B. Devlin

B. Devlin, S. Bacanu, A. Bergen, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Mixture models for linkage analysis of affected sibling pairs and covariates

K. Roeder, B. Devlin, S. Bacanu, 2002, Genetic epidemiology.

Unbiased methods for population‐based association studies

K. Roeder, B. Devlin, S. Bacanu, 2001, Genetic epidemiology.

Using Dimension Reduction Techniques to Model Genetic Relationships for Association Studies Thesis Proposal for

Ann B. Lee, A. Rinaldo, B. Devlin, 2010 .

Sex Differences in the Human Brain Transcriptome of Cases With Schizophrenia

Kelsey S. Montgomery, B. Devlin, A. Chess, 2020, Biological Psychiatry.

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

Ryan L. Collins, Ryan M. Layer, Jeffrey D. Mandell, 2018, Nature Genetics.

Refining the role of de novo protein truncating variants in neurodevelopmental disorders using population reference samples

Stephan J Sanders, K. Roeder, M. Daly, 2016, Nature Genetics.

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.

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.

An interactome perturbation framework prioritizes damaging missense mutations for developmental disorders

K. Roeder, L. Klei, B. Devlin, 2018, Nature Genetics.

Global landscape and genetic regulation of RNA editing in cortical samples from individuals with schizophrenia

Kelsey S. Montgomery, David Bruce Lewis, L. Klei, 2019, Nature Neuroscience.

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.

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

Hae Kyung Im, Solveig K Sieberts, Kiran Girdhar, 2019, Nature Genetics.

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.

Genetic Risk for Schizophrenia and Psychosis in Alzheimer Disease

B Devlin, L. Klei, B. Devlin, 2017, Molecular Psychiatry.

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

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

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

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

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

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

Identifying tissues implicated in Anorexia Nervosa using Transcriptomic Imputation

Hunna J. Watson, I. Ntalla, E. Zeggini, 2018, bioRxiv.

Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS

Benjamin A. Logsdon, Kristen K. Dang, Benjamin S. Glicksberg, 2018, American journal of human genetics.

Of Genes and IQ

K. Roeder, B. Devlin, Michael J. Daniels, 1997 .

Association study of brain‐derived neurotrophic factor in adults with a history of childhood onset mood disorder

B Devlin, B. Devlin, J. Kennedy, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Systematic evaluation of genome sequencing as a first-tier diagnostic test for prenatal and pediatric disorders

Ryan L. Collins, Stephan J Sanders, D. MacArthur, 2020 .

The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer’s disease

B. Devlin, G. Schellenberg, J. Trojanowski, 2013, Acta Neuropathologica Communications.

Functional annotation of rare structural variation in the human brain

Kelsey S. Montgomery, P. Sullivan, L. Klei, 2020, Nature Communications.

Investigating Shared Genetic Basis Across Tourette Syndrome and Comorbid Neurodevelopmental Disorders Along the Impulsivity-Compulsivity Spectrum

N. Wray, B. Franke, B. Devlin, 2021, Biological Psychiatry.

Gene expression imputation across multiple brain regions reveals schizophrenia risk throughout development

Hoang T. Nguyen, M. O’Donovan, P. Sullivan, 2017, bioRxiv.

Resting-State Functional Network Organization Is Stable Across Adolescent Development for Typical and Psychosis Spectrum Youth.

K. Roeder, B. Devlin, B. Luna, 2019, Schizophrenia bulletin.

De novo structural mutation rates and gamete-of-origin biases revealed through genome sequencing of 2,396 families

Brent S. Pedersen, Jonathan R. Belyeu, Thomas J. Nicholas, 2020, bioRxiv.

