Genetic variation in NOS1AP is associated with sudden cardiac death: evidence from the Rotterdam Study

By Eijgelsheim Mark   Newton-Cheh Christopher   Aarnoudse Adrianus L.H.J.   van Noord Charlotte   Witteman Jacqueline C.M.   Hofman Albert   Uitterlinden Andr G.   Stricker Bruno H.C.  

Human Molecular Genetics, Vol. 18, Iss. 21, 2009-11 ,pp. : 4213-4218

Oxford University Press

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A non-synonymous variant in ADH1B is strongly associated with prenatal alcohol use in a European sample of pregnant women

By Zuccolo Luisa   Fitz-Simon Nicola   Gray Ron   Ring Susan M.   Sayal Kapil   Smith George Davey   Lewis Sarah J.  

Human Molecular Genetics, Vol. 18, Iss. 22, 2009-11 ,pp. : 4457-4466

Oxford University Press

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Common variants in the SLCO1B3 locus are associated with bilirubin levels and unconjugated hyperbilirubinemia

By Sanna Serena   Busonero Fabio   Maschio Andrea   McArdle Patrick F.   Usala Gianluca   Dei Mariano   Lai Sandra   Mulas Antonella   Piras Maria Grazia   Perseu Lucia   Masala Marco   Marongiu Mara   Crisponi Laura   Naitza Silvia   Galanello Renzo   Abecasis Gonalo R.   Shuldiner Alan R.   Schlessinger David   Cao Antonio   Uda Manuela  

Human Molecular Genetics, Vol. 18, Iss. 14, 2009-07 ,pp. : 2711-2718

Oxford University Press

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Dystonia associated with mutation of the neuronal sodium channel Scn8a and identification of the modifier locus Scnm1 on mouse chromosome 3

By Sprunger L.K.  

Human Molecular Genetics, Vol. 8, Iss. 3, 1999-03 ,pp. : 471-479

Oxford University Press

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Common variation at the adiponectin locus is not associated with colorectal cancer risk in the UK

By Carvajal-Carmona Luis G.   Spain Sarah   Kerr David   Houlston Richard   Cazier Jean-Baptiste   Tomlinson Ian  

Human Molecular Genetics, Vol. 18, Iss. 10, 2009-05 ,pp. : 1889-1892

Oxford University Press

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