List of works - Benjamin Glaser

68Ga-DOTA-NOC PET/CT imaging of neuroendocrine tumors: comparison with ¹¹¹In-DTPA-octreotide (OctreoScan®).

scientific article published in June 2011

A Genome Scan for Type 2 Diabetes Susceptibility Loci in a Genetically Isolated Population

scientific article published on 01 March 2001

A Spot Sample Test for the Estimation of Urinary or Nephrogenous cAMP in the Evaluation of Parathyroid Function

scientific article published on 01 January 1983

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.

scientific article published in April 2004

A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism

scientific article published on 01 November 1997

A single-nucleotide polymorphism in the RAD51 gene modifies breast cancer risk in BRCA2 carriers, but not in BRCA1 carriers or noncarriers

scientific article published on May 2004

ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia ⬇️

scientific article (publication date: October 2011)

Abrogation of Autophagy by Chloroquine Alone or in Combination with mTOR Inhibitors Induces Apoptosis in Neuroendocrine Tumor Cells.

scientific article published on December 2015

Adenosine diphosphate as an intracellular regulator of insulin secretion.

scientific article

Aging-Dependent Demethylation of Regulatory Elements Correlates with Chromatin State and Improved β Cell Function

scientific article published on 26 August 2015

Ashkenazi Jewish mtDNA haplogroup distribution varies among distinct subpopulations: lessons of population substructure in a closed group

scientific article

Beta Cell Death by Cell-Free DNA and Outcome after Clinical Islet Transplantation

scientific article published on 11 January 2018

Beta cell heterogeneity: an evolving concept.

scientific article

Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy

scientific article published on 01 August 2000

CT of the Ear in Pendred Syndrome

article

Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism

scientific article

Cellular immune functions in patients with primary hyperparathyroidism: Effects of histamine and cimetidine

scientific article published on 01 April 1985

Common variants in WFS1 confer risk of type 2 diabetes

scientific article published on July 2007

Comprehensive human cell-type methylation atlas reveals origins of circulating cell-free DNA in health and disease

scientific article published in Nature Communications

Control of pancreatic β cell regeneration by glucose metabolism.

scientific article published on April 2011

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

correction of a scientific article; published on 30 May 2019

Cross-sectional and longitudinal study of the pituitary-thyroid axis in patients with thalassaemia major.

scientific article published in January 1993

Detailed investigation of the role of common and low-frequency WFS1 variants in type 2 diabetes risk

scientific article

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Diagnosis of ABCC8 congenital hyperinsulinism of infancy in a 20 year-old man evaluated for factitious hypoglycemia

scientific article published on 01 February 2017

Differences in mtDNA haplogroup distribution among 3 Jewish populations alter susceptibility to T2DM complications.

scientific article published on 29 April 2008

Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health.

scientific article

Distinct Imprinting Signatures and Biased Differentiation of Human Androgenetic and Parthenogenetic Embryonic Stem Cells

scientific article published on 01 September 2019

Do cyclic AMP concentrations in saliva reflect PTH biologic activity?

scientific article published on 01 June 1985

Dominant SUR1 mutation causing autosomal dominant type 2 diabetes

scientific article published in The Lancet

Dynamical compensation in physiological circuits

scientific article published on 8 November 2016

Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations

scientific article

Early intensive insulin treatment for induction of long-term glycaemic control in type 2 diabetes.

scientific article

Effect of 6 months' gliclazide treatment on insulin release and sensitivity to endogenous insulin in NIDDM: role of initial CSII-induced normoglycemia ⬇️

scientific article published on January 1, 1991

Effect of Acute Cimetidine Administration on Indices of Parathyroid Hormone Action in Healthy Subjects and Patients with Primary and Secondary Hyperparathyroidism

scientific article published on 01 November 1984

Effects of Moderate Intensity Glycemic Control After Cardiac Surgery ⬇️

scientific article published on December 1, 2010

Effects of ageing and senescence on pancreatic β-cell function

scientific article published on September 2016

Elevated brain-derived cell-free DNA among patients with first psychotic episode – a proof-of-concept study

scientific article published in 2022

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

scientific article published on 23 January 2018

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

article by Jason Flannick et al published 22 May 2019 in Nature

FOXP3 mutations causing early-onset insulin-requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.

