Benjamin Glaser
Benjamin Glaser
Hadassah-Hebrew University Medical Center
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Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)
LA Everett, B Glaser, JC Beck, JR Idol, A Buchs, F Adawi, E Hazani, ...
Nature genetics 17 (4), 411-422, 1997
The genetic architecture of type 2 diabetes
C Fuchsberger, J Flannick, TM Teslovich, A Mahajan, V Agarwala, ...
Nature 536 (7614), 41-47, 2016
p57KIP2 expression in normal islet cells and in hyperinsulinism of infancy
SA Kassem, I Ariel, PS Thornton, K Hussain, V Smith, KJ Lindley, ...
Diabetes 50 (12), 2763-2769, 2001
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
Induction of long-term glycemic control in newly diagnosed type 2 diabetic patients by transient intensive insulin treatment
H Ilkova, B Glaser, A Tunškale, N Bagriašik, E Cerasi
Diabetes care 20 (9), 1353-1356, 1997
Adenosine diphosphate as an intracellular regulator of insulin secretion
CG Nichols, SL Shyng, A Nestorowicz, B Glaser, JPT Clement, ...
Science 272 (5269), 1785-1787, 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
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
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
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
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
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
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
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
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
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
Mutations in the sulfonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews
A Nestorowicz, BA Wilson, KP Schoor, H Inoue, B Glaser, H Landau, ...
Human Molecular Genetics 5 (11), 1813-1822, 1996
A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4α gene on chromosome 20q is associated with type 2 diabetes and appears to contribute toá…
LD Love-Gregory, J Wasson, J Ma, CH Jin, B Glaser, BK Suarez, ...
Diabetes 53 (4), 1134-1140, 2004
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
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), 1-12, 2018
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