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A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly

Clinical genetics, 2015-07, Vol.88 (1), p.E1-E4

2015

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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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An X-Linked Haplotype of Neandertal Origin Is Present Among All Non-African Populations

Molecular biology and evolution, 2011-07, Vol.28 (7), p.1957-1962

2011

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Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion

Neurology, 2000-06, Vol.54 (12), p.2322

2000

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Prostate cancer susceptibility genes: lessons learned and challenges posed

Endocrine-related cancer, 2003-06, Vol.10 (2), p.225-259

2003

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Genetic susceptibility to breast cancer in French‐Canadians: Role of carcinogen‐metabolizing enzymes and gene–environment interactions

International journal of cancer, 2001-04, Vol.92 (2), p.220-225

2001

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Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations

Journal of medical genetics, 2008-04, Vol.45 (4), p.200-209

2008

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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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Fraction of Informative Recombinations: A Heuristic Approach to Analyze Recombination Rates

Genetics (Austin), 2008-04, Vol.178 (4), p.2069-2079

2008

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Analysis of nucleotide diversity of NAT2 coding region reveals homogeneity across Native American populations and high intra-population diversity

The pharmacogenomics journal, 2007-04, Vol.7 (2), p.144-152

2007

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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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Ethiopia: between Sub‐Saharan Africa and Western Eurasia

Annals of human genetics, 2005-05, Vol.69 (3), p.275-287

2005

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Is selection responsible for the low level of variation in the last intron of the ZFY locus?

Molecular biology and evolution, 1999-11, Vol.16 (11), p.1633-1640

1999

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Ethiopia: between Sub-Saharan Africa and Western Eurasia

Annals of human genetics, 2005-05, Vol.69 (3), p.275-287

2005

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Polymorphisms in Genes Encoding Drugs and Xenobiotic Metabolizing Enzymes, DNA Repair Enzymes, and Response to Treatment of Childhood Acute Lymphoblastic Leukemia

Clinical cancer research, 2002-03, Vol.8 (3), p.802-810

2002

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Childhood acute lymphoblastic leukemia: genetic determinants of susceptibility and disease outcome

Reviews on environmental health, 2001, Vol.16 (4), p.263

2001

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Alu RNA secondary structure consists of two independent 7 SL RNA-like folding units

The Journal of biological chemistry, 1991-05, Vol.266 (14), p.8675-8678

1991

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Frequent loss of heterozygosity at the DNA mismatch-repair loci hMLH1 and hMSH3 in sporadic breast cancer

British journal of cancer, 1999-03, Vol.79 (7-8), p.1012-1017

1999

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A survey of genetic and epigenetic variation affecting human gene expression

Physiological genomics, 2004-01, Vol.16 (2), p.184-193

2004

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Risk of Childhood Leukemia Associated with Exposure to Pesticides and with Gene Polymorphisms

Epidemiology (Cambridge, Mass.), 1999-09, Vol.10 (5), p.481-487

1999

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Susceptibility to Childhood Acute Lymphoblastic Leukemia: Influence of CYP1A1, CYP2D6, GSTM1, and GSTT1 Genetic Polymorphisms

Blood, 1999-03, Vol.93 (5), p.1496-1501

1999

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CORE-SINEs: Eukaryotic Short Interspersed Retroposing Elements with Common Sequence Motifs

Proceedings of the National Academy of Sciences - PNAS, 1999-03, Vol.96 (6), p.2869-2874

1999

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Role of NQO1, MPO and CYP2E1 genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia

International journal of cancer, 2002-01, Vol.97 (2), p.230-236

2002

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Splice-Mediated Insertion of an Alu Sequence Inactivates Ornithine δ-Aminotransferase: A Role for Alu Elements in Human Mutation

Proceedings of the National Academy of Sciences - PNAS, 1991-02, Vol.88 (3), p.815-819

1991

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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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A homozygous mutation in SLC1A4 in siblings with severe intellectual disability and microcephaly

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

An X-Linked Haplotype of Neandertal Origin Is Present Among All Non-African Populations

Unique origin and specific ethnic distribution of the Friedreich ataxia GAA expansion

Prostate cancer susceptibility genes: lessons learned and challenges posed

Genetic susceptibility to breast cancer in French‐Canadians: Role of carcinogen‐metabolizing enzymes and gene–environment interactions

Age and origin of major Smith-Lemli-Opitz syndrome (SLOS) mutations in European populations

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

Fraction of Informative Recombinations: A Heuristic Approach to Analyze Recombination Rates

Analysis of nucleotide diversity of NAT2 coding region reveals homogeneity across Native American populations and high intra-population diversity

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

Ethiopia: between Sub‐Saharan Africa and Western Eurasia

Is selection responsible for the low level of variation in the last intron of the ZFY locus?

Ethiopia: between Sub-Saharan Africa and Western Eurasia

Polymorphisms in Genes Encoding Drugs and Xenobiotic Metabolizing Enzymes, DNA Repair Enzymes, and Response to Treatment of Childhood Acute Lymphoblastic Leukemia

Childhood acute lymphoblastic leukemia: genetic determinants of susceptibility and disease outcome

Alu RNA secondary structure consists of two independent 7 SL RNA-like folding units

Frequent loss of heterozygosity at the DNA mismatch-repair loci hMLH1 and hMSH3 in sporadic breast cancer

A survey of genetic and epigenetic variation affecting human gene expression

Risk of Childhood Leukemia Associated with Exposure to Pesticides and with Gene Polymorphisms

Susceptibility to Childhood Acute Lymphoblastic Leukemia: Influence of CYP1A1, CYP2D6, GSTM1, and GSTT1 Genetic Polymorphisms

CORE-SINEs: Eukaryotic Short Interspersed Retroposing Elements with Common Sequence Motifs

Role of NQO1, MPO and CYP2E1 genetic polymorphisms in the susceptibility to childhood acute lymphoblastic leukemia

Splice-Mediated Insertion of an Alu Sequence Inactivates Ornithine δ-Aminotransferase: A Role for Alu Elements in Human Mutation

Evolutionary inventions and continuity of CORE-SINEs in mammals

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