-
1
-
-
84882448216
-
Genomic imprinting and parent-of-origin effects on complex traits
-
H.A. Lawson, J.M. Cheverud, and J.B. Wolf Genomic imprinting and parent-of-origin effects on complex traits Nat. Rev. Genet. 14 2013 609 617
-
(2013)
Nat. Rev. Genet.
, vol.14
, pp. 609-617
-
-
Lawson, H.A.1
Cheverud, J.M.2
Wolf, J.B.3
-
2
-
-
84892752841
-
The architecture of parent-of-origin effects in mice
-
R. Mott, W. Yuan, P. Kaisaki, X. Gan, J. Cleak, A. Edwards, A. Baud, and J. Flint The architecture of parent-of-origin effects in mice Cell 156 2014 332 342
-
(2014)
Cell
, vol.156
, pp. 332-342
-
-
Mott, R.1
Yuan, W.2
Kaisaki, P.3
Gan, X.4
Cleak, J.5
Edwards, A.6
Baud, A.7
Flint, J.8
-
3
-
-
84856489941
-
Parent of origin effects
-
A. Guilmatre, and A.J. Sharp Parent of origin effects Clin. Genet. 81 2012 201 209
-
(2012)
Clin. Genet.
, vol.81
, pp. 201-209
-
-
Guilmatre, A.1
Sharp, A.J.2
-
4
-
-
73349115848
-
The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes
-
C. Wallace, D.J. Smyth, M. Maisuria-Armer, N.M. Walker, J.A. Todd, and D.G. Clayton The imprinted DLK1-MEG3 gene region on chromosome 14q32.2 alters susceptibility to type 1 diabetes Nat. Genet. 42 2010 68 71
-
(2010)
Nat. Genet.
, vol.42
, pp. 68-71
-
-
Wallace, C.1
Smyth, D.J.2
Maisuria-Armer, M.3
Walker, N.M.4
Todd, J.A.5
Clayton, D.G.6
-
5
-
-
72449122779
-
Parental origin of sequence variants associated with complex diseases
-
A. Kong, V. Steinthorsdottir, G. Masson, G. Thorleifsson, P. Sulem, S. Besenbacher, A. Jonasdottir, A. Sigurdsson, K.T. Kristinsson, A. Jonasdottir, et al. DIAGRAM Consortium Parental origin of sequence variants associated with complex diseases Nature 462 2009 868 874
-
(2009)
Nature
, vol.462
, pp. 868-874
-
-
Kong, A.1
Steinthorsdottir, V.2
Masson, G.3
Thorleifsson, G.4
Sulem, P.5
Besenbacher, S.6
Jonasdottir, A.7
Sigurdsson, A.8
Kristinsson, K.T.9
Jonasdottir, A.10
-
6
-
-
84897958382
-
Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment
-
R. Nudel, N.H. Simpson, G. Baird, A. O'Hare, G. Conti-Ramsden, P.F. Bolton, E.R. Hennessy, S.M. Ring, G. Davey Smith, C. Francks, et al. SLI Consortium Genome-wide association analyses of child genotype effects and parent-of-origin effects in specific language impairment Genes Brain Behav. 13 2014 418 429
-
(2014)
Genes Brain Behav.
, vol.13
, pp. 418-429
-
-
Nudel, R.1
Simpson, N.H.2
Baird, G.3
O'Hare, A.4
Conti-Ramsden, G.5
Bolton, P.F.6
Hennessy, E.R.7
Ring, S.M.8
Davey Smith, G.9
Francks, C.10
-
7
-
-
84926223357
-
Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance
-
J. Esparza-Gordillo, A. Matanovic, I. Marenholz, A. Bauerfeind, K. Rohde, K. Nemat, M.A. Lee-Kirsch, M. Nordenskjöld, M.C. Winge, T. Keil, and et al. Maternal filaggrin mutations increase the risk of atopic dermatitis in children: an effect independent of mutation inheritance PLoS Genet. 11 2015 e1005076
-
(2015)
PLoS Genet.
