Human Genome Epidemiology Literature Finder
Records 1 - 11 (of 11 Records) |
Query Trace: Sclerosis and KIF1B[original query] |
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Genetic variation in the KIF1B locus influences susceptibility to multiple sclerosis.
![]() Nature genetics 2008 Dec 40 (12): 1402-3. Aulchenko Yurii S, Hoppenbrouwers Ilse A, Ramagopalan Sreeram V, Broer Linda, Jafari Naghmeh, Hillert Jan, Link Jenny, Lundström Wangko, Greiner Eva, Dessa Sadovnick A, Goossens Dirk, Van Broeckhoven Christine, Del-Favero Jurgen, Ebers George C, Oostra Ben A, van Duijn Cornelia M, Hintzen Rogier |
Hexose-6-phosphate dehydrogenase: a new risk gene for multiple sclerosis. European journal of human genetics : EJHG 2010 May 18 (5): 618-20. Alcina Antonio, Ramagopalan Sreeram V, Fernández Oscar, Catalá-Rabasa Antonio, Fedetz María, Ndagire Dorothy, Leyva Laura, Arnal Carmen, Delgado Concepción, Lucas Miguel, Izquierdo Guillermo, Ebers George C, Matesanz Fuencis |
Lack of support for association between the KIF1B rs10492972[C] variant and multiple sclerosis. Nature genetics 2010 Jun 42 (6): 469-70; author reply 470-1. , Booth David R, Heard Robert N, Stewart Graeme J, Cox Mathew, Scott Rodney J, Lechner-Scott Jeannette, Goris An, Dobosi Rita, Dubois Bénédicte, Saarela Janna, Leppä Virpi, Peltonen Leena, Pirttila Tuula, Cournu-Rebeix Isabelle, Fontaine Bertrand, Bergamaschi Laura, D'Alfonso Sandra, Leone Maurizio, Lorentzen Aslaug R, Harbo Hanne F, Celius Elisabeth G, Spurkland Anne, Link Jenny, Kockum Ingrid, Olsson Tomas, Hillert Jan, Ban Maria, Baker Amie, Kemppinen Anu, Sawcer Stephen, Compston Alastair, Robertson Neil P, De Jager Philip L, Hafler David A, Barcellos Lisa F, Ivinson Adrian J, McCauley Jacob L, Pericak-Vance Margaret A, Oksenberg Jorge R, Hauser Stephen L, Sexton David, Haines Jonath |
Lack of replication of KIF1B gene in an Italian primary progressive multiple sclerosis cohort. European journal of neurology 2010 May 17 (5): 740-5. Martinelli-Boneschi F, Esposito F, Scalabrini D, Fenoglio C, Rodegher M E, Brambilla P, Colombo B, Ghezzi A, Capra R, Collimedaglia L, Coniglio G, De Riz M, Serpente M, Cantoni C, Scarpini E, Martinelli V, Galimberti D, Comi |
Polymorphic locus rs10492972 of the KIF1B gene association with multiple sclerosis in Russia: case control study. Molecular genetics and metabolism 2011 Nov 104 (3): 390-4. Kudryavtseva Ekaterina A, Rozhdestvenskii Aleksei S, Kakulya Anastasia V, Khanokh Elena V, Delov Roman A, Malkova Nadezhda A, Korobko Denis S, Platonov Fedor A, Aref Eva Elena G, Zagorskaya Natalia N, Aliferova Valentina M, Titova Marina A, Babenko Sergei A, Smagina Inna V, El Chaninova Svetlana A, Zolovkina Anna G, Lifshits G I, Puzyrev Valerii P, Filipenko Maxim |
When is the absence of evidence, evidence of absence? Use of equivalence-based analyses in genetic epidemiology and a conclusion for the KIF1B rs10492972*C allelic association in multiple sclerosis. Genetic epidemiology 2011 Sep 35 (6): 568-71. Gourraud Pierre-Antoine, |
[The effect of genetic factors on the phenotypic expression of multiple sclerosis]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinsko? promyshlennosti Rossi?sko? Federatsii, Vserossi?skoe obshchestvo nevrologov [i] Vserossi?skoe obshchestvo psikhiatrov 2013 113 (2 Pt 2): 10-6. Korobko D S, Malkova N A, Bulatova E V, Babenko L A, Sazonov D V, Sokolova E A, Filipenko M |
[Clinical and electrophysiological and molecular genetic characteristics of the course of relapsing-remitting multiple sclerosis]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova / Ministerstvo zdravookhraneniia i meditsinsko? promyshlennosti Rossi?sko? Federatsii, Vserossi?skoe obshchestvo nevrologov [i] Vserossi?skoe obshchestvo psikhiatrov 2013 113 (10): 55-9. Delov R A, Rozhdestvenski? A S, Marks E A, Smialovski? V E, Khanokh E V, Kakulia A V, Sokolova E A, Agapova O |
Molecular analysis and clinical diversity of distal hereditary motor neuropathy. European journal of neurology 2020 4 27 (7): 1319-1326. Liu X, Duan X, Zhang Y, Sun A, Fan |
[Associations of single nucleotide polymorphisms of KIF1B gene with the severity of clinical manifestations of multiple sclerosis]. Zhurnal nevrologii i psikhiatrii imeni S.S. Korsakova 2019 119 (10. Vyp. 2): 58-62. Arbusova E E, Selyanina N V, Karakulova Yu |
[Risk of Multiple Sclerosis: Analysis of Interactions Between Variants of Nuclear and Mitochondrial Genomes]. Molekuliarnaia biologiia 0 55 (6): 956-964. Kozin M S, Kiselev I S, Baulina N M, Pavlova G V, Boyko A N, Kulakova O G, Favorova O |
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