A selective inference approach for false discovery rate control using multiomics covariates yields insights into disease risk

K. Roeder, B. Devlin, Max G'sell, 2020, Proceedings of the National Academy of Sciences.

How rare and common risk variation jointly affect liability for autism spectrum disorder

K. Roeder, L. Klei, J. Buxbaum, 2020, Molecular Autism.

Dynamic landscape and genetic regulation of RNA editing in schizophrenia

J. Buxbaum, B. Devlin, A. Chess, 2018, bioRxiv.

Co-localization of Conditional eQTL and GWAS Signatures in Schizophrenia

D. Pinto, B. Devlin, P. Sklar, 2017, bioRxiv.

Analysis of Shared Haplotypes amongst Palauans Maps Loci for Psychotic Disorders to 4q28 and 5q23-q31

K. Roeder, L. Klei, B. Devlin, 2016, Molecular Neuropsychiatry.

Application of post-selection inference to multi-omics data yields insights into the etiologies of human diseases

K. Roeder, B. Devlin, Max G'sell, 2019, bioRxiv.

Cross-disorder GWAS meta-analysis for Attention Deficit/Hyperactivity Disorder, Autism Spectrum Disorder, Obsessive Compulsive Disorder, and Tourette Syndrome

N. Wray, M. Daly, B. Franke, 2019 .

Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5‐years apart

Finnegan J. Calabro, K. Roeder, L. Klei, 2020, Human brain mapping.

Cognitive and default mode networks support developmental stability in functional connectome fingerprinting through adolescence

Finnegan J. Calabro, K. Roeder, L. Klei, 2019, bioRxiv.

Functional connectome fingerprinting accuracy in youths and adults is similar when examined on the same day and 1.5 years apart

K. Roeder, L. Klei, B. Devlin, 2020 .

Rare Copy Number Variants in Tourette Syndrome Disrupt Genes in Histaminergic Pathways and Overlap with Autism

Joseph T. Glessner, Stephan J Sanders, J. Glessner, 2012, Biological Psychiatry.

Adjusting Head Circumference for Covariates in Autism: Clinical Correlates of a Highly Heritable Continuous Trait

Stephan J Sanders, Donna M. Martin, D. Ledbetter, 2013, Biological Psychiatry.

Heritable Variation, With Little or No Maternal Effect, Accounts for Recurrence Risk to Autism Spectrum Disorder in Sweden

K. Roeder, L. Klei, J. Buxbaum, 2017, Biological Psychiatry.

Cohort profile: Epidemiology and Genetics of Obsessive–compulsive disorder and chronic tic disorders in Sweden (EGOS)

L. Klei, J. Buxbaum, B. Devlin, 2020, Social Psychiatry and Psychiatric Epidemiology.

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

Ryan L. Collins, Gabor T. Marth, Stephan J Sanders, 2018, Science.

Limited contribution of rare, noncoding variation to autism spectrum disorder from sequencing of 2,076 genomes in quartet families

Ryan L. Collins, Ryan M. Layer, Gabor T. Marth, 2017, bioRxiv.

No association of psychosis in Alzheimer disease with neurodegenerative pathway genes

L. Klei, B. Devlin, R. Sweet, 2011, Neurobiology of Aging.

Alcohol use disorder comorbidity in eating disorders: a multicenter study.

B. Devlin, C. Bulik, L. Thornton, 2004, The Journal of clinical psychiatry.

Genome-Wide Association Identifies the First Risk Loci for Psychosis in Alzheimer Disease

S. Djurovic, O. Andreassen, L. Klei, 2020, Molecular Psychiatry.

Multiple Recurrent De Novo Copy Number Variations , Including Duplications of the 7 q 11 . 23 Williams-Beuren Syndrome Region , Are Associated with Autism

Rebecca, Michael J. DiCola, Stephan J Sanders, 2011 .

A UNIFIED STATISTICAL FRAMEWORK FOR SINGLE CELL AND BULK RNA SEQUENCING DATA.

K. Roeder, B. Devlin, Jing Lei, 2016, The annals of applied statistics.

The genetic architecture of obsessive-compulsive disorder: alleles across the frequency spectrum contribute liability to OCD

K. Roeder, L. Klei, J. Buxbaum, 2021, medRxiv.

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.

