Header Logo

Connection

Swapan Nath to Genes, Dominant

This is a "connection" page, showing publications Swapan Nath has written about Genes, Dominant.
Connection Strength

0.299
  1. Genome-wide linkage and copy number variation analysis reveals 710 kb duplication on chromosome 1p31.3 responsible for autosomal dominant omphalocele. J Med Genet. 2012 Apr; 49(4):270-6.
    View in: PubMed
    Score: 0.098
  2. Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing. Invest Ophthalmol Vis Sci. 2011 Aug 29; 52(9):6814-9.
    View in: PubMed
    Score: 0.094
  3. Ectrodactyly with aplasia of long bones (OMIM; 119100) in a large inbred Arab family with an apparent autosomal dominant inheritance and reduced penetrance: clinical and genetic analysis. Am J Med Genet A. 2006 Jul 01; 140(13):1440-6.
    View in: PubMed
    Score: 0.066
  4. Hidradenitis suppurativa (or Acne inversa) with autosomal dominant inheritance is not linked to chromosome 1p21.1-1q25.3 region. Exp Dermatol. 2010 Sep; 19(9):851-3.
    View in: PubMed
    Score: 0.022
  5. Linkage disequilibrium analysis of biallelic DNA markers, human quantitative trait loci, and threshold-defined case and control subjects. Am J Hum Genet. 2000 Nov; 67(5):1208-18.
    View in: PubMed
    Score: 0.011
  6. Schizophrenia susceptibility loci on chromosomes 13q32 and 8p21. Nat Genet. 1998 Sep; 20(1):70-3.
    View in: PubMed
    Score: 0.010
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.