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Genomes and GenesSpecies | Torben HansenSummaryAffiliation: University of Copenhagen Country: Denmark Publications
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Publications
Pancreatic beta-cell stimulation tests in transient and persistent congenital hyperinsulinismH B Christesen
Department of Paediatrics, Odense University Hospital, Denmark
Acta Paediatr 90:1116-20. 2001..In vivo beta-cell stimulation tests may contribute to the characterization of the HI subtypes...
The second activating glucokinase mutation (A456V): implications for glucose homeostasis and diabetes therapyHenrik B T Christesen
Department of Pediatrics, Odense University Hospital, Odense, Denmark
Diabetes 51:1240-6. 2002..Mathematical modeling predicted a markedly lowered GSIR threshold of 1.5 mmol/l. The theoretical and practical implications are manifold and significant...
A novel syndrome of autosomal-dominant hyperinsulinemic hypoglycemia linked to a mutation in the human insulin receptor geneKurt Højlund
Diabetes Research Centre, Department of Endocrinology, Odense University Hospital, Kloevervaenget 6, DK 5000, Odense C, Denmark
Diabetes 53:1592-8. 2004....
Association of polymorphisms of the CHI3L1 gene with asthma and atopy: a populations-based study of 6514 Danish adultsCamilla Noelle Rathcke
Department of Endocrinology, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark
PLoS ONE 4:e6106. 2009..The objective of the present study was to investigate the association of common variation in the CHI3L1 locus with asthma, atopy and lung function in a large population-based sample of adults...
High prevalence of type 2 diabetes and pre-diabetes in adult offspring of women with gestational diabetes mellitus or type 1 diabetes: the role of intrauterine hyperglycemiaTine D Clausen
Department of Obstetrics, Copenhagen Center for Pregnant Women with Diabetes, Copenhagen University Hospital, Rigshospitalet, Denmark
Diabetes Care 31:340-6. 2008..We studied glucose tolerance in adult offspring of women with either gestational diabetes mellitus (GDM) or type 1 diabetes, taking the impact of both intrauterine hyperglycemia and genetic predisposition to type 2 diabetes into account...
Genetic evidence that HNF-1alpha-dependent transcriptional control of HNF-4alpha is essential for human pancreatic beta cell functionSara K Hansen
Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Denmark
J Clin Invest 110:827-33. 2002..Furthermore, they indicate that this regulation is essential to maintain normal pancreatic function...
Variation in CHI3LI in relation to type 2 diabetes and related quantitative traitsCamilla Noelle Rathcke
Department of Endocrinology, Herlev Hospital, University of Copenhagen, Copenhagen, Denmark
PLoS ONE 4:e5469. 2009..The aim of the present study was to investigate the putative association between SNPs and haplotype blocks of CHI3LI and T2D and T2D related quantitative traits...
Overweight and the metabolic syndrome in adult offspring of women with diet-treated gestational diabetes mellitus or type 1 diabetesTine D Clausen
Center for Pregnant Women with Diabetes, Department of Obstetrics, Rigshospitalet, The Capital Region of Denmark, Faculty of Health Sciences, University of Copenhagen, 2100 Copenhagen, Denmark
J Clin Endocrinol Metab 94:2464-70. 2009..In animal studies, exposure to intrauterine hyperglycemia increases the risk of cardiovascular disease through only partly understood epigenetic mechanisms. Human long-term follow-up studies on the same topic are few...
Impact of two common polymorphisms in the PPARgamma gene on glucose tolerance and plasma insulin profiles in monozygotic and dizygotic twins: thrifty genotype, thrifty phenotype, or both?Pernille Poulsen
Department of Endocrinology, Odense University Hospital, Odense C, Denmark
Diabetes 52:194-8. 2003..Accordingly, our study simultaneously supports a role for both the intrauterine environment (thrifty phenotype) and for genetics (thrifty genotype) in the etiology of insulin resistance and perhaps glucose intolerance in twins...