scientific article published on 29 November 2017

Familial hyperinsulinism caused by an activating glucokinase mutation

Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant

scientific article published on 01 January 1998

Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy ⬇️

scientific article published on July 1, 1998

G0-G1 transition and the restriction point in pancreatic β-cells in vivo

scientific article published on 15 October 2013

Ga-68 DOTA-NOC Uptake in the Pancreas

article

Gastrin: a distinct fate of neurogenin3 positive progenitor cells in the embryonic pancreas

scientific article published in 2013

Gastrointestinal/pancreatic hormone concentrations in the portal venous system of nine patients with organic hyperinsulinism ⬇️

scientific article published on October 1, 1981

Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population

scientific article

Genetic activation of α-cell glucokinase in mice causes enhanced glucose-suppression of glucagon secretion during normal and diabetic states

scientific article published on 19 February 2021

Genetic heterogeneity in familial hyperinsulinism.

scientific article

Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs

article

Genetics of neonatal hyperinsulinism.

scientific article

Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood

scientific article

Germline Fumarate Hydratase Mutations in Families with Multiple Cutaneous and Uterine Leiomyomata

scientific article published on 01 October 2003

Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata

article

Glucagonoma and the glucagonoma syndrome - cumulative experience with an elusive endocrine tumour.

scientific article

Glucose metabolism: key endogenous regulator of β‐cell replication and survival ⬇️

scientific article published on October 1, 2012

Glucose regulates cyclin D2 expression in quiescent and replicating pancreatic β-cells through glycolysis and calcium channels

scientific article

Glycosylated serum protein levels assayed with highly sensitive immunoradiometric assay accurately reflect glycemic control of diabetic patients

scientific article published on May 1, 1992

Growth hormone reserve in adult beta thalassemia patients

scientific article published on 01 February 2007

Growth-hormone-binding protein in patients with acromegaly

scientific article published on January 1, 1992

Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews ⬇️

scientific article published on June 1, 1998

Hyperglycaemia induces metabolic dysfunction and glycogen accumulation in pancreatic β-cells

scientific article

Hyperinsulinemic Hypoglycemia in Beckwith-Wiedemann Syndrome due to Defects in the Function of Pancreatic β-Cell Adenosine Triphosphate-Sensitive Potassium Channels

scientific article published on 05 April 2005

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene

scientific article

Hyperinsulinism of infancy: the regulated release of insulin by KATP channel-independent pathways.

scientific article

IGF-1 levels may increase paradoxically with dopamine agonist treatment for prolactinomas

scientific article published on 01 August 2018

Identification of a G-Protein Subunit-α11 Gain-of-Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2)

scientific article published on 28 January 2016

Identification of a SIRT1 mutation in a family with type 1 diabetes

scientific article published on March 2013

Identification of tissue-specific cell death using methylation patterns of circulating DNA

scientific article published on 14 March 2016

Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation

scientific article published on 21 June 2008

Induction of Long-Term Glycemic Control in Newly Diagnosed Type 2 Diabetic Patients by Transient Intensive Insulin Treatment

scientific article published on 01 September 1997

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

preprint published 25 September 2016

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

scientific article

Insulin mutations in diabetes: the clinical spectrum

scientific article published on 01 April 2008

Insulin receptor alternative splicing is regulated by insulin signaling and modulates beta cell survival.

scientific article published on 16 August 2016

Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism

scientific article published in January 1999

Isolation and characterization of the human AKT1 gene, identification of 13 single nucleotide polymorphisms (SNPs), and their lack of association with Type II diabetes.

scientific article

Isolation and characterization of the human PAX4 gene

scientific article

Large Islets, Beta-Cell Proliferation, and a Glucokinase Mutation

scientific article published on 8 April 2010

Lessons in human biology from a monogenic pancreatic β cell disease

scientific article published on October 2011

Long-acting somatostatin analogues are an effective treatment for type 1 gastric carcinoid tumours.

scientific article

Long-term neurodevelopmental outcome in conservatively treated congenital hyperinsulinism

scientific article

Loss of Liver Kinase B1 (LKB1) in Beta Cells Enhances Glucose-stimulated Insulin Secretion Despite Profound Mitochondrial Defects

scientific article

Loss-of-function mutations in SLC30A8 protect against type 2 diabetes

scientific article

Mapping of the human insulin receptor substrate-2 gene, identification of a linked polymorphic marker and linkage analysis in families with Type II diabetes: no evidence for a major susceptibility role.

