Human Genome Epidemiology Literature Finder
Records 1 - 7 (of 7 Records) |
Query Trace: Birth Weight and ABCC8[original query] |
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Anthropometry, carbohydrate and lipid metabolism in the East Flanders Prospective Twin Survey: linkage of candidate genes using two sib-pair based variance components analyses. Twin research and human genetics : the official journal of the International Society for Twin Studies 2008 Oct 11 (5): 505-16. Souren Nicole Y, Zeegers Maurice P, Janssen Rob G J H, Steyls Anja, Gielen Marij, Loos Ruth J F, Beunen Gaston, Fagard Robert, Stassen Alphons P M, Aerssens Jeroen, Derom Catherine, Vlietinck Robert, Paulussen Aimee D |
Diazoxide-responsive hyperinsulinemic hypoglycemia caused by HNF4A gene mutations. European journal of endocrinology / European Federation of Endocrine Societies 2010 May 162 (5): 987-92. Flanagan S E, Kapoor R R, Mali G, Cody D, Murphy N, Schwahn B, Siahanidou T, Banerjee I, Akcay T, Rubio-Cabezas O, Shield J P H, Hussain K, Ellard |
Clinical and molecular characterisation of hyperinsulinaemic hypoglycaemia in infants born small-for-gestational age. Archives of disease in childhood. Fetal and neonatal edition 2013 Jan . Arya VB, Flanagan SE, Kumaran A, Shield JP, Ellard S, Hussain K, Kapoor RR |
Clinical characteristics and phenotype-genotype analysis in Turkish patients with congenital hyperinsulinism; predominance of recessive KATP channel mutations. European journal of endocrinology / European Federation of Endocrine Societies 2014 Jun 170 (6): 885-92. Demirbilek Huseyin, Arya Ved Bhushan, Ozbek Mehmet Nuri, Akinci Aysehan, Dogan Murat, Demirel Fatma, Houghton Jayne, Kaba Sultan, Guzel Fatma, Baran Riza Taner, Unal Sevim, Tekkes Selahattin, Flanagan Sarah E, Ellard Sian, Hussain Khal |
ABCC8 R1420H Loss-of-Function Variant in a Southwest American Indian Community: Association With Increased Birth Weight and Doubled Risk of Type 2 Diabetes. Diabetes 2015 Aug . Baier Leslie J, Muller Yunhua Li, Remedi Maria Sara, Traurig Michael, Piaggi Paolo, Wiessner Gregory, Huang Ke, Stacy Alyssa, Kobes Sayuko, Krakoff Jonathan, Bennett Peter H, Nelson Robert G, Knowler William C, Hanson Robert L, Nichols Colin G, Bogardus Clift |
A homozygous mutation in the insulin gene (INS) causing autosomal recessive neonatal diabetes in Saudi families. Annals of pediatric endocrinology & metabolism 2020 4 25 (1): 42-45. Shaikh Adnan Al, Shirah Bader, Alzelaye Soma |
Birth weight and diazoxide unresponsiveness strongly predict the likelihood of congenital hyperinsulinism due to a mutation in ABCC8 or KCNJ11. European journal of endocrinology 2021 10 185 (6): 813-818. Hewat Thomas I, Yau Daphne, Jerome Joseph C S, Laver Thomas W, Houghton Jayne A L, Shields Beverley M, Flanagan Sarah E, Patel Kashyap |
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