Drugs: endocrine system

VEGF polymorphisms and severity of atherosclerosis
W M Howell, S Ali, M J Rose-Zerilli, S Ye

Journal of Medical Genetics Jun 2005, 42 (6) 485-490; DOI: 10.1136/jmg.2004.025734
Phenotype–genotype correlation in a familial IGF1R microdeletion case
D C M Veenma, H J Eussen, L C P Govaerts, S W K de Kort, R J Odink, C H Wouters, A C S Hokken-Koelega, A de Klein

Journal of Medical Genetics Jul 2010, 47 (7) 492-498; DOI: 10.1136/jmg.2009.070730
Interleukin 12 gene polymorphisms enhance gastric cancer risk in H pylori infected individuals
F Navaglia, D Basso, C-F Zambon, E Ponzano, L Caenazzo, N Gallo, A Falda, C Belluco, P Fogar, E Greco, F Di Mario, M Rugge, M Plebani

Journal of Medical Genetics Jun 2005, 42 (6) 503-510; DOI: 10.1136/jmg.2004.022723
SLC39A5 mutations interfering with the BMP/TGF-β pathway in non-syndromic high myopia
Hui Guo, Xuemin Jin, Tengfei Zhu, Tianyun Wang, Ping Tong, Lei Tian, Yu Peng, Liangdan Sun, Anran Wan, Jingjing Chen, Yanling Liu, Ying Li, Qi Tian, Lu Xia, Lusi Zhang, Yongcheng Pan, Lina Lu, Qiong Liu, Lu Shen, Yunping Li, Wei Xiong, Jiada Li, Beisha Tang, Yong Feng, Xuejun Zhang, Zhuohua Zhang, Qian Pan, Zhengmao Hu, Kun Xia

Journal of Medical Genetics Aug 2014, 51 (8) 518-525; DOI: 10.1136/jmedgenet-2014-102351
Low expression VEGF haplotype increases the risk for tetralogy of Fallot: a family based association study
D Lambrechts, K Devriendt, D A Driscoll, E Goldmuntz, M Gewillig, R Vlietinck, D Collen, P Carmeliet

Journal of Medical Genetics Jun 2005, 42 (6) 519-522; DOI: 10.1136/jmg.2004.026443
TNFα and IL10 SNPs act together to predict disease behaviour in Crohn’s disease
E V Fowler, R Eri, G Hume, S Johnstone, N Pandeya, D Lincoln, D Templeton, G L Radford-Smith

Journal of Medical Genetics Jun 2005, 42 (6) 523-528; DOI: 10.1136/jmg.2004.027425
Congenital hyperinsulinism in children with paternal 11p uniparental isodisomy and Beckwith–Wiedemann syndrome
Jennifer M Kalish, Kara E Boodhansingh, Tricia R Bhatti, Arupa Ganguly, Laura K Conlin, Susan A Becker, Stephanie Givler, Lindsey Mighion, Andrew A Palladino, N Scott Adzick, Diva D De León, Charles A Stanley, Matthew A Deardorff

Journal of Medical Genetics Jan 2016, 53 (1) 53-61; DOI: 10.1136/jmedgenet-2015-103394
Characterisation of the growth regulating gene IMP3, a candidate for Silver-Russell syndrome
D Monk, L Bentley, C Beechey, M Hitchins, J Peters, M A Preece, P Stanier, G E Moore

Journal of Medical Genetics Aug 2002, 39 (8) 575-581; DOI: 10.1136/jmg.39.8.575
A genome-wide association study of men with symptoms of testicular dysgenesis syndrome and its network biology interpretation
Marlene D Dalgaard, Nils Weinhold, Daniel Edsgärd, Jeremy D Silver, Tune H Pers, John E Nielsen, Niels Jørgensen, Anders Juul, Thomas A Gerds, Aleksander Giwercman, Yvonne L Giwercman, Gabriella Cohn-Cedermark, Helena E Virtanen, Jorma Toppari, Gedske Daugaard, Thomas S Jensen, Søren Brunak, Ewa Rajpert-De Meyts, Niels E Skakkebæk, Henrik Leffers, Ramneek Gupta

Journal of Medical Genetics Jan 2012, 49 (1) 58-65; DOI: 10.1136/jmedgenet-2011-100174
Twelve novel FBN1 mutations in Marfan syndrome and Marfan related phenotypes test the feasibility of FBN1 mutation testing in clinical practice
D J Halliday, S Hutchinson, L Lonie, J A Hurst, H Firth, P A Handford, P Wordsworth

Journal of Medical Genetics Aug 2002, 39 (8) 589-593; DOI: 10.1136/jmg.39.8.589

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