TY  - JOUR
A1  - Blom, H J
A1  - Shaw, G M
A1  - den, H 
A1  - Finnell, R H
T1  - Neural tube defects and folate: case far from closed.
Y1  - 2006/09/
N1  - R828292
VL  - 7
IS  - 9
SP  - 724
EP  - 731
ER  - 


TY  - JOUR
A1  - Carmichael, S L
A1  - Shaw, G M
A1  - Yang, W 
A1  - Lammer, E J
T1  - Limb deficiency defects, <em>MSX1</em>, and exposure to tobacco smoke.
Y1  - 2004/03/15
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS PART A
VL  - 125A
IS  - 3
SP  - 285
EP  - 289
ER  - 


TY  - JOUR
A1  - Carmichael, S L
A1  - Shaw, G M
A1  - Laurent, C 
A1  - Lammer, E J
T1  - Hypospadias and maternal exposures to cigarette smoke.
Y1  - 2005//
N1  - R828292
JF  - PEDIATRIC AND PRENATAL EPIDEMIOLOGY
ER  - 


TY  - JOUR
A1  - Carmichael, S L
A1  - Shaw, G M
A1  - Iovannisci, D M
A1  - Yang, W 
A1  - Finnell, R H
A1  - Cheng, S 
A1  - Lammer, E J
T1  - Risks of human limb deficiency anomalies associated with 29 SNPs of genes involved in homocysteine metabolism, coagulation, cell-cell interactions, inflammatory response, and blood pressure regulation.
Y1  - 2006/11/15
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS PART A
VL  - 140A
IS  - 22
SP  - 2433
EP  - 2440
ER  - 


TY  - JOUR
A1  - Carmichael, S L
A1  - Shaw, G M
A1  - Yang, W 
A1  - Iovannisci, D M
A1  - Lammer, E 
T1  - Risk of limb deficiency defects associated with <em>NAT1</em>, <em>NAT2</em>, <em>GSTT1</em>, <em>GSTM1</em>, and <em>NOS3</em> genetic variants, maternal smoking, and vitamin supplement intake.
Y1  - 2006/09/15
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS PART A
VL  - 140A
IS  - 18
SP  - 1915
EP  - 1922
ER  - 


TY  - JOUR
A1  - Finnell, R H
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Brandt, K L
A1  - Carmichael, S L
A1  - Rosenquist, T H
T1  - Gene-nutrient interactions: importance of folates and retinoids during early embryogenesis.
Y1  - 2004/07/15
N1  - R828292
JF  - TOXICOLOGY AND APPLIED PHARMACOLOGY
J1  - TOXICOL APPL PHARM
J2  - Toxicol.Appl.Pharmacol.
J3  - Toxicol Appl Pharmacol
J4  - Toxicology and Applied Pharmacology
VL  - 198
IS  - 2
SP  - 75
EP  - 85
ER  - 


TY  - JOUR
A1  - Graham, J 
A1  - Shaw, G M
T1  - Gene-environment interactions in rare diseases that include common birth defects.
Y1  - 2005/11/
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A: CLINICAL AND MOLECULAR TERATOLOGY
VL  - 73
IS  - 11
SP  - 865
EP  - 867
ER  - 


TY  - JOUR
A1  - Gupta, T 
A1  - Yang, W 
A1  - Lovannisci, D 
A1  - Carmichal, S 
A1  - Stevenson, D 
A1  - Shaw, G 
A1  - Lammer, E 
T1  - Considering the vascular hypothesis for the pathogenesis of small intestinal atresia: A case control study of genetic factors
Y1  - 2013//01
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS PART A
VL  - 161A
IS  - 4
SP  - 702
EP  - 710
ER  - 


TY  - JOUR
A1  - Iovannisci, D M
A1  - Kupperman, S O
A1  - Lloyd, E W
A1  - Lammer, E J
T1  - The READIT™ assay as a method for genotyping NAT1*10 polymorphisms.
Y1  - 2002//
N1  - R828292
JF  - GENETIC TESTING
J1  - GENET TEST
VL  - 6
IS  - 4
SP  - 245
EP  - 253
ER  - 


