-
1
-
-
73149102059
-
Prevalence of autism spectrum disorders-autism and developmental disabilities monitoring network, United States
-
Prevalence of autism spectrum disorders-autism and developmental disabilities monitoring network, United States, 2006. MMWR Surveill Summ. 2009;58:1-20.
-
(2006)
MMWR Surveill Summ
, vol.2009
, Issue.58
, pp. 1-20
-
-
-
2
-
-
67349152455
-
The rise in autism and the role of age at diagnosis
-
Hertz-Picciotto I, Delwiche L. The rise in autism and the role of age at diagnosis. Epidemiology. 2009;20:84-90.
-
(2009)
Epidemiology
, vol.20
, pp. 84-90
-
-
Hertz-Picciotto, I.1
Delwiche, L.2
-
3
-
-
34249735268
-
The epidemiology of autism spectrum disorders
-
DOI 10.1146/annurev.publhealth.28.021406.144007
-
Newschaffer CJ, Croen LA, Daniels J, et al. The epidemiology of autism spectrum disorders. Annu Rev Public Health. 2007;28:235-258. (Pubitemid 46833342)
-
(2007)
Annual Review of Public Health
, vol.28
, pp. 235-258
-
-
Newschaffer, C.J.1
Croen, L.A.2
Daniels, J.3
Giarelli, E.4
Grether, J.K.5
Levy, S.E.6
Mandell, D.S.7
Miller, L.A.8
Pinto-Martin, J.9
Reaven, J.10
Reynolds, A.M.11
Rice, C.E.12
Schendel, D.13
Windham, G.C.14
-
4
-
-
79551532813
-
Closely spaced pregnancies are associated with increased odds of autism in California sibling births
-
Cheslack-Postava K, Liu K, Bearman PS. Closely spaced pregnancies are associated with increased odds of autism in California sibling births. Pediatrics. 2011;127:246-253.
-
(2011)
Pediatrics
, vol.127
, pp. 246-253
-
-
Cheslack-Postava, K.1
Liu, K.2
Bearman, P.S.3
-
5
-
-
0029990539
-
Embryological origin for autism: Developmental anomalies of the cranial nerve motor nuclei
-
DOI 10.1002/(SICI)1096-9861(19960624)370:2<247::AID-CNE8>3.0.CO;2-2
-
Rodier PM, Ingram JL, Tisdale B, Nelson S, Romano J. Embryological origin for autism: developmental anomalies of the cranial nerve motor nuclei. J Comp Neurol. 1996;370:247-261. (Pubitemid 26227148)
-
(1996)
Journal of Comparative Neurology
, vol.370
, Issue.2
, pp. 247-261
-
-
Rodier, P.M.1
Ingram, J.L.2
Tisdale, B.3
Nelson, S.4
Romano, J.5
-
6
-
-
0025863475
-
Prevention of neural tube defects: Results of the Medical Research Council Vitamin Study
-
MRC Vitamin Study Research Group
-
MRC Vitamin Study Research Group.Prevention of neural tube defects: results of the Medical Research Council Vitamin Study. Lancet 1991; 338:131-137.
-
(1991)
Lancet
, vol.338
, pp. 131-137
-
-
-
7
-
-
77953033904
-
Folate and methionine metabolism in autism: A systematic review
-
Main PA, Angley MT, Thomas P, O'Doherty CE, Fenech M. Folate and methionine metabolism in autism: a systematic review. Am J Clin Nutr. 2010;91:1598-1620.
