FIND

researchers

DISCOVER

relevant articles

PROMOTE

your research

now for free

Benjamin Glaser

Research Profile

Disorders

Physiology

Chemicals & Drugs

Living Beings

Anatomy

Concepts & Ideas

Pedigree

Genes & Molecular Sequences

Alleles

Co-author Network

Publications

TOP 3
Yuval Dor; Benjamin Glaser
β-cell dedifferentiation and type 2 diabetes.
Miri Stolovich-Rain; Benjamin Glaser; Joseph Grimsby; Ayat Hija; Yuval Dor
Pancreatic beta cells in very old mice retain capacity for compensatory proliferation.
Benjamin Glaser
Lessons in human biology from a monogenic pancreatic β cell disease.

Register for free to view:

Visualized networks:

See your personal network in
sophisticated graphical views

GeoTargeted Searches:

Locate experts around the world
and connect with global collaborators

Research Profiles:

See the research activity
of experts around the globe

Geonetwork of Benjamin Glaser (preview)

Cities where this author has publications
Cities where co-authors of this author have publications

Flash Player Required

All Publications

2013: Yuval Dor; Benjamin Glaser
β-cell dedifferentiation and type 2 diabetes.
The New England journal of medicine 2013;368(6):572-3.
2012: Miri Stolovich-Rain; Benjamin Glaser; Joseph Grimsby; Ayat Hija; Yuval Dor
Pancreatic beta cells in very old mice retain capacity for compensatory proliferation.
The Journal of biological chemistry 2012;287(33):27407-14.
2011: Benjamin Glaser
Lessons in human biology from a monogenic pancreatic β cell disease.
The Journal of clinical investigation 2011;121(10):3821-5.
2011: Benjamin Glaser; Yocheved Krakinovsky; Heddy Landau; Kineret Mazor-Aronovitch; Ilana Blech; Josef Ekstein; David Gillis; Dvorah Abeliovich
ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia.
Genetics in medicine : official journal of the American College of Medical Genetics 2011;13(10):891-4.
2011: Chamutal Gur; Sameer A Kassem; Judith Magenheim; Hagit Achdout; Yuval Dor; Jonatan Enk; Benjamin Glaser; Yaakov Naparstek; Tomer Nir; Angel Porgador; James Shapiro; Miri Stolovich-Rain; Yaron Suissa; Ofer Mandelboim
Recognition and killing of human and murine pancreatic beta cells by the NK receptor NKp46.
Journal of immunology (Baltimore, Md. : 1950) 2011;187(6):3096-103.
2011: Seth J Salpeter; A M James Shapiro; Noa Weinberg-Corem; Amir Eden; Benjamin Glaser; Zvi Granot; Joseph Grimsby; Agnes Klochendler; Mark Magnuson; Shay Porat; Yuval Dor
Glucose regulates cyclin D2 expression in quiescent and replicating pancreatic β-cells through glycolysis and calcium channels.
Endocrinology 2011;152(7):2589-98.
2011: Yodphat Krausz; Nanette Freedman; Rina Rubinstein; Efraim Lavie; Marina Orevi; Sagi Tshori; Asher Salmon; Benjamin Glaser; Roland Chisin; Eyal Mishani; David J Gross
68Ga-DOTA-NOC PET/CT imaging of neuroendocrine tumors: comparison with ¹¹¹In-DTPA-octreotide (OctreoScan®).
Molecular imaging and biology : MIB : the official publication of the Academy of Molecular Imaging 2011;13(3):583-93.
2011: Roy Eldor; Benjamin Glaser; Merav Fraenkel; Victoria Doviner; Asher Salmon; David J Gross
Glucagonoma and the glucagonoma syndrome - cumulative experience with an elusive endocrine tumour.
Clinical endocrinology 2011;74(5):593-8.
2011: Ilana Blech; Mark Katzenellenbogen; Alexandra Katzenellenbogen; Julio Wainstein; Ardon Rubinstein; Ilana Harman-Boehm; Joseph Cohen; Toni I Pollin; Benjamin Glaser
Predicting diabetic nephropathy using a multifactorial genetic model.
PloS one 2011;6(4):e18743.
2010: Benjamin Glaser
Genetic analysis of complex disease--a roadmap to understanding or a colossal waste of money.
Pediatric endocrinology reviews : PER 2010;7(3):258-65.
