Bernie Devlin - Researcher Profile | RDL Research Database

Publications

5 shown

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

Kaitlin E. Samocha , Elise Robinson , Stephan Sanders +23 more

2014 Nature Genetics 1091 citations

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

Jung‐Ying Tzeng , William Byerley , Bernie Devlin +2 more

We define a statistic, called the <em>matching statistic</em>, for locating regions of the genome that exhibit excess similarity among cases when compared to controls. Such regi...

2003 Journal of the American Statistical A... 33 citations

Combined Analysis from Eleven Linkage Studies of Bipolar Disorder Provides Strong Evidence of Susceptibility Loci on Chromosomes 6q and 8q

Matthew B. McQueen , Bernie Devlin , Stephen V. Faraone +50 more

2005 The American Journal of Human Genetics 244 citations

Identification of common genetic risk variants for autism spectrum disorder

Jakob Grove , Stephan Ripke , Thomas D. Als +73 more

2019 Nature Genetics 2404 citations

Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism

F. Kyle Satterstrom , Jack A. Kosmicki , Jiebiao Wang +97 more

2020 Cell 2225 citations

Frequent Co-Authors

Researcher Info

h-index: 5
Publications: 5
Citations: 5,997
Institution: University of Pittsburgh

External Links

ORCID Profile Google Scholar

Identifiers

ORCID: 0000-0003-2524-4290

Impact Metrics

h-index 5

h-index: Number of publications with at least h citations each.