-
1
-
-
19444374276
-
Orofacial clefting: Recent insights into a complex trait
-
DOI 10.1016/j.gde.2005.03.003, PII S0959437X05000511
-
Jugessur A, Murray JC. Orofacial clefting: recent insights into a complex trait. Curr Opin Genet, 2005, 15 : 270-278. (Pubitemid 40726050)
-
(2005)
Current Opinion in Genetics and Development
, vol.15
, Issue.3 SPEC. ISS
, pp. 270-278
-
-
Jugessur, A.1
Murray, J.C.2
-
2
-
-
0242670655
-
Epidemiology of oral clefts: An international perspective
-
Wyszynski DF, ed. New York: Oxford University Press
-
Mossey P, Little J. Epidemiology of oral clefts: an international perspective. In: Wyszynski DF, ed. Cleft Lip and Palate: From Origin to Treatment. New York: Oxford University Press, 2002. 127-157.
-
(2002)
Cleft Lip and Palate: From Origin to Treatment
, pp. 127-157
-
-
Mossey, P.1
Little, J.2
-
3
-
-
0036556368
-
Gene/environment causes of cleft lip and/or palate
-
DOI 10.1034/j.1399-0004.2002.610402.x
-
Murray JC. Gene/environment causes of cleft lip and/or palate. Clin Genet, 2002, 61 : 248-256. (Pubitemid 36372641)
-
(2002)
Clinical Genetics
, vol.61
, Issue.4
, pp. 248-256
-
-
Murray, J.C.1
-
4
-
-
34548484598
-
Human genetic factors in nonsyndromic cleft lip and palate: An update
-
DOI 10.1016/j.ijporl.2007.06.007, PII S0165587607002583
-
Carinci F, Scapoli L, Palmieri A, et al. Human genetic factors in nonsyndromic cleft lip and palate: An update. Int J Pediatr Otorhinolaryngol, 2007, 71 : 1509-1519. (Pubitemid 47376750)
-
(2007)
International Journal of Pediatric Otorhinolaryngology
, vol.71
, Issue.10
, pp. 1509-1519
-
-
Carinci, F.1
Scapoli, L.2
Palmieri, A.3
Zollino, I.4
Pezzetti, F.5
-
5
-
-
42649095999
-
The effect of polymorphisms of MTHFR C677T, A1298C, MS A2756G and CBS 844ins68bp on plasma total homocysteine level and the risk of ischemic stroke in Thai children
-
DOI 10.1016/j.thromres.2007.09.012, PII S0049384807003702
-
Sirachainan N, Sasanakul W, Visudtibhan A, et al. The effect of polymorphisms of MTHFR C677T, A1298C, MS A2756G and CBS 844ins68bp on plasma total homocysteine level and the risk of ischemicstroke in Thai children. Thrombosis Res, 2008, 122 : 33-37. (Pubitemid 351601851)
-
(2008)
Thrombosis Research
, vol.122
, Issue.1
, pp. 33-37
-
-
Sirachainan, N.1
Sasanakul, W.2
Visudtibhan, A.3
Tapanapruksakul, P.4
Charoenkwan, P.5
Kadegasem, P.6
Udomsubpayakul, U.7
Chuansumrit, A.8
-
6
-
-
5144219676
-
Effects of methionine synthase gene variation in parents on occurence of congenital heart disease in offspring
-
Zhu WL, Dao JJ, Cheng J, et al. Effects of methionine synthase gene variation in parents on occurence of congenital heart disease in offspring. J Peking Univ (Health Sci), 2004, 36 : 254-259.
-
(2004)
J Peking Univ (Health Sci)
, vol.36
, pp. 254-259
-
-
Zhu, W.L.1
Dao, J.J.2
Cheng, J.3
-
7
-
-
0027377799
-
Transmission test for linkage disequilibrium: The insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
Spielman RS, McGinnis RE, Ewens WJ, et al. Transmission test for linkage disequilibrium: the insulin gene region and insulin- dependent diabetes mellitus (IDDM). Am J Hum Genet, 1993, 65 : 578-580. (Pubitemid 23311321)
-
(1993)
American Journal of Human Genetics
, vol.52
, Issue.3
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
8
-
-
0026494911
-
A haplotype-based 'haplotype relative risk' approach to detecting allelic associations
-
Terwilliger JD, Ott J. A haplotype-based 'haplotype relative risk' approach to detecting allelic associations. Hum Hered, 1992, 42 : 337-346.
