Items where the Publication is European journal of human genetics
Number of items: 17.
2017
Suggestive association between variants in IL1RAPL and asthma symptoms in Latin American children. (2017)
Marques, Cintia Rodrigues; Costa, Gustavo No; da Silva, Thiago Magalhães; Oliveira, Pablo; Cruz, Alvaro A; Alcantara-Neves, Neuza Maria; Fiaccone, Rosemeire L; Horta, Bernardo L; Hartwig, Fernando Pires; Burchard, Esteban G; Pino-Yanes, Maria; Rodrigues, Laura C; Lima-Costa, Maria Fernanda; Pereira, Alexandre C; Gouveia, Mateus H; Sant Anna, Hanaisa P; Tarazona-Santos, Eduardo; Lima Barreto, Maurício; Figueiredo, Camila Alexandrina
2015
Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array. (2015)
Rodriguez, Santiago; Gaunt, Tom R; Guo, Yiran; Zheng, Jie; Barnes, Michael R; Tang, Weihang; Danish, Fazal; Johnson, Andrew; Castillo, Berta A; Li, Yun R; Hakonarson, Hakon; Buxbaum, Sarah G; Palmer, Tom; Tsai, Michael Y; Lange, Leslie A; Ebrahim, Shah; Davey Smith, George; Lawlor, Debbie A; Folsom, Aaron R; Hoogeveen, Ron; Reiner, Alex; Keating, Brendan; Day, Ian NM
2010
A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis. (2010)
Mero, Inger-Lise; Lorentzen, Aslaug R; Ban, Maria; Smestad, Cathrine; Celius, Elisabeth G; Aarseth, Jan H; Myhr, Kjell-Morten; Link, Jenny; Hillert, Jan; Olsson, Tomas; Kockum, Ingrid; Masterman, Thomas; Oturai, Annette Bang; Søndergaard, Helle Bach; Sellebjerg, Finn; Saarela, Janna; Kemppinen, Anu; Elovaara, Irina; Spurkland, Anne; Dudbridge, Frank; Lie, Benedicte A; Harbo, Hanne F
Evidence for both copy number and allelic (NA1/NA2) risk at the FCGR3B locus in systemic lupus erythematosus. (2010)
Morris, David L; Roberts, Amy L; Witherden, Abigail S; Tarzi, Ruth; Barros, Paula; Whittaker, John C; Cook, Terence H; Aitman, Timothy J; Vyse, Timothy J
2009
Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. (2009)
Ban, Maria; Goris, An; Lorentzen, Aslaug R; Baker, Amie; Mihalova, Tania; Ingram, Gillian; Booth, David R; Heard, Robert N; Stewart, Graeme J; Bogaert, Elke; Dubois, Bénédicte; Harbo, Hanne F; Celius, Elisabeth G; Spurkland, Anne; Strange, Richard; Hawkins, Clive; Robertson, Neil P; Dudbridge, Frank; Wason, James; De Jager, Philip L; Hafler, David; Rioux, John D; Ivinson, Adrian J; McCauley, Jacob L; Pericak-Vance, Margaret; Oksenberg, Jorge R; Hauser, Stephen L; Sexton, David; Haines, Jonathan; Sawcer, Stephen; Wellcome Trust Case-Control Consortium (WTCCC); Compston, Alastair
Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility. (2009)
Clark, Taane G; Fry, Andrew E; Auburn, Sarah; Campino, Susana; Diakite, Mahamadou; Green, Angela; Richardson, Anna; Teo, Yik Y; Small, Kerrin; Wilson, Jonathan; Jallow, Muminatou; Sisay-Joof, Fatou; Pinder, Margaret; Sabeti, Pardis; Kwiatkowski, Dominic P; Rockett, Kirk A
Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) and BMI. (2009)
Shugart, Yin Yao; Chen, Lina; Day, Ian NM; Lewis, Sarah J; Timpson, Nicholas J; Yuan, Wei; Abdollahi, Mohammad Reza; Ring, Sue M; Ebrahim, Shah; Golding, Jean; Lawlor, Debbie A; Davey-Smith, George
Lactase persistence-related genetic variant: population substructure and health outcomes. (2009)
Smith, George Davey; Lawlor, Debbie A; Timpson, Nic J; Baban, Jamil; Kiessling, Matt; Day, Ian NM; Ebrahim, Shah
MET and autism susceptibility: family and case-control studies. (2009)
Sousa, Inês; Clark, Taane G; Toma, Claudio; Kobayashi, Kazuhiro; Choma, Maja; Holt, Richard; Sykes, Nuala H; Lamb, Janine A; Bailey, Anthony J; Battaglia, Agatino; Maestrini, Elena; Monaco, Anthony P; International Molecular Genetic Study of Autism Consortium (IMGS
A genome-wide scan of 10 000 gene-centric variants and colorectal cancer risk. (2009)
Webb, Emily; Broderick, Peter; Lubbe, Steven; Chandler, Ian; Tomlinson, Ian; Houlston, Richard S
2008
Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation. (2008)
Bagnall, RD; Roberts, RG; Mirza, MM; Torigoe, T; Prescott, NJ; Mathew, CG
Deciphering the genetics of hereditary non-syndromic colorectal cancer. (2008)
Papaemmanuil, Eli; Carvajal-Carmona, Luis; Sellick, Gabrielle S; Kemp, Zoe; Webb, Emily; Spain, Sarah; Sullivan, Kate; Barclay, Ella; Lubbe, Steven; Jaeger, Emma; Vijayakrishnan, Jayaram; Broderick, Peter; Gorman, Maggie; Martin, Lynn; Lucassen, Anneke; Bishop, D Timothy; Evans, D Gareth; Maher, Eamonn R; Steinke, Verena; Rahner, Nils; Schackert, Hans K; Goecke, Timm O; Holinski-Feder, Elke; Propping, Peter; Van Wezel, Tom; Wijnen, Juul; Cazier, Jean-Baptiste; Thomas, Huw; Houlston, Richard S; Tomlinson, Ian; CORGI Consortium
2007
Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels. (2007)
Barber, Thomas M; Bennett, Amanda J; Gloyn, Anna L; Groves, Christopher J; Sovio, Ulla; Ruokonen, Aimo; Martikainen, Hannu; Pouta, Anneli; Taponen, Saara; Weedon, Michael N; Hartikainen, Anna-Liisa; Wass, John AH; Järvelin, Marjo-Riitta; Zeggini, Eleftheria; Franks, Stephen; McCarthy, Mark I
Linkage and association analysis of CACNG3 in childhood absence epilepsy. (2007)
Everett, Kate V; Chioza, Barry; Aicardi, Jean; Aschauer, Harald; Brouwer, Oebele; Callenbach, Petra; Covanis, Athanasios; Dulac, Olivier; Eeg-Olofsson, Orvar; Feucht, Martha; Friis, Mogens; Goutieres, Françoise; Guerrini, Renzo; Heils, Armin; Kjeldsen, Marianne; Lehesjoki, Anna-Elina; Makoff, Andrew; Nabbout, Rima; Olsson, Ingrid; Sander, Thomas; Sirén, Auli; McKeigue, Paul; Robinson, Robert; Taske, Nichole; Rees, Michele; Gardiner, Mark