Lawrence C Brody

Lawrence C Brody

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Lawrence C Brody

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Lessons learned from two decades of BRCA1 and BRCA2 genetic testing: the evolution of data sharing and variant classification.

Genet Med 2019 07 26;21(7):1476-1480. Epub 2018 Nov 26.

National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1038/s41436-018-0370-4DOI Listing
July 2019

ComPaSS-GWAS: A method to reduce type I error in genome-wide association studies when replication data are not available.

Genet Epidemiol 2019 02 18;43(1):102-111. Epub 2018 Oct 18.

Genometrics Section, Computational and Statistical Genomics Branch, National Human Genome Research Institute/National Institutes of Health (NHGRI/NIH), Baltimore, Maryland.

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http://dx.doi.org/10.1002/gepi.22168DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6330131PMC
February 2019

Providing Individual Research Results to Participants.

JAMA 2018 12;320(24):2600-2601

Division of Genomics and Society, National Human Genome Research Institute, Bethesda, Maryland.

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http://dx.doi.org/10.1001/jama.2018.18099DOI Listing
December 2018

Functional and phylogenetic characterization of noncanonical vitamin B-binding proteins in zebrafish suggests involvement in cobalamin transport.

J Biol Chem 2018 11 20;293(45):17606-17621. Epub 2018 Sep 20.

From the Gene and Environment Interaction Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892 and

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http://dx.doi.org/10.1074/jbc.RA118.005323DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6231144PMC
November 2018

Mice lacking the transcobalamin-vitamin B12 receptor, CD320, suffer from anemia and reproductive deficits when fed vitamin B12-deficient diet.

Hum Mol Genet 2018 10;27(20):3627-3640

Division of Intramural Research, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

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https://academic.oup.com/hmg/article/27/20/3627/5067847
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http://dx.doi.org/10.1093/hmg/ddy267DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6168973PMC
October 2018

The impact of common genetic variants in the mitochondrial glycine cleavage system on relevant metabolites.

Mol Genet Metab Rep 2018 Sep 11;16:20-22. Epub 2018 Jun 11.

Department of Clinical Medicine, School of Medicine, Trinity College Dublin 2, Ireland.

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http://dx.doi.org/10.1016/j.ymgmr.2018.05.006DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6034155PMC
September 2018

Prioritizing diversity in human genomics research.

Nat Rev Genet 2018 03 20;19(3):175-185. Epub 2017 Nov 20.

National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892-2152, USA.

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http://dx.doi.org/10.1038/nrg.2017.89DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6532668PMC
March 2018

Copy number variants in Ebstein anomaly.

PLoS One 2017 7;12(12):e0188168. Epub 2017 Dec 7.

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0188168PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5720705PMC
January 2018

Copy-number variants and candidate gene mutations in isolated split hand/foot malformation.

J Hum Genet 2017 Oct 25;62(10):877-884. Epub 2017 May 25.

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1038/jhg.2017.56DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5612852PMC
October 2017

Genetic Risk Factors for Folate-Responsive Neural Tube Defects.

Annu Rev Nutr 2017 08 19;37:269-291. Epub 2017 Jun 19.

Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, Maryland 20892; email: ,

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http://dx.doi.org/10.1146/annurev-nutr-071714-034235DOI Listing
August 2017

Traceback: A Proposed Framework to Increase Identification and Genetic Counseling of BRCA1 and BRCA2 Mutation Carriers Through Family-Based Outreach.

J Clin Oncol 2017 Jul 11;35(20):2329-2337. Epub 2017 Apr 11.

