-
1
-
-
0344132050
-
A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13
-
Arngrimsson a, Sigurard tS, Frigge ML, Bjarnadottir RI, Jonsson T, Stefansson H, et al. A genome-wide scan reveals a maternal susceptibility locus for pre-eclampsia on chromosome 2p13. Hum Mol Genet 1999; 8:1799-805.
-
(1999)
Hum Mol Genet
, vol.8
-
-
Arngrimsson, A.1
Sigurard, T.S.2
Frigge, M.L.3
Bjarnadottir, R.I.4
Jonsson, T.5
Stefansson, H.6
-
2
-
-
0037219649
-
Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families
-
Laivuori H, Lahermo P, Ollikainen V, Widen E, Haiva-Mallinen L, Sundstrom H, et al. Susceptibility loci for preeclampsia on chromosomes 2p25 and 9p13 in Finnish families. Am J Hum Genet 2003; 72:168-77.
-
(2003)
Am J Hum Genet
, vol.72
, pp. 1633-1617
-
-
Laivuori, H.1
Lahermo, P.2
Ollikainen, V.3
Widen, E.4
Haiva-Mallinen, L.5
Sundstrom, H.6
-
3
-
-
18944388998
-
Fine mapping and SNP analysis of positional candidates at the preeclampsia susceptibility locus (PREG1) on chromosome 2
-
Fitzpatrick E, Goring HH, Liu H, Borg A, Forrest S, Cooper DW, et al. Fine mapping and SNP analysis of positional candidates at the preeclampsia susceptibility locus (PREG1) on chromosome 2. Hum Biol 2004; 76:849-62.
-
(2004)
Hum Biol
, vol.76
, pp. 8433-8486
-
-
Fitzpatrick, E.1
Goring, H.H.2
Liu, H.3
Borg, A.4
Forrest, S.5
Cooper, D.W.6
-
4
-
-
58349118696
-
Association between the candidate susceptibility gene ACVR2A on chromo-some 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study)
-
Roten LT, Johnson MP, Forsmo S, Fitzpatrick E, Dyer TD, Brennecke SP, et al. Association between the candidate susceptibility gene ACVR2A on chromo-some 2q22 and pre-eclampsia in a large Norwegian population-based study (the HUNT study). Eur J Hum Genet 2009; 17:250-7.
-
(2009)
Eur J Hum Genet
, vol.17
, pp. 250-257
-
-
Roten, L.T.1
Johnson, M.P.2
Forsmo, S.3
Fitzpatrick, E.4
Dyer, T.D.5
Brennecke, S.P.6
-
5
-
-
0034748125
-
A genome-wide scan for preeclampsia in the Netherlands
-
Lachmeijer AM, Arngrimsson R, Bastiaans EJ, Frigge ML, Pals G, Sigurdardottir S, et al. A genome-wide scan for preeclampsia in the Netherlands. Eur J Hum Genet 2001; 9:758-64.
-
(2001)
Eur J Hum Genet
, vol.9
, pp. 7533-7576
-
-
Lachmeijer, A.M.1
Arngrimsson, R.2
Bastiaans, E.J.3
Frigge, M.L.4
Pals, G.5
Sigurdardottir, S.6
-
6
-
-
4344708984
-
The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with downregulated expression in androgenetic placentas
-
Oudejans CB, Mulders J, Lachmeijer AM, van Dijk M, Konst AA, Westerman BA, et al. The parent-of-origin effect of 10q22 in pre-eclamptic females coincides with two regions clustered for genes with downregulated expression in androgenetic placentas. Mol Hum Reprod 2004; 10:589-98.
-
(2004)
Mol Hum Reprod
, vol.10
, pp. 5833-5859
-
-
Oudejans, C.B.1
Mulders, J.2
Lachmeijer, A.M.3
van Dijk, M.4
Konst, A.A.5
Westerman, B.A.6
-
7
-
-
8844267643
-
Differential downregulation of alphaT-catenin expression in placenta: Trophoblast cell type-dependent imprinting of the CTNNA3 gene
-
van Dijk M, Mulders J, Konst A, Janssens B, van Roy F, Blankenstein M, et al. Differential downregulation of alphaT-catenin expression in placenta: trophoblast cell type-dependent imprinting of the CTNNA3 gene. Gene Expr Patterns 2004; 5:61-5.