-
(2010)
Am J Clin Nutr
, vol.91
, pp. 1598-1620
-
-
Main, P.A.1
Angley, M.T.2
Thomas, P.3
O'doherty, C.E.4
Fenech, M.5
-
8
-
-
34447643277
-
Preliminary evidence for involvement of the folate gene polymorphism 19 bp deletion-DHFR in occurrence of autism
-
DOI 10.1016/j.neulet.2007.05.025, PII S0304394007005988
-
Adams M, Lucock M, Stuart J, Fardell S, Baker K, Ng X. Preliminary evidence for involvement of the folate gene polymorphism 19bp deletion- DHFR in occurrence of autism. Neurosci Lett. 2007;422:24-29. (Pubitemid 47086296)
-
(2007)
Neuroscience Letters
, vol.422
, Issue.1
, pp. 24-29
-
-
Adams, M.1
Lucock, M.2
Stuart, J.3
Fardell, S.4
Baker, K.5
Ng, X.6
-
10
-
-
33845438146
-
Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism
-
DOI 10.1002/ajmg.b.30366
-
James SJ, Melnyk S, Jernigan S, et al. Metabolic endophenotype and related genotypes are associated with oxidative stress in children with autism. Am J Med Genet B Neuropsychiatr Genet. 2006;141:947-956. (Pubitemid 44905454)
-
(2006)
American Journal of Medical Genetics, Part B: Neuropsychiatric Genetics
, vol.141
, Issue.8
, pp. 947-956
-
-
James, S.J.1
Melnyk, S.2
Jernigan, S.3
Cleves, M.A.4
Halsted, C.H.5
Wong, D.H.6
Cutler, P.7
Bock, K.8
Boris, M.9
Bradstreet, J.J.10
Baker, S.M.11
Gaylor, D.W.12
-
11
-
-
77956111572
-
A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism
-
James SJ, Melnyk S, Jernigan S, et al. A functional polymorphism in the reduced folate carrier gene and DNA hypomethylation in mothers of children with autism. Am J Med Genet B Neuropsychiatr Genet. 2010; 153B:1209-1220.
-
(2010)
Am J Med Genet B Neuropsychiatr Genet
, vol.153 B
, pp. 1209-1220
-
-
James, S.J.1
Melnyk, S.2
Jernigan, S.3
-
12
-
-
0036126756
-
12, and the 5,10- methylenetetrahydrofolate reductase 677C→T variant
-
DOI 10.1067/mob.2002.121105
-
Molloy AM, Mills JL, McPartlin J, Kirke PN, Scott JM, Daly S. Maternal and fetal plasma homocysteine concentrations at birth: the influence of folate, vitamin B12, and the 5,10-methylenetetrahydrofolate reductase 677C->T variant. Am J Obstet Gynecol. 2002;186:499-503. (Pubitemid 34234164)
-
(2002)
American Journal of Obstetrics and Gynecology
, vol.186
, Issue.3
, pp. 499-503
-
-
Molloy, A.M.1
Mills, J.L.2
McPartlin, J.3
Kirke, P.N.4
Scott, J.M.5
Daly, S.6
-
13
-
-
33745787015
-
The CHARGE study: An epidemiologic investigation of genetic and environmental factors contributing to autism
-
DOI 10.1289/ehp.8483
-
Hertz-Picciotto I, Croen LA, Hansen R, Jones CR, van de Water J, Pessah IN. The CHARGE study: an epidemiologic investigation of genetic and environmental factors contributing to autism. Environ Health Perspect. 2006;114:1119-1125. (Pubitemid 44018911)
-
(2006)
Environmental Health Perspectives
, vol.114
, Issue.7
, pp. 1119-1125
-
-
Hertz-Picciotto, I.1
Croen, L.A.2
Hansen, R.3
Jones, C.R.4
Van De Water, J.5
Pessah, I.N.6
-
14
-
-
0027997172
-
Autism diagnostic interview-revised: A revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders
-
DOI 10.1007/BF02172145
-
Lord C, Rutter M, Le Couteur A. Autism diagnostic interview-revised: a revised version of a diagnostic interview for caregivers of individuals with possible pervasive developmental disorders. J Autism Dev Disord. 1994;24:659-685. (Pubitemid 24309810)
-
(1994)
Journal of Autism and Developmental Disorders
, vol.24
, Issue.5
, pp. 659-685
-
-
Lord, C.1
Rutter, M.2
Couteur, A.L.3
-
15
-
-
0033802632
-
The autism diagnostic observation schedule-generic: A standard measure of social and communication deficits associated with the spectrum of autism
-
Lord C, Risi S, Lambrecht L, et al. The autism diagnostic observation schedule-generic: a standard measure of social and communication deficits associated with the spectrum of autism. J Autism Dev Disord. 2000;30:205-223.
