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Number of items: 14.
C
Carvajal-Carmona, LG;
O'Mara, TA;
Painter, JN;
Lose, FA;
Dennis, J;
Michailidou, K;
Tyrer, JP;
Ahmed, S;
Ferguson, K;
Healey, CS;
+84 more...
Pooley, K;
Beesley, J;
Cheng, T;
Jones, A;
Howarth, K;
Martin, L;
Gorman, M;
Hodgson, S;
National Study of Endometrial Cancer Genetics Group (NSECG);
Australian National Endometrial Cancer Study Group (ANECS);
Wentzensen, N;
Fasching, PA;
Hein, A;
Beckmann, MW;
Renner, SP;
Dörk, T;
Hillemanns, P;
Dürst, M;
Runnebaum, I;
Lambrechts, D;
Coenegrachts, L;
Schrauwen, S;
Amant, F;
Winterhoff, B;
Dowdy, SC;
Goode, EL;
Teoman, A;
Salvesen, HB;
Trovik, J;
Njolstad, TS;
Werner, HM;
Scott, RJ;
Ashton, K;
Proietto, T;
Otton, G;
Wersäll, O;
Mints, M;
Tham, E;
RENDOCAS;
Hall, P;
Czene, K;
Liu, J;
Li, J;
Hopper, JL;
Southey, MC;
Australian Ovarian Cancer Study (AOCS);
Ekici, AB;
Ruebner, M;
Johnson, N;
Peto, J;
Burwinkel, B;
Marme, F;
Brenner, H;
Dieffenbach, AK;
Meindl, A;
Brauch, H;
GENICA Network;
Lindblom, A;
Depreeuw, J;
Moisse, M;
Chang-Claude, J;
Rudolph, A;
Couch, FJ;
Olson, JE;
Giles, GG;
Bruinsma, F;
Cunningham, JM;
Fridley, BL;
Børresen-Dale, AL;
Kristensen, VN;
Cox, A;
Swerdlow, AJ;
Orr, N;
Bolla, MK;
Wang, Q;
Weber, RP;
Chen, Z;
Shah, M;
Pharoah, PD;
Dunning, AM;
Tomlinson, I;
Easton, DF;
Spurdle, AB;
Thompson, DJ;
(2014)
Candidate locus analysis of the TERT-CLPTM1L cancer risk region on chromosome 5p15 identifies multiple independent variants associated with endometrial cancer risk.
Human genetics, 134 (2).
pp. 231-45.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-014-1515-4
D
Diakite, M;
Clark, TG;
Auburn, S;
Campino, S;
Fry, AE;
Green, A;
Morris, AP;
Richardson, A;
Jallow, M;
Sisay-Joof, F;
+3 more...
Pinder, M;
Kwiatkowski, DP;
Rockett, KA;
(2009)
A genetic association study in the Gambia using tagging polymorphisms in the major histocompatibility complex class III region implicates a HLA-B associated transcript 2 polymorphism in severe malaria susceptibility.
Human genetics, 125 (1).
pp. 105-9.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-008-0597-2
Full text not available from this repository.
E
Ebrahim, S;
Smith, GD;
(2008)
Mendelian randomization: can genetic epidemiology help redress the failures of observational epidemiology?
Human genetics, 123 (1).
pp. 15-33.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-007-0448-6
Full text not available from this repository.
G
Goncalves, A;
Makalo, P;
Joof, H;
Burr, S;
Ramadhani, A;
Massae, P;
Malisa, A;
Mtuy, T;
Derrick, T;
Last, AR;
+11 more...
Nabicassa, M;
Cassama, E;
Houghton, J;
Palmer, CD;
Pickering, H;
Burton, MJ;
Mabey, DC;
Bailey, RL;
Goodier, MR;
Holland, MJ;
Roberts, CH;
(2016)
Differential frequency of NKG2C/KLRC2 deletion in distinct African populations and susceptibility to Trachoma: a new method for imputation of KLRC2 genotypes from SNP genotyping data.
Human genetics, 135 (8).
pp. 939-51.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-016-1694-2
H
Higgins, CD;
Swerdlow, AJ;
Schoemaker, MJ;
Wright, AF;
Jacobs, PA;
On behalf of the UK clinical cytogenetics group;
(2007)
Mortality and cancer incidence in males with Y polysomy in Britain: a cohort study.
Human genetics, 121 (6).
pp. 691-6.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-007-0365-8
Full text not available from this repository.
Houlston, RS;
Peto, J;
(2003)
The future of association studies of common cancers.
Human genetics, 112 (4).
pp. 434-435.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-002-0902-4
Full text not available from this repository.
L
Lei, J;
Rudolph, A;
Moysich, KB;
Behrens, S;
Goode, EL;
Bolla, MK;
Dennis, J;
Dunning, AM;
Easton, DF;
Wang, Q;
+80 more...
