-
1
-
-
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, Mattews RG, Boers GJ, den Heijer M, Kluijtmans LA, van der Heuvel LP, Rozen R (1995) A candidate genetic risk factor for vascular disease: a common mutation in methylenetetrahydrofolate reductase. Nat Genet 10:111-113
-
(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
Mattews, R.G.6
Boers, G.J.7
Den Heijer, M.8
Kluijtmans, L.A.9
Van Der Heuvel, L.P.10
Rozen, R.11
-
2
-
-
0035313224
-
Biological and clinical implications of the mthfr c677t polymorphism
-
Ueland PM, Hustad S, Schneede J, Refsum H, Vollset SE (2001) Biological and clinical implications of the MTHFR C677T polymorphism. Trends Pharmacol Sci 22:195-201
-
(2001)
Trends Pharmacol Sci
, vol.22
, pp. 195-201
-
-
Ueland, P.M.1
Hustad, S.2
Schneede, J.3
Refsum, H.4
Vollset, S.E.5
-
3
-
-
0029921114
-
Hyperhomocysteinemia as a risk factor for deep-vein thrombosis
-
den Heijer M, Koster T, Blom HJ, Bos GM, Briet E, Reitsma PH, Vandenbroucke JP, Rosendaal FR (1996) Hyperhomocysteinemia as a risk factor for deep-vein thrombosis. N Engl J Med 334:759-762
-
(1996)
N Engl J Med
, vol.334
, pp. 759-762
-
-
Den Heijer, M.1
Koster, T.2
Blom, H.J.3
Bos, G.M.4
Briet, E.5
Reitsma, P.H.6
Vandenbroucke, J.P.7
Rosendaal, F.R.8
-
4
-
-
0031454443
-
Hyperhomocysteinemia and venous thromboembolic disease
-
D'Angelo A, Mazzola G, Crippa L, Fermo I, Vigano D'Angelo S (1997) Hyperhomocysteinemia and venous thromboembolic disease. Haematologica 82:211-219
-
(1997)
Haematologica
, vol.82
, pp. 211-219
-
-
D'Angelo, A.1
Mazzola, G.2
Crippa, L.3
Fermo, I.4
Vigano D'Angelo, S.5
-
5
-
-
0028833677
-
Homocysteine metabolism in pregnancies complicated by neural tube defects
-
Mills JL, McPartlin JM, Kirke PN, Lee YJ, Conley MR, Weir DG, Scott JM (1995) Homocysteine metabolism in pregnancies complicated by neural tube defects. Lancet 345:149-151
-
(1995)
Lancet
, vol.345
, pp. 149-151
-
-
Mills, J.L.1
McPartlin, J.M.2
Kirke, P.N.3
Lee, Y.J.4
Conley, M.R.5
Weir, D.G.6
Scott, J.M.7
-
6
-
-
0027330937
-
Hyperhomocysteinemia: A risk factor in women with unexplained recurrent early pregnancy loss
-
Wouters MG, Boers GH, Blom HJ, Trijbels FJ, Thomas CM, Borm GF, Steegers-Theunissen RP, Eskes TK (1993) Hyperhomocysteinemia: a risk factor in women with unexplained recurrent early pregnancy loss. Fertil Steril 60:820-825
-
(1993)
Fertil Steril
, vol.60
, pp. 820-825
-
-
Wouters, M.G.1
Boers, G.H.2
Blom, H.J.3
Trijbels, F.J.4
Thomas, C.M.5
Borm, G.F.6
Steegers-Theunissen, R.P.7
Eskes, T.K.8
-
7
-
-
0028487161
-
Human methylenetetrahydrofolate reductase: Isolation of cdna, mapping and mutation identification
-
Goyette P, Sumner JS, Milos R, Duncan AM, Rosenblatt DS, Matthews RG, Rozen R (1994) Human methylenetetrahydrofolate reductase: isolation of cDNA, mapping and mutation identification. Nat Genet 7:195-200
-
(1994)
Nat Genet
, vol.7
, pp. 195-200
-
-
Goyette, P.1
Sumner, J.S.2
Milos, R.3
Duncan, A.M.4
Rosenblatt, D.S.5
Matthews, R.G.6
Rozen, R.7
-
8
