Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome.
, 2010 Sep: 790-3
Exome sequencing identifies the cause of a mendelian disorder.
, 2010 Jan: 30-5
Ribosomal mutations cause p53-mediated dark skin and pleiotropic effects.
, 2008 Aug: 963-70
A near null variant of 12/15-LOX encoded by a novel SNP in ALOX15 and the risk of coronary artery disease.
, 2008 May: 136-44
Common polymorphisms of ALOX5 and ALOX5AP and risk of coronary artery disease.
, 2008 May: 399-408
Polymorphisms in hypoxia inducible factor 1 and the initial clinical presentation of coronary disease.
American heart journal
, 2007 Dec: 1035-42
Ethical implications of array comparative genomic hybridization in complex phenotypes: points to consider in research.
Genetics in medicine : official journal of the American College of Medical Genetics
, 2007 Sep: 626-31
Candidate-gene approaches for studying complex genetic traits: practical considerations.
Nature reviews. Genetics
, 2002 May: 391-7
Lack of association between HoxA1 and HoxB1 gene variants and autism in 110 multiplex families.
American journal of medical genetics
, 2002 Jan 8: 24-30