-
(1992)
Hum Hered
, vol.42
, pp. 337-346
-
-
Terwilliger, J.D.1
Ott, J.2
-
9
-
-
0033814928
-
Implementing a unified approach to family based tests of association
-
Laird N, Horvath S, Xu X, et al. Implementing a unified approach to family based tests of association. Genet Epidemiol, 2000, 19 (Suppl 1) : 36-42.
-
(2000)
Genet Epidemiol
, vol.19
, Issue.SUPPL. 1
, pp. 36-42
-
-
Laird, N.1
Horvath, S.2
Xu, X.3
-
11
-
-
0022728801
-
Effects of misspecifying genetic parameters in lod score analysis
-
Clerget-Darpoux F, Bonaiti-Pellie C, Hochez J, et al. Effects of misspecifying genetic parameters in lod score analysis. Biometrics, 1986, 42 : 393-399.
-
(1986)
Biometrics
, vol.42
, pp. 393-399
-
-
Clerget-Darpoux, F.1
Bonaiti-Pellie, C.2
Hochez, J.3
-
12
-
-
33748653166
-
Genomewide scan for nonsyndromic cleft lip and palate in multigenerational Indian families reveals significant evidence of linkage at 13q33.1-34
-
DOI 10.1086/507487
-
Radhakrishna U, Ratnamala U, Gaines M, et al. Genomewide scan for nonsyndromic cleft lip and palate in multigenerational indian families reveals significant evidence of linkage at 13q33. 1- 34. Am J Hum Genet, 2006, 79 : 580-585. (Pubitemid 44384269)
-
(2006)
American Journal of Human Genetics
, vol.79
, Issue.3
, pp. 580-585
-
-
Radhakrishna, U.1
Ratnamala, U.2
Gaines, M.3
Beiraghi, S.4
Hutchings, D.5
Golla, J.6
Husain, S.A.7
Gambhir, P.S.8
Sheth, J.J.9
Sheth, F.J.10
Chetan, G.K.11
Naveed, M.12
Solanki, J.V.13
Patel, U.C.14
Master, D.C.15
Memon, R.16
Antonarakis, G.S.17
Antonarakis, S.E.18
Nath, S.K.19
-
13
-
-
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
-
-
-
14
-
-
0032130079
-
Focusing on folic acid. Task force organizing to promote consumption of folic acid
-
Berry A. Focusing on folic acid. Task force organizing to promote consumption of folic acid. AWHONN Lifelines, 1998, 2 : 19-20.
-
(1998)
AWHONN Lifelines
, vol.2
, pp. 19-20
-
-
Berry, A.1
-
15
-
-
0033547432
-
Neural-tube defects
-
DOI 10.1056/NEJM199911113412006
-
Botto LD, Moore CA, Khoury MJ, et al. Neural-tube defects. N Engl J Med, 1999, 341 : 1509-1519. (Pubitemid 29526355)
-
(1999)
New England Journal of Medicine
, vol.341
, Issue.20
, pp. 1509-1519
-
-
Botto, L.D.1
Moore, C.A.2
Khoury, M.J.3
Erickson, J.D.4
-
16
-
-
3242893075
-
Maternal nutrition and oral clefts
-
Wyszynski DF ed. Oxford: Oxford University Press
-
Munger RG. Maternal nutrition and oral clefts. In: Wyszynski DF ed. Cleft lip and palate: From origin to treatment. Oxford: Oxford University Press, 2002. 170-192.
