16 Vitamin–Genome Interactions

[1]  J. Zvárová,et al.  Rare allelic variants determine folate status in an unsupplemented European population. , 2012, The Journal of nutrition.

[2]  Claudio J. Verzilli,et al.  An Abundance of Rare Functional Variants in 202 Drug Target Genes Sequenced in 14,002 People , 2012, Science.

[3]  Jaume Bertranpetit,et al.  Human Genetic Variation, Shared and Private , 2012, Science.

[4]  Jacob A. Tennessen,et al.  Evolution and Functional Impact of Rare Coding Variation from Deep Sequencing of Human Exomes , 2012, Science.

[5]  D. Fouad,et al.  The modifying effect of selenium and vitamins A, C, and E on the genotoxicity induced by sunset yellow in male mice. , 2012, Mutation research.

[6]  Michael Fenech,et al.  Folate (vitamin B9) and vitamin B12 and their function in the maintenance of nuclear and mitochondrial genome integrity. , 2012, Mutation research.

[7]  S. Zeisel Dietary choline deficiency causes DNA strand breaks and alters epigenetic marks on DNA and histones. , 2012, Mutation research.

[8]  P. Stover Polymorphisms in 1-Carbon Metabolism, Epigenetics and Folate-Related Pathologies , 2012, Lifestyle Genomics.

[9]  P. Stover,et al.  Serine Hydroxymethyltransferase Anchors de Novo Thymidylate Synthesis Pathway to Nuclear Lamina for DNA Synthesis* , 2012, The Journal of Biological Chemistry.

[10]  D. Corella,et al.  Association between a SLC23A2 gene variation, plasma vitamin C levels, and risk of glaucoma in a Mediterranean population , 2011, Molecular vision.

[11]  B. Sjöberg,et al.  DNA building blocks: keeping control of manufacture , 2011, Critical reviews in biochemistry and molecular biology.

[12]  K. Ye,et al.  Recent advances in understanding the role of nutrition in human genome evolution. , 2011, Advances in nutrition.

[13]  G. Block,et al.  Serum vitamin C and other biomarkers differ by genotype of phase 2 enzyme genes GSTM1 and GSTT1. , 2011, The American journal of clinical nutrition.

[14]  L. Curtin,et al.  Biomarkers of folate status in NHANES: a roundtable summary123456 , 2011, The American journal of clinical nutrition.

[15]  L. Curtin,et al.  Biomarkers of vitamin B-12 status in NHANES: a roundtable summary , 2011, The American journal of clinical nutrition.

[16]  L. Cahill,et al.  Haptoglobin genotype modifies the association between dietary vitamin C and serum ascorbic acid deficiency. , 2010, The American journal of clinical nutrition.

[17]  J. Mill,et al.  Allele-specific methylation in the human genome , 2010, Epigenetics.

[18]  A. Furano,et al.  The mutational spectrum of non-CpG DNA varies with CpG content. , 2010, Genome research.

[19]  F. Spronsen Phenylketonuria management from an European perspective: a commentary. , 2010 .

[20]  F. Collins,et al.  Genomic medicine--an updated primer. , 2010, The New England journal of medicine.

[21]  David B. Witonsky,et al.  Human adaptations to diet, subsistence, and ecoregion are due to subtle shifts in allele frequency , 2010, Proceedings of the National Academy of Sciences.

[22]  F. Vermeylen,et al.  Choline intake exceeding current dietary recommendations preserves markers of cellular methylation in a genetic subgroup of folate-compromised men. , 2010, The Journal of nutrition.

[23]  J. Venter,et al.  Multiple personal genomes await , 2010, Nature.

[24]  D. Smiraglia,et al.  Mild folate deficiency induces genetic and epigenetic instability and phenotype changes in prostate cancer cells , 2010, BMC Biology.

[25]  M. Hurles,et al.  Copy number variation in human health, disease, and evolution. , 2009, Annual review of genomics and human genetics.

[26]  P. Stover,et al.  SHMT1 and SHMT2 Are Functionally Redundant in Nuclear De novo Thymidylate Biosynthesis , 2009, PloS one.

[27]  Andrew G. Clark,et al.  Darwinian and demographic forces affecting human protein coding genes. , 2009, Genome research.

[28]  K. Frazer,et al.  Human genetic variation and its contribution to complex traits , 2009, Nature Reviews Genetics.

[29]  S. Tishkoff,et al.  African genetic diversity: implications for human demographic history, modern human origins, and complex disease mapping. , 2008, Annual review of genomics and human genetics.

[30]  M. Caudill,et al.  Genetic and epigenetic contributions to human nutrition and health: managing genome-diet interactions. , 2008, Journal of the American Dietetic Association.

[31]  R. Weindruch,et al.  A methyl‐deficient diet modifies histone methylation and alters Igf2 and H19 repression in the prostate , 2008, The Prostate.

[32]  L. Ferguson,et al.  Nutrition and mutagenesis. , 2008, Annual review of nutrition.

[33]  Francis S Collins,et al.  A HapMap harvest of insights into the genetics of common disease. , 2008, The Journal of clinical investigation.

[34]  M. Caudill,et al.  Folate intake at RDA levels is inadequate for Mexican American men with the methylenetetrahydrofolate reductase 677TT genotype , 2008, The Journal of nutrition.

[35]  Pardis C Sabeti,et al.  Genome-wide detection and characterization of positive selection in human populations , 2007, Nature.

[36]  Fernando A. Villanea,et al.  Diet and the evolution of human amylase gene copy number variation , 2007, Nature Genetics.

