Harvard Catalyst Profiles

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Richard Louis Maas, M.D.,Ph.D.

Co-Author

This page shows the publications co-authored by Richard Maas and Fowzan Alkuraya.
Connection Strength

0.844
  1. SUMO1 haploinsufficiency leads to cleft lip and palate. Science. 2006 Sep 22; 313(5794):1751.
    View in: PubMed
    Score: 0.339
  2. Identification of a Recognizable Progressive Skeletal Dysplasia Caused by RSPRY1 Mutations. Am J Hum Genet. 2015 Oct 01; 97(4):608-15.
    View in: PubMed
    Score: 0.158
  3. Deficiency of the cytoskeletal protein SPECC1L leads to oblique facial clefting. Am J Hum Genet. 2011 Jul 15; 89(1):44-55.
    View in: PubMed
    Score: 0.118
  4. Mutations in the RNA granule component TDRD7 cause cataract and glaucoma. Science. 2011 Mar 25; 331(6024):1571-6.
    View in: PubMed
    Score: 0.116
  5. NFIA haploinsufficiency is associated with a CNS malformation syndrome and urinary tract defects. PLoS Genet. 2007 May 25; 3(5):e80.
    View in: PubMed
    Score: 0.089
  6. Characterization of apparently balanced chromosomal rearrangements from the developmental genome anatomy project. Am J Hum Genet. 2008 Mar; 82(3):712-22.
    View in: PubMed
    Score: 0.023
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.
Funded by the NIH National Center for Advancing Translational Sciences through its Clinical and Translational Science Awards Program, grant number UL1TR002541.