Hypertension

Admixture mapping of ankle–arm index: identification of a candidate locus associated with peripheral arterial disease
M L Scherer, M A Nalls, L Pawlikowska, E Ziv, G Mitchell, S Huntsman, D Hu, K Sutton-Tyrrell, E G Lakatta, W-C Hsueh, A B Newman, A Tandon, L Kim, P-Y Kwok, A Sung, R Li, B Psaty, A P Reiner, T Harris

Journal of Medical Genetics Jan 2010, 47 (1) 1-7; DOI: 10.1136/jmg.2008.064808
Genetic association analysis of inositol polyphosphate phosphatase-like 1 (INPPL1, SHIP2) variants with essential hypertension
Ana Carolina Braga Marçano, Beverley Burke, Johannie Gungadoo, Chris Wallace, Pamela J Kaisaki, Peng Y Woon, Martin Farrall, David Clayton, Morris Brown, Anna Dominiczak, John M Connell, John Webster, Mark Lathrop, Mark Caulfield, Nilesh Samani, Dominique Gauguier, Patricia B Munroe

Journal of Medical Genetics Sep 2007, 44 (9) 603-605; DOI: 10.1136/jmg.2007.049718
A genome-wide scan for genes involved in primary vesicoureteric reflux
H Kelly, C M Molony, J M Darlow, M E Pirker, A Yoneda, A J Green, P Puri, D E Barton

Journal of Medical Genetics Nov 2007, 44 (11) 710-717; DOI: 10.1136/jmg.2007.051086
Current needs for human and medical genomics research infrastructure in low and middle income countries
Diego A Forero, Ambroise Wonkam, Wei Wang, Paul Laissue, Catalina López-Correa, Juan C Fernández-López, Raja Mugasimangalam, George Perry

Journal of Medical Genetics Jul 2016, 53 (7) 438-440; DOI: 10.1136/jmedgenet-2015-103631
Expansion of the clinical phenotype associated with mutations in activity-dependent neuroprotective protein
Matthew F Pescosolido, Matthew Schwede, Ashley Johnson Harrison, Michael Schmidt, Ece D Gamsiz, Wendy S Chen, John P Donahue, Natasha Shur, Beth A Jerskey, Chanika Phornphutkul, Eric M Morrow

Journal of Medical Genetics Sep 2014, 51 (9) 587-589; DOI: 10.1136/jmedgenet-2014-102444
Genetic loci associated with lipid concentrations and cardiovascular risk factors in the Korean population
Mi-Hyun Park, NamHee Kim, Jong-Young Lee, Hyun-Young Park

Journal of Medical Genetics Jan 2011, 48 (1) 10-15; DOI: 10.1136/jmg.2010.081000
Acrofacial dysostosis in a patient with the TSC2-PKD1 contiguous gene syndrome
J G Dauwerse, K Bouman, A J van Essen, A H van der Hout, G Kolsters, M H Breuning, D J M Peters

Journal of Medical Genetics Feb 2002, 39 (2) 136-141; DOI: 10.1136/jmg.39.2.136
Relationship between microsatellite polymorphism in the haem oxygenase-1 gene promoter and longevity of the normal Japanese population
M Yamaya, K Nakayama, S Ebihara, H Hirai, S Higuchi, H Sasaki

Journal of Medical Genetics Feb 2003, 40 (2) 146-148; DOI: 10.1136/jmg.40.2.146
Haptoglobin and its association with the HELLP syndrome
M T M Raijmakers, E M Roes, R H M te Morsche, E A P Steegers, W H M Peters

Journal of Medical Genetics Mar 2003, 40 (3) 214-216; DOI: 10.1136/jmg.40.3.214
Genetic risk for myocardial infarction determined by polymorphisms of candidate genes in a Japanese population
Y Yamada, K Kato, M Oguri, T Fujimaki, K Yokoi, H Matsuo, S Watanabe, N Metoki, H Yoshida, K Satoh, S Ichihara, Y Aoyagi, A Yasunaga, H Park, M Tanaka, Y Nozawa

Journal of Medical Genetics Apr 2008, 45 (4) 216-221; DOI: 10.1136/jmg.2007.054387

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