scientific article published on November 1998

Metabolic Stress and Compromised Identity of Pancreatic Beta Cells.

scientific article published on 21 February 2017

Missense polymorphism in the human carboxypeptidase E gene alters enzymatic activity.

scientific article

Molecular basis and characterization of the hyperinsulinism/hyperammonemia syndrome: predominance of mutations in exons 11 and 12 of the glutamate dehydrogenase gene. HI/HA Contributing Investigators

article

Monilethrix: Mutational Hotspot in the Helix Termination Motif of the Human Hair Basic Keratin 6

scientific article published on 01 September 2000

Monitoring liver damage using hepatocyte-specific methylation markers in cell-free circulating DNA

scientific article published on 21 June 2018

Mutations in the sulonylurea receptor gene are associated with familial hyperinsulinism in Ashkenazi Jews.

scientific article

Neonatal Hyperinsulinism.

scientific article published on March 1999

Non-invasive detection of human cardiomyocyte death using methylation patterns of circulating DNA.

scientific article

Normal proinsulin processing despite beta-cell dysfunction in persistent hyperinsulinaemic hypoglycaemia of infancy (nesidioblastosis).

scientific article published in November 1996

Novel de novo mutation in sulfonylurea receptor 1 presenting as hyperinsulinism in infancy followed by overt diabetes in early adolescence

scientific article published on 4 April 2008

PERSISTENT HYPERINSULINAEMIC HYPOGLYCAEMIA OF INFANCY: LONG-TERM TREATMENT WITH THE SOMATOSTATIN ANALOGUE SANDOSTATIN

scientific article published on 01 July 1989

Pancreatic Beta Cells in Very Old Mice Retain Capacity for Compensatory Proliferation ⬇️

scientific article published on June 27, 2012

Pancreatic beta-cell glucokinase: closing the gap between theoretical concepts and experimental realities.

scientific article

Pancreatic polypeptide-producing tumors. Silent lesions of the pancreas?

scientific article published on May 1984

Pancreatic β-Cells Express the Fetal Islet Hormone Gastrin in Rodent and Human Diabetes

scientific article published on 18 November 2016

Parental diabetes status reveals association of mitochondrial DNA haplogroup J1 with type 2 diabetes

scientific article published on 18 June 2009

Pendred syndrome is caused by mutations in a putative sulphate transporter gene (PDS)

scientific article

Pendred syndrome maps to chromosome 7q21-34 and is caused by an intrinsic defect in thyroid iodine organification

scientific article

Percutaneous Transhepatic Venous Sampling of Gastrin

scientific article published on 01 July 1982

Persistent hyperinsulinemic hypoglycemia of infancy (“nesidioblastosis”): Autosomal recessive inheritance in 7 pedigrees

scientific article published on 01 December 1990

Persistent hyperinsulinemic hypoglycemia of infancy: Long-term octreotide treatment without pancreatectomy

scientific article published on 01 October 1993

Plasma Human Pancreatic Polypeptide Responses to Administered Secretin: Effects of Surgical Vagotomy, Cholinergic Blockade, and Chronic Pancreatitis*

article

Polyglutamine repeat length in theAIB1 gene modifies breast cancer susceptibility inBRCA1 carriers

article

Polymorphisms of the HDL receptor gene associated with HDL cholesterol levels in diabetic kindred from three populations.

scientific article published in January 2003

Population-specific risk of type 2 diabetes conferred by HNF4A P2 promoter variants: a lesson for replication studies

scientific article published on 26 August 2008

Post genome-wide association studies of novel genes associated with type 2 diabetes show gene-gene interaction and high predictive value

scientific article published in 2008

Postnatal Exocrine Pancreas Growth by Cellular Hypertrophy Correlates with a Shorter Lifespan in Mammals

scientific article published on 01 June 2018

Predicting Diabetic Nephropathy Using a Multifactorial Genetic Model ⬇️

scientific article published on April 14, 2011

Preliminary evidence that a functional polymorphism in type 1 deiodinase is associated with enhanced potentiation of the antidepressant effect of sertraline by triiodothyronine.