Association testing of novel type 2 diabetes risk alleles in the JAZF1, CDC123/CAMK1D, TSPAN8, THADA, ADAMTS9, and NOTCH2 loci with insulin release, insulin sensitivity, and obesity in a population-based sample of 4,516 glucose-tolerant middle-aged DanesNiels Grarup
Steno Diabetes Center, Copenhagen, Denmark
Diabetes 57:2534-40. 2008....
Refining the impact of TCF7L2 gene variants on type 2 diabetes and adaptive evolutionAgnar Helgason
deCODE Genetics, 101 Reykjavik, Iceland
Nat Genet 39:218-25. 2007....
The HADHSC gene encoding short-chain L-3-hydroxyacyl-CoA dehydrogenase (SCHAD) and type 2 diabetes susceptibility: the DAMAGE studyEls C van Hove
Leiden University Medical Center, Department of Molecular Cell Biology, Building 2, Room R2 005, Postal Zone S1 P, P O Box 9600, 2300 RC Leiden, Netherlands
Diabetes 55:3193-6. 2006..We conclude that it is unlikely that variation in HADHSC plays a major role in the pathogenesis of type 2 diabetes in the examined cohorts...
Lens fluorescence in relation to glucose tolerance and genetic predisposition to type 2 diabetes mellitus in a population-based studyPernille Koefoed Theil
Department of Ophthalmology, Glostrup Hospital, University of Copenhagen, Denmark
Curr Eye Res 31:733-8. 2006..Fasting blood glucose measurement remains the method of choice for type 2 diabetes screening...
The -250G>A promoter variant in hepatic lipase associates with elevated fasting serum high-density lipoprotein cholesterol modulated by interaction with physical activity in a study of 16,156 Danish subjectsNiels Grarup
Steno Diabetes Center, Niels Steensens Vej 1, Gentofte, Denmark
J Clin Endocrinol Metab 93:2294-9. 2008..Hepatic lipase plays a pivotal role in the metabolism of high-density lipoprotein (HDL) and low-density lipoprotein by involvement in reverse cholesterol transport and the formation of atherogenic small dense low-density lipoprotein...
A novel -192c/g mutation in the proximal P2 promoter of the hepatocyte nuclear factor-4 alpha gene (HNF4A) associates with late-onset diabetesJakob Ek
Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Denmark
Diabetes 55:1869-73. 2006..In conclusion, a rare, novel mutation that disrupts a protein binding site in the pancreatic HNF4A promoter associates with late-onset diabetes...
A -30G>A polymorphism of the beta-cell-specific glucokinase promoter associates with hyperglycemia in the general population of whitesChristian S Rose
Steno Diabetes Center, DK 2820 Gentofte, Denmark
Diabetes 54:3026-31. 2005..17-2.24]). In conclusion, the GCK -30G>A polymorphism associates with elevated fasting and post-OGTT glycemia in the middle-aged general population of whites, as well as with IGR and other features of the WHO-defined metabolic syndrome...
Common variation in LMNA increases susceptibility to type 2 diabetes and associates with elevated fasting glycemia and estimates of body fat and height in the general population: studies of 7,495 Danish whitesLise Wegner
Steno Diabetes Center, Niels Steensens Vej 2, NSP1 03, DK 2820 Gentofte, Denmark
Diabetes 56:694-8. 2007....
Studies of association of variants near the HHEX, CDKN2A/B, and IGF2BP2 genes with type 2 diabetes and impaired insulin release in 10,705 Danish subjects: validation and extension of genome-wide association studiesNiels Grarup
Steno Diabetes Center, Niels Steensens Vej 1, NLC2 14, 2820 Gentofte, Denmark
Diabetes 56:3105-11. 2007..Furthermore, we aimed to characterize quantitative metabolic risk phenotypes of the four variants...
Two variants on chromosome 17 confer prostate cancer risk, and the one in TCF2 protects against type 2 diabetesJulius Gudmundsson
deCODE Genetics, Sturlugata 8, 101 Reykjavik, Iceland
Nat Genet 39:977-83. 2007..Results from eight case-control groups, including one West African and one Chinese, demonstrate that this variant confers protection against type 2 diabetes...
