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Stephan Menzel
Stephan Menzel
Senior Lecturer, King's College London
在 kcl.ac.uk 的电子邮件经过验证
标题
引用次数
引用次数
年份
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
22271996
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
8291996
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
6132009
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
6022007
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
3742001
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
3732007
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
3731996
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
3182009
Discovering the genetics underlying foetal haemoglobin production in adults
SL Thein, S Menzel
British journal of haematology 145 (4), 455-467, 2009
2552009
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
2322001
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
2262014
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
2122006
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
2111997
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
1872011
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
1721998
Environmental determinants of severity in sickle cell disease
S Tewari, V Brousse, FB Piel, S Menzel, DC Rees
Haematologica 100 (9), 1108, 2015
1692015
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
1522009
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
1502011
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
1242011
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
1122007
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