Devlin, Bernie

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

Liu, L., Sabo, A., Neale, B. M., Nagaswamy, U., Stevens, C., Lim, E., Bodea, C. A., Muzny, D., Reid, J. G., Banks, E., et al. (2013) · PLoS Genetics

Autism Spectrum Disorder ResearchGenomics and Rare Diseases

Cited by 135

On the Use of General Control Samples for Genome-wide Association Studies: Genetic Matching Highlights Causal Variants

Luca, D., Ringquist, S., Klei, L., Lee, A. B., Gieger, C., Wichmann, H.-E., Schreiber, S., Krawczak, M., Lu, Y., Styche, A., et al. (2008) · The American Journal of Human Genetics

Genetic Associations and EpidemiologyGenetic Mapping and Diversity in Plants and Animals

Cited by 128

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

Kaye, W. H., Lilenfeld, L. R., Berrettini, W. H., Strober, M., Devlin, B., Klump, K. L., Goldman, D., Bulik, C. M., Halmi, K. A., Fichter, M. M., et al. (2000) · Biological Psychiatry

Eating Disorders and BehaviorsGenetic Associations and Epidemiology

Cited by 116

Discovering genetic ancestry using spectral graph theory

Lee, A. B., Luca, D., Klei, L., Devlin, B., & Roeder, K. (2010) · Genetic Epidemiology

Forensic and Genetic ResearchGenetic Associations and Epidemiology

Cited by 108

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

Devlin, B., Melhem, N., & Roeder, K. (2011) · Brain Research

Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology

Cited by 105

Common risk variants identified in autism spectrum disorder

Grove, J., Ripke, S., Als, T. D., Mattheisen, M., Walters, R., Won, H., Pallesen, J., Agerbo, E., Andreassen, O. A., Anney, R., et al. (2017) · bioRxiv (Cold Spring Harbor Laboratory)

Autism Spectrum Disorder ResearchGenetic Associations and Epidemiology

Cited by 89

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

Gilbert, A. R., Akkal, D., Almeida, J. R. C., Mataix-Cols, D., Kalas, C., Devlin, B., Birmaher, B., & Phillips, M. L. (2009) · Journal of the American Academy of Child & Adolescent Psychiatry

Obsessive-Compulsive Spectrum DisordersNeural and Behavioral Psychology Studies

Cited by 86

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

Gamsiz, E. D., Viscidi, E. W., Frederick, A. M., Nagpal, S., Sanders, S. J., Murtha, M. T., Schmidt, M., Triche, E. W., Geschwind, D. H., State, M. W., et al. (2013) · The American Journal of Human Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 79

Genome-wide association identifies the first risk loci for psychosis in Alzheimer disease

DeMichele-Sweet, M. A. A., Klei, L., Creese, B., Harwood, J. C., Weamer, E. A., McClain, L., Sims, R., Hernandez, I., Moreno-Grau, S., Tárraga, L., et al. (2021) · Molecular Psychiatry

Dementia and Cognitive Impairment ResearchAlzheimer's disease research and treatments

Cited by 64

Modest Impact on Risk for Autism Spectrum Disorder of Rare Copy Number Variants at 15 q 11.2, Specifically Breakpoints 1 to 2

Chaste, P., Sanders, S. J., Mohan, K. N., Klei, L., Song, Y., Murtha, M. T., Hus, V., Lowe, J. K., Willsey, A. J., Moreno‐De‐Luca, D., et al. (2014) · Autism Research

Genomic variations and chromosomal abnormalitiesAutism Spectrum Disorder Research

Cited by 61

Heritable variation, with little or no maternal effect, accounts for recurrence risk to autism spectrum disorder in Sweden

Yip, B. H. K., Bai, D., Mahjani, B., Klei, L., Pawitan, Y., Hultman, C. M., Grice, D. E., Roeder, K., Buxbaum, J. D., Devlin, B., et al. (2018) · Biological Psychiatry

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 46

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

Brune, C. W., Korvatska, E., Allen‐Brady, K., Cook, E. H., Dawson, G., Devlin, B., Estes, A., Hennelly, M., Hyman, S. L., McMahon, W. M., et al. (2008) · American Journal of Medical Genetics Part B: Neuropsychiatric Genetics

Autism Spectrum Disorder ResearchGenetics and Neurodevelopmental Disorders

Cited by 40

Maternal Effects as Causes of Risk for Obsessive-Compulsive Disorder

Mahjani, B., Klei, L., Hultman, C. M., Larsson, H., Devlin, B., Buxbaum, J. D., Sandin, S., & Grice, D. E. (2020) · Biological Psychiatry

Obsessive-Compulsive Spectrum DisordersGenetic Associations and Epidemiology

Cited by 36

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

Yurko, R., Roeder, K., Devlin, B., & G'Sell, M. (2021) · Annals of Human Genetics

Genetic Associations and EpidemiologyBioinformatics and Genomic Networks

Cited by 23

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

Crossett, A., Kent, B. P., Klei, L., Ringquist, S., Trucco, M., Roeder, K., & Devlin, B. (2010) · Statistics in Medicine

Genetic Associations and EpidemiologyForensic and Genetic Research

Cited by 15