IFRD1 is a candidate gene for SMNA on chromosome
7q22-q23.
American journal of human
genetics
, 2009 May: 692-7
Pharmacology and genetics of autism: implications for
diagnosis and treatment.
Personalized medicine
, 2008 Nov: 599-607
Genome scan of a nonword repetition phenotype in families
with dyslexia: evidence for multiple loci.
Behavior genetics
, 2008 Sep: 462-75
Evaluation of candidate genes for DYX1 and DYX2 in
families with dyslexia.
American journal of medical genetics. Part B,
Neuropsychiatric genetics : the official publication of the
International Society of Psychiatric Genetics
, 2007 Jun 5: 556-60
Genomewide scan for real-word reading subphenotypes of
dyslexia: novel chromosome 13 locus and genetic
complexity.
American journal of medical genetics. Part B,
Neuropsychiatric genetics : the official publication of the
International Society of Psychiatric Genetics
, 2006 Jan 5: 15-27
Genetic determinants of addiction to opioids and
cocaine.
Harvard review of psychiatry
, 2005 Jul-Aug: 218-32
Linkage analyses of four regions previously implicated in
dyslexia: confirmation of a locus on chromosome 15q.
American journal of medical genetics. Part B,
Neuropsychiatric genetics : the official publication of the
International Society of Psychiatric Genetics
, 2004 Nov 15: 67-75
Missense mutations in the regulatory domain of PKC gamma:
a new mechanism for dominant nonepisodic cerebellar
ataxia.
American journal of human
genetics
, 2003 Apr: 839-49
Prazosin in PTSD.
Journal of the American Academy of Child and
Adolescent Psychiatry
, 2003 Apr: 384-5
A new dominant spinocerebellar ataxia linked to chromosome
19q13.4-qter.
Archives of neurology
, 2002 Aug: 1291-5
Autosomal dominant sensory/motor neuropathy with Ataxia
(SMNA): Linkage to chromosome 7q22-q32.
American journal of medical
genetics
, 2002 May 8: 450-7