scientific article

Premature aging of leukocyte DNA methylation is associated with type 2 diabetes prevalence

scientific article

Recognition and Killing of Human and Murine Pancreatic Cells by the NK Receptor NKp46

scientific article published on 17 August 2011

Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews

article

Recombinant mapping of the familial hyperinsulinism gene to an 0.8 cM region on chromosome 11p15.1 and demonstration of a founder effect in Ashkenazi Jews

Recurrence-associated mortality in patients with differentiated thyroid carcinoma

scientific article published on 01 March 1993

Regulation of insulin release in persistent hyperinsulinaemic hypoglycaemia of infancy studied in long-term culture of pancreatic tissue.

scientific article published in August 1990

Relative expression of a dominant mutated ABCC8 allele determines the clinical manifestation of congenital hyperinsulinism.

scientific article published on 21 November 2011

Reproducibility of glucose measurements using the glucose sensor.

scientific article published in July 2002

Safety and efficacy of oral octreotide in acromegaly: results of a multicenter phase III trial.

scientific article published on 9 February 2015

Searching for Type 2 Diabetes Genes on Chromosome 20

article

Sebum Measurements for Rapid Identification of Hyperandrogenism Due to an Ovarian Leydig Cell Tumor

scientific article published on 01 April 1991

Secretion of pancreatic polypeptide in man in response to beef ingestion is mediated in part by an extravagal cholinergic mechanism

scientific article published on 01 January 1983

Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

scientific article published on 19 December 2017

Sex Difference in the Sensitivity of the Human Pancreatic Polypeptide Cell to Autonomic Nervous Stimulation in Man*

scientific article published on 01 January 1983

Sodium valproate and metyrapone for pituitary-dependent Cushing's disease.

scientific article published in September 1984

Somatostatin Receptor Scintigraphy for Early Detection of Regional and Distant Metastases of Medullary Carcinoma of the Thyroid

scientific article published on 01 April 1999

Somatostatin-Receptor Imaging of Medullary Thyroid Carcinoma

scientific article published on 01 May 1994

Somatostatin-receptor scintigraphy in the management of gastroenteropancreatic tumors

scientific article published on 01 January 1998

Studies in psychoneuroimmunology: psychological, immunological, and neuroendocrinological parameters in Israeli civilians during and after a period of Scud missile attacks.

scientific article published in January 1996

Sulfate transport is not impaired in pendred syndrome thyrocytes

scientific article published on 01 July 1999

Sulfonylurea-Responsive Diabetes in Childhood

scientific article published on 01 May 2007

Systemic regulation of the age-related decline of pancreatic β-cell replication. Diabetes 2013;62:2843–2848.

scientific article

TRUNCAL VAGOTOMY ABOLISHES THE SOMATOSTATIN RESPONSE TO INSULIN-INDUCED HYPOGLYCEMIA IN MAN

article

Targeted demethylation at the CDKN1C/p57 induces human β cell replication

article

Targeting the cell cycle inhibitor p57Kip2 promotes adult human β cell replication.

scientific article published on 16 January 2014

The Genetic Program of Pancreatic β-Cell Replication In Vivo

scientific article published on 18 March 2016

The H syndrome: a genodermatosis characterized by indurated, hyperpigmented, and hypertrichotic skin with systemic manifestations.

scientific article published on 14 April 2008

The Plastic Pancreas ⬇️

scientific article published on July 15, 2013

The expression of the beta cell-derived autoimmune ligand for the killer receptor nkp46 is attenuated in type 2 diabetes

scientific article

The genetic architecture of type 2 diabetes

scientific article (publication date: 11 July 2016)

Thyroidectomy Practice After Implementation of the 2015 American Thyroid Association Guidelines on Surgical Options for Patients With Well-Differentiated Thyroid Carcinoma.

scientific article published on 29 March 2018

Type 2 diabetes and congenital hyperinsulinism cause DNA double-strand breaks and p53 activity in β cells

scientific article published on 12 December 2013

Type 2 diabetes genetic loci informed by multi-trait associations point to disease mechanisms and subtypes: A soft clustering analysis

scientific article published on 21 September 2018

Type 2 diabetes: hypoinsulinism, hyperinsulinism, or both?

scientific article

Uncontrolled insulin secretion from a childhood pancreatic beta-cell adenoma is not due to the functional loss of ATP-sensitive potassium channels.