, vol.11
-
-
Esparza-Gordillo, J.1
Matanovic, A.2
Marenholz, I.3
Bauerfeind, A.4
Rohde, K.5
Nemat, K.6
Lee-Kirsch, M.A.7
Nordenskjöld, M.8
Winge, M.C.9
Keil, T.10
-
8
-
-
48449083270
-
Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis
-
S.E. Jamieson, L.A. de Roubaix, M. Cortina-Borja, H.K. Tan, E.J. Mui, H.J. Cordell, M.J. Kirisits, E.N. Miller, C.S. Peacock, A.C. Hargrave, and et al. Genetic and epigenetic factors at COL2A1 and ABCA4 influence clinical outcome in congenital toxoplasmosis PLoS ONE 3 2008 e2285
-
(2008)
PLoS ONE
, vol.3
-
-
Jamieson, S.E.1
De Roubaix, L.A.2
Cortina-Borja, M.3
Tan, H.K.4
Mui, E.J.5
Cordell, H.J.6
Kirisits, M.J.7
Miller, E.N.8
Peacock, C.S.9
Hargrave, A.C.10
-
9
-
-
31344467988
-
A method for using incomplete triads to test maternally mediated genetic effects and parent-of-origin effects in relation to a quantitative trait
-
E.O. Kistner, C. Infante-Rivard, and C.R. Weinberg A method for using incomplete triads to test maternally mediated genetic effects and parent-of-origin effects in relation to a quantitative trait Am. J. Epidemiol. 163 2006 255 261
-
(2006)
Am. J. Epidemiol.
, vol.163
, pp. 255-261
-
-
Kistner, E.O.1
Infante-Rivard, C.2
Weinberg, C.R.3
-
10
-
-
38049025721
-
Quantitative trait association in parent offspring trios: Extension of case/pseudocontrol method and comparison of prospective and retrospective approaches
-
E. Wheeler, and H.J. Cordell Quantitative trait association in parent offspring trios: Extension of case/pseudocontrol method and comparison of prospective and retrospective approaches Genet. Epidemiol. 31 2007 813 833
-
(2007)
Genet. Epidemiol.
, vol.31
, pp. 813-833
-
-
Wheeler, E.1
Cordell, H.J.2
-
11
-
-
77149160020
-
A powerful genome-wide feasible approach to detect parent-of-origin effects in studies of quantitative traits
-
N.M. Belonogova, T.I. Axenovich, and Y.S. Aulchenko A powerful genome-wide feasible approach to detect parent-of-origin effects in studies of quantitative traits Eur. J. Hum. Genet. 18 2010 379 384
-
(2010)
Eur. J. Hum. Genet.
, vol.18
, pp. 379-384
-
-
Belonogova, N.M.1
Axenovich, T.I.2
Aulchenko, Y.S.3
-
12
-
-
84905474692
-
Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index
-
C.J. Hoggart, G. Venturini, M. Mangino, F. Gomez, G. Ascari, J.H. Zhao, A. Teumer, T.W. Winkler, N. Tšernikova, J. Luan, et al. Generation Scotland Consortium LifeLines Cohort study GIANT Consortium Novel approach identifies SNPs in SLC2A10 and KCNK9 with evidence for parent-of-origin effect on body mass index PLoS Genet. 10 2014 e1004508
-
(2014)
PLoS Genet.
, vol.10
-
-
Hoggart, C.J.1
Venturini, G.2
Mangino, M.3
Gomez, F.4
Ascari, G.5
Zhao, J.H.6
Teumer, A.7
Winkler, T.W.8
Tšernikova, N.9
Luan, J.10
-
13
-
-
84929751447
-
Review of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits
-
S. Connolly, and E.A. Heron Review of statistical methodologies for the detection of parent-of-origin effects in family trio genome-wide association data with binary disease traits Brief. Bioinform. 16 2015 429 448
-
(2015)
Brief. Bioinform.
, vol.16
, pp. 429-448
-
-
Connolly, S.1
Heron, E.A.2
-
14
-
-
34548292504
-
PLINK: a tool set for whole-genome association and population-based linkage analyses
-
S. Purcell, B. Neale, K. Todd-Brown, L. Thomas, M.A. Ferreira, D. Bender, J. Maller, P. Sklar, P.I. de Bakker, M.J. Daly, and P.C. Sham PLINK: a tool set for whole-genome association and population-based linkage analyses Am. J. Hum. Genet. 81 2007 559 575
-
(2007)
Am. J. Hum. Genet.