-
(2000)
J Autism Dev Disord
, vol.30
, pp. 205-223
-
-
Lord, C.1
Risi, S.2
Lambrecht, L.3
-
16
-
-
33748417617
-
Combining information from multiple sources in the diagnosis of autism spectrum disorders
-
DOI 10.1097/01.chi.0000227880.42780.0e, PII 0000458320060900000009
-
Risi S, Lord C, Gotham K, et al. Combining information from multiple sources in the diagnosis of autism spectrum disorders. J Am Acad Child Adolesc Psychiatry. 2006;45:1094-1103. (Pubitemid 44343065)
-
(2006)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.45
, Issue.9
, pp. 1094-1103
-
-
Risi, S.1
Lord, C.2
Gotham, K.3
Corsello, C.4
Chrysler, C.5
Szatmari, P.6
Cook, E.H.7
Leventhal, B.L.8
Pickles, A.9
-
17
-
-
25444463596
-
A hybrid design for studying genetic influences on risk of diseases with onset early in life
-
DOI 10.1086/496900
-
Weinberg CR, Umbach DM. A hybrid design for studying genetic influences on risk of diseases with onset early in life. Am J Hum Genet. 2005;77:627-636. (Pubitemid 41361609)
-
(2005)
American Journal of Human Genetics
, vol.77
, Issue.4
, pp. 627-636
-
-
Weinberg, C.R.1
Umbach, D.M.2
-
18
-
-
33947432843
-
Survey research methods in evaluation and case-control studies
-
DOI 10.1002/sim.2796
-
Kalton G, Piesse A. Survey research methods in evaluation and casecontrol studies. Stat Med. 2007;26:1675-1687. (Pubitemid 46455627)
-
(2007)
Statistics in Medicine
, vol.26
, Issue.8
, pp. 1675-1687
-
-
Kalton, G.1
Piesse, A.2
-
21
-
-
77449157341
-
Maternal folic acid supplement use in early pregnancy and child behavioural problems: The Generation R Study
-
Roza SJ, van Batenburg-Eddes T, Steegers EA, et al. Maternal folic acid supplement use in early pregnancy and child behavioural problems: The Generation R Study. Br J Nutr. 2010;103:445-452.
-
(2010)
Br J Nutr
, vol.103
, pp. 445-452
-
-
Roza, S.J.1
Van Batenburg-Eddes, T.2
Steegers, E.A.3
-
22
-
-
63449111562
-
Maternal use of folic acid supplements during pregnancy and four-yearold neurodevelopment in a population-based birth cohort
-
Julvez J, Fortuny J, Mendez M, Torrent M, Ribas-Fito N, Sunyer J. Maternal use of folic acid supplements during pregnancy and four-yearold neurodevelopment in a population-based birth cohort. Paediatr Perinat Epidemiol. 2009;23:199-206.
-
(2009)
Paediatr Perinat Epidemiol
, vol.23
, pp. 199-206
-
-
Julvez, J.1
Fortuny, J.2
Mendez, M.3
Torrent, M.4
Ribas-Fito, N.5
Sunyer, J.6
-
23
-
-
77950405455
-
Lower maternal folate status in early pregnancy is associated with childhood hyperactivity and peer problems in offspring
-
Schlotz W, Jones A, Phillips DI, Gale CR, Robinson SM, Godfrey KM. Lower maternal folate status in early pregnancy is associated with childhood hyperactivity and peer problems in offspring. J Child Psychol Psychiatry. 2010;51:594-602.
-
(2010)
J Child Psychol Psychiatry
, vol.51
, pp. 594-602
-
-
Schlotz, W.1
Jones, A.2
Phillips, D.I.3
Gale, C.R.4
Robinson, S.M.5
Godfrey, K.M.6
-
24
-
-
0035234557
-
Genomic imprinting: Parental influence on the genome
-
DOI 10.1038/35047554
-
Reik W, Walter J. Genomic imprinting: parental influence on the genome. Nat Rev Genet. 2001;2:21-32. (Pubitemid 33674766)
-
(2001)
Nature Reviews Genetics
, vol.2
, Issue.1
, pp. 21-32
-
-
Reik, W.1
Walter, J.2
-
25
-
-
0036322831
-
Maternal methyl supplements in mice affect epigenetic variation and DNA methylation of offspring
-
Cooney CA, Dave AA, Wolff GL. Maternal methyl supplements in mice affect epigenetic variation and DNA methylation of offspring. J Nutr2002;132(suppl 8):2393S-2400S. (Pubitemid 34848114)
-
(2002)
Journal of Nutrition
, vol.132
, Issue.8 SUPPL.
