-
1
-
-
0029029002
-
Incidence of congenital heart disease I. Postnatal incidence
-
Hoffman JI. Incidence of congenital heart disease: I. Postnatal incidence. Pediatr Cardiol 1995;16:103-13.
-
(1995)
Pediatr Cardiol
, vol.16
, pp. 103-113
-
-
Hoffman, J.I.1
-
2
-
-
0029000773
-
Incidence of congenital heart disease: II Prenatal incidence
-
Hoffman JI. Incidence of congenital heart disease: II. Prenatal incidence. Pediatr Cardiol 1995;16:155-65.
-
(1995)
Pediatr Cardiol
, vol.16
, pp. 155-165
-
-
Hoffman, J.I.1
-
3
-
-
0027154167
-
Causes of congenital heart diseases: Old and new modes, mechanisms, and models
-
DOI 10.1016/0002-8703(93)91014-6
-
Nora JJ. Causes of congenital heart diseases: Old and new modes, mechanisms, and models. Am Heart J 1993;125: 1409-19. (Pubitemid 23134549)
-
(1993)
American Heart Journal
, vol.125
, Issue.5
, pp. 1409-1419
-
-
Nora, J.J.1
-
4
-
-
0032583944
-
Recurrence risks in offspring of adults with major heart defects: Results from first cohort of British collaborative study
-
DOI 10.1016/S0140-6736(97)06486-6
-
Burn J, Brennan P, Little J, Holloway S, Coffey R, Somerville J, et al. Recurrence risks in offspring of adults with major heart defects: Results from first cohort of British collaborative study. Lancet 1998;351:311-6. (Pubitemid 28052695)
-
(1998)
Lancet
, vol.351
, Issue.9099
, pp. 311-316
-
-
Burn, J.1
Brennan, P.2
Little, J.3
Holloway, S.4
Coffey, R.5
Somerville, J.6
Dennis, N.R.7
Allan, L.8
Arnold, R.9
Deanfield, J.E.10
Godman, M.11
Houston, A.12
Keeton, B.13
Oakley, C.14
Scott, O.15
Silove, E.16
Wilkinson, J.17
Pembrey, M.18
Hunter, A.S.19
-
5
-
-
0017840201
-
The evolution of specific genetic and environmental counseling in congenital heart diseases
-
Nora JJ, Nora AH. The evolution of specific genetic and environmental counseling in congenital heart diseases. Circulation 1978;57:205-13. (Pubitemid 8277770)
-
(1978)
Circulation
, vol.57
, Issue.2
, pp. 205-213
-
-
Nora, J.J.1
Nora, A.H.2
-
6
-
-
0028487161
-
Erratum: Human methylenetetrahydrofolate reductase: Isolation of cDNA, mapping and mutation identification (Nature Genetics (1994) 7 (195-200))
-
Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, et al. Human methylenetetrahydrofolate reductase: Isolation of cDNA mapping and mutation identification. Nat Genet 1994;7:551. (Pubitemid 24308346)
-
(1994)
Nature Genetics
, vol.7
, Issue.4
, pp. 551
-
-
Goyette, P.1
Sumner, J.S.2
Milos, R.3
Duncan, A.M.V.4
Rosenblatt, D.S.5
Matthews, R.G.6
Rozen, R.7
-
7
-
-
0031904465
-
Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR)
-
DOI 10.1007/s003359900838
-
Goyette P, Pai A, Milos R, Frosst P, Tran P, Chen Z, et al. Gene structure of human and mouse methylenetetrahydrofolate reductase (MTHFR). Mamm Genome 1998;9:652-6. (Pubitemid 28355328)
-
(1998)
Mammalian Genome
, vol.9
, Issue.8
, pp. 652-656
-
-
Goyette, P.1
Pai, A.2
Milos, R.3
Frosst, P.4
Tran, P.5
Chen, Z.6
Chan, M.7
Rozen, R.8
-
8
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, Goyette P, Sheppard CA, Matthews RG, et al. A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995;10:111-3.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
Goyette, P.4
Sheppard, C.A.5
Matthews, R.G.6
-
9
-
-
0029738540
-
The common 'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia
