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Number of items: 45.
2016
Figueroa, JD;
Middlebrooks, CD;
Banday, AR;
Ye, Y;
Garcia-Closas, M;
Chatterjee, N;
Koutros, S;
Kiemeney, LA;
Rafnar, T;
Bishop, T;
+117 more...
Furberg, H;
Matullo, G;
Golka, K;
Gago-Dominguez, M;
Taylor, JA;
Fletcher, T;
Siddiq, A;
Cortessis, VK;
Kooperberg, C;
Cussenot, O;
Benhamou, S;
Prescott, J;
Porru, S;
Dinney, CP;
Malats, N;
Baris, D;
Purdue, MP;
Jacobs, EJ;
Albanes, D;
Wang, Z;
Chung, CC;
Vermeulen, SH;
Aben, KK;
Galesloot, TE;
Thorleifsson, G;
Sulem, P;
Stefansson, K;
Kiltie, AE;
Harland, M;
Teo, M;
Offit, K;
Vijai, J;
Bajorin, D;
Kopp, R;
Fiorito, G;
Guarrera, S;
Sacerdote, C;
Selinski, S;
Hengstler, JG;
Gerullis, H;
Ovsiannikov, D;
Blaszkewicz, M;
Esteban Castelao, J;
Calaza, M;
Martinez, ME;
Cordeiro, P;
Xu, Z;
Panduri, V;
Kumar, R;
Gurzau, E;
Koppova, K;
Bueno-de-Mesquita, HB;
Ljungberg, B;
Clavel-Chapelon, F;
Weiderpass, E;
Krogh, V;
Dorronsoro, M;
Travis, RC;
Tjonneland, A;
Brennan, P;
Chang-Claude, J;
Riboli, E;
Conti, D;
Stern, MC;
Pike, MC;
van Den Berg, D;
Yuan, J.-, M;
Hohensee, C;
Jeppson, RP;
Cancel-Tassin, G;
Roupret, M;
Comperat, E;
Turman, C;
de Vivo, I;
Giovannucci, E;
Hunter, DJ;
Kraft, P;
Lindstrom, S;
Carta, A;
Pavanello, S;
Arici, C;
Mastrangelo, G;
Kamat, AM;
Zhang, L;
Gong, Y;
Pu, X;
Hutchinson, A;
Burdett, L;
Wheeler, WA;
Karagas, MR;
Johnson, A;
Schned, A;
Hosain, GMM;
Schwenn, M;
Kogevinas, M;
Tardon, A;
Serra, C;
Carrato, A;
Garcia-Closas, R;
Lloreta, J;
Andriole, G., Jr;
Grubb, R., III;
Black, A;
Diver, WR;
Gapstur, SM;
Weinstein, S;
Virtamo, J;
Haiman, CA;
Landi, MT;
Caporaso, NE;
Fraumeni, J.F., Jr;
Vineis, P;
Wu, X;
Chanock, SJ;
Silverman, DT;
Prokunina-Olsson, L;
Rothman, N;
(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: https://doi.org/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...
Hopper, JL;
Southey, MC;
Schmidt, MK;
Broeks, A;
Muir, K;
Lophatananon, A;
Fasching, PA;
Beckmann, MW;
Peto, J;
Dos-Santos-Silva, I;
Sawyer, EJ;
Tomlinson, I;
Burwinkel, B;
Marme, F;
Guénel, P;
Truong, T;
Bojesen, SE;
Nordestgaard, BG;
González-Neira, A;
Benitez, J;
Neuhausen, SL;
Brenner, H;
Dieffenbach, AK;
Meindl, A;
Schmutzler, RK;
Brauch, H;
GENICA Network;
Nevanlinna, H;
Khan, S;
Matsuo, K;
Ito, H;
Dörk, T;
Bogdanova, NV;
Lindblom, A;
Margolin, S;
Mannermaa, A;
Kosma, VM;
kConFab Investigators;
Australian Ovarian Cancer Study Group;
Wu, AH;
Van Den Berg, D;
Lambrechts, D;
Wildiers, H;
Chang-Claude, J;
Rudolph, A;
Radice, P;
Peterlongo, P;
Couch, FJ;
Olson, JE;
Giles, GG;
Milne, RL;
Haiman, CA;
Henderson, BE;
Dumont, M;
Teo, SH;
Wong, TY;
Kristensen, V;
Zheng, W;
Long, J;
Winqvist, R;
Pylkäs, K;
Andrulis, IL;
Knight, JA;
Devilee, P;
Seynaeve, C;
García-Closas, M;
Figueroa, J;
Klevebring, D;
Czene, K;
Hooning, MJ;
van den Ouweland, AM;
Darabi, H;
Shu, XO;
Gao, YT;
Cox, A;
Blot, W;
Signorello, LB;
Shah, M;
Kang, D;
Choi, JY;
Hartman, M;
Miao, H;
Hamann, U;
Jakubowska, A;
Lubinski, J;
Sangrajrang, S;
McKay, J;
Toland, AE;
Yannoukakos, D;
Shen, CY;
Wu, PE;
Swerdlow, A;
Orr, N;
Simard, J;
Pharoah, PD;
Dunning, AM;
Chenevix-Trench, G;
Hall, P;
Bandera, E;
Amos, C;
Ambrosone, C;
Easton, DF;
Cole, MD;
(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: https://doi.org/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...
Whiley, P;
Blanco, A;
Raponi, M;
Hauke, J;
Wappenschmidt, B;
Becker, A;
Hansen, TV;
Behar, R;
KConFaB investigators;
Niederacher, D;
Arnold, N;
Dworniczak, B;
Steinemann, D;
Faust, U;
Rubinstein, W;
Hulick, PJ;
Houdayer, C;
Caputo, SM;
Castera, L;
Pesaran, T;
Chao, E;
Brewer, C;
Southey, MC;
van Asperen, CJ;
Singer, CF;
Sullivan, J;
Poplawski, N;
Mai, P;
Peto, J;
Johnson, N;
Burwinkel, B;
Surowy, H;
Bojesen, SE;
Flyger, H;
Lindblom, A;
Margolin, S;
Chang-Claude, J;
Rudolph, A;
Radice, P;
Galastri, L;
Olson, JE;
Hallberg, E;
Giles, GG;
Milne, RL;
Andrulis, IL;
Glendon, G;
Hall, P;
Czene, K;
Blows, F;
Shah, M;
Wang, Q;
Dennis, J;
Michailidou, K;
McGuffog, L;
Bolla, MK;
Antoniou, AC;
Easton, DF;
Couch, FJ;
Tavtigian, S;
Vreeswijk, M;
Parsons, M;
Meeks, H;
Martins, A;
Goldgar, DE;
Spurdle, AB;
(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: https://doi.org/10.1093/hmg/ddw094
Full text not available from this repository.
2015
Felix, JF;
Bradfield, JP;
Monnereau, C;
van der Valk, RJ;
Stergiakouli, E;
Chesi, A;
Gaillard, R;
Feenstra, B;
Thiering, E;
Kreiner-Møller, E;
+113 more...