Principal Components of Heritability From Neurocognitive Domains Differ Between Families With Schizophrenia and Control Subjects

L. Klei, B. Devlin, R. Gur, 2012, Schizophrenia bulletin.

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

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

Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder

L. Klei, J. Buxbaum, B. Devlin, 2020, Biological Psychiatry.

Not All Autism Genes Are Created Equal: A Response to Myers et al.

Stephan J Sanders, K. Roeder, M. Daly, 2020, American journal of human genetics.

Title : Genetic maternal effects contributes to the risk of Tourette ' s disorder

L. Klei, J. Buxbaum, B. Devlin, 2020 .

Shedding new light on genetic dark matter

B. Devlin, N. Melhem, 2010, Genome Medicine.

Schizophrenia-associated differential DNA methylation in brain is distributed across the genome and annotated to MAD1L1, a locus at which DNA methylation and transcription phenotypes share genetic variation with schizophrenia risk

L. Klei, B. Devlin, Jiebiao Wang, 2022, Translational Psychiatry.

Rare coding variation provides insight into the genetic architecture and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2022, Nature Genetics.

Systematic evaluation of genome sequencing for the assessment of fetal structural anomalies

Ryan L. Collins, Jack M. Fu, Christopher W. Whelan, 2020, bioRxiv.

A framework for the interpretation of de novo mutation in human disease

Stephan J Sanders, K. Roeder, M. DePristo, 2014, Nature Genetics.

Prevalence and Phenotypic Impact of Rare Likely Pathogenic Variants in Autism Spectrum Disorder

Jack M. Fu, K. Roeder, L. Klei, 2020 .

Not All Autism Genes Are Created Equal: A Response to Myers et al.

Stephan J Sanders, K. Roeder, M. Daly, 2020, American journal of human genetics.

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

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

Comment on: What genes are differentially expressed in individuals with schizophrenia? A systematic review

D. Geschwind, B. Devlin, D. Weinberger, 2022, Molecular Psychiatry.

Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk

B. Devlin, F. Dickerson, R. Yolken, 2007, Schizophrenia Research.

Most genetic risk for autism resides with common variation

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

Semisoft clustering of single-cell data

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

Semi-soft Clustering of Single Cell Data

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

Evaluation of a Susceptibility Gene for Schizophrenia: Genotype Based Meta-Analysis of RGS4 Polymorphisms from Thirteen Independent Samples

D. Collier, D. Clair, G. Kirov, 2006, Biological Psychiatry.

Trajectories of cognitive decline in Alzheimer's disease

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

Meta-analysis of GWAS of over 16,000 individuals with autism spectrum disorder highlights a novel locus at 10q24.32 and a significant overlap with schizophrenia

Christopher S. Poultney, Stephan J Sanders, Stephen J. Guter, 2017, Molecular Autism.

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.

Genome-wide association study identifies new locus associated with OCD

Dan J Stein, Ben D. Greenberg, M. S. Artigas, 2021, medRxiv.

H‐MAGMA, inheriting a shaky statistical foundation, yields excess false positives

K. Roeder, B. Devlin, Ronald Yurko, 2020, Annals of human genetics.

H-MAGMA, inheriting a shaky statistical foundation, yields excess false positives

K. Roeder, B. Devlin, Ronald Yurko, 2020, bioRxiv.

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

Kathryn Roeder, Ronald Yurko, Bernie Devlin, 2019 .

Patterns and rates of exonic de novo mutations in autism spectrum disorders

Evan T. Geller, Emily L. Crawford, K. Roeder, 2012, Nature.

Age dependent association of inbreeding with risk for schizophrenia in Egypt

L. Klei, Shawn Wood, B. Devlin, 2020, Schizophrenia Research.

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

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

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.

Rare coding variation illuminates the allelic architecture, risk genes, cellular expression patterns, and phenotypic context of autism

Ryan L. Collins, Jack M. Fu, Stephan J Sanders, 2021, medRxiv.

The Yin and Yang of Autism Genetics: How Rare De Novo and Common Variations Affect Liability.