-
-
Cooney, C.A.1
Dave, A.A.2
Wolff, G.L.3
-
26
-
-
70649097099
-
Periconceptional maternal folic acid use of 400 microg per day is related to increased methylation of the IGF2 gene in the very young child
-
Steegers-Theunissen RP, Obermann-Borst SA, Kremer D, et al. Periconceptional maternal folic acid use of 400 microg per day is related to increased methylation of the IGF2 gene in the very young child. PLoS One. 2009;4:e7845.
-
(2009)
PLoS One
, vol.4
-
-
Steegers-Theunissen, R.P.1
Obermann-Borst, S.A.2
Kremer, D.3
-
27
-
-
33749007122
-
Epigenetics of autism spectrum disorders
-
DOI 10.1093/hmg/ddl213
-
Schanen NC. Epigenetics of autism spectrum disorders. Hum Mol Genet. 2006;15(spec no 2):R138-R150. (Pubitemid 44446787)
-
(2006)
Human Molecular Genetics
, vol.15
, Issue.SUPPL. 2
-
-
Schanen, N.C.1
-
28
-
-
65349184462
-
Folic acid, methylation and neural tube closure in humans
-
Blom HJ. Folic acid, methylation and neural tube closure in humans. Birth Defects Res A Clin Mol Teratol. 2009;85:295-302.
-
(2009)
Birth Defects Res A Clin Mol Teratol
, vol.85
, pp. 295-302
-
-
Blom, H.J.1
-
29
-
-
59149091750
-
The role of iron in neurodevelopment: Fetal iron deficiency and the developing hippocampus
-
Georgieff MK. The role of iron in neurodevelopment: fetal iron deficiency and the developing hippocampus. Biochem Soc Trans. 2008; 36(pt 6):1267-1271.
-
(2008)
Biochem Soc Trans
, vol.36
, Issue.PART 6
, pp. 1267-1271
-
-
Georgieff, M.K.1
-
30
-
-
34247589073
-
The methylenetetrahydrofolate reductase 677C→T polymorphism as a modulator of a B vitamin network with major effects on homocysteine metabolism
-
DOI 10.1086/513520
-
Hustad S, Midttun O, Schneede J, Vollset SE, Grotmol T, Ueland PM. The methylenetetrahydrofolate reductase 677C->T polymorphism as a modulator of a B vitamin network with major effects on homocysteine metabolism. Am J Hum Genet. 2007;80:846-855. (Pubitemid 46668453)
-
(2007)
American Journal of Human Genetics
, vol.80
, Issue.5
, pp. 846-855
-
-
Hustad, S.1
Midttun, O.2
Schneede, J.3
Vollset, S.E.4
Grotmol, T.5
Ueland, P.M.6
-
31
-
-
54049150738
-
Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates
-
Lopreato FR, Stabler SP, Carvalho FR, et al. Relationships between gene polymorphisms of folate-related proteins and vitamins and metabolites in pregnant women and neonates. Clin Chim Acta. 2008;398:134-139.
-
(2008)
Clin Chim Acta
, vol.398
, pp. 134-139
-
-
Lopreato, F.R.1
Stabler, S.P.2
Carvalho, F.R.3
-
32
-
-
33749428869
-
Neural tube defects and folate pathway genes: Family-based association tests of gene-gene and gene-environment interactions
-
DOI 10.1289/ehp.9166
-
Boyles AL, Billups AV, Deak KL, et al. Neural tube defects and folate pathway genes: family-based association tests of gene-gene and geneenvironment interactions. Environ Health Perspect. 2006;114:1547-1552. (Pubitemid 44509653)
-
(2006)
Environmental Health Perspectives
, vol.114
, Issue.10
, pp. 1547-1552
-
-
Boyles, A.L.1
Billups, A.V.2
Deak, K.L.3
Siegel, D.G.4
Mehltretter, L.5
Slifer, S.H.6
Bassuk, A.G.7
Kessler, J.A.8
Reed, M.C.9
Nijhout, H.F.10
George, T.M.11
Enterline, D.S.12
Gilbert, J.R.13
Speer, M.C.14
Aben, J.15
Alysworth, A.16
Bodurtha, J.17
Brei, T.18
Buran, C.19
Iskandar, B.20
Ito, J.21
Lasarsky, N.22
Mack, P.23
Meeropol, E.24
Mackey, J.25
McLone, D.26
Oakes, W.J.27
Powell, C.28
Sawin, K.29
Walker, M.30
Worley, G.31
more..
