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Browsing by Author Walters, RG
Showing results 2 to 4 of 4
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| Issue Date | Title | Author(s) |
|---|---|---|
| 2013 | Rare Genomic Structural Variants in Complex Disease: Lessons from the Replication of Associations with Obesity | Walters, RG; Coin, LJM; Ruokonen, A; de Smith, AJ; Moustafa, JSE-S; Jacquemont, S; Elliott, P; Esko, T; Hartikainen, A-L; Laitinen, J; Maennik, K; Martinet, D; Meyre, D; Nauck, M; Schurmann, C; Sladek, R; Thorleifsson, G; Thorsteinsdottir, U; Valsesia, A; Waeber, G; Zufferey, F; Balkau, B; Pattou, F; Metspalu, A; Voelzke, H; Vollenweider, P; Stefansson, K; Jarvelin, M-R; Beckmann, JS; Froguel, P; Blakemore, AIF |
| 2008 | Small Deletion Variants Have Stable Breakpoints Commonly Associated with Alu Elements | de Smith, AJ; Walters, RG; Coin, LJM; Steinfeld, I; Yakhini, Z; Sladek, R; Froguel, P; Blakemore, AIF |
| 2015 | Truncating Homozygous Mutation of Carboxypeptidase E (CPE) in a Morbidly Obese Female with Type 2 Diabetes Mellitus, Intellectual Disability and Hypogonadotrophic Hypogonadism | Alsters, SIM; Goldstone, AP; Buxton, JL; Zekavati, A; Sosinsky, A; Yiorkas, AM; Holder, S; Klaber, RE; Bridges, N; van Haelst, MM; le Roux, CW; Walley, AJ; Walters, RG; Mueller, M; Blakemore, AIF |