-
-
0031687887
-
A second genetic polymorphism in methylenetehydrofolate reductase (mthfr) association with decreased enzyme activity
-
Weiberg I, Tran P, Christensen B, Sibani S, Rozen R (1998) A second genetic polymorphism in methylenetehydrofolate reductase (MTHFR) association with decreased enzyme activity. Mol Genet Metab 64:169-172
-
(1998)
Mol Genet Metab
, vol.64
, pp. 169-172
-
-
Weiberg, I.1
Tran, P.2
Christensen, B.3
Sibani, S.4
Rozen, R.5
-
9
-
-
0037117501
-
A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic dna methylation through an interaction with folate status
-
Friso S, Choi S, Girelli D, Mason JB, Dolnikowski GG, Bagley PJ, Olivieri O, Jacques PF, Rosenberg IH, Corrocher R, Seihub J (2002) A common mutation in the 5,10-methylenetetrahydrofolate reductase gene affects genomic DNA methylation through an interaction with folate status. Proc Natl Acad Sci USA 99:5606-5611
-
(2002)
Proc Natl Acad Sci USA
, vol.99
, pp. 5606-5611
-
-
Friso, S.1
Choi, S.2
Girelli, D.3
Mason, J.B.4
Dolnikowski, G.G.5
Bagley, P.J.6
Olivieri, O.7
Jacques, P.F.8
Rosenberg, I.H.9
Corrocher, R.10
Seihub, J.11
-
10
-
-
0031971515
-
A second common mutation in the methylenetetrahydrofolate reductase gene: An additional risk factor for neural tube defects?
-
van der Put NMJ, Gabreels F, Stevens EM, Smeitink JA, Trijbels FJ, Eskes TK, van den Heuvel LP, Blom HJ (1998) A second common mutation in the methylenetetrahydrofolate reductase gene: an additional risk factor for neural tube defects? Am J Hum Genet 62:1044-1051
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1044-1051
-
-
Van Der Put, N.M.J.1
Gabreels, F.2
Stevens, E.M.3
Smeitink, J.A.4
Trijbels, F.J.5
Eskes, T.K.6
Van Den Heuvel, L.P.7
Blom, H.J.8
-
11
-
-
0034994203
-
Mthfr gene polymorphism, homocysteine and cardiovascular disease
-
Cortese C, Motti C (2001) MTHFR gene polymorphism, homocysteine and cardiovascular disease. Public Health Nutr 4:493-497
-
(2001)
Public Health Nutr
, vol.4
, pp. 493-497
-
-
Cortese, C.1
Motti, C.2
-
12
-
-
2942608990
-
Common gene polymorphisms in the metabolic folate and methylation pathway and the risk of acute lymphoblastic leukemia and non-hodgkin's lymphoma in adults
-
Gemmati D, Ongaro A, Scapoli GL, Porta MD, Tognazzo S, Serino ML, Di Bona E, Rodeghiero F, Gilli G, Reverberi R, Caruso A, Pasello M, Pellati A, De Mattei M (2004) Common gene polymorphisms in the metabolic folate and methylation pathway and the risk of acute lymphoblastic leukemia and non-Hodgkin's lymphoma in adults. Cancer Epidemiol Biomarkers Prev 13:787-794
-
(2004)
Cancer Epidemiol Biomarkers Prev
, vol.13
, pp. 787-794
-
-
Gemmati, D.1
Ongaro, A.2
Scapoli, G.L.3
Porta, M.D.4
Tognazzo, S.5
Serino, M.L.6
Di Bona, E.7
Rodeghiero, F.8
Gilli, G.9
Reverberi, R.10
Caruso, A.11
Pasello, M.12
Pellati, A.13
De Mattei, M.14
-
13
-
-
0029855024
-
A methylenetetrahydrofolate reductase polymorphism and the risk of colorectal cancer
-