Mahajan, A;
Pitkänen, N;
Joro, R;
Cavadino, A;
Huikari, V;
Franks, S;
Groen-Blokhuis, MM;
Cousminer, DL;
Marsh, JA;
Lehtimäki, T;
Curtin, JA;
Vioque, J;
Ahluwalia, TS;
Myhre, R;
Price, TS;
Vilor-Tejedor, N;
Yengo, L;
Grarup, N;
Ntalla, I;
Ang, W;
Atalay, M;
Bisgaard, H;
Blakemore, AI;
Bonnefond, A;
Carstensen, L;
Bone Mineral Density in Childhood Study (BMDCS);
Early Genetics and Lifecourse Epidemiology (EAGLE) consortium;
Eriksson, J;
Flexeder, C;
Franke, L;
Geller, F;
Geserick, M;
Hartikainen, AL;
Haworth, CM;
Hirschhorn, JN;
Hofman, A;
Holm, JC;
Horikoshi, M;
Hottenga, JJ;
Huang, J;
Kadarmideen, HN;
Kähönen, M;
Kiess, W;
Lakka, HM;
Lakka, TA;
Lewin, AM;
Liang, L;
Lyytikäinen, LP;
Ma, B;
Magnus, P;
McCormack, SE;
McMahon, G;
Mentch, FD;
Middeldorp, CM;
Murray, CS;
Pahkala, K;
Pers, TH;
Pfäffle, R;
Postma, DS;
Power, C;
Simpson, A;
Sengpiel, V;
Tiesler, CM;
Torrent, M;
Uitterlinden, AG;
van Meurs, JB;
Vinding, R;
Waage, J;
Wardle, J;
Zeggini, E;
Zemel, BS;
Dedoussis, GV;
Pedersen, O;
Froguel, P;
Sunyer, J;
Plomin, R;
Jacobsson, B;
Hansen, T;
Gonzalez, JR;
Custovic, A;
Raitakari, OT;
Pennell, CE;
Widén, E;
Boomsma, DI;
Koppelman, GH;
Sebert, S;
Järvelin, MR;
Hyppönen, E;
McCarthy, MI;
Lindi, V;
Harri, N;
Körner, A;
Bønnelykke, K;
Heinrich, J;
Melbye, M;
Rivadeneira, F;
Hakonarson, H;
Ring, SM;
Smith, GD;
Sørensen, TI;
Timpson, NJ;
Grant, SF;
Jaddoe, VW;
Early Growth Genetics (EGG) Consortium;
Bone Mineral Density in Childhood Study BMDCS;
, COLLABORATORS;
Kalkwarf, HJ;
Lappe, JM;
Gilsanz, V;
Oberfield, SE;
Shepherd, JA;
Kelly, A;
Zemel, BS;
(2015)
Genome-wide association analysis identifies three new susceptibility loci for childhood body mass index.
Human molecular genetics, 25 (2).
pp. 389-403.
ISSN 0964-6906
DOI: https://doi.org/10.1093/hmg/ddv472
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...
Apicella, C;
Stone, J;
Schmidt, MK;
Broeks, A;
Van't Veer, LJ;
Hogervorst, FB;
Fasching, PA;
Haeberle, L;
Ekici, AB;
Beckmann, MW;
Gibson, L;
Aitken, Z;
Warren, H;
Sawyer, E;
Tomlinson, I;
Kerin, MJ;
Miller, N;
Burwinkel, B;
Marme, F;
Schneeweiss, A;
Sohn, C;
Guénel, P;
Truong, T;
Cordina-Duverger, E;
Sanchez, M;
Bojesen, SE;
Nordestgaard, BG;
Nielsen, SF;
Flyger, H;
Benitez, J;
Zamora, MP;
Arias Perez, JI;
Menéndez, P;
Anton-Culver, H;
Neuhausen, SL;
Brenner, H;
Dieffenbach, AK;
Arndt, V;
Stegmaier, C;
Hamann, U;
Brauch, H;
Justenhoven, C;
Brüning, T;
Ko, YD;
Nevanlinna, H;
Aittomäki, K;
Blomqvist, C;
Khan, S;
Bogdanova, N;
Dörk, T;
Lindblom, A;
Margolin, S;
Mannermaa, A;
Kataja, V;
Kosma, VM;
Hartikainen, JM;
Chenevix-Trench, G;
Beesley, J;
Lambrechts, D;
Moisse, M;
Floris, G;
Beuselinck, B;
Chang-Claude, J;
Rudolph, A;
Seibold, P;
Flesch-Janys, D;
Radice, P;
Peterlongo, P;
Peissel, B;
Pensotti, V;
Couch, FJ;
Olson, JE;
Slettedahl, S;
Vachon, C;
Giles, GG;
Milne, RL;
McLean, C;
Haiman, CA;
Henderson, BE;
Schumacher, F;
Le Marchand, L;
Simard, J;
Goldberg, MS;
Labrèche, F;
Dumont, M;
Kristensen, V;
Alnæs, GG;
Nord, S;
Borresen-Dale, AL;
Zheng, W;
Deming-Halverson, S;
Shrubsole, M;
Long, J;
Winqvist, R;
Pylkäs, K;
Jukkola-Vuorinen, A;
Grip, M;
Andrulis, IL;
Knight, JA;
Glendon, G;
Tchatchou, S;
Devilee, P;
Tollenaar, RA;
Seynaeve, CM;
Van Asperen, CJ;
Garcia-Closas, M;
Figueroa, J;
Chanock, SJ;
Lissowska, J;
Czene, K;
Darabi, H;
Eriksson, M;
Klevebring, D;
Hooning, MJ;
Hollestelle, A;
van Deurzen, CH;
Kriege, M;
Hall, P;
Li, J;
Liu, J;
Humphreys, K;
Cox, A;
Cross, SS;
Reed, MW;
Pharoah, PD;
Dunning, AM;
Shah, M;
Perkins, BJ;
Jakubowska, A;
Lubinski, J;
Jaworska-Bieniek, K;
Durda, K;
Ashworth, A;
Swerdlow, A;
Jones, M;
Schoemaker, MJ;
Meindl, A;
Schmutzler, RK;
Olswold, C;
Slager, S;
Toland, AE;
Yannoukakos, D;
Muir, K;
Lophatananon, A;
Stewart-Brown, S;
Siriwanarangsan, P;
Matsuo, K;
Ito, H;
Iwata, H;
Ishiguro, J;
Wu, AH;
Tseng, CC;
Van Den Berg, D;
Stram, DO;
Teo, SH;
Yip, CH;
Kang, P;
Ikram, MK;
Shu, XO;
Lu, W;
Gao, YT;
Cai, H;
Kang, D;
Choi, JY;
Park, SK;
Noh, DY;
Hartman, M;
Miao, H;
Lim, WY;
Lee, SC;
Sangrajrang, S;
Gaborieau, V;
Brennan, P;
Mckay, J;
Wu, PE;
Hou, MF;
Yu, JC;
Shen, CY;
Blot, W;
Cai, Q;
Signorello, LB;
Luccarini, C;
Bayes, C;
Ahmed, S;
Maranian, M;
Healey, CS;
González-Neira, A;
Pita, G;
Alonso, MR;
Álvarez, N;
Herrero, D;
Tessier, DC;
Vincent, D;
Bacot, F;
Hunter, DJ;
Lindstrom, S;
Dennis, J;
Michailidou, K;
Bolla, MK;
Easton, DF;
dos Santos Silva, I;
Fletcher, O;
Peto, J;
GENICA Network;
kConFab Investigators;
Australian Ovarian Cancer Study Group;
(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: https://doi.org/10.1093/hmg/ddv035
2014
Lin, WY;
Camp, NJ;
Ghoussaini, M;
Beesley, J;
Michailidou, K;
Hopper, JL;
Apicella, C;
Southey, MC;
Stone, J;
Schmidt, MK;
+215 more...
