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Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry

Diabetologia, 2013-07, Vol.56 (7), p.1512-1519

2013

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Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development

Journal of medical genetics, 2011-12, Vol.48 (12), p.825-830

2011

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Single-base insertions in the VNTR of the carboxyl ester lipase gene Ц A role in pancreatic disease?

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2022-11, Vol.22, p.e47-e47

2022

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Lack of pancreatic body and tail in HNF1B mutation carriers

Diabetic medicine, 2008-07, Vol.25 (7), p.782-787

2008

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New insights into the role of CEL-HYB in chronic pancreatitis: Protein aggregation and ER stress

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2020-11, Vol.20, p.S60-S60

2020

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To test, or not to test: time for a MODY calculator?

Diabetologia, 2012-05, Vol.55 (5), p.1231-1234

2012

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The genetic risk factor CEL-HYB causes chronic pancreatitis in mice

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2021-07, Vol.21, p.S9-S9

2021

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The CEL-MODY mouse: A new genetic model for chronic pancreatitis

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2020-11, Vol.20, p.S24-S25

2020

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Independent mutational events in the hypervariable region of the carboxyl ester lipase gene: Identification of two new CEL-MODY families from Sweden and the Czech Republic

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2020-11, Vol.20, p.S100-S101

2020

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The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes

Diabetes research and clinical practice, 2017-11, Vol.133, p.142-149

2017

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Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study)

Diabetologia, 2008-06, Vol.51 (6), p.971-977

2008

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Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young (HNF1B-MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas

Diabetic medicine, 2013-08, Vol.30 (8), p.946-955

2013

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Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study)

Diabetic medicine, 2008-07, Vol.25 (7), p.775-781

2008

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Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder

Molecular psychiatry, 2004-06, Vol.9 (6), p.621-629

2004

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The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy

Clinical genetics, 2009-05, Vol.75 (5), p.440-448

2009

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Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Nature communications, 2018-11, Vol.9 (1), p.4774-10, Article 4774

2018

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Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene

FEBS letters, 1996-08, Vol.392 (1), p.30-34

1996

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A frame-shift mutation in the carboxyl-ester lipase gene alters the intracellular localization of the CEL protein

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2012-11, Vol.12 (6), p.540-541

2012

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Wolcott–Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome

Journal of inherited metabolic disease, 2008-12, Vol.31 (Suppl 2), p.293-297

2008

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Copy number variants of the carboxyl ester lipase gene in pancreatic disease

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2012-11, Vol.12 (6), p.549-549

2012

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Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases

The journal of clinical endocrinology and metabolism, 2022-04, Vol.107 (4), p.e1455-e1466

2022

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Lymphomas diagnosed in Uganda during the HIV/AIDS pandemic

East African medical journal, 2009-05, Vol.86 (5), p.226-232

2009

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Secretin-stimulated duodenal markers associated with increased risk for pancreatic ductal adenocarcinoma

Pancreatology : official journal of the International Association of Pancreatology (IAP) ... [et al.], 2012-11, Vol.12 (6), p.551-551

2012

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A human myo-inositol monophosphatase gene (IMPA2) localized in a putative susceptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patients

Molecular psychiatry, 2000-03, Vol.5 (2), p.172-180

2000

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Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

Nature genetics, 2006-01, Vol.38 (1), p.54-62

2006

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Prevalence of monogenic diabetes in the population-based Norwegian Childhood Diabetes Registry

Disruption of a long distance regulatory region upstream of SOX9 in isolated disorders of sex development

Single-base insertions in the VNTR of the carboxyl ester lipase gene Ц A role in pancreatic disease?

Lack of pancreatic body and tail in HNF1B mutation carriers

New insights into the role of CEL-HYB in chronic pancreatitis: Protein aggregation and ER stress

To test, or not to test: time for a MODY calculator?

The genetic risk factor CEL-HYB causes chronic pancreatitis in mice

The CEL-MODY mouse: A new genetic model for chronic pancreatitis

Independent mutational events in the hypervariable region of the carboxyl ester lipase gene: Identification of two new CEL-MODY families from Sweden and the Czech Republic

The HNF1A mutant Ala180Val: Clinical challenges in determining causality of a rare HNF1A variant in familial diabetes

Genetic analysis of recently identified type 2 diabetes loci in 1,638 unselected patients with type 2 diabetes and 1,858 control participants from a Norwegian population-based cohort (the HUNT study)

Exocrine pancreatic function in hepatocyte nuclear factor 1β-maturity-onset diabetes of the young (HNF1B-MODY) is only moderately reduced: compensatory hypersecretion from a hypoplastic pancreas

Prevalence of HNF1A (MODY3) mutations in a Norwegian population (the HUNT2 Study)

Examination of IMPA1 and IMPA2 genes in manic-depressive patients: association between IMPA2 promoter polymorphisms and bipolar disorder

The spectrum of ABCC8 mutations in Norwegian patients with congenital hyperinsulinism of infancy

Novel pleiotropic risk loci for melanoma and nevus density implicate multiple biological pathways

Ultrarapid metabolizers of debrisoquine: Characterization and PCR-based detection of alleles with duplication of the CYP2D6 gene

A frame-shift mutation in the carboxyl-ester lipase gene alters the intracellular localization of the CEL protein

Wolcott–Rallison syndrome with 3-hydroxydicarboxylic aciduria and lethal outcome

Copy number variants of the carboxyl ester lipase gene in pancreatic disease

Two New Mutations in the CEL Gene Causing Diabetes and Hereditary Pancreatitis: How to Correctly Identify MODY8 Cases

Lymphomas diagnosed in Uganda during the HIV/AIDS pandemic

Secretin-stimulated duodenal markers associated with increased risk for pancreatic ductal adenocarcinoma

A human myo-inositol monophosphatase gene (IMPA2) localized in a putative susceptibility region for bipolar disorder on chromosome 18p11.2: genomic structure and polymorphism screening in manic-depressive patients

Mutations in the CEL VNTR cause a syndrome of diabetes and pancreatic exocrine dysfunction

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