-
1
-
-
57449085114
-
Noninvasive prenatal detection of fetal chromosomal aneuploidies by maternal plasma nucleic acid analysis: A review of the current state of the art
-
10.1111/j.1471-0528.2008.02010.x 19076946
-
Noninvasive prenatal detection of fetal chromosomal aneuploidies by maternal plasma nucleic acid analysis: a review of the current state of the art. Lo YM, BJOG 2009 116 2 152 157 10.1111/j.1471-0528.2008.02010.x 19076946
-
(2009)
BJOG
, vol.116
, Issue.2
, pp. 152-157
-
-
Lo, Y.M.1
-
2
-
-
27744477773
-
First-trimester or second-trimester screening, or both, for Down's syndrome
-
10.1056/NEJMoa043693 16282175
-
First-trimester or second-trimester screening, or both, for Down's syndrome. Malone FD, Canick JA, Ball RH, Nyberg DA, Comstock CH, Bukowski R, Berkowitz RL, Gross SJ, Dugoff L, Craigo SD, et al. N Engl J Med 2005 353 19 2001 2011 10.1056/NEJMoa043693 16282175
-
(2005)
N Engl J Med
, vol.353
, Issue.19
, pp. 2001-2011
-
-
Malone, F.D.1
Canick, J.A.2
Ball, R.H.3
Nyberg, D.A.4
Comstock, C.H.5
Bukowski, R.6
Berkowitz, R.L.7
Gross, S.J.8
Dugoff, L.9
Craigo, S.D.10
-
3
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
10.1016/S0140-6736(97)02174-0 9274585
-
Presence of fetal DNA in maternal plasma and serum. Lo YM, Corbetta N, Chamberlain PF, Rai V, Sargent IL, Redman CW, Wainscoat JS, Lancet 1997 350 9076 485 487 10.1016/S0140-6736(97)02174-0 9274585
-
(1997)
Lancet
, vol.350
, Issue.9076
, pp. 485-487
-
-
Lo, Y.M.1
Corbetta, N.2
Chamberlain, P.F.3
Rai, V.4
Sargent, I.L.5
Redman, C.W.6
Wainscoat, J.S.7
-
4
-
-
0037447089
-
MRNA of placental origin is readily detectable in maternal plasma
-
10.1073/pnas.0637450100 12644709
-
mRNA of placental origin is readily detectable in maternal plasma. Ng EK, Tsui NB, Lau TK, Leung TN, Chiu RW, Panesar NS, Lit LC, Chan KW, Lo YM, Proc Natl Acad Sci U S A 2003 100 8 4748 4753 10.1073/pnas.0637450100 12644709
-
(2003)
Proc Natl Acad Sci U S A
, vol.100
, Issue.8
, pp. 4748-4753
-
-
Ng, E.K.1
Tsui, N.B.2
Lau, T.K.3
Leung, T.N.4
Chiu, R.W.5
Panesar, N.S.6
Lit, L.C.7
Chan, K.W.8
Lo, Y.M.9
-
5
-
-
2642529740
-
Systematic micro-array based identification of placental mRNA in maternal plasma: Towards non-invasive prenatal gene expression profiling
-
10.1136/jmg.2003.016881 15173234
-
Systematic micro-array based identification of placental mRNA in maternal plasma: towards non-invasive prenatal gene expression profiling. Tsui NB, Chim SS, Chiu RW, Lau TK, Ng EK, Leung TN, Tong YK, Chan KC, Lo YM, J Med Genet 2004 41 6 461 467 10.1136/jmg.2003.016881 15173234
-
(2004)
J Med Genet
, vol.41
, Issue.6
, pp. 461-467
-
-
Tsui, N.B.1
Chim, S.S.2
Chiu, R.W.3
Lau, T.K.4
Ng, E.K.5
Leung, T.N.6
Tong, Y.K.7
Chan, K.C.8
Lo, Y.M.9
-
6
-
-
0036140193
-
Differential DNA methylation between fetus and mother as a strategy for detecting fetal DNA in maternal plasma
-
11751536
-
Differential DNA methylation between fetus and mother as a strategy for detecting fetal DNA in maternal plasma. Poon LL, Leung TN, Lau TK, Chow KC, Lo YM, Clin Chem 2002 48 1 35 41 11751536
-
(2002)
Clin Chem
, vol.48
, Issue.1
, pp. 35-41
-
-
Poon, L.L.1
Leung, T.N.2
Lau, T.K.3
Chow, K.C.4
Lo, Y.M.5
-
7
-
-
37349014758
-