-
(2004)
Gene Expr Patterns
, vol.5
, pp. 61-65
-
-
van Dijk, M.1
Mulders, J.2
Konst, A.3
Janssens, B.4
van Roy, F.5
Blankenstein, M.6
-
8
-
-
18144377731
-
Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family
-
van Dijk M, Mulders J, Poutsma A, Konst AA, Lachmeijer AM, Dekker GA, et al. Maternal segregation of the Dutch preeclampsia locus at 10q22 with a new member of the winged helix gene family. Nat Genet 2005; 37:514-9.
-
(2005)
Nat Genet
, vol.37
, pp. 514-519
-
-
van Dijk, M.1
Mulders, J.2
Poutsma, A.3
Konst, A.A.4
Lachmeijer, A.M.5
Dekker, G.A.6
-
9
-
-
33947669482
-
Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample
-
Kivinen K, Peterson H, Hiltunen L, Laivuori H, Heino S, Tiala I, et al. Evaluation of STOX1 as a preeclampsia candidate gene in a population-wide sample. Eur J Hum Genet 2007; 15:494-7.
-
(2007)
Eur J Hum Genet
, vol.15
, pp. 494-497
-
-
Kivinen, K.1
Peterson, H.2
Hiltunen, L.3
Laivuori, H.4
Heino, S.5
Tiala, I.6
-
10
-
-
33847295115
-
STOX1 is not imprinted and is not likely to be involved in preeclampsia
-
Iglesias-Platas I, Monk D, Jebbink J, Buimer M, Boer K, van der Post J, et al. STOX1 is not imprinted and is not likely to be involved in preeclampsia. Nat Genet 2007; 39:279-80.
-
(2007)
Nat Genet
, vol.39
, pp. 2733-2728
-
-
Iglesias-Platas, I.1
Monk, D.2
Jebbink, J.3
Buimer, M.4
Boer, K.5
van der Post, J.6
-
11
-
-
34547850904
-
STOX1 gene in pre-eclampsia and intrauterine growth restriction
-
Berends AL, Bertoli-Avella AM, de Groot CJ, van Duijn CM, Oostra BA, Steegers EA. STOX1 gene in pre-eclampsia and intrauterine growth restriction. BJOG 2007; 114:1163-7.
-
(2007)
BJOG
, vol.114
, pp. 1163-1167
-
-
Berends, A.L.1
Bertoli-Avella, A.M.2
de Groot, C.J.3
van Duijn, C.M.4
Oostra, B.A.5
Steegers, E.A.6
-
12
-
-
33847317325
-
Reply to "STOX1 is not imprinted and is not likely to be involved in preeclampsia"
-
van Dijk M, van Bezu J, Chim SS, Lo YM, Blankenstein MA, Oudejans CB. Reply to "STOX1 is not imprinted and is not likely to be involved in preeclampsia". Nat Genet 2007; 39:280-1.
-
(2007)
Nat Genet
, vol.39
, pp. 280-281
-
-
van Dijk, M.1
van Bezu, J.2
Chim, S.S.3
Lo, Y.M.4
Blankenstein, M.A.5
Oudejans, C.B.6
-
13
-
-
36749083455
-
A new class of tissue-specifically methylated regions involving entire CpG islands in the mouse
-
Suzuki M, Sato S, Arai Y, Shinohara T, Tanaka S, Greally JM, et al. A new class of tissue-specifically methylated regions involving entire CpG islands in the mouse. Genes Cells 2007; 12:1305-14.
-
(2007)
Genes Cells
, vol.12
, pp. 1305-1314
-
-
Suzuki, M.1
Sato, S.2
Arai, Y.3
Shinohara, T.4
Tanaka, S.5
Greally, J.M.6
-
14
-
-
44449149683
-
Monozygotic twins reveal germline contribution to allelic expression differences
-
Cheung VG, Bruzel A, Burdick JT, Morley M, Devlin JL, Spielman RS. Monozygotic twins reveal germline contribution to allelic expression differences. Am J Hum Genet 2008; 82:1357-60.