2010: Rosalind J Neuman; Jon Wasson; Gil Atzmon; Julio Wainstein; Yair Yerushalmi; Joseph Cohen; Nir Barzilai; Ilana Blech; Benjamin Glaser; M Alan Permutt
Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population.
PloS one 2010;5(3):e9903.
2009: Rena Cooper-Kazaz; Wendy M van der Deure; Marco Medici; Theo J Visser; Ana Alkelai; Benjamin Glaser; Robin P Peeters; Bernard Lerer
Preliminary evidence that a functional polymorphism in type 1 deiodinase is associated with enhanced potentiation of the antidepressant effect of sertraline by triiodothyronine.
Journal of affective disorders 2009;116(1-2):113-6.
2009: Jeanette Feder; Ofer Ovadia; Ilana Blech; Josef Cohen; Julio Wainstein; Ilana Harman-Boehm; Benjamin Glaser; Dan Mishmar
Parental diabetes status reveals association of mitochondrial DNA haplogroup J1 with type 2 diabetes.
BMC medical genetics 2009;10():60.
2008: Vered Molho-Pessach; Ziad Agha; Suhail Aamar; Benjamin Glaser; Victoria Doviner; Nurith Hiller; David H Zangen; Annick Raas-Rothschild; Ziva Ben-Neriah; Shaher Shweiki; Orly Elpeleg; Abraham Zlotogorski
The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations.
Journal of the American Academy of Dermatology 2008;59(1):79-85.
2008: Maha Abdulhadi-Atwan; Jeremy Bushman; Jeremy Bushmann; Sharona Tornovsky-Babaey; Avital Perry; Abdulsalam Abu-Libdeh; Benjamin Glaser; Show-Ling Shyng; David H Zangen
Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence.
Diabetes 2008;57(7):1935-40.
2008: Benjamin Glaser
Insulin mutations in diabetes: the clinical spectrum.
Diabetes 2008;57(4):799-800.
2008: Jeanette Feder; Ilana Blech; Ofer Ovadia; Shirly Amar; Julio Wainstein; Itamar Raz; Sarah Dadon; Dan E Arking; Benjamin Glaser; Dan Mishmar
Differences in mtDNA haplogroup distribution among 3 Jewish populations alter susceptibility to T2DM complications.
BMC genomics 2008;9():198.
2007: K Mazor-Aronovitch; D Gillis; D Lobel; Harry J Hirsch; Orit Pinhas-Hamiel; Dalit Modan-Moses; Benjamin Glaser; Heddy Landau
Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism.
European journal of endocrinology / European Federation of Endocrine Societies 2007;157(4):491-7.
2007: Carlos A Benbassat; Sara Mechlis-Frish; Hadassah Guttmann; Benjamin Glaser; Yodphat Krausz
Current concepts in the follow-up of patients with differentiated thyroid cancer.
The Israel Medical Association journal : IMAJ 2007;9(7):540-5.
2007: Rena Cooper-Kazaz; Jeffrey T Apter; Revital Cohen; Leonid Karagichev; Said Muhammed-Moussa; Daniel Grupper; Taly Drori; Michael E Newman; Harold A Sackeim; Benjamin Glaser; Bernard Lerer
Combined treatment with sertraline and liothyronine in major depression: a randomized, double-blind, placebo-controlled trial.
Archives of general psychiatry 2007;64(6):679-88.
2007: Hila Elinav; Zemira Wolf; Auryan Szalat; Tali Bdolah-Abram; Benjamin Glaser; Itamar Raz; Gil Leibowitz
In-hospital treatment of hyperglycemia: effects of intensified subcutaneous insulin treatment.
Current medical research and opinion 2007;23(4):757-65.
2007: Benjamin Glaser
Type 2 diabetes: hypoinsulinism, hyperinsulinism, or both?
PLoS medicine 2007;4(4):e148.
2005: Liran Horev; Tamara Potikha; Sharon Ayalon; Vered Molho-Pessach; Arieh Ingber; Mohamad Abdel Gany; Basel Sad Edin; Benjamin Glaser; Abraham Zlotogorski
A novel splice-site mutation in ECM-1 gene in a consanguineous family with lipoid proteinosis.
Experimental dermatology 2005;14(12):891-7.
2005: Khalid Hussain; Karen E Cosgrove; Ruth M Shepherd; A Luharia; Virpi V Smith; Sameer Kassem; John W Gregory; A Sivaprasadarao; Henrik Christesen; Bendt Brock Jacobsen; Klaus Brusgaard; Benjamin Glaser; E A Maher; Keith J Lindley; Peter Hindmarsh; Mehul T Dattani; Mark J Dunne