K. Roeder, B. Devlin, P. Chaste, 2017, Annual review of genomics and human genetics.

Architecture of the Genetic Risk for Autism

B. Devlin, P. Chaste, 2015 .

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.

Transcriptional consequences of 16p11.2 deletion and duplication in mouse cortex and multiplex autism families.

K. Roeder, J. Levin, L. Klei, 2014, American journal of human genetics.

Whole exome sequencing reveals minimal differences between cell line and whole blood derived DNA.

K. Roeder, M. Daly, Seungtai Yoon, 2013, Genomics.

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.

De Novo Insertions and Dele tions of Predominantly Paternal Origin Are Associated with Autism Spectrum Disorder Graphical

Jeffrey D. Mandell, Michael F. Walker, Michael J. DiCola, 2022 .

Intellectual disability is associated with increased runs of homozygosity in simplex autism.

Stephan J Sanders, D. Geschwind, E. Cook, 2013, American journal of human genetics.

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

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

Identification of common genetic risk variants for autism spectrum disorder

Alicia R. Martin, K. Roeder, M. Daly, 2019, Nature Genetics.

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.

Exome Analyses Reveal New Autism Genes in Synaptic, Transcriptional, and Chromatin Networks Supplementary Methods

Christopher S. Poultney, Stephan J Sanders, Evan T. Geller, 2022 .

Prevalence and phenotypic impact of rare potentially damaging variants in autism spectrum disorder

Jack M. Fu, K. Roeder, L. Klei, 2021, Molecular Autism.

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

M. Owen, M. O’Donovan, P. Sullivan, 2019, Nature Genetics.

Large eQTL meta-analysis reveals differing patterns between cerebral cortical and cerebellar brain regions

Kara H. Woo, Cory C. Funk, Kelsey S. Montgomery, 2020, Scientific Data.

Genetic analysis of bulimia nervosa: methods and sample description.

B. Devlin, S. Bacanu, A. Bergen, 2004, The International journal of eating disorders.

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

K. Roeder, B. Devlin, Ronald Yurko, 2021, bioRxiv.

Association studies for quantitative traits in structured populations

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

CommonMind Consortium provides transcriptomic and epigenomic data for Schizophrenia and Bipolar Disorder

Kelsey S. Montgomery, P. Sullivan, J. Buxbaum, 2019, Scientific Data.

The MAOA promoter polymorphism, disruptive behavior disorders, and early onset substance use disorder: gene–environment interaction

B. Devlin, B. Maher, R. Ferrell, 2007, Psychiatric genetics.

Amino Acid Position 11 of HLA-DRβ1 is a Major Determinant of Chromosome 6p Association with Ulcerative Colitis

K. Roeder, L. Klei, B. Devlin, 2011, Genes and Immunity.

Expansion of RNA sequence diversity and RNA editing rates throughout human cortical development

Stephan J Sanders, K. Roeder, J. Buxbaum, 2021, bioRxiv.

Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15q11.2, Specifically Breakpoints 1 to 2

Stephan J Sanders, Donna M. Martin, D. Ledbetter, 2014, Autism research : official journal of the International Society for Autism Research.

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

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

ADLAPH: A molecular haplotyping method based on allele-discriminating long-range PCR.

B. Devlin, G. Schellenberg, Chang-En Yu, 2004, Genomics.

Convergent patterns of association between phenylalanine hydroxylase variants and schizophrenia in four independent samples

G. Kirov, M. Owen, M. O’Donovan, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Population-level variation in enhancer expression identifies disease mechanisms in the human brain

Kelsey S. Montgomery, L. Klei, J. Buxbaum, 2022, Nature Genetics.

Statistical and functional convergence of common and rare genetic influences on autism at chromosome 16p

Evan Z. Macosko, Jack M. Fu, Jessica B. Girault, 2022, Nature Genetics.