[37]  R. Waterland,et al.  Epigenetic epidemiology of the developmental origins hypothesis. , 2007, Annual review of nutrition.

[38]  S. Berger The complex language of chromatin regulation during transcription , 2007, Nature.

[39]  D. Altshuler,et al.  Completing the map of human genetic variation , 2007, Nature.

[40]  P. Stover Human Nutrition and Genetic Variation , 2007, Food and nutrition bulletin.

[41]  D. Conrad,et al.  Global variation in copy number in the human genome , 2006, Nature.

[42]  R. Redon,et al.  Copy number variation: new insights in genome diversity. , 2006, Genome research.

[43]  P. Stover Influence of human genetic variation on nutritional requirements. , 2006, The American journal of clinical nutrition.

[44]  H. McNulty,et al.  Riboflavin Lowers Homocysteine in Individuals Homozygous for the MTHFR 677C→T Polymorphism , 2005, Circulation.

[45]  S. Hunt,et al.  Genome-Wide Associations of Gene Expression Variation in Humans , 2005, PLoS genetics.

[46]  T. Milewicz,et al.  Uracil misincorporation into DNA of leukocytes of young women with positive folate balance depends on plasma vitamin B12 concentrations and methylenetetrahydrofolate reductase polymorphisms. A pilot study. , 2005, The Journal of nutritional biochemistry.

[47]  Y. Saijo,et al.  Genetic factors in fetal growth restriction and miscarriage. , 2005, Seminars in thrombosis and hemostasis.

[48]  B. Ames,et al.  Folate deficiency and ionizing radiation cause DNA breaks in primary human lymphocytes: a comparison , 2004, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

[49]  M. Adams,et al.  Inferring Nonneutral Evolution from Human-Chimp-Mouse Orthologous Gene Trios , 2003, Science.

[50]  Sarah A Tishkoff,et al.  Patterns of human genetic diversity: implications for human evolutionary history and disease. , 2003, Annual review of genomics and human genetics.

[51]  J. Diamond,et al.  The double puzzle of diabetes , 2003, Nature.

[52]  Wen-Hsiung Li,et al.  Molecular evolution meets the genomics revolution , 2003, Nature Genetics.

[53]  M. Caudill,et al.  Heterogeneity in the prevalence of methylenetetrahydrofolate reductase gene polymorphisms in women of different ethnic groups. , 2003, Journal of the American Dietetic Association.

[54]  G. Wray,et al.  Abundant raw material for cis-regulatory evolution in humans. , 2002, Molecular biology and evolution.

[55]  H. McNulty,et al.  Impaired functioning of thermolabile methylenetetrahydrofolate reductase is dependent on riboflavin status: implications for riboflavin requirements. , 2002, The American journal of clinical nutrition.

[56]  Debabrata Banerjee,et al.  Novel aspects of resistance to drugs targeted to dihydrofolate reductase and thymidylate synthase. , 2002, Biochimica et biophysica acta.

[57]  M. Batzer,et al.  Alu repeats and human genomic diversity , 2002, Nature Reviews Genetics.

[58]  T. Rossman,et al.  Reduction of spontaneous mutagenesis in mismatch repair-deficient and proficient cells by dietary antioxidants. , 2001, Mutation research.

[59]  Andrew G. Clark,et al.  Haplotype Diversity and Linkage Disequilibrium at Human G6PD: Recent Origin of Alleles That Confer Malarial Resistance , 2001, Science.

[60]  M. Nachman,et al.  Estimate of the mutation rate per nucleotide in humans. , 2000, Genetics.

[61]  B. Ames,et al.  Folate deficiency causes uracil misincorporation into human DNA and chromosome breakage: implications for cancer and neuronal damage. , 1997, Proceedings of the National Academy of Sciences of the United States of America.

[62]  R. Edwards Recent scientific and medical advances in assisted human conception. , 1997, The International journal of developmental biology.

[63]  W. Willett,et al.  Methylenetetrahydrofolate reductase polymorphism, dietary interactions, and risk of colorectal cancer. , 1997, Cancer research.

[64]  H. Blom,et al.  Is the common 677C-->T mutation in the methylenetetrahydrofolate reductase gene a risk factor for neural tube defects? A meta-analysis. , 1997, QJM : monthly journal of the Association of Physicians.

[65]  B. Ames,et al.  Ascorbic acid protects against endogenous oxidative DNA damage in human sperm. , 1991, Proceedings of the National Academy of Sciences of the United States of America.

[66]  P. Little,et al.  Analysis of thymidylate synthase gene amplification and of mRNA levels in the cell cycle. , 1987, The Journal of biological chemistry.

[67]  D. Edmonds,et al.  Early embryonic mortality in women , 1982 .

[68]  M. Fenech,et al.  Genetic polymorphisms of genes involved in DNA repair and metabolism influence micronucleus frequencies in human peripheral blood lymphocytes. , 2011, Mutagenesis.

[69]  R. Jaenisch,et al.  Folate deficiency induces genomic uracil misincorporation and hypomethylation but does not increase DNA point mutations. , 2009, Gastroenterology.

[70]  P. Stover,et al.  Folate-mediated one-carbon metabolism. , 2008, Vitamins and hormones.

[71]  Holly M. Mortensen,et al.  Convergent adaptation of human lactase persistence in Africa and Europe , 2007, Nature Genetics.

[72]  S. Sommer,et al.  Spontaneous mutation frequency and pattern in Big Blue® mice fed a vitamin E‐supplemented diet , 1999, Environmental and molecular mutagenesis.