-
1
-
-
0038167547
-
Recent developments in orofacial cleft genetics
-
Carinci F, Pezzetti F, Scapoli L, et al. Recent developments in orofacial cleft genetics. J Craniofac Surg 2003; 14: 130-143.
-
(2003)
J Craniofac Surg
, vol.14
, pp. 130-143
-
-
Carinci, F.1
Pezzetti, F.2
Scapoli, L.3
-
2
-
-
0035716321
-
Nonsyndromic cleft lip and palate: Complex genetics and environmental effects
-
Prescott NJ, Winter RM, Malcolm S. Nonsyndromic cleft lip and palate: complex genetics and environmental effects. Ann Hum Genet 2001; 65: 505-515.
-
(2001)
Ann Hum Genet
, vol.65
, pp. 505-515
-
-
Prescott, N.J.1
Winter, R.M.2
Malcolm, S.3
-
3
-
-
33847786727
-
Folic acid supplements and risk of facial clefts: National population based case-control study
-
Wilcox AJ, Lie RT, Solvoll K, et al. Folic acid supplements and risk of facial clefts: national population based case-control study. BMJ 2007; 334: 464.
-
(2007)
BMJ
, vol.334
, pp. 464
-
-
Wilcox, A.J.1
Lie, R.T.2
Solvoll, K.3
-
4
-
-
33845984049
-
Folic acid-containing supplement consumption during pregnancy and risk for oral clefts: A meta-analysis
-
Badovinac RL, Werler MM, Williams PL, Kelsey K T, Hayes C. Folic acid-containing supplement consumption during pregnancy and risk for oral clefts: a meta-analysis. Birth Defects Res A Clin Mol Teratol 2007; 79: 8-15.
-
(2007)
Birth Defects Res a Clin Mol Teratol
, vol.79
, pp. 8-15
-
-
Badovinac, R.L.1
Werler, M.M.2
Williams, P.L.3
Kelsey, K.T.4
Hayes, C.5
-
5
-
-
0034634007
-
Homocysteine inhibits retinoic acid synthesis: A mechanism for homocysteine-induced congenital defects
-
Limpach A, Dalton M, Miles R, Gadson P. Homocysteine inhibits retinoic acid synthesis: a mechanism for homocysteine-induced congenital defects. Exp Cell Res 2000; 260: 166-174.
-
(2000)
Exp Cell Res
, vol.260
, pp. 166-174
-
-
Limpach, A.1
Dalton, M.2
Miles, R.3
Gadson, P.4
-
6
-
-
0037295535
-
Homocysteine is embryotoxic but does not cause neural tube defects in mouse embryos
-
Greene ND, Dunlevy LE, Copp AJ. Homocysteine is embryotoxic but does not cause neural tube defects in mouse embryos. Anat Embryol (Berl) 2003; 206: 185-191.
-
(2003)
Anat Embryol (Berl)
, vol.206
, pp. 185-191
-
-
Greene, N.D.1
Dunlevy, L.E.2
Copp, A.J.3
-
7
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
Van der Put NM, Steegers-Theunissen R P, Frosst P, et al. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 1995; 346: 1070-1071.
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van der Put, N.M.1
Steegers-Theunissen, R.P.2
Frosst, P.3
-
8
-
-
0031971515
-
A second common mutation in the methylenetetrahydrofolate reductase gene: An additional risk factor for neural-tube defects?
-
Van der Put NM, Gabreels F, Stevens EM, et al. A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural-tube defects? Am J Hum Genet 1998; 62: 1044-1051.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1044-1051
-
-
Van der Put, N.M.1
Gabreels, F.2
Stevens, E.M.3
-
9
-
-
0034935450
-
Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease
-
Junker R, Kotthoff S, Vielhaber H, et al. Infant methylenetetrahydrofolate reductase 677TT genotype is a risk factor for congenital heart disease. Cardiovasc Res 2001; 51: 251-254.
-
(2001)
Cardiovasc Res
, vol.51
, pp. 251-254
-
-
Junker, R.1
Kotthoff, S.2
Vielhaber, H.3
-
10
-
-
0032802054
-
Methylenetetrahydrofolate reductase thermolabile variant and oral clefts
-
Mills JL, Kirke PN, Molloy AM, et al. Methylenetetrahydrofolate reductase thermolabile variant and oral clefts. Am J Med Genet 1999; 86: 71-74.
-
(1999)
Am J Med Genet
, vol.86
, pp. 71-74
-
-
Mills, J.L.1
Kirke, P.N.2
Molloy, A.M.3
-
11
-
-
0036096518
-
Maternal MTHFR genotype contributes to the risk of non-syndromic cleft lip and palate
-
Prescott NJ, Winter RM, Malcolm S. Maternal MTHFR genotype contributes to the risk of non-syndromic cleft lip and palate. J Med Genet 2002; 39: 368-369.
