonuclease Family Member 3 (ERI3) with Schizophrenia

Neuropsychopharmacology (New York, N.Y.), 2017-12, Vol.42 (13), p.2471-2471

2017

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Single Nucleus Transcriptome Data from Alzheimer's Disease Mouse Models Yield New Insight into Pathophysiology

Journal of Alzheimer's disease, 2022-01, Vol.90 (3), p.1233-1247

2022

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Investigation of long interspersed element‐1 retrotransposons as potential risk factors for idiopathic temporal lobe epilepsy

Epilepsia (Copenhagen), 2021-06, Vol.62 (6), p.1329-1342

2021

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Association between Polymorphisms in the Vesicular Monoamine Transporter 1 Gene (VMAT1/SLC18A1) on Chromosome 8p and Schizophrenia

Neuropsychobiology, 2008-01, Vol.57 (1-2), p.55-60

2008

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The imperative of clinical and molecular research on neonatal opioid withdrawal syndrome

Molecular psychiatry, 2019-11, Vol.24 (11), p.1568-1571

2019

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Somatic DNA Variation in Brain as a Source of Risk for CNS Diseases

Neuropsychopharmacology (New York, N.Y.), 2016-01, Vol.41 (1), p.386-387

2016

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Differential expression and transcription factor binding associated with genotype at a pharmacogenetic variant in OPRD1

The American journal of drug and alcohol abuse, 2021-09, Vol.47 (5), p.581-589

2021

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Assessment of Probable Opioid Use Disorder Using Electronic Health Record Documentation

JAMA network open, 2020-09, Vol.3 (9), p.e2015909

2020

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Pharmacogenetic analysis of opioid dependence treatment dose and dropout rate

The American journal of drug and alcohol abuse, 2018-01, Vol.44 (4), p.431-440

2018

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Genetic variants in the cocaine- and amphetamine-regulated transcript gene ( CARTPT) and cocaine dependence

Neuroscience letters, 2008-08, Vol.440 (3), p.280-283

2008

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Identification and functional significance of polymorphisms in the μ-opioid receptor gene ( Oprm) promoter of C57BL/6 and DBA/2 mice

Neuroscience research, 2006-07, Vol.55 (3), p.244-254

2006

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Inherited L1 Retrotransposon Insertions Associated With Risk for Schizophrenia and Bipolar Disorder

Schizophrenia bulletin open, 2021-01, Vol.2 (1), p.sgab031-sgab031

2021

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Reading LINEs within the cocaine addicted brain

Brain and behavior, 2017-05, Vol.7 (5), p.e00678-n/a

2017

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Identification of CHRNA5 rare variants in African-American heavy smokers

Psychiatric genetics, 2014-06, Vol.24 (3), p.102-109

2014

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Re-sequencing of ankyrin 3 exon 48 and case-control association analysis of rare variants in bipolar disorder type I

Bipolar disorders, 2012-12, Vol.14 (8), p.809-821

2012

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Reading LINE s within the cocaine addicted brain

Brain and behavior, 2017-05, Vol.7 (5)

2017

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Analysis of differential gene expression and transcript usage in hippocampus of Apoe null mutant mice: Implications for Alzheimer’s disease

Analysis of single-cell transcriptome data from a mouse model implicates protein synthesis dysfunction in schizophrenia

Replication of the pharmacogenetic effect of rs678849 on buprenorphine efficacy in African-Americans with opioid use disorder

Genetics and prescription opioid use (GaPO): study design for consenting a cohort from an existing biobank to identify clinical and genetic factors influencing prescription opioid use and abuse

Restriction Enzyme Based Enriched L1Hs Sequencing (REBELseq): A Scalable Technique for Detection of Ta Subfamily L1Hs in the Human Genome

Mammary tumor induction in transgenic mice expressing an RNA-binding protein

In vitro and ex vivo analysis of CHRNA3 and CHRNA5 haplotype expression

Analysis of LINE-1 Elements in DNA from Postmortem Brains of Individuals with Schizophrenia

Neonatal Opioid Withdrawal Syndrome (NOWS): A Transgenerational Echo of the Opioid Crisis

Failure to Replicate an Association of a LINE-1 Element in ERI1 Exoribonuclease Family Member 3 (ERI3) with Schizophrenia

Single Nucleus Transcriptome Data from Alzheimer's Disease Mouse Models Yield New Insight into Pathophysiology

Investigation of long interspersed element‐1 retrotransposons as potential risk factors for idiopathic temporal lobe epilepsy

Association between Polymorphisms in the Vesicular Monoamine Transporter 1 Gene (VMAT1/SLC18A1) on Chromosome 8p and Schizophrenia

The imperative of clinical and molecular research on neonatal opioid withdrawal syndrome

Somatic DNA Variation in Brain as a Source of Risk for CNS Diseases

Differential expression and transcription factor binding associated with genotype at a pharmacogenetic variant in OPRD1

Assessment of Probable Opioid Use Disorder Using Electronic Health Record Documentation

Pharmacogenetic analysis of opioid dependence treatment dose and dropout rate

Genetic variants in the cocaine- and amphetamine-regulated transcript gene ( CARTPT) and cocaine dependence

Identification and functional significance of polymorphisms in the μ-opioid receptor gene ( Oprm) promoter of C57BL/6 and DBA/2 mice

Inherited L1 Retrotransposon Insertions Associated With Risk for Schizophrenia and Bipolar Disorder

Reading LINEs within the cocaine addicted brain

Identification of CHRNA5 rare variants in African-American heavy smokers

Re-sequencing of ankyrin 3 exon 48 and case-control association analysis of rare variants in bipolar disorder type I

Reading LINE s within the cocaine addicted brain

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