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Connection

Amanda Krause to Founder Effect

This is a "connection" page, showing publications Amanda Krause has written about Founder Effect.
Connection Strength

0,981
  1. Common and Founder Mutations for Monogenic Traits in Sub-Saharan African Populations. Annu Rev Genomics Hum Genet. 2018 08 31; 19:149-175.
    View in: PubMed
    Score: 0,617
  2. Endocrine profiling in patients with Fanconi anemia, homozygous for a FANCG founder mutation. Mol Genet Genomic Med. 2020 08; 8(8):e1351.
    View in: PubMed
    Score: 0,174
  3. Phenotypic consequences in black South African Fanconi anemia patients homozygous for a founder mutation. Genet Med. 2014 May; 16(5):400-6.
    View in: PubMed
    Score: 0,110
  4. Feasibility of prenatal diagnosis and carrier detection in South African haemophilia A patients. Br J Haematol. 1997 Jun; 97(3):558-60.
    View in: PubMed
    Score: 0,035
  5. Clinical and genetic characterization of a founder PKHD1 mutation in Afrikaners with ARPKD. Pediatr Nephrol. 2015 Feb; 30(2):273-9.
    View in: PubMed
    Score: 0,029
  6. A common Fanconi anemia mutation in black populations of sub-Saharan Africa. Blood. 2005 May 01; 105(9):3542-4.
    View in: PubMed
    Score: 0,015
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.