-
(2002)
J Med Genet
, vol.39
, pp. 368-369
-
-
Prescott, N.J.1
Winter, R.M.2
Malcolm, S.3
-
12
-
-
0031785528
-
Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip
-
Shaw GM, Rozen R, Finnell RH, Todoroff K, Lammer EJ. Infant C677T mutation in MTHFR, maternal periconceptional vitamin use, and cleft lip. Am J Med Genet 1998; 80: 196-198.
-
(1998)
Am J Med Genet
, vol.80
, pp. 196-198
-
-
Shaw, G.M.1
Rozen, R.2
Finnell, R.H.3
Todoroff, K.4
Lammer, E.J.5
-
13
-
-
0042415793
-
Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip
-
Shotelersuk V, Ittiwut C, Siriwan P, Angspatt A. Maternal 677CT/1298AC genotype of the MTHFR gene as a risk factor for cleft lip. J Med Genet 2003; 40: e64.
-
(2003)
J Med Genet
, vol.40
-
-
Shotelersuk, V.1
Ittiwut, C.2
Siriwan, P.3
Angspatt, A.4
-
14
-
-
0032751289
-
Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: Results from a case-control study in Brazil
-
Gaspar DA, Pavanello RC, Zatz M, et al. Role of the C677T polymorphism at the MTHFR gene on risk to nonsyndromic cleft lip with/without cleft palate: results from a case-control study in Brazil. Am J Med Genet 1999; 87: 197-199.
-
(1999)
Am J Med Genet
, vol.87
, pp. 197-199
-
-
Gaspar, D.A.1
Pavanello, R.C.2
Zatz, M.3
-
15
-
-
0037100024
-
MTHFR is not a risk factor in the development of isolated nonsyndromic cleft lip and palate
-
Blanton SH, Patel S, Hecht JT, Mulliken JB. MTHFR is not a risk factor in the development of isolated nonsyndromic cleft lip and palate. Am J Med Genet 2002; 110: 404-405.
-
(2002)
Am J Med Genet
, vol.110
, pp. 404-405
-
-
Blanton, S.H.1
Patel, S.2
Hecht, J.T.3
Mulliken, J.B.4
-
16
-
-
0038315197
-
Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian case-parent triads
-
Jugessur A, Wilcox AJ, Lie RT, et al. Exploring the effects of methylenetetrahydrofolate reductase gene variants C677T and A1298C on the risk of orofacial clefts in 261 Norwegian case-parent triads. Am J Epidemiol 2003; 157: 1083-1091.
-
(2003)
Am J Epidemiol
, vol.157
, pp. 1083-1091
-
-
Jugessur, A.1
Wilcox, A.J.2
Lie, R.T.3
-
17
-
-
0035254496
-
C677T variant form at the MTHFR gene and CL/P: A risk factor for mothers?
-
Martinelli M, Scapoli L, Pezzetti F, et al. C677T variant form at the MTHFR gene and CL/P: a risk factor for mothers? Am J Med Genet 2001; 98: 357-360.
-
(2001)
Am J Med Genet
, vol.98
, pp. 357-360
-
-
Martinelli, M.1
Scapoli, L.2
Pezzetti, F.3
-
18
-
-
7244219970
-
Maternal MTHFR variant forms increase the risk in offspring of isolated nonsyndromic cleft lip with or without cleft palate
-
Pezzetti F, Martinelli M, Scapoli L, et al. Maternal MTHFR variant forms increase the risk in offspring of isolated nonsyndromic cleft lip with or without cleft palate. Hum Mutat 2004; 24: 104-105.
-
(2004)
Hum Mutat
, vol.24
, pp. 104-105
-
-
Pezzetti, F.1
Martinelli, M.2
Scapoli, L.3
-
19
-
-
0242600545
-
Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate?
-
van Rooij IA, Vermeij-Keers C, Kluijtmans LA, et al. Does the interaction between maternal folate intake and the methylenetetrahydrofolate reductase polymorphisms affect the risk of cleft lip with or without cleft palate? Am J Epidemiol 2003; 157: 583-591.
-
(2003)
Am J Epidemiol
, vol.157
, pp. 583-591
-
-
van Rooij, I.A.1
Vermeij-Keers, C.2
Kluijtmans, L.A.3
-
20
-
-
33846807689
-
Fetal and maternal MTHFR C677T genotype, maternal folate intake and the risk of nonsyndromic oral clefts
-
Chevrier C, Perret C, Bahuau M, et al. Fetal and maternal MTHFR C677T genotype, maternal folate intake and the risk of nonsyndromic oral clefts. Am J Med Genet A 2007; 143: 248-257.
-
(2007)
Am J Med Genet A
, vol.143
, pp. 248-257
-
-
Chevrier, C.1
Perret, C.2
Bahuau, M.3
-
21
-
-
0034068966
-
Spina bifida and common mutations at the homocysteine metabolism pathway
-
Akar N, Akar E, Deda G, Arsan S. Spina bifida and common mutations at the homocysteine metabolism pathway. Clin Genet 2000; 57: 230-231.
