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Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects

Journal of human genetics, 2003-04, Vol.48 (4), p.190-193

2003

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A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects: Report of the Birth Defects Research Group

American journal of human genetics, 2002-11, Vol.71 (5), p.1207-1215

2002

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Targeted Disruption of the Methionine Synthase Gene in Mice

Molecular and Cellular Biology, 2001-02, Vol.21 (4), p.1058-1065

2001

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Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population

American journal of medical genetics. Part A, 2008-10, Vol.146A (20), p.2617-2625

2008

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Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population

Birth defects research. A Clinical and molecular teratology, 2005-04, Vol.73 (4), p.239-244

2005

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Analysis of the human folate receptor β gene for an association with neural tube defects

Molecular genetics and metabolism, 2003-06, Vol.79 (2), p.129-133

2003

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PHR1 Encodes an Abundant, Pleckstrin Homology Domain-containing Integral Membrane Protein in the Photoreceptor Outer Segments

The Journal of biological chemistry, 1999-12, Vol.274 (50), p.35676-35685

1999

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Identification and Characterization of the Human Ortholog of Rat STXBP1, a Protein Implicated in Vesicle Trafficking and Neurotransmitter Release

Genomics (San Diego, Calif.), 1998-03, Vol.48 (3), p.373-376

1998

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Mammalian orthologs of C. elegans unc-119 highly expressed in photoreceptors

Investigative ophthalmology & visual science, 1998-10, Vol.39 (11), p.2085-2094

1998

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A Ubiquitin C-Terminal Hydrolase Gene on the Proximal Short Arm of the X Chromosome: Implications for X-Linked Retinal Disorders

Human molecular genetics, 1996-04, Vol.5 (4), p.533-538

1996

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Methionine Synthase: High-Resolution Mapping of the Human Gene and Evaluation as a Candidate Locus for Neural Tube Defects

Molecular genetics and metabolism, 1999-08, Vol.67 (4), p.324-333

1999

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A differential hybridization scheme to identify photoreceptor-specific genes

Genome research, 1997-05, Vol.7 (5), p.513

1997

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Gene Order Is Conserved within the Human Chromosome 21 Linkage Group on Mouse Chromosome 10

Genomics (San Diego, Calif.), 1994-05, Vol.21 (1), p.144-149

1994

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Expression and processing of human ornithine-δ-aminotransferase in Saccharomyces cerevisiae

Human molecular genetics, 1993-11, Vol.2 (11), p.1835-1840

1993

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Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA

American journal of human genetics, 2016-01, Vol.98 (1), p.58-74

2016

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The relation of bilingual cognitive skills to the second language writing performance of primary grade students

Journal of experimental child psychology, 2024-02, Vol.238, p.105776-105776, Article 105776

2024

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Assessment of the Reliability of Standard Automated Perimetry in Regions of Glaucomatous Damage

Ophthalmology (Rochester, Minn.), 2014-07, Vol.121 (7), p.1359-1369

2014

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Randomized Phase III Noninferiority Study Comparing Two Radiotherapy Fractionation Schedules in Patients With Low-Risk Prostate Cancer

Journal of clinical oncology, 2016-07, Vol.34 (20), p.2325-2332

2016

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Mechanisms of Cardiac and Renal Dysfunction in Patients Dying of Sepsis

American journal of respiratory and critical care medicine, 2013-03, Vol.187 (5), p.509-517

2013

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Cognition and Writing Development in Early Adolescent English Learners

Journal of educational psychology, 2022-07, Vol.114 (5), p.1136-1155

2022

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Uncovering the essential genes of the human malaria parasite Plasmodium falciparum by saturation mutagenesis

Science (American Association for the Advancement of Science), 2018-05, Vol.360 (6388)

2018

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Organic Radical Contrast Agents for Magnetic Resonance Imaging

Journal of the American Chemical Society, 2012-09, Vol.134 (38), p.15724-15727

2012

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Antidepressant dose, age, and the risk of deliberate self-harm

JAMA internal medicine, 2014-06, Vol.174 (6), p.899

2014

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Microglial activation induced by brain trauma is suppressed by post-injury treatment with a PARP inhibitor

Journal of neuroinflammation, 2012-02, Vol.9 (1), p.31-31, Article 31

2012

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Evidence of Positive Selection Acting at the Human Dopamine Receptor D4 Gene Locus

Proceedings of the National Academy of Sciences - PNAS, 2002-01, Vol.99 (1), p.309-314

2002

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Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects

A Polymorphism, R653Q, in the Trifunctional Enzyme Methylenetetrahydrofolate Dehydrogenase/Methenyltetrahydrofolate Cyclohydrolase/Formyltetrahydrofolate Synthetase Is a Maternal Genetic Risk Factor for Neural Tube Defects: Report of the Birth Defects Research Group

Targeted Disruption of the Methionine Synthase Gene in Mice

Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population

Evaluation of transcobalamin II polymorphisms as neural tube defect risk factors in an Irish population

Analysis of the human folate receptor β gene for an association with neural tube defects

PHR1 Encodes an Abundant, Pleckstrin Homology Domain-containing Integral Membrane Protein in the Photoreceptor Outer Segments

Identification and Characterization of the Human Ortholog of Rat STXBP1, a Protein Implicated in Vesicle Trafficking and Neurotransmitter Release

Mammalian orthologs of C. elegans unc-119 highly expressed in photoreceptors

A Ubiquitin C-Terminal Hydrolase Gene on the Proximal Short Arm of the X Chromosome: Implications for X-Linked Retinal Disorders

Methionine Synthase: High-Resolution Mapping of the Human Gene and Evaluation as a Candidate Locus for Neural Tube Defects

A differential hybridization scheme to identify photoreceptor-specific genes

Gene Order Is Conserved within the Human Chromosome 21 Linkage Group on Mouse Chromosome 10

Expression and processing of human ornithine-δ-aminotransferase in Saccharomyces cerevisiae

Genome Sequencing of Autism-Affected Families Reveals Disruption of Putative Noncoding Regulatory DNA

The relation of bilingual cognitive skills to the second language writing performance of primary grade students

Assessment of the Reliability of Standard Automated Perimetry in Regions of Glaucomatous Damage

Randomized Phase III Noninferiority Study Comparing Two Radiotherapy Fractionation Schedules in Patients With Low-Risk Prostate Cancer

Mechanisms of Cardiac and Renal Dysfunction in Patients Dying of Sepsis

Cognition and Writing Development in Early Adolescent English Learners

Uncovering the essential genes of the human malaria parasite Plasmodium falciparum by saturation mutagenesis

Organic Radical Contrast Agents for Magnetic Resonance Imaging

Antidepressant dose, age, and the risk of deliberate self-harm

Microglial activation induced by brain trauma is suppressed by post-injury treatment with a PARP inhibitor

Evidence of Positive Selection Acting at the Human Dopamine Receptor D4 Gene Locus

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