, vol.81
, pp. 559-575
-
-
Purcell, S.1
Neale, B.2
Todd-Brown, K.3
Thomas, L.4
Ferreira, M.A.5
Bender, D.6
Maller, J.7
Sklar, P.8
De Bakker, P.I.9
Daly, M.J.10
Sham, P.C.11
-
15
-
-
0027377799
-
Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM)
-
R.S. Spielman, R.E. McGinnis, and W.J. Ewens Transmission test for linkage disequilibrium: the insulin gene region and insulin-dependent diabetes mellitus (IDDM) Am. J. Hum. Genet. 52 1993 506 516
-
(1993)
Am. J. Hum. Genet.
, vol.52
, pp. 506-516
-
-
Spielman, R.S.1
McGinnis, R.E.2
Ewens, W.J.3
-
16
-
-
0033362236
-
Methods for detection of parent-of-origin effects in genetic studies of case-parents triads
-
C.R. Weinberg Methods for detection of parent-of-origin effects in genetic studies of case-parents triads Am. J. Hum. Genet. 65 1999 229 235
-
(1999)
Am. J. Hum. Genet.
, vol.65
, pp. 229-235
-
-
Weinberg, C.R.1
-
17
-
-
0031949066
-
A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting
-
C.R. Weinberg, A.J. Wilcox, and R.T. Lie A log-linear approach to case-parent-triad data: assessing effects of disease genes that act either directly or through maternal effects and that may be subject to parental imprinting Am. J. Hum. Genet. 62 1998 969 978
-
(1998)
Am. J. Hum. Genet.
, vol.62
, pp. 969-978
-
-
Weinberg, C.R.1
Wilcox, A.J.2
Lie, R.T.3
-
18
-
-
33846635400
-
A simple method for detection of imprinting effects based on case-parents trios
-
J.Y. Zhou, Y.Q. Hu, and W.K. Fung A simple method for detection of imprinting effects based on case-parents trios Heredity (Edinb) 98 2007 85 91
-
(2007)
Heredity (Edinb)
, vol.98
, pp. 85-91
-
-
Zhou, J.Y.1
Hu, Y.Q.2
Fung, W.K.3
-
19
-
-
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
-
H.J. Cordell, B.J. Barratt, and D.G. Clayton 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. 26 2004 167 185
-
(2004)
Genet. Epidemiol.
, vol.26
, pp. 167-185
-
-
Cordell, H.J.1
Barratt, B.J.2
Clayton, D.G.3
-
20
-
-
78650311616
-
Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring
-
H.F. Ainsworth, J. Unwin, D.L. Jamison, and H.J. Cordell Investigation of maternal effects, maternal-fetal interactions and parent-of-origin effects (imprinting), using mothers and their offspring Genet. Epidemiol. 35 2011 19 45
-
(2011)
Genet. Epidemiol.
, vol.35
, pp. 19-45
-
-
Ainsworth, H.F.1
Unwin, J.2
Jamison, D.L.3
Cordell, H.J.4
-
21
-
-
84862747876
-
PREMIM and EMIM: tools for estimation of maternal, imprinting and interaction effects using multinomial modelling
-
R. Howey, and H.J. Cordell PREMIM and EMIM: tools for estimation of maternal, imprinting and interaction effects using multinomial modelling BMC Bioinformatics 13 2012 149
-
(2012)
BMC Bioinformatics
, vol.13
, pp. 149
-
-
Howey, R.1
Cordell, H.J.2
-
22
-
-
33750621366
-
Detection of parent-of-origin effects in nuclear families using haplotype analysis
-
T. Becker, M.P. Baur, and M. Knapp Detection of parent-of-origin effects in nuclear families using haplotype analysis Hum. Hered. 62 2006 64 76
-
(2006)
Hum. Hered.
