| Issue Date | Title | Author(s) |
| 2015-03-17 | Rare variants in neuronal excitability genes influence risk for bipolar disorder | Ament, SA; Szelinger, S; Glusman, G; Ashworth, J; Hou, L; Akula, N; Shekhtman, T; Badner, JA; Brunkow, ME; Mauldin, DE; Stittrich, AB; Rouleau, K; Detera-Wadleigh, SD; Nurnberger, JI; Edenberg, HJ; Gershon, ES; Schork, N; Price, ND; Gelinas, R; Hood, L; Craig, D; McMahon, FJ; Kelsoe, JR; Roach, JC |
| 2018-03-01 | Integrating exome sequencing into a diagnostic pathway for epileptic encephalopathy: Evidence of clinical utility and cost effectiveness | Palmer, EE; Schofield, D; Shrestha, R; Kandula, T; Macintosh, R; Lawson, JA; Andrews, I; Sampaio, H; Johnson, AM; Farrar, MA; Cardamone, M; Mowat, D; Elakis, G; Lo, W; Zhu, Y; Ying, K; Morris, P; Tao, J; Dias, KR; Buckley, M; Dinger, ME; Cowley, MJ; Roscioli, T; Kirk, EP; Bye, A; Sachdev, RK |
| 2012-02-01 | A single nucleotide polymorphism in EXO1 gene is associated with cervical cancer susceptibility in chinese patients | Luo, X; Hong, XS; Xiong, XD; Zeng, LQ; Lim, CED |
| 2000-08 | Survey of the allelic frequency of a NOS2A promoter microsatellite in human populations: assessment of the NOS2A gene and predisposition to infectious disease. | Xu, W; Humphries, S; Tomita, M; Okuyama, T; Matsuki, M; Burgner, D; Kwiatkowski, D; Liu, L; Charles, IG |
| 2018-02-22 | A Mild PUM1 Mutation Is Associated with Adult-Onset Ataxia, whereas Haploinsufficiency Causes Developmental Delay and Seizures | Gennarino, VA; Palmer, EE; McDonell, LM; Wang, L; Adamski, CJ; Koire, A; See, L; Chen, CA; Schaaf, CP; Rosenfeld, JA; Panzer, JA; Moog, U; Hao, S; Bye, A; Kirk, EP; Stankiewicz, P; Breman, AM; McBride, A; Kandula, T; Dubbs, HA; Macintosh, R; Cardamone, M; Zhu, Y; Ying, K; Dias, KR; Cho, MT; Henderson, LB; Baskin, B; Morris, P; Tao, J; Cowley, MJ; Dinger, ME; Roscioli, T; Caluseriu, O; Suchowersky, O; Sachdev, RK; Lichtarge, O; Tang, J; Boycott, KM; Holder, JL; Zoghbi, HY |
| 2014-01-01 | The heritability of abortion in pedigree Charollais flocks | Darlay, R; Stear, MJ; Mason, S; Smith, J; Shaw, MA |
| 2004-02 | Genetic background affects susceptibility in nonfatal pneumococcal bronchopneumonia. | Preston, JA; Beagley, KW; Gibson, PG; Hansbro, PM |
| 2014-10 | ZAP-70 genotype disrupts the relationship between microbiota and host, leading to spondyloarthritis and ileitis in SKG mice. | Rehaume, LM; Mondot, S; Aguirre de Cárcer, D; Velasco, J; Benham, H; Hasnain, SZ; Bowman, J; Ruutu, M; Hansbro, PM; McGuckin, MA; Morrison, M; Thomas, R |