Polymorphisms in the 3' UTR in the neurocalcin delta gene affect mRNA stability, and confer susceptibility to diabetic nephropathyMasumi Kamiyama
Laboratory for Diabetic Nephropathy, SNP Research Centre, Institute of Physical and Chemical Research, 1 7 22 Suehiro cho, Tsurumi ku, Yokohama, Kanagawa 230 0045, Japan
Hum Genet 122:397-407. 2007..G, P = 0.03, odds ratio = 1.91, 95% CI 1.07-3.42). These results suggest that the NCALD gene is a likely candidate for conferring susceptibility to diabetic nephropathy...
Studies of association of the CASQ1 rs2275703 polymorphism in relation to type 2 diabetes and related quantitative metabolic traits among 7,088 Danish whitesThomas Sparsø
Steno Diabetes Center, Niels Steensens Vej 1, NLC2 13, DK 2820, Gentofte, Denmark
Mol Genet Metab 92:278-82. 2007....
A candidate type 2 diabetes polymorphism near the HHEX locus affects acute glucose-stimulated insulin release in European populations: results from the EUGENE2 studyHarald Staiger
Internal Medicine IV, Medical Clinic Tübingen, Otfried Muller Str 10, D 72076 Tubingen, Germany
Diabetes 57:514-7. 2008..Based on HHEX's function during embryonic development of the ventral pancreas in mice, we investigated whether these SNPs affect beta-cell function in humans...
Association of variants in the sterol regulatory element-binding factor 1 (SREBF1) gene with type 2 diabetes, glycemia, and insulin resistance: a study of 15,734 Danish subjectsNiels Grarup
Steno Diabetes Center, Copenhagen, Denmark
Diabetes 57:1136-42. 2008..Due to the previous inconclusive quantitative trait associations, we also did studies of intermediate quantitative phenotypes...
Single-nucleotide polymorphism rs7754840 of CDKAL1 is associated with impaired insulin secretion in nondiabetic offspring of type 2 diabetic subjects and in a large sample of men with normal glucose toleranceAlena Stancakova
Department of Medicine, University of Kuopio and University Hospital, 70210 Kuopio, Finland
J Clin Endocrinol Metab 93:1924-30. 2008..CDKAL1 is a recently discovered susceptibility gene for type 2 diabetes...
Seven mutations in the human insulin gene linked to permanent neonatal/infancy-onset diabetes mellitusCarlo Colombo
Laboratory of Molecular Endocrinology and Metabolism, Bambino Gesu Children s Hospital, Scientific Institute and Department of Internal Medicine, University of Tor Vergata, Rome, Italy
J Clin Invest 118:2148-56. 2008..Similarly transfected INS-1E insulinoma cells had diminished viability compared with those expressing WT proinsulin. In conclusion, we find that mutations in the insulin gene that promote proinsulin misfolding may cause PNDM...
A prevalent amino acid polymorphism at codon 98 (Ala98Val) of the hepatocyte nuclear factor-1alpha is associated with maturity-onset diabetes of the young and younger age at onset of type 2 diabetes in Asian IndiansShekher Anuradha
Dr Mohans MV Diabetes Specialties Centre and Madras Diabetes Research Foundation, Gopalapuram, Chennai, India
Diabetes Care 28:2430-5. 2005..The aim of this study was to estimate the prevalence of Ala98Val polymorphism of the HNF1alpha gene in different types of diabetes in Asian Indians...
Studies of variations of the cyclin-dependent kinase inhibitor 1C and the cyclin-dependent kinase 4 genes in relation to type 2 diabetes mellitus and related quantitative traitsEva Maria D Nielsen
Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Copenhagen, Denmark
J Mol Med (Berl) 83:353-61. 2005..02) and altered fasting plasma glucose (P=0.03). However, these later findings could not be replicated in additional studies. In conclusion, variants in CDKN1C may contribute to the inter-individual variation in birth weight...
