Zobrazeno 1 - 2
of 2
pro vyhledávání: '"genetic [European Continental Ancestry Group]"'
Autor:
Mario Pirastu, Ginevra Biino, Ozren Polasek, Laura Portas, Igor Rudan, Marina Ciullo, Sheila Ulivi, Nicola Pirastu, Paolo Gasparini, Giorgia Girotto, Nicholas D. Hastie, Rossella Sorice, Alan F. Wright, Teresa Nutile, Harry Campbell, Adamo Pio d'Adamo, Caroline Hayward, Tatijana Zemunik
Publikováno v:
Journal of medical genetics
48 (2011): 369–374. doi:10.1136/jmg.2010.088310
info:cnr-pdr/source/autori:Girotto G, Pirastu N, Sorice R, Biino G, Campbell H, d'Adamo AP, Hastie ND, Nutile T, Polasek O, Portas L, Rudan I, Ulivi S, Zemunik T, Wright AF, Ciullo M, Hayward C, Pirastu M, Gasparini P./titolo:Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways./doi:10.1136%2Fjmg.2010.088310/rivista:Journal of medical genetics (Print)/anno:2011/pagina_da:369/pagina_a:374/intervallo_pagine:369–374/volume:48
Journal of Medical Genetics
Journal of Medical Genetics, BMJ Publishing Group, 2011, 48 (6), pp.369. ⟨10.1136/jmg.2010.088310⟩
48 (2011): 369–374. doi:10.1136/jmg.2010.088310
info:cnr-pdr/source/autori:Girotto G, Pirastu N, Sorice R, Biino G, Campbell H, d'Adamo AP, Hastie ND, Nutile T, Polasek O, Portas L, Rudan I, Ulivi S, Zemunik T, Wright AF, Ciullo M, Hayward C, Pirastu M, Gasparini P./titolo:Hearing function and thresholds: a genome-wide association study in European isolated populations identifies new loci and pathways./doi:10.1136%2Fjmg.2010.088310/rivista:Journal of medical genetics (Print)/anno:2011/pagina_da:369/pagina_a:374/intervallo_pagine:369–374/volume:48
Journal of Medical Genetics
Journal of Medical Genetics, BMJ Publishing Group, 2011, 48 (6), pp.369. ⟨10.1136/jmg.2010.088310⟩
BACKGROUND: Hearing is a complex trait, but until now only a few genes are known to contribute to variability of this process. In order to discover genes and pathways that underlie auditory function, a genome-wide association study was carried out wi
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::e6699d351494c8e9151d42a5145398c7
http://hdl.handle.net/11368/2489175
http://hdl.handle.net/11368/2489175
Autor:
Thomas Meitinger, T. Piskackova, Leena Peltonen, Draga Toncheva, Christelle Borel, Sena Karachanak, Liene Nikitina-Zake, Xavier Estivill, Béla Melegh, Daniela Toniolo, Janis Klovins, Mari Nelis, Andrey Khrunin, H-Erich Wichmann, Raquel Rabionet, Michael Krawczak, Ivan Balascak, Stefan Schreiber, Tõnu Esko, Jūratė Kasnauskienė, Alexander Zimprich, Paolo Gasparini, Pilar Galan, Fritz Zimprich, Karola Rehnström, Simon Heath, Pio D'Adamo, Antonio Julià, Sara Marsal, Arne Pfeufer, Stylianos E. Antonarakis, Eveliina Jakkula, Svetlana A. Limborska, Noémi Polgár, Reedik Mägi, Samuel Deutsch, Tadeusz Dębniak, Homa Attar, Jan Lubinski, Vaidutis Kučinskas, Maryline Gagnebin, Mark Lathrop, Milan Macek, Andres Metspalu, Maido Remm
Publikováno v:
PLOS ONE, Vol. 4, No 5 (2009) P. e5472
PLoS ONE, Vol 4, Iss 5, p e5472 (2009)
PLoS ONE
PloS one
PLoS ONE; Vol 4
PLoS ONE, Vol 4, Iss 5, p e5472 (2009)
PLoS ONE
PloS one
PLoS ONE; Vol 4
Using principal component (PC) analysis, we studied the genetic constitution of 3,112 individuals from Europe as portrayed by more than 270,000 single nucleotide polymorphisms (SNPs) genotyped with the Illumina Infinium platform. In cohorts where the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::5589440a1ebd026aa6ae87c29bbd6f9d
https://archive-ouverte.unige.ch/unige:9227
https://archive-ouverte.unige.ch/unige:9227