sameAs
P184
Genome-wide association scan meta-analysis identifies three Loci influencing adiposity and fat distributionIntegrated genetic and epigenetic analysis identifies haplotype-specific methylation in the FTO type 2 diabetes and obesity susceptibility locusGenetic studies of body mass index yield new insights for obesity biologyEvidence for haploinsufficiency of the human HNF1alpha gene revealed by functional characterization of MODY3-associated mutationsAn in-frame deletion at the polymerase active site of POLD1 causes a multisystem disorder with lipodystrophyRfx6 directs islet formation and insulin production in mice and humansGenetic variations in the gene encoding TFAP2B are associated with type 2 diabetes mellitusHypomethylation of multiple imprinted loci in individuals with transient neonatal diabetes is associated with mutations in ZFP57Mutations in PTF1A cause pancreatic and cerebellar agenesisInsights into the biochemical and genetic basis of glucokinase activation from naturally occurring hypoglycemia mutationsMolecular basis of Kir6.2 mutations associated with neonatal diabetes or neonatal diabetes plus neurological featurestRNA methyltransferase homolog gene TRMT10A mutation in young onset diabetes and primary microcephaly in humansA common variant of HMGA2 is associated with adult and childhood height in the general populationTwelve type 2 diabetes susceptibility loci identified through large-scale association analysisCommon variation in the FTO gene alters diabetes-related metabolic traits to the extent expected given its effect on BMIGenome-wide association study of CNVs in 16,000 cases of eight common diseases and 3,000 shared controlsHundreds of variants clustered in genomic loci and biological pathways affect human heightCommon variants near MC4R are associated with fat mass, weight and risk of obesitySix new loci associated with body mass index highlight a neuronal influence on body weight regulationAssociation scan of 14,500 nonsynonymous SNPs in four diseases identifies autoimmunity variantsA common variant in the FTO gene is associated with body mass index and predisposes to childhood and adult obesityA mutation (R826W) in nucleotide-binding domain 1 of ABCC8 reduces ATPase activity and causes transient neonatal diabetesGenetic variants in Apolipoprotein AV alter triglyceride concentrations in pregnancyA heterozygous activating mutation in the sulphonylurea receptor SUR1 (ABCC8) causes neonatal diabetes.Permanent neonatal diabetes caused by dominant, recessive, or compound heterozygous SUR1 mutations with opposite functional effects.Regulation of apolipoprotein M gene expression by MODY3 gene hepatocyte nuclear factor-1alpha: haploinsufficiency is associated with reduced serum apolipoprotein M levelsGenetic cause of hyperglycaemia and response to treatment in diabetesPremature birth and low birth weight associated with nonautoimmune hyperthyroidism due to an activating thyrotropin receptor gene mutationNew genetic loci implicated in fasting glucose homeostasis and their impact on type 2 diabetes riskLarge-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetesThe fat mass- and obesity-associated locus and dietary intake in childrenMacrosomia and hyperinsulinaemic hypoglycaemia in patients with heterozygous mutations in the HNF4A geneLower Circulating B12 Is Associated with Higher Obesity and Insulin Resistance during Pregnancy in a Non-Diabetic White British PopulationCan clinical features be used to differentiate type 1 from type 2 diabetes? A systematic review of the literatureLow-frequency and rare exome chip variants associate with fasting glucose and type 2 diabetes susceptibilityUrine C-peptide creatinine ratio can be used to assess insulin resistance and insulin production in people without diabetes: an observational studyReplication of genome-wide association signals in UK samples reveals risk loci for type 2 diabetesThe role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancyA genome-wide association search for type 2 diabetes genes in African AmericansLinkage disequilibrium mapping of the replicated type 2 diabetes linkage signal on chromosome 1q