-
(2002)
Cleft Lip and Palate: From Origin to Treatment
, pp. 170-192
-
-
Munger, R.G.1
-
17
-
-
33847786727
-
Folic acid supplements and risk of facial clefts: National population based case-control study
-
DOI 10.1136/bmj.39079.618287.0B
-
Wilcox AJ, Lie RT, Solvoll K, et al. Drevon CA. Folic acid supplements and risk of facial clefts: National population based case-control study. BMJ, 2007, 334 : 464-470. (Pubitemid 46586604)
-
(2007)
British Medical Journal
, vol.334
, Issue.7591
, pp. 464-467
-
-
Wilcox, A.J.1
Lie, R.T.2
Solvoll, K.3
Taylor, J.4
McConnaughey, D.R.5
Abyholm, F.6
Vindenes, H.7
Vollset, S.E.8
Drevon, C.A.9
-
18
-
-
33845984049
-
Folic acid-containing supplement consumption during pregnancy and risk for oral clefts: A meta-analysis
-
DOI 10.1002/bdra.20315
-
Badovinac RL, Werler MM, Williams PL, et al. 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. (Pubitemid 46053405)
-
(2007)
Birth Defects Research Part a - Clinical and Molecular Teratology
, vol.79
, Issue.1
, pp. 8-15
-
-
Badovinac, R.L.1
Werler, M.M.2
Williams, P.L.3
Kelsey, K.T.4
Hayes, C.5
-
19
-
-
38849187271
-
Folate and one-carbon metabolism gene polymorphisms and their associations with oral facial clefts
-
DOI 10.1002/ajmg.a.32162
-
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, 146 : 440-449. (Pubitemid 351206814)
-
(2008)
American Journal of Medical Genetics, Part a
, vol.146
, Issue.4
, pp. 440-449
-
-
Boyles, A.L.1
Wilcox, A.J.2
Taylor, J.A.3
Meyer, K.4
Fredriksen, A.5
Ueland, P.M.6
Drevon, C.A.7
Vollset, S.E.8
Lie, R.T.9
-
20
-
-
34250354391
-
Methylenetetrahydrofolate reductase and methionine synthase polymorphisms and risk of bladder cancer in a Tunisian population
-
DOI 10.1016/j.cancergencyto.2007.03.007, PII S0165460807001501
-
Ouerhani S, Oliveira E, Marrakchi R, et al. Methylenetetrahydrofolate reductase and methionine synthase polymorphisms and risk of bladder cancer in a Tunisian population. Cancer Genet Cytogenet, 2007, 176 : 48-53. (Pubitemid 46908831)
-
(2007)
Cancer Genetics and Cytogenetics
, vol.176
, Issue.1
, pp. 48-53
-
-
Ouerhani, S.1
Oliveira, E.2
Marrakchi, R.3
Ben Slama, M.R.4
Sfaxi, M.5
Ayed, M.6
Chebil, M.7
Amorim, A.8
El Gaaied, A.B.9
Prata, M.J.10
-
21
-
-
10044281662
-
Polymorphism in folate- And methionine-metabolizing enzyme and aberrant CpG island hypermethylation in uterine cervical cancer
-
DOI 10.1016/j.ygyno.2004.09.031, PII S0090825804007917
-
Kanga S, Kima JW, Kang GH, et al. Polymorphism in folate-and methionine-metabolizing enzyme and aberrant CpG island hypermethylation in uterine cervical cancer. Gynecol Oncol, 2005, 96 : 173-180. (Pubitemid 39612433)
-
(2005)
Gynecologic Oncology
, vol.96
, Issue.1
, pp. 173-180
-
-
Kang, S.1
Kim, J.W.2
Kang, G.H.3
Park, N.H.4
Song, Y.S.5
Kang, S.B.6
Lee, H.P.7
-
22
-
-
0035500262
-
Gene polymorphisms of homocysteine metabolism-related enzymes in chinese patients with occlusive coronary artery or cerebral vascular diseases
-
DOI 10.1016/S0049-3848(01)00352-8, PII S0049384801003528
-
Zhang GS, Dai CW. Gene Polymorphisms of homocysteine metabolism-related enzymes in Chinese patients with occlusive coronary artery or cerebral vascular diseases. Thrombosis Res, 2001, 104 : 187-195. (Pubitemid 32973760)
-
(2001)
Thrombosis Research
, vol.104
, Issue.3
, pp. 187-195
-
-
Zhang, G.1
Dai, C.2
-
23
-
-
3142769010
-
Relations of methionine synthase gene variation with congenital heart disease
-
Zhu WL, Dao JJ, Cheng J, et al. Relations of methionine synthase gene variation with congenital heart disease. J Hygiene Res, 2004, 33 : 66-69.