Chen J, Giovannucci E, Kelsey K, Rimm EB, Stampfer MJ, Colditz GA, Spiegelman D, Willett WC, Hunter DJ (1996) A methylenetetrahydrofolate reductase polymorphism and the risk of colorectal cancer. Cancer Res 56:4862-4864
-
(1996)
Cancer Res
, vol.56
, pp. 4862-4864
-
-
Chen, J.1
Giovannucci, E.2
Kelsey, K.3
Rimm, E.B.4
Stampfer, M.J.5
Colditz, G.A.6
Spiegelman, D.7
Willett, W.C.8
Hunter, D.J.9
-
14
-
-
84855207949
-
Polymorphisms and haplotypes in methylenetetrahydrofolate reductase gene and head and neck squamous cell carcinoma risk
-
Galbiatti AL, Ruiz MT, Rodrigues JO, Raposo LS, Maníglia JV, Pavarino EC, Goloni-Bertollo EM (2012) Polymorphisms and haplotypes in methylenetetrahydrofolate reductase gene and head and neck squamous cell carcinoma risk. Mol Biol Rep 39: 635-643
-
(2012)
Mol Biol Rep
, vol.39
, pp. 635-643
-
-
Galbiatti, A.L.1
Ruiz, M.T.2
Rodrigues, J.O.3
Raposo, L.S.4
Maníglia, J.V.5
Pavarino, E.C.6
Goloni-Bertollo, E.M.7
-
15
-
-
84855250577
-
Epistatic interactions between loci of one-carbon metabolism modulate susceptibility to breast cancer
-
Naushad SM, Pavani A, Digumarti RR, Gottumukkala SR, Kutala VK (2011) Epistatic interactions between loci of one-carbon metabolism modulate susceptibility to breast cancer. Mol Biol Rep 38:4893-4901
-
(2011)
Mol Biol Rep
, vol.38
, pp. 4893-4901
-
-
Naushad, S.M.1
Pavani, A.2
Digumarti, R.R.3
Gottumukkala, S.R.4
Kutala, V.K.5
-
16
-
-
79951581547
-
The association between methylene-Tetrahydrofolate reductase gene polymorphism and lung cancer risk
-
Arslan S, Karadayi S, YildirimME,Ozdemir O,Akkurt I (2011) The association between methylene-Tetrahydrofolate reductase gene polymorphism and lung cancer risk. Mol Biol Rep 38:991-996
-
(2011)
Mol Biol Rep
, vol.38
, pp. 991-996
-
-
Arslan, S.1
Karadayi, S.2
Yildirim, M.E.3
Ozdemir, O.4
Akkurt, I.5
-
17
-
-
84455188556
-
Mthfr 677c[t and 1298a[c polymorphisms and male infertility risk: A meta-Analysis
-
doi:10.1007/s11033-011-0946-4
-
Wei B, Xu Z, Ruan J, Zhu M, Jin K, Zhou D, Xu Z, Hu Q, Wang Q, Wang Z (2011) MTHFR 677C[T and 1298A[C polymorphisms and male infertility risk: a meta-Analysis. Mol Biol Rep. doi:10.1007/s11033-011-0946-4
-
(2011)
Mol Biol Rep
-
-
Wei, B.1
Xu, Z.2
Ruan, J.3
Zhu, M.4
Jin, K.5
Zhou, D.6
Xu, Z.7
Hu, Q.8
Wang, Q.9
Wang, Z.10
-
18
-
-
32544441595
-
Thrombophilia in pregnancy: A systematic review
-
Robertson L, Wu O, Langhorne P, Twaddle S, Clark P, Lowe GD, Walker ID, Greaves M, Brenkel I, Regan L, Greer IA (2006) Thrombophilia in pregnancy: A systematic review. Br J Haematol 132:171-196
-
(2006)
Br J Haematol
, vol.132
, pp. 171-196
-
-
Robertson, L.1
Wu, O.2
Langhorne, P.3
Twaddle, S.4
Clark, P.5
Lowe, G.D.6
Walker, I.D.7
Greaves, M.8
Brenkel, I.9
Regan, L.10
Greer, I.A.11
-
19
-
-
33244479387
-
Methylenetehydrofolate reductase c677t and a1298c polymorphism and changes in homocysteine concentration in women with idiopathic recurrent pregnancy losses
-
