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Sarah E. Calvo, Ph.D.

Co-Author

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This page shows the publications co-authored by Sarah Calvo and Jeremy Schmahmann.
Sarah Calvo
Connection Strength
0.102
Jeremy Schmahmann
  1. Next generation sequencing with copy number variant detection expands the phenotypic spectrum of HSD17B4-deficiency. BMC Med Genet. 2014 Mar 06; 15:30.
    View in: PubMed
    Score: 0.037
  2. Targeted exome sequencing of suspected mitochondrial disorders. Neurology. 2013 May 07; 80(19):1762-70.
    View in: PubMed
    Score: 0.034
  3. Atypical case of Wolfram syndrome revealed through targeted exome sequencing in a patient with suspected mitochondrial disease. BMC Med Genet. 2012 Jan 06; 13:3.
    View in: PubMed
    Score: 0.031
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.
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Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.