-
(2000)
Clin Genet
, vol.57
, pp. 230-231
-
-
Akar, N.1
Akar, E.2
Deda, G.3
Arsan, S.4
-
22
-
-
0032587430
-
Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects
-
Boduroglu K, Alikasifoglu M, Anar B, Tuncbilek E. Association of the 677C-->T mutation on the methylenetetrahydrofolate reductase gene in Turkish patients with neural tube defects. J Child Neurol 1999; 14: 159-161.
-
(1999)
J Child Neurol
, vol.14
, pp. 159-161
-
-
Boduroglu, K.1
Alikasifoglu, M.2
Anar, B.3
Tuncbilek, E.4
-
23
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ. Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM). Am J Hum Genet 1993; 52: 506-516.
-
(1993)
Am J Hum Genet
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
24
-
-
77949272183
-
The maternal homocysteine pathway is influenced by riboflavin intake and MTHFR polymorphisms without affecting the risk of orofacial clefts in the offspring
-
Vujkovic M, Steegers EA, van Meurs J, et al. The maternal homocysteine pathway is influenced by riboflavin intake and MTHFR polymorphisms without affecting the risk of orofacial clefts in the offspring. Eur J Clin Nutr 2010; 64: 266-273.
-
(2010)
Eur J Clin Nutr
, vol.64
, pp. 266-273
-
-
Vujkovic, M.1
Steegers, E.A.2
van Meurs, J.3
-
25
-
-
38849187271
-
Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts
-
Boyles AL, Wilcox AJ, Taylor JA, et al. Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts. Am J Med Genet A 2008; 146A: 440-449.
-
(2008)
Am J Med Genet A
, vol.146 A
, pp. 440-449
-
-
Boyles, A.L.1
Wilcox, A.J.2
Taylor, J.A.3
-
26
-
-
34247844422
-
Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: A meta-analysis
-
Verkleij-Hagoort A, Bliek J, Sayed-Tabatabaei F, et al. Hyperhomocysteinemia and MTHFR polymorphisms in association with orofacial clefts and congenital heart defects: a meta-analysis. Am J Med Genet A 2007; 143A: 952-960.
-
(2007)
Am J Med Genet A
, vol.143 A
, pp. 952-960
-
-
Verkleij-Hagoort, A.1
Bliek, J.2
Sayed-Tabatabaei, F.3
-
27
-
-
75449117469
-
MTHFR, TGFB3, and TGFA polymorphisms and their association with the risk of non-syndromic cleft lip and cleft palate in China
-
Zhu J, Hao L, Li S, Bailey LB, Tian Y, Li Z. MTHFR, TGFB3, and TGFA polymorphisms and their association with the risk of non-syndromic cleft lip and cleft palate in China. Am J Med Genet A 2010; 152A: 291-298.
-
(2010)
Am J Med Genet A
, vol.152 A
, pp. 291-298
-
-
Zhu, J.1
Hao, L.2
Li, S.3
Bailey, L.B.4
Tian, Y.5
Li, Z.6
-
28
-
-
33644859355
-
Variable contribution of the MTHFR C677T polymorphism to non-syndromic cleft lip and palate risk in China
-
Zhu J, Ren A, Hao L, et al. Variable contribution of the MTHFR C677T polymorphism to non-syndromic cleft lip and palate risk in China. Am J Med Genet A 2006; 140: 551-557.
-
(2006)
Am J Med Genet A
, vol.140
, pp. 551-557
-
-
Zhu, J.1
Ren, A.2
Hao, L.3
-
29
-
-
33750731645
-
Folic acid rivals methylenetetrahydrofolate reductase (MTHFR) gene-silencing effect on MEPM cell proliferation and apoptosis
-
Xiao WL, Wu M, Shi B. Folic acid rivals methylenetetrahydrofolate reductase (MTHFR) gene-silencing effect on MEPM cell proliferation and apoptosis. Mol Cell Biochem 2006; 292: 145-154.
-
(2006)
Mol Cell Biochem
, vol.292
, pp. 145-154
-
-
Xiao, W.L.1
Wu, M.2
Shi, B.3
-
30
-
-
79955846242
-
Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defects
-
Blom HJ, Smulders Y. Overview of homocysteine and folate metabolism. With special references to cardiovascular disease and neural tube defects. J Inherit Metab Dis 2011; 34: 75-81.
-
(2011)
J Inherit Metab Dis
, vol.34
, pp. 75-81
-
-
Blom, H.J.1
Smulders, Y.2
-
31
-
-
0034743914
-
The 1298A->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): In vitro expression and association with homocysteine
-
Weisberg IS, Jacques P F, Selhub J, et al. The 1298A->C polymorphism in methylenetetrahydrofolate reductase (MTHFR): in vitro expression and association with homocysteine. Atherosclerosis 2001; 156: 409-415.
-
(2001)
Atherosclerosis
, vol.156
, pp. 409-415
-
-
Weisberg, I.S.1
Jacques, P.F.2
Selhub, J.3
|