Bernie Devlin

发表

Semi-soft Clustering of Single Cell Data

Kathryn Roeder, Jing Lei, Lingxue Zhu, 2018, bioRxiv.

A Method to Exploit the Structure of Genetic Ancestry Space to Enhance Case-Control Studies.

Kathryn Roeder, Stephan Ripke, Bernie Devlin, 2016, American journal of human genetics.

TESTING HIGH-DIMENSIONAL COVARIANCE MATRICES, WITH APPLICATION TO DETECTING SCHIZOPHRENIA RISK GENES.

Kathryn Roeder, Lingxue Zhu, Bernie Devlin, 2016, The annals of applied statistics.

Wringing The Bell Curve: A Cautionary Tale about the Relationships among Race, Genes, and IQ

Stephen E. Fienberg, Kathryn Roeder, Daniel P. Resnick, 1995 .

Using multiple measurements of tissue to estimate subject- and cell-type-specific gene expression

Kathryn Roeder, Jiebiao Wang, Bernie Devlin, 2019, Bioinform..

A method to exploit the structure of genetic ancestry space to enhance case-control studies

Kathryn Roeder, Stephan Ripke, Benjamin M. Neale, 2016 .

Semisoft clustering of single-cell data

Kathryn Roeder, Lingxue Zhu, Bernie Devlin, 2018, Proceedings of the National Academy of Sciences.

A selective inference approach for FDR control using multi-omics covariates yields insights into disease risk

Kathryn Roeder, Ronald Yurko, Bernie Devlin, 2019 .

A United Statistical Framework for Single Cell and Bulk Sequencing Data

Kathryn Roeder, Jing Lei, Lingxue Zhu, 2017, bioRxiv.

A United Statistical Framework for Single Cell and Bulk Sequencing Data

Kathryn Roeder, Lingxue Zhu, Bernie Devlin, 2016, bioRxiv.

An approach to gene-based testing accounting for dependence of tests among nearby genes

Kathryn Roeder, Ronald Yurko, Bernie Devlin, 2021, Briefings Bioinform..

Identification of common variants influencing risk of the tauopathy Progressive Supranuclear Palsy

Andrew J. Lees, Allissa Dillman, Li-San Wang, 2011, Nature Genetics.

REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING.

Kathryn Roeder, Ann B. Lee, Bernie Devlin, 2012, The annals of applied statistics.

Project among African-Americans to explore risks for schizophrenia (PAARTNERS): evidence for impairment and heritability of neurocognitive functioning in families of schizophrenia patients.

Raquel E Gur, Ruben C Gur, Bernie Devlin, 2010, The American journal of psychiatry.

A Genome-wide Association Study of Autism Using the Simons Simplex Collection: Does Reducing Phenotypic Heterogeneity in Autism Increase Genetic Homogeneity?

Eric M. Morrow, Shrikant M. Mane, Edwin H. Cook, 2015, Biological Psychiatry.

Analysis of Rare, Exonic Variation amongst Subjects with Autism Spectrum Disorders and Population Controls

Kathryn Roeder, Stephan Ripke, Shannon Gross, 2013, PLoS genetics.

Joint Analysis of Psychiatric Disorders Increases Accuracy of Risk Prediction for Schizophrenia, Bipolar Disorder, and Major Depressive Disorder

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, American journal of human genetics.

Differential Activity of Transcribed Enhancers in the Prefrontal Cortex of 537 cases with Schizophrenia and Controls

Kathryn Roeder, Manuel Mattheisen, Claudia Giambartolomei, 2018, Molecular Psychiatry.

Genome-wide transcriptome profiling reveals the functional impact of rare de novo and recurrent CNVs in autism spectrum disorders.

Yuan Tian, Matthew E Hurles, Irina Voineagu, 2012, American journal of human genetics.

Common genetic variants in the CLDN2 and PRSS1-PRSS2 loci alter risk for alcohol-related and sporadic pancreatitis

Robert C. Green, Andrew J. Saykin, Liana G. Apostolova, 2012, Nature Genetics.

"Intelligence, Genes, and Success": Scientists Respond To The Bell Curve

Bernie Devlin, B. Devlin, 1997 .

Integration of association statistics over genomic regions using Bayesian adaptive regression splines

Kathryn Roeder, Bernie Devlin, Garrick Wallstrom, 2003, Human Genomics.

Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

Kathryn Roeder, Murim Choi, Eric M. Morrow, 2011, Neuron.

Coexpression Networks Implicate Human Midfetal Deep Cortical Projection Neurons in the Pathogenesis of Autism

Wei Niu, Kathryn Roeder, Mingfeng Li, 2013, Cell.

Rare Complete Knockouts in Humans: Population Distribution and Significant Role in Autism Spectrum Disorders

Kathryn Roeder, Stephan Ripke, Shannon Gross, 2013, Neuron.

Common risk variants identified in autism spectrum disorder

Jakob Grove, Esben Agerbo, Anders D. Børglum, 2017, bioRxiv.

Using ancestry matching to combine family‐based and unrelated samples for genome‐wide association studies

Kathryn Roeder, Massimo Trucco, Bernie Devlin, 2010, Statistics in medicine.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Thomas Bourgeron, Alberto Segre, Alberto Maria Segre, 2007, Nature Genetics.