scientific article published in December 2002

Weaning triggers a maturation step of pancreatic β cells

scientific article published on 5 February 2015

p16(Ink4a)-induced senescence of pancreatic beta cells enhances insulin secretion.

scientific article published on 07 March 2016

p57KIP2 Expression in Normal Islet Cells and in Hyperinsulinism of Infancy ⬇️

scientific article published on December 1, 2001

p57Kip2 (cdkn1c): sequence, splice variants and unique temporal and spatial expression pattern in the rat pancreas

scientific article published on 01 March 2005

β-Cell DNA Damage Response Promotes Islet Inflammation in Type 1 Diabetes

scientific article published on 27 August 2018

β-Cells are not uniform after all-Novel insights into molecular heterogeneity of insulin-secreting cells

scientific article

β-cell dedifferentiation and type 2 diabetes.

scientific article published in February 2013

List of works by Benjamin Glaser

68Ga-DOTA-NOC PET/CT imaging of neuroendocrine tumors: comparison with ¹¹¹In-DTPA-octreotide (OctreoScan®).

A Genome Scan for Type 2 Diabetes Susceptibility Loci in a Genetically Isolated Population

A Spot Sample Test for the Estimation of Urinary or Nephrogenous cAMP in the Evaluation of Parathyroid Function

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.

A nonsense mutation in the inward rectifier potassium channel gene, Kir6.2, is associated with familial hyperinsulinism

A single-nucleotide polymorphism in the RAD51 gene modifies breast cancer risk in BRCA2 carriers, but not in BRCA1 carriers or noncarriers

ABCC8 mutation allele frequency in the Ashkenazi Jewish population and risk of focal hyperinsulinemic hypoglycemia ⬇️

Abrogation of Autophagy by Chloroquine Alone or in Combination with mTOR Inhibitors Induces Apoptosis in Neuroendocrine Tumor Cells.

Adenosine diphosphate as an intracellular regulator of insulin secretion.

Aging-Dependent Demethylation of Regulatory Elements Correlates with Chromatin State and Improved β Cell Function

Ashkenazi Jewish mtDNA haplogroup distribution varies among distinct subpopulations: lessons of population substructure in a closed group

Beta Cell Death by Cell-Free DNA and Outcome after Clinical Islet Transplantation

Beta cell heterogeneity: an evolving concept.

Beta-cell proliferation and apoptosis in the developing normal human pancreas and in hyperinsulinism of infancy

CT of the Ear in Pendred Syndrome

Calcium-stimulated insulin secretion in diffuse and focal forms of congenital hyperinsulinism

Cellular immune functions in patients with primary hyperparathyroidism: Effects of histamine and cimetidine

Common variants in WFS1 confer risk of type 2 diabetes

Comprehensive human cell-type methylation atlas reveals origins of circulating cell-free DNA in health and disease

Control of pancreatic β cell regeneration by glucose metabolism.

Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Cross-sectional and longitudinal study of the pituitary-thyroid axis in patients with thalassaemia major.

Detailed investigation of the role of common and low-frequency WFS1 variants in type 2 diabetes risk

Determinants of penetrance and variable expressivity in monogenic metabolic conditions across 77,184 exomes

Diagnosis of ABCC8 congenital hyperinsulinism of infancy in a 20 year-old man evaluated for factitious hypoglycemia

Differences in mtDNA haplogroup distribution among 3 Jewish populations alter susceptibility to T2DM complications.

Disrupting mitochondrial-nuclear coevolution affects OXPHOS complex I integrity and impacts human health.

Distinct Imprinting Signatures and Biased Differentiation of Human Androgenetic and Parthenogenetic Embryonic Stem Cells

Do cyclic AMP concentrations in saliva reflect PTH biologic activity?

Dominant SUR1 mutation causing autosomal dominant type 2 diabetes

Dynamical compensation in physiological circuits

Dysregulation of insulin secretion in children with congenital hyperinsulinism due to sulfonylurea receptor mutations

Early intensive insulin treatment for induction of long-term glycaemic control in type 2 diabetes.