-
Harmon DL, Woodside JV, Yarnell JW, McMaster D, Young IS, McCrum EE, et al. The common'thermolabile' variant of methylene tetrahydrofolate reductase is a major determinant of mild hyperhomocysteinaemia. QJM 1996;89:571-7. (Pubitemid 26278868)
-
(1996)
QJM - Monthly Journal of the Association of Physicians
, vol.89
, Issue.8
, pp. 571-577
-
-
Harmon, D.L.1
Woodside, J.V.2
Yarnell, J.W.G.3
McMaster, D.4
Young, I.S.5
McCrum, E.E.6
Gey, K.F.7
Whitehead, A.S.8
Evans, A.E.9
-
10
-
-
0029816188
-
Molecular genetics of methylenetetrahydrofolate reductase deficiency
-
Rozen R. Molecular genetics of methylenetetrahydrofolate reductase deficiency. J Inherit Metab Dis 1996;19:589-94. (Pubitemid 26315907)
-
(1996)
Journal of Inherited Metabolic Disease
, vol.19
, Issue.5
, pp. 589-594
-
-
Rozen, R.1
-
11
-
-
20544456441
-
Folic acid supplementation and the occurrence of congenital heart defects, orofacial clefts, multiple births, and miscarriage
-
Bailey LB, Berry RJ. Folic acid supplementation and the occurrence of congenital heart defects, orofacial clefts, multiple births, and miscarriage. Am J Clin Nutr 2005;81:1213S-7S. (Pubitemid 41724972)
-
(2005)
American Journal of Clinical Nutrition
, vol.81
, Issue.5
-
-
Bailey, L.B.1
Berry, R.J.2
-
12
-
-
64149102559
-
Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations
-
Tanaka T, Scheet P, Giusti B, Bandinelli S, Piras MG, Usala G, et al. Genome-wide association study of vitamin B6, vitamin B12, folate, and homocysteine blood concentrations. Am J Hum Genet 2009;84:477-82.
-
(2009)
Am J Hum Genet
, vol.84
, pp. 477-482
-
-
Tanaka, T.1
Scheet, P.2
Giusti, B.3
Bandinelli, S.4
Piras, M.G.5
Usala, G.6
-
13
-
-
77953617511
-
MTHFR c.1793G) A polymorphism is associated with congenital cardiac disease in a Chinese population
-
Xu J, Xu X, Xue L, Liu X, Gu H, Cao H, et al. MTHFR c.1793G) A polymorphism is associated with congenital cardiac disease in a Chinese population. Cardiol Young 2010; 20:318-26.
-
(2010)
Cardiol Young
, vol.20
, pp. 318-326
-
-
Xu, J.1
Xu, X.2
Xue, L.3
Liu, X.4
Gu, H.5
Cao, H.6
-
14
-
-
70350319243
-
The methylenetetrahydrofolate reductase gene variant (C677T) as a susceptibility gene for tetralogy of Fallot
-
Marinho C, Alho I, Guerra A, Rego C, Areias J, Bicho M. The methylenetetrahydrofolate reductase gene variant (C677T) as a susceptibility gene for tetralogy of Fallot. Rev Port Cardiol 2009;28:809-12.
-
(2009)
Rev Port Cardiol
, vol.28
, pp. 809-812
-
-
Marinho, C.1
Alho, I.2
Guerra, A.3
Rego, C.4
Areias, J.5
Bicho, M.6
-
15
-
-
33645096433
-
Maternal and offspring MTHFR gene C677T polymorphism as predictors of congenital atrial septal defect and patent ductus arteriosus
-
Zhu WL, Li Y, Yan L, Dao J, Li S. Maternal and offspring MTHFR gene C677T polymorphism as predictors of congenital atrial septal defect and patent ductus arteriosus. Mol Hum Reprod 2006;12:51-4.
-
(2006)
Mol Hum Reprod
, vol.12
, pp. 51-54
-
-
Zhu, W.L.1
Li, Y.2
Yan, L.3
Dao, J.4
Li, .S.5
-
16
-
-
28344454474
-
Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases
-
Lee CN, Su YN, Cheng WF, Lin MT, Wang JK, Wu MH, et al. Association of the C677T methylenetetrahydrofolate reductase mutation with congenital heart diseases. Acta Obstet Gyn Scan 2005;84:1134-40.
