| Issue Date | Title | Author(s) |
| 1998-10-10 | Inducible nitric oxide synthase polymorphism and fatal cerebral malaria. | Burgner, D; Xu, W; Rockett, K; Gravenor, M; Charles, IG; Hill, AV; Kwiatkowski, D |
| 2017-03-21 | Genetic correlation between amyotrophic lateral sclerosis and schizophrenia | McLaughlin, RL; Schijven, D; Van Rheenen, W; Van Eijk, KR; O'Brien, M; Kahn, RS; Ophoff, RA; Goris, A; Bradley, DG; Al-Chalabi, A; Van Den Berg, LH; Luykx, JJ; Hardiman, O; Veldink, JH; Shatunov, A; Dekker, AM; Diekstra, FP; Pulit, SL; Van Der Spek, RAA; Van Doormaal, PTC; Sproviero, W; Jones, AR; Nicholson, GA; Rowe, DB; Pamphlett, R; Kiernan, MC; Bauer, D; Kahlke, T; Williams, K; Eftimov, F; Fogh, I; Ticozzi, N; Lin, K; Millecamps, S; Salachas, F; Meininger, V; Carvalho, MD; Pinto, S; Mora, JS; Rojas-Garcyá, R; Polak, M; Chandran, S; Colville, S; Swingler, R; Morrison, KE; Shaw, PJ; Hardy, J; Orrell, RW; Pittman, A; Sidle, K; Fratta, P; Malaspina, A; Petri, S; Abdulla, S; Drepper, C; Sendtner, M; Meyer, T; Wiedau-Pazos, M; Lomen-Hoerth, C; Deerlin, VMV; Trojanowski, JQ; Elman, L; McCluskey, L; Basak, N; Meitinger, T; Lichtner, P; Blagojevic-Radivojkov, M; Andres, CR; Maurel, C; Bensimon, G; Landwehrmeyer, B; Brice, A; Payan, CAM; Saker-Delye, S; Durr, A; Wood, N; Tittmann, L; Lieb, W; Franke, A; Rietschel, M; Cichon, S; Nothen, MM; Amouyel, P; Tzourio, C; Dartigues, JF; Uitterlinden, AG; Rivadeneira, F; Estrada, K; Hofman, A; Curtis, C; Derkooi, AJV; De Visser, M; Weber, M; Shaw, CE; Smith, BN; Pansarasa, O; Cereda, C; Bo, RD; Comi, GP; D'Alfonso, 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 |
| 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 |
| 2021-07 | Variation in the risk of colorectal cancer in families with Lynch syndrome: a retrospective cohort study. | International Mismatch Repair Consortium, |
| 2019-06-01 | Genetic and antigenic variation of foot-and-mouth disease virus during persistent infection in naturally infected cattle and Asian buffalo in India | Biswal, JK; Ranjan, R; Subramaniam, S; Mohapatra, JK; Patidar, S; Sharma, MK; Bertram, MR; Brito, B; Rodriguez, LL; Pattnaik, B; Arzt, J |
