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Number of items: 46.

2017

Mullin, BH; Hua Zhao, J; Brown, SJ; Perry, JRB; Luan, J; Zheng, HF; Langenberg, C; Dudbridge, F; Scott, R; Wareham, NJ; +4 more... Spector, TD; Brent Richards, J; Walsh, JP; Wilson, SG; (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: https://doi.org/10.1093/hmg/ddx174
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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
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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
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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; +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
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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
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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
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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
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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
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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... 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
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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... 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
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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... 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
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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: https://doi.org/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... 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.

This list was generated on Tue Nov 13 12:20:07 2018 GMT.