-
(2005)
Acta Obstet Gyn Scan
, vol.84
, pp. 1134-1140
-
-
Lee, C.N.1
Su, Y.N.2
Cheng, W.F.3
Lin, M.T.4
Wang, J.K.5
Wu, M.H.6
-
17
-
-
24344454621
-
Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes
-
DOI 10.1002/ajmg.a.30924
-
Shaw GM, Iovannisci DM, Yang W, Finnell RH, Carmichael SL, Cheng S, et al. Risks of human conotruncal heart defects associated with 32 single nucleotide polymorphisms of selected cardiovascular disease-related genes. Am J Med Genet A 2005; 138:21-6. (Pubitemid 41262639)
-
(2005)
American Journal of Medical Genetics
, vol.138 A
, Issue.1
, pp. 21-26
-
-
Shaw, G.M.1
Iovannisci, D.M.2
Yang, W.3
Finnell, R.H.4
Carmichael, S.L.5
Cheng, S.6
Lammer, E.J.7
-
18
-
-
37549037491
-
The MTHFR 677C-)T polymorphism and the risk of congenital heart defects: A literature review and meta-analysis
-
van Beynum IM, den Heijer M, Blom HJ, Kapusta L. The MTHFR 677C-)T polymorphism and the risk of congenital heart defects: A literature review and meta-analysis. QJM 2007;100:743-53.
-
(2007)
QJM
, vol.100
, pp. 743-753
-
-
Van Beynum, I.M.1
Den Heijer, M.2
Blom, H.J.3
Kapusta, L.4
-
19
-
-
34247844422
-
Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: A meta-analysis
-
DOI 10.1002/ajmg.a.31684
-
Verkleij-Hagoort A, Bliek J, Sayed-Tabatabaei F, Ursem N, Steegers E, Steegers-Theunissen R. Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: A meta-analysis. Am J Med Genet A 2007;143A:952-60. (Pubitemid 46700901)
-
(2007)
American Journal of Medical Genetics, Part A
, vol.143
, Issue.9
, pp. 952-960
-
-
Verkleij-Hagoort, A.1
Bliek, J.2
Sayed-Tabatabaei, F.3
Ursem, N.4
Steegers, E.5
Steegers-Theunissen, R.6
-
20
-
-
77955152092
-
Maternal folate-related gene environment interactions and congenital heart defects
-
Hobbs CA, Cleves MA, Karim MA, Zhao W, MacLeod SL. Maternal folate-related gene environment interactions and congenital heart defects. Obstet Gynecol 2010;116:316-22.
-
(2010)
Obstet Gynecol
, vol.116
, pp. 316-322
-
-
Hobbs, C.A.1
Cleves, M.A.2
Karim, M.A.3
Zhao, W.4
MacLeod, S.L.5
-
21
-
-
34547807717
-
Association of congenital cardiac defects and the C677T methylenetetrahydrofolate reductase polymorphism
-
DOI 10.1002/pd.1761
-
Wintner S, Hafner E, Stonek F, Stuempflen I, Metzenbauer M, Philipp K. Association of congenital cardiac defects and the C677T methylenetetrahydrofolate reductase polymorphism. Prenatal Diag 2007;27:704-8. (Pubitemid 47242399)
-
(2007)
Prenatal Diagnosis
, vol.27
, Issue.8
, pp. 704-708
-
-
Wintner, S.1
Hafner, E.2
Stonek, F.3
Stuempflen, I.4
Metzenbauer, M.5
Philipp, K.6
-
22
-
-
77953415047
-
MTHFR polymorphisms in Puerto Rican children with isolated congenital heart disease and their mothers
-
Garcia-Fragoso L, Garcia-Garcia I, Leavitt G, Renta J, Ayala MA, Cadilla CL. MTHFR polymorphisms in Puerto Rican children with isolated congenital heart disease and their mothers. Int J Genet Mol Biol 2010;2:43-7.