| 2020-06-16 | Germline HOXB13 mutations p.G84E and p.R217C do not confer an increased breast cancer risk. | Liu, J; Prager-van der Smissen, WJC; Collée, JM; Bolla, MK; Wang, Q; Michailidou, K; Dennis, J; Ahearn, TU; Aittomäki, K; Ambrosone, CB; Andrulis, IL; Anton-Culver, H; Antonenkova, NN; Arndt, V; Arnold, N; Aronson, KJ; Augustinsson, A; Auvinen, P; Becher, H; Beckmann, MW; Behrens, S; Bermisheva, M; Bernstein, L; Bogdanova, NV; Bogdanova-Markov, N; Bojesen, SE; Brauch, H; Brenner, H; Briceno, I; Brucker, SY; Brüning, T; Burwinkel, B; Cai, Q; Cai, H; Campa, D; Canzian, F; Castelao, JE; Chang-Claude, J; Chanock, SJ; Choi, J-Y; Christiaens, M; Clarke, CL; NBCS Collaborators,; Couch, FJ; Czene, K; Daly, MB; Devilee, P; Dos-Santos-Silva, I; Dwek, M; Eccles, DM; Eliassen, AH; Fasching, PA; Figueroa, J; Flyger, H; Fritschi, L; Gago-Dominguez, M; Gapstur, SM; García-Closas, M; García-Sáenz, JA; Gaudet, MM; Giles, GG; Goldberg, MS; Goldgar, DE; Guénel, P; Haiman, CA; Håkansson, N; Hall, P; Harrington, PA; Hart, SN; Hartman, M; Hillemanns, P; Hopper, JL; Hou, M-F; Hunter, DJ; Huo, D; ABCTB Investigators,; Ito, H; Iwasaki, M; Jakimovska, M; Jakubowska, A; John, EM; Kaaks, R; Kang, D; Keeman, R; Khusnutdinova, E; Kim, S-W; Kraft, P; Kristensen, VN; Kurian, AW; Le Marchand, L; Li, J; Lindblom, A; Lophatananon, A; Luben, RN; Lubiński, J; Mannermaa, A; Manoochehri, M; Manoukian, S; Margolin, S; Mariapun, S; Matsuo, K; Maurer, T; Mavroudis, D; Meindl, A; Menon, U; Milne, RL; Muir, K; Mulligan, AM; Neuhausen, SL; Nevanlinna, H; Offit, K; Olopade, OI; Olson, JE; Olsson, H; Orr, N; Park, SK; Peterlongo, P; Peto, J; Plaseska-Karanfilska, D; Presneau, N; Rack, B; Rau-Murthy, R; Rennert, G; Rennert, HS; Rhenius, V; Romero, A; Ruebner, M; Saloustros, E; Schmutzler, RK; Schneeweiss, A; Scott, C; Shah, M; Shen, C-Y; Shu, X-O; Simard, J; Sohn, C; Southey, MC; Spinelli, JJ; Tamimi, RM; Tapper, WJ; Teo, SH; Terry, MB; Torres, D; Truong, T; Untch, M; Vachon, CM; van Asperen, CJ; Wolk, A; Yamaji, T; Zheng, W; Ziogas, A; Ziv, E; Torres-Mejía, G; Dörk, T; Swerdlow, AJ; Hamann, U; Schmidt, MK; Dunning, AM; Pharoah, PDP; Easton, DF; Hooning, MJ; Martens, JWM; Hollestelle, A |
| 2021-02-17 | A case-only study to identify genetic modifiers of breast cancer risk for BRCA1/BRCA2 mutation carriers. | Coignard, J; Lush, M; Beesley, J; O'Mara, TA; Dennis, J; Tyrer, JP; Barnes, DR; McGuffog, L; Leslie, G; Bolla, MK; Adank, MA; Agata, S; Ahearn, T; Aittomäki, K; Andrulis, IL; Anton-Culver, H; Arndt, V; Arnold, N; Aronson, KJ; Arun, BK; Augustinsson, A; Azzollini, J; Barrowdale, D; Baynes, C; Becher, H; Bermisheva, M; Bernstein, L; Białkowska, K; Blomqvist, C; Bojesen, SE; Bonanni, B; Borg, A; Brauch, H; Brenner, H; Burwinkel, B; Buys, SS; Caldés, T; Caligo, MA; Campa, D; Carter, BD; Castelao, JE; Chang-Claude, J; Chanock, SJ; Chung, WK; Claes, KBM; Clarke, CL; GEMO