-
33
-
-
0032937206
-
Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects
-
DOI 10.1002/(SICI)1096-8628(19990521)84:2<151::AID-AJMG12>3.0.CO;2- T
-
Christensen B, Arbour L, Tran P, et al. Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects. Am J Med Genet. 1999;84:151-157. (Pubitemid 29201082)
-
(1999)
American Journal of Medical Genetics
, vol.84
, Issue.2
, pp. 151-157
-
-
Christensen, B.1
Arbour, L.2
Tran, P.3
Leclerc, D.4
Sabbaghian, N.5
Platt, R.6
Gilfix, B.M.7
Rosenblatt, D.S.8
Gravel, R.A.9
Forbes, P.10
Rozen, R.11
-
34
-
-
0032856882
-
12) increases risk for spina bifida
-
DOI 10.1006/mgme.1999.2879
-
Wilson A, Platt R, Wu Q, et al. A common variant in methionine synthase reductase combined with low cobalamin (vitamin B12) increases risk for spina bifida. Mol Genet Metab. 1999;67:317-323. (Pubitemid 29406795)
-
(1999)
Molecular Genetics and Metabolism
, vol.67
, Issue.4
, pp. 317-323
-
-
Wilson, A.1
Platt, R.2
Wu, Q.3
Leclerc, D.4
Christensen, B.5
Yang, H.6
Gravel, R.A.7
Rozen, R.8
-
35
-
-
0019417904
-
Decreased transmethylation of biogenic amines after in vivo elevation of brain S-adenosyl-L-homocysteine
-
DOI 10.1111/j.1471-4159.1981.tb00426.x
-
Schatz RA, Wilens TE, Sellinger OZ. Decreased transmethylation of biogenic amines after in vivo elevation of brain S-adenosyl-l-homocysteine. J Neurochem. 1981;36:1739-1748. (Pubitemid 11083547)
-
(1981)
Journal of Neurochemistry
, vol.36
, Issue.5
, pp. 1739-1748
-
-
Schatz, R.A.1
Wilens, T.E.2
Sellinger, O.Z.3
-
36
-
-
0014237840
-
Catechol-O-methyl transferase and monoamine oxidase activities in the heart and liver of the embryonic and developing chick
-
Ignarro LJ, Shideman FE. Catechol-O-methyl transferase and monoamine oxidase activities in the heart and liver of the embryonic and developing chick. J Pharmacol Exp Ther. 1968;159:29-37.
-
(1968)
J Pharmacol Exp Ther
, vol.159
, pp. 29-37
-
-
Ignarro, L.J.1
Shideman, F.E.2
-
37
-
-
60349116939
-
Impact of interacting functional variants in COMT on regional gray matter volume in human brain
-
Honea R, Verchinski BA, Pezawas L, et al. Impact of interacting functional variants in COMT on regional gray matter volume in human brain. Neuroimage. 2009;45:44-51.
-
(2009)
Neuroimage
, vol.45
, pp. 44-51
-
-
Honea, R.1
Verchinski, B.A.2
Pezawas, L.3
-
38
-
-
0035810850
-
108/158 Met genotype on frontal lobe function and risk for schizophrenia
-
DOI 10.1073/pnas.111134598
-
Egan MF, Goldberg TE, Kolachana BS, et al. Effect of COMT Val108/ 158 Met genotype on frontal lobe function and risk for schizophrenia. Proc Natl Acad Sci U S A. 2001;98:6917-6922. (Pubitemid 32538317)
-
(2001)
Proceedings of the National Academy of Sciences of the United States of America
, vol.98
, Issue.12
, pp. 6917-6922
-
-
Egan, M.F.1
Goldberg, T.E.2
Kolachana, B.S.3
Callicott, J.H.4
Mazzanti, C.M.5
Straub, R.E.6
Goldman, D.7
Weinberger, D.R.8
-
39
-
-
0242637444
-
BDNF gene expression is reduced in the frontal cortex of dopamine transporter knockout mice
-
Fumagalli F, Racagni G, Colombo E, Riva MA. BDNF gene expression is reduced in the frontal cortex of dopamine transporter knockout mice. Mol Psychiatry. 2003;8:898-899.