Hyperinsulinemic hypoglycemia in Beckwith-Wiedemann syndrome due to defects in the function of pancreatic beta-cell adenosine triphosphate-sensitive potassium channels.
The Journal of clinical endocrinology and metabolism 2005;90(7):4376-82.
2005: Moshe Goldfeld; Benjamin Glaser; Elias Nassir; John Moshe Gomori; Elitsur Hazani; Nassir Bishara
CT of the ear in Pendred syndrome.
Radiology 2005;235(2):537-40.
2005: Gary S Chuang; Amalia Martinez-Mir; Adam S Geyer; Danielle E Engler; Benjamin Glaser; Peter B Cserhalmi-Friedman; Derek Gordon; Liran Horev; Barbara Lukash; Eric Herman; Manuel Prieto Cid; Sarah Brenner; Marina Landau; Eli Sprecher; Maria Pilar Garcia Muret; Angela M Christiano; Abraham Zlotogorski
Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata.
Journal of the American Academy of Dermatology 2005;52(3 Pt 1):410-6.
2005: Tamara Potikha; Sameer Kassem; Esther P Haber; Ilana Ariel; Benjamin Glaser
p57Kip2 (cdkn1c): sequence, splice variants and unique temporal and spatial expression pattern in the rat pancreas.
Laboratory investigation; a journal of technical methods and pathology 2005;85(3):364-75.
2004: Sharona Tornovsky; Ana Crane; Karen E Cosgrove; Khalid Hussain; Judith Lavie; Ma'ayan Heyman; Yaron Nesher; Na'ama Kuchinski; Etti Ben-Shushan; Olga Shatz; Efrat Nahari; Tamara Potikha; David H Zangen; Yardena Tenenbaum-Rakover; Liat de Vries; Jesús Argente; Ricardo Gracia; Heddy Landau; Alon Eliakim; Keith J Lindley; Mark J Dunne; Lydia Aguilar-Bryan; Benjamin Glaser
Hyperinsulinism of infancy: novel ABCC8 and KCNJ11 mutations and evidence for additional locus heterogeneity.
The Journal of clinical endocrinology and metabolism 2004;89(12):6224-34.
2004: Luna Kadouri; Zsofia Kote-Jarai; Ayala Hubert; Francine Durocher; Dvorah Abeliovich; Benjamin Glaser; Tamar Hamburger; Rosalind A Eeles; Tamar Peretz
A single-nucleotide polymorphism in the RAD51 gene modifies breast cancer risk in BRCA2 carriers, but not in BRCA1 carriers or noncarriers.
British journal of cancer 2004;90(10):2002-5.
2004: Latisha Love-Gregory; Jonathon Wasson; Jiyan Ma; Carol H Jin; Benjamin Glaser; Brian K Suarez; M Alan Permutt
A common polymorphism in the upstream promoter region of the hepatocyte nuclear factor-4 alpha gene on chromosome 20q is associated with type 2 diabetes and appears to contribute to the evidence for linkage in an ashkenazi jewish population.
Diabetes 2004;53(4):1134-40.
2004: Luna Kadouri; Zsofia Kote-Jarai; Douglas F Easton; Ayala Hubert; Rifat A Hamoudi; Benjamin Glaser; Dvorah Abeliovich; Tamar Peretz; Rosalind A Eeles
Polyglutamine repeat length in the AIB1 gene modifies breast cancer susceptibility in BRCA1 carriers.
International journal of cancer. Journal international du cancer 2004;108(3):399-403.
2004: Philippe Ruszniewski; Sophia Ish-Shalom; Machteld Wymenga; Dermot O'Toole; Rudolf Arnold; Paola Tomassetti; Nigel Bax; Martyn E Caplin; Barbro Eriksson; Benjamin Glaser; Michel Ducreux; Catherine Lombard-Bohas; Wouter W de Herder; Gianfranco Delle Fave; Nick Reed; Jean François Seitz; Eric Van Cutsem; Ashley Grossman; Philippe Rougier; Wolfgang Schmidt; Bertram Wiedenmann
Rapid and sustained relief from the symptoms of carcinoid syndrome: results from an open 6-month study of the 28-day prolonged-release formulation of lanreotide.
Neuroendocrinology 2004;80(4):244-51.
2003: Benjamin Glaser
Pendred syndrome.
Pediatric endocrinology reviews : PER 2003;1 Suppl 2():199-204; discussion 204.
2003: Amalia Martinez-Mir; Benjamin Glaser; Gary S Chuang; Liran Horev; Arie Waldman; Danielle E Engler; Derek Gordon; Lynda J Spelman; Ioannis Hatzibougias; Jack Green; Angela M Christiano; Abraham Zlotogorski