Study Collaborators,; EMBRACE Collaborators,; Collée, JM; Conroy, DM; Czene, K; Daly, MB; Devilee, P; Diez, O; Ding, YC; Domchek, SM; Dörk, T; Dos-Santos-Silva, I; Dunning, AM; Dwek, M; Eccles, DM; Eliassen, AH; Engel, C; Eriksson, M; Evans, DG; Fasching, PA; Flyger, H; Fostira, F; Friedman, E; Fritschi, L; Frost, D; Gago-Dominguez, M; Gapstur, SM; Garber, J; Garcia-Barberan, V; García-Closas, M; García-Sáenz, JA; Gaudet, MM; Gayther, SA; Gehrig, A; Georgoulias, V; Giles, GG; Godwin, AK; Goldberg, MS; Goldgar, DE; González-Neira, A; Greene, MH; Guénel, P; Haeberle, L; Hahnen, E; Haiman, CA; Håkansson, N; Hall, P; Hamann, U; Harrington, PA; Hart, SN; He, W; Hogervorst, FBL; Hollestelle, A; Hopper, JL; Horcasitas, DJ; Hulick, PJ; Hunter, DJ; Imyanitov, EN; KConFab Investigators,; HEBON Investigators,; ABCTB Investigators,; Jager, A; Jakubowska, A; James, PA; Jensen, UB; John, EM; Jones, ME; Kaaks, R; Kapoor, PM; Karlan, BY; Keeman, R; Khusnutdinova, E; Kiiski, JI; Ko, Y-D; Kosma, V-M; Kraft, P; Kurian, AW; Laitman, Y; Lambrechts, D; Le Marchand, L; Lester, J; Lesueur, F; Lindstrom, T; Lopez-Fernández, A; Loud, JT; Luccarini, C; Mannermaa, A; Manoukian, S; Margolin, S; Martens, JWM; Mebirouk, N; Meindl, A; Miller, A; Milne, RL; Montagna, M; Nathanson, KL; Neuhausen, SL; Nevanlinna, H; Nielsen, FC; O'Brien, KM; Olopade, OI; Olson, JE; Olsson, H; Osorio, A; Ottini, L; Park-Simon, T-W; Parsons, MT; Pedersen, IS; Peshkin, B; Peterlongo, P; Peto, J; Pharoah, PDP; Phillips, K-A; Polley, EC; Poppe, B; Presneau, N; Pujana, MA; Punie, K; Radice, P; Rantala, J; Rashid, MU; Rennert, G; Rennert, HS; Robson, M; Romero, A; Rossing, M; Saloustros, E; Sandler, DP; Santella, R; Scheuner, MT; Schmidt, MK; Schmidt, G; Scott, C; Sharma, P; Soucy, P; Southey, MC; Spinelli, JJ; Steinsnyder, Z; Stone, J; Stoppa-Lyonnet, D; Swerdlow, A; Tamimi, RM; Tapper, WJ; Taylor, JA; Terry, MB; Teulé, A; Thull, DL; Tischkowitz, M; Toland, AE; Torres, D; Trainer, AH; Truong, T; Tung, N; Vachon, CM; Vega, A; Vijai, J; Wang, Q; Wappenschmidt, B; Weinberg, CR; Weitzel, JN; Wendt, C; Wolk, A; Yadav, S; Yang, XR; Yannoukakos, D; Zheng, W; Ziogas, A; Zorn, KK; Park, SK; Thomassen, M; Offit, K; Schmutzler, RK; Couch, FJ; Simard, J; Chenevix-Trench, G; Easton, DF; Andrieu, N; Antoniou, AC |
