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Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population

American journal of human genetics, 2012-04, Vol.90 (4), p.693-700

2012

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Mutability of Y-Chromosomal Microsatellites: Rates, Characteristics, Molecular Bases, and Forensic Implications

American journal of human genetics, 2010-09, Vol.87 (3), p.341-353

2010

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Nonsense Mutations in BAG3 are Associated With Early-Onset Dilated Cardiomyopathy in French Canadians

Canadian journal of cardiology, 2014-12, Vol.30 (12), p.1655-1661

2014

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Evolutionary inventions and continuity of CORE-SINEs in mammals

Journal of molecular biology, 2000-05, Vol.298 (3), p.365-377

2000

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Alu sequences in the coding regions of mRNA: a source of protein variability

Trends in genetics, 1994-06, Vol.10 (6), p.188-193

1994

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In vitro evolution of RNA aptamers recognizing carcinogenic aromatic amines

Biochemical and biophysical research communications, 2004-01, Vol.313 (4), p.1004-1008

2004

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Haplotypes in the Dystrophin DNA Segment Point to a Mosaic Origin of Modern Human Diversity

American journal of human genetics, 2003-11, Vol.73 (5), p.994-1015

2003

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Self-priming arrest by modified random oligonucleotides facilitates the quality control of whole genome amplification

Analytical biochemistry, 2005-04, Vol.339 (2), p.345-347

2005

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Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies

American journal of human genetics, 2018-12, Vol.103 (6), p.893-906

2018

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Rapid Detection of CYP1A1, CYP2D6, and NAT Variants by Multiplex Polymerase Chain Reaction and Allele-Specific Oligonucleotide Assay

Analytical biochemistry, 1999-11, Vol.275 (1), p.84-92

1999

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Genome Fingerprinting by Simple Sequence Repeat (SSR)-Anchored Polymerase Chain Reaction Amplification

Genomics (San Diego, Calif.), 1994-03, Vol.20 (2), p.176-183

1994

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Female-to-Male Breeding Ratio in Modern Humans—an Analysis Based on Historical Recombinations

American journal of human genetics, 2010-03, Vol.86 (3), p.353-363

2010

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Distribution of the mammalian-wide interspersed repeats (MIRs) in the isochores of the human genome

FEBS letters, 1998-11, Vol.439 (1), p.63-65

1998

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Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas

American journal of human genetics, 2003-09, Vol.73 (3), p.524-539

2003

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Response to Lohmueller et al

American journal of human genetics, 2010-07, Vol.86 (6), p.980-981

2010

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Dynamic allele-specific oligonucleotide hybridization on solid support

Analytical biochemistry, 2004-01, Vol.324 (2), p.309-311

2004

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Female-to-Male Breeding Ratio in Modern Humans—an Analysis Based on Historical Recombinations

American journal of human genetics, 2010-06, Vol.86 (6), p.982-982

2010

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Phylogenetic and Familial Estimates of Mitochondrial Substitution Rates: Study of Control Region Mutations in Deep-Rooting Pedigrees

American journal of human genetics, 2001-11, Vol.69 (5), p.1113-1126

2001

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The Genetic Clock and the Age of the Founder Effect in Growing Populations: A Lesson from French Canadians and Ashkenazim

American journal of human genetics, 1997-09, Vol.61 (3), p.768-771

1997

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Phi29-based amplification of small genomes

Analytical biochemistry, 2006-07, Vol.354 (1), p.154-156

2006

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Human Mitochondrial HMG CoA Synthase: Liver cDNA and Partial Genomic Cloning, Chromosome Mapping to 1p12-p13, and Possible Role in Vertebrate Evolution

Genomics (San Diego, Calif.), 1994-10, Vol.23 (3), p.552-559

1994

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Linkage disequilibrium analysis in young populations : Pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

American journal of human genetics, 1996-09, Vol.59 (3), p.633-643

1996

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Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes

Genomics (San Diego, Calif.), 2006-06, Vol.87 (6), p.704-710

2006

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A “ Fille du Roy” Introduced the T14484C Leber Hereditary Optic Neuropathy Mutation in French Canadians

American journal of human genetics, 2005-08, Vol.77 (2), p.313-317

2005

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Mutations in C5ORF42 Cause Joubert Syndrome in the French Canadian Population

Mutability of Y-Chromosomal Microsatellites: Rates, Characteristics, Molecular Bases, and Forensic Implications

Nonsense Mutations in BAG3 are Associated With Early-Onset Dilated Cardiomyopathy in French Canadians

Evolutionary inventions and continuity of CORE-SINEs in mammals

Alu sequences in the coding regions of mRNA: a source of protein variability

In vitro evolution of RNA aptamers recognizing carcinogenic aromatic amines

Haplotypes in the Dystrophin DNA Segment Point to a Mosaic Origin of Modern Human Diversity

Self-priming arrest by modified random oligonucleotides facilitates the quality control of whole genome amplification

Inferring Transmission Histories of Rare Alleles in Population-Scale Genealogies

Rapid Detection of CYP1A1, CYP2D6, and NAT Variants by Multiplex Polymerase Chain Reaction and Allele-Specific Oligonucleotide Assay

Joubert Syndrome in French Canadians and Identification of Mutations in CEP104

Genome Fingerprinting by Simple Sequence Repeat (SSR)-Anchored Polymerase Chain Reaction Amplification

Female-to-Male Breeding Ratio in Modern Humans—an Analysis Based on Historical Recombinations

Distribution of the mammalian-wide interspersed repeats (MIRs) in the isochores of the human genome

Y-Chromosome Evidence for Differing Ancient Demographic Histories in the Americas

Response to Lohmueller et al

Dynamic allele-specific oligonucleotide hybridization on solid support

Female-to-Male Breeding Ratio in Modern Humans—an Analysis Based on Historical Recombinations

Phylogenetic and Familial Estimates of Mitochondrial Substitution Rates: Study of Control Region Mutations in Deep-Rooting Pedigrees

The Genetic Clock and the Age of the Founder Effect in Growing Populations: A Lesson from French Canadians and Ashkenazim

Phi29-based amplification of small genomes

Human Mitochondrial HMG CoA Synthase: Liver cDNA and Partial Genomic Cloning, Chromosome Mapping to 1p12-p13, and Possible Role in Vertebrate Evolution

Linkage disequilibrium analysis in young populations : Pseudo-vitamin D-deficiency rickets and the founder effect in French Canadians

Detection and characterization of DNA variants in the promoter regions of hundreds of human disease candidate genes

A “ Fille du Roy” Introduced the T14484C Leber Hereditary Optic Neuropathy Mutation in French Canadians

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