Broeks, A;
Van't Veer, LJ;
Th Rutgers, EJ;
Muir, K;
Lophatananon, A;
Stewart-Brown, S;
Siriwanarangsan, P;
Fasching, PA;
Haeberle, L;
Ekici, AB;
Beckmann, MW;
Peto, J;
Dos-Santos-Silva, I;
Fletcher, O;
Johnson, N;
Bolla, MK;
Wang, Q;
Dennis, J;
Sawyer, EJ;
Cheng, T;
Tomlinson, I;
Kerin, MJ;
Miller, N;
Marmé, F;
Surowy, HM;
Burwinkel, B;
Guénel, P;
Truong, T;
Menegaux, F;
Mulot, C;
Bojesen, SE;
Nordestgaard, BG;
Nielsen, SF;
Flyger, H;
Benitez, J;
Zamora, MP;
Arias Perez, JI;
Menéndez, P;
González-Neira, A;
Pita, G;
Alonso, MR;
Alvarez, N;
Herrero, D;
Anton-Culver, H;
Brenner, H;
Dieffenbach, AK;
Arndt, V;
Stegmaier, C;
Meindl, A;
Lichtner, P;
Schmutzler, RK;
Müller-Myhsok, B;
Brauch, H;
Brüning, T;
Ko, YD;
GENICA Network;
Tessier, DC;
Vincent, D;
Bacot, F;
Nevanlinna, H;
Aittomäki, K;
Blomqvist, C;
Khan, S;
Matsuo, K;
Ito, H;
Iwata, H;
Horio, A;
Bogdanova, NV;
Antonenkova, NN;
Dörk, T;
Lindblom, A;
Margolin, S;
Mannermaa, A;
Kataja, V;
Kosma, VM;
Hartikainen, JM;
kConFab Investigators;
Australian Ovarian Cancer Study Group;
Wu, AH;
Tseng, CC;
Van Den Berg, D;
Stram, DO;
Neven, P;
Wauters, E;
Wildiers, H;
Lambrechts, D;
Chang-Claude, J;
Rudolph, A;
Seibold, P;
Flesch-Janys, D;
Radice, P;
Peterlongo, P;
Manoukian, S;
Bonanni, B;
Couch, FJ;
Wang, X;
Vachon, C;
Purrington, K;
Giles, GG;
Milne, RL;
Mclean, C;
Haiman, CA;
Henderson, BE;
Schumacher, F;
Le Marchand, L;
Simard, J;
Goldberg, MS;
Labrèche, F;
Dumont, M;
Teo, SH;
Yip, CH;
Hassan, N;
Vithana, EN;
Kristensen, V;
Zheng, W;
Deming-Halverson, S;
Shrubsole, MJ;
Long, J;
Winqvist, R;
Pylkäs, K;
Jukkola-Vuorinen, A;
Kauppila, S;
Andrulis, IL;
Knight, JA;
Glendon, G;
Tchatchou, S;
Devilee, P;
Tollenaar, RA;
Seynaeve, C;
Van Asperen, CJ;
García-Closas, M;
Figueroa, J;
Lissowska, J;
Brinton, L;
Czene, K;
Darabi, H;
Eriksson, M;
Brand, JS;
Hooning, MJ;
Hollestelle, A;
Van Den Ouweland, AM;
Jager, A;
Li, J;
Liu, J;
Humphreys, K;
Shu, XO;
Lu, W;
Gao, YT;
Cai, H;
Cross, SS;
Reed, MW;
Blot, W;
Signorello, LB;
Cai, Q;
Pharoah, PD;
Perkins, B;
Shah, M;
Blows, FM;
Kang, D;
Yoo, KY;
Noh, DY;
Hartman, M;
Miao, H;
Chia, KS;
Putti, TC;
Hamann, U;
Luccarini, C;
Baynes, C;
Ahmed, S;
Maranian, M;
Healey, CS;
Jakubowska, A;
Lubinski, J;
Jaworska-Bieniek, K;
Durda, K;
Sangrajrang, S;
Gaborieau, V;
Brennan, P;
Mckay, J;
Slager, S;
Toland, AE;
Yannoukakos, D;
Shen, CY;
Hsiung, CN;
Wu, PE;
Ding, SL;
Ashworth, A;
Jones, M;
Orr, N;
Swerdlow, AJ;
Tsimiklis, H;
Makalic, E;
Schmidt, DF;
Bui, QM;
Chanock, SJ;
Hunter, DJ;
Hein, R;
Dahmen, N;
Beckmann, L;
Aaltonen, K;
Muranen, TA;
Heikkinen, T;
Irwanto, A;
Rahman, N;
Turnbull, CA;
Breast and Ovarian Cancer Susceptibility (BOCS) Study;
Waisfisz, Q;
Meijers-Heijboer, HE;
Adank, MA;
Van Der Luijt, RB;
Hall, P;
Chenevix-Trench, G;
Dunning, A;
Easton, DF;
Cox, A;
(2014)
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: https://doi.org/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;
+43 more...
Peto, J;
Kote-Jarai, Z;
Muir, K;
Nsengimana, J;
UKTCC;
Stratton, MR;
Easton, DF;
Bishop, DT;
Huddart, RA;
Rahman, N;
Turnbull, C;
UKTCC;
, COLLABORATORS;
Pugh, J;
Linger, R;
Marke, J;
Hughes, D;
Pernet, D;
Hall, P;
Easton, DF;
Berchuck, A;
Eeles, R;
Chenevix-Trench, G;
Dennis, J;
Dunning, AM;
Lee, A;
Dicks, E;
Easton, DF;
Benitez, J;
Gonzalez-Neira, A;
Simard, J;
Tessier, DC;
Bacot, F;
Vincent, D;
LaBoissière, S;
Robidoux, F;
Bojesen, SE;
Nielsen, SF;
Nordestgaard, BG;
Cunningham, JM;
Windebank, SA;
Hilker, CA;
Meyer, J;
(2014)
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: https://doi.org/10.1093/hmg/ddu511
Full text not available from this repository.
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...
Alonso, MR;
Dennis, J;
Wang, Q;
Bolla, MK;
Swerdlow, A;
Ashworth, A;
Orr, N;
Schoemaker, M;
Ko, YD;
Brauch, H;
Hamann, U;
GENICA Network;
Andrulis, IL;
Knight, JA;
Glendon, G;
Tchatchou, S;
kConFab Investigators;
Australian Ovarian Cancer Study Group;
Matsuo, K;
Ito, H;
Iwata, H;
Tajima, K;
Li, J;
Brand, JS;
Brenner, H;
Dieffenbach, AK;
Arndt, V;
Stegmaier, C;
Lambrechts, D;
Peuteman, G;
Christiaens, MR;
Smeets, A;
Jakubowska, A;
Lubinski, J;
Jaworska-Bieniek, K;
Durda, K;
Hartman, M;
Hui, M;
Yen Lim, W;
Wan Chan, C;
Marme, F;
Yang, R;
Bugert, P;
Lindblom, A;
Margolin, S;
García-Closas, M;
Chanock, SJ;
Lissowska, J;
Figueroa, JD;
Bojesen, SE;
Nordestgaard, BG;
Flyger, H;
Hooning, MJ;
Kriege, M;
van den Ouweland, AM;
Koppert, LB;
Fletcher, O;
Johnson, N;
dos-Santos-Silva, I;
Peto, J;
Zheng, W;
Deming-Halverson, S;
Shrubsole, MJ;
Long, J;
Chang-Claude, J;
Rudolph, A;
Seibold, P;
Flesch-Janys, D;
Winqvist, R;
Pylkäs, K;
Jukkola-Vuorinen, A;
Grip, M;
Cox, A;
Cross, SS;
Reed, MW;
Schmidt, MK;
Broeks, A;
Cornelissen, S;
Braaf, L;
Kang, D;
Choi, JY;
Park, SK;
Noh, DY;
Simard, J;
Dumont, M;
Goldberg, MS;
Labrèche, F;
Fasching, PA;
Hein, A;
Ekici, AB;
Beckmann, MW;
Radice, P;
Peterlongo, P;
Azzollini, J;
Barile, M;
Sawyer, E;
Tomlinson, I;
Kerin, M;
Miller, N;
Hopper, JL;
Schmidt, DF;
Makalic, E;
Southey, MC;
Hwang Teo, S;
Har Yip, C;
Sivanandan, K;
Tay, WT;
Shen, CY;
Hsiung, CN;
Yu, JC;
Hou, MF;
Guénel, P;
Truong, T;
Sanchez, M;
Mulot, C;
Blot, W;
Cai, Q;
Nevanlinna, H;
Muranen, TA;
Aittomäki, K;
Blomqvist, C;
Wu, AH;
Tseng, CC;
Van Den Berg, D;
Stram, DO;
Bogdanova, N;
Dörk, T;
Muir, K;
Lophatananon, A;
Stewart-Brown, S;
Siriwanarangsan, P;
Mannermaa, A;
Kataja, V;
Kosma, VM;
Hartikainen, JM;
Shu, XO;
Lu, W;
Gao, YT;
Zhang, B;
Couch, FJ;
Toland, AE;
TNBCC;
Yannoukakos, D;
Sangrajrang, S;
McKay, J;
Wang, X;
Olson, JE;
Vachon, C;
Purrington, K;
Severi, G;
Baglietto, L;
Haiman, CA;
Henderson, BE;
Schumacher, F;
Le Marchand, L;
Devilee, P;
Tollenaar, RA;
Seynaeve, C;
Czene, K;
Eriksson, M;
Humphreys, K;
Darabi, H;
Ahmed, S;
Shah, M;
Pharoah, PD;
Hall, P;
Giles, GG;
Benítez, J;
Dunning, AM;
Chenevix-Trench, G;
Easton, DF;
(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: https://doi.org/10.1093/hmg/ddu311
Painter, JN;
O'Mara, TA;
Batra, J;
Cheng, T;
Lose, FA;
Dennis, J;
Michailidou, K;
Tyrer, JP;
Ahmed, S;
Ferguson, K;
+443 more...