Maturity-onset diabetes of the young with end-stage nephropathy: a new indication for simultaneous pancreas and kidney transplantation?Frantisek Saudek
Diabetes Center, Institute for Clinical and Experimental Medicine, Praha, Czech Republic
Transplantation 77:1298-301. 2004..A hyperglycemic clamp test showed a normal beta-cell function. CONCLUSION: Identification of MODY3 among all C-peptide-positive patients with advanced diabetic nephropathy might help to select a specific group profiting from SPK...
Increasing incidence of diabetes after gestational diabetes: a long-term follow-up in a Danish populationJeannet Lauenborg
Department of Obstetrics, Rigshospitalet, Copenhagen University Hospital, Copenhagen, Denmark
Diabetes Care 27:1194-9. 2004....
Type 2 diabetes mellitus--a multifactorial diseaseTorben Hansen
Steno Diabetes Center, Hagedorn Research Institute, Copenhagen, Denmark
Ann Univ Mariae Curie Sklodowska [Med] 57:544-9. 2002..Understanding of diabetes pathogenesis is essential to the development of new methods of treatment and strategies of effective prevention of this disease...
Evidence for an association between the Leu162Val polymorphism of the PPARalpha gene and decreased fasting serum triglyceride levels in glucose tolerant subjectsEva Maria D Nielsen
Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Copenhagen, Denmark
Pharmacogenetics 13:417-23. 2003..In conclusion, the Leu162Val polymorphism of PPARalpha is associated with a decreased level of fasting serum triglyceride in glucose tolerant white subjects...
A genome-wide scan in families with maturity-onset diabetes of the young: evidence for further genetic heterogeneityTimothy M Frayling
Department of Diabetes and Vascular Medicine, Postgraduate School of Medicine and Health Science, University of Exeter, Exeter, U.K
Diabetes 52:872-81. 2003..88 at 169-175 cM), and to chromosomes 3 (heterogeneity LOD [HLOD] score 1.27 at 124 cM) and 5 (HLOD score 1.22 at 175 cM) in 14 more strictly defined families. Our results provide evidence for further heterogeneity in MODY...
The E23K variant of Kir6.2 associates with impaired post-OGTT serum insulin response and increased risk of type 2 diabetesEva Maria D Nielsen
Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Copenhagen, Denmark
Diabetes 52:573-7. 2003..49, P = 0.00022). In conclusion, the widespread E23K polymorphism may have a diabetogenic effect by impairing glucose-induced insulin release and increasing BMI...
Mutational analysis of the UCP2 core promoter and relationships of variants with obesityLouise T Dalgaard
Steno Diabetes Center and Statens Serum Institute, 5 Artillerivej, Gentofte, DK 2300 Copenhagen, Denmark
Obes Res 11:1420-7. 2003..To identify polymorphisms in the human uncoupling protein 2 gene (UCP2) promoter and to investigate whether these were associated with obesity or weight gain...
Variants within the calpain-10 gene on chromosome 2q37 (NIDDM1) and relationships to type 2 diabetes, insulin resistance, and impaired acute insulin secretion among Scandinavian CaucasiansSøren K Rasmussen
Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Denmark
Diabetes 51:3561-7. 2002....
The functional Thr130Ile and Val255Met polymorphisms of the hepatocyte nuclear factor-4alpha (HNF4A): gene associations with type 2 diabetes or altered beta-cell function among DanesJakob Ek
Steno Diabetes Center and Hagedorn Research Institute, Niels Steensens Vej 6, NSK1 14, DK 2820 Gentofte, Denmark
J Clin Endocrinol Metab 90:3054-9. 2005....
[Chasing the genetic determinants of the presumed polygenic forms of type 2 diabetes. Status and perspectives]Oluf Borbye Pedersen
Steno Diabetes Center, Niels Steensens Vej 2, DK-2820 Gentofte
Ugeskr Laeger 164:2163-6. 2002
Characterization of the Met326Ile variant of phosphatidylinositol 3-kinase p85alphaKatrine Almind
Research Division, Joslin Diabetes Center and Department of Medicine, Harvard Medical School, Boston, MA 02215, USA
Proc Natl Acad Sci U S A 99:2124-8. 2002..Thus, the Met-326Ile variant of p85alpha is functional for intracellular signaling and adipocyte differentiation but has small alterations in protein expression and activity that could play a role in modifying insulin action...
