Hypertension

A novel genetic locus for low renin hypertension: familial hyperaldosteronism type II maps to chromosome 7 (7p22)
Antony R Lafferty, David J Torpy, Michael Stowasser, Susan E Taymans, Jing Ping Lin, Philip Huggard, Richard D Gordon, Constantine A Stratakis

Journal of Medical Genetics Nov 2000, 37 (11) 831-835; DOI: 10.1136/jmg.37.11.831
Molecular and functional analysis identifies ALK-1 as the predominant cause of pulmonary hypertension related to hereditary haemorrhagic telangiectasia
R E Harrison, J A Flanagan, M Sankelo, S A Abdalla, J Rowell, R D Machado, C G Elliott, I M Robbins, H Olschewski, V McLaughlin, E Gruenig, F Kermeen, T Laitinen, N W Morrell, R C Trembath

Journal of Medical Genetics Dec 2003, 40 (12) 865-871; DOI: 10.1136/jmg.40.12.865
APOE and TGF-β1 genes are associated with obesity phenotypes
J-R Long, P-Y Liu, Y-J Liu, Y Lu, D-H Xiong, L Elze, R R Recker, H-W Deng

Journal of Medical Genetics Dec 2003, 40 (12) 918-924; DOI: 10.1136/jmg.40.12.918
Inbreeding and risk of late onset complex disease
I Rudan, D Rudan, H Campbell, A Carothers, A Wright, N Smolej-Narancic, B Janicijevic, L Jin, R Chakraborty, R Deka, P Rudan

Journal of Medical Genetics Dec 2003, 40 (12) 925-932; DOI: 10.1136/jmg.40.12.925
Association of single nucleotide polymorphisms in the oxidised LDL receptor 1 (OLR1) gene in patients with acute myocardial infarction
R Mango, F Clementi, P Borgiani, G B Forleo, M Federici, G Contino, E Giardina, L Garza, I E Fahdi, R Lauro, J L Mehta, G Novelli, F Romeo

Journal of Medical Genetics Dec 2003, 40 (12) 933-936; DOI: 10.1136/jmg.40.12.933
Genetic causes of familial hypercholesterolaemia in patients in the UK: relation to plasma lipid levels and coronary heart disease risk
S E Humphries, R A Whittall, C S Hubbart, S Maplebeck, J A Cooper, A K Soutar, R Naoumova, G R Thompson, M Seed, P N Durrington, J P Miller, D J B Betteridge, H A W Neil

Journal of Medical Genetics Dec 2006, 43 (12) 943-949; DOI: 10.1136/jmg.2006.038356
Further support for digenic inheritance in Bardet-Biedl syndrome
S Fauser, M Munz, D Besch

Journal of Medical Genetics Aug 2003, 40 (8) e104; DOI: 10.1136/jmg.40.8.e104
Low frequency of BMPR2 mutations in a German cohort of patients with sporadic idiopathic pulmonary arterial hypertension
R Koehler, E Grünig, M W Pauciulo, M M Hoeper, H Olschewski, H Wilkens, M Halank, J Winkler, R Ewert, H Bremer, S Kreuscher, B Janssen, W C Nichols

Journal of Medical Genetics Dec 2004, 41 (12) e127; DOI: 10.1136/jmg.2004.023101
Mapping of the human genes (SLC23A2 andSLC23A1) coding for vitamin C transporters 1 and 2 (SVCT1 and SVCT2) to 5q23 and 20p12, respectively
CONSTANTINE A STRATAKIS, SUSAN E TAYMANS, RUSHAD DARUWALA, JIAN SONG, MARK LEVINE

Journal of Medical Genetics Sep 2000, 37 (9) e20; DOI: 10.1136/jmg.37.9.e20
Partial trisomy 22 in a liveborn resulting from a rearrangement between chromosomes 6 and 22
GHAZALA MIRZA, KIYOSHI IMAIZUMI, JIANNIS RAGOUSSIS

Journal of Medical Genetics Sep 2000, 37 (9) e22; DOI: 10.1136/jmg.37.9.e22

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