-
(2004)
J Hygiene Res
, vol.33
, pp. 66-69
-
-
Zhu, W.L.1
Dao, J.J.2
Cheng, J.3
-
24
-
-
0027992091
-
Comparison of statistics for candidate-gene association studies using cases and parents
-
Schaid DJ, Sommer SS. Comparison of statistics for candidate- gene association studies using cases and parents. Am J Hum Genet, 1994, 55 : 402-409. (Pubitemid 24233226)
-
(1994)
American Journal of Human Genetics
, vol.55
, Issue.2
, pp. 402-409
-
-
Schaid, D.J.1
Sommer, S.S.2
-
25
-
-
0036079141
-
Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families
-
DOI 10.1086/341944
-
Marazita ML, Field LL, Cooper ME, et al. Genome scan for loci involved in cleft lip with or without cleft palate, in Chinese multiplex families. Am J Hum Genet, 2002, 71 : 349-364. (Pubitemid 34800251)
-
(2002)
American Journal of Human Genetics
, vol.71
, Issue.2
, pp. 349-364
-
-
Marazita, M.L.1
Field, L.L.2
Cooper, M.E.3
Tobias, R.4
Maher, B.S.5
Peanchitlertkajorn, S.6
Liu, Y.-E.7
-
26
-
-
34249885875
-
A genome-wide association study of type 2 diabetes in finns detects multiple susceptibility variants
-
DOI 10.1126/science.1142382
-
Scott LJ, Mohlke M, Bonnycastle LL, et al. A genome-wide association study of type 2 diabetes in finns detects multiple susceptibility variants. Science, 2007, 316 : 1341-1345. (Pubitemid 46871655)
-
(2007)
Science
, vol.316
, Issue.5829
, pp. 1341-1345
-
-
Scott, L.J.1
Mohlke, K.L.2
Bonnycastle, L.L.3
Willer, C.J.4
Li, Y.5
Duren, W.L.6
Erdos, M.R.7
Stringham, H.M.8
Chines, P.S.9
Jackson, A.U.10
Prokunina-Olsson, L.11
Ding, C.-J.12
Swift, A.J.13
Narisu14
Hu, T.15
Pruim, R.16
Xiao, R.17
Li, X.-Y.18
Conneely, K.N.19
Riebow, N.L.20
Sprau, A.G.21
Tong, M.22
White, P.P.23
Hetrick, K.N.24
Barnhart, M.W.25
Bark, C.W.26
Goldstein, J.L.27
Watkins, L.28
Xiang, F.29
Saramies, J.30
Buchanan, T.A.31
Watanabe, R.M.32
Valle, T.T.33
Kinnunen, L.34
Abecasis, G.R.35
Pugh, E.W.36
Doheny, K.F.37
Bergman, R.N.38
Tuomilehto, J.39
Collins, F.S.40
Boehnke, M.41
more..
-
27
-
-
34249888775
-
Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels
-
DOI 10.1126/science.1142358
-
Saxena R, Voight BF, Lyssenko V, et al. Genome-wide association analysis identifies loci for type 2 diabetes and triglyceride levels. Science, 2007, 316 : 1331-1336. (Pubitemid 46871653)
-
(2007)
Science
, vol.316
, Issue.5829
, pp. 1331-1336
-
-
Saxena, R.1
Voight, B.F.2
Lyssenko, V.3
Burtt, N.P.4
De Bakker, P.I.W.5
Chen, H.6
Roix, J.J.7
Kathiresan, S.8
Hirschhorn, J.N.9
Daly, M.J.10
Hughes, T.E.11
Groop, L.12
Altshuler, D.13
-
28
-
-
34250001297
-
A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer
-
DOI 10.1038/ng2075, PII NG2075
-
Hunter DJ, Kraft P, Jacobs KB, et al. A genome-wide association study identifies alleles in FGFR2 associated with risk of sporadic postmenopausal breast cancer. Nat Genet, 2007, 39 : 870-874. (Pubitemid 47014500)
-
(2007)
Nature Genetics
, vol.39
, Issue.7
, pp. 870-874
-
-
Hunter, D.J.1
Kraft, P.2
Jacobs, K.B.3
Cox, D.G.4
Yeager, M.5
Hankinson, S.E.6
Wacholder, S.7
Wang, Z.8
Welch, R.9
Hutchinson, A.10
Wang, J.11
Yu, K.12
Chatterjee, N.13
Orr, N.14
Willett, W.C.15
Colditz, G.A.16
Ziegler, R.G.17
Berg, C.D.18
Buys, S.S.19
McCarty, C.A.20
Feigelson, H.S.21
Calle, E.E.22
Thun, M.J.23
Hayes, R.B.24
Tucker, M.25
Gerhard, D.S.26
Fraumeni, J.F.27
Hoover, R.N.28
Thomas, G.29
Chanock, S.J.30
more..
|