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Number of items: 43.

2017

Mullin, BH; Hua Zhao, J; Brown, SJ; Perry, JRB; Luan, J; Zheng, HF; Langenberg, C; Dudbridge, F; Scott, R; Wareham, NJ; +4 more... (2017) Genome-wide association study meta-analysis for quantitative ultrasound parameters of bone identifies five novel loci for broadband ultrasound attenuation. Human molecular genetics. ISSN 0964-6906 DOI: 10.1093/hmg/ddx174 Full text not available from this repository.

2016

Figueroa, JD; Middlebrooks, CD; Banday, AR; Ye, Y; Garcia-Closas, M; Chatterjee, N; Koutros, S; Kiemeney, LA; Rafnar, T; Bishop, T; +117 more... (2016) Identification of a novel susceptibility locus at 13q34 and refinement of the 20p12.2 region as a multi-signal locus associated with bladder cancer risk in individuals of European ancestry. Human molecular genetics, 25 (6). pp. 1203-1214. ISSN 0964-6906 DOI: 10.1093/hmg/ddv492 Full text not available from this repository.

Wyszynski, A; Hong, CC; Lam, K; Michailidou, K; Lytle, C; Yao, S; Zhang, Y; Bolla, MK; Wang, Q; Dennis, J; +103 more... (2016) An intergenic risk locus containing an enhancer deletion in 2q35 modulates breast cancer risk by deregulating IGFBP5 expression. Human molecular genetics, 25 (17). pp. 3863-3876. ISSN 0964-6906 DOI: 10.1093/hmg/ddw223 Full text not available from this repository.

de la Hoya, M; Soukarieh, O; López-Perolio, I; Vega, A; Walker, LC; van Ierland, Y; Baralle, D; Santamariña, M; Lattimore, V; Wijnen, J; +65 more... (2016) Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms. Human molecular genetics. ISSN 0964-6906 DOI: 10.1093/hmg/ddw094 Full text not available from this repository.

2015

Lin, WY; Camp, NJ; Ghoussaini, M; Beesley, J; Michailidou, K; Hopper, JL; Apicella, C; Southey, MC; Stone, J; Schmidt, MK; +215 more... (2015) Identification and characterisation of novel associations in the CASP8/ALS2CR12 region on chromosome 2 with breast cancer risk. Human molecular genetics, 24 (1). pp. 285-98. ISSN 0964-6906 DOI: 10.1093/hmg/ddu431 Full text not available from this repository.

Litchfield, K; Sultana, R; Renwick, A; Dudakia, D; Seal, S; Ramsay, E; Powell, S; Elliott, A; Warren-Perry, M; Eeles, R; +12 more... (2015) Multi-stage genome wide association study identifies new susceptibility locus for testicular germ cell tumour on chromosome 3q25. Human molecular genetics, 24 (4). pp. 1169-76. ISSN 0964-6906 DOI: 10.1093/hmg/ddu511 Full text not available from this repository.

Orr, N; Dudbridge, F; Dryden, N; Maguire, S; Novo, D; Perrakis, E; Johnson, N; Ghoussaini, M; Hopper, JL; Southey, MC; +206 more... (2015) Fine-mapping identifies two additional breast cancer susceptibility loci at 9q31.2. Human molecular genetics, 24 (10). pp. 2966-84. ISSN 0964-6906 DOI: 10.1093/hmg/ddv035
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Painter, JN; O'Mara, TA; Batra, J; Cheng, T; Lose, FA; Dennis, J; Michailidou, K; Tyrer, JP; Ahmed, S; Ferguson, K; +109 more... (2015) Fine-mapping of the HNF1B multicancer locus identifies candidate variants that mediate endometrial cancer risk. Human molecular genetics, 24 (5). pp. 1478-92. ISSN 0964-6906 DOI: 10.1093/hmg/ddu552
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2014

Milne, RL; Burwinkel, B; Michailidou, K; Arias-Perez, JI; Zamora, MP; Menéndez-Rodríguez, P; Hardisson, D; Mendiola, M; González-Neira, A; Pita, G; +171 more... (2014) Common non-synonymous SNPs associated with breast cancer susceptibility: findings from the Breast Cancer Association Consortium. Human molecular genetics, 23 (22). pp. 6096-111. ISSN 0964-6906 DOI: 10.1093/hmg/ddu311
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Milne, RL; Herranz, J; Michailidou, K; Dennis, J; Tyrer, JP; Zamora, MP; Arias-Perez, JI; González-Neira, A; Pita, G; Alonso, MR; +137 more... (2014) A large-scale assessment of two-way SNP interactions in breast cancer susceptibility using 46 450 cases and 42 461 controls from the breast cancer association consortium. Human molecular genetics, 23 (7). pp. 1934-46. ISSN 0964-6906 DOI: 10.1093/hmg/ddt581 Full text not available from this repository.