Quantitative aberrations of hypermethylated RASSF1A gene sequences in maternal plasma in pre-eclampsia
-
10.1002/pd.1897 17994635
-
Quantitative aberrations of hypermethylated RASSF1A gene sequences in maternal plasma in pre-eclampsia. Tsui DW, Chan KC, Chim SS, Chan LW, Leung TY, Lau TK, Lo YM, Chiu RW, Prenat Diagn 2007 27 13 1212 1218 10.1002/pd.1897 17994635
-
(2007)
Prenat Diagn
, vol.27
, Issue.13
, pp. 1212-1218
-
-
Tsui, D.W.1
Chan, K.C.2
Chim, S.S.3
Chan, L.W.4
Leung, T.Y.5
Lau, T.K.6
Lo, Y.M.7
Chiu, R.W.8
-
8
-
-
35648987069
-
Detection of restriction enzyme-digested target DNA by PCR amplification using a stem-loop primer: Application to the detection of hypomethylated fetal DNA in maternal plasma
-
10.1373/clinchem.2007.092619 17901110
-
Detection of restriction enzyme-digested target DNA by PCR amplification using a stem-loop primer: application to the detection of hypomethylated fetal DNA in maternal plasma. Tong YK, Chiu RW, Leung TY, Ding C, Lau TK, Leung TN, Lo YM, Clin Chem 2007 53 11 1906 1914 10.1373/clinchem.2007.092619 17901110
-
(2007)
Clin Chem
, vol.53
, Issue.11
, pp. 1906-1914
-
-
Tong, Y.K.1
Chiu, R.W.2
Leung, T.Y.3
Ding, C.4
Lau, T.K.5
Leung, T.N.6
Lo, Y.M.7
-
9
-
-
65649095218
-
Sites of differential DNA methylation between placenta and peripheral blood: Molecular markers for noninvasive prenatal diagnosis of aneuploidies
-
10.2353/ajpath.2009.081038 19349366
-
Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies. Papageorgiou EA, Fiegler H, Rakyan V, Beck S, Hulten M, Lamnissou K, Carter NP, Patsalis PC, Am J Pathol 2009 174 5 1609 1618 10.2353/ajpath.2009.081038 19349366
-
(2009)
Am J Pathol
, vol.174
, Issue.5
, pp. 1609-1618
-
-
Papageorgiou, E.A.1
Fiegler, H.2
Rakyan, V.3
Beck, S.4
Hulten, M.5
Lamnissou, K.6
Carter, N.P.7
Patsalis, P.C.8
-
10
-
-
79953739378
-
Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21
-
10.1038/nm.2312 21378977
-
Fetal-specific DNA methylation ratio permits noninvasive prenatal diagnosis of trisomy 21. Papageorgiou EA, Karagrigoriou A, Tsaliki E, Velissariou V, Carter NP, Patsalis PC, Nat Med 2011 17 4 510 513 10.1038/nm.2312 21378977
-
(2011)
Nat Med
, vol.17
, Issue.4
, pp. 510-513
-
-
Papageorgiou, E.A.1
Karagrigoriou, A.2
Tsaliki, E.3
Velissariou, V.4
Carter, N.P.5
Patsalis, P.C.6
-
11
-
-
33745700202
-
Genome-wide profiling of CpG methylation identifies novel targets of aberrant hypermethylation in myeloid leukemia
-
10.1158/0008-5472.CAN-06-0376 16778185
-
Genome-wide profiling of CpG methylation identifies novel targets of aberrant hypermethylation in myeloid leukemia. Gebhard C, Schwarzfischer L, Pham TH, Schilling E, Klug M, Andreesen R, Rehli M, Cancer Res 2006 66 12 6118 6128 10.1158/0008-5472.CAN-06-0376 16778185
-
(2006)
Cancer Res
, vol.66
, Issue.12
, pp. 6118-6128
-
-
Gebhard, C.1
Schwarzfischer, L.2
Pham, T.H.3
Schilling, E.4
Klug, M.5
Andreesen, R.6
Rehli, M.7
-
12
-
-
33748055105
-
MIRA-assisted microarray analysis, a new technology for the determination of DNA methylation patterns, identifies frequent methylation of homeodomain-containing genes in lung cancer cells
-
10.1158/0008-5472.CAN-06-1888 16912168
-