TY  - JOUR
A1  - Iovannisci, D M
A1  - Ha, T T
A1  - Shaw, G M
T1  - Recovery of genomic DNA from residual frozen archival blood clots suitable for amplification and use in genotyping assays.
Y1  - 2006//
N1  - R828292
JF  - GENETIC TESTING
J1  - GENET TEST
VL  - 10
IS  - 1
SP  - 44
EP  - 49
ER  - 


TY  - JOUR
A1  - Kuehl, K 
A1  - Loffredo, C 
A1  - Lammer, E 
A1  - Lovannisci, D 
A1  - Snaw, G 
T1  - Association of Congenital Cardiovascular Malformations with 33 Single Nucleotide Polymorphisms of Selected Cardiovascular Disease-Related Genes
Y1  - 2010//01
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A-CLINICAL AND MOLECULAR TERATOLOGY
VL  - 88
IS  - 2
SP  - 101
EP  - 110
ER  - 


TY  - JOUR
A1  - Lammer, E J
A1  - Shaw, G M
A1  - Iovannisci, D M
A1  - Van Waes, J 
T1  - Maternal smoking and the risk of orofacial clefts: susceptibility with <em>NAT1</em> and <em>NAT2</em> polymorphisms.
Y1  - 2004/03/
N1  - R828292
JF  - EPIDEMIOLOGY
J1  - EPIDEMIOLOGY
VL  - 15
IS  - 2
SP  - 150
EP  - 156
ER  - 


TY  - JOUR
A1  - Lammer, E J
A1  - Shaw, G M
A1  - Iovannisci, D M
A1  - Finnell, R H
T1  - Periconceptional multivitamin intake during early pregnancy, genetic variation of acetyl-<em>N</em>-transferase (<em>NAT1</em>), and risk for orofacial clefts.
Y1  - 2004/11/
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A: CLINICAL AND MOLECULAR TERATOLOGY
VL  - 70
IS  - 11
SP  - 846
EP  - 852
ER  - 


TY  - JOUR
A1  - Lammer, E J
A1  - Shaw, G M
A1  - Iovannisci, D M
A1  - Finnell, R H
T1  - Maternal smoking genetic variation of glutathione <em>S</em>-transferases, and risk for orofacial clefts.
Y1  - 2005/09/
N1  - R828292
JF  - EPIDEMIOLOGY
J1  - EPIDEMIOLOGY
VL  - 16
IS  - 5
SP  - 698
EP  - 701
ER  - 


TY  - JOUR
A1  - Lu, W 
A1  - Volcik, K A
A1  - Zhu, H 
A1  - Wen, S 
A1  - Yang, W 
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Finnell, R H
T1  - Genetic variation in the proto-oncogene <em>SKI </em> and risk for orofacial clefting.
Y1  - 2005/11/
N1  - R828292
JF  - MOLECULAR GENETICS AND METABOLISM
J1  - MOL GENET METAB
VL  - 86
IS  - 3
SP  - 412
EP  - 416
ER  - 


TY  - JOUR
A1  - Lu, W 
A1  - Zhu, H 
A1  - Wen, S 
A1  - Laurent, C 
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Finnell, R H
T1  - Screening for novel <em>PAX3</em> polymorphisms and risks of spina bifida.
Y1  - 2007/01/
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A: CLINICAL AND MOLECULAR TERATOLOGY
VL  - 79
IS  - 1
SP  - 45
EP  - 49
ER  - 


TY  - JOUR
A1  - Miller, S P
A1  - Wu, Y W
A1  - Lee, J 
A1  - Lammer, E J
A1  - Iovannisci, D M
A1  - Glidden, D V
A1  - Bonifacio, S L
A1  - Collins, A 
A1  - Shaw, G M
A1  - Barkovich, A J
A1  - Ferriero, D M
T1  - Candidate gene polymorphisms do not differ between newborns with stroke and normal controls.
Y1  - 2006/11/
N1  - R828292
JF  - STROKE
J1  - STROKE
VL  - 37
IS  - 11
SP  - 2678
EP  - 2683
ER  - 


