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Number of items: 17.

2018

2017

Marques, CR; Costa, GN; da Silva, TM; Oliveira, P; Cruz, AA; Alcantara-Neves, NM; Fiaccone, RL; Horta, BL; Hartwig, FP; Burchard, EG; +9 more... Pino-Yanes, M; Rodrigues, LC; Lima-Costa, MF; Pereira, AC; Gouveia, MH; Sant Anna, HP; Tarazona-Santos, E; Lima Barreto, M; Figueiredo, CA; (2017) Suggestive association between variants in IL1RAPL and asthma symptoms in Latin American children. European journal of human genetics, 25 (4). pp. 439-445. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2016.197 Full text not available from this repository.

2016

Moosajee, M; Yu-Wai-Man, P; Rouzier, C; Bitner-Glindzicz, M; Bowman, R; (2016) Clinical utility gene card for: Wolfram syndrome. European journal of human genetics, 24 (11). ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2016.49
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2015

Rodriguez, S; Gaunt, TR; Guo, Y; Zheng, J; Barnes, MR; Tang, W; Danish, F; Johnson, A; Castillo, BA; Li, YR; +13 more... Hakonarson, H; Buxbaum, SG; Palmer, T; Tsai, MY; Lange, LA; Ebrahim, S; Davey Smith, G; Lawlor, DA; Folsom, AR; Hoogeveen, R; Reiner, A; Keating, B; Day, IN; (2015) Lipids, obesity and gallbladder disease in women: insights from genetic studies using the cardiovascular gene-centric 50K SNP array. European journal of human genetics. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2015.63
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2013

Gaunt, TR; Lowe, GD; Lawlor, DA; Casas, JP; Day, IN; (2013) A gene-centric analysis of activated partial thromboplastin time and activated protein C resistance using the HumanCVD focused genotyping array. European journal of human genetics, 21 (7). pp. 779-83. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2012.242
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2010

Mero, IL; Lorentzen, AR; Ban, M; Smestad, C; Celius, EG; Aarseth, JH; Myhr, KM; Link, J; Hillert, J; Olsson, T; +12 more... Kockum, I; Masterman, T; Oturai, AB; S?ndergaard, HB; Sellebjerg, F; Saarela, J; Kemppinen, A; Elovaara, I; Spurkland, A; Dudbridge, F; Lie, BA; Harbo, HF; (2010) A rare variant of the TYK2 gene is confirmed to be associated with multiple sclerosis. European journal of human genetics, 18 (4). pp. 502-4. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2009.195 Full text not available from this repository.

Morris, DL; Roberts, AL; Witherden, AS; Tarzi, R; Barros, P; Whittaker, JC; Cook, TH; Aitman, TJ; Vyse, TJ; (2010) Evidence for both copy number and allelic (NA1/NA2) risk at the FCGR3B locus in systemic lupus erythematosus. European journal of human genetics, 18 (9). pp. 1027-1031. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2010.56 Full text not available from this repository.

2009

Ban, M; Goris, A; Lorentzen, AR; Baker, A; Mihalova, T; Ingram, G; Booth, DR; Heard, RN; Stewart, GJ; Bogaert, E; +22 more... Dubois, B; Harbo, HF; Celius, EG; Spurkland, A; Strange, R; Hawkins, C; Robertson, NP; Dudbridge, F; Wason, J; De Jager, PL; Hafler, D; Rioux, JD; Ivinson, AJ; McCauley, JL; Pericak-Vance, M; Oksenberg, JR; Hauser, SL; Sexton, D; Haines, J; Sawcer, S; Wellcome Trust Case-Control Consortium (WTCCC); Compston, A; (2009) Replication analysis identifies TYK2 as a multiple sclerosis susceptibility factor. European journal of human genetics, 17 (10). pp. 1309-13. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2009.41 Full text not available from this repository.

Clark, TG; Fry, AE; Auburn, S; Campino, S; Diakite, M; Green, A; Richardson, A; Teo, YY; Small, K; Wilson, J; +6 more... Jallow, M; Sisay-Joof, F; Pinder, M; Sabeti, P; Kwiatkowski, DP; Rockett, KA; (2009) Allelic heterogeneity of G6PD deficiency in West Africa and severe malaria susceptibility. European journal of human genetics, 17 (8). pp. 1080-5. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2009.8 Full text not available from this repository.

