Author

Jason A. O’Rawe

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Genetics· 1

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Research Focus:database / resource· 1 Research Focus:differential expression· 1 Approach:experimental assay· 1 Research Focus:gene regulatory network inference· 1 Organism:human· 1 Research Focus:variant calling· 1 Assay:whole-genome sequencing· 1

Frequent Co-Authors

David Mittelman· 1 shared Gareth Highnam· 1 shared Gholson J. LyoniD· 1 shared Han FangiD· 1 shared Laura T. Jiménez-Barrón· 1 shared Margaret Yoon· 1 shared Yiyang Wu· 1 shared

Activity by Year

2015-2015 · peak 1/yr

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7 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

David Mittelman

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1 paper

Recent·Most cited

GeneticsbioRxivPreprintMay 11, 2015

Whole genome analysis of an extended pedigree with Prader–Willi Syndrome, hereditary hemochromatosis, and dysautonomia-like symptoms

Han Fang, Yiyang Wu, Margaret Yoon…·Gholson J. Lyon

This paper reports whole genome sequencing of a family with PWS, HH, and dysautonomia-like symptoms, identifying genetic variants and highlighting the importance of standardized phenotypic and genomic data.

DOI 10.1101/019182

humanwhole-genome sequencing

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