Healey, CS;
Kaufmann, S;
Hillman, KM;
Walpole, C;
Moya, L;
Pollock, P;
Jones, A;
Howarth, K;
Martin, L;
Gorman, M;
Hodgson, S;
National Study of Endometrial Cancer Genetics Group (NSECG);
CHIBCHA Consortium;
De Polanco, MM;
Sans, M;
Carracedo, A;
Castellvi-Bel, S;
Rojas-Martinez, A;
Santos, E;
Teixeira, MR;
Carvajal-Carmona, L;
Shu, XO;
Long, J;
Zheng, W;
Xiang, YB;
Australian National Endometrial Cancer Study Group (ANECS);
Montgomery, GW;
Webb, PM;
Scott, RJ;
McEvoy, M;
Attia, J;
Holliday, E;
Martin, NG;
Nyholt, DR;
Henders, AK;
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;
Ashton, K;
Proietto, T;
Otton, G;
Tzortzatos, G;
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;
French, JD;
Pharoah, PD;
Dunning, AM;
Tomlinson, I;
Easton, DF;
Edwards, SL;
Thompson, DJ;
Spurdle, AB;
, COLLABORATORS;
Spurdle, AB;
Webb, PM;
Young, J;
McQuire, L;
Baron-Hay, S;
Bell, D;
Bonaventura, A;
Brand, A;
Braye, S;
Carter, J;
Chan, F;
Dalrymple, C;
Ferrier, A;
Gard, G;
Hacker, N;
Hogg, R;
Houghton, R;
Marsden, D;
McIlroy, K;
Otton, G;
Pather, S;
Proietto, A;
Robertson, G;
Scurry, J;
Sharma, R;
Wain, G;
Wong, F;
Armes, J;
Crandon, A;
Cummings, M;
Land, R;
Nicklin, J;
Perrin, L;
Obermair, A;
Ward, B;
Davy, M;
Dodd, T;
Miller, J;
Oehler, M;
Paramasivum, S;
Pierides, J;
Whitehead, F;
Blomfield, P;
Challis, D;
Neesham, D;
Pyman, J;
Quinn, M;
Rome, R;
Weitzer, M;
Brennan, B;
Hammond, I;
Leung, Y;
McCartney, A;
Stewart, C;
Thompson, J;
O'Brien, S;
Moore, S;
Ferguson, K;
Walsh, M;
Cicero, R;
Green, L;
Griffith, J;
Jackman, L;
Ranieri, B;
O'Brien, M;
Schultz, P;
Alexander, B;
Baxter, C;
Croy, H;
Fitzgerald, A;
Herron, E;
Hill, C;
Jones, M;
Maidens, J;
Marshall, A;
Martin, K;
Mayhew, J;
Minehan, E;
Roffe, D;
Shirley, H;
Steane, H;
Stenlake, A;
Ward, A;
Webb, S;
White, J;
de Polanco, M;
Bohórquez, ME;
Prieto, R;
Criollo, A;
Ramírez, C;
Estrada, AP;
Suárez, JJ;
Martinez, AR;
Rogatto, S;
Jnr, SA;
Santos, EM;
Sans, M;
Colistro, V;
Hidalgo, PC;
Mut, P;
Carracedo, A;
Ponte, CR;
Garcia, IQ;
Castellvi-Bel, S;
Teixeira, M;
de Almeida, AB;
Hamann, U;
Gilbert, M;
Tomlinson, I;
Adams, M;
Al-Samarraie, A;
Anwar, S;
Athavale, R;
Awad, S;
Bali, A;
Barnes, A;
Cawdell, G;
Chan, S;
Chin, K;
Cornes, P;
Crawford, M;
Cullimore, J;
Ghaem-Maghami, S;
Gornall, R;
Green, J;
Hall, M;
Harvey, M;
Hawe, J;
Head, A;
Herod, J;
Hingorani, M;
Hocking, M;
Holland, C;
Hollingsworth, T;
Hollingworth, J;
Ind, T;
Irvine, R;
Irwin, C;
Katesmark, M;
Kehoe, S;
Kheng-Chew, G;
Lankester, K;
Linder, A;
Luesley, D;
B-Lynch, C;
McFarlane, V;
Naik, R;
Nicholas, N;
Nugent, D;
Oates, S;
Oladipo, A;
Papadopoulos, A;
Pearson, S;
Radstone, D;
Raju, S;
Rathmell, A;
Redman, C;
Rymer, M;
Sarhanis, P;
Sparrow, G;
Stuart, N;
Sundar, S;
Thompson, A;
Tinkler, S;
Trent, S;
Tristram, A;
Walji, N;
Woolas, R;
Lindblom, A;
Tzortzatos, G;
Mints, M;
Tham, E;
Castro, O;
Gemzell-Danielsson, K;
Baker, H;
Baynes, C;
Conroy, D;
Curzon, B;
Harrington, P;
Irvine, S;
Luccarini, C;
Mayes, R;
Munday, H;
Perkins, B;
Pharoah, D;
Platte, R;
Stafford, A;
West, J;
Shu, XO;
Zheng, W;
Long, J;
Cai, Q;
Dai, Q;
Cai, H;
Delahanty, R;
Li, C;
Xiang, YB;
Gao, Y;
Xu, WH;
Lu, W;
Zheng, Y;
Gu, K;
Stuart-Harris, R;
Kirsten, F;
Rutovitz, J;
Clingan, P;
Glasgow, A;
Proietto, A;
Braye, S;
Otton, G;
Shannon, J;
Bonaventura, T;
Stewart, J;
Begbie, S;
Friedlander, M;
Bell, D;
Baron-Hay, S;
Ferrier, A;
Gard, G;
Nevell, D;
Pavlakis, N;
Valmadre, S;
Young, B;
Camaris, C;
Crouch, R;
Edwards, L;
Hacker, N;
Marsden, D;
Robertson, G;
Beale, P;
Beith, J;
Carter, J;
Dalrymple, C;
Houghton, R;
Russell, P;
Anderson, L;
Links, M;
Grygiel, J;
Hill, J;
Brand, A;
Byth, K;
Jaworski, R;
Harnett, P;
Sharma, R;
Wain, G;
Purdie, D;
Whiteman, D;
Ward, B;
Papadimos, D;
Crandon, A;
Cummings, M;
Horwood, K;
Obermair, A;
Perrin, L;
Wyld, D;
Nicklin, J;
Davy, M;
Oehler, MK;
Hall, C;
Dodd, T;
Healy, T;
Pittman, K;
Henderson, D;
Miller, J;
Pierdes, J;
Achan, A;
Blomfield, P;
Challis, D;
McIntosh, R;
Parker, A;
Brown, B;
Rome, R;
Allen, D;
Grant, P;
Hyde, S;
Robbie, RL;
Healy, D;
Jobling, T;
Manolitsas, T;
McNealage, J;
Rogers, P;
Susil, B;
Sumithran, E;
Simpson, I;
Haviv, I;
Phillips, K;
Rischin, D;
Fox, S;
Johnson, D;
Lade, S;
Waring, P;
Loughrey, M;
O'Callaghan, N;
Murray, B;
Mileshkin, L;
Allan, P;
Billson, V;
Pyman, J;
Neesham, D;
Quinn, M;
Hamilton, A;
Underhill, C;
Bell, R;
Ng, LF;
Blum, R;
Ganju, V;
Hammond, I;
McCartney, A;
Stewart, C;
Leung, Y;
Buck, M;
Zeps, N;
Bowtell, DD;
Green, AC;
Chenevix-Trench, G;
deFazio, A;
Gertig, D;
Webb, PM;
Bugert, P;
Arndt, V;
Müller, H;
Stegmaier, C;
Lo, WY;
Justenhoven, C;
Hamann, U;
Brüning, T;
Pesch, B;
Ko, YD;
Rabstein, S;
Lotz, A;
Baisch, C;
Fischer, HP;
Harth, V;
(2014)
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: https://doi.org/10.1093/hmg/ddu552
Purrington, KS;
Slettedahl, S;
Bolla, MK;
Michailidou, K;
Czene, K;
Nevanlinna, H;
Bojesen, SE;
Andrulis, IL;
Cox, A;
Hall, P;
+157 more...
