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John Martin Scott

Institution

Trinity College Dublin

Contact

Subjects

Biochemistry

Medicine & Nursing

Details
Publications 80
As first author 13
As last author 43
Unique topics 421
Collaborations 38
Patents 2
Sources 11
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All
2019
2015
2014
2013
2012
2011
2010
2009
2008
Earlier
All
2019
2015
2014
2013
2012
2011
2010
2009
2008
Earlier

2019

A scoping review to map empirical evidence regarding key domains and questions in the clinical pathway of delirium in palliative care
2015

Evidence from a Randomized Trial That Exposure to Supplemental Folic Acid at Recommended Levels during Pregnancy Does Not Lead to Increased Unmetabolized Folic Acid Concentrations in Maternal or Cord Blood.
2015

Impact of voluntary fortification and supplement use on dietary intakes and biomarker status of folate and vitamin B-12 in Irish adults.
2014

Replication and exploratory analysis of 24 candidate risk polymorphisms for neural tube defects.
2013

Is low iron status a risk factor for neural tube defects?
2012

Unmetabolized folic acid prevalence is widespread in the older Irish population despite the lack of a mandatory fortification program.
2011

Folic acid consumption throughout pregnancy: differentiation between trimesters.
2011

Genotyping of a tri-allelic polymorphism by a novel melting curve assay in MTHFD1L: an association study of nonsyndromic Cleft in Ireland.
2010

A genome-wide association study of cleft lip with and without cleft palate identifies risk variants near MAFB and ABCA4.
2010

Testing reported associations of genetic risk factors for oral clefts in a large Irish study population.
2010

Transcobalamin II receptor polymorphisms are associated with increased risk for neural tube defects.
2009

A common variant in MTHFD1L is associated with neural tube defects and mRNA splicing efficiency
2009

Analysis of the MTHFD1 promoter and risk of neural tube defects
2009

Cobalamin, folic acid, and homocysteine
2009

Folate/homocysteine phenotypes and MTHFR 677C>T genotypes are associated with serum levels of monocyte chemoattractant protein-1.
2009

Lack of Association between Folate-Receptor Autoantibodies and Neural-Tube Defects
2009

Maternal vitamin B12 status and risk of neural tube defects in a population with high neural tube defect prevalence and no folic Acid fortification
2009

Persistent circulating unmetabolised folic acid in a setting of liberal voluntary folic acid fortification. Implications for further mandatory fortification?
2009

Personalised nutrition Genetic variation and disease risk: new advances
2009

The reduced folate carrier (SLC19A1) c.80G>A polymorphism is associated with red cell folate concentrations among women.
2009

Uncoupling protein 2 polymorphisms as risk factors for NTDs
2008

Analysis of the MTHFD1 promoter and risk of neural tube defects.
2008

Construction of a high resolution linkage disequilibrium map to evaluate common genetic variation in TP53 and neural tube defect risk in an Irish population.
2008

Effects of folate and vitamin B12 deficiencies during pregnancy on fetal, infant, and child development.
2008

Folate-related gene polymorphisms as risk factors for cleft lip and cleft palate.
2008

Homocysteine concentration, related B vitamins, and betaine in pregnant women recruited to the Seychelles Child Development Study.
2008

Persistent circulating unmetabolised folic acid in a setting of liberal voluntary folic acid fortification. Implications for further mandatory fortification?
2008

Vascular biomarkers of cognitive performance in a community-based elderly population: the Dublin Healthy Ageing study.
2007

Detection of vitamin B12 deficiency in older people by measuring vitamin B12 or the active fraction of vitamin B12, holotranscobalamin.
2007

Effect of a voluntary food fortification policy on folate, related B vitamin status, and homocysteine in healthy adults.
2007

Evidence of unmetabolised folic acid in cord blood of newborn and serum of 4-day-old infants
2007

Folic acid fortification and public health: report on threshold doses above which unmetabolised folic acid appear in serum
2007

Reduced folate status is common and increases disease risk. It can be corrected by daily ingestion of supplements or fortification.
2007

The 19-bp deletion polymorphism in intron-1 of dihydrofolate reductase (DHFR) may decrease rather than increase risk for spina bifida in the Irish population.
2006

Clinical relevance of low serum vitamin B12 concentrations in older people: the Banbury B12 study.
2006

Confirmation of the R653Q polymorphism of the trifunctional C1-synthase enzyme as a maternal risk for neural tube defects in the Irish population.
2006

Riboflavin lowers homocysteine in individuals homozygous for the MTHFR 677C->T polymorphism.
2005

A common insertion/deletion polymorphism of the thymidylate synthase (TYMS) gene is a determinant of red blood cell folate and homocysteine concentrations
2005