Variations in Genes Related to Sleep Patterns in Children With Autism Spectrum Disorder

B. Devlin, J. Dorman, E. Chasens, 2019, Biological research for nursing.

New mutations, old statistical challenges

P. Visscher, N. Wray, K. Roeder, 2017, bioRxiv.

Haplotypes of the monoamine oxidase genes and the risk for substance use disorders

B. Devlin, B. Maher, R. Ferrell, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Joint evaluation of serum C-Reactive Protein levels and polygenic risk scores as risk factors for schizophrenia

L. Klei, B. Devlin, F. Dickerson, 2018, Psychiatry Research.

Transcriptomic Imputation of Bipolar Disorder and Bipolar subtypes reveals 29 novel associated genes

Hoang T. Nguyen, B. Devlin, E. Gamazon, 2017, bioRxiv.

Consanguinity associated with increased risk for bipolar I disorder in Egypt

L. Klei, B. Devlin, M. Talkowski, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Bayesian estimation of cell type–specific gene expression with prior derived from single-cell data

K. Roeder, B. Devlin, Jiebiao Wang, 2021, Genome research.

Heritability of fearful-anxious endophenotypes in infant rhesus macaques: a preliminary report

Silviu-Alin Bacanu, Neal D Ryan, B. Devlin, 2003, Biological Psychiatry.

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.

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

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

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

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

A controlled family history study of childhood-onset depressive disorder.

B. Devlin, M. Kovács, P. Mukerji, 1997, Archives of general psychiatry.

Internalizing disorders in childhood.

B. Devlin, M. Kovács, 1998, Journal of child psychology and psychiatry, and allied disciplines.

Runs of homozygosity, copy number variation, and risk for depression and suicidal behavior in an Arab Bedouin kindred

L. Klei, Shawn Wood, B. Devlin, 2017, Psychiatric genetics.

Consanguinity and increased risk for schizophrenia in Egypt

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

Copy Number Variants for Schizophrenia and Related Psychotic Disorders in Oceanic Palau: Risk and Transmission in Extended Pedigrees

K. Roeder, L. Klei, B. Devlin, 2011, Biological Psychiatry.

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

D. Kupfer, B. Devlin, T. Monk, 2006, Genes, brain, and behavior.

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

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

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.

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.

Alleles of a reelin CGG repeat do not convey liability to autism in a sample from the CPEA network

G. Dawson, W. McMahon, N. Minshew, 2004, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

No evidence for linkage of liability to autism to HOXA1 in a sample from the CPEA network.

G. Dawson, W. McMahon, E. Cook, 2002, American journal of medical genetics.

Project among African-Americans to explore risks for schizophrenia (PAARTNERS): Recruitment and assessment methods

B. Devlin, J. Ragland, R. Gur, 2006, Schizophrenia Research.

Genome-Wide Association Identifies the First Risk Loci for Psychosis in Alzheimer Disease

S. Djurovic, O. Andreassen, L. Klei, 2020, Molecular Psychiatry.

REFINING GENETICALLY INFERRED RELATIONSHIPS USING TREELET COVARIANCE SMOOTHING.

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

Transcriptome alterations are enriched for synapse-associated genes in the striatum of subjects with obsessive-compulsive disorder

L. Klei, B. Devlin, Jiebiao Wang, 2020, bioRxiv.

Characterizing runs of homozygosity and their impact on risk for psychosis in a population isolate

K. Roeder, L. Klei, Shawn Wood, 2014, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Linkage analysis of anorexia nervosa incorporating behavioral covariates.

B. Devlin, S. Bacanu, C. Bulik, 2002, Human molecular genetics.

The genetics of anorexia nervosa collaborative study: methods and sample description.

B. Devlin, C. Bulik, L. Thornton, 2008, The International journal of eating disorders.

Association and linkage analyses of RGS4 polymorphisms in schizophrenia.

B. Devlin, F. Middleton, P. Levitt, 2002, Human molecular genetics.

Linkage disequilibrium mapping of the chromosome 6q21–22.31 bipolar I disorder susceptibility locus

B. Devlin, N. Laird, J. Calabrese, 2009, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The AVPR1A Gene and Substance Use Disorders: Association, Replication, and Functional Evidence

Vladimir I. Vladimirov, Shawn J Latendresse, P. Muglia, 2011, Biological Psychiatry.

