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Bradley P. Coe

Women's Hospital(US)Bayhealth Foundation(US)CS Diagnostics(DE)Drexel University(US)

Publications by Year

Research Areas

Genomic variations and chromosomal abnormalities, Genomics and Rare Diseases, Genetics and Neurodevelopmental Disorders, Autism Spectrum Disorder Research, Cancer Genomics and Diagnostics

Most-Cited Works

→ Sporadic autism exomes reveal a highly interconnected protein network of de novo mutations(2012)2,212 cited
→ Genome structural variation discovery and genotyping(2011)1,696 cited
→ A copy number variation morbidity map of developmental delay(2011)1,390 cited
→ Multiplex Targeted Sequencing Identifies Recurrently Mutated Genes in Autism Spectrum Disorders(2012)1,283 cited
→ Disruptive CHD8 Mutations Define a Subtype of Autism Early in Development(2014)800 cited
→ Refining analyses of copy number variation identifies specific genes associated with developmental delay(2014)744 cited
→

Copy number variation detection and genotyping from exome sequence data

(2012)

668 cited

→ A tiling resolution DNA microarray with complete coverage of the human genome(2004)629 cited

→ Excess of rare, inherited truncating mutations in autism(2015)628 cited

→ Phenotypic Heterogeneity of Genomic Disorders and Rare Copy-Number Variants(2012)626 cited