Goli Samimi, Charlisse F. Caga-anan, Michael Dean, Leah E. Mechanic, Lori M. Minasian, and Mark E. Sherman, National Cancer Institute; Lawrence C. Brody, National Human Genome Research Institute, Bethesda, MD; Marcus Q. Bernardini, Stephanie Lheureux, Patricia A. Shaw, Princess Margaret Cancer Centre, Toronto, Ontario; Janice S. Kwon, University of British Columbia; British Columbia Cancer Agency, Vancouver, British Columbia, Canada; Ian G. Campbell, Paul A. James, Masataka Takenaka, and David D. Bowtell, Peter MacCallum Cancer Centre; David D. Bowtell, University of Melbourne, Melbourne, Victoria; Georgia Chenevix-Trench, QIMR Berghofer Medical Research Institute, Brisbane, Queensland; Michael Friedlander, The Prince of Wales Hospital; Susan J. Ramus, University of New South Wales; Susan J. Ramus and David D. Bowtell, Garvan Institute of Medical Research, Sydney, New South Wales, Australia; Fergus J. Couch, Mayo Clinic, Rochester, MN; Joanne A. de Hullu and Marline G. Harmsen, Radboud University Medical Center, Nijmegen, the Netherlands; Susan M. Domchek and Ronny Drapkin, University of Pennsylvania, Philadelphia; Phuong L. Mai, Magee-Women's Hospital of the University of Pittsburgh Medical Center, Pittsburgh, PA; Heather Spencer Feigelson, Kaiser Permanente Institute for Health Research, Denver, CO; Mia M. Gaudet, American Cancer Society, Atlanta, GA; Karen Hurley and Mark E. Robson, Memorial Sloan Kettering Cancer Center; Mark E. Robson, Weill Cornell Medical College, New York, NY; Felicitas Lacbawan, Quest Diagnostics Nichols Institute, San Juan Capistrano; Thomas P. Slavin, City of Hope, Duarte, CA; Evan R. Myers, Duke University Medical Center, Durham, NC; Lisa F. Rezende, FORCE: Facing Our Risk of Cancer Empowered, Tampa; Mark E. Sherman, Mayo Clinic, Jacksonville, FL; and Elizabeth M. Swisher, University of Washington Medical Center, Seattle, WA.

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http://dx.doi.org/10.1200/JCO.2016.70.3439DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5501360PMC
July 2017

Moderately Elevated Homocysteine Does Not Contribute to Thoracic Aortic Aneurysm in Mice.

J Nutr 2017 07 24;147(7):1290-1295. Epub 2017 May 24.

National Human Genome Research Institute, NIH, Bethesda, MD;

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http://dx.doi.org/10.3945/jn.117.251173DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5483969PMC
July 2017

Genetic Variants in Isolated Ebstein Anomaly Implicated in Myocardial Development Pathways.

PLoS One 2016 27;11(10):e0165174. Epub 2016 Oct 27.

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0165174PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5082909PMC
June 2017

Copy number variants in a population-based investigation of Klippel-Trenaunay syndrome.

Am J Med Genet A 2017 Feb 30;173(2):352-359. Epub 2016 Nov 30.

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/ajmg.a.37868DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205266PMC
February 2017

Rare copy number variants in a population-based investigation of hypoplastic right heart syndrome.

Birth Defects Res 2017 01;109(1):8-15

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/bdra.23586DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5388571PMC
January 2017

Generating Exome Enriched Sequencing Libraries from Formalin-Fixed, Paraffin-Embedded Tissue DNA for Next-Generation Sequencing.

Curr Protoc Hum Genet 2017 01 11;92:18.10.1-18.10.25. Epub 2017 Jan 11.

Center for Inherited Disease Research, McKusick-Nathans Institute of Genetic Medicine, Johns Hopkins University, Baltimore, Maryland.

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http://dx.doi.org/10.1002/cphg.27DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5228582PMC
January 2017

Copy-number variant analysis of classic heterotaxy highlights the importance of body patterning pathways.

Hum Genet 2016 12 15;135(12):1355-1364. Epub 2016 Sep 15.

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, 6100 Executive Boulevard, Bethesda, MD, 20892, USA.

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http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5065782PMC
http://dx.doi.org/10.1007/s00439-016-1727-xDOI Listing
December 2016

Association of a transcobalamin II genetic variant with falsely low results for the holotranscobalamin immunoassay.

Eur J Clin Invest 2016 May 15;46(5):434-9. Epub 2016 Apr 15.

Medical Genomics and Metabolic Genetics Branch, National Human Genome Research Institute, Bethesda, MD, USA.

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http://dx.doi.org/10.1111/eci.12617DOI Listing
May 2016

Rare copy number variants implicated in posterior urethral valves.

Am J Med Genet A 2016 Mar 14;170(3):622-33. Epub 2015 Dec 14.

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland.

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http://dx.doi.org/10.1002/ajmg.a.37493DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6205289PMC
March 2016

r2VIM: A new variable selection method for random forests in genome-wide association studies.

BioData Min 2016 1;9. Epub 2016 Feb 1.

