Bradley P Coe
Bradley P Coe
Laboratory Scientist, BC Children's and Women's Hospital
Verified email at
Cited by
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Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations
BJ O’Roak, L Vives, S Girirajan, E Karakoc, N Krumm, BP Coe, R Levy, ...
Nature 485 (7397), 246-250, 2012
Genome structural variation discovery and genotyping
C Alkan, BP Coe, EE Eichler
Nature reviews genetics 12 (5), 363-376, 2011
A copy number variation morbidity map of developmental delay
GM Cooper, BP Coe, S Girirajan, JA Rosenfeld, TH Vu, C Baker, ...
Nature genetics 43 (9), 838-846, 2011
Multiplex targeted sequencing identifies recurrently mutated genes in autism spectrum disorders
BJ O’Roak, L Vives, W Fu, JD Egertson, IB Stanaway, IG Phelps, G Carvill, ...
Science 338 (6114), 1619-1622, 2012
A tiling resolution DNA microarray with complete coverage of the human genome
AS Ishkanian, CA Malloff, SK Watson, RJ DeLeeuw, B Chi, BP Coe, ...
Nature genetics 36 (3), 299-303, 2004
Disruptive CHD8 mutations define a subtype of autism early in development
R Bernier, C Golzio, B Xiong, HA Stessman, BP Coe, O Penn, ...
Cell 158 (2), 263-276, 2014
A higher mutational burden in females supports a “female protective model” in neurodevelopmental disorders
S Jacquemont, BP Coe, M Hersch, MH Duyzend, N Krumm, S Bergmann, ...
The American Journal of Human Genetics 94 (3), 415-425, 2014
Copy number variation detection and genotyping from exome sequence data
N Krumm, PH Sudmant, A Ko, BJ O'Roak, M Malig, BP Coe, AR Quinlan, ...
Genome research 22 (8), 1525-1532, 2012
Refining analyses of copy number variation identifies specific genes associated with developmental delay
BP Coe, K Witherspoon, JA Rosenfeld, BWM Van Bon, ...
Nature genetics 46 (10), 1063-1071, 2014
Excess of rare, inherited truncating mutations in autism
N Krumm, TN Turner, C Baker, L Vives, K Mohajeri, K Witherspoon, ...
Nature genetics 47 (6), 582-588, 2015
Phenotypic heterogeneity of genomic disorders and rare copy-number variants
S Girirajan, JA Rosenfeld, BP Coe, S Parikh, N Friedman, A Goldstein, ...
New England Journal of Medicine 367 (14), 1321-1331, 2012
Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases
HAF Stessman, BO Xiong, BP Coe, T Wang, K Hoekzema, M Fenckova, ...
Nature genetics 49 (4), 515-526, 2017
Global diversity, population stratification, and selection of human copy-number variation
PH Sudmant, S Mallick, BJ Nelson, F Hormozdiari, N Krumm, ...
Science 349 (6253), aab3761, 2015
Relative burden of large CNVs on a range of neurodevelopmental phenotypes
S Girirajan, Z Brkanac, BP Coe, C Baker, L Vives, TH Vu, N Shafer, ...
PLoS genetics 7 (11), e1002334, 2011
A SWI/SNF-related autism syndrome caused by de novo mutations in ADNP
C Helsmoortel, AT Vulto-van Silfhout, BP Coe, G Vandeweyer, L Rooms, ...
Nature genetics 46 (4), 380-384, 2014
Genomic patterns of de novo mutation in simplex autism
TN Turner, BP Coe, DE Dickel, K Hoekzema, BJ Nelson, MC Zody, ...
Cell 171 (3), 710-722. e12, 2017
De novo genic mutations among a Chinese autism spectrum disorder cohort
T Wang, H Guo, B Xiong, HAF Stessman, H Wu, BP Coe, TN Turner, Y Liu, ...
Nature communications 7 (1), 13316, 2016
Refinement and discovery of new hotspots of copy-number variation associated with autism spectrum disorder
S Girirajan, MY Dennis, C Baker, M Malig, BP Coe, CD Campbell, K Mark, ...
The American Journal of Human Genetics 92 (2), 221-237, 2013
Estimates of penetrance for recurrent pathogenic copy-number variations
JA Rosenfeld, BP Coe, EE Eichler, H Cuckle, LG Shaffer
Genetics in Medicine 15 (6), 478-481, 2013
Neurodevelopmental disease genes implicated by de novo mutation and copy number variation morbidity
BP Coe, HAF Stessman, A Sulovari, MR Geisheker, TE Bakken, AM Lake, ...
Nature genetics 51 (1), 106-116, 2019
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