Hypertension

Displaying results 1-10 of 56

• Mosaic ACVRL1 and ENG mutations in hereditary haemorrhagic telangiectasia patients

  • D Hunter Best,
  • Cecily Vaughn,
  • Jamie McDonald,
  • Kristy Damjanovich,
  • James R Runo,
  • Jason M Chibuk,
  • Pinar Bayrak-Toydemir

  J. Med. Genet.  2011;48:358-360  doi:10.1136/jmg.2010.088286
  • [Abstract]
  • [Full text]
  • [PDF]
  • [Web Only Data]

• 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

  J. Med. Genet.  2011;48:10-15  doi:10.1136/jmg.2010.081000
  • [Abstract]
  • [Full text]
  • [PDF]
  • [Web Only Data]
• Short report:

  Co-segregation of Norrie disease and idiopathic pulmonary hypertension in a family with a microdeletion of the NDP region at Xp11.3-p11.4

  • John F Staropoli,
  • Winnie Xin,
  • Katherine B Sims

  J. Med. Genet.  2010;47:786-790  doi:10.1136/jmg.2010.079301
  • [Abstract]
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• Heritability of metabolic syndrome traits among healthy younger adults: a population based study in China

  • B F Luo,
  • L Du,
  • J X Li,
  • B Y Pan,
  • J M Xu,
  • J Chen,
  • X Y Yin,
  • YQ Ren,
  • F Zhang

  J. Med. Genet.  2010;47:415-420  doi:10.1136/jmg.2009.068932
  • [Abstract]
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  • [PDF]

• 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

  J. Med. Genet.  2010;47:1-7  doi:10.1136/jmg.2008.064808
  • [Abstract]
  • [Full text]
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• Letters to JMG:

  Do mutations of the Pendred syndrome gene, SLC26A4, confer resistance to asthma and hypertension?

  • A C Madeo,
  • A Manichaikul,
  • S P Pryor,
  • A J Griffith

  J. Med. Genet.  2009;46:405-406  doi:10.1136/jmg.2008.063610
  • [Abstract]
  • [Full text]
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• Original articles:

  A new nonsense mutation of SMAD8 associated with pulmonary arterial hypertension

  • M Shintani,
  • H Yagi,
  • T Nakayama,
  • T Saji,
  • R Matsuoka

  J. Med. Genet.  2009;46:331-337  doi:10.1136/jmg.2008.062703
  • [Abstract]
  • [Full text]
  • [PDF]
  • [Web only appendices]
• Original articles:

  Genetic analysis of 56 polymorphisms in 17 genes involved in methionine metabolism in patients with abdominal aortic aneurysm

  • B Giusti,
  • C Saracini,
  • P Bolli,
  • A Magi,
  • I Sestini,
  • E Sticchi,
  • G Pratesi,
  • R Pulli,
  • C Pratesi,
  • R Abbate

  J. Med. Genet.  2008;45:721-730  doi:10.1136/jmg.2008.057851
  • [Abstract]
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  • [web only appendices]
• Original articles:

  Prevalence and heritability of the metabolic syndrome and its individual components in a Dutch isolate: the Erasmus Rucphen Family study

  • P Henneman,
  • Y S Aulchenko,
  • R R Frants,
  • K W van Dijk,
  • B A Oostra,
  • C M van Duijn

  J. Med. Genet.  2008;45:572-577  doi:10.1136/jmg.2008.058388
  • [Abstract]
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• Original articles:

  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

  J. Med. Genet.  2008;45:216-221  doi:10.1136/jmg.2007.054387
  • [Abstract]
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  • [web only table]