MIRA-assisted microarray analysis, a new technology for the determination of DNA methylation patterns, identifies frequent methylation of homeodomain-containing genes in lung cancer cells. Rauch T, Li H, Wu X, Pfeifer GP, Cancer Res 2006 66 16 7939 7947 10.1158/0008-5472.CAN-06-1888 16912168
-
(2006)
Cancer Res
, vol.66
, Issue.16
, pp. 7939-7947
-
-
Rauch, T.1
Li, H.2
Wu, X.3
Pfeifer, G.P.4
-
13
-
-
34248361968
-
Homeobox gene methylation in lung cancer studied by genome-wide analysis with a microarray-based methylated CpG island recovery assay
-
10.1073/pnas.0701059104 17369352
-
Homeobox gene methylation in lung cancer studied by genome-wide analysis with a microarray-based methylated CpG island recovery assay. Rauch T, Wang Z, Zhang X, Zhong X, Wu X, Lau SK, Kernstine KH, Riggs AD, Pfeifer GP, Proc Natl Acad Sci U S A 2007 104 13 5527 5532 10.1073/pnas.0701059104 17369352
-
(2007)
Proc Natl Acad Sci U S A
, vol.104
, Issue.13
, pp. 5527-5532
-
-
Rauch, T.1
Wang, Z.2
Zhang, X.3
Zhong, X.4
Wu, X.5
Lau, S.K.6
Kernstine, K.H.7
Riggs, A.D.8
Pfeifer, G.P.9
-
14
-
-
20044362416
-
Epigenome analyses using BAC microarrays identify evolutionary conservation of tissue-specific methylation of SHANK3
-
10.1038/ng1563 15895082
-
Epigenome analyses using BAC microarrays identify evolutionary conservation of tissue-specific methylation of SHANK3. Ching TT, Maunakea AK, Jun P, Hong C, Zardo G, Pinkel D, Albertson DG, Fridlyand J, Mao JH, Shchors K, et al. Nat Genet 2005 37 6 645 651 10.1038/ng1563 15895082
-
(2005)
Nat Genet
, vol.37
, Issue.6
, pp. 645-651
-
-
Ching, T.T.1
Maunakea, A.K.2
Jun, P.3
Hong, C.4
Zardo, G.5
Pinkel, D.6
Albertson, D.G.7
Fridlyand, J.8
Mao, J.H.9
Shchors, K.10
-
15
-
-
37549066863
-
Discovery of epigenetically silenced genes by methylated DNA immunoprecipitation in colon cancer cells
-
10.1158/0008-5472.CAN-07-2687 18089774
-
Discovery of epigenetically silenced genes by methylated DNA immunoprecipitation in colon cancer cells. Jacinto FV, Ballestar E, Ropero S, Esteller M, Cancer Res 2007 67 24 11481 11486 10.1158/0008-5472.CAN-07-2687 18089774
-
(2007)
Cancer Res
, vol.67
, Issue.24
, pp. 11481-11486
-
-
Jacinto, F.V.1
Ballestar, E.2
Ropero, S.3
Esteller, M.4
-
16
-
-
23044514626
-
Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells
-
10.1038/ng1598 16007088
-
Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells. Weber M, Davies JJ, Wittig D, Oakeley EJ, Haase M, Lam WL, Schubeler D, Nat Genet 2005 37 8 853 862 10.1038/ng1598 16007088
-
(2005)
Nat Genet
, vol.37
, Issue.8
, pp. 853-862
-
-
Weber, M.1
Davies, J.J.2
Wittig, D.3
Oakeley, E.J.4
Haase, M.5
Lam, W.L.6
Schubeler, D.7
-
17
-
-
61449322942
-
The MIRA method for DNA methylation analysis
-
10.1007/978-1-59745-522-0-6 18987807
-
The MIRA method for DNA methylation analysis. Rauch TA, Pfeifer GP, Methods Mol Biol 2009 507 65 75 10.1007/978-1-59745-522-0-6 18987807
-
(2009)
Methods Mol Biol
, vol.507
, pp. 65-75
-
-
Rauch, T.A.1
Pfeifer, G.P.2
-
18
-
-
0035942271
-
Significance analysis of microarrays applied to the ionizing radiation response
-
10.1073/pnas.091062498 11309499
-
Significance analysis of microarrays applied to the ionizing radiation response. Tusher VG, Tibshirani R, Chