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Author Details

Andrei Verner
1995
27
20
PMIDPaper TitleJournal TitlePublished Year
17805225Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.Eur J Hum Genet2008
17142250Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica.Hum Mol Genet2007
17943131Genome-wide detection and characterization of positive selection in human populations.Nature2007
17943122A second generation human haplotype map of over 3.1 million SNPs.Nature2007
17099076Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica.Thorax2007
17024367Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica.Hum Genet2007
16281286Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype.Hum Mutat2006
17033958Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome).Am J Hum Genet2006
15668823An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22.Hum Genet2005
14583597A survey of genetic and epigenetic variation affecting human gene expression.Physiol Genomics2004
15591281Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8.J Med Genet2004
14741197The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians.Mol Genet Metab2004
14737177Susceptibility to leprosy is associated with PARK2 and PACRG.Nature2004
14699422Genome-wide scan in Portuguese Island families identifies 5q31-5q35 as a susceptibility locus for schizophrenia and psychosis.Mol Psychiatry2004
15108176Genome-wide scan in Portuguese Island families implicates multiple loci in bipolar disorder: fine mapping adds support on chromosomes 6 and 11.Am J Med Genet B Neuropsychiatr Genet2004
12577057Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population.Nat Genet2003
11992121Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.Nat Genet2002
11156534A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.Am J Hum Genet2001
11704926Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.Am J Hum Genet2001
11179024A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.Am J Hum Genet2001
10628993Sex-of-offspring-specific transmission ratio distortion on mouse chromosome X.Genetics2000
10820129Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.Am J Hum Genet2000
10337624The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om.Mamm Genome1999
9887372Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human.Eur J Hum Genet1998
9271664Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal "DDK syndrome" genes are linked.Mamm Genome1997
8846906Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome.Genetics1996
8565326Transmission-ratio distortion of X chromosomes among male offspring of females with skewed X-inactivation.Dev Genet1995
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Collaborators

Ontario Institute for Cancer Research
Co-authored papers 17
McGill University and Genome Quebec Innovation Centre
Co-authored papers 5
University of Utah
Co-authored papers 4
Massachusetts General Hospital
Co-authored papers 4
University of North Carolina
Co-authored papers 4
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Brigham and Women's Hospital
Co-authored papers 3
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Co-authored papers 2
Nanfang Hospital and Basic Medical College, Southern Medical University
Co-authored papers 2
McGill University Health Center
Co-authored papers 2
Co-authored papers 2
McGill University, Canada Montreal Neurological Institute and Hospital
Co-authored papers 2
Center for Cerebrovascular Research
Co-authored papers 2
23andMe Inc.
Co-authored papers 2
Center for Statistical Genetics, Columbia University Medical Center
Co-authored papers 2
Adaptive Biotechnologies
Co-authored papers 2
Fudan University
Co-authored papers 2
Wellcome Trust Sanger Institute
Co-authored papers 2
Harvard Medical School, Vanderbilt University, Yale University Yale Law School
Co-authored papers 2
First Hospital of Xingtai
Co-authored papers 2
McGill University
Co-authored papers 2
William Harvey Research Institute, Queen Mary University of London
Co-authored papers 2
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Illumina Inc.
Co-authored papers 2
Newcastle University
Co-authored papers 2