Mtiraoui N, Zammiti W, Ghazouani L, Braham NJ, Saidi S, Finan RR, Almawi WY, Mahjoub T (2006) Methylenetehydrofolate reductase C677T and A1298C polymorphism and changes in homocysteine concentration in women with idiopathic recurrent pregnancy losses. Reproduction 131:395-401
-
(2006)
Reproduction
, vol.131
, pp. 395-401
-
-
Mtiraoui, N.1
Zammiti, W.2
Ghazouani, L.3
Braham, N.J.4
Saidi, S.5
Finan, R.R.6
Almawi, W.Y.7
Mahjoub, T.8
-
20
-
-
75649091533
-
Mthfr c677t and factor v leiden in recurrent pregnancy loss: A study among an endogamous group in north india
-
Mukhopadhyay R, Saraswathy KN, Ghosh PK (2009) MTHFR C677T and factor V Leiden in recurrent pregnancy loss: a study among an endogamous group in north India. Genet Test Mol Biomarkers 13:861-865
-
(2009)
Genet Test Mol Biomarkers
, vol.13
, pp. 861-865
-
-
Mukhopadhyay, R.1
Saraswathy, K.N.2
Ghosh, P.K.3
-
22
-
-
0032231408
-
Heterogeneity in world distribution of the thermolabile c677t mutation in 5,10-methylenetetrahydrofolate reductase
-
Pepe G, Camacho VO, Giusti B, Brunelli T, Marcucci R, Atanasio M, Rickards O, De Stefano GF, Prisco D, Geusini GF, Abbate R (1998) Heterogeneity in world distribution of the thermolabile C677T mutation in 5,10- methylenetetrahydrofolate reductase. Am J Hum Genet 63:917-920
-
(1998)
Am J Hum Genet
, vol.63
, pp. 917-920
-
-
Pepe, G.1
Camacho, V.O.2
Giusti, B.3
Brunelli, T.4
Marcucci, R.5
Atanasio, M.6
Rickards, O.7
De Stefano, G.F.8
Prisco, D.9
Geusini, G.F.10
Abbate, R.11
-
23
-
-
0031961002
-
Worldwide distribution of a common methylenetetrahydrofolate reductase mutation
-
Schneider JA, Rees DC, Liu YT, Clegg JB (1998) Worldwide distribution of a common methylenetetrahydrofolate reductase mutation. Am J Hum Genet 62:1258-1260
-
(1998)
Am J Hum Genet
, vol.62
, pp. 1258-1260
-
-
Schneider, J.A.1
Rees, D.C.2
Liu, Y.T.3
Clegg, J.B.4
-
24
-
-
0041326346
-
Geographical and ethnic variation of the 677c[t allele of 5,10 methylenetetrahydrofolate reductase (mthfr): Findings from over 7000 newborns from 16 areas worldwide
-
Wilcken B, Bamforth F, Li Z, Zhu H, Ritvanen A, Redlund M, Stoll C, Alembik Y, Dott B, Czeizel AE, Gelman-Kohan Z, Scarano G, Bianca S, Ettore G, Tenconi R, Bellato S, Scala I, Mutchinick OM, Lopez MA, de Walle H, Hofstra R, Joutchenko L, Kavteladze L, Bermejo E, Martinez-Frians ML, Gallagher M, Erickson J, Vollset SE, Mastroiacovo P, Andria G, Botto LD (2003) Geographical and ethnic variation of the 677C[T allele of 5,10 methylenetetrahydrofolate reductase (MTHFR): findings from over 7000 newborns from 16 areas worldwide. J Med Genet 40:619-625
-
(2003)
J Med Genet
, vol.40
, pp. 619-625
-
-
Wilcken, B.1
Bamforth, F.2
Li, Z.3
Zhu, H.4
Ritvanen, A.5
Redlund, M.6
Stoll, C.7
Alembik, Y.8
Dott, B.9
Czeizel, A.E.10
Gelman-Kohan, Z.11
Scarano, G.12
Bianca, S.13
Ettore, G.14
Tenconi, R.15
Bellato, S.16
Scala, I.17
Mutchinick, O.M.18
Lopez, M.A.19
De Walle, H.20
Hofstra, R.21
Joutchenko, L.22
Kavteladze, L.23
Bermejo, E.24
Martinez-Frians, M.L.25
Gallagher, M.26
Erickson, J.27
Vollset, S.E.28
Mastroiacovo, P.29
Andria, G.30
Botto, L.D.31
more..
