Drugs: endocrine system

Genomewide scans of red cell indices suggest linkage on chromosome 6q23
A Iliadou, D M Evans, G Zhu, D L Duffy, I H Frazer, G W Montgomery, N G Martin

Journal of Medical Genetics Jan 2007, 44 (1) 24-30; DOI: 10.1136/jmg.2006.043521
Association of oestrogen receptor α gene polymorphisms with postmenopausal bone loss, bone mass, and quantitative ultrasound properties of bone
O M E Albagha, U Pettersson, A Stewart, F E A McGuigan, H M MacDonald, D M Reid, S H Ralston

Journal of Medical Genetics Mar 2005, 42 (3) 240-246; DOI: 10.1136/jmg.2004.023895
Congenital hyperinsulinism and mosaic abnormalities of the ploidy
I Giurgea, D Sanlaville, J-C Fournet, C Sempoux, C Bellanné-Chantelot, G Touati, L Hubert, M-S Groos, F Brunelle, J Rahier, J-C Henquin, M J Dunne, F Jaubert, J-J Robert, C Nihoul-Fékété, M Vekemans, C Junien, P de Lonlay

Journal of Medical Genetics Mar 2006, 43 (3) 248-254; DOI: 10.1136/jmg.2005.034116
Phenotypic and population differences in the association between CILP and lumbar disc disease
I M Virtanen, Y Q Song, K M C Cheung, L Ala-Kokko, J Karppinen, D W H Ho, K D K Luk, S P Yip, J C Y Leong, K S E Cheah, P Sham, D Chan

Journal of Medical Genetics Apr 2007, 44 (4) 285-288; DOI: 10.1136/jmg.2006.047076
Inflammation, genetics, and longevity: further studies on the protective effects in men of IL-10 −1082 promoter SNP and its interaction with TNF-α −308 promoter SNP
D Lio, L Scola, A Crivello, G Colonna-Romano, G Candore, M Bonafé, L Cavallone, F Marchegiani, F Olivieri, C Franceschi, C Caruso

Journal of Medical Genetics Apr 2003, 40 (4) 296-299; DOI: 10.1136/jmg.40.4.296
A case control and family based association study of the neuregulin1 gene and schizophrenia
X Zhao, Y Shi, J Tang, R Tang, L Yu, N Gu, G Feng, S Zhu, H Liu, Y Xing, S Zhao, H Sang, Y Guan, D St Clair, L He

Journal of Medical Genetics Jan 2004, 41 (1) 31-34; DOI: 10.1136/jmg.2003.014977
A PDGFRA promoter polymorphism, which disrupts the binding of ZNF148, is associated with primitive neuroectodermal tumours and ependymomas
C De Bustos, A Smits, B Strömberg, V P Collins, M Nistér, G Afink

Journal of Medical Genetics Jan 2005, 42 (1) 31-37; DOI: 10.1136/jmg.2004.024034
Positional mapping of PRKD1, NRP1 and PRDM1 as novel candidate disease genes in truncus arteriosus
Ranad Shaheen, Amal Al Hashem, Mohammed H Alghamdi, Mohammed Zain Seidahmad, Salma M Wakil, Khalid Dagriri, Bernard Keavney, Judith Goodship, Saad Alyousif, Fahad M Al-Habshan, Khalid Alhussein, Agaadir Almoisheer, Niema Ibrahim, Fowzan S Alkuraya

Journal of Medical Genetics May 2015, 52 (5) 322-329; DOI: 10.1136/jmedgenet-2015-102992
A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension
M Shintani, H Yagi, T Nakayama, T Saji, R Matsuoka

Journal of Medical Genetics May 2009, 46 (5) 331-337; DOI: 10.1136/jmg.2008.062703
Comprehensive genomic analysis of PKHD1 mutations in ARPKD cohorts
A M Sharp, L M Messiaen, G Page, C Antignac, M-C Gubler, L F Onuchic, S Somlo, G G Germino, L M Guay-Woodford

Journal of Medical Genetics Apr 2005, 42 (4) 336-349; DOI: 10.1136/jmg.2004.024489

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