Deriving behavioural phenotypes in an international, multi-centre study of eating disorders

B. Devlin, S. Bacanu, D. Goldman, 2001, Psychological Medicine.

Genetic liability to schizophrenia in Oceanic Palau: a search in the affected and maternal generation

K. Roeder, L. Klei, B. Devlin, 2007, Human Genetics.

Do common variants play a role in risk for autism? Evidence and theoretical musings

K. Roeder, B. Devlin, N. Melhem, 2011, Brain Research.

Neural correlates of symptom dimensions in pediatric obsessive-compulsive disorder: a functional magnetic resonance imaging study.

B. Devlin, M. Phillips, D. Akkal, 2009, Journal of the American Academy of Child and Adolescent Psychiatry.

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.

Circadian Phase Variation in Bipolar I Disorder

D. Kupfer, B. Devlin, M. Thase, 2005, Chronobiology international.

Association of FKBP5 polymorphisms with suicidal events in the Treatment of Resistant Depression in Adolescents (TORDIA) study.

B. Devlin, N. Ryan, B. Birmaher, 2010, The American journal of psychiatry.

Linkage analysis of schizophrenia in African-American families

L. Klei, B. Devlin, R. Gur, 2009, Schizophrenia Research.

Brain-derived neurotrophic factor variants are associated with childhood-onset mood disorder: confirmation in a Hungarian sample

B. Devlin, J. Kennedy, M. Kovács, 2005, Molecular Psychiatry.

Are exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia?

B. Devlin, R. Yolken, S. Bacanu, 2007, Annals of medicine.

Linkage analysis of a completely ascertained sample of familial schizophrenics and bipolars from Palau, Micronesia

L. Klei, B. Devlin, S. Bacanu, 2005, Human Genetics.

Psychotic symptoms in Alzheimer disease: evidence for a distinct phenotype

B. Devlin, D. Jeste, R. Sweet, 2003, Molecular Psychiatry.

Evaluation of HLA polymorphisms in relation to schizophrenia risk and infectious exposure.

L. Klei, B. Devlin, R. Yolken, 2012, Schizophrenia bulletin.

Catechol-O-methyltransferase haplotypes are associated with psychosis in Alzheimer disease

B. Devlin, B. Pollock, S. DeKosky, 2005, Molecular Psychiatry.

Genetics in psychiatry: common variant association studies

J. Buxbaum, B. Devlin, S. Baron-Cohen, 2010, Molecular autism.

Sequence variation in the primate dopamine transporter gene and its relationship to social dominance.

B. Devlin, S. Manuck, R. Ferrell, 2007, Molecular biology and evolution.

Personality in men with eating disorders.

B. Devlin, S. Bacanu, C. Bulik, 2004, Journal of psychosomatic research.

A Pleiotropic Missense Variant in SLC39A8 Is Associated With Crohn's Disease and Human Gut Microbiome Composition.

Judy H. Cho, M. Daly, L. Klei, 2016, Gastroenterology.

A pleiotropic missense variant in SLC 39 A 8 is associated with Crohn ’ s disease and human gut microbiome composition Short Title : SLC 39 A 8 associated with CD and gut microbiome

Judy H. Cho, M. Daly, L. Klei, 2016 .

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

Kristen K. Dang, D. A. Lewis, C. Spencer, 2019, Nature Genetics.

G-BLUP Prediction of ASD Risk 3 . 1 Linear Random Effects Model

K. Roeder, B. Devlin, Lingxue Zhu, 2017 .

Persistent infection with neurotropic herpes viruses and cognitive impairment

L. Klei, B. Devlin, R. Yolken, 2012, Psychological Medicine.

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.