Statistical Genetics Section, Inherited Disease Research Branch, National Human Genome Research Institute, National Institutes of Health, 333 Cassell Dr, 21224 Baltimore, USA.

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http://dx.doi.org/10.1186/s13040-016-0087-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4736152PMC
February 2016

Association of Transcobalamin II (TCN2) and Transcobalamin II-Receptor (TCblR) Genetic Variations With Cobalamin Deficiency Parameters in Elderly Women.

Biol Res Nurs 2015 Jul 5;17(4):444-54. Epub 2015 Feb 5.

Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA

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http://journals.sagepub.com/doi/ 10.1177/1099800415569506
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http://dx.doi.org/10.1177/1099800415569506DOI Listing
July 2015

Novel copy-number variants in a population-based investigation of classic heterotaxy.

Genet Med 2015 May 18;17(5):348-57. Epub 2014 Sep 18.

Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1038/gim.2014.112DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5901701PMC
May 2015

Maternal choline concentrations during pregnancy and choline-related genetic variants as risk factors for neural tube defects.

Am J Clin Nutr 2014 Oct 13;100(4):1069-74. Epub 2014 Aug 13.

From the Division of Intramural Population Health Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development (JLM, RF, AL, and YW), and Genome Technology Branch, National Human Genome Research Institute (LCB), NIH, Bethesda, MD; the Department of Clinical Science, University of Bergen and Laboratory of Clinical Biochemistry, Haukeland University Hospital, Bergen, Norway (PMU); the Health Research Board of Ireland, Dublin, Ireland (PNK); the University of California, Berkeley, Berkeley, CA (BS); and the Department of Clinical Medicine, School of Medicine, Trinity College Dublin, Dublin, Ireland (AMM).

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http://www.folk.uib.no/mfapu/Pages/papers%20pdf/2014/mills_2
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http://ajcn.nutrition.org/cgi/doi/10.3945/ajcn.113.079319
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http://dx.doi.org/10.3945/ajcn.113.079319DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4163794PMC
October 2014

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

BMC Med Genet 2014 Oct 8;15:102. Epub 2014 Oct 8.

Molecular Pathogenesis Section, Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Room 5306, 50 South Drive, Bethesda, MD, 20892-8004, USA.

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http://dx.doi.org/10.1186/s12881-014-0102-9DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4411759PMC
October 2014

Genomics of CpG methylation in developing and developed zebrafish.

G3 (Bethesda) 2014 Mar 21;4(5):861-9. Epub 2014 Mar 21.

Molecular Pathogenesis Section, Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland

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http://dx.doi.org/10.1534/g3.113.009514DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4025485PMC
March 2014

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

Birth Defects Res A Clin Mol Teratol 2014 Feb 18;100(2):100-6. Epub 2014 Feb 18.

The Institute of Molecular Medicine, School of Medicine, Trinity College Dublin, Ireland.

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http://dx.doi.org/10.1002/bdra.23223DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4018583PMC
February 2014

Anorectal atresia and variants at predicted regulatory sites in candidate genes.

Ann Hum Genet 2013 Jan 6;77(1):31-46. Epub 2012 Nov 6.

Division of Epidemiology, Statistics, and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda 20892, MD, USA.

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http://dx.doi.org/10.1111/j.1469-1809.2012.00734.xDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3535506PMC
January 2013

Hirschsprung's disease and variants in genes that regulate enteric neural crest cell proliferation, migration and differentiation.

J Hum Genet 2012 Aug 31;57(8):485-93. Epub 2012 May 31.

Department of Health and Human Services, Division of Epidemiology, Statistics, and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1038/jhg.2012.54DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503526PMC
August 2012

Differential analysis of ovarian and endometrial cancers identifies a methylator phenotype.

PLoS One 2012 5;7(3):e32941. Epub 2012 Mar 5.

DIR/GTB Genomic Functional Analysis Section, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland, United States of America.

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http://journals.plos.org/plosone/article?id=10.1371/journal.pone.0032941PLOS
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3293923PMC
July 2012

Patients' understanding of and responses to multiplex genetic susceptibility test results.

Genet Med 2012 Jul;14(7):681-7

Division of Public Health Sciences, Department of Surgery, Washington University School of Medicine, St. Louis, MO, USA.