PGC-1alpha Gly482Ser polymorphism associates with hypertension among Danish whitesGitte Andersen
Steno Diabetes Center, Niels Steensens Vej 2, NSH2 16, DK 2820 Gentofte, Denmark
Hypertension 45:565-70. 2005..001). In conclusion, the Ser allele of PGC-1alpha Gly482Ser confers a significantly reduced risk of hypertension in whites. Further studies are needed to elucidate the differential role of this polymorphism in men and women...
[Maturity-onset diabetes of the young--MODY. Molecular-genetic, pathophysiological and clinical characteristics]Torben Hansen
Steno Diabetes Center, Niels Steensens Vej 2, DK-2820 Gentofte
Ugeskr Laeger 164:2017-22. 2002..The identification of MODY genes also opens new perspectives in the understanding of the molecular basis of diabetes and may probably contribute to the definition of novel targets for drug development and gene therapy...
Role of transcription factor KLF11 and its diabetes-associated gene variants in pancreatic beta cell functionBernadette Neve
Centre National de la Recherche Scientifique, Unité Mixte de Recherche 8090, Institute Pasteur de Lille, F 59019 Lille, France
Proc Natl Acad Sci U S A 102:4807-12. 2005..Thus, both functional and genetic analyses reveal that KLF11 plays a role in the regulation of pancreatic beta cell physiology, and its variants may contribute to the development of diabetes...
The BIGTT test: a novel test for simultaneous measurement of pancreatic beta-cell function, insulin sensitivity, and glucose toleranceTorben Hansen
Steno Diabetes Center, Niels Steensens Vej 2, DK 2820 Gentofte, Denmark
Diabetes Care 30:257-62. 2007....
Low physical activity accentuates the effect of the FTO rs9939609 polymorphism on body fat accumulationCamilla H Andreasen
Steno Diabetes Center, Niels Steensens Vej 1, NLC2 13, DK 2820 Gentofte, Denmark
Diabetes 57:95-101. 2008..In the present study, the effect of FTO variation on metabolic traits including obesity, type 2 diabetes, and related quantitative phenotypes was examined...
The same sequence variant on 9p21 associates with myocardial infarction, abdominal aortic aneurysm and intracranial aneurysmAnna Helgadottir
deCODE Genetics, Sturlugata 8, IS 101 Reykjavik, Iceland
Nat Genet 40:217-24. 2008..These findings extend our insight into the role of the sequence variant tagged by rs10757278-G and show that it is not confined to atherosclerotic diseases...
The KCNMB1 Glu65Lys polymorphism associates with reduced systolic and diastolic blood pressure in the Inter99 study of 5729 DanesTrine Nielsen
Steno Diabetes Center, Gentofte, Denmark
J Hypertens 26:2142-6. 2008..The previous studies have, however, been conflicting, and the aim of the present study was to clarify the impact of the Glu65Lys polymorphism on hypertension at the population level of middle-aged people...
AHSG tag single nucleotide polymorphisms associate with type 2 diabetes and dyslipidemia: studies of metabolic traits in 7,683 white Danish subjectsGitte Andersen
Steno Diabetes Center, Niels Steensens Vej 1, NLC2 12, DK 2820 Gentofte, Denmark
Diabetes 57:1427-32. 2008..We related seven frequent AHSG tag single nucleotide polymorphisms to a range of metabolic traits, including type 2 diabetes, obesity, and dyslipidemia...
Association of the calpain-10 gene with type 2 diabetes in Europeans: results of pooled and meta-analysesTakafumi Tsuchiya
Departments of Medicine and Human Genetics, The University of Chicago, 5841 S Maryland Ave, MC1027, Chicago, IL 60637, USA
Mol Genet Metab 89:174-84. 2006..68 (1.33-2.11), P=0.00001). The pooled and meta-analyses as well as the linkage disequilibrium and haplotype diversity studies suggest a role for genetic variation in CAPN10 affecting risk of T2D in Europeans...
