-
1
-
-
0034190659
-
5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: A HuGe review
-
Botto LD, Yang Q. 5,10-Methylenetetrahydrofolate reductase gene variants and congenital anomalies: a HuGe review. Am J Epidemiol 2000; 151: 862-877.
-
(2000)
Am J Epidemiol
, vol.151
, pp. 862-877
-
-
Botto, L.D.1
Yang, Q.2
-
2
-
-
0027409267
-
Center for Disease Control and Prevention (CDCP) recommendations for use of folic acid to reduce number of spina bifida cases and other neural tube defects
-
Center for Disease Control and Prevention (CDCP) recommendations for use of folic acid to reduce number of spina bifida cases and other neural tube defects. JAMA 1993; 269: 1233-1238.
-
(1993)
JAMA
, vol.269
, pp. 1233-1238
-
-
-
3
-
-
0033156107
-
Neural tube defects in Turkey: Prevalence, distribution and risk factors
-
Tuncbilek E, Boduroglu K, Alikasifoglu M. Neural tube defects in Turkey: prevalence, distribution and risk factors. Turk J Pediatr 1999; 41: 299-305.
-
(1999)
Turk J Pediatr
, vol.41
, pp. 299-305
-
-
Tuncbilek, E.1
Boduroglu, K.2
Alikasifoglu, M.3
-
4
-
-
0027080461
-
Prevention of the first occurrence of neural tube defects by periconceptional vitamin supplementation
-
Czeizel AE, Dudas I. Prevention of the first occurrence of neural tube defects by periconceptional vitamin supplementation. N Engl J Med 1992; 327: 1832-1835.
-
(1992)
N Engl J Med
, vol.327
, pp. 1832-1835
-
-
Czeizel, A.E.1
Dudas, I.2
-
5
-
-
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; 341: 131-137.
-
(1991)
Lancet
, vol.341
, pp. 131-137
-
-
-
6
-
-
0032906750
-
Polymorphisms of methylenetet rahydrofolate reductase and other enzymes: Metabolic significance, risks, and impact on folate requirement
-
Bailey LB, Gregory J. Polymorphisms of methylenetet rahydrofolate reductase and other enzymes: metabolic significance, risks, and impact on folate requirement. J Nutr 1999; 129: 919-922.
-
(1999)
J Nutr
, vol.129
, pp. 919-922
-
-
Bailey, L.B.1
Gregory, J.2
-
7
-
-
0029049553
-
A candidate genetic risk factor for vascular disease: A common mutation in methylenetetrahydrofolate reductase
-
Frosst P, Blom HJ, Milos R, et al. A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 1995; 10: 111-113.
-
(1995)
Nat Genet
, vol.10
, pp. 111-113
-
-
Frosst, P.1
Blom, H.J.2
Milos, R.3
-
8
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
van der Put NM, Steegers-Theunissen RP, 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
-
9
-
-
0028803474
-
A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects
-
Whitehead AS, Gallagher P, Mills JL, et al. A genetic defect in 5,10 methylenetetrahydrofolate reductase in neural tube defects. Q J Med 1995; 88: 763-766.
-
(1995)
Q J Med
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
-
10
-
-
0030018760
-
5,10 methyle netetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
-
Ou CY, Stevenson RE, Brown VY, et al. 5,10 methyle netetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. Am J Med Genet 1996; 63: 610-614.
-
(1996)
Am J Med Genet
, vol.63
, pp. 610-614
-
-
Ou, C.Y.1
Stevenson, R.E.2
Brown, V.Y.3
-
11
-
-
0032937206
-
Genetic polymorphisms in methylenetetrahydrofolate reductase and methionine synthase, folate levels in red blood cells, and risk of neural tube defects
-
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.
-
(1999)
Am J Med Genet
, vol.84
, pp. 151-157
-
-
Christensen, B.1
Arbour, L.2
Tran, P.3
-
12
-
-
17344370082
-
The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy
-
de Francis R, Buoninconti A, Mandato C, et al. The C677T mutation of the 5,10-methylenetetrahydrofolate reductase gene is a moderate risk factor for spina bifida in Italy. J Med Genet 1998; 35: 1009-1013.
-
(1998)
J Med Genet
, vol.35
, pp. 1009-1013
-
-
de Francis, R.1
Buoninconti, A.2
Mandato, C.3
-
13
-
-
0033365197
-
The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: An evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother
-
Shields DC, Kirke PN, Mills JL, et al. The "thermolabile" variant of methylenetetrahydrofolate reductase and neural tube defects: an evaluation of genetic risk and the relative importance of the genotypes of the embryo and the mother. Am J Hum Genet 1999; 64: 1045-1055.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1045-1055
-
-
Shields, D.C.1
Kirke, P.N.2
Mills, J.L.3
-
14
-
-
0032587430
-
Association of the 677C→T mutation on the methylenetetrahydro folate reductase gene in Turkish patients with neural tube defects
-
Boduroglu K, Alikasifoglu M, Anar B, et al. Association of the 677C→T mutation on the methylenetetrahydro folate 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
-
15
-
-
0031429097
-
Screening of the C677T mutation on the methylenetetrahydrof olate reductase gene in French patients with neural tube defects
-
Mornet E, Muller F, Lenvoisé-Furet A, et al. Screening of the C677T mutation on the methylenetetrahydrof olate reductase gene in French patients with neural tube defects. Hum Genet 1997; 100: 512-514.
-
(1997)
Hum Genet
, vol.100
, pp. 512-514
-
-
Mornet, E.1
Muller, F.2
Lenvoisé-Furet, A.3
-
16
-
-
0032448182
-
Susceptibility to spina bifida; an association study of five candidate genes
-
Morrison K, Papapetrou C, Hol FA, et al. Susceptibility to spina bifida; an association study of five candidate genes. Ann Hum Genet 1998; 62: 379-396.
