| Mutations in the hepatocyte nuclear factor-1α gene in maturity-onset diabetes of the young (MODY3) K Yamagata, N Oda, PJ Kaisaki, S Menzel, H Furuta, M Vaxillaire, ... Nature 384 (6608), 455-458, 1996 | 2227 | 1996 |
| A genome–wide search for human non–insulin–dependent (type 2) diabetes genes reveals a major susceptibility locus on chromosome 2 CL Hanis, E Boerwinkle, R Chakraborty, DL Ellsworth, P Concannon, ... Nature genetics 13 (2), 161-166, 1996 | 829 | 1996 |
| A genome-wide meta-analysis identifies 22 loci associated with eight hematological parameters in the HaemGen consortium N Soranzo, TD Spector, M Mangino, B Kühnel, A Rendon, A Teumer, ... Nature genetics 41 (11), 1182-1190, 2009 | 613 | 2009 |
| A QTL influencing F cell production maps to a gene encoding a zinc-finger protein on chromosome 2p15 S Menzel, C Garner, I Gut, F Matsuda, M Yamaguchi, S Heath, M Foglio, ... Nature genetics 39 (10), 1197-1199, 2007 | 602 | 2007 |
| A genomewide scan for loci predisposing to type 2 diabetes in a UK population (the Diabetes UK Warren 2 Repository): analysis of 573 pedigrees provides independent replication … S Wiltshire, AT Hattersley, GA Hitman, M Walker, JC Levy, M Sampson, ... The American Journal of Human Genetics 69 (3), 553-569, 2001 | 374 | 2001 |
| Intergenic variants of HBS1L-MYB are responsible for a major quantitative trait locus on chromosome 6q23 influencing fetal hemoglobin levels in adults SL Thein, S Menzel, X Peng, S Best, J Jiang, J Close, N Silver, ... Proceedings of the National Academy of Sciences 104 (27), 11346-11351, 2007 | 373 | 2007 |
| Altered insulin secretory responses to glucose in diabetic and nondiabetic subjects with mutations in the diabetes susceptibility gene MODY3 on chromosome 12 MM Byrne, J Sturis, S Menzel, K Yamagata, SS Fajans, MJ Dronsfield, ... Diabetes 45 (11), 1503-1510, 1996 | 373 | 1996 |
| Control of fetal hemoglobin: new insights emerging from genomics and clinical implications SL Thein, S Menzel, M Lathrop, C Garner Human molecular genetics 18 (R2), R216-R223, 2009 | 318 | 2009 |
| Discovering the genetics underlying foetal haemoglobin production in adults SL Thein, S Menzel British journal of haematology 145 (4), 455-467, 2009 | 255 | 2009 |
| Studies of association between the gene for calpain-10 and type 2 diabetes mellitus in the United Kingdom JC Evans, TM Frayling, PG Cassell, PJ Saker, GA Hitman, M Walker, ... The American Journal of Human Genetics 69 (3), 544-552, 2001 | 232 | 2001 |
| HBS1L-MYB intergenic variants modulate fetal hemoglobin via long-range MYB enhancers R Stadhouders, S Aktuna, S Thongjuea, A Aghajanirefah, F Pourfarzad, ... The Journal of clinical investigation 124 (4), 1699-1710, 2014 | 226 | 2014 |
| cMYB is involved in the regulation of fetal hemoglobin production in adults J Jiang, S Best, S Menzel, N Silver, MI Lai, GL Surdulescu, TD Spector, ... Blood 108 (3), 1077-1083, 2006 | 212 | 2006 |
| Mutations in the hepatocyte nuclear factor-1α gene in MODY and early-onset NIDDM: evidence for a mutational hotspot in exon 4 PJ Kaisaki, S Menzel, T Lindner, N Oda, I Rjasanowski, J Sahm, ... Diabetes 46 (3), 528-535, 1997 | 211 | 1997 |
| Systematic documentation and analysis of human genetic variation in hemoglobinopathies using the microattribution approach B Giardine, J Borg, DR Higgs, KR Peterson, S Philipsen, D Maglott, ... Nature genetics 43 (4), 295-301, 2011 | 187 | 2011 |
| A low renal threshold for glucose in diabetic patients with a mutation in the hepatocyte nuclear factor‐1α (HNF‐1α) gene R Menzel, PJ Kaisaki, I Rjasanowski, P Heinke, W Kerner, S Menzel Diabetic Medicine 15 (10), 816-820, 1998 | 172 | 1998 |
| Environmental determinants of severity in sickle cell disease S Tewari, V Brousse, FB Piel, S Menzel, DC Rees Haematologica 100 (9), 1108, 2015 | 169 | 2015 |
| A novel variant on chromosome 7q22. 3 associated with mean platelet volume, counts, and function N Soranzo, A Rendon, C Gieger, CI Jones, NA Watkins, S Menzel, ... Blood, The Journal of the American Society of Hematology 113 (16), 3831-3837, 2009 | 152 | 2009 |
| Multiple loci are associated with white blood cell phenotypes MA Nalls, DJ Couper, T Tanaka, FJA van Rooij, MH Chen, AV Smith, ... PLoS genetics 7 (6), e1002113, 2011 | 150 | 2011 |
| Genetics of fetal hemoglobin in Tanzanian and British patients with sickle cell anemia J Makani, S Menzel, S Nkya, SE Cox, E Drasar, D Soka, AN Komba, ... Blood, The Journal of the American Society of Hematology 117 (4), 1390-1392, 2011 | 124 | 2011 |
| The HBS1L-MYB intergenic region on chromosome 6q23.3 influences erythrocyte, platelet, and monocyte counts in humans S Menzel, J Jiang, N Silver, J Gallagher, J Cunningham, G Surdulescu, ... Blood, The Journal of the American Society of Hematology 110 (10), 3624-3626, 2007 | 112 | 2007 |