Purrington, KS; Slettedahl, S; Bolla, MK; Michailidou, K; Czene, K; Nevanlinna, H; Bojesen, SE; Andrulis, IL; Cox, A; Hall, P; +157 more... (2014) Genetic variation in mitotic regulatory pathway genes is associated with breast tumor grade. Human molecular genetics, 23 (22). pp. 6034-46. ISSN 0964-6906 DOI: 10.1093/hmg/ddu300 Full text not available from this repository.

2013

Cousminer, DL; Berry, DJ; Timpson, NJ; Ang, W; Thiering, E; Byrne, EM; Taal, HR; Huikari, V; Bradfield, JP; Kerkhof, M; +61 more... (2013) Genome-wide association and longitudinal analyses reveal genetic loci linking pubertal height growth, pubertal timing and childhood adiposity. Human molecular genetics, 22 (13). pp. 2735-2747. ISSN 0964-6906 DOI: 10.1093/hmg/ddt104 Full text not available from this repository.

2012

Cornes, BK; Khor, CC; Nongpiur, ME; Xu, L; Tay, WT; Zheng, Y; Lavanya, R; Li, Y; Wu, R; Sim, X; +14 more... (2012) Identification of four novel variants that influence central corneal thickness in multi-ethnic Asian populations. Human molecular genetics, 21 (2). pp. 437-45. ISSN 0964-6906 DOI: 10.1093/hmg/ddr463 Full text not available from this repository.

Mead, S; Uphill, J; Beck, J; Poulter, M; Campbell, T; Lowe, J; Adamson, G; Hummerich, H; Klopp, N; Ruckert, IM; +11 more... (2012) Genome-wide association study in multiple human prion diseases suggests genetic risk factors additional to PRNP. Human molecular genetics, 21 (8). pp. 1897-1906. ISSN 0964-6906 DOI: 10.1093/hmg/ddr607 Full text not available from this repository.

Siddiq, A; Couch, FJ; Chen, GK; Lindström, S; Eccles, D; Millikan, RC; Michailidou, K; Stram, DO; Beckmann, L; Rhie, SK; +133 more... (2012) A meta-analysis of genome-wide association studies of breast cancer identifies two novel susceptibility loci at 6q14 and 20q11. Human molecular genetics, 21 (24). pp. 5373-84. ISSN 0964-6906 DOI: 10.1093/hmg/dds381 Full text not available from this repository.

Vimaleswaran, KS; Tachmazidou, I; Zhao, JH; Hirschhorn, JN; Dudbridge, F; Loos, RJF; (2012) Candidate genes for obesity-susceptibility show enriched association within a large genome-wide association study for BMI. Human molecular genetics, 21 (20). pp. 4537-4542. ISSN 0964-6906 DOI: 10.1093/hmg/dds283 Full text not available from this repository.

Wu, XF; Scelo, G; Purdue, MP; Rothman, N; Johansson, M; Ye, YQ; Wang, ZM; Zelenika, D; Moore, LE; Wood, CG; +82 more... (2012) A genome-wide association study identifies a novel susceptibility locus for renal cell carcinoma on 12p11.23. Human molecular genetics, 21 (2). pp. 456-462. ISSN 0964-6906 DOI: 10.1093/hmg/ddr479 Full text not available from this repository.

2011

Figueroa, JD; Garcia-Closas, M; Humphreys, M; Platte, R; Hopper, JL; Southey, MC; Apicella, C; Hammet, F; Schmidt, MK; Broeks, A; +137 more... (2011) Associations of common variants at 1p11.2 and 14q24.1 (RAD51L1) with breast cancer risk and heterogeneity by tumor subtype: findings from the Breast Cancer Association Consortium. Human molecular genetics, 20 (23). pp. 4693-706. ISSN 0964-6906 DOI: 10.1093/hmg/ddr368 Full text not available from this repository.

Khor, CC; Ramdas, WD; Vithana, EN; Cornes, BK; Sim, X; Tay, WT; Saw, SM; Zheng, Y; Lavanya, R; Wu, R; +15 more... (2011) Genome-wide association studies in Asians confirm the involvement of ATOH7 and TGFBR3, and further identify CARD10 as a novel locus influencing optic disc area. Human molecular genetics, 20 (9). pp. 1864-72. ISSN 0964-6906 DOI: 10.1093/hmg/ddr060 Full text not available from this repository.