Genome-wide Association Study of Alzheimer’s disease with Psychotic Symptoms

Brian Lawlor, Oscar L. Lopez, David Craig, 2011, Molecular Psychiatry.

Gene expression imputation across multiple brain regions provides insights into schizophrenia risk

Benjamin A. Logsdon, Hae Kyung Im, Solveig K Sieberts, 2019, Nature Genetics.

Consanguinity and increased risk for schizophrenia in Egypt

Vishwajit L. Nimgaonkar, Annie Watson, Bernie Devlin, 2010, Schizophrenia Research.

A search for susceptibility loci for anorexia nervosa: methods and sample description

David Goldman, Bernie Devlin, B. Devlin, 2000, Biological Psychiatry.

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Jianxin Shi, Susmita Datta, Aribert Rothenberger, 2013, Nature Genetics.

Common genetic variants, acting additively, are a major source of risk for autism

Kathryn Roeder, Timothy W Yu, Bernie Devlin, 2012, Molecular Autism.

Comprehensive analysis of APOE and selected proximate markers for late-onset Alzheimer's disease: patterns of linkage disequilibrium and disease/marker association.

Ellen M Wijsman, Bernie Devlin, Howard Seltman, 2007, Genomics.

Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia

Joel Dudley, Kathryn Roeder, A. Ercument Cicek, 2016 .

Genetic architecture in autism spectrum disorder.

Bernie Devlin, Stephen W Scherer, S. Scherer, 2012, Current opinion in genetics & development.

Integrated Model of De Novo and Inherited Genetic Variants Yields Greater Power to Identify Risk Genes

Kathryn Roeder, Xin He, Richard A. Gibbs, 2013, PLoS genetics.

Most genetic risk for autism resides with common variation

Kathryn Roeder, Ann B. Lee, Stephan Ripke, 2014, Nature Genetics.

The impact of the metabotropic glutamate receptor and other gene family interaction networks on autism

Thomas Bourgeron, Ellen M. Wijsman, Gillian Baird, 2014, Nature Communications.

Association study of 21 circadian genes with bipolar I disorder, schizoaffective disorder, and schizophrenia.

Matcheri Keshavan, Ellen Frank, David J Miklowitz, 2009, Bipolar disorders.

Genome-wide association study of corticobasal degeneration identifies risk variants shared with progressive supranuclear palsy

Murray Grossman, Jordan Grafman, Nilüfer Ertekin-Taner, 2015, Nature Communications.

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Jakob Grove, Anders D. Børglum, Aysu Okbay, 2016, Nature Genetics.

Association studies for quantitative traits in structured populations

Kathryn Roeder, Bernie Devlin, Silviu-Alin Bacanu, 2002, Genetic epidemiology.

Trajectories of cognitive decline in Alzheimer's disease

Oscar L Lopez, Bernie Devlin, B. Devlin, 2009, International Psychogeriatrics.

Outlier Detection and False Discovery Rates for Whole-Genome DNA Matching

Larry Wasserman, Kathryn Roeder, Jung-Ying Tzeng, 2003 .

GemTools: A fast and efficient approach to estimating genetic ancestry

Kathryn Roeder, Bernie Devlin, Lambertus Klei, 2011, 1104.1162.

Heterogeneous association between engrailed‐2 and autism in the CPEA network

Geraldine Dawson, Kristina Allen-Brady, Bernie Devlin, 2008, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Psychiatric genome-wide association study analyses implicate neuronal, immune and histone pathways

Laura J. Scott, Naomi R. Wray, Margaret A. Pericak-Vance, 2015, Nature Neuroscience.

Identification of genetic loci underlying the phenotypic constructs of autism spectrum disorders.

Ellen M Wijsman, Bernie Devlin, Edwin H Cook, 2011, Journal of the American Academy of Child and Adolescent Psychiatry.

Does Staying in School Make You Smarter

Stephen E. Fienberg, Kathryn Roeder, Christopher Winship, 1997 .

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Robert T. Schultz, Takeshi Sakurai, Joseph Piven, 2009, Nature.

Polygenic transmission disequilibrium confirms that common and rare variation act additively to create risk for autism spectrum disorders

Jakob Grove, Anders D. Børglum, Aysu Okbay, 2016 .

De novo insertions and deletions of predominantly paternal origin are associated with autism spectrum disorder.

Kathryn Roeder, Liping Wei, Jeanselle Dea, 2014, Cell reports.

Individual common variants exert weak effects on the risk for autism spectrum disorders

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2012, Human molecular genetics.

A genome-wide scan for common alleles affecting risk for autism

Margaret A. Pericak-Vance, Kathryn Roeder, Thomas Bourgeron, 2010, Human molecular genetics.

DAWN: a framework to identify autism genes and subnetworks using gene expression and genetics

Kathryn Roeder, Avi Ma’ayan, Mingfeng Li, 2014, Molecular Autism.

A network of dopaminergic gene variations implicated as risk factors for schizophrenia.

Michael E Talkowski, Bernie Devlin, Michael J Owen, 2008, Human molecular genetics.