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Scholar Results 1 - 10 of about 59 citing Relton: Gene-gene interaction in folate-related genes and risk of neural tube defects in.... (0.10 sec) 

Genetics, statistics and human disease: analytical retooling for complexity

- luc.edu [PDF] 
TA Thornton-Wells, JH Moore, JL Haines - TRENDS in Genetics, 2004 - Elsevier
Molecular biologists and geneticists alike now acknowledge that most common
human diseases with a genetic component are likely to have complex etiologies.
Yet despite this belief, many statistical geneticists continue applying, in ...
Cited by 135 - Related articles - All 6 versions

Metabolic endophenotype and related genotypes are associated with oxidative stress in …


SJ James, S Melnyk, S Jernigan, MA Cleves, … - American journal of medical genetics. Part B, …, 2006 - pubmedcentral.nih.gov
Cited by 94 - Related articles - BL Direct - All 6 versions

[PDF] Etiology, pathogenesis and prevention of neural tube defects


R Padmanabhan - Congenital anomalies, 2006 - rc.kfshrc.edu.sa
Correspondence: Rengasamy Padmanabhan, MS, PhD, Cbiol, FIBiol (Lond), DSc (med),
Department of Anatomy, Faculty of Medicine and Health Sciences, UAE University,
PO Box 17666, Al Ain, United Arab Emirates. Email: padmanabhanr@uaeu.ac.ae ...
Cited by 49 - Related articles - View as HTML - BL Direct - All 8 versions

The merits of testing Hardy-Weinberg equilibrium in the analysis of unmatched case-control …


GY Zou, A Donner - Ann Hum Genet, 2006 - interscience.wiley.com
Testing for departures from the assumption of Hardy-Weinberg equilibrium (HWE)
has been widely recommended as a preliminary step in the analysis of genetic
case-control studies. Some authors suggest using a two-stage procedure in ...
Cited by 45 - Related articles - BL Direct - All 3 versions

Investigations into the etiology of neural tube defects


RM Cabrera, DS Hill, AJ Etheredge, RH … - Birth Defects Research Part C Embryo Today Reviews, 2004 - interscience.wiley.com
It is also possible that your web browser is not configured or not able to
display style sheets. In this case, although the visual presentation will be
degraded, the site should continue to be functional. We recommend using the ...
Cited by 30 - Related articles - All 3 versions

The methionine synthase reductase 66A> G polymorphism is a maternal risk factor for spina …


IJM van der Linden, M den Heijer, LA Afman, … - Journal of Molecular Medicine, 2006 - Springer
Page 1. ORIGINAL ARTICLE The methionine synthase reductase 66A>G polymorphism
is a maternal risk factor for spina bifida Ivon JM ...
Cited by 30 - Related articles - All 6 versions

Genetic variation in genes of folate metabolism and neural-tube defect risk


IJM van der Linden, LA Afman, SG Heil, HJ … - Proceedings of the Nutrition Society, 2007 - Cambridge Univ Press
Page 1. A meeting hosted by the Irish Section of the Nutrition Society
was held at Queen's University Belfast on 15–17 June 2005 ...
Cited by 24 - Related articles - BL Direct - All 10 versions

[PDF] Acquired and inherited disorders of cobalamin and folate in children


VM Whitehead… - Br J Haematol, 2006 - rc.kfshrc.edu.sa
Cobalamin deficiency in the newborn usually results from cobalamin deficiency in
the mother. Megaloblastic anaemia, pancytopenia and failure to thrive can be
present, accompan- ied by neurological deficits if the diagnosis is ...
Cited by 23 - Related articles - View as HTML - BL Direct - All 6 versions

Folate-mediated one-carbon metabolism and neural tube defects: balancing genome …


AE Beaudin, PJ Stover - BIRTH DEFECTS RESEARCH PART C EMBRYO …, 2007 - interscience.wiley.com
Neural tube defects (NTDs) refer to a cluster of neurodevelopmental conditions
associated with failure of neural tube closure during embryonic development.
Worldwide prevalence of NTDs ranges from approximately 0.5 to 60 per 10,000 ...
Cited by 19 - Related articles - BL Direct - All 2 versions

Metabolic derangement of methionine and folate metabolism in mice deficient in methionine …

- nih.gov
CL Elmore, X Wu, D Leclerc, ED Watson, T … - Molecular genetics and metabolism, 2007 - Elsevier
Hyperhomocyst(e)inemia is a metabolic derangement that is linked to the
distribution of folate pools, which provide one-carbon units for biosynthesis of
purines and thymidylate and for remethylation of homocysteine to form ...
Cited by 20 - Related articles - All 4 versions


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