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Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

Nature genetics, 2002-06, Vol.31 (2), p.184-189

2002

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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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Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population

Nature genetics, 2003-03, Vol.33 (3), p.412-415

2003

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A Novel Syndrome Affecting Multiple Mitochondrial Functions, Located by Microcell-Mediated Transfer to Chromosome 2p14-2p13

American journal of human genetics, 2001-02, Vol.68 (2), p.386-396

2001

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A haplotype map of the human genome

Nature, 2005-10, Vol.437 (7063), p.1299-1320

2005

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The International HapMap Project

Nature, 2003-12, Vol.426 (6968), p.789-796

2003

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Susceptibility to leprosy is associated with PARK2 and PACRG

Nature, 2004-02, Vol.427 (6975), p.636-640

2004

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Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q

American journal of human genetics, 2001-12, Vol.69 (6), p.1266-1270

2001

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Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype

Human mutation, 2006-01, Vol.27 (1), p.31-43

2006

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Integrating ethics and science in the International HapMap Project

Nature reviews. Genetics, 2004-06, Vol.5 (6), p.467-475

Foster, Morris W

2004

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Sex-of-Offspring-Specific Transmission Ratio Distortion on Mouse Chromosome X

Genetics (Austin), 2000-01, Vol.154 (1), p.343-350

2000

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Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal “DDK syndrome” genes are linked

Mammalian genome, 1997-09, Vol.8 (9), p.642-646

1997

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Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)

American journal of human genetics, 2006-11, Vol.79 (5), p.807-819

2006

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Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica

Human molecular genetics, 2007-02, Vol.16 (3), p.243-253

2007

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129-P: Automated microarray processing using Prodigy™ instrument

Human immunology, 2008, Vol.69, p.S72-S72

2008

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Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica

Human genetics, 2007-01, Vol.120 (5), p.691-699

2007

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Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica

Thorax, 2007-03, Vol.62 (3), p.224-230

2007

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An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22

Human genetics, 2005-02, Vol.116 (3), p.167-171

2005

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Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population

European journal of human genetics : EJHG, 2008-01, Vol.16 (1), p.105-114

2008

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A Progressive Autosomal Recessive Cataract Locus Maps to Chromosome 9q13-q22

American journal of human genetics, 2001-03, Vol.68 (3), p.772-777

2001

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Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human

European journal of human genetics : EJHG, 1998-11, Vol.6 (6), p.552-562

1998

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The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians

Molecular genetics and metabolism, 2004-02, Vol.81 (2), p.140-143

2004

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Localization of a Recessive Gene for North American Indian Childhood Cirrhosis to Chromosome Region 16q22—and Identification of a Shared Haplotype

American journal of human genetics, 2000-07, Vol.67 (1), p.222-228

2000

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maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om

Mammalian genome, 1999-05, Vol.10 (5), p.492-497

1999

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The population history of northeastern Siberia since the Pleistocene

Nature (London), 2019-06, Vol.570 (7760), p.182-188

2019

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Mutation of GABRA1 in an autosomal dominant form of juvenile myoclonic epilepsy

A survey of genetic and epigenetic variation affecting human gene expression

Chromosome 6q25 is linked to susceptibility to leprosy in a Vietnamese population

A Novel Syndrome Affecting Multiple Mitochondrial Functions, Located by Microcell-Mediated Transfer to Chromosome 2p14-2p13

A haplotype map of the human genome

The International HapMap Project

Susceptibility to leprosy is associated with PARK2 and PACRG

Identification of a Major Susceptibility Locus for Restless Legs Syndrome on Chromosome 12q

Spectrum of mutations in mut methylmalonic acidemia and identification of a common Hispanic mutation and haplotype

Integrating ethics and science in the International HapMap Project

Sex-of-Offspring-Specific Transmission Ratio Distortion on Mouse Chromosome X

Confirmation of maternal transmission ratio distortion at Om and direct evidence that the maternal and paternal “DDK syndrome” genes are linked

Mutations in TMEM76 Cause Mucopolysaccharidosis IIIC (Sanfilippo C Syndrome)

Sex-specific linkage to total serum immunoglobulin E in families of children with asthma in Costa Rica

129-P: Automated microarray processing using Prodigy™ instrument

Significant linkage to airway responsiveness on chromosome 12q24 in families of children with asthma in Costa Rica

Genome-wide linkage analysis of pulmonary function in families of children with asthma in Costa Rica

An atypical form of erythrokeratodermia variabilis maps to chromosome 7q22

Identification of a chromosome 8p locus for early-onset coronary heart disease in a French Canadian population

A Progressive Autosomal Recessive Cataract Locus Maps to Chromosome 9q13-q22

Genetic mapping of X-linked loci involved in skewing of X chromosome inactivation in the human

The c.419-420insA in the MTP gene is associated with abetalipoproteinemia among French-Canadians

Localization of a Recessive Gene for North American Indian Childhood Cirrhosis to Chromosome Region 16q22—and Identification of a Shared Haplotype

maternal DDK syndrome phenotype is determined by modifier genes that are not linked to Om

The population history of northeastern Siberia since the Pleistocene

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