[Genetics in non-autoimmune diabetes. The Danish Society of Endocrinology]Torben Hansen
Steno Diabetes Center, DK-2820 Gentofte
Ugeskr Laeger 170:1021. 2008
Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetesEleftheria Zeggini
Wellcome Trust Centre for Human Genetics, University of Oxford, Oxford, UK
Nat Genet 40:638-45. 2008..1 x 10(-9)), ADAMTS9 (P = 1.2 x 10(-8)) and NOTCH2 (P = 4.1 x 10(-8)) gene regions. Our results illustrate the value of large discovery and follow-up samples for gaining further insights into the inherited basis of T2D...
Genetic variation of the GLUT10 glucose transporter (SLC2A10) and relationships to type 2 diabetes and intermediary traitsGitte Andersen
Steno Diabetes Center and Hagedorn Research Institute, Gentofte, Denmark
Diabetes 52:2445-8. 2003..However, the codon 206 polymorphism may be related to the interindividual variation in fasting and oral glucose-induced serum insulin levels...
Evidence that the mitochondrial leucyl tRNA synthetase (LARS2) gene represents a novel type 2 diabetes susceptibility geneLeen M 't Hart
Leiden University Medical Center, Department of Molecular Cell Biology, Wassenaarseweg 72, 2333 AL Leiden, Netherlands
Diabetes 54:1892-5. 2005..This is the first report of association between an aminoacyl tRNA synthetase gene and disease. Our results further highlight the important role of mitochondria in glucose homeostasis...
Novel variants in the putative peroxisome proliferator-activated receptor {gamma} promoter and relationships with obesity in menThomas M Larsen
Department of Human Nutrition, LMC Royal Veterinary and Agricultural University, Rolighedsvej 30, 1958 Frederiksberg C, Denmark
Obes Res 13:953-8. 2005..In conclusion, the identified novel variants in the PPARgamma2 promoter region do not explain the reported discrepancies in the association of previously identified variants with obesity and type 2 diabetes...
Evidence of an association between the Arg72 allele of the peptide YY and increased risk of type 2 diabetesSigne S Torekov
Steno Diabetes Center, Niels Steensens Vej 2, DK 2820, Gentofte, Denmark
Diabetes 54:2261-5. 2005..03), and a lower insulinogenic index (P = 0.01). In conclusion, the common Arg allele of the PYY Arg72Thr variant modestly associates with type 2 diabetes and with type 2 diabetes-related quantitative traits...
Analysis of separate and combined effects of common variation in KCNJ11 and PPARG on risk of type 2 diabetesSara K Hansen
Steno Diabetes Center and Hagedorn Research Institute, Niels Steensens Vej 2, DK 2820 Gentofte, Denmark
J Clin Endocrinol Metab 90:3629-37. 2005..In conclusion, our results showed no evidence of a synergistic interaction between the KCNJ11 Glu(23)Lys and PPARG Pro(12)Ala polymorphisms, but indicated that they may act in an additive manner to increase the risk of type 2 diabetes...
Variation in CAPN10 in relation to type 2 diabetes, obesity and quantitative metabolic traits: studies in 6018 whitesDorit P Jensen
Steno Diabetes Center, Niels Steensens Vej 2, DK 2820 Gentofte, Copenhagen, Denmark
Mol Genet Metab 89:360-7. 2006....
Grey-box modelling of pharmacokinetic/pharmacodynamic systemsChristoffer W Tornøe
Informatics and Mathematical Modelling, Technical University of Denmark, Lyngby, Denmark
J Pharmacokinet Pharmacodyn 31:401-17. 2004....
Studies of the common DIO2 Thr92Ala polymorphism and metabolic phenotypes in 7342 Danish white subjectsNiels Grarup
Steno Diabetes Center, Niels Steensens Vej 2, 2820 Gentofte, Denmark
J Clin Endocrinol Metab 92:363-6. 2007..A Thr92Ala polymorphism in the gene encoding D2 (DIO2) has been reported to associate with insulin resistance...