TY  - JOUR
A1  - Olshan, A F
A1  - Shaw, G M
A1  - Millikan, R 
A1  - Laurent, C 
A1  - Finnell, R H
T1  - Polymorphisms in DNA repair genes as risk factors for spina bifida and orofacial clefts.
Y1  - 2005/06/15
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS PART A
VL  - 135A
IS  - 3
SP  - 268
EP  - 273
ER  - 


TY  - JOUR
A1  - Rull, R P
A1  - Ritz, B 
A1  - Shaw, G M
T1  - Validation of self-reported proximity to agricultural crops in a case-control study of neural tube defects.
Y1  - 2006/03/
N1  - R828292
JF  - JOURNAL OF EXPOSURE ANALYSIS AND ENVIRONMENTAL EPIDEMIOLOGY
J1  - J EXPO ANAL ENV EPID
J2  - J.Expo.Anal.Environ.Epidemiol.
J3  - J Expo Anal Environ Epidemiol
VL  - 16
IS  - 2
SP  - 147
EP  - 155
ER  - 


TY  - JOUR
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Zhu, H 
A1  - Baker, M W
A1  - Neri, E 
A1  - Finnell, R H
T1  - Maternal periconceptional vitamin use, genetic variation of infant reduced folate carrier (A80G), and risk of spina bifida.
Y1  - 2002//
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS
J1  - AM J MED GENET
VL  - 108
IS  - 1
SP  - 1
EP  - 6
ER  - 


TY  - JOUR
A1  - Shaw, G M
A1  - Nelson, V 
A1  - Iovannisci, D M
A1  - Finnell, R H
A1  - Lammer, E J
T1  - Maternal occupational chemical exposures and biotransformation genotypes as risk factors for selected congenital anomalies.
Y1  - 2003/03/15
N1  - R828292
JF  - AMERICAN JOURNAL OF EPIDEMIOLOGY
J1  - AM J EPIDEMIOL
J2  - Am.J.Epidemiol.
J3  - American Journal of Epidemiology
J4  - American Journal of Epidemiology
VL  - 157
IS  - 6
SP  - 475
EP  - 484
ER  - 


TY  - JOUR
A1  - Shaw, G M
A1  - Zhu, H 
A1  - Lammer, E J
A1  - Yang, W 
A1  - Finnell, R H
T1  - Genetic variation of infant reduced folate carrier (A80G) and risk of orofacial and conotruncal heart defects.
Y1  - 2003/10/15
N1  - R828292
JF  - AMERICAN JOURNAL OF EPIDEMIOLOGY
J1  - AM J EPIDEMIOL
J2  - Am.J.Epidemiol.
J3  - American Journal of Epidemiology
J4  - American Journal of Epidemiology
VL  - 158
IS  - 8
SP  - 747
EP  - 752
ER  - 


TY  - JOUR
A1  - Shaw, G M
A1  - Quach, T 
A1  - Nelson, V 
A1  - Carmichael, S L
A1  - Schaffer, D M
A1  - Selvin, S 
T1  - Neural tube defects in offspring associated with maternal periconceptional dietary intake of simple sugars and glycemic index.
Y1  - 2003//
N1  - R828292
JF  - AMERICAN JOURNAL OF CLINICAL NUTRITION
J1  - AM J CLIN NUTR
VL  - 78
IS  - 5
SP  - 972
EP  - 978
ER  - 


TY  - JOUR
A1  - Shaw, G M
A1  - Carmichael, S L
A1  - Yang, W 
A1  - Selvin, S 
T1  - Periconceptional dietary intake of choline and betaine and neural tube defects in offspring.
Y1  - 2004/07/15
N1  - R828292
JF  - AMERICAN JOURNAL OF EPIDEMIOLOGY
J1  - AM J EPIDEMIOL
J2  - Am.J.Epidemiol.
J3  - American Journal of Epidemiology
J4  - American Journal of Epidemiology
VL  - 160
IS  - 2
SP  - 102
EP  - 109
ER  - 