, vol.62
, pp. 64-76
-
-
Becker, T.1
Baur, M.P.2
Knapp, M.3
-
23
-
-
57449096200
-
Detection of parent-of-origin effects in complete and incomplete nuclear families with multiple affected children using multiple tightly linked markers
-
J.Y. Zhou, S. Lin, W.K. Fung, and Y.Q. Hu Detection of parent-of-origin effects in complete and incomplete nuclear families with multiple affected children using multiple tightly linked markers Hum. Hered. 67 2009 116 127
-
(2009)
Hum. Hered.
, vol.67
, pp. 116-127
-
-
Zhou, J.Y.1
Lin, S.2
Fung, W.K.3
Hu, Y.Q.4
-
24
-
-
33645727811
-
Case-parent triads: estimating single- and double-dose effects of fetal and maternal disease gene haplotypes
-
H.K. Gjessing, and R.T. Lie Case-parent triads: estimating single- and double-dose effects of fetal and maternal disease gene haplotypes Ann. Hum. Genet. 70 2006 382 396
-
(2006)
Ann. Hum. Genet.
, vol.70
, pp. 382-396
-
-
Gjessing, H.K.1
Lie, R.T.2
-
25
-
-
65449146360
-
Using case-parent triads to estimate relative risks associated with a candidate haplotype
-
M. Shi, D.M. Umbach, and C.R. Weinberg Using case-parent triads to estimate relative risks associated with a candidate haplotype Ann. Hum. Genet. 73 2009 346 359
-
(2009)
Ann. Hum. Genet.
, vol.73
, pp. 346-359
-
-
Shi, M.1
Umbach, D.M.2
Weinberg, C.R.3
-
26
-
-
12744269459
-
HAPLORE: a program for haplotype reconstruction in general pedigrees without recombination
-
K. Zhang, F. Sun, and H. Zhao HAPLORE: a program for haplotype reconstruction in general pedigrees without recombination Bioinformatics 21 2005 90 103
-
(2005)
Bioinformatics
, vol.21
, pp. 90-103
-
-
Zhang, K.1
Sun, F.2
Zhao, H.3
-
27
-
-
41649094148
-
Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data
-
F. Dudbridge Likelihood-based association analysis for nuclear families and unrelated subjects with missing genotype data Hum. Hered. 66 2008 87 98
-
(2008)
Hum. Hered.
, vol.66
, pp. 87-98
-
-
Dudbridge, F.1
-
28
-
-
26844482093
-
A fine-scale map of recombination rates and hotspots across the human genome
-
S. Myers, L. Bottolo, C. Freeman, G. McVean, and P. Donnelly A fine-scale map of recombination rates and hotspots across the human genome Science 310 2005 321 324
-
(2005)
Science
, vol.310
, pp. 321-324
-
-
Myers, S.1
Bottolo, L.2
Freeman, C.3
McVean, G.4
Donnelly, P.5
-
29
-
-
35348983887
-
A second generation human haplotype map of over 3.1 million SNPs
-
K.A. Frazer, D.G. Ballinger, D.R. Cox, D.A. Hinds, L.L. Stuve, R.A. Gibbs, J.W. Belmont, A. Boudreau, P. Hardenbol, S.M. Leal, et al. International HapMap Consortium A second generation human haplotype map of over 3.1 million SNPs Nature 449 2007 851 861
-
(2007)
Nature
, vol.449
, pp. 851-861
-
-
Frazer, K.A.1
Ballinger, D.G.2
Cox, D.R.3
Hinds, D.A.4
Stuve, L.L.5
Gibbs, R.A.6
Belmont, J.W.7
Boudreau, A.8
Hardenbol, P.9
Leal, S.M.10
-
30
-
-
77953808087
-
Genotype imputation for genome-wide association studies
-
J. Marchini, and B. Howie Genotype imputation for genome-wide association studies Nat. Rev. Genet. 11 2010 499 511
-
(2010)
Nat. Rev. Genet.