Spencer, CCA; Plagnol, V; Strange, A; Gardner, M; Paisan-Ruiz, C; Band, G; Barker, RA; Bellenguez, C; Bhatia, K; Blackburn, H; +39 more... (2011) Dissection of the genetics of Parkinson's disease identifies an additional association 5 ' of SNCA and multiple associated haplotypes at 17q21. Human molecular genetics, 20 (2). pp. 345-353. ISSN 0964-6906 DOI: 10.1093/hmg/ddq469
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Vithana, EN; Aung, T; Khor, CC; Cornes, BK; Tay, WT; Sim, X; Lavanya, R; Wu, R; Zheng, Y; Hibberd, ML; +6 more... (2011) Collagen-related genes influence the glaucoma risk factor, central corneal thickness. Human molecular genetics, 20 (4). pp. 649-58. ISSN 0964-6906 DOI: 10.1093/hmg/ddq511 Full text not available from this repository.

2010

Niederer, HA; Willcocks, LC; Rayner, TF; Yang, W; Lau, YL; Williams, TN; Scott, JA; Urban, BC; Peshu, N; Dunstan, SJ; +10 more... (2010) Copy number, linkage disequilibrium and disease association in the FCGR locus. Human molecular genetics, 19 (16). pp. 3282-94. ISSN 0964-6906 DOI: 10.1093/hmg/ddq216
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2009

Drenos, F; Talmud, PJ; Casas, JP; Smeeth, L; Palmen, J; Humphries, SE; Hingorani, AD; (2009) Integrated associations of genotypes with multiple blood biomarkers linked to coronary heart disease risk. Human molecular genetics, 18 (12). pp. 2305-16. ISSN 0964-6906 DOI: 10.1093/hmg/ddp159
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Dunning, AM; Healey, CS; Baynes, C; Maia, AT; Scollen, S; Vega, A; Rodriguez, R; Barbosa-Morais, NL; Ponder, BAJ; Low, YL; +60 more... (2009) Association of ESR1 gene tagging SNPs with breast cancer risk. Human molecular genetics, 18 (6). pp. 1131-1139. ISSN 0964-6906 DOI: 10.1093/hmg/ddn429 Full text not available from this repository.

Flanagan, JM; Munoz-Alegre, M; Henderson, S; Tang, T; Sun, P; Johnson, N; Fletcher, O; Silva, ID; Peto, J; Boshoff, C; +2 more... (2009) Gene-body hypermethylation of ATM in peripheral blood DNA of bilateral breast cancer patients. Human molecular genetics, 18 (7). pp. 1332-1342. ISSN 0964-6906 DOI: 10.1093/hmg/ddp033
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Fry, AE; Ghansa, A; Small, KS; Palma, A; Auburn, S; Diakite, M; Green, A; Campino, S; Teo, YY; Clark, TG; +18 more... (2009) Positive selection of a CD36 nonsense variant in sub-Saharan Africa, but no association with severe malaria phenotypes. Human molecular genetics, 18 (14). pp. 2683-92. ISSN 0964-6906 DOI: 10.1093/hmg/ddp192
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Zuccolo, L; Fitz-Simon, N; Gray, R; Ring, SM; Sayal, K; Smith, GD; Lewis, SJ; (2009) A non-synonymous variant in ADH1B is strongly associated with prenatal alcohol use in a European sample of pregnant women. Human molecular genetics, 18 (22). pp. 4457-66. ISSN 0964-6906 DOI: 10.1093/hmg/ddp388
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2008

Benzinou, M; Chèvre, JC; Ward, KJ; Lecoeur, C; Dina, C; Lobbens, S; Durand, E; Delplanque, J; Horber, FF; Heude, B; +7 more... (2008) Endocannabinoid receptor 1 gene variations increase risk for obesity and modulate body mass index in European populations. Human molecular genetics, 17 (13). pp. 1916-21. ISSN 0964-6906 DOI: 10.1093/hmg/ddn089 Full text not available from this repository.

Bethke, L; Webb, E; Murray, A; Schoemaker, M; Johansen, C; Christensen, HC; Muir, K; McKinney, P; Hepworth, S; Dimitropoulou, P; +11 more... (2008) Comprehensive analysis of the role of DNA repair gene polymorphisms on risk of glioma. Human molecular genetics, 17 (6). pp. 800-5. ISSN 0964-6906 DOI: 10.1093/hmg/ddm351 Full text not available from this repository.

Palles, C; Johnson, N; Coupland, B; Taylor, C; Carvajal, J; Holly, J; Fentiman, IS; Dos Santos Silva, I; Ashworth, A; Peto, J; +1 more... (2008) Identification of genetic variants that influence circulating IGF1 levels: a targeted search strategy. Human molecular genetics, 17 (10). pp. 1457-64. ISSN 0964-6906 DOI: 10.1093/hmg/ddn034 Full text not available from this repository.

Pittman, AM; Webb, E; Carvajal-Carmona, L; Howarth, K; di Bernardo, MC; Broderick, P; Spain, S; Walther, A; Price, A; Sullivan, K; +54 more... (2008) Refinement of the basis and impact of common 11q23.1 variation to the risk of developing colorectal cancer. Human molecular genetics, 17 (23). pp. 3720-3727. ISSN 0964-6906 DOI: 10.1093/hmg/ddn267 Full text not available from this repository.

