1 - 25 of 214 results for author:"Hattersley A.T." in Literature citations
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| Mosaic PPM1D mutations are associated with predisposition to breast and ovarian cancer. Wellcome Trust Case Control Consortium Nature 493:406-410(2013) · Mapped (6) |
| GATA6 mutations cause a broad phenotypic spectrum of diabetes from pancreatic agenesis to adult-onset diabetes without exocrine insufficiency. International NDM Consortium Diabetes 62:993-997(2013) · Mapped (3) |
| Genome-wide association study for type 2 diabetes in Indians identifies a new susceptibility locus at 2q21. Tabassum R., Chauhan G., Dwivedi O.P., Mahajan A., Jaiswal A., Kaur I., Bandesh K., Singh T., Mathai B.J., Pandey Y. et al. Diabetes 62:977-986(2013) · Mapped (2) |
| A genome-wide association study identifies GRK5 and RASGRP1 as type 2 diabetes loci in Chinese Hans. DIAGRAM Consortium Diabetes 62:291-298(2013) · Mapped (10) |
| Paradoxical lower serum triglyceride levels and higher type 2 diabetes mellitus susceptibility in obese individuals with the PNPLA3 148M variant. Palmer C.N., Maglio C., Pirazzi C., Burza M.A., Adiels M., Burch L., Donnelly L.A., Colhoun H., Doney A.S., Dillon J.F. et al. PLoS ONE 7:e39362-e39362(2012) · Mapped (1) |
| SLC2A2 mutations can cause neonatal diabetes, suggesting GLUT2 may have a role in human insulin secretion. Sansbury F.H., Flanagan S.E., Houghton J.A., Shuixian Shen F.L., Al-Senani A.M., Habeb A.M., Abdullah M., Kariminejad A., Ellard S., Hattersley A.T. Diabetologia 55:2381-2385(2012) · Mapped (3) |
| Amino acid properties may be useful in predicting clinical outcome in patients with Kir6.2 neonatal diabetes. Fraser C.S., Rubio-Cabezas O., Littlechild J.A., Ellard S., Hattersley A.T., Flanagan S.E. Eur. J. Endocrinol. 167:417-421(2012) · Mapped (3) |
| A genome-wide association meta-analysis identifies new childhood obesity loci. Early Growth Genetics Consortium Nat. Genet. 44:526-531(2012) · Mapped (3) |
| The role of inflammatory pathway genetic variation on maternal metabolic phenotypes during pregnancy. Urbanek M., Hayes M.G., Lee H., Freathy R.M., Lowe L.P., Ackerman C., Jafari N., Dyer A.R., Cox N.J., Dunger D.B. et al. PLoS ONE 7:e32958-e32958(2012) · Mapped (15) |
| Recessive SLC19A2 mutations are a cause of neonatal diabetes mellitus in thiamine-responsive megaloblastic anaemia. Shaw-Smith C., Flanagan S.E., Patch A.M., Grulich-Henn J., Habeb A.M., Hussain K., Pomahacova R., Matyka K., Abdullah M., Hattersley A.T. et al. Pediatr Diabetes 13:314-321(2012) · Mapped (3) |
| GATA6 haploinsufficiency causes pancreatic agenesis in humans. Allen H.L., Flanagan S.E., Shaw-Smith C., De Franco E., Akerman I., Caswell R., Ferrer J., Hattersley A.T., Ellard S. |
| Heterozygous ABCC8 mutations are a cause of MODY. Bowman P., Flanagan S.E., Edghill E.L., Damhuis A., Shepherd M.H., Paisey R., Hattersley A.T., Ellard S. Diabetologia 55:123-127(2012) · Mapped (3) |
| KATP channel mutations in infants with permanent diabetes diagnosed after 6 months of life. Rubio-Cabezas O., Flanagan S.E., Damhuis A., Hattersley A.T., Ellard S. Pediatr Diabetes 13:322-325(2012) · Mapped (6) |
| The Lin28/let-7 axis regulates glucose metabolism. DIAGRAM Consortium Cell 147:81-94(2011) · Mapped (11) |
| Mutations of the same conserved glutamate residue in NBD2 of the sulfonylurea receptor 1 subunit of the KATP channel can result in either hyperinsulinism or neonatal diabetes. Mannikko R., Flanagan S.E., Sim X., Segal D., Hussain K., Ellard S., Hattersley A.T., Ashcroft F.M. Diabetes 60:1813-1822(2011) · Mapped (3) |
| The previously reported T342P GCK missense variant is not a pathogenic mutation causing MODY. Steele A.M., Tribble N.D., Caswell R., Wensley K.J., Hattersley A.T., Gloyn A.L., Ellard S. Diabetologia 54:2202-2205(2011) · UniProtKB (1) · Mapped (2) |
| Genetic variation at CHRNA5-CHRNA3-CHRNB4 interacts with smoking status to influence body mass index. Freathy R.M., Kazeem G.R., Morris R.W., Johnson P.C., Paternoster L., Ebrahim S., Hattersley A.T., Hill A., Hingorani A.D., Holst C. et al. Int J Epidemiol 40:1617-1628(2011) · Mapped (15) |
| Identification of an imprinted master trans regulator at the KLF14 locus related to multiple metabolic phenotypes. GIANT Consortium Nat. Genet. 43:561-564(2011) · Mapped (2) |
| A conserved tryptophan at the membrane-water interface acts as a gatekeeper for Kir6.2/SUR1 channels and causes neonatal diabetes when mutated. Mannikko R., Stansfeld P.J., Ashcroft A.S., Hattersley A.T., Sansom M.S., Ellard S., Ashcroft F.M. J. Physiol. (Lond.) 589:3071-3083(2011) · Mapped (6) |
| Permanent Neonatal Diabetes and Enteric Anendocrinosis Associated With Biallelic Mutations in NEUROG3. Rubio-Cabezas O., Jensen J.N., Hodgson M.I., Codner E., Ellard S., Serup P., Hattersley A.T. Diabetes 60:1349-1353(2011) · Mapped (2) |
| A meta-analysis of the associations between common variation in the PDE8B gene and thyroid hormone parameters, including assessment of longitudinal stability of associations over time and effect of thyroid hormone replacement. Taylor P.N., Panicker V., Sayers A., Shields B., Iqbal A., Bremner A.P., Beilby J.P., Leedman P.J., Hattersley A.T., Vaidya B. et al. Eur. J. Endocrinol. 164:773-780(2011) · Mapped (5) |
| Identification of ADAMTS7 as a novel locus for coronary atherosclerosis and association of ABO with myocardial infarction in the presence of coronary atherosclerosis: two genome-wide association studies. Myocardial Infarction Genetics Consortium Lancet 377:383-392(2011) · Mapped (5) |
| Novel GLIS3 mutations demonstrate an extended multisystem phenotype. Dimitri P., Warner J.T., Minton J.A., Patch A.M., Ellard S., Hattersley A.T., Barr S., Hawkes D., Wales J.K., Gregory J.W. Eur. J. Endocrinol. 164:437-443(2011) · UniProtKB (1) |
| Association analyses of 249,796 individuals reveal 18 new loci associated with body mass index. Procardis Consortium Nat. Genet. 42:937-948(2010) · Mapped (6) |
| Meta-analysis identifies 13 new loci associated with waist-hip ratio and reveals sexual dimorphism in the genetic basis of fat distribution. Heid I.M., Jackson A.U., Randall J.C., Winkler T.W., Qi L., Steinthorsdottir V., Thorleifsson G., Zillikens M.C., Speliotes E.K., Magi R. et al. Nat. Genet. 42:949-960(2010) · Mapped (57) |