Benitez, J;
Hopper, JL;
Southey, MC;
Schmidt, MK;
Broeks, A;
Fasching, PA;
Haeberle, L;
Peto, J;
Dos-Santos-Silva, I;
Sawyer, EJ;
Tomlinson, I;
Burwinkel, B;
Marmé, F;
Guénel, P;
Truong, T;
Bojesen, SE;
Flyger, H;
Nielsen, SF;
Nordestgaard, BG;
González-Neira, A;
Menéndez, P;
Anton-Culver, H;
Neuhausen, SL;
Brenner, H;
Arndt, V;
Meindl, A;
Schmutzler, RK;
Brauch, H;
Hamann, U;
Nevanlinna, H;
Fagerholm, R;
Dörk, T;
Bogdanova, NV;
Mannermaa, A;
Hartikainen, JM;
Australian Ovarian Study Group;
kConFab Investigators;
Van Dijck, L;
Smeets, A;
Flesch-Janys, D;
Eilber, U;
Radice, P;
Peterlongo, P;
Couch, FJ;
Hallberg, E;
Giles, GG;
Milne, RL;
Haiman, CA;
Schumacher, F;
Simard, J;
Goldberg, MS;
Kristensen, V;
Borresen-Dale, AL;
Zheng, W;
Beeghly-Fadiel, A;
Winqvist, R;
Grip, M;
Andrulis, IL;
Glendon, G;
García-Closas, M;
Figueroa, J;
Czene, K;
Brand, JS;
Darabi, H;
Eriksson, M;
Hall, P;
Li, J;
Cox, A;
Cross, SS;
Pharoah, PD;
Shah, M;
Kabisch, M;
Torres, D;
Jakubowska, A;
Lubinski, J;
Ademuyiwa, F;
Ambrosone, CB;
Swerdlow, A;
Jones, M;
Chang-Claude, J;
(2015)
Genetic variation in the immunosuppression pathway genes and breast cancer susceptibility: a pooled analysis of 42,510 cases and 40,577 controls from the Breast Cancer Association Consortium.
Human genetics, 135 (1).
pp. 137-54.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-015-1616-8
M
Molokhia, M;
Hoggart, C;
Patrick, AL;
Shriver, M;
Parra, E;
Ye, J;
Silman, AJ;
McKeigue, PM;
(2003)
Relation of risk of systemic lupus erythematosus to west African admixture in a Caribbean population.
Human genetics, 112 (3).
pp. 310-8.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-002-0883-3
Full text not available from this repository.
R
Rhodes, B;
Morris, DL;
Subrahmanyan, L;
Aubin, C;
de Leon, CFM;
Kelly, JF;
Evans, DA;
Whittaker, JC;
Oksenberg, JR;
de Jager, PL;
+1 more...
Vyse, TJ;
(2008)
Fine-mapping the genetic basis of CRP regulation in African Americans: a Bayesian approach.
Human genetics, 123 (6).
pp. 633-642.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-008-0517-5
Full text not available from this repository.
S
Sellick, GS;
Coleman, RJ;
Webb, EL;
Chow, J;
Bevan, S;
Rosbotham, JL;
Houlston, RS;
(2005)
Dominantly inherited cutaneous small-vessel lymphocytic vasculitis maps to chromosome 6q26-q27.
Human genetics, 118 (1).
pp. 82-6.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-005-0022-z
Full text not available from this repository.
Shriver, MD;
Parra, EJ;
Dios, S;
Bonilla, C;
Norton, H;
Jovel, C;
Pfaff, C;
Jones, C;
Massac, A;
Cameron, N;
+7 more...
Baron, A;
Jackson, T;
Argyropoulos, G;
Jin, L;
Hoggart, CJ;
McKeigue, PM;
Kittles, RA;
(2003)
Skin pigmentation, biogeographical ancestry and admixture mapping.
Human genetics, 112 (4).
pp. 387-399.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-002-0896-y
Full text not available from this repository.
Sirugo, G;
Hennig, BJ;
Adeyemo, AA;
Matimba, A;
Newport, MJ;
Ibrahim, ME;
Ryckman, KK;
Tacconelli, A;
Mariani-Costantini, R;
Novelli, G;
+5 more...
Soodyall, H;
Rotimi, CN;
Ramesar, RS;
Tishkoff, SA;
Williams, SM;
(2008)
Genetic studies of African populations: an overview on disease susceptibility and response to vaccines and therapeutics.
Human genetics, 123 (6).
pp. 557-98.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-008-0511-y
Full text not available from this repository.
Swerdlow, AJ;
Schoemaker, MJ;
Higgins, CD;
Wright, AF;
Jacobs, PA;
(2005)
Mortality and cancer incidence in women with extra X chromosomes: a cohort study in Britain.
Human genetics, 118 (2).
pp. 255-60.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-005-0043-7
Full text not available from this repository.
Swerdlow, AJ;
Schoemaker, MJ;
Higgins, CD;
Wright, AF;
Jacobs, PA;
UK Clinical Cytogenetics Group;
(2008)
Mortality risks in patients with constitutional autosomal chromosome deletions in Britain: a cohort study.
Human genetics, 123 (2).
pp. 215-24.
ISSN 0340-6717
DOI: https://doi.org/10.1007/s00439-008-0465-0
Full text not available from this repository.