-
25
-
-
41449106682
-
High prevalence of mthfr gene a1298c polymorphism in lebanon
-
Sabbagh AS, Mahfoud Z, Taher A, Ghazi Z, Daher R, Mahfouz RAR (2008) High prevalence of MTHFR gene A1298C polymorphism in Lebanon. Genet Test 12:75-80
-
(2008)
Genet Test
, vol.12
, pp. 75-80
-
-
Sabbagh, A.S.1
Mahfoud, Z.2
Taher, A.3
Ghazi, Z.4
Daher, R.5
Mahfouz, R.A.R.6
-
26
-
-
0033794925
-
Neonatal and fetal methylenetetrahydrofolate reductase genetic polymorphisms: An examination of c677t and a1298c mutations
-
Isotalo AP, Wells GA, Donnelly JG (2000) Neonatal and fetal Methylenetetrahydrofolate reductase genetic polymorphisms: an examination of C677T and A1298C mutations. Am J Hum Genet 67:986-990
-
(2000)
Am J Hum Genet
, vol.67
, pp. 986-990
-
-
Isotalo, A.P.1
Wells, G.A.2
Donnelly, J.G.3
-
27
-
-
44149107150
-
Genetic landscape of the people of india: A canvas for disease gene exploration
-
Indian Genome Variation Consortium (2008) Genetic landscape of the people of India: a canvas for disease gene exploration. J Genet 87:3-20
-
(2008)
J Genet
, vol.87
, pp. 3-20
-
-
-
28
-
-
84864287623
-
-
A database of G. A, Calcutta. Accessed 10 Jan 2011
-
A database of G. A. Grierson's linguistic survey of India, 1904-1928, Calcutta. http://www.joao-roiz.jp/LSI/. Accessed 10 Jan 2011
-
(1904)
Grierson's linguistic survey of India
-
-
-
29
-
-
0024284028
-
A simple salting out procedure for extracting dna from human nucleated cells
-
Miller SA, Dykes DD, Polesky HF (1988) A simple salting out procedure for extracting DNA from human nucleated cells. Nucleic Acids Res 16:1215
-
(1988)
Nucleic Acids Res
, vol.16
, pp. 1215
-
-
Miller, S.A.1
Dykes, D.D.2
Polesky, H.F.3
-
30
-
-
0030610090
-
The mutation ala677-val in the methylene tetrahydrofolate reductase gene: A risk factor for arterial disease and venous thrombosis
-
Arruda VR, von Zuben PM, Chiaparini LC, Annichino-Bizzzacchi JM, Costa FF (1997) The mutation Ala677-Val in the methylene tetrahydrofolate reductase gene: a risk factor for arterial disease and venous thrombosis. Thromb Haemost 77: 818-821
-
(1997)
Thromb Haemost
, vol.77
, pp. 818-821
-
-
Arruda, V.R.1
Von Zuben, P.M.2
Chiaparini, L.C.3
Annichino-Bizzzacchi, J.M.4
Costa, F.F.5
-
31
-
-
78049251351
-
Methylenetetrahydrofolate reductase polymorphism: An independent risk determinant of coronary heart disease in an endogamous population from delhi (india
-
Sinha E, Walia GK, Mukhopadhyay R, Samtani R, Gupta BP, Ghosh PK, Saraswathy KN (2010) Methylenetetrahydrofolate reductase polymorphism: An independent risk determinant of coronary heart disease in an endogamous population from Delhi (India). e-spen 5(5):e213-e218
-
(2010)
E-spen
, vol.5
, Issue.5
-
-
Sinha, E.1
Walia, G.K.2
Mukhopadhyay, R.3
Samtani, R.4
Gupta, B.P.5
Ghosh, P.K.6
Saraswathy, K.N.7
-
34
-
-
77950878526
-
Allelic and haplotypic structure at the drd2 locus among five north indian caste populations
-
Saraswathy KN, Meitei SY, Gupta V, Murry B, Sachdeva MP, Ghosh PK (2010) Allelic and haplotypic structure at the DRD2 Locus among five north Indian caste populations. Am J Physical Anthropol 141:651-657
-
(2010)
Am J Physical Anthropol
, vol.141
, pp. 651-657