-
(2010)
Int J Genet Mol Biol
, vol.2
, pp. 43-47
-
-
Garcia-Fragoso, L.1
Garcia-Garcia, I.2
Leavitt, G.3
Renta, J.4
Ayala, M.A.5
Cadilla, C.L.6
-
23
-
-
77956235500
-
Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome
-
Locke AE, Dooley KJ, Tinker SW, Cheong SY, Feingold E, Allen EG, et al. Variation in folate pathway genes contributes to risk of congenital heart defects among individuals with Down syndrome. Genet Epidemiol 2010;34:613-23.
-
(2010)
Genet Epidemiol
, vol.34
, pp. 613-623
-
-
Locke, A.E.1
Dooley, K.J.2
Tinker, S.W.3
Cheong, S.Y.4
Feingold, E.5
Allen, E.G.6
-
24
-
-
76749142411
-
Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes
-
Kuehl K, Loffredo C, Lammer EJ, Iovannisci DM, Shaw GM. Association of congenital cardiovascular malformations with 33 single nucleotide polymorphisms of selected cardiovascular disease-related genes. Birth Defects Res A Clin Mol Teratol 2010;88:101-10.
-
(2010)
Birth Defects Res A Clin Mol Teratol
, vol.88
, pp. 101-110
-
-
Kuehl, K.1
Loffredo, C.2
Lammer, E.J.3
Iovannisci, D.M.4
Shaw, G.M.5
-
25
-
-
78651302650
-
Congenital heart defects and biomarkers of methylation in children: A case-control study
-
Obermann-Borst SA, Van Driel LM, Helbing WA, De Jonge R, Wildhagen MF, Steegers EA, et al. Congenital heart defects and biomarkers of methylation in children: A case-control study. Eur J Clin Invest 2011;41:143-50.
-
(2011)
Eur J Clin Invest
, vol.41
, pp. 143-150
-
-
Obermann-Borst, S.A.1
Van Driel, L.M.2
Helbing, W.A.3
De Jonge, R.4
Wildhagen, M.F.5
Steegers, E.A.6
-
26
-
-
46449086503
-
Two MTHFR polymorphisms, maternal B-vitamin intake, and CHDs
-
DOI 10.1002/bdra.20463
-
van Driel LM, Verkleij-Hagoort AC, de Jonge R, Uitterlinden AG, Steegers EA, van Duijn CM, et al. Two MTHFR polymorphisms, maternal B-vitamin intake, and CHDs. Birth Defects Res A Clin Mol Teratol 2008;82:474-81. (Pubitemid 351928452)
-
(2008)
Birth Defects Research Part A - Clinical and Molecular Teratology
, vol.82
, Issue.6
, pp. 474-481
-
-
Van Driel, L.M.J.W.1
Verkleij-Hagoort, A.C.2
De Jonge, R.3
Uitterlinden, A.G.4
Steegers, E.A.P.5
Van Duijn, C.M.6
Steegers-Theunissen, R.P.M.7
-
27
-
-
33846177202
-
Homocysteine concentrations and molecular analysis in patients with congenital heart defects
-
DOI 10.1016/j.arcmed.2006.09.012, PII S0188440906003420
-
Galdieri LC, Arrieta SR, Silva CM, Pedra CA, D'Almeida V. Homocysteine concentrations and molecular analysis in patients with congenital heart defects. Arch Med Res 2007;38:212-8. (Pubitemid 46080545)
-
(2007)
Archives of Medical Research
, vol.38
, Issue.2
, pp. 212-218
-
-
Galdieri, L.C.1
Arrieta, S.R.2
Silva, C.M.C.3
Pedra, C.A.C.4
D'Almeida, V.5
-
28
-
-
33645473405
-
Maternal MTHFR 677C)T is a risk factor for congenital heart defects: Effect modification by periconceptional folate supplementation
-
van Beynum IM, Kapusta L, den Heijer M, Vermeulen SH, Kouwenberg M, Daniels O, et al. Maternal MTHFR 677C)T is a risk factor for congenital heart defects: Effect modification by periconceptional folate supplementation. Eur Heart J 2006; 27:981-7.