2007

Brennan, P; McKay, J; Moore, L; Zaridze, D; Mukeria, A; Szeszenia-Dabrowska, N; Lissowska, J; Rudnai, P; Fabianova, E; Mates, D; +15 more... (2007) Uncommon CHEK2 mis-sense variant and reduced risk of tobacco-related cancers: case-control study. Human molecular genetics, 16 (15). pp. 1794-1801. ISSN 0964-6906 DOI: 10.1093/hmg/ddm127 Full text not available from this repository.

Matakidou, A; el Galta, R; Webb, EL; Rudd, MF; Bridle, H; GELCAPS Consortium; Eisen, T; Houlston, RS; (2007) Genetic variation in the DNA repair genes is predictive of outcome in lung cancer. Human molecular genetics, 16 (19). pp. 2333-40. ISSN 0964-6906 DOI: 10.1093/hmg/ddm190 Full text not available from this repository.

Natividad, A; Holland, MJ; Rockett, KA; Forton, J; Faal, N; Joof, HM; Mabey, DC; Bailey, RL; Kwiatkowski, DP; (2007) Susceptibility to sequelae of human ocular chlamydial infection associated with allelic variation in IL-10 cis-regulation. Human molecular genetics, 17 (2). pp. 323-9. ISSN 0964-6906 DOI: 10.1093/hmg/ddm310 Full text not available from this repository.

2006

Graham, DS; Wong, AK; McHugh, NJ; Whittaker, JC; Vyse, TJ; (2006) Evidence for unique association signals in SLE at the CD28-CTLA4-ICOS locus in a family-based study. Human molecular genetics, 15 (21). pp. 3195-205. ISSN 0964-6906 DOI: 10.1093/hmg/ddl395 Full text not available from this repository.

Kemp, Z; Carvajal-Carmona, L; Spain, S; Barclay, E; Gorman, M; Martin, L; Jaeger, E; Brooks, N; Bishop, DT; Thomas, H; +10 more... (2006) Evidence for a colorectal cancer susceptibility locus on chromosome 3q21-q24 from a high-density SNP genome-wide linkage scan. Human molecular genetics, 15 (19). pp. 2903-10. ISSN 0964-6906 DOI: 10.1093/hmg/ddl231 Full text not available from this repository.

Webb, EL; Rudd, MF; Sellick, GS; el Galta, R; Bethke, L; Wood, W; Fletcher, O; Penegar, S; Withey, L; Qureshi, M; +5 more... (2006) Search for low penetrance alleles for colorectal cancer through a scan of 1467 non-synonymous SNPs in 2575 cases and 2707 controls with validation by kin-cohort analysis of 14 704 first-degree relatives. Human molecular genetics, 15 (21). pp. 3263-3271. ISSN 0964-6906 DOI: 10.1093/hmg/ddl401 Full text not available from this repository.

2004

Mauvais-Jarvis, F; Smith, SB; May, CL; Leal, SM; Gautier, JF; Molokhia, M; Riveline, JP; Rajan, AS; Kevorkian, JP; Zhang, S; +3 more... (2004) PAX4 gene variations predispose to ketosis-prone diabetes. Human molecular genetics, 13 (24). pp. 3151-9. ISSN 0964-6906 DOI: 10.1093/hmg/ddh341 Full text not available from this repository.

Russell, AI; Cunninghame Graham, DS; Shepherd, C; Roberton, CA; Whittaker, J; Meeks, J; Powell, RJ; Isenberg, DA; Walport, MJ; Vyse, TJ; (2004) Polymorphism at the C-reactive protein locus influences gene expression and predisposes to systemic lupus erythematosus. Human molecular genetics, 13 (1). pp. 137-47. ISSN 0964-6906 DOI: 10.1093/hmg/ddh021 Full text not available from this repository.

2003

Chowers, I; Liu, D; Farkas, RH; Gunatilaka, TL; Hackam, AS; Bernstein, SL; Campochiaro, PA; Parmigiani, G; Zack, DJ; (2003) Gene expression variation in the adult human retina. Human molecular genetics, 12 (22). pp. 2881-93. ISSN 0964-6906 DOI: 10.1093/hmg/ddg326 Full text not available from this repository.

2002

Cervino, ACL; Lakiss, S; Sow, O; Bellamy, R; Beyers, N; Hoal-van Helden, E; van Helden, P; McAdam, KPWJ; Hill, AVS; (2002) Fine mapping of a putative tuberculosis susceptibility locus on chromosome 15q11-13 in African families. Human molecular genetics, 11 (14). pp. 1599-603. ISSN 0964-6906 DOI: 10.1093/hmg/11.14.1599 Full text not available from this repository.

This list was generated on Tue Aug 22 19:53:07 2017 BST.