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Connection

Kevin Strauss to Genetic Diseases, Inborn

This is a "connection" page, showing publications Kevin Strauss has written about Genetic Diseases, Inborn.
Connection Strength

1.075
  1. Williams KB, Brigatti KW, Puffenberger EG, Gonzaga-Jauregui C, Griffin LB, Martinez ED, Wenger OK, Yoder MA, Kandula VVR, Fox MD, Demczko MM, Poskitt L, Furuya KN, Reid JG, Overton JD, Baras A, Miles L, Radhakrishnan K, Carson VJ, Antonellis A, Jinks RN, Strauss KA. Homozygosity for a mutation affecting the catalytic domain of tyrosyl-tRNA synthetase (YARS) causes multisystem disease. Hum Mol Genet. 2019 02 15; 28(4):525-538.
    View in: PubMed
    Score: 0.628
  2. Strauss KA, Puffenberger EG, Morton DH. One community's effort to control genetic disease. Am J Public Health. 2012 Jul; 102(7):1300-6.
    View in: PubMed
    Score: 0.393
  3. Morton DH, Morton CS, Strauss KA, Robinson DL, Puffenberger EG, Hendrickson C, Kelley RI. Pediatric medicine and the genetic disorders of the Amish and Mennonite people of Pennsylvania. Am J Med Genet C Semin Med Genet. 2003 Aug 15; 121C(1):5-17.
    View in: PubMed
    Score: 0.054
Connection Strength

The connection strength for concepts is the sum of the scores for each matching publication.

Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.