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A new locus for spinocerebellar ataxia (SCA21) maps to chromosome 7p21.3-p15.1.
Vuillaume I, Devos D, Schraen-Maschke S, Dina C, Lemainque A, Vasseur F, Bocquillon G, Devos P, Kocinski C, Marzys C, Destée A, Sablonnière B. Vuillaume I, et al. Among authors: lemainque a. Ann Neurol. 2002 Nov;52(5):666-70. doi: 10.1002/ana.10344. Ann Neurol. 2002. PMID: 12402269
Genome-wide scan for genes involved in bipolar affective disorder in 70 European families ascertained through a bipolar type I early-onset proband: supportive evidence for linkage at 3p14.
Etain B, Mathieu F, Rietschel M, Maier W, Albus M, McKeon P, Roche S, Kealey C, Blackwood D, Muir W, Bellivier F, Henry C, Dina C, Gallina S, Gurling H, Malafosse A, Preisig M, Ferrero F, Cichon S, Schumacher J, Ohlraun S, Borrmann-Hassenbach M, Propping P, Abou Jamra R, Schulze TG, Marusic A, Dernovsek ZM, Giros B, Bourgeron T, Lemainque A, Bacq D, Betard C, Charon C, Nöthen MM, Lathrop M, Leboyer M. Etain B, et al. Among authors: lemainque a. Mol Psychiatry. 2006 Jul;11(7):685-94. doi: 10.1038/sj.mp.4001815. Epub 2006 Mar 14. Mol Psychiatry. 2006. PMID: 16534504 Free PMC article.
Genome screen in the French EGEA study: detection of linked regions shared or not shared by allergic rhinitis and asthma.
Dizier MH, Bouzigon E, Guilloud-Bataille M, Bétard C, Bousquet J, Charpin D, Gormand F, Hochez J, Just J, Lemainque A, Le Moual N, Matran R, Neukirch F, Oryszczyn MP, Paty E, Pin I, Vervloet D, Kauffmann F, Lathrop M, Demenais F, Annesi-Maesano I. Dizier MH, et al. Among authors: lemainque a. Genes Immun. 2005 Mar;6(2):95-102. doi: 10.1038/sj.gene.6364163. Genes Immun. 2005. PMID: 15674395
Clustering patterns of LOD scores for asthma-related phenotypes revealed by a genome-wide screen in 295 French EGEA families.
Bouzigon E, Dizier MH, Krähenbühl C, Lemainque A, Annesi-Maesano I, Betard C, Bousquet J, Charpin D, Gormand F, Guilloud-Bataille M, Just J, Le Moual N, Maccario J, Matran R, Neukirch F, Oryszczyn MP, Paty E, Pin I, Rosenberg-Bourgin M, Vervloet D, Kauffmann F, Lathrop M, Demenais F. Bouzigon E, et al. Among authors: lemainque a. Hum Mol Genet. 2004 Dec 15;13(24):3103-13. doi: 10.1093/hmg/ddh340. Epub 2004 Oct 27. Hum Mol Genet. 2004. PMID: 15509591
Linkage of benign familial infantile convulsions to chromosome 16p12-q12 suggests allelism to the infantile convulsions and choreoathetosis syndrome.
Caraballo R, Pavek S, Lemainque A, Gastaldi M, Echenne B, Motte J, Genton P, Cersósimo R, Humbertclaude V, Fejerman N, Monaco AP, Lathrop MG, Rochette J, Szepetowski P. Caraballo R, et al. Among authors: lemainque a. Am J Hum Genet. 2001 Mar;68(3):788-94. doi: 10.1086/318805. Epub 2001 Feb 13. Am J Hum Genet. 2001. PMID: 11179027 Free PMC article.
Existence of a genetic risk factor on chromosome 5q in Italian coeliac disease families.
Greco L, Babron MC, Corazza GR, Percopo S, Sica R, Clot F, Fulchignoni-Lataud MC, Zavattari P, Momigliano-Richiardi P, Casari G, Gasparini P, Tosi R, Mantovani V, De Virgiliis S, Iacono G, D'Alfonso A, Selinger-Leneman H, Lemainque A, Serre JL, Clerget-Darpoux F. Greco L, et al. Among authors: lemainque a. Ann Hum Genet. 2001 Jan;65(Pt 1):35-41. doi: 10.1046/j.1469-1809.2001.6510035.x. Ann Hum Genet. 2001. PMID: 11415521
47 results