-
(2006)
Eur Heart J
, vol.27
, pp. 981-987
-
-
Van Beynum, I.M.1
Kapusta, L.2
Den Heijer, M.3
Vermeulen, S.H.4
Kouwenberg, M.5
Daniels, O.6
-
29
-
-
0037256945
-
Association between 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and conotruncal heart defects
-
DOI 10.1515/CCLM.2003.043
-
Storti S, Vittorini S, Lascone MR, Sacchelli M, Collavoli A, Ripoli A, et al. Association between 5,10-methylenetetrahydrofolate reductase C677T and A1298C polymorphisms and conotruncal heart defects. Clin Chem Lab Med 2003;41:276-80. (Pubitemid 36432832)
-
(2003)
Clinical Chemistry and Laboratory Medicine
, vol.41
, Issue.3
, pp. 276-280
-
-
Storti, S.1
Vittorini, S.2
Iascone, M.R.3
Sacchelli, M.4
Collavoli, A.5
Ripoli, A.6
Cocchi, G.7
Biagini, A.8
Clerico, A.9
-
30
-
-
0034935450
-
Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease
-
DOI 10.1016/S0008-6363(01)00286-3, PII S0008636301002863
-
Junker R, Kotthoff S, Vielhaber H, Halimeh S, Kosch A, Koch HG, et al. Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease. Cardiovasc Res 2001;51:251-4. (Pubitemid 32695535)
-
(2001)
Cardiovascular Research
, vol.51
, Issue.2
, pp. 251-254
-
-
Junker, R.1
Kotthoff, S.2
Vielhaber, H.3
Halimeh, S.4
Kosch, A.5
Koch, H.-G.6
Kassenbohmer, R.7
Heineking, B.8
Nowak-Gottl, U.9
-
31
-
-
67649209221
-
118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects
-
Shaw GM, Lu W, Zhu H, Yang W, Briggs FB, Carmichael SL, et al. 118 SNPs of folate-related genes and risks of spina bifida and conotruncal heart defects. BMC Med Genet 2009;10:49.
-
(2009)
BMC Med Genet
, vol.10
, pp. 49
-
-
Shaw, G.M.1
Lu, W.2
Zhu, H.3
Yang, W.4
Briggs, F.B.5
Carmichael, S.L.6
-
32
-
-
0035064154
-
Association of the C677T methylenetetrahydrofolate reductase mutation and elevated homocysteine levels with congenital cardiac malformations
-
discussion12-7
-
Wenstrom KD, Johanning GL, Johnston KE, DuBard M. Association of the C677T methylenetetrahydrofolate reductase mutation and elevated homocysteine levels with congenital cardiac malformations. Am J Obstet Gynecol 2001;184:806-12; discussion 12-7.
-
(2001)
Am J Obstet Gynecol
, vol.184
, pp. 806-812
-
-
Wenstrom, K.D.1
Johanning, G.L.2
Johnston, K.E.3
Dubard, M.4
-
33
-
-
84960989652
-
On estimating the relation between blood group and disease
-
Woolf B. On estimating the relation between blood group and disease. Ann Hum Genet 1955;19:251-3.
-
(1955)
Ann Hum Genet
, vol.19
, pp. 251-253
-
-
Woolf, B.1
-
34
-
-
84959801619
-
Statistical aspects of the analysis of data from retrospective studies of disease
-
Mantel N, Haenszel W. Statistical aspects of the analysis of data from retrospective studies of disease. J Natl Cancer Inst 1959;22:719-48.
-
(1959)
J Natl Cancer Inst
, vol.22
, pp. 719-748
-
-
Mantel, N.1
Haenszel, W.2
-
35
-
-
0022992740
-
Meta-analysis in clinical trials
-
DOI 10.1016/0197-2456(86)90046-2
-
DerSimonian R, Laird N. Meta-analysis in clinical trials. Control Clin Trials 1986;7:177-88. (Pubitemid 17189972)
-
(1986)
Controlled Clinical Trials
, vol.7
, Issue.3
, pp. 177-188
-
-
DerSimonian, R.1
Laird, N.2
-
37
-
-
0030922816
-
Bias in meta-analysis detected by a simple, graphical test
-
Egger M, Davey Smith G, Schneider M, Minder C. Bias in meta-analysis detected by a simple, graphical test. BMJ 1997; 315:629-34. (Pubitemid 27387172)
-
(1997)
British Medical Journal
, vol.315
, Issue.7109
, pp. 629-634
-
-
Egger, M.1
Smith, G.D.2
Schneider, M.3
Minder, C.4
|