Germline fumarate hydratase mutations in families with multiple cutaneous and uterine leiomyomata.
The Journal of investigative dermatology 2003;121(4):741-4.
2003: Benjamin Glaser
Dominant SUR1 mutation causing autosomal dominant type 2 diabetes.
Lancet 2003;361(9354):272-3.
2002: Khalid Hussain; Karen E Cosgrove; Ruth M Shepherd; JC Chapman; S M Swift; Virpi V Smith; Sameer Kassem; Benjamin Glaser; Keith J Lindley; Al Aynsley-Green; Mark J Dunne
Uncontrolled insulin secretion from a childhood pancreatic beta-cell adenoma is not due to the functional loss of ATP-sensitive potassium channels.
Endocrine-related cancer 2002;9(4):221-6.
2002: M Alan Permutt; Jonathon Wasson; Latisha Love-Gregory; Jiyan Ma; Gary Skolnick; Brian K Suarez; Jennifer Lin; Benjamin Glaser
Searching for type 2 diabetes genes on chromosome 20.
Diabetes 2002;51 Suppl 3():S308-15.
2002: Muriel Metzger; Gil Leibowitz; Julio Wainstein; Benjamin Glaser; Itamar Raz
Reproducibility of glucose measurements using the glucose sensor.
Diabetes care 2002;25(7):1185-91.
2002: Benjamin Dekel; Daniel Lubin; Dalit Modan-Moses; Jacob Quint; Benjamin Glaser; Joseph Meyerovitch
Compound heterozygosity for the common sulfonylurea receptor mutations can cause mild diazoxide-sensitive hyperinsulinism.
Clinical pediatrics 2002;41(3):183-6.
2001: Sameer Kassem; Ilana Ariel; Paul S Thornton; Khalid Hussain; V Smith; Keith J Lindley; Al Aynsley-Green; Benjamin Glaser
p57(KIP2) expression in normal islet cells and in hyperinsulinism of infancy.
Diabetes 2001;50(12):2763-9.
2001: Yodphat Krausz; Beatrice Uziely; R Nesher; Roland Chisin; Benjamin Glaser
Recombinant thyroid-stimulating hormone in differentiated thyroid cancer.
The Israel Medical Association journal : IMAJ 2001;3(11):843-9.
2001: Luna Kadouri; Douglas F Easton; S Edwards; Ayala Hubert; Zsofia Kote-Jarai; Benjamin Glaser; Francine Durocher; Dvorah Abeliovich; Tamar Peretz; Rosalind A Eeles
CAG and GGC repeat polymorphisms in the androgen receptor gene and breast cancer susceptibility in BRCA1/2 carriers and non-carriers.
British journal of cancer 2001;85(1):36-40.
2001: Susanne G Straub; Karen E Cosgrove; C Ammälä; Ruth M Shepherd; RE O'Brien; Philippa D Barnes; N Kuchinski; JC Chapman; M Schaeppi; Benjamin Glaser; Keith J Lindley; Geoffrey W G Sharp; Al Aynsley-Green; Mark J Dunne
Hyperinsulinism of infancy: the regulated release of insulin by KATP channel-independent pathways.
Diabetes 2001;50(2):329-39.
2000: Maria Bitner-Glindzicz; Keith J Lindley; Paul Rutland; Diana Blaydon; Virpi V Smith; P J Milla; Khalid Hussain; J Furth-Lavi; Karen E Cosgrove; Ruth M Shepherd; Philippa D Barnes; RE O'Brien; P A Farndon; Jane C Sowden; Xue Zhong Liu; M J Scanlan; Sue Malcolm; Mark J Dunne; Al Aynsley-Green; Benjamin Glaser
A recessive contiguous gene deletion causing infantile hyperinsulinism, enteropathy and deafness identifies the Usher type 1C gene.
Nature genetics 2000;26(1):56-60.
2000: Liran Horev; Benjamin Glaser; Aryeh Metzker; Dan Ben-Amitai; D Vardy; Abraham Zlotogorski
Monilethrix: mutational hotspot in the helix termination motif of the human hair basic keratin 6.
Human heredity 2000;50(5):325-30.
2000: Sameer Kassem; Ilana Ariel; Paul S Thornton; I Scheimberg; Benjamin Glaser
Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy.
Diabetes 2000;49(8):1325-33.
2000: Benjamin Glaser
Hyperinsulinism of the newborn.
Seminars in perinatology 2000;24(2):150-63.
2000: Benjamin Glaser; Paul Thornton; Timo Otonkoski; C Junien
Genetics of neonatal hyperinsulinism.
Archives of disease in childhood. Fetal and neonatal edition 2000;82(2):F79-86.
2000: Benjamin Glaser
[Hyperinsulinemia, a heterogeneous illness].
Journées annuelles de diabétologie de l'Hôtel-Dieu 2000;():25-38.