GemTools: A fast and efficient approach to estimating genetic ancestry

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

Novel, Replicated Associations Between Dopamine D3 Receptor Gene Polymorphisms and Schizophrenia in Two Independent Samples

B. Devlin, M. Talkowski, B. Thelma, 2006, Biological Psychiatry.

Avoiding stratification in association studies

K. Roeder, B. Devlin, 2005 .

Genomic control for association studies: a semiparametric test to detect excess-haplotype sharing.

B Devlin, K Roeder, L Wasserman, 2000, Biostatistics.

Heritability of functioning in families with schizophrenia in relation to neurocognition

B. Devlin, R. Gur, M. Calkins, 2012, Schizophrenia Research.

Linkage analysis of anorexia and bulimia nervosa cohorts using selected behavioral phenotypes as quantitative traits or covariates

B. Devlin, S. Bacanu, A. Bergen, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

TOMM40 poly-T repeat lengths, age of onset and psychosis risk in Alzheimer disease

K. Roeder, B. Devlin, R. Sweet, 2011, Neurobiology of Aging.

Linkage analysis of Alzheimer disease with psychosis

B. Devlin, S. DeKosky, S. Bacanu, 2002, Neurology.

Personality characteristics of women before and after recovery from an eating disorder

B. Devlin, C. Bulik, L. Thornton, 2004, Psychological Medicine.

29 BRAINVAR DATA SET: WHOLE-GENOME AND RNA SEQUENCING REVEAL VARIATION AND TRANSCRIPTOMIC COORDINATION IN THE DEVELOPING HUMAN PREFRONTAL CORTEX

Stephan J Sanders, K. Roeder, B. Devlin, 2019, European Neuropsychopharmacology.

Alcohol Use Disorder Comorbidity in Eating

B. Devlin, C. Bulik, L. Thornton, 2004 .

Temperament and character in women with anorexia nervosa.

Fichter, B. Devlin, M. Shabbout, 2000, The Journal of nervous and mental disease.

Increased familial risk of the psychotic phenotype of Alzheimer disease

B. Devlin, O. Lopez, S. DeKosky, 2002, Neurology.

Direct additive genetics and maternal effect contribute to the risk of Tourette disorder

L. Klei, J. Buxbaum, B. Devlin, 2023, Journal of Neurology, Neurosurgery, and Psychiatry.

Heritability of psychosis in Alzheimer disease.

B. Devlin, S. DeKosky, S. Bacanu, 2005, The American journal of geriatric psychiatry : official journal of the American Association for Geriatric Psychiatry.

Title No evidence for linkage of liability to autism to HOXA 1 in a sample from the CPEA network Permalink

G. Dawson, W. McMahon, E. Cook, 2002 .

Using linkage information to weight a genome‐wide association of bipolar disorder

B. Devlin, N. Laird, D. Howrigan, 2011, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

The unfolded protein response is activated in disease-affected brain regions in progressive supranuclear palsy and Alzheimer’s disease

B. Devlin, G. Schellenberg, J. Trojanowski, 2013, Acta neuropathologica communications.

Neuregulin‐1 polymorphism in late onset Alzheimer's disease families with psychoses

B. Devlin, D. Blacker, S. Bassett, 2005, American journal of medical genetics. Part B, Neuropsychiatric genetics : the official publication of the International Society of Psychiatric Genetics.

Incomplete response in late-life depression: getting to remission

B. Devlin, B. Pollock, B. Mulsant, 2008, Dialogues in Clinical Neuroscience.

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

Bernie Devlin, B. Devlin, 1997 .

Association of Multiple DRD2 Polymorphisms with Anorexia Nervosa

B. Devlin, M. Yeager, R. Welch, 2005, Neuropsychopharmacology.

Intelligence, Genes, and Success

S. Fienberg, K. Roeder, B. Devlin, 1997 .

Bayesian estimation of cell-type-specific gene expression per bulk sample with prior derived from single-cell data

K. Roeder, B. Devlin, Jiebiao Wang, 2020, bioRxiv.

Genetic maternal effects contributes to the risk of Tourette's disorder

L. Klei, J. Buxbaum, B. Devlin, 2020, medRxiv.