P50
Q21092459-3A0967E8-0706-43F1-A039-F85E7C5CF977Q21136048-EC3AB612-4D9A-4FBB-80AA-0BBA66D0B8D1Q22305005-DE6E8F5B-56AB-486B-A200-675A554781D3Q24292735-C33BF224-A85A-496A-9E52-C43FDAFA0FCAQ24295141-F20743AC-256F-4B43-897F-C5E27F50186EQ24298978-B7094020-564A-44A1-81C6-43E8180A6788Q24304627-DCFAEDD5-F29F-4E67-9CE8-FC70C035D741Q24312925-977B3162-C51B-4777-91BC-0CDFCF1A0DB0Q24314872-D888B457-B925-46CB-9BEE-0FFFDA542351Q24318505-2100D44F-4C42-4A8F-A96C-D2AA26F4A61DQ24320031-48D52FDD-C054-499E-80E1-5557B1CBCFE7Q24339464-34C7887D-9594-4591-8E0E-30E7F370A06EQ24603211-BD54BC11-563B-4A06-A274-422C96C10023Q24609915-3DB2A520-98CC-4467-AA17-8F453381F9B6Q24621500-21B3F008-3DB3-4A88-B8AB-B2814BD68726Q24628710-FB2AC70E-0616-49F7-968B-2D61C071C6CBQ24630979-E6348B3C-ED45-4DF9-9577-2F3A34216706Q24641880-FF33AEA6-8628-4E88-85B5-7CA2EF4873E5Q24646434-4F2CBF0A-9483-4FA3-8DF0-597DD9BF4730Q24646663-D2D7DDBB-4372-4999-B808-726B8165EFF8Q24650037-1C0664BB-9721-4937-B1E8-32ADAFAD1E99Q24656945-CB8D2361-29CC-48D3-AD5D-67671A1883A1Q24797224-E92302A8-47EC-4CF3-9D44-D75EFAD9A204Q27863920-08B51A80-573A-4961-80F6-464CF553E606Q27865195-68B3B13A-DCD6-40B5-A4E7-AD4952E57D53Q28186484-478D3C83-71AE-4E48-A91A-60BB5D8F556AQ28212185-589833E5-F9B8-42A7-8E7D-B787D8B5B85DQ28263474-D4FB3165-8CEE-4753-9487-C3845473C353Q28270700-D0681E8D-55B2-4682-9DB2-2E400D96D5F7Q28272915-27BF409A-30F1-462E-AB45-463A5407EF39Q28296347-B4B6252C-F45C-444E-A136-AFEB8895E4ECQ28469173-6E58B130-8027-4052-B4B5-A0982B9D5EDCQ28547361-3BE2D9F1-6DED-4070-937A-9108E3D66974Q28607704-A36DFE01-83C7-47FC-81E3-C9BB7CD009B0Q28651068-49363079-0779-40CF-AC59-CEADA2A16A2AQ28660810-BD7F6747-FE64-475B-AE5A-4AB32F1B11C5Q28680760-261C2E1B-A79C-4B72-9F1D-C696C106CF22Q28730838-B67629B7-DA91-4079-B020-74AC36384AAFQ28740367-86593371-EE23-4C05-99FB-1467689D798FQ28752440-F2B92AC2-A77D-4CDE-86F5-170E756F8A6F
P50
description
Professor of Molecular Medicine at the University of Exeter
@en
onderzoeker
@nl
հետազոտող
@hy
name
Andrew Tym Hattersley
@af
Andrew Tym Hattersley
@an
Andrew Tym Hattersley
@ast
Andrew Tym Hattersley
@ay
Andrew Tym Hattersley
@az
Andrew Tym Hattersley
@br
Andrew Tym Hattersley
@ca
Andrew Tym Hattersley
@ce
Andrew Tym Hattersley
@ceb
Andrew Tym Hattersley
@co
type
label
Andrew Tym Hattersley
@af
Andrew Tym Hattersley
@an
Andrew Tym Hattersley
@ast
Andrew Tym Hattersley
@ay
Andrew Tym Hattersley
@az
Andrew Tym Hattersley
@br
Andrew Tym Hattersley
@ca
Andrew Tym Hattersley
@ce
Andrew Tym Hattersley
@ceb
Andrew Tym Hattersley
@co
altLabel
A T Hattersley
@en
Andrew Hattersley
@af
Andrew Hattersley
@an
Andrew Hattersley
@ast
Andrew Hattersley
@ay
Andrew Hattersley
@az
Andrew Hattersley
@br
Andrew Hattersley
@ca
Andrew Hattersley
@ce
Andrew Hattersley
@ceb
prefLabel
Andrew Tym Hattersley
@af
Andrew Tym Hattersley
@an
Andrew Tym Hattersley
@ast
Andrew Tym Hattersley
@ay
Andrew Tym Hattersley
@az
Andrew Tym Hattersley
@br
Andrew Tym Hattersley
@ca
Andrew Tym Hattersley
@ce
Andrew Tym Hattersley
@ceb
Andrew Tym Hattersley
@co
P166
P106
P1153
7102760992
P185
P2070
andrew-hattersley-11591
P21
P31
P463
P496
0000-0001-5620-473X
P569
1958-01-01T00:00:00Z