Carpenter, J;
Yannoukakos, D;
Haiman, CA;
Fasching, PA;
Mannermaa, A;
Winqvist, R;
Brenner, H;
Lindblom, A;
Chenevix-Trench, G;
Benitez, J;
Swerdlow, A;
Kristensen, V;
Guénel, P;
Meindl, A;
Darabi, H;
Eriksson, M;
Fagerholm, R;
Aittomäki, K;
Blomqvist, C;
Nordestgaard, BG;
Nielsen, SF;
Flyger, H;
Wang, X;
Olswold, C;
Olson, JE;
Mulligan, AM;
Knight, JA;
Tchatchou, S;
Reed, MW;
Cross, SS;
Liu, J;
Li, J;
Humphreys, K;
Clarke, C;
Scott, R;
ABCTB Investigators;
Fostira, F;
Fountzilas, G;
Konstantopoulou, I;
Henderson, BE;
Schumacher, F;
Le Marchand, L;
Ekici, AB;
Hartmann, A;
Beckmann, MW;
Hartikainen, JM;
Kosma, VM;
Kataja, V;
Jukkola-Vuorinen, A;
Pylkäs, K;
Kauppila, S;
Dieffenbach, AK;
Stegmaier, C;
Arndt, V;
Margolin, S;
Australian Ovarian Cancer Study Group;
kConFab Investigators;
Balleine, R;
Arias Perez, JI;
Pilar Zamora, M;
Menéndez, P;
Ashworth, A;
Jones, M;
Orr, N;
Arveux, P;
Kerbrat, P;
Truong, T;
Bugert, P;
Toland, AE;
Ambrosone, CB;
Labrèche, F;
Goldberg, MS;
Dumont, M;
Ziogas, A;
Lee, E;
Dite, GS;
Apicella, C;
Southey, MC;
Long, J;
Shrubsole, M;
Deming-Halverson, S;
Ficarazzi, F;
Barile, M;
Peterlongo, P;
Durda, K;
Jaworska-Bieniek, K;
Tollenaar, RA;
Seynaeve, C;
GENICA Network;
Brüning, T;
Ko, YD;
Van Deurzen, CH;
Martens, JW;
Kriege, M;
Figueroa, JD;
Chanock, SJ;
Lissowska, J;
Tomlinson, I;
Kerin, MJ;
Miller, N;
Schneeweiss, A;
Tapper, WJ;
Gerty, SM;
Durcan, L;
Mclean, C;
Milne, RL;
Baglietto, L;
dos Santos Silva, I;
Fletcher, O;
Johnson, N;
Van'T Veer, LJ;
Cornelissen, S;
Försti, A;
Torres, D;
Rüdiger, T;
Rudolph, A;
Flesch-Janys, D;
Nickels, S;
Weltens, C;
Floris, G;
Moisse, M;
Dennis, J;
Wang, Q;
Dunning, AM;
Shah, M;
Brown, J;
Simard, J;
Anton-Culver, H;
Neuhausen, SL;
Hopper, JL;
Bogdanova, N;
Dörk, T;
Zheng, W;
Radice, P;
Jakubowska, A;
Lubinski, J;
Devillee, P;
Brauch, H;
Hooning, M;
García-Closas, M;
Sawyer, E;
Burwinkel, B;
Marmee, F;
Eccles, DM;
Giles, GG;
Peto, J;
Schmidt, M;
Broeks, A;
Hamann, U;
Chang-Claude, J;
Lambrechts, D;
Pharoah, PD;
Easton, D;
Pankratz, VS;
Slager, S;
Vachon, CM;
Couch, FJ;
(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: https://doi.org/10.1093/hmg/ddu300
Full text not available from this repository.
van der Valk, RJ;
Kreiner-Møller, E;
Kooijman, MN;
Guxens, M;
Stergiakouli, E;
Sääf, A;
Bradfield, JP;
Geller, F;
Hayes, MG;
Cousminer, DL;
+110 more...
Körner, A;
Thiering, E;
Curtin, JA;
Myhre, R;
Huikari, V;
Joro, R;
Kerkhof, M;
Warrington, NM;
Pitkänen, N;
Ntalla, I;
Horikoshi, M;
Veijola, R;
Freathy, RM;
Teo, YY;
Barton, SJ;
Evans, DM;
Kemp, JP;
St Pourcain, B;
Ring, SM;
Davey Smith, G;
Bergström, A;
Kull, I;
Hakonarson, H;
Mentch, FD;
Bisgaard, H;
Chawes, B;
Stokholm, J;
Waage, J;
Eriksen, P;
Sevelsted, A;
Melbye, M;
Early Genetics and Lifecourse Epidemiology (EAGLE) Consortium;
van Duijn, CM;
Medina-Gomez, C;
Hofman, A;
de Jongste, JC;
Taal, HR;
Uitterlinden, AG;
Genetic Investigation of ANthropometric Traits (GIANT) Consortiu;
Armstrong, LL;
Eriksson, J;
Palotie, A;
Bustamante, M;
Estivill, X;
Gonzalez, JR;
Llop, S;
Kiess, W;
Mahajan, A;
Flexeder, C;
Tiesler, CM;
Murray, CS;
Simpson, A;
Magnus, P;
Sengpiel, V;
Hartikainen, AL;
Keinanen-Kiukaanniemi, S;
Lewin, A;
Da Silva Couto Alves, A;
Blakemore, AI;
Buxton, JL;
Kaakinen, M;
Rodriguez, A;
Sebert, S;
Vaarasmaki, M;
Lakka, T;
Lindi, V;
Gehring, U;
Postma, DS;
Ang, W;
Newnham, JP;
Lyytikäinen, LP;
Pahkala, K;
Raitakari, OT;
Panoutsopoulou, K;
Zeggini, E;
Boomsma, DI;
Groen-Blokhuis, M;
Ilonen, J;
Franke, L;
Hirschhorn, JN;
Pers, TH;
Liang, L;
Huang, J;
Hocher, B;
Knip, M;
Saw, SM;
Holloway, JW;
Melén, E;
Grant, SF;
Feenstra, B;
Lowe, WL;
Widén, E;
Sergeyev, E;
Grallert, H;
Custovic, A;
Jacobsson, B;
Jarvelin, MR;
Atalay, M;
Koppelman, GH;
Pennell, CE;
Niinikoski, H;
Dedoussis, GV;
Mccarthy, MI;
Frayling, TM;
Sunyer, J;
Timpson, NJ;
Rivadeneira, F;
Bønnelykke, K;
Jaddoe, VW;
Early Growth Genetics (EGG) Consortium;
(2014)
A novel common variant in DCST2 is associated with length in early life and height in adulthood.
Human molecular genetics, 24 (4).
pp. 1155-68.
ISSN 0964-6906
DOI: https://doi.org/10.1093/hmg/ddu510
2013
Cousminer, DL;
Berry, DJ;
Timpson, NJ;
Ang, W;
Thiering, E;
Byrne, EM;
Taal, HR;
Huikari, V;
Bradfield, JP;
Kerkhof, M;
+61 more...
