Hypertension

Citations 11-20 of 51 total displayed.

Letters to JMG
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 for the Simon Broome Familial Hyperlipidaemia Register Group and Scientific Steering Committee
J. Med. Genet. 2006; 43: 943-949. [Abstract] [Full text] [PDF] [Request Permissions] [ web only appendix ]  

Electronic letters
Divergent phenotypes in Gaucher disease implicate the role of modifiers

O Goker-Alpan, K S Hruska, E Orvisky, P S Kishnani, B K Stubblefield, R Schiffmann, E Sidransky
J. Med. Genet. 2005; 42: e37. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
A rare variant of the leptin gene has large effects on blood pressure and carotid intima-medial thickness: a study of 1428 individuals in 248 families

N Gaukrodger, B M Mayosi, H Imrie, P Avery, M Baker, J M C Connell, H Watkins, M Farrall, B Keavney
J. Med. Genet. 2005; 42: 474-478. [Abstract] [Full text] [PDF] [Request Permissions]  

Original articles
Angiotensin II type I receptor gene polymorphism: anthropometric and metabolic syndrome traits

M R Abdollahi, T R Gaunt, H E Syddall, C Cooper, D I W Phillips, S Ye, I N M Day
J. Med. Genet. 2005; 42: 396-401. [Abstract] [Full text] [PDF] [Request Permissions]  

Letters to JMG
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
J. Med. Genet. 2005; 42: 336-349. [Extract] [Full text] [PDF] [Request Permissions] [ Web-only tables ]  

Letters to JMG
Evidence for a gene influencing haematocrit on chromosome 6q23–24: genomewide scan in the Framingham Heart Study

J-P Lin, C J O’Donnell, D Levy, L A Cupples
J. Med. Genet. 2005; 42: 75-79. [Extract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
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
J. Med. Genet. 2004; 41: e127. [Extract] [Full text] [PDF] [Request Permissions]  

Electronic letters
Evidence of differing genotypic effects of PPAR in women and men

Q H Khan, D E Pontefract, S Iyengar, S Ye
J. Med. Genet. 2004; 41: e79. [Extract] [Full text] [PDF] [Request Permissions]  

Online mutation reports
Complement factor I: a susceptibility gene for atypical haemolytic uraemic syndrome

V Fremeaux-Bacchi, M-A Dragon-Durey, J Blouin, C Vigneau, D Kuypers, B Boudailliez, C Loirat, E Rondeau, W H Fridman
J. Med. Genet. 2004; 41: e84. [Extract] [Full text] [PDF] [Request Permissions]  

Original articles
Large scale association analysis for identification of genes underlying premature coronary heart disease: cumulative perspective from analysis of 111 candidate genes

J J McCarthy, A Parker, R Salem, D J Moliterno, Q Wang, E F Plow, S Rao, G Shen, W J Rogers, L K Newby, R Cannata, K Glatt, E J Topol
J. Med. Genet. 2004; 41: 334-341. [Abstract] [Full text] [PDF] [Request Permissions] [ Web-only Table ]