-
1
-
-
0028844492
-
Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida
-
van der Put NMJ, Steegers-Theunissen RPM, Frosst P, et al. Mutated methylenetetrahydrofolate reductase as a risk factor for spina bifida. Lancet 1995;346:1070-1.
-
(1995)
Lancet
, vol.346
, pp. 1070-1071
-
-
Van Der Put, N.M.J.1
Steegers-Theunissen, R.P.M.2
Frosst, P.3
-
2
-
-
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. QJM 1995;88:763-6.
-
(1995)
QJM
, vol.88
, pp. 763-766
-
-
Whitehead, A.S.1
Gallagher, P.2
Mills, J.L.3
-
3
-
-
0030018760
-
5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects
-
Ou CY, Stevenson RE, Brown VK, et al. 5,10 Methylenetetrahydrofolate reductase genetic polymorphism as a risk factor for neural tube defects. Am J Med Genet 1996;63:610-14.
-
(1996)
Am J Med Genet
, vol.63
, pp. 610-614
-
-
Ou, C.Y.1
Stevenson, R.E.2
Brown, V.K.3
-
4
-
-
0029968027
-
Is mutated MTHFR a risk factor for neural tube defects?
-
Posey DL, Khoury MJ, Mulinare J, et al. Is mutated MTHFR a risk factor for neural tube defects? Lancet 1996;347:686-9.
-
(1996)
Lancet
, vol.347
, pp. 686-689
-
-
Posey, D.L.1
Khoury, M.J.2
Mulinare, J.3
-
5
-
-
0030938599
-
Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium
-
Mitchell LE. Differentiating between fetal and maternal genotypic effects, using the transmission test for linkage disequilibrium. Am J Hum Genet 1997;60:1006-7.
-
(1997)
Am J Hum Genet
, vol.60
, pp. 1006-1007
-
-
Mitchell, L.E.1
-
6
-
-
0032211487
-
Distinguishing the effects of maternal and offspring genes through studies of "case-parent triads"
-
Wilcox AJ, Weinberg CR, Lie RT. Distinguishing the effects of maternal and offspring genes through studies of "case-parent triads." Am J Epidemiol 1998;148:893-901.
-
(1998)
Am J Epidemiol
, vol.148
, pp. 893-901
-
-
Wilcox, A.J.1
Weinberg, C.R.2
Lie, R.T.3
-
7
-
-
0031949066
-
A log-linear approach to case-parent-triad data: Assessing the effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting
-
Weinberg CR, Wilcox AJ, Lie RT. A log-linear approach to case-parent-triad data: assessing the effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting. Am J Hum Genet 1998;62:969-78.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 969-978
-
-
Weinberg, C.R.1
Wilcox, A.J.2
Lie, R.T.3
-
8
-
-
0037318735
-
Studying parents and grandparents to assess genetic contributions to early-onset disease
-
Weinberg CR. Studying parents and grandparents to assess genetic contributions to early-onset disease. Am J Hum Genet 2003;72:438-47.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 438-447
-
-
Weinberg, C.R.1
-
9
-
-
1842483890
-
Case/pseudocontrol analysis in genetic association studies: A unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects
-
Cordell HJ, Barratt BJ, Clayton DG. Case/pseudocontrol analysis in genetic association studies: a unified framework for detection of genotype and haplotype associations, gene-gene and gene-environment interactions, and parent-of-origin effects. Genet Epidemiol 2004;26:167-85.
-
(2004)
Genet Epidemiol
, vol.26
, pp. 167-185
-
-
Cordell, H.J.1
Barratt, B.J.2
Clayton, D.G.3
-
10
-
-
0002629270
-
Maximum likelihood from incomplete data via the EM algorithm
-
Dempster AP, Laird NM, Rubin DB. Maximum likelihood from incomplete data via the EM algorithm. J R Stat Soc (B) 1977;39:1-28.
-
(1977)
J R Stat Soc (B)
, vol.39
, pp. 1-28
-
-
Dempster, A.P.1
Laird, N.M.2
Rubin, D.B.3
-
11
-
-
0004215245
-
-
Cary, NC: SAS Institute, Inc
-
SAS Institute, Inc. SAS computer program, version 8.01. Cary, NC: SAS Institute, Inc, 1999.
-
(1999)
SAS Computer Program, Version 8.01
-
-
-
12
-
-
0033362166
-
Allowing for missing parents in genetic studies of case-parent triads
-
Weinberg CR. Allowing for missing parents in genetic studies of case-parent triads. Am J Hum Genet 1999;64:1186-93.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 1186-1193
-
-
Weinberg, C.R.1
-
13
-
-
0036517472
-
A comprehensive review of genetic association studies
-
Hirschhorn JN, Lohmueller K, Byrne E, et al. A comprehensive review of genetic association studies. Genet Med 2002;4:45-61.