-
-
Saraswathy, K.N.1
Meitei, S.Y.2
Gupta, V.3
Murry, B.4
Sachdeva, M.P.5
Ghosh, P.K.6
-
35
-
-
84864279623
-
-
Accessed 7 Jan
-
http://alfred.med.yale.edu/alfred/SiteTable1A-working.asp?site uid=SI001032G. Accessed 7 Jan 2011
-
(2011)
-
-
-
36
-
-
42949134479
-
Methylenetetrahydrofolate reductase gene polymorphisms in 13 chinese ethnic populations
-
Mao R, Fan Y, Chen F, Sun D, Bai J, Fu S (2008) Methylenetetrahydrofolate reductase gene polymorphisms in 13 Chinese ethnic populations. Cell Biochem Funct 26:352-358
-
(2008)
Cell Biochem Funct
, vol.26
, pp. 352-358
-
-
Mao, R.1
Fan, Y.2
Chen, F.3
Sun, D.4
Bai, J.5
Fu, S.6
-
37
-
-
0018180775
-
Skin color and nutrient photolysis: An evolutionary hypothesis
-
Branda RF, Eaton JW (1978) Skin color and nutrient photolysis: an evolutionary hypothesis. Science 18:625-626
-
(1978)
Science
, vol.18
, pp. 625-626
-
-
Branda, R.F.1
Eaton, J.W.2
-
38
-
-
33750912762
-
Ultraviolet radiation represents an evolutionary selective pressure for the south-To-north gradient of the mthfr 677tt genotype
-
Cordain L, Hickey MS (2006) Ultraviolet radiation represents an evolutionary selective pressure for the south-To-north gradient of the MTHFR 677TT genotype. Am J Clin Nutr 84:1243
-
(2006)
Am J Clin Nutr
, vol.84
, pp. 1243
-
-
Cordain, L.1
Hickey, M.S.2
-
39
-
-
0032941095
-
Cobalamine and folate deficiency: Acquired and hereditary disorders in children
-
Rosenblatt DS, Whitehead VM (1999) Cobalamine and folate deficiency: acquired and hereditary disorders in children. Semin Hematol 36:19-34
-
(1999)
Semin Hematol
, vol.36
, pp. 19-34
-
-
Rosenblatt, D.S.1
Whitehead, V.M.2
-
40
-
-
0036798246
-
Implications on human fertility of the 677c[t and 1298a[c polymorphisms of the mthfr gene: Consequences of a possible genetic selection
-
Reyes-Engel A, Munoz E, Gaitan MJ, Fabre E, Gallo M, Dieguez JL, Ruiz M, Morell M (2002) Implications on human fertility of the 677C[T and 1298A[C polymorphisms of the MTHFR gene: consequences of a possible genetic selection. Mol Hum Reprod 8:952-957
-
(2002)
Mol Hum Reprod
, vol.8
, pp. 952-957
-
-
Reyes-Engel, A.1
Munoz, E.2
Gaitan, M.J.3
Fabre, E.4
Gallo, M.5
Dieguez, J.L.6
Ruiz, M.7
Morell, M.8
-
41
-
-
0036178211
-
The frequent 5,10-methylenetetrahydrofolate reductase c677t polymorphism is associated with a common haplotype in whites, japanese, and africans
-
Rosenberg N, Murata M, Ikeda Y, Opare-Sem O, Zivelin A, Geffen E, Seligsohn U (2002) The frequent 5,10-methylenetetrahydrofolate reductase C677T polymorphism is associated with a common haplotype in Whites, Japanese, and Africans. Am J Hum Genet 70:758-762
-
(2002)
Am J Hum Genet
, vol.70
, pp. 758-762
-
-
Rosenberg, N.1
Murata, M.2
Ikeda, Y.3
Opare-Sem, O.4
Zivelin, A.5
Geffen, E.6
Seligsohn, U.7
-
42
-
-
84864288693
-
-
Accessed 7 Jan
-
http://alfred.med.yale.edu/alfred/SiteTable1A-working.asp?siteu id=SI003687Y. Accessed 7 Jan 2011
-
(2011)
-
-
-
43
-
-
38049125769
-
Mthfr c677t polymorphisms among the ahirs and jats of haryana (india
-
Saraswathy KN, Mukhopadhaya R, Sinha E, Aggarwal S, Sachdeva MP, Kalla AK (2007) MTHFR C677T polymorphisms among the Ahirs and Jats of Haryana (India). Am J Hum Biol 20:116-117
