Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS) LA Everett, B Glaser, JC Beck, JR Idol, A Buchs, M Heyman, F Adawi, ... Nature genetics 17 (4), 411-422, 1997 | 1401 | 1997 |
The genetic architecture of type 2 diabetes C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ... Nature 536 (7614), 41-47, 2016 | 1243 | 2016 |
Familial hyperinsulinism caused by an activating glucokinase mutation B Glaser, P Kesavan, M Heyman, E Davis, A Cuesta, A Buchs, CA Stanley, ... New England Journal of Medicine 338 (4), 226-230, 1998 | 767 | 1998 |
Comprehensive human cell-type methylation atlas reveals origins of circulating cell-free DNA in health and disease J Moss, J Magenheim, D Neiman, H Zemmour, N Loyfer, A Korach, ... Nature communications 9 (1), 5068, 2018 | 709 | 2018 |
Induction of long-term glycemic control in newly diagnosed type 2 diabetic patients by transient intensive insulin treatment H Ilkova, B Glaser, A Tunçkale, N Bagriaçik, E Cerasi Diabetes care 20 (9), 1353-1356, 1997 | 672 | 1997 |
Identification of tissue-specific cell death using methylation patterns of circulating DNA R Lehmann-Werman, D Neiman, H Zemmour, J Moss, J Magenheim, ... Proceedings of the National Academy of Sciences 113 (13), E1826-E1834, 2016 | 605 | 2016 |
Adenosine diphosphate as an intracellular regulator of insulin secretion CG Nichols, SL Shyng, A Nestorowicz, B Glaser, JP Clement Iv, ... Science 272 (5269), 1785-1787, 1996 | 581 | 1996 |
Loss-of-function mutations in SLC30A8 protect against type 2 diabetes J Flannick, G Thorleifsson, NL Beer, SBR Jacobs, N Grarup, NP Burtt, ... Nature genetics 46 (4), 357-363, 2014 | 535 | 2014 |
Common variants in WFS1 confer risk of type 2 diabetes MS Sandhu, MN Weedon, KA Fawcett, J Wasson, SL Debenham, A Daly, ... Nature genetics 39 (8), 951-953, 2007 | 470 | 2007 |
Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy. SA Kassem, I Ariel, PS Thornton, I Scheimberg, B Glaser Diabetes 49 (8), 1325-1333, 2000 | 458 | 2000 |
Pancreatic beta-cell glucokinase: closing the gap between theoretical concepts and experimental realities. FM Matschinsky, B Glaser, MA Magnuson Diabetes 47 (3), 307-315, 1998 | 440 | 1998 |
Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: a soft clustering analysis MS Udler, J Kim, M von Grotthuss, S Bonàs-Guarch, JB Cole, J Chiou, ... PLoS medicine 15 (9), e1002654, 2018 | 417 | 2018 |
Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood G Toperoff, D Aran, JD Kark, M Rosenberg, T Dubnikov, B Nissan, ... Human molecular genetics 21 (2), 371-383, 2012 | 384 | 2012 |
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene M Bitner-Glindzicz, KJ Lindley, P Rutland, D Blaydon, VV Smith, PJ Milla, ... Nature genetics 26 (1), 56-60, 2000 | 367 | 2000 |
Control of pancreatic β cell regeneration by glucose metabolism S Porat, N Weinberg-Corem, S Tornovsky-Babaey, R Schyr-Ben-Haroush, ... Cell metabolism 13 (4), 440-449, 2011 | 349 | 2011 |
Reproducibility of glucose measurements using the glucose sensor M Metzger, G Leibowitz, J Wainstein, B Glaser, I Raz Diabetes Care 25 (7), 1185-1191, 2002 | 318 | 2002 |
p16Ink4a-induced senescence of pancreatic beta cells enhances insulin secretion A Helman, A Klochendler, N Azazmeh, Y Gabai, E Horwitz, S Anzi, ... Nature medicine 22 (4), 412-420, 2016 | 316 | 2016 |
A nonsense mutation in the inward rectifier potassium channel gene, Kir6. 2, is associated with familial hyperinsulinism A Nestorowicz, N Inagaki, T Gonoi, KP Schoor, BA Wilson, B Glaser, ... Diabetes 46 (11), 1743-1748, 1997 | 292 | 1997 |
Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls J Flannick, JM Mercader, C Fuchsberger, MS Udler, A Mahajan, J Wessel, ... Nature 570 (7759), 71-76, 2019 | 284 | 2019 |
Genetics of neonatal hyperinsulinism B Glaser, P Thornton, T Otonkoski, C Junien Archives of Disease in Childhood-Fetal and Neonatal Edition 82 (2), F79-F86, 2000 | 277 | 2000 |