, vol.11
, pp. 499-511
-
-
Marchini, J.1
Howie, B.2
-
31
-
-
84856478855
-
A linear complexity phasing method for thousands of genomes
-
O. Delaneau, J. Marchini, and J.F. Zagury A linear complexity phasing method for thousands of genomes Nat. Methods 9 2012 179 181
-
(2012)
Nat. Methods
, vol.9
, pp. 179-181
-
-
Delaneau, O.1
Marchini, J.2
Zagury, J.F.3
-
32
-
-
84871952176
-
Improved whole-chromosome phasing for disease and population genetic studies
-
O. Delaneau, J.F. Zagury, and J. Marchini Improved whole-chromosome phasing for disease and population genetic studies Nat. Methods 10 2013 5 6
-
(2013)
Nat. Methods
, vol.10
, pp. 5-6
-
-
Delaneau, O.1
Zagury, J.F.2
Marchini, J.3
-
33
-
-
27544433613
-
SimPed: a simulation program to generate haplotype and genotype data for pedigree structures
-
S.M. Leal, K. Yan, and B. Müller-Myhsok SimPed: a simulation program to generate haplotype and genotype data for pedigree structures Hum. Hered. 60 2005 119 122
-
(2005)
Hum. Hered.
, vol.60
, pp. 119-122
-
-
Leal, S.M.1
Yan, K.2
Müller-Myhsok, B.3
-
34
-
-
78651100696
-
Data quality control in genetic case-control association studies
-
C.A. Anderson, F.H. Pettersson, G.M. Clarke, L.R. Cardon, A.P. Morris, and K.T. Zondervan Data quality control in genetic case-control association studies Nat. Protoc. 5 2010 1564 1573
-
(2010)
Nat. Protoc.
, vol.5
, pp. 1564-1573
-
-
Anderson, C.A.1
Pettersson, F.H.2
Clarke, G.M.3
Cardon, L.R.4
Morris, A.P.5
Zondervan, K.T.6
-
35
-
-
84875272446
-
Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot
-
H.J. Cordell, A. Töpf, C. Mamasoula, A.V. Postma, J. Bentham, D. Zelenika, S. Heath, G. Blue, C. Cosgrove, J. Granados Riveron, and et al. Genome-wide association study identifies loci on 12q24 and 13q32 associated with tetralogy of Fallot Hum. Mol. Genet. 22 2013 1473 1481
-
(2013)
Hum. Mol. Genet.
, vol.22
, pp. 1473-1481
-
-
Cordell, H.J.1
Töpf, A.2
Mamasoula, C.3
Postma, A.V.4
Bentham, J.5
Zelenika, D.6
Heath, S.7
Blue, G.8
Cosgrove, C.9
Granados Riveron, J.10
-
36
-
-
0032714352
-
Genomic control for association studies
-
B. Devlin, and K. Roeder Genomic control for association studies Biometrics 55 1999 997 1004
-
(1999)
Biometrics
, vol.55
, pp. 997-1004
-
-
Devlin, B.1
Roeder, K.2
-
38
-
-
33644877450
-
The imprinted gene and parent-of-origin effect database now includes parental origin of de novo mutations
-
R.L. Glaser, J.P. Ramsay, and I.M. Morison The imprinted gene and parent-of-origin effect database now includes parental origin of de novo mutations Nucleic Acids Res. 34 2006 D29 D31
-
(2006)
Nucleic Acids Res.
, vol.34
, pp. D29-D31
-
-
Glaser, R.L.1
Ramsay, J.P.2
Morison, I.M.3
-
39
-
-
0034774633
-
Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region
-
D. Kotzot Comparative analysis of isodisomic and heterodisomic segments in cases with maternal uniparental disomy 14 suggests more than one imprinted region Clin. Genet. 60 2001 226 231
-
(2001)
Clin. Genet.
, vol.60
, pp. 226-231
-
-
Kotzot, D.1
-
40
-
-
0034726689
-
Search for imprinted regions on chromosome 14: comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion
-
V.R. Sutton, and L.G. Shaffer Search for imprinted regions on chromosome 14: comparison of maternal and paternal UPD cases with cases of chromosome 14 deletion Am. J. Med. Genet. 93 2000 381 387
-
(2000)
Am. J. Med. Genet.
, vol.93
, pp. 381-387
-
-
Sutton, V.R.1
Shaffer, L.G.2
|