Relationships between the functional PPARalpha Leu162Val polymorphism and obesity, type 2 diabetes, dyslipidaemia, and related quantitative traits in studies of 5799 middle-aged white peopleThomas Sparsø
Steno Diabetes Center, 521, Niels Steensens Vej 2, 2820 Gentofte, Denmark
Mol Genet Metab 90:205-9. 2007..If replicated, the Val162Val variant may, however, confer an increase in fasting levels of serum lipids...
Variation in the interleukin-6 receptor gene associates with type 2 diabetes in Danish whitesYasmin H Hamid
Steno Diabetes Center, Hagedorn Research Institute, Gentofte, Copenhagen, Denmark
Diabetes 53:3342-5. 2004..In conclusion, the Asp358Ala polymorphism of the IL6R associates with type 2 diabetes in Danish whites...
The functional Pro129Thr variant of the FAAH gene is not associated with various fat accumulation phenotypes in a population-based cohort of 5,801 whitesDorit P Jensen
Steno Diabetes Center, Niels Steensens Vej 2, 2820, Gentofte, Denmark
J Mol Med (Berl) 85:445-9. 2007..In conclusion, in a large study sample, we were unable to find robust evidence of an association of the Pro129Thr FAAH variant with overweight, obesity, and any related quantitative traits among the examined whites...
Mutation analysis of the preproghrelin gene: no association with obesity and type 2 diabetesLesli H Larsen
Steno Diabetes Center and Hagedorn Research Institute, Copenhagen, Denmark
Clin Biochem 38:420-4. 2005..To investigate the preproghrelin gene for variants and their association with obesity and type 2 diabetes...
Variation in NCB5OR: studies of relationships to type 2 diabetes, maturity-onset diabetes of the young, and gestational diabetes mellitusGitte Andersen
Steno Diabetes Center and Hagedorn Research Institute, Niels Steensens Vej 2, NSH2 16, DK 2820 Gentofte, Denmark
Diabetes 53:2992-7. 2004..Thus, variation in the coding region of NCB5OR is not a major contributor in the pathogenesis of nonautoimmune diabetes...
A variant in CDKAL1 influences insulin response and risk of type 2 diabetesValgerdur Steinthorsdottir
deCODE Genetics, Sturlugata 8, 101 Reykjavik, Iceland
Nat Genet 39:770-5. 2007..The insulin response for homozygotes was approximately 20% lower than for heterozygotes or noncarriers, suggesting that this variant confers risk of T2D through reduced insulin secretion...
A common haplotype in the G-protein-coupled receptor gene GPR74 is associated with leanness and increased lipolysisIngrid Dahlman
Department of Medicine, Karolinska University Hospital, Huddinge, Stockholm, Sweden
Am J Hum Genet 80:1115-24. 2007..The latter involves a cross-talk between GPR74 and beta -adrenoceptor signaling to lipolysis in fat cells...
Melanocortin 4 receptor mutations in obese Czech children: studies of prevalence, phenotype development, weight reduction response, and functional analysisIrena Hainerova
Department of Pediatrics and Center for Research of Diabetes, Metabolism, and Nutrition, Third Faculty of Medicine, Charles University, 100 34 Prague 10, Czech Republic
J Clin Endocrinol Metab 92:3689-96. 2007..Mutations in the melanocortin 4 receptor gene (MC4R) represent the most common known cause of monogenic human obesity...
A P387L variant in protein tyrosine phosphatase-1B (PTP-1B) is associated with type 2 diabetes and impaired serine phosphorylation of PTP-1B in vitroSøren M Echwald
Steno Diabetes Center and Hagedorn Research Institute, Copenhagen, Denmark
Diabetes 51:1-6. 2002..7 (CI 1.26-10.93, P = 0.02) genotype relative risk of type 2 diabetes in the examined population of Danish Caucasian subjects and results in impaired in vitro serine phosphorylation of the PTP-1B peptide...