-
(2002)
Genet Med
, vol.4
, pp. 45-61
-
-
Hirschhorn, J.N.1
Lohmueller, K.2
Byrne, E.3
-
15
-
-
0042881041
-
Mathematical multi-locus approaches to localizing complex human trait genes
-
Hoh J, Ott J. Mathematical multi-locus approaches to localizing complex human trait genes. Nat Rev Genet 2003;4:701-9.
-
(2003)
Nat Rev Genet
, vol.4
, pp. 701-709
-
-
Hoh, J.1
Ott, J.2
-
16
-
-
0345411335
-
The ubiquitous nature of epistasis in determining susceptibility to common human diseases
-
Moore JH. The ubiquitous nature of epistasis in determining susceptibility to common human diseases. Hum Hered 2003;56:73-82.
-
(2003)
Hum Hered
, vol.56
, pp. 73-82
-
-
Moore, J.H.1
-
17
-
-
0037433052
-
Multifactorial dimensionality reduction software for detecting gene-gene and gene-environment interactions
-
Hahn LW, Ritchie MD, Moore JH. Multifactorial dimensionality reduction software for detecting gene-gene and gene-environment interactions. Bioinformatics 2003;19:376-82.
-
(2003)
Bioinformatics
, vol.19
, pp. 376-382
-
-
Hahn, L.W.1
Ritchie, M.D.2
Moore, J.H.3
-
18
-
-
0346101571
-
Power estimation for multiple SNP association test of case-control study and application
-
Hao K, Xu X, Laird N, et al. Power estimation for multiple SNP association test of case-control study and application. Genet Epidemiol 2004;26:22-30.
-
(2004)
Genet Epidemiol
, vol.26
, pp. 22-30
-
-
Hao, K.1
Xu, X.2
Laird, N.3
-
19
-
-
0345689434
-
Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers
-
Wille A, Hoh J, Ott J. Sum statistics for the joint detection of multiple disease loci in case-control association studies with SNP markers. Genet Epidemiol 2003;25:350-9.
-
(2003)
Genet Epidemiol
, vol.25
, pp. 350-359
-
-
Wille, A.1
Hoh, J.2
Ott, J.3
-
20
-
-
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;151:862-77.
-
(2000)
Am J Epidemiol
, vol.151
, pp. 862-877
-
-
Botto, L.D.1
Yang, Q.2
-
21
-
-
0003463062
-
-
Hyattsville, MD: National Center for Health Statistics, Centers for Disease Control and Prevention
-
US Department of Health and Human Services. Vital statistics of the United States, 1999: natality. Hyattsville, MD: National Center for Health Statistics, Centers for Disease Control and Prevention, 2001. (http://www.cdc.gov/nchs/datawh/statab/unpubd/natality/natab99.htm).
-
(2001)
Vital Statistics of the United States, 1999: Natality
-
-
-
22
-
-
0036918343
-
RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility
-
Palmer CGS, Turuunen JA, Sinsheimer JS, et al. RHD maternal-fetal genotype incompatibility increases schizophrenia susceptibility. Am J Hum Genet 2002;71:1312-19.
-
(2002)
Am J Hum Genet
, vol.71
, pp. 1312-1319
-
-
Palmer, C.G.S.1
Turuunen, J.A.2
Sinsheimer, J.S.3
-
24
-
-
3142714601
-
Maternal and fetal variants of genetic thrombophilias and the risk of preeclampsia
-
Vefring H, Lie RT, Odegard R, et al. Maternal and fetal variants of genetic thrombophilias and the risk of preeclampsia. Epidemiology 2004;15:317-22.
-
(2004)
Epidemiology
, vol.15
, pp. 317-322
-
-
Vefring, H.1
Lie, R.T.2
Odegard, R.3
-
25
-
-
0842346181
-
Lipoprotein concentrations in newborns are associated with allelic variants in their mothers
-
Descamps OS, Bruniaux M, Guilmot PF, et al. Lipoprotein concentrations in newborns are associated with allelic variants in their mothers. Atherosclerosis 2004;172:287-98.
-
(2004)
Atherosclerosis
, vol.172
, pp. 287-298
-
-
Descamps, O.S.1
Bruniaux, M.2
Guilmot, P.F.3
-
26
-
-
0036271829
-
Oocyte-specific genes regulate follicle formation, fertility and early mouse development
-
Dean J. Oocyte-specific genes regulate follicle formation, fertility and early mouse development. J Reprod Immunol 2002;53:171-80.
-
(2002)
J Reprod Immunol
, vol.53
, pp. 171-180
-
-
Dean, J.1
-
27
-
-
0037313184
-
Zygote arrest 1 (Zar1) is a novel maternal-effect gene critical for the oocyte-to-embryo transition
-
Wu X, Viveiros MM, Eppig JJ, et al. Zygote arrest 1 (Zar1) is a novel maternal-effect gene critical for the oocyte-to-embryo transition. Nat Genetic 2003;33:187-91.
-
(2003)
Nat Genetic
, vol.33
, pp. 187-191
-
-
Wu, X.1
Viveiros, M.M.2
Eppig, J.J.3
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