TY  - JOUR
A1  - Shaw, G M
A1  - Iovannisci, D M
A1  - Yang, W 
A1  - Finnell, R H
T1  - Endothelial nitric oxide synthase (<em>NOS3</em>) genetic variants, maternal smoking, vitamin use, and risk of human orofacial clefts.
Y1  - 2005/12/15
N1  - R828292
JF  - AMERICAN JOURNAL OF EPIDEMIOLOGY
J1  - AM J EPIDEMIOL
J2  - Am.J.Epidemiol.
J3  - American Journal of Epidemiology
J4  - American Journal of Epidemiology
VL  - 162
IS  - 12
SP  - 1207
EP  - 1214
ER  - 


TY  - JOUR
A1  - Shaw, G M
A1  - Carmichael, S L
A1  - Yang, W 
A1  - Schaffer, D M
T1  - Periconceptional dietary intake of myo-inositol and neural tube defects in offspring.
Y1  - 2005/03/
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A: CLINICAL AND MOLECULAR TERATOLOGY
VL  - 73
IS  - 3
SP  - 184
EP  - 187
ER  - 


TY  - JOUR
A1  - Shaw, G M
A1  - Iovannisci, D M
A1  - Yang, W 
A1  - Finnell, R H
A1  - Carmichael, S L
A1  - Cheng, S 
A1  - Lammer, E J
T1  - Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes.
Y1  - 2005/09/15
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS PART A
VL  - 138A
IS  - 19
SP  - 21
EP  - 26
ER  - 


TY  - JOUR
A1  - Shaw, G M
A1  - Carmichael, S L
A1  - Laurent, C 
A1  - Rasmussen, S A
T1  - Maternal nutrient intakes and risk of orofacial clefts.
Y1  - 2006/05/
N1  - R828292
JF  - EPIDEMIOLOGY
J1  - EPIDEMIOLOGY
VL  - 17
IS  - 3
SP  - 285
EP  - 291
ER  - 


TY  - JOUR
A1  - Torfs, C P
A1  - Christianson, R E
A1  - Iovannisci, D M
A1  - Shaw, G M
A1  - Lammer, E J
T1  - Selected gene polymorphisms and their interaction with maternal smoking, as risk factors for gastroschisis.
Y1  - 2006/10/
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A: CLINICAL AND MOLECULAR TERATOLOGY
VL  - 76
IS  - 10
SP  - 723
EP  - 730
ER  - 


TY  - JOUR
A1  - Volcik, K A
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Zhu, H 
A1  - Finnell, R H
T1  - Evaluation of infant methylenetetrahydrofolate reductase genotype, maternal vitamin use, and risk of high versus low level spina bifida defects.
Y1  - 2003/03/
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A: CLINICAL AND MOLECULAR TERATOLOGY
VL  - 67
IS  - 3
SP  - 154
EP  - 157
ER  - 


TY  - JOUR
A1  - Volcik, K A
A1  - Shaw, G M
A1  - Zhu, H 
A1  - Lammer, E J
A1  - Finnell, R H
T1  - Risk factors for neural tube defects: associations between uncoupling protein 2 polymorphisms and spina bifida.
Y1  - 2003/03/
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A: CLINICAL AND MOLECULAR TERATOLOGY
VL  - 67
IS  - 3
SP  - 158
EP  - 161
ER  - 


TY  - JOUR
A1  - Volcik, K A
A1  - Shaw, G M
A1  - Zhu, H 
A1  - Lammer, E J
A1  - Laurent, C 
A1  - Finnell, R H
T1  - Associations between polymorphisms within the thymidylate synthase gene and spina bifida.
Y1  - 2003/11/
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A: CLINICAL AND MOLECULAR TERATOLOGY
VL  - 67
IS  - 11
SP  - 924
EP  - 928
ER  - 