Groen-Blokhuis, MM;
Kreiner-Moller, E;
Marinelli, M;
Holst, C;
Leinonen, JT;
Perry, JRB;
Surakka, I;
Pietilainen, O;
Kettunen, J;
Anttila, V;
Kaakinen, M;
Sovio, U;
Pouta, A;
Das, S;
Lagou, V;
Power, C;
Prokopenko, I;
Evans, DM;
Kemp, JP;
St Pourcain, B;
Ring, S;
Palotie, A;
Kajantie, E;
Osmond, C;
Lehtimaki, T;
Viikari, JS;
Kahonen, M;
Warrington, NM;
Lye, SJ;
Palmer, LJ;
Tiesler, CMT;
Flexeder, C;
Montgomery, GW;
Medland, SE;
Hofman, A;
Hakonarson, H;
Guxens, M;
Bartels, M;
Salomaa, V;
Murabito, JM;
Kaprio, J;
Sorensen, TIA;
Ballester, F;
Bisgaard, H;
Boomsma, DI;
Koppelman, GH;
Grant, SFA;
Jaddoe, VWV;
Martin, NG;
Heinrich, J;
Pennell, CE;
Raitakari, OT;
Eriksson, JG;
Smith, GD;
Hypponen, E;
Jarvelin, MR;
McCarthy, MI;
Ripatti, S;
Widen, E;
Reprogen, Consortium;
Early Growth Genetics, EGG;
(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: https://doi.org/10.1093/hmg/ddt104
Full text not available from this repository.
Milne, RL;
Herranz, J;
Michailidou, K;
Dennis, J;
Tyrer, JP;
Zamora, MP;
Arias-Perez, JI;
González-Neira, A;
Pita, G;
Alonso, MR;
+137 more...
Wang, Q;
Bolla, MK;
Czene, K;
Eriksson, M;
Humphreys, K;
Darabi, H;
Li, J;
Anton-Culver, H;
Neuhausen, SL;
Ziogas, A;
Clarke, CA;
Hopper, JL;
Dite, GS;
Apicella, C;
Southey, MC;
Chenevix-Trench, G;
kConFab Investigators;
Australian Ovarian Cancer Study Group;
Swerdlow, A;
Ashworth, A;
Orr, N;
Schoemaker, M;
Jakubowska, A;
Lubinski, J;
Jaworska-Bieniek, K;
Durda, K;
Andrulis, IL;
Knight, JA;
Glendon, G;
Mulligan, AM;
Bojesen, SE;
Nordestgaard, BG;
Flyger, H;
Nevanlinna, H;
Muranen, TA;
Aittomäki, K;
Blomqvist, C;
Chang-Claude, J;
Rudolph, A;
Seibold, P;
Flesch-Janys, D;
Wang, X;
Olson, JE;
Vachon, C;
Purrington, K;
Winqvist, R;
Pylkäs, K;
Jukkola-Vuorinen, A;
Grip, M;
Dunning, AM;
Shah, M;
Guénel, P;
Truong, T;
Sanchez, M;
Mulot, C;
Brenner, H;
Dieffenbach, AK;
Arndt, V;
Stegmaier, C;
Lindblom, A;
Margolin, S;
Hooning, MJ;
Hollestelle, A;
Collée, JM;
Jager, A;
Cox, A;
Brock, IW;
Reed, MW;
Devilee, P;
Tollenaar, RA;
Seynaeve, C;
Haiman, CA;
Henderson, BE;
Schumacher, F;
Le Marchand, L;
Simard, J;
Dumont, M;
Soucy, P;
Dörk, T;
Bogdanova, NV;
Hamann, U;
Försti, A;
Rüdiger, T;
Ulmer, HU;
Fasching, PA;
Häberle, L;
Ekici, AB;
Beckmann, MW;
Fletcher, O;
Johnson, N;
dos Santos Silva, I;
Peto, J;
Radice, P;
Peterlongo, P;
Peissel, B;
Mariani, P;
Giles, GG;
Severi, G;
Baglietto, L;
Sawyer, E;
Tomlinson, I;
Kerin, M;
Miller, N;
Marme, F;
Burwinkel, B;
Mannermaa, A;
Kataja, V;
Kosma, VM;
Hartikainen, JM;
Lambrechts, D;
Yesilyurt, BT;
Floris, G;
Leunen, K;
Alnæs, GG;
Kristensen, V;
Børresen-Dale, AL;
García-Closas, M;
Chanock, SJ;
Lissowska, J;
Figueroa, JD;
Schmidt, MK;
Broeks, A;
Verhoef, S;
Rutgers, EJ;
Brauch, H;
Brüning, T;
Ko, YD;
GENICA Network;
Couch, FJ;
Toland, AE;
TNBCC;
Yannoukakos, D;
Pharoah, PD;
Hall, P;
Benítez, J;
Malats, N;
Easton, DF;
(2013)
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: https://doi.org/10.1093/hmg/ddt581
Full text not available from this repository.
2012
Adams, MK;
Simpson, JA;
Richardson, AJ;
Guymer, RH;
Williamson, E;
Cantsilieris, S;
English, DR;
Aung, KZ;
Makeyeva, GA;
Giles, GG;
+3 more...
Hopper, J;
Robman, LD;
Baird, PN;
(2012)
Can genetic associations change with age? CFH and age-related macular degeneration.
Human molecular genetics, 21 (23).
pp. 5229-36.
ISSN 0964-6906
DOI: https://doi.org/10.1093/hmg/dds364
Full text not available from this repository.
Cornes, BK;
Khor, CC;
Nongpiur, ME;
Xu, L;
Tay, WT;
Zheng, Y;
Lavanya, R;
Li, Y;
Wu, R;
Sim, X;
+14 more...
Wang, YX;
Chen, P;
Teo, YY;
Chia, KS;
Seielstad, M;
Liu, J;
Hibberd, ML;
Cheng, CY;
Saw, SM;
Tai, ES;
Jonas, JB;
Vithana, EN;
Wong, TY;
Aung, T;
(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: https://doi.org/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...
Wichmann, HE;
Azazi, D;
Plagnol, V;
Pako, WH;
Whitfield, J;
Alpers, MP;
Whittaker, J;
Balding, DJ;
Zerr, I;
Kretzschmar, H;
Collinge, J;
(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: https://doi.org/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...
Ambrosone, CB;
Aittomäki, K;
Amiano, P;
Apicella, C;
Australian Breast Cancer Tissue Bank Investigators;
Baglietto, L;
Bandera, EV;
Beckmann, MW;
Berg, CD;
Bernstein, L;
Blomqvist, C;
Brauch, H;
Brinton, L;
Bui, QM;
Buring, JE;
Buys, SS;
Campa, D;
Carpenter, JE;
Chasman, DI;
Chang-Claude, J;
Chen, C;
Clavel-Chapelon, F;
Cox, A;
Cross, SS;
Czene, K;
Deming, SL;
Diasio, RB;
Diver, WR;
Dunning, AM;
Durcan, L;
Ekici, AB;
Fasching, PA;
Familial Breast Cancer Study;
Feigelson, HS;
Fejerman, L;
Figueroa, JD;
Fletcher, O;
Flesch-Janys, D;
Gaudet, MM;
GENICA Consortium;
Gerty, SM;
Rodriguez-Gil, JL;
Giles, GG;
van Gils, CH;
Godwin, AK;
Graham, N;
Greco, D;
Hall, P;
Hankinson, SE;
Hartmann, A;
Hein, R;
Heinz, J;
Hoover, RN;
Hopper, JL;
Hu, JJ;
Huntsman, S;
Ingles, SA;
Irwanto, A;
Isaacs, C;
Jacobs, KB;
John, EM;
Justenhoven, C;
Kaaks, R;
Kolonel, LN;
Coetzee, GA;
Lathrop, M;
Le Marchand, L;
Lee, AM;
Lee, IM;
Lesnick, T;
Lichtner, P;
Liu, J;
Lund, E;
Makalic, E;
Martin, NG;
McLean, CA;
Meijers-Heijboer, H;
Meindl, A;
Miron, P;
Monroe, KR;
Montgomery, GW;
Müller-Myhsok, B;
Nickels, S;
Nyante, SJ;
Olswold, C;
Overvad, K;
Palli, D;
Park, DJ;
Palmer, JR;
Pathak, H;
Peto, J;
Pharoah, P;
Rahman, N;
Rivadeneira, F;
Schmidt, DF;
Schmutzler, RK;
Slager, S;
Southey, MC;
Stevens, KN;
Sinn, HP;
Press, MF;
Ross, E;
Riboli, E;
Ridker, PM;
Schumacher, FR;
Severi, G;
Dos Santos Silva, I;
Stone, J;
Sund, M;
Tapper, WJ;
Thun, MJ;
Travis, RC;
Turnbull, C;
Uitterlinden, AG;
Waisfisz, Q;
Wang, X;
Wang, Z;
Weaver, J;
Schulz-Wendtland, R;
Wilkens, LR;
Van Den Berg, D;
Zheng, W;
Ziegler, RG;
Ziv, E;
Nevanlinna, H;
Easton, DF;
Hunter, DJ;
Henderson, BE;
Chanock, SJ;
Garcia-Closas, M;
Kraft, P;
Haiman, CA;
Vachon, CM;
(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: https://doi.org/10.1093/hmg/dds381
Full text not available from this repository.
