Browsing Centre for Genomics and Child Health by Author "Durbin, R"
Now showing items 1-5 of 5
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Estimating the human mutation rate from autozygous segments reveals population differences in human mutational processes
Narasimhan, VM; Rahbari, R; Scally, A; Wuster, A; Mason, D; Xue, Y; Wright, J; Trembath, RC; Maher, ER; van Heel, DA (2017-08-21) -
Health and population effects of rare gene knockouts in adult humans with related parents
Narasimhan, VM; Hunt, KA; Mason, D; Baker, CL; Karczewski, KJ; Barnes, MER; Barnett, AH; Bates, C; Bellary, S; Bockett, NA (2016-04-22) -
Steroid receptor coactivator-1 modulates the function of Pomc neurons and energy homeostasis
Yang, Y; van der Klaauw, AA; Zhu, L; Cacciottolo, TM; He, Y; Stadler, LKJ; Wang, C; Xu, P; Saito, K; Hinton, A (2019-04-12) -
The UK10K project identifies rare variants in health and disease
Walter, K; Min, JL; Huang, J; Crooks, L; Memari, Y; McCarthy, S; Perry, JRB; Xu, C; Futema, M; Lawson, D (2015-10-01) -
Whole-Genome Sequencing Coupled to Imputation Discovers Genetic Signals for Anthropometric Traits
Tachmazidou, I; Suveges, D; Min, JL; Ritchie, GRS; Steinberg, J; Walter, K; Iotchkova, V; Schwartzentruber, J; Huang, J; Memari, Y (2017-06-01)