Shugart, YY; Chen, L; Day, IN; Lewis, SJ; Timpson, NJ; Yuan, W; Abdollahi, MR; Ring, SM; Ebrahim, S; Golding, J; +2 more... Lawlor, DA; Davey-Smith, G; (2009) Two British women studies replicated the association between the Val66Met polymorphism in the brain-derived neurotrophic factor (BDNF) and BMI. European journal of human genetics, 17 (8). pp. 1050-5. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2008.272 Full text not available from this repository.

Smith, GD; Lawlor, DA; Timpson, NJ; Baban, J; Kiessling, M; Day, INM; Ebrahim, S; (2009) Lactase persistence-related genetic variant: population substructure and health outcomes. European journal of human genetics, 17 (3). pp. 357-367. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2008.156 Full text not available from this repository.

Sousa, I; Clark, TG; Toma, C; Kobayashi, K; Choma, M; Holt, R; Sykes, NH; Lamb, JA; Bailey, AJ; Battaglia, A; +3 more... Maestrini, E; Monaco, AP; International Molecular Genetic Study of Autism Consortium (IMGS; (2009) MET and autism susceptibility: family and case-control studies. European journal of human genetics, 17 (6). pp. 749-58. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2008.215 Full text not available from this repository.

Webb, E; Broderick, P; Lubbe, S; Chandler, I; Tomlinson, I; Houlston, RS; (2009) A genome-wide scan of 10 000 gene-centric variants and colorectal cancer risk. European journal of human genetics, 17 (11). pp. 1507-14. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2009.92 Full text not available from this repository.

2008

Bagnall, RD; Roberts, RG; Mirza, MM; Torigoe, T; Prescott, NJ; Mathew, CG; (2008) Novel isoforms of the CARD8 (TUCAN) gene evade a nonsense mutation. European journal of human genetics, 23. p. 23. ISSN 1018-4813 http://researchonline.lshtm.ac.uk/id/eprint/4286 Full text not available from this repository.

Papaemmanuil, E; Carvajal-Carmona, L; Sellick, GS; Kemp, Z; Webb, E; Spain, S; Sullivan, K; Barclay, E; Lubbe, S; Jaeger, E; +21 more... Vijayakrishnan, J; Broderick, P; Gorman, M; Martin, L; Lucassen, A; Bishop, DT; Evans, DG; Maher, ER; Steinke, V; Rahner, N; Schackert, HK; Goecke, TO; Holinski-Feder, E; Propping, P; Van Wezel, T; Wijnen, J; Cazier, JB; Thomas, H; Houlston, RS; Tomlinson, I; CORGI Consortium; (2008) Deciphering the genetics of hereditary non-syndromic colorectal cancer. European journal of human genetics, 16 (12). pp. 1477-86. ISSN 1018-4813 DOI: https://doi.org/10.1038/ejhg.2008.129 Full text not available from this repository.

2007

Barber, TM; Bennett, AJ; Gloyn, AL; Groves, CJ; Sovio, U; Ruokonen, A; Martikainen, H; Pouta, A; Taponen, S; Weedon, MN; +6 more... Hartikainen, AL; Wass, JA; J?rvelin, MR; Zeggini, E; Franks, S; McCarthy, MI; (2007) Relationship between E23K (an established type II diabetes-susceptibility variant within KCNJ11), polycystic ovary syndrome and androgen levels. European journal of human genetics, 15 (6). pp. 679-84. ISSN 1018-4813 DOI: https://doi.org/10.1038/sj.ejhg.5201802 Full text not available from this repository.

Everett, KV; Chioza, B; Aicardi, J; Aschauer, H; Brouwer, O; Callenbach, P; Covanis, A; Dulac, O; Eeg-Olofsson, O; Feucht, M; +16 more... Friis, M; Goutieres, F; Guerrini, R; Heils, A; Kjeldsen, M; Lehesjoki, AE; Makoff, A; Nabbout, R; Olsson, I; Sander, T; Siren, A; McKeigue, P; Robinson, R; Taske, N; Rees, M; Gardiner, M; (2007) Linkage and association analysis of CACNG3 in childhood absence epilepsy. European journal of human genetics, 15 (4). pp. 463-472. ISSN 1018-4813 DOI: https://doi.org/10.1038/sj.ejhg.5201783 Full text not available from this repository.

This list was generated on Fri Nov 16 15:08:16 2018 GMT.