Tyrrell, J;
Huikari, V;
Christie, JT;
Cavadino, A;
Bakker, R;
Brion, MJ;
Geller, F;
Paternoster, L;
Myhre, R;
Potter, C;
+34 more...
Johnson, PC;
Ebrahim, S;
Feenstra, B;
Hartikainen, AL;
Hattersley, AT;
Hofman, A;
Kaakinen, M;
Lowe, LP;
Magnus, P;
McConnachie, A;
Melbye, M;
Ng, JW;
Nohr, EA;
Power, C;
Ring, SM;
Sebert, SP;
Sengpiel, V;
Taal, HR;
Watt, GC;
Sattar, N;
Relton, CL;
Jacobsson, B;
Frayling, TM;
Sørensen, TI;
Murray, JC;
Lawlor, DA;
Pennell, CE;
Jaddoe, VW;
Hypponen, E;
Lowe, WLJr;
Jarvelin, MR;
Smith, GD;
Freathy, RM;
for the Early Growth Genetics (EGG) Consortium;
(2012)
Genetic variation in the 15q25 nicotinic acetylcholine receptor gene cluster (CHRNA5-CHRNA3-CHRNB4) interacts with maternal self-reported smoking status during pregnancy to influence birth weight.
Human molecular genetics.
ISSN 0964-6906
DOI: https://doi.org/10.1093/hmg/dds372
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: https://doi.org/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...
Prokhortchouk, E;
Gaborieau, V;
Jacobs, KB;
Chow, WH;
Toro, JR;
Zaridze, D;
Lin, J;
Lubinski, J;
Trubicka, J;
Szeszenia-Dabrowska, N;
Lissowska, J;
Rudnai, P;
Fabianova, E;
Mates, D;
Jinga, V;
Bencko, V;
Slamova, A;
Holcatova, I;
Navratilova, M;
Janout, V;
Boffetta, P;
Colt, JS;
Davis, FG;
Schwartz, KL;
Banks, RE;
Selby, PJ;
Harnden, P;
Berg, CD;
Hsing, AW;
Grubb, RL;
Boeing, H;
Vineis, P;
Clavel-Chapelon, F;
Palli, D;
Tumino, R;
Krogh, V;
Panico, S;
Duell, EJ;
Quiros, JR;
Sanchez, MJ;
Navarro, C;
Ardanaz, E;
Dorronsoro, M;
Khaw, KT;
Allen, NE;
Bueno-de-Mesquita, HB;
Peeters, PHM;
Trichopoulos, D;
Linseisen, J;
Ljungberg, B;
Overvad, K;
Tjonneland, A;
Romieu, I;
Riboli, E;
Stevens, VL;
Thun, MJ;
Diver, WR;
Gapstur, SM;
Pharoah, PD;
Easton, DF;
Albanes, D;
Virtamo, J;
Vatten, L;
Hveem, K;
Fletcher, T;
Koppova, K;
Cussenot, O;
Cancel-Tassin, G;
Benhamou, S;
Hildebrandt, MA;
Pu, X;
Foglio, M;
Lechner, D;
Hutchinson, A;
Yeager, M;
Fraumeni, JF;
Lathrop, M;
Skryabin, KG;
McKay, JD;
Gu, J;
Brennan, P;
Chanock, SJ;
(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: https://doi.org/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...
Tollenaar, RA;
Van't Veer, LJ;
Fasching, PA;
Beckmann, MW;
Ekici, AB;
Strick, R;
Peto, J;
dos Santos Silva, I;
Fletcher, O;
Johnson, N;
Sawyer, E;
Tomlinson, I;
Kerin, M;
Burwinkel, B;
Marme, F;
Schneeweiss, A;
Sohn, C;
Bojesen, S;
Flyger, H;
Nordestgaard, BG;
Benítez, J;
Milne, RL;
Ignacio Arias, J;
Zamora, MP;
Brenner, H;
Müller, H;
Arndt, V;
Rahman, N;
Turnbull, C;
Seal, S;
Renwick, A;
Brauch, H;
Justenhoven, C;
Brüning, T;
GENICA Network;
Chang-Claude, J;
Hein, R;
Wang-Gohrke, S;
Dörk, T;
Schürmann, P;
Bremer, M;
Hillemanns, P;
Nevanlinna, H;
Heikkinen, T;
Aittomäki, K;
Blomqvist, C;
Bogdanova, N;
Antonenkova, N;
Rogov, YI;
Karstens, JH;
Bermisheva, M;
Prokofieva, D;
Gantcev, SH;
Khusnutdinova, E;
Lindblom, A;
Margolin, S;
Chenevix-Trench, G;
Beesley, J;
Chen, X;
kConFab AOCS Management Group;
Mannermaa, A;
Kosma, VM;
Soini, Y;
Kataja, V;
Lambrechts, D;
Yesilyurt, BT;
Chrisiaens, MR;
Peeters, S;
Radice, P;
Peterlongo, P;
Manoukian, S;
Barile, M;
Couch, F;
Lee, AM;
Diasio, R;
Wang, X;
Giles, GG;
Severi, G;
Baglietto, L;
Maclean, C;
Offit, K;
Robson, M;
Joseph, V;
Gaudet, M;
John, EM;
Winqvist, R;
Pylkäs, K;
Jukkola-Vuorinen, A;
Grip, M;
Andrulis, I;
Knight, JA;
Mulligan, AM;
O'Malley, FP;
Brinton, LA;
Sherman, ME;
Lissowska, J;
Chanock, SJ;
Hooning, M;
Martens, JW;
van den Ouweland, AM;
Collée, JM;
Hall, P;
Czene, K;
Cox, A;
Brock, IW;
Reed, MW;
Cross, SS;
Pharoah, P;
Dunning, AM;
Kang, D;
Yoo, KY;
Noh, DY;
Ahn, SH;
Jakubowska, A;
Lubinski, J;
Jaworska, K;
Durda, K;
Sangrajrang, S;
Gaborieau, V;
Brennan, P;
McKay, J;
Shen, CY;
Ding, SL;
Hsu, HM;
Yu, JC;
Anton-Culver, H;
Ziogas, A;
Ashworth, A;
Swerdlow, A;
Jones, M;
Orr, N;
Trentham-Dietz, A;
Egan, K;
Newcomb, P;
Titus-Ernstoff, L;
Easton, D;
Spurdle, AB;
(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: https://doi.org/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...
Wang, JJ;
Mitchell, P;
Uitterlinden, AG;
Rivadeneira, F;
Teo, YY;
Chia, KS;
Seielstad, M;
Hibberd, M;
Vingerling, JR;
Klaver, CC;
Jansonius, NM;
Tai, ES;
Wong, TY;
van Duijn, CM;
Aung, T;
(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: https://doi.org/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...
Blackwell, JM;
Bramon, E;
Brown, MA;
Burn, D;
Casas, JP;
Chinnery, PF;
Clarke, CE;
Corvin, A;
Craddock, N;
Deloukas, P;
Edkins, S;
Evans, J;
Freeman, C;
Gray, E;
Hardy, J;
Hudson, G;
Hunt, S;
Jankowski, J;
Langford, C;
Lees, AJ;
Markus, HS;
Mathew, CG;
McCarthy, MI;
Morrison, KE;
Palmer, CNA;
Pearson, JP;
Peltonen, L;
Pirinen, M;
Plomin, R;
Potter, S;
Rautanen, A;
Sawcer, SJ;
Su, Z;
Trembath, RC;
Viswanathan, AC;
Williams, NW;
Morris, HR;
Donnelly, P;
Wood, NW;
(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: https://doi.org/10.1093/hmg/ddq469
2010
Niederer, HA;
Willcocks, LC;
Rayner, TF;
Yang, W;
Lau, YL;
Williams, TN;
Scott, JA;
Urban, BC;
Peshu, N;
Dunstan, SJ;
+10 more...