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http://dx.doi.org/10.1038/gim.2012.22DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3417078PMC
July 2012

Folate and vitamin B12-related genes and risk for omphalocele.

Hum Genet 2012 May 25;131(5):739-46. Epub 2011 Nov 25.

Division of Epidemiology, Statistics and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, NIH, DHHS, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1007/s00439-011-1117-3DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3374579PMC
May 2012

Do high blood folate concentrations exacerbate metabolic abnormalities in people with low vitamin B-12 status?

Am J Clin Nutr 2011 Aug 8;94(2):495-500. Epub 2011 Jun 8.

Division of Epidemiology, Statistics, and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.3945/ajcn.111.014621DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3142724PMC
August 2011

Participation in genetic testing research varies by social group.

Public Health Genomics 2011 18;14(2):85-93. Epub 2010 Mar 18.

Henry Ford Hospital, Detroit, MI 48208, USA.

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http://dx.doi.org/10.1159/000294277DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3214933PMC
June 2011

Evaluation of 64 candidate single nucleotide polymorphisms as risk factors for neural tube defects in a large Irish study population.

Am J Med Genet A 2011 Jan 10;155A(1):14-21. Epub 2010 Dec 10.

Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland 20892-7510, USA.

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http://dx.doi.org/10.1002/ajmg.a.33755DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503244PMC
January 2011

Polymorphisms in the adenomatous polyposis coli (APC) gene and advanced colorectal adenoma risk.

Eur J Cancer 2010 Sep 24;46(13):2457-66. Epub 2010 May 24.

Department of Health and Human Services, Division of Cancer Epidemiology and Genetics, National Cancer Institute, NIH, Rockville, MD, USA.

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http://dx.doi.org/10.1016/j.ejca.2010.04.020DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2924917PMC
September 2010

Screening student athletes for sickle cell trait--a social and clinical experiment.

N Engl J Med 2010 Sep;363(11):997-9

Social and Behavioral Research Branch, National Human Genome Research Institute, Bethesda, MD, USA.

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http://dx.doi.org/10.1056/NEJMp1007639DOI Listing
September 2010

Consumers' use of web-based information and their decisions about multiplex genetic susceptibility testing.

J Med Internet Res 2010 Sep 29;12(3):e41. Epub 2010 Sep 29.

Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.2196/jmir.1587DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2956320PMC
September 2010

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

Birth Defects Res A Clin Mol Teratol 2010 Feb;88(2):84-93

Division of Epidemiology, Statistics, and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Department of Health and Human Services, Bethesda, Maryland, USA.

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http://dx.doi.org/10.1002/bdra.20639DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3503531PMC
February 2010

Characteristics of users of online personalized genomic risk assessments: implications for physician-patient interactions.

Genet Med 2009 Aug;11(8):582-7

Social and Behavioral Research Branch, National Human Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1097/GIM.0b013e3181b22c3aDOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC3341609PMC
August 2009

The search for genetic polymorphisms in the homocysteine/folate pathway that contribute to the etiology of human neural tube defects.

Birth Defects Res A Clin Mol Teratol 2009 Apr;85(4):285-94

School of Biochemistry and Immunology, Trinity College, Dublin, Ireland.

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http://dx.doi.org/10.1002/bdra.20566DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC6129971PMC
April 2009

Uncoupling protein 2 polymorphisms as risk factors for NTDs.

Birth Defects Res A Clin Mol Teratol 2009 Feb;85(2):156-60

Molecular Pathogenesis Section, Genome Technology Branch, National Human Genome Research Institute, 50 South Drive, Bethesda, MD 20892-8004, USA.

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http://dx.doi.org/10.1002/bdra.20520DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2724655PMC
February 2009

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

Birth Defects Res A Clin Mol Teratol 2008 Sep;82(9):636-43

Division of Epidemiology, Statistics and Prevention Research, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, MD 20892, USA.

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http://doi.wiley.com/10.1002/bdra.20491
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http://dx.doi.org/10.1002/bdra.20491DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2670560PMC
September 2008

Putting science over supposition in the arena of personalized genomics.

Nat Genet 2008 Aug;40(8):939-42

Social and Behavioral Research Branch, National Genome Research Institute, National Institutes of Health, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1038/ng0808-939DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2531214PMC
August 2008

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

Food Nutr Bull 2008 Jun;29(2 Suppl):S101-11; discussion S112-5

School of Medicine, Trinity College Dublin, Ireland.

