Evgeny Rogaev to Mutation
This is a "connection" page, showing publications Evgeny Rogaev has written about Mutation.
Connection Strength
2.195
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Manakhov AD, Mintseva MY, Andreev IA, Uralsky LI, Andreeva TV, Trapezov OV, Rogaev EI. Genome analysis of American minks reveals link of mutations in Ras-related protein-38 gene to Moyle brown coat phenotype. Sci Rep. 2020 09 28; 10(1):15876.
Score: 0.406
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Manakhov AD, Andreeva TV, Rogaev EI. The curly coat phenotype of the Ural Rex feline breed is associated with a mutation in the lipase H gene. Anim Genet. 2020 Aug; 51(4):584-589.
Score: 0.396
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Manakhov AD, Andreeva TV, Trapezov OV, Kolchanov NA, Rogaev EI. Genome analysis identifies the mutant genes for common industrial Silverblue and Hedlund white coat colours in American mink. Sci Rep. 2019 03 14; 9(1):4581.
Score: 0.364
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Borinskaya S, Kal'ina N, Marusin A, Faskhutdinova G, Morozova I, Kutuev I, Koshechkin V, Khusnutdinova E, Stepanov V, Puzyrev V, Yankovsky N, Rogaev E. Distribution of the alcohol dehydrogenase ADH1B*47His allele in Eurasia. Am J Hum Genet. 2009 Jan; 84(1):89-92; author reply 92-4.
Score: 0.180
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Burmistrova OA, Goltsov AY, Abramova LI, Kaleda VG, Orlova VA, Rogaev EI. MicroRNA in schizophrenia: genetic and expression analysis of miR-130b (22q11). Biochemistry (Mosc). 2007 May; 72(5):578-82.
Score: 0.160
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Protasova MS, Andreeva TV, Klyushnikov SA, Illarioshkin SN, Rogaev EI. Genetic Variant in GRM1 Underlies Congenital Cerebellar Ataxia with No Obvious Intellectual Disability. Int J Mol Sci. 2023 Jan 12; 24(2).
Score: 0.119
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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.
Score: 0.113
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Protasova MS, Gusev FE, Andreeva TV, Klyushnikov SA, Illarioshkin SN, Rogaev EI. Novel genes bearing mutations in rare cases of early-onset ataxia with cerebellar hypoplasia. Eur J Hum Genet. 2022 06; 30(6):703-711.
Score: 0.112
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Rogaev EI, Sherrington R, Rogaeva EA, Levesque G, Ikeda M, Liang Y, Chi H, Lin C, Holman K, Tsuda T, et al. Familial Alzheimer's disease in kindreds with missense mutations in a gene on chromosome 1 related to the Alzheimer's disease type 3 gene. Nature. 1995 Aug 31; 376(6543):775-8.
Score: 0.071
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Plotnikova OV, Kondrashov FA, Vlasov PK, Grigorenko AP, Ginter EK, Rogaev EI. Conversion and compensatory evolution of the gamma-crystallin genes and identification of a cataractogenic mutation that reverses the sequence of the human CRYGD gene to an ancestral state. Am J Hum Genet. 2007 Jul; 81(1):32-43.
Score: 0.040
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Grigorenko AP, Rogaev EI. [Molecular basics of Alzheimer's disease]. Mol Biol (Mosk). 2007 Mar-Apr; 41(2):331-45.
Score: 0.040
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Pankov IuA, Iatsyshina SB, Karpova SK, Chekhranova MK, Popova IuP, Grigorian ON, Rogaev EI. [Screening of mutations in genes of pro-opiomelanocortin in patients with constitutional exogenous obesity]. Vopr Med Khim. 2002 Jan-Feb; 48(1):121-30.
Score: 0.028
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Rogaeva EA, Fafel KC, Song YQ, Medeiros H, Sato C, Liang Y, Richard E, Rogaev EI, Frommelt P, Sadovnick AD, Meschino W, Rockwood K, Boss MA, Mayeux R, St George-Hyslop P. Screening for PS1 mutations in a referral-based series of AD cases: 21 novel mutations. Neurology. 2001 Aug 28; 57(4):621-5.
Score: 0.027
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Rogaev EI. [Genetic factors and a polygenic model of Alzheimer's disease]. Genetika. 1999 Nov; 35(11):1558-71.
Score: 0.024
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Rogaev EI. [Genetic basis for Alzheimer's disease and other dementias and prospects of molecular diagnosis]. Vestn Ross Akad Med Nauk. 1999; (1):33-9.
Score: 0.022
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Rogaev EI. [Presenilins: detection and characterization of Alzheimer's disease genes]. Mol Biol (Mosk). 1998 Jan-Feb; 32(1):71-83.
Score: 0.021
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Korovaitseva GI, Bukina A, Farrer LA, Rogaev EI. Presenilin polymorphisms in Alzheimer's disease. Lancet. 1997 Sep 27; 350(9082):959.
Score: 0.021
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Tsuda T, Chi H, Liang Y, Rogaeva EA, Sherrington R, Levesque G, Ikeda M, Rogaev EI, Pollen D, Freedman M, et al. Failure to detect missense mutations in the S182 gene in a series of late-onset Alzheimer's disease cases. Neurosci Lett. 1995 Dec 08; 201(2):188-90.
Score: 0.018
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Sherrington R, Rogaev EI, Liang Y, Rogaeva EA, Levesque G, Ikeda M, Chi H, Lin C, Li G, Holman K, Tsuda T, Mar L, Foncin JF, Bruni AC, Montesi MP, Sorbi S, Rainero I, Pinessi L, Nee L, Chumakov I, Pollen D, Brookes A, Sanseau P, Polinsky RJ, Wasco W, Da Silva HA, Haines JL, Perkicak-Vance MA, Tanzi RE, Roses AD, Fraser PE, Rommens JM, St George-Hyslop PH. Cloning of a gene bearing missense mutations in early-onset familial Alzheimer's disease. Nature. 1995 Jun 29; 375(6534):754-60.
Score: 0.018
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Nicolaou M, Song YQ, Sato CA, Orlacchio A, Kawarai T, Medeiros H, Liang Y, Sorbi S, Richard E, Rogaev EI, Moliaka Y, Bruni AC, Jorge R, Percy M, Duara R, Farrer LA, St Georg-Hyslop P, Rogaeva EA. Mutations in the open reading frame of the beta-site APP cleaving enzyme (BACE) locus are not a common cause of Alzheimer's disease. Neurogenetics. 2001 Oct; 3(4):203-6.
Score: 0.007
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Sorbi S, Nacmias B, Forleo P, Piacentini S, Sherrington R, Rogaev E, St George Hyslop P, Amaducci L. Missense mutation of S182 gene in Italian families with early-onset Alzheimer's disease. Lancet. 1995 Aug 12; 346(8972):439-40.
Score: 0.004
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St George-Hyslop P, McLachlan DC, Tsuda T, Rogaev E, Karlinsky H, Lippa CF, Pollen D, Tuda T. Alzheimer's disease and possible gene interaction. Science. 1994 Jan 28; 263(5146):537.
Score: 0.004