Hien, TT;
Phu, NH;
Padyukov, L;
Gunnarsson, I;
Svenungsson, E;
Savage, CO;
Watts, RA;
Lyons, PA;
Clayton, DG;
Smith, KG;
(2010)
Copy number, linkage disequilibrium and disease association in the FCGR locus.
Human molecular genetics, 19 (16).
pp. 3282-94.
ISSN 0964-6906
DOI: https://doi.org/10.1093/hmg/ddq216
Vithana, EN;
Aung, T;
Khor, CC;
Cornes, BK;
Tay, WT;
Sim, X;
Lavanya, R;
Wu, R;
Zheng, Y;
Hibberd, ML;
+6 more...
Chia, KS;
Seielstad, M;
Goh, LK;
Saw, SM;
Tai, ES;
Wong, TY;
(2010)
Collagen-related genes influence the glaucoma risk factor, central corneal thickness.
Human molecular genetics, 20 (4).
pp. 649-58.
ISSN 0964-6906
DOI: https://doi.org/10.1093/hmg/ddq511
Full text not available from this repository.
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: https://doi.org/10.1093/hmg/ddp159
Dunning, AM;
Healey, CS;
Baynes, C;
Maia, AT;
Scollen, S;
Vega, A;
Rodriguez, R;
Barbosa-Morais, NL;
Ponder, BAJ;
Low, YL;
+60 more...
Bingham, S;
Haiman, CA;
le Marchand, L;
Broeks, A;
Schmidt, MK;
Hopper, J;
Southey, M;
Beckmann, MW;
Fasching, PA;
Peto, J;
Johnson, N;
Bojesen, SE;
Nordestgaard, B;
Milne, RL;
Benitez, J;
Hamann, U;
Ko, Y;
Schmutzler, RK;
Burwinkel, B;
Schurmann, P;
Dork, T;
Heikkinen, T;
Nevanlinna, H;
Lindblom, A;
Margolin, S;
Mannermaa, A;
Kosma, VM;
Chen, XQ;
Spurdle, A;
Change-Claude, J;
Flesch-Janys, D;
Couch, FJ;
Olson, JE;
Severi, G;
Baglietto, L;
Brresen-Dale, AL;
Kristensen, V;
Hunter, DJ;
Hankinson, SE;
Devilee, P;
Vreeswijk, M;
Lissowska, J;
Brinton, L;
Liu, JJ;
Hall, P;
Kang, D;
Yoo, KY;
Shen, CY;
Yu, JC;
Anton-Culver, H;
Ziogoas, A;
Sigurdson, A;
Struewing, J;
Easton, DF;
Garcia-Closas, M;
Humphreys, MK;
Morrison, J;
Pharoah, PDP;
Pooley, KA;
Chenevix-Trench, G;
(2009)
Association of ESR1 gene tagging SNPs with breast cancer risk.
Human molecular genetics, 18 (6).
pp. 1131-1139.
ISSN 0964-6906
DOI: https://doi.org/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...
Narod, S;
Petronis, A;
(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: https://doi.org/10.1093/hmg/ddp033
Fry, AE;
Ghansa, A;
Small, KS;
Palma, A;
Auburn, S;
Diakite, M;
Green, A;
Campino, S;
Teo, YY;
Clark, TG;
+18 more...
Jeffreys, AE;
Wilson, J;
Jallow, M;
Sisay-Joof, F;
Pinder, M;
Griffiths, MJ;
Peshu, N;
Williams, TN;
Newton, CR;
Marsh, K;
Molyneux, ME;
Taylor, TE;
Koram, KA;
Oduro, AR;
Rogers, WO;
Rockett, KA;
Sabeti, PC;
Kwiatkowski, DP;
(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: https://doi.org/10.1093/hmg/ddp192
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: https://doi.org/10.1093/hmg/ddp388
2008
Benzinou, M;
Chèvre, JC;
Ward, KJ;
Lecoeur, C;
Dina, C;
Lobbens, S;
Durand, E;
Delplanque, J;
Horber, FF;
Heude, B;
+7 more...
Balkau, B;
Borch-Johnsen, K;
Jørgensen, T;
Hansen, T;
Pedersen, O;
Meyre, D;
Froguel, P;
(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: https://doi.org/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...
Lophatananon, A;
Feychting, M;
Lönn, S;
Ahlbom, A;
Malmer, B;
Henriksson, R;
Auvinen, A;
Kiuru, A;
Salminen, T;
Swerdlow, A;
Houlston, R;
(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: https://doi.org/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...
Fletcher, O;
(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: https://doi.org/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...
Twiss, P;
Fielding, S;
Rowan, A;
Jaeger, E;
Vijayakrishnan, J;
Chandler, I;
Penegar, S;
Qureshi, M;
Lubbe, S;
Domingo, E;
Kemp, Z;
Barclay, E;
Wood, W;
Martin, L;
Gorman, M;
Thomas, H;
Peto, J;
Bishop, T;
Gray, R;
Maher, ER;
Lucassen, A;
Kerr, D;
Evans, GR;
van Wezel, T;
Morreau, H;
Wijnen, JT;
Hopper, JL;
Southey, MC;
Giles, GG;
Severi, G;
Castellvi-Bel, S;
Ruiz-Ponte, C;
Carracedo, A;
Castells, A;
Forsti, A;
Hemminki, K;
Vodicka, P;
Naccarati, A;
Lipton, L;
Ho, JWC;
Cheng, KK;
Sham, PC;
Luk, J;
Agundez, JAG;
Ladero, JM;
de la Hoya, M;
Caldes, T;
Niitymaki, I;
Tuupanen, S;
Karhu, A;
Aaltonen, LA;
Cazier, JB;
Tomlinson, IPM;
Houlston, RS;
(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: https://doi.org/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...
Bencko, V;
Foretova, L;
Janout, V;
Chow, WH;
Rothman, N;
Chabrier, A;
Gaborieau, V;
Odefrey, F;
Southey, M;
Hashibe, M;
Hall, J;
Boffetta, P;
Peto, J;
Peto, R;
Hung, RJ;
(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: https://doi.org/10.1093/hmg/ddm127
Full text not available from this repository.
Johnson, N;
Fletcher, O;
Palles, C;
Rudd, M;
Webb, E;
Sellick, G;
dos Santos Silva, I;
McCormack, V;
Gibson, L;
Fraser, A;
+6 more...
Leonard, A;
Gilham, C;
Tavtigian, SV;
Ashworth, A;
Houlston, R;
Peto, J;
(2007)
Counting potentially functional variants in BRCA1, BRCA2 and ATM predicts breast cancer susceptibility.
Human molecular genetics, 16 (9).
pp. 1051-7.
ISSN 0964-6906
DOI: https://doi.org/10.1093/hmg/ddm050
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: https://doi.org/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: https://doi.org/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: https://doi.org/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...
Tomlinson, I;
Papaemmanuil, E;
Webb, E;
Sellick, GS;
Wood, W;
Evans, G;
Lucassen, A;
Maher, ER;
Houlston, RS;
ColoRectal tumour Gene Identification (CoRGI) Study Consortium;
(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: https://doi.org/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...
Johnson, N;
Tomlinson, I;
Gray, R;
Peto, J;
Houlston, RS;
(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: https://doi.org/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...
Vexiau, P;
German, MS;
Vaisse, C;
(2004)
PAX4 gene variations predispose to ketosis-prone diabetes.
Human molecular genetics, 13 (24).
pp. 3151-9.
ISSN 0964-6906
DOI: https://doi.org/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: https://doi.org/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: https://doi.org/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: https://doi.org/10.1093/hmg/11.14.1599
Full text not available from this repository.