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http://fnb.sagepub.com/content/29/2_suppl1/S101.full.pdf
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http://dx.doi.org/10.1177/15648265080292S114DOI Listing
June 2008

Point: genetic risk feedback for common disease time to test the waters.

Cancer Epidemiol Biomarkers Prev 2007 Sep;16(9):1724-6

National Human Genome Research Institute, NIH, 31 Center Drive, Building 31, Room B2B37, Bethesda, MD 20892-2030, USA.

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http://dx.doi.org/10.1158/1055-9965.EPI-07-0102DOI Listing
September 2007

Genetic and nutritional deficiencies in folate metabolism influence tumorigenicity in Apcmin/+ mice.

J Nutr Biochem 2007 May 11;18(5):305-12. Epub 2006 Sep 11.

Department of Human Genetics, McGill University-Montreal Children's Hospital Research Institute, Montreal, Quebec, Canada.

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http://linkinghub.elsevier.com/retrieve/pii/S095528630600157
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http://dx.doi.org/10.1016/j.jnutbio.2006.06.001DOI Listing
May 2007

Clinical and molecular features associated with biallelic mutations in FANCD1/BRCA2.

J Med Genet 2007 Jan 6;44(1):1-9. Epub 2006 Jul 6.

Clinical Genetics Branch, Division of Cancer Epidemiology and Genetics, National Cancer Institute, 6120 Executive Blvd, Executive Plaza South, Room 7020, Rockville, MD 20852-7231, USA.

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http://dx.doi.org/10.1136/jmg.2006.043257DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2597904PMC
January 2007

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

Mol Genet Metab 2006 Jul 18;88(3):290-4. Epub 2006 Apr 18.

School of Biochemistry and Immunology, Trinity College Dublin, Ireland.

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http://dx.doi.org/10.1016/j.ymgme.2006.02.011DOI Listing
July 2006

Reduced folate carrier polymorphisms and neural tube defect risk.

Mol Genet Metab 2006 Apr 15;87(4):364-9. Epub 2005 Dec 15.

Department of Biochemistry, Trinity College Dublin, Ireland.

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http://dx.doi.org/10.1016/j.ymgme.2005.09.024DOI Listing
April 2006

Screening for new MTHFR polymorphisms and NTD risk.

Am J Med Genet A 2005 Oct;138A(2):99-106

Department of Biochemistry, Trinity College Dublin, Dublin, Ireland.

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http://dx.doi.org/10.1002/ajmg.a.30846DOI Listing
October 2005

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

Am J Clin Nutr 2005 Oct;82(4):836-42

Department of Clinical Medicine and the National Human Genome Research Institute, the National Institutes of Health, Bethesda, MD, USA.

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http://dx.doi.org/10.1093/ajcn/82.4.836DOI Listing
October 2005

Treating cancer by targeting a weakness.

Authors:
Lawrence C Brody

N Engl J Med 2005 Sep;353(9):949-50

Genome Technology Branch of the National Human Genome Research Institute, National Institutes of Health, Bethesda, Md, USA.

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http://www.nejm.org/doi/abs/10.1056/NEJMcibr052331
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http://dx.doi.org/10.1056/NEJMcibr052331DOI Listing
September 2005

Folate-related genes and omphalocele.

Am J Med Genet A 2005 Jul;136(1):8-11

Division of Epidemiology, Statistics and Prevention Research, NICHD, NIH, DHHS, Bethesda, Maryland 20892, USA.

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http://dx.doi.org/10.1002/ajmg.a.30772DOI Listing
July 2005

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

Birth Defects Res A Clin Mol Teratol 2005 Apr;73(4):239-44

Genome Technology Branch, National Human Genome Research Institute, National Institutes of Health, Department of Health and Human Services, Bethesda, MD 20892, USA.

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http://dx.doi.org/10.1002/bdra.20122DOI Listing
April 2005

Functional characterization of BRCA1 sequence variants using a yeast small colony phenotype assay.

Cancer Biol Ther 2004 May 18;3(5):453-7. Epub 2004 May 18.

Department of Biochemistry and Molecular Genetics, University of Virginia Health Sciences Center, Charlottesville, Virginia, USA.

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http://dx.doi.org/10.4161/cbt.3.5.809DOI Listing
May 2004