Effect of 6 months' gliclazide treatment on insulin release and sensitivity to endogenous insulin in NIDDM: role of initial CSII-induced normoglycemia ⬇️

Effect of Acute Cimetidine Administration on Indices of Parathyroid Hormone Action in Healthy Subjects and Patients with Primary and Secondary Hyperparathyroidism

Effects of Moderate Intensity Glycemic Control After Cardiac Surgery ⬇️

Effects of ageing and senescence on pancreatic β-cell function

Elevated brain-derived cell-free DNA among patients with first psychotic episode – a proof-of-concept study

Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls

Exome sequencing of 20,791 cases of type 2 diabetes and 24,440 controls

FOXP3 mutations causing early-onset insulin-requiring diabetes but without other features of immune dysregulation, polyendocrinopathy, enteropathy, X-linked syndrome.

Familial hyperinsulinism caused by an activating glucokinase mutation

Familial hyperinsulinism with apparent autosomal dominant inheritance: Clinical and genetic differences from the autosomal recessive variant

Functional analyses of novel mutations in the sulfonylurea receptor 1 associated with persistent hyperinsulinemic hypoglycemia of infancy ⬇️

G0-G1 transition and the restriction point in pancreatic β-cells in vivo

Ga-68 DOTA-NOC Uptake in the Pancreas

Gastrin: a distinct fate of neurogenin3 positive progenitor cells in the embryonic pancreas

Gastrointestinal/pancreatic hormone concentrations in the portal venous system of nine patients with organic hyperinsulinism ⬇️

Gene-gene interactions lead to higher risk for development of type 2 diabetes in an Ashkenazi Jewish population

Genetic activation of α-cell glucokinase in mice causes enhanced glucose-suppression of glucagon secretion during normal and diabetic states

Genetic heterogeneity in familial hyperinsulinism.

Genetics of NIDDM in France: studies with 19 candidate genes in affected sib pairs

Genetics of neonatal hyperinsulinism.

Genome-wide survey reveals predisposing diabetes type 2-related DNA methylation variations in human peripheral blood

Germline Fumarate Hydratase Mutations in Families with Multiple Cutaneous and Uterine Leiomyomata

Germline fumarate hydratase mutations and evidence for a founder mutation underlying multiple cutaneous and uterine leiomyomata

Glucagonoma and the glucagonoma syndrome - cumulative experience with an elusive endocrine tumour.

Glucose metabolism: key endogenous regulator of β‐cell replication and survival ⬇️

Glucose regulates cyclin D2 expression in quiescent and replicating pancreatic β-cells through glycolysis and calcium channels

Glycosylated serum protein levels assayed with highly sensitive immunoradiometric assay accurately reflect glycemic control of diabetic patients

Growth hormone reserve in adult beta thalassemia patients

Growth-hormone-binding protein in patients with acromegaly

Hepatocyte nuclear factor 1alpha coding mutations are an uncommon contributor to early-onset type 2 diabetes in Ashkenazi Jews ⬇️

Hyperglycaemia induces metabolic dysfunction and glycogen accumulation in pancreatic β-cells

Hyperinsulinemic Hypoglycemia in Beckwith-Wiedemann Syndrome due to Defects in the Function of Pancreatic β-Cell Adenosine Triphosphate-Sensitive Potassium Channels

Hyperinsulinism caused by paternal-specific inheritance of a recessive mutation in the sulfonylurea-receptor gene

Hyperinsulinism of infancy: the regulated release of insulin by KATP channel-independent pathways.

IGF-1 levels may increase paradoxically with dopamine agonist treatment for prolactinomas

Identification of a G-Protein Subunit-α11 Gain-of-Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2)

Identification of a SIRT1 mutation in a family with type 1 diabetes

Identification of tissue-specific cell death using methylation patterns of circulating DNA

Impact of polymorphisms in WFS1 on prediabetic phenotypes in a population-based sample of middle-aged people with normal and abnormal glucose regulation

Induction of Long-Term Glycemic Control in Newly Diagnosed Type 2 Diabetic Patients by Transient Intensive Insulin Treatment

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population

Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population.

Insulin mutations in diabetes: the clinical spectrum

Insulin receptor alternative splicing is regulated by insulin signaling and modulates beta cell survival.

Intragenic single nucleotide polymorphism haplotype analysis of SUR1 mutations in familial hyperinsulinism

Isolation and characterization of the human AKT1 gene, identification of 13 single nucleotide polymorphisms (SNPs), and their lack of association with Type II diabetes.