-
(2003)
Mol Psychiatry
, vol.8
, pp. 898-899
-
-
Fumagalli, F.1
Racagni, G.2
Colombo, E.3
Riva, M.A.4
-
40
-
-
78649622917
-
Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism
-
Correia CT, Coutinho AM, Sequeira AF, et al. Increased BDNF levels and NTRK2 gene association suggest a disruption of BDNF/TrkB signaling in autism. Genes Brain Behav. 2010;9:841-848.
-
(2010)
Genes Brain Behav
, vol.9
, pp. 841-848
-
-
Correia, C.T.1
Coutinho, A.M.2
Sequeira, A.F.3
-
41
-
-
0030004521
-
Human catechol-O-methyltransferase pharmacogenetics: Description of a functional polymorphism and its potential application to neuropsychiatric disorders
-
DOI 10.1097/00008571-199606000-00007
-
Lachman HM, Papolos DF, Saito T, Yu YM, Szumlanski CL, Weinshilboum RM. Human catechol-O-methyltransferase pharmacogenetics: description of a functional polymorphism and its potential application to neuropsychiatric disorders. Pharmacogenetics. 1996;6:243-250. (Pubitemid 26226317)
-
(1996)
Pharmacogenetics
, vol.6
, Issue.3
, pp. 243-250
-
-
Lachman, H.M.1
Papolos, D.F.2
Saito, T.3
Yu, Y.-M.4
Szumlanski, C.L.5
Weinshilboum, R.M.6
-
42
-
-
33646344731
-
The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: Evidence and lessons
-
Craddock N, Owen MJ, O'Donovan MC. The catechol-O-methyl transferase (COMT) gene as a candidate for psychiatric phenotypes: evidence and lessons. Mol Psychiatry. 2006;11:446-458.
-
(2006)
Mol Psychiatry
, vol.11
, pp. 446-458
-
-
Craddock, N.1
Owen, M.J.2
O'donovan, M.C.3
-
43
-
-
33748426974
-
The 22q11.2 deletion in children: High rate of autistic disorders and early onset of psychotic symptoms
-
DOI 10.1097/01.chi.0000228131.56956.c1, PII 0000458320060900000010
-
Vorstman JA, Morcus ME, Duijff SN, et al. The 22q11.2 deletion in children: high rate of autistic disorders and early onset of psychotic symptoms. J Am Acad Child Adolesc Psychiatry. 2006;45:1104-1113. (Pubitemid 44343066)
-
(2006)
Journal of the American Academy of Child and Adolescent Psychiatry
, vol.45
, Issue.9
, pp. 1104-1113
-
-
Vorstman, J.A.S.1
Morcus, M.E.J.2
Duijff, S.N.3
Klaassen, P.W.J.4
Heineman-De Boer, J.A.5
Beemer, F.A.6
Swaab, H.7
Kahn, R.S.8
Van Engeland, H.9
-
44
-
-
25444478031
-
Use of dietary supplements containing folic acid among women of childbearing age: United States
-
Centers for Disease Control and Prevention
-
Centers for Disease Control and Prevention. Use of dietary supplements containing folic acid among women of childbearing age: United States, 2005. Morb Mortal Wkly Rep. 2005;54:955-958.
-
(2005)
Morb Mortal Wkly Rep
, vol.2005
, Issue.54
, pp. 955-958
-
-
-
45
-
-
0024534022
-
Reporting accuracy among mothers of malformed and nonmalformed infants
-
Werler MM, Pober BR, Nelson K, Holmes LB. Reporting accuracy among mothers of malformed and nonmalformed infants. Am J Epidemiol. 1989;129:415-421. (Pubitemid 19047007)
-
(1989)
American Journal of Epidemiology
, vol.129
, Issue.2
, pp. 415-421
-
-
Werler, M.M.1
Pober, B.R.2
Nelson, K.3
Holmes, L.B.4
-
46
-
-
73649084816
-
Reproducibility of reported nutrient intake and supplement use during a past pregnancy: A report from the Children's Oncology Group
-
Bosco JL, Tseng M, Spector LG, Olshan AF, Bunin GR. Reproducibility of reported nutrient intake and supplement use during a past pregnancy: a report from the Children's Oncology Group. Paediatr Perinat Epidemiol. 2010;24:93-101.
-
(2010)
Paediatr Perinat Epidemiol
, vol.24
, pp. 93-101
-
-
Bosco, J.L.1
Tseng, M.2
Spector, L.G.3
Olshan, A.F.4
Bunin, G.R.5
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