-
(2007)
Am J Hum Biol
, vol.20
, pp. 116-117
-
-
Saraswathy, K.N.1
Mukhopadhaya, R.2
Sinha, E.3
Aggarwal, S.4
Sachdeva, M.P.5
Kalla, A.K.6
-
44
-
-
4444305073
-
Prevalence of mthfr gene polymorphisms (c677t and a1298c) among tamilians
-
Angeline T, Jeyaraj N, Granito S, Tsongalis GJ (2004) Prevalence of MTHFR gene polymorphisms (C677T and A1298C) among Tamilians. Exp Mol Pathol 77:85-88
-
(2004)
Exp Mol Pathol
, vol.77
, pp. 85-88
-
-
Angeline, T.1
Jeyaraj, N.2
Granito, S.3
Tsongalis, G.J.4
-
45
-
-
58149112276
-
Human genetic selection on the mthfr 677c[t polymorphism
-
Mayor-Olea A ́ , Callejón G, Palomares AR, Jiménez AJ, Gaitán MJ, Rodríguez A, Ruiz M, Reyes-Engel A (2008) Human genetic selection on the MTHFR 677C[T polymorphism. BMC Med Genet 9:104-110
-
(2008)
BMC Med Genet
, vol.9
, pp. 104-110
-
-
Mayor-Olea A ́1
Callejón, G.2
Palomares, A.R.3
Jiménez, A.J.4
Gaitán, M.J.5
Rodríguez, A.6
Ruiz, M.7
Reyes-Engel, A.8
-
46
-
-
0141893992
-
Genotype frequencies and linkage disequilibrium in the ceph human diversity panel for variants in folate pathway genes mthfr, mthfd, mtrr, rfc1, and gcp2
-
Shi M, Caprau D, Romitti P, Christensen K, Murray JC (2003) Genotype frequencies and linkage disequilibrium in the CEPH Human diversity Panel for variants in folate pathway genes MTHFR, MTHFD, MTRR, RFC1, and GCP2. Birth Defect Res A 67:545-549
-
(2003)
Birth Defect Res A
, vol.67
, pp. 545-549
-
-
Shi, M.1
Caprau, D.2
Romitti, P.3
Christensen, K.4
Murray, J.C.5
-
47
-
-
0037276240
-
Genotype and haplotype distributions of mthfr 677c[t and 1298 a[c single nucleotide polymorphisms: A meta-Analysis
-
Ogino S, Wilson RB (2003) Genotype and haplotype distributions of MTHFR 677C[T and 1298 A[C single nucleotide polymorphisms: a meta-Analysis. J Hum Genet 48:1-7
-
(2003)
J Hum Genet
, vol.48
, pp. 1-7
-
-
Ogino, S.1
Wilson, R.B.2
-
48
-
-
0032822750
-
Methylenetetrahydrofolate reductage (mthfr): The incidence of mutations c677t and a1298c in the ashkenazi jewish population
-
Rady PL, Tyring SK, Hudnall SD, Vargas T, Kellner LH, Nitowsky H, Matalon RK (1999) Methylenetetrahydrofolate reductage (MTHFR): the incidence of mutations C677T and A1298C in the Ashkenazi Jewish population. Am J Med Genet 86:380-384
-
(1999)
Am J Med Genet
, vol.86
, pp. 380-384
-
-
Rady, P.L.1
Tyring, S.K.2
Hudnall, S.D.3
Vargas, T.4
Kellner, L.H.5
Nitowsky, H.6
Matalon, R.K.7
-
49
-
-
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, Kohlschmidt N, Schroter B, Ermert A, Koch MC (1999) 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 87:23-29
-
(1999)
Am J Med Genet
, vol.87
, pp. 23-29
-
-
Stegmann, K.1
Ziegler, A.2
Ngo, E.T.3
Kohlschmidt, N.4
Schroter, B.5
Ermert, A.6
Koch, M.C.7
-
50
-
-
27644488218
-
Prevalence of genetic risk factors for coronary artery disease in corsica island (france
-
Falchi A, Giovannoni L, Piras IS, Calo CM, Moral P, Vona G, Varesi (2005) Prevalence of genetic risk factors for coronary artery disease in Corsica Island (France). Exp Mol Pathol 79:210-213
-
(2005)
Exp Mol Pathol
, vol.79
, pp. 210-213
-
-
Falchi, A.1
Giovannoni, L.2
Piras, I.S.3
Calo, C.M.4
Moral, P.5
Vona G Varesi6
|