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Vandana Gupta, Ph.D.

Co-Author

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This page shows the publications co-authored by Vandana Gupta and Fowzan Alkuraya.
Vandana Gupta
Connection Strength
0.607
Fowzan Alkuraya
  1. GOLGA2, encoding a master regulator of golgi apparatus, is mutated in a patient with a neuromuscular disorder. Hum Genet. 2016 Feb; 135(2):245-251.
    View in: PubMed
    Score: 0.162
  2. Mutation of the mitochondrial carrier SLC25A42 causes a novel form of mitochondrial myopathy in humans. Hum Genet. 2016 Jan; 135(1):21-30.
    View in: PubMed
    Score: 0.160
  3. ZBTB42 mutation defines a novel lethal congenital contracture syndrome (LCCS6). Hum Mol Genet. 2014 Dec 15; 23(24):6584-93.
    View in: PubMed
    Score: 0.146
  4. Identification of KLHL41 Mutations Implicates BTB-Kelch-Mediated Ubiquitination as an Alternate Pathway to Myofibrillar Disruption in Nemaline Myopathy. Am J Hum Genet. 2013 Dec 05; 93(6):1108-17.
    View in: PubMed
    Score: 0.139
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.
© 2022 President and Fellows of Harvard College
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.