TY  - JOUR
A1  - Volcik, K A
A1  - Zhu, H 
A1  - Shaw, G M
A1  - Canfield, M 
A1  - Lammer, E J
A1  - Finnell, R H
T1  - Evaluation of the CITED2 gene and risk for spina bifida and congenital heart defects.
Y1  - 2004//
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS
J1  - AM J MED GENET
ER  - 


TY  - JOUR
A1  - Volcik, K A
A1  - Zhu, H 
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Finnell, R H
T1  - Jumonji gene and risk for spina bifida and congenital heart defects.
Y1  - 2004//
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS
J1  - AM J MED GENET
ER  - 


TY  - JOUR
A1  - Zhang, J 
A1  - Zhu, H 
A1  - Yang, W 
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Finnell, R H
T1  - Phosphatidylethanolamine <em>N</em>-methyltransferase (<em>PEMT</em>) gene polymorphisms and risk of spina bifida.
Y1  - 2006/04/01
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS PART A
VL  - 140A
IS  - 7
SP  - 785
EP  - 789
ER  - 


TY  - JOUR
A1  - Zhu, H P
A1  - Barber, R 
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Finnell, R H
T1  - Is Sonic hedgehog (SHH) a candidate gene for spina bifida? A pilot study.
Y1  - 2003/02/15
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS
J1  - AM J MED GENET
VL  - 117A
IS  - 1
SP  - 87
EP  - 88
ER  - 


TY  - JOUR
A1  - Zhu, H P
A1  - Wicker, N J
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Hendricks, K 
A1  - Suarez, L 
A1  - Canfield, M 
A1  - Finnell, R H
T1  - Homocysteine remethylation enzyme polymorphisms and increased risks for neural tube defects.
Y1  - 2003/03/
N1  - R828292
JF  - MOLECULAR GENETICS AND METABOLISM
J1  - MOL GENET METAB
VL  - 78
IS  - 3
SP  - 216
EP  - 221
ER  - 


TY  - JOUR
A1  - Zhu, H P
A1  - Wicker, N J
A1  - Volcik, K 
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Suarez, L 
A1  - Canfield, M 
A1  - Finnell, R H
T1  - Promoter haplotype combinations for the human <em>PDGFRA</em> gene are associated with risk of neural tube defects.
Y1  - 2004/02/
N1  - R828292
JF  - MOLECULAR GENETICS AND METABOLISM
J1  - MOL GENET METAB
VL  - 81
IS  - 2
SP  - 127
EP  - 132
ER  - 


TY  - JOUR
A1  - Zhu, H P
A1  - Curry, S 
A1  - Wen, S 
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Yang, W 
A1  - Jafarov, T 
A1  - Finnell, R H
T1  - Are the betaine-homocysteine methyltransferase (<em>BHMT</em> and <em>BHMT2</em>) genes risk factors for spina bifida and orofacial clefts?
Y1  - 2005/06/15
N1  - R828292
JF  - AMERICAN JOURNAL OF MEDICAL GENETICS PART A
VL  - 135A
IS  - 3
SP  - 274
EP  - 277
ER  - 


TY  - JOUR
A1  - Zhu, H P
A1  - Yang, W 
A1  - Lu, W 
A1  - Zhang, J 
T1  - A known functional polymorphism (Ile120Val) of the human <em>PCMT1</em> gene and risk of spina bifida.
Y1  - 2006/01/
N1  - R828292
JF  - MOLECULAR GENETICS AND METABOLISM
J1  - MOL GENET METAB
VL  - 87
IS  - 1
SP  - 66
EP  - 70
ER  - 


TY  - JOUR
A1  - Zhu, H 
A1  - Lu, W 
A1  - Laurent, C 
A1  - Shaw, G M
A1  - Lammer, E J
A1  - Finnell, R H
T1  - Genes encoding catalytic subunits of protein kinase A and risk of spina bifida.
Y1  - 2005//
N1  - R828292
JF  - BIRTH DEFECTS RESEARCH PART A: CLINICAL AND MOLECULAR TERATOLOGY
ER  -