-
(1998)
Ann Hum Genet
, vol.62
, pp. 379-396
-
-
Morrison, K.1
Papapetrou, C.2
Hol, F.A.3
-
17
-
-
0035067094
-
Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population
-
Richter B, Stegmann K, Röper B, et al. Interaction of folate and homocysteine pathway genotypes evaluated in susceptibility to neural tube defects (NTD) in a German population. J Hum Genet 2001; 46: 105-109.
-
(2001)
J Hum Genet
, vol.46
, pp. 105-109
-
-
Richter, B.1
Stegmann, K.2
Röper, B.3
-
18
-
-
0033623867
-
The effect of 677C→T and 1298A→C mutations on plasma homocysteine and 5,10- methylenetetrahydrofolate reductase activity in healthy subjects
-
Chango A, Boisson F, Barbe F, et al. The effect of 677C→T and 1298A→C mutations on plasma homocysteine and 5,10- methylenetetrahydrofolate reductase activity in healthy subjects. Br J Nutr 2000; 83: 593-596.
-
(2000)
Br J Nutr
, vol.83
, pp. 593-596
-
-
Chango, A.1
Boisson, F.2
Barbe, F.3
-
19
-
-
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 BE, 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, B.E.3
-
20
-
-
0037908697
-
Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects
-
Parle-McDermott A, Mills JL, Kirke PN, et al. Analysis of the MTHFR 1298A→C and 677C→T polymorphisms as risk factors for neural tube defects. J Hum Genet 2003; 48: 190-193.
-
(2003)
J Hum Genet
, vol.48
, pp. 190-193
-
-
Parle-McDermott, A.1
Mills, J.L.2
Kirke, P.N.3
-
21
-
-
0041320771
-
Methyle netetrahydrofolate reductase (MTHFR): Incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida
-
Perez ABA, D'Almeida V, Vergani N, et al. Methyle netetrahydrofolate reductase (MTHFR): incidence of mutations C677T and A1298C in Brazilian population and its correlation with plasma homocysteine levels in spina bifida. Am J Med Genet 2003; 119A: 20-25.
-
(2003)
Am J Med Genet
, vol.119 A
, pp. 20-25
-
-
Perez, A.B.A.1
D'Almeida, V.2
Vergani, N.3
-
22
-
-
0035987006
-
Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population
-
De Marco P, Calevo MG, Moroni A, et al. Study of MTHFR and MS polymorphisms as risk factors for NTD in the Italian population. J Hum Genet 2002; 47: 319-324.
-
(2002)
J Hum Genet
, vol.47
, pp. 319-324
-
-
De Marco, P.1
Calevo, M.G.2
Moroni, A.3
-
23
-
-
0032845227
-
Abnormal folate metabolism and mutation in the methylenete trahydrofolate reductase gene may be maternal risk factors for Down syndrome
-
James SJ, Pogribna M, Pogribny IP, et al. Abnormal folate metabolism and mutation in the methylenete trahydrofolate reductase gene may be maternal risk factors for Down syndrome. Am J Clin Nutr 1999; 70: 495-501.
-
(1999)
Am J Clin Nutr
, vol.70
, pp. 495-501
-
-
James, S.J.1
Pogribna, M.2
Pogribny, I.P.3
-
24
-
-
0033527788
-
Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects (NTD)
-
Stegmann K, Ziegler A, Ngo ET, et al. Linkage disequilibrium of MTHFR genotypes 677C/T-1298A/C in the German population and association studies in probands with neural tube defects (NTD). Am J Med Genet 1999; 87: 23-29.
-
(1999)
Am J Med Genet
, vol.87
, pp. 23-29
-
-
Stegmann, K.1
Ziegler, A.2
Ngo, E.T.3
-
25
-
-
0031687887
-
A second genetic polymorphism in methylenete trahydrofolate reductase (MTHFR) associated with decreased enzyme activity
-
Weisberg I, Tran P, Christensen B, Sibani S, Rozen R. A second genetic polymorphism. in methylenete trahydrofolate reductase (MTHFR) associated with decreased enzyme activity. Molec Genet Metabol 1998; 63: 169-172.
-
(1998)
Molec Genet Metabol
, vol.63
, pp. 169-172
-
-
Weisberg, I.1
Tran, P.2
Christensen, B.3
Sibani, S.4
Rozen, R.5
-
26
-
-
0035864690
-
The effect of the C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase gene on homocysteine levels in elderly men and women from the British regional heart study
-
Dekou V, Whincup P, Papacosta O, et al. The effect of the C677T and A1298C polymorphisms in the methylenetetrahydrofolate reductase gene on homocysteine levels in elderly men and women from the British regional heart study. Atherosclerosis 2001; 154: 659-666.
-
(2001)
Atherosclerosis
, vol.154
, pp. 659-666
-
-
Dekou, V.1
Whincup, P.2
Papacosta, O.3
-
27
-
-
0035870245
-
Methylenetetrahydrofola te reductase polymorphisms increase risk of esophageal squamous cell carcinoma in a Chinese population
-
Song C, Xing D, Tan W, et al. Methylenetetrahydrofola te reductase polymorphisms increase risk of esophageal squamous cell carcinoma in a Chinese population. Cancer Res 2001; 61: 3272-3275.
-
(2001)
Cancer Res
, vol.61
, pp. 3272-3275
-
-
Song, C.1
Xing, D.2
Tan, W.3
-
28
-
-
0034068966
-
Spina bifida and common mutations at the homocysteine metabolism pathway
-
Akar N, Akar E, Deda G, et al. 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
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