1999: Benjamin Glaser; Fergus Ryan; Marc Y Donath; Heddy Landau; Charles A Stanley; L Baker; David Barton; Paul S Thornton
Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene.
Diabetes 1999;48(8):1652-7.
1999: Zaki Kraiem; R Heinrich; Orit Sadeh; Eitan Shiloni; Elias Nassir; Elitsur Hazani; Benjamin Glaser
Sulfate transport is not impaired in pendred syndrome thyrocytes.
The Journal of clinical endocrinology and metabolism 1999;84(7):2574-6.
1999: Yodphat Krausz; A Rosler; Hadassah Guttmann; Sophia Ish-Shalom; N Shibley; Roland Chisin; Benjamin Glaser
Somatostatin receptor scintigraphy for early detection of regional and distant metastases of medullary carcinoma of the thyroid.
Clinical nuclear medicine 1999;24(4):256-60.
1999: Benjamin Glaser; J Furth; Charles A Stanley; L Baker; Paul S Thornton; Heddy Landau; M Alan Permutt
Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism.
Human mutation 1999;14(1):23-9.
1998: Benjamin Glaser; Paul S Thornton; KC Herold; Charles A Stanley
Clinical and molecular heterogeneity of familial hyperinsulinism.
The Journal of pediatrics 1998;133(6):801-2.
1998: Fergus Ryan; D Devaney; C Joyce; A Nestorowicz; M Alan Permutt; Benjamin Glaser; David Barton; Paul S Thornton
Hyperinsulinism: molecular aetiology of focal disease.
Archives of disease in childhood 1998;79(5):445-7.
1998: Abraham Zlotogorski; Liran Horev; Benjamin Glaser
Monilethrix: a keratin hHb6 mutation is co-dominant with variable expression.
Experimental dermatology 1998;7(5):268-72.
1998: Show-Ling Shyng; T Ferrigni; J B Shepard; A Nestorowicz; Benjamin Glaser; M Alan Permutt; Colin G Nichols
Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy.
Diabetes 1998;47(7):1145-51.
1998: A Nestorowicz; Benjamin Glaser; B A Wilson; Show-Ling Shyng; Colin G Nichols; Charles A Stanley; Paul S Thornton; M Alan Permutt
Genetic heterogeneity in familial hyperinsulinism.
Human molecular genetics 1998;7(7):1119-28.
1998: Franz M Matschinsky; Benjamin Glaser; Mark Magnuson
Pancreatic beta-cell glucokinase: closing the gap between theoretical concepts and experimental realities.
Diabetes 1998;47(3):307-15.
1998: Benjamin Glaser; P Kesavan; M Heyman; E Davis; A Cuesta; Adina Buchs; Charles A Stanley; Paul S Thornton; M Alan Permutt; Franz M Matschinsky; KC Herold
Familial hyperinsulinism caused by an activating glucokinase mutation.
The New England journal of medicine 1998;338(4):226-30.
1998: M Alan Permutt; K Chiu; J Ferrer; Benjamin Glaser; H Inoue; A Nestorowicz; Charles A Stanley; Y Tanizawa
Genetics of type II diabetes.
Recent progress in hormone research 1998;53():201-16.
1998: Paul S Thornton; MS Satin-Smith; KC Herold; Benjamin Glaser; K C Chiu; A Nestorowicz; M Alan Permutt; L Baker; Charles A Stanley
Familial hyperinsulinism with apparent autosomal dominant inheritance: clinical and genetic differences from the autosomal recessive variant.
The Journal of pediatrics 1998;132(1):9-14.
1998: Yodphat Krausz; Jacob Bar-Ziv; R B de Jong; Sophia Ish-Shalom; Roland Chisin; N Shibley; Benjamin Glaser
Somatostatin-receptor scintigraphy in the management of gastroenteropancreatic tumors.
The American journal of gastroenterology 1998;93(1):66-70.
1997: L A Everett; Benjamin Glaser; J C Beck; Jacquelyn R Idol; Adina Buchs; M Heyman; F Adawi; Elitsur Hazani; Elias Nassir; Andreas D Baxevanis; Val C Sheffield; Eric Green
Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS).
Nature genetics 1997;17(4):411-22.
1997: A Nestorowicz; N Inagaki; T Gonoi; K P Schoor; B A Wilson; Benjamin Glaser; Heddy Landau; Charles A Stanley; Paul S Thornton; S Seino; M Alan Permutt
A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism.
Diabetes 1997;46(11):1743-8.