A polymorphism in the MTHFD1 gene increases a mother's risk of having an unexplained second trimester pregnancy loss.
2005

Analysis of methionine synthase reductase polymorphisms for neural tube defects risk association.
2005

Choline and homocysteine interrelations in umbilical cord and maternal plasma at delivery.
2005

MTHFD1 R653Q polymorphism is a maternal genetic risk factor for severe abruptio placentae.
2005

Reduced folate carrier polymorphisms and neural tube defect risk.
2005

Screening for new MTHFR polymorphisms and NTD risk.
2005

The MTHFR 1298CC and 677TT genotypes have opposite associations with red cell folate levels.
2004

Determining bioavailability of food folates in a controlled intervention study
2004

Facts and recommendations about total homocysteine determinations: an expert opinion
2004

Impact of the MTHFR C677T polymorphism on risk of neural tube defects:case-control study
2004

Maternal homocysteine before conception and throughout pregnancy predicts fetal homocysteine and birth weight.
2004

The short-term bioavailabilities of [6S]-5-methyltetrahydrofolate and folic acid are equivalent in men.
2003

Analysis of the human folate receptor beta gene for an association with neural tube defects.
2003

Elevated plasma homocysteine in early pregnancy: a risk factor for the development of nonsevere preeclampsia.
2003

Folate, vitamin B12 and birth defects.
2003

Genetic and nutritional factors contributing to hyperhomocysteinemia in young adults
2003

Polymorphisms within the vitamin B12 dependent methylmalonyl-coA mutase are not risk factors for neural tube defects.
2003

Screening for vitamin B-12 and folate deficiency in older persons
2002

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
2002

Analysis of the MTHFR 1298A-->C and 677C-->T polymorphisms as risk factors for neural tube defects.
2002

Impaired functioning of thermolabile methylenetetrahydrofolate reductase is dependent on riboflavin status: implications for riboflavin requirements
2002

Maternal and fetal plasma homocysteine concentrations at birth: the influence of folate, vitamin B12, and the 5,10-methylenetetrahydrofolate reductase 677C-->T variant.
2002

Riboflavin, flavin mononucleotide, and flavin adenine dinucleotide in human plasma and erythrocytes at baseline and after low-dose riboflavin supplementation
2002

The pregnancy-related decrease in fasting plasma homocysteine is not explained by folic acid supplementation, hemodilution, or a decrease in albumin in a longitudinal study
2001

Folates and prevention of disease.
2000

Association between historically high frequencies of neural tube defects and the human T homologue of mouse T (Brachyury).
1999

Folate status and neural tube defects.
1999

Homocysteine, folate enzymes and neural tube defects
1999

The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother.
1998

Folic acid, homocysteine and one-carbon metabolism: a review of the essential biochemistry.
1998

Low blood folates in NTD pregnancies are only partly explained by thermolabile 5,10-methylenetetrahydrofolate reductase: low folate status alone may be the critical factor.
1997

Microbiological assay for serum, plasma, and red cell folate using cryopreserved, microtiter plate method.
1995

A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects.
1995

An abnormal methylation ratio induces hypomethylation in vitro in the brain of pig and man, but not in rat.
1995

Demonstration of hypomethylation of proteins in the brain of pigs (but not in rats) associated with chronic vitamin B12 inactivation.
1995

Folate levels and neural tube defects. Implications for prevention.
1994

Deriving a useful packed cell volume estimate from haemoglobin analysis
1994

Folate/vitamin B12 inter-relationships.
1993

Characterization of betaine efflux from rat liver mitochondria.
1993

Folate metabolism in pregnancy.
1992

Choline transport into rat liver mitochondria. Characterization and kinetics of a specific transporter.
1990

The role of nutrition in neural tube defects.

These arethe11 unique sources for John Martin Scott's 80 publications. A single publication may appear in multiple sources. Click on a name or publication count to see the publications for a particular source.

Source #
Ireland -> Dublin City University 5
Ireland -> Dublin City University -> PubMed 4
Ireland -> Royal College of Surgeons in Ireland 2
Ireland -> Royal College of Surgeons in Ireland -> PubMed 2
Ireland -> Trinity College Dublin 71
Ireland -> Trinity College Dublin -> PubMed 29
Ireland -> University College Cork 1
Ireland -> University College Cork -> PubMed 1
Ireland -> University College Dublin 3
Ireland -> University College Dublin -> PubMed 3
Ireland -> University of Limerick 1
Aug 27, 2008

USE OF RIBOFLAVIN IN THE TREATMENT OF HYPERTENSION
+
Jan 4, 2007

METHODS AND MATERIALS FOR IDENTIFYING POLYMORPHIC VARIANTS, DIAGNOSING SUSCEPTIBILITIES, AND TREATING DISEASE
+

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