Steven G. Hershman, Ph.D.

Affiliations: 
2013 Systems Biology Harvard University, Cambridge, MA, United States 
Area:
Genetics, Bioinformatics Biology, Medicine and Surgery
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"Steven Hershman"

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Vamsi Mootha grad student 2013 Harvard
 (Personal Genomics and Mitochondrial Disease.)
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Publications

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Bianchi MT, Hershman S, Bahadoran M, et al. (2014) The challenge of undiagnosed sleep apnea in low-risk populations: a decision analysis. Military Medicine. 179: 47-54
Lieber DS, Hershman SG, Slate NG, et al. (2014) Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency. Bmc Medical Genetics. 15: 30
Lieber DS, Calvo SE, Shanahan K, et al. (2013) Targeted exome sequencing of suspected mitochondrial disorders. Neurology. 80: 1762-70
Calvo SE, Compton AG, Hershman SG, et al. (2012) Molecular diagnosis of infantile mitochondrial disease with targeted next-generation sequencing. Science Translational Medicine. 4: 118ra10
Tucker EJ, Hershman SG, Köhrer C, et al. (2011) Mutations in MTFMT underlie a human disorder of formylation causing impaired mitochondrial translation. Cell Metabolism. 14: 428-34
Ryvkin P, Hershman SG, Wang LS, et al. (2010) Computational approaches to the detection and analysis of sequences with intramolecular G-quadruplex forming potential. Methods in Molecular Biology (Clifton, N.J.). 608: 39-50
Hershman SG, Chen Q, Lee JY, et al. (2008) Genomic distribution and functional analyses of potential G-quadruplex-forming sequences in Saccharomyces cerevisiae. Nucleic Acids Research. 36: 144-56
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