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Folate metabolism genes, dietary folate and response to antidepressant medications in late-life depression

International journal of geriatric psychiatry, 2013-09, Vol.28 (9), p.925-932

2013

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Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects

Birth defects research. A Clinical and molecular teratology, 2008-10, Vol.82 (10), p.662-669

2008

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Candidate gene analysis in human neural tube defects

American journal of medical genetics. Part C, Seminars in medical genetics, 2005-05, Vol.135C (1), p.9-23

2005

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Native American myopathy: Congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia

American journal of medical genetics. Part A, 2008-07, Vol.146A (14), p.1832-1841

2008

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Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE)

Birth defects research. A Clinical and molecular teratology, 2012-09, Vol.94 (9), p.683-692

2012

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Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15

American journal of medical genetics. Part A, 2006-12, Vol.140A (24), p.2776-2785

2006

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Genetic Association Analyses of Nitric Oxide Synthase Genes and Neural Tube Defects Vary by Phenotype

Birth defects research. Part B. Developmental and reproductive toxicology, 2013-10, Vol.98 (5), p.365-373

2013

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Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2

Birth defects research. A Clinical and molecular teratology, 2005-11, Vol.73 (11), p.868-875

2005

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Harnessing the Power of the Pedigree

Journal of midwifery & women's health, 2005-05, Vol.50 (3), p.189-196

2005

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Refinement of 2q and 7p loci in a large multiplex NTD family

Birth defects research. A Clinical and molecular teratology, 2008-06, Vol.82 (6), p.441-452

2008

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Investigation of Notch3 as a candidate gene for bipolar disorder using brain hyperintensities as an endophenotype

American journal of medical genetics, 2002-08, Vol.114 (6), p.652-658

2002

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High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35

Birth defects research. A Clinical and molecular teratology, 2006-06, Vol.76 (6), p.499-505

2006

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Speaking the Language of Genetics: A Primer

Journal of midwifery & women's health, 2005-05, Vol.50 (3), p.184-188

2005

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The role of genetics and cigarette smoking in the development of pulmonary fibrosis

Respirology (Carlton, Vic.), 2006-01, Vol.11 (s1), p.S23-S23

2006

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TERC is not a major gene in human neural tube defects

Birth defects research. A Clinical and molecular teratology, 2004-08, Vol.70 (8), p.531-533

2004

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Genetic Association Analyses of Nitric Oxide Synthase Genes and Neural Tube Defects Vary by Phenotype

Birth defects research. Part B. Developmental and reproductive toxicology, 2013, Vol.98 (5), p.364-372

2013

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Data simulation for GAW9 problems 1 and 2

Genetic epidemiology, 1995, Vol.12 (6), p.561-564

1995

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Genetic mapping of a novel familial form of infantile hemangioma

American journal of medical genetics, 1999-01, Vol.82 (1), p.77-83

1999

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Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects

Clinical genetics, 2003-03, Vol.63 (3), p.210-214

2003

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High Density SNP Screen in A Large Multiplex Neural Tube Defect Family Refines Linkage to Loci at 7p21-Pter And 2q33.1-35

Birth defects research. A Clinical and molecular teratology, 2006-06, Vol.76 (6), p.499-505

2006

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High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35

Birth defects research. A Clinical and molecular teratology, 2006-06, Vol.76 (6), p.499-505

2006

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Analysis ofALDH1A2,CYP26A1,CYP26B1,CRABP1, andCRABP2 in human neural tube defects suggests a possible association with alleles inALDH1A2

Birth defects research. A Clinical and molecular teratology, 2005-11, Vol.73 (11), p.868-875

2005

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Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2

Birth defects research. A Clinical and molecular teratology, 2005-11, Vol.73 (11), p.868-875

2005

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Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects

Clinical genetics, 1999-08, Vol.56 (2), p.142-144

1999

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T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families

American journal of medical genetics, 2002-07, Vol.110 (3), p.215-218

2002

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Folate metabolism genes, dietary folate and response to antidepressant medications in late-life depression

Further evidence for a maternal genetic effect and a sex-influenced effect contributing to risk for human neural tube defects

Candidate gene analysis in human neural tube defects

Native American myopathy: Congenital myopathy with cleft palate, skeletal anomalies, and susceptibility to malignant hyperthermia

Transcriptome profiling of genes involved in neural tube closure during human embryonic development using long serial analysis of gene expression (long-SAGE)

Phenotypic definition of Chiari type I malformation coupled with high-density SNP genome screen shows significant evidence for linkage to regions on chromosomes 9 and 15

Genetic Association Analyses of Nitric Oxide Synthase Genes and Neural Tube Defects Vary by Phenotype

Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2

Harnessing the Power of the Pedigree

Refinement of 2q and 7p loci in a large multiplex NTD family

Investigation of Notch3 as a candidate gene for bipolar disorder using brain hyperintensities as an endophenotype

High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35

Speaking the Language of Genetics: A Primer

The role of genetics and cigarette smoking in the development of pulmonary fibrosis

TERC is not a major gene in human neural tube defects

Genetic Association Analyses of Nitric Oxide Synthase Genes and Neural Tube Defects Vary by Phenotype

Data simulation for GAW9 problems 1 and 2

Genetic mapping of a novel familial form of infantile hemangioma

Updated investigations of the role of methylenetetrahydrofolate reductase in human neural tube defects

High Density SNP Screen in A Large Multiplex Neural Tube Defect Family Refines Linkage to Loci at 7p21-Pter And 2q33.1-35

High-density single nucleotide polymorphism screen in a large multiplex neural tube defect family refines linkage to loci at 7p21.1-pter and 2q33.1-q35

Analysis ofALDH1A2,CYP26A1,CYP26B1,CRABP1, andCRABP2 in human neural tube defects suggests a possible association with alleles inALDH1A2

Analysis of ALDH1A2, CYP26A1, CYP26B1, CRABP1, and CRABP2 in human neural tube defects suggests a possible association with alleles in ALDH1A2

Possible interaction of genotypes at cystathionine β-synthase and methylenetetrahydrofolate reductase (MTHFR) in neural tube defects

T locus shows no evidence for linkage disequilibrium or mutation in American Caucasian neural tube defect families

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