-
(2008)
Am J Hum Genet
, vol.82
, pp. 1357-1360
-
-
Cheung, V.G.1
Bruzel, A.2
Burdick, J.T.3
Morley, M.4
Devlin, J.L.5
Spielman, R.S.6
-
15
-
-
0034173022
-
Efficient, rapid and reliable establishment of human trophoblast cell lines using poly-L-ornithine
-
Choy MY, St. Whitley G, Manyonda IT. Efficient, rapid and reliable establishment of human trophoblast cell lines using poly-L-ornithine. Early Pregnancy 2000; 4:124-43.
-
(2000)
Early Pregnancy
, vol.4
, pp. 1233-1214
-
-
Choy, M.Y.1
St. Whitley, G.2
Manyonda, I.T.3
-
16
-
-
77049089715
-
The pre-eclampsia gene STOX1 controls a conserved pathway in placenta and brain upregulated in late-onset Alzheimer's disease
-
van Dijk M, van Bezu J, Poutsma A, Veerhuis R, Rozemuller AJ, Scheper W, et al. The pre-eclampsia gene STOX1 controls a conserved pathway in placenta and brain upregulated in late-onset Alzheimer's disease. J Alzheimers Dis 2010; 19:673-9.
-
(2010)
J Alzheimers Dis
, vol.19
, pp. 673-679
-
-
van Dijk, M.1
van Bezu, J.2
Poutsma, A.3
Veerhuis, R.4
Rozemuller, A.J.5
Scheper, W.6
-
17
-
-
77954162320
-
The STOX1 genotype associated with pre-eclampsia leads to a reduction of trophoblast invasion by alpha-T-catenin upregulation
-
DOI: 10.1093/ hmg/ddq152
-
van Dijk M, van Bezu J, van Abel D, Dunk C, Blankenstein MA, Oudejans CB, et al. The STOX1 genotype associated with pre-eclampsia leads to a reduction of trophoblast invasion by alpha-T-catenin upregulation. Hum Mol Genet 2010; DOI: 10.1093/ hmg/ddq152.
-
(2010)
Hum Mol Genet
-
-
van Dijk, M.1
van Bezu, J.2
van Abel, D.3
Dunk, C.4
Blankenstein, M.A.5
Oudejans, C.B.6
-
18
-
-
46249117780
-
Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation
-
Kerkel K, Spadola A, Yuan E, Kosek J, Jiang L, Hod E, et al. Genomic surveys by methylation-sensitive SNP analysis identify sequence-dependent allele-specific DNA methylation. Nat Genet 2008; 40:904-8.
-
(2008)
Nat Genet
, vol.40
, pp. 904-908
-
-
Kerkel, K.1
Spadola, A.2
Yuan, E.3
Kosek, J.4
Jiang, L.5
Hod, E.6
-
19
-
-
77954238686
-
Allele-specific methylation is prevalent and is contributed by CpG-SNPs in the human genome
-
Shoemaker R, Deng J, Wang W, Zhang K. Allele-specific methylation is prevalent and is contributed by CpG-SNPs in the human genome. Genome Res 2010; 20:883-9.
-
(2010)
Genome Res
, vol.20
, pp. 883-889
-
-
Shoemaker, R.1
Deng, J.2
Wang, W.3
Zhang, K.4
-
20
-
-
0035111294
-
Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: Relation to expression and imprinting
-
Weber M, Milligan L, Delalbre A, Antoine E, Brunel C, Cathala G, et al. Extensive tissue-specific variation of allelic methylation in the Igf2 gene during mouse fetal development: relation to expression and imprinting. Mech Dev 2001; 101:133-41.
-
(2001)
Mech Dev
, vol.101
, pp. 1333-1314
-
-
Weber, M.1
Milligan, L.2
Delalbre, A.3
Antoine, E.4
Brunel, C.5
Cathala, G.6
|