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Connection

Evgeny Rogaev to Mutation, Missense

This is a "connection" page, showing publications Evgeny Rogaev has written about Mutation, Missense.
Connection Strength

1.880
  1. Manakhov AD, Mintseva MY, Andreeva TV, Trapezov OV, Rogaev EI. Shadow coat colour in American mink associated with a missense mutation in the KIT gene. Anim Genet. 2022 Aug; 53(4):522-525.
    View in: PubMed
    Score: 0.741
  2. Andreeva TV, Tyazhelova TV, Rykalina VN, Gusev FE, Goltsov AY, Zolotareva OI, Aliseichik MP, Borodina TA, Grigorenko AP, Reshetov DA, Ginter EK, Amelina SS, Zinchenko RA, Rogaev EI. Whole exome sequencing links dental tumor to an autosomal-dominant mutation in ANO5 gene associated with gnathodiaphyseal dysplasia and muscle dystrophies. Sci Rep. 2016 05 24; 6:26440.
    View in: PubMed
    Score: 0.491
  3. Protasova MS, Grigorenko AP, Tyazhelova TV, Andreeva TV, Reshetov DA, Gusev FE, Laptenko AE, Kuznetsova IL, Goltsov AY, Klyushnikov SA, Illarioshkin SN, Rogaev EI. Whole-genome sequencing identifies a novel ABCB7 gene mutation for X-linked congenital cerebellar ataxia in a large family of Mongolian ancestry. Eur J Hum Genet. 2016 Apr; 24(4):550-5.
    View in: PubMed
    Score: 0.465
  4. Rogaev EI. Different Pathways to Neurodegeneration. Biochemistry (Mosc). 2018 Sep; 83(9):1007-1008.
    View in: PubMed
    Score: 0.144
  5. Rogaev EI, Zinchenko RA, Dvoryachikov G, Sherbatich T, Ginter EK. Total hypotrichosis: genetic form of alopecia not linked to hairless gene. Lancet. 1999 Sep 25; 354(9184):1097-8.
    View in: PubMed
    Score: 0.039
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.