|Blackburn, NB and Meikle, PJ and Peralta, JM and Kumar, S and Leandro, AC and Bellinger, MA and Giles, C and Huynh, K and Mahaney, MC and Goring, HHH and VandeBerg, JL and Williams-Blangero, S and Glahn, DC and Duggirala, R and Blangero, J and Michael, LF and Curran, JE, Identifying the lipidomic effects of a rare loss-of-function deletion in ANGPTL3, Circulation. Genomic and Precision Medicine ISSN 2574-8300 (2021) [Refereed Article]|
|Landi, MT and Bishop, DT and MacGregor, S and Machiela, MJ and Stratigos, AJ and Ghiorzo, P and Brossard, M and Calista, D and Choi, J and Fargnoli, MC and Zhang, T and Rodolfo, M and Trower, AJ and Menin, C and Martinez, J and Hadjisavvas, A and Song, L and Stefanaki, I and Scolyer, R and Yang, R and Goldstein, AM and Potrony, M and Kypreou, KP and Pastorino, L and Queirolo, P and Pellegrini, C and Cattaneo, L and Zawistowski, M and Gimenez-Xavier, P and Rodriguez, A and Elefanti, L and Manoukian, S and Rivoltini, L and Smith, BH and Loizidou, MA and Del Regno, L and Massi, D and Mandala, M and Khosrotehrani, K and Akslen, LA and Amos, CI and Andresen, PA and Avril, MF and Azizi, E and Soyer, HP and Bataille, V and Dalmasso, B and Bowdler, LM and Burdon, KP and Chen, WV and Codd, V and Craig, JE and Debniak, T and Falchi, M and Fang, S and Friedman, E and Simi, S and Galan, P and Garcia-Casado, Z and Gillanders, EM and Gordon, S and Green, A and Gruis, NA and Hansson, J and Harland, M and Harris, J and Helsing, P and Henders, A and Hocevar, M and Hoiom, V and Hunter, D and Ingvar, C and Kumar, R and Lang, J and Lathrop, GM and Lee, JE and Li, X and Lubinski, J and Mackie, RM and Malt, M and Malvehy, J and McAloney, K and Mohamdi, H and Molven, A and Moses, EK and Neale, RE and Novakovic, S and Nyholt, DR and Olsson, H and Orr, N and Fritsche, LG and Puig-Butille, JA and Qureshi, AA and Radford-Smith, GL and Randerson-Moor, J and Requena, C and Rowe, C and Samani, NJ and Sanna, M and Schadendorf, D, Genome-wide association meta-analyses combining multiple risk phenotypes provide insights into the genetic architecture of cutaneous melanoma susceptibility, Nature Genetics, 52, (5) pp. 494-504. ISSN 1061-4036 (2020) [Refereed Article]|
|Blackburn, AN and Blondell, L and Kos, MZ and Blackburn, NB and Peralta, JM and Stevens, PT and Lehman, DM and Blangero, J and Goring, HHH, Genotype phasing in pedigrees using whole-genome sequence data, European Journal of Human Genetics, 28, (6) pp. 790-803. ISSN 1018-4813 (2020) [Refereed Article]|
|Hansen, RL and Safabakhsh, S and Curtis, JM and Hsueh, W-C and Jones, LI and Aflague, TF and Duenas Sarmiento, J and Kumar, S and Blackburn, NB and Curran, JE and Mahkee, D and Baier, LJ and Knowler, WC and Nelson, RG, Association of CREBRF variants with obesity and diabetes in Pacific Islanders from Guam and Saipan, Diabetologia, 62, (9) pp. 1647-1652. ISSN 0012-186X (2019) [Refereed Article]|
|Blackburn, NB and Porto, A and Peralta, JM and Blangero, J, Heritability and genetic associations of triglyceride and HDL-C levels using pedigree-based and empirical kinships, BMC Proceedings, 12, (Suppl 9) pp. 129-258. ISSN 1753-6561 (2018) [Refereed Article]|
|Porto, A and Peralta, JM and Blackburn, NB and Blangero, J, Reliability of genomic predictions of complex human phenotypes, BMC Proceedings, 12, (Suppl 9) pp. 157-258. ISSN 1753-6561 (2018) [Refereed Article]|
This list was generated on Mon Aug 15 20:49:41 2022.