Skip directly to search Skip directly to A to Z list Skip directly to navigation Skip directly to page options Skip directly to site content

Public Health Genomics and Precision Health Knowledge Base (v6.2)

Note: Javascript is disabled or is not supported by your browser. For this reason, some items on this page will be unavailable. For more information about this message, please visit this page: About CDC.gov.

HuGE Navigator|HuGE Literature Finder|PHGKB

HuGE Literature Finder

Records 1-12

Query Trace: HADH[orginal query]

Analysis on the pathogenic genes of 60 Chinese children with congenital hyperinsulinemia. Endocrine connections 2018 11 7 (12): 1251-1261. Xu Zi-Di, Zhang Wei, Liu Min, Wang Huan-Min, Hui Pei-Pei, Liang Xue-Jun, Yan Jie, Wu Yu-Jun, Sang Yan-Mei, Zhu Cheng, Ni Gui-Ch Similar articles in PubMed
Genome-scale identification of microRNA-related SNPs associated with risk of head and neck squamous cell carcinoma. Carcinogenesis 2017 Jun . Wilkins Owen M, Titus Alexander J, Gui Jiang, Eliot Melissa, Butler Rondi A, Sturgis Erich M, Li Guojun, Kelsey Karl T, Christensen Brock Similar articles in PubMed
Possible involvement of ACSS2 gene in alcoholism. Journal of neural transmission (Vienna, Austria : 1996) 2017 09 124 (9): 1151-1158. Ribeiro Andrea Frozino, de Lacerda Roseli Boerngen, Correia Diego, Brunialti-Godard Ana Lúcia, de Miranda Débora Marques, Campos Valdir Ribeiro, de Souza Valéria Fernandes, Ribeiro Angela Mar Similar articles in PubMed
Clinical, genetic characteristics, management and long-term follow up of Turkish patients with congenital hyperinsulinism. Journal of clinical research in pediatric endocrinology 2015 Dec . Güven Ayla, Cebeci Ay?e Nurcan, Ellard Sian, Flanagan Sarah Similar articles in PubMed
Uncovering the molecular pathogenesis of congenital hyperinsulinism by panel gene sequencing in 32 Chinese patients. Molecular genetics & genomic medicine 2015 Nov 3 (6): 526-36. Fan Zi-Chuan, Ni Jin-Wen, Yang Lin, Hu Li-Yuan, Ma Si-Min, Mei Mei, Sun Bi-Jun, Wang Hui-Jun, Zhou Wen-H Similar articles in PubMed
High incidence of heterozygous ABCC8 and HNF1A mutations in Czech patients with congenital hyperinsulinism. The Journal of clinical endocrinology and metabolism 2015 Oct jc20152763. Rozenkova Klara, Malikova Jana, Nessa Azizun, Dusatkova Lenka, Bjørkhaug Lise, Obermannova Barbora, Dusatkova Petra, Kytnarova Jitka, Aukrust Ingvild, Najmi Laeya, Rypackova Blanka, Sumnik Zdenek, Lebl Jan, Njølstad Pål R, Hussain Khalid, Pruhova Stepan Similar articles in PubMed
Clinical and Molecular Characterisation of 300 patients with Congenital Hyperinsulinism. European journal of endocrinology / European Federation of Endocrine Societies 2013 Jan . Kapoor RR, Flanagan SE, Arya VB, Shield JP, Ellard S, Hussain K Similar articles in PubMed
Next-generation sequencing reveals deep intronic cryptic ABCC8 and HADH splicing founder mutations causing hyperinsulinism by pseudoexon activation. American journal of human genetics 2013 Jan 92 (1): 131-6. Flanagan Sarah E, Xie Weijia, Caswell Richard, Damhuis Annet, Vianey-Saban Christine, Akcay Teoman, Darendeliler Feyza, Bas Firdevs, Guven Ayla, Siklar Zeynep, Ocal Gonul, Berberoglu Merih, Murphy Nuala, O'Sullivan Maureen, Green Andrew, Clayton Peter E, Banerjee Indraneel, Clayton Peter T, Hussain Khalid, Weedon Michael N, Ellard Si Similar articles in PubMed
Genotype and Phenotype Correlations in 417 Children With Congenital Hyperinsulinism. The Journal of clinical endocrinology and metabolism 2012 Dec . Snider KE, Becker S, Boyajian L, Shyng SL, Macmullen C, Hughes N, Ganapathy K, Bhatti T, Stanley CA, Ganguly A Similar articles in PubMed
A systematic gene-based screen of chr4q22-q32 identifies association of a novel susceptibility gene, DKK2, with the quantitative trait of alcohol dependence symptom counts. Human molecular genetics 2010 Jun 19 (12): 2497-506. Kalsi Gursharan, Kuo Po-Hsiu, Aliev Fazil, Alexander Jeffry, McMichael Omari, Patterson Diana G, Walsh Dermot, Zhao Zhongming, Schuckit Marc, Nurnberger John, Edenberg Howard, Kramer John, Hesselbrock Victor, Tischfield Jay A, Vladimirov Vladimir, Prescott Carol A, Dick Danielle M, Kendler Kenneth S, Riley Brien Similar articles in PubMed
Genetic variants in nuclear-encoded mitochondrial genes influence AIDS progression. PloS one 2010 5 (9): e12862. Hendrickson Sher L, Lautenberger James A, Chinn Leslie Wei, Malasky Michael, Sezgin Efe, Kingsley Lawrence A, Goedert James J, Kirk Gregory D, Gomperts Edward D, Buchbinder Susan P, Troyer Jennifer L, O'Brien Stephen Similar articles in PubMed
The HADHSC gene encoding short-chain L-3-hydroxyacyl-CoA dehydrogenase (SCHAD) and type 2 diabetes susceptibility: the DAMAGE study. Diabetes 2006 Nov 55 (11): 3193-6. van Hove Els C, Hansen Torben, Dekker Jacqueline M, Reiling Erwin, Nijpels Giel, Jørgensen Torben, Borch-Johnsen Knut, Hamid Yasmin H, Heine Robert J, Pedersen Oluf, Maassen J Antonie, 't Hart Leen Similar articles in PubMed

File Formats Help:

How do I view different file formats (PDF, DOC, PPT, MPEG) on this site?

Page last reviewed:Mar 16, 2019
Page last updated:Apr 02, 2020
Content source:

TOP