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Human Genome Epidemiology Literature Finder|Home|PHGKB

Human Genome Epidemiology Literature Finder


Last data update: Jan 25, 2025. (Total: 235671Documents)
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Records 1 - 9 (of 9 Records)

Query Trace: Birth Weight and KCNJ11[original query]
Examination of type 2 diabetes loci implicates CDKAL1 as a birth weight gene.
Diabetes 2009 Jul .
Zhao J, Li M, Bradfield JP, Wang K, Zhang H, Sleiman P, Kim CE, Annaiah K, Glaberson W, Glessner JT, Otieno GF, Thomas KA, Garris M, Hou C, Frackelton EC, Chiavacci RM, Berkowitz RI, Hakonarson H, Grant SF
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
Frequency of the E23K polymorphism of the KCNJ11 gene in children born small for gestational age and its influence on auxological and metabolic parameters in the prepubertal period.
Journal of pediatric endocrinology & metabolism : JPEM 2013 26 (5-6): 457-62.
Stawerska Renata, Sza?apska Ma?gorzata, Borowiec Maciej, M?ynarski Wojciech, Antosik Karolina, Hilczer Maciej, Lewi?ski Andrz
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
Analysis of clinical and genetic characteristics of Chinese children with congenital hyperinsulinemia that is spontaneously relieved.
Endocrine 2021 1 72 (1): 116-123.
Xu Zi-di, Hui Pei-Pei, Zhang Wei, Zeng Qiao, Zhang Lin, Liu Min, Yan Jie, Wu Yu-Jun, Sang Yan-M
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