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Author Details
Full Name
Andrei Verner
Affiliation
ORCID
Career Start Year
1995
Papers
27
H Index
20
Expertise
CM4AI Collaborator
PMID
Paper Title
Journal Title
Published Year
17805225
Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population.
Eur J Hum Genet
2008
17142250
Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica.
Hum Mol Genet
2007
17943131
Genome-wide detection and characterization of positive selection in human populations.
Nature
2007
17943122
A second generation human haplotype map of over 3.1 million SNPs.
Nature
2007
17099076
Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica.
Thorax
2007
17024367
Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica.
Hum Genet
2007
16281286
Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype.
Hum Mutat
2006
17033958
Mutations in TMEM76* cause mucopolysaccharidosis IIIC (Sanfilippo C syndrome).
Am J Hum Genet
2006
15668823
An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22.
Hum Genet
2005
14583597
A survey of genetic and epigenetic variation affecting human gene expression.
Physiol Genomics
2004
15591281
Localisation of a gene for mucopolysaccharidosis IIIC to the pericentromeric region of chromosome 8.
J Med Genet
2004
14741197
The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians.
Mol Genet Metab
2004
14737177
Susceptibility to leprosy is associated with PARK2 and PACRG.
Nature
2004
14699422
Genome-wide scan in Portuguese Island families identifies 5q31-5q35 as a susceptibility locus for schizophrenia and psychosis.
Mol Psychiatry
2004
15108176
Genome-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 Genet
2004
12577057
Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population.
Nat Genet
2003
11992121
Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy.
Nat Genet
2002
11156534
A novel syndrome affecting multiple mitochondrial functions, located by microcell-mediated transfer to chromosome 2p14-2p13.
Am J Hum Genet
2001
11704926
Identification of a major susceptibility locus for restless legs syndrome on chromosome 12q.
Am J Hum Genet
2001
11179024
A progressive autosomal recessive cataract locus maps to chromosome 9q13-q22.
Am J Hum Genet
2001
10628993
Sex-of-offspring-specific transmission ratio distortion on mouse chromosome X.
Genetics
2000
10820129
Localization of a recessive gene for North American Indian childhood cirrhosis to chromosome region 16q22-and identification of a shared haplotype.
Am J Hum Genet
2000
10337624
The maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om.
Mamm Genome
1999
9887372
Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human.
Eur J Hum Genet
1998
9271664
Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal "DDK syndrome" genes are linked.
Mamm Genome
1997
8846906
Transmission-ratio distortion through F1 females at chromosome 11 loci linked to Om in the mouse DDK syndrome.
Genetics
1996
8565326
Transmission-ratio distortion of X chromosomes among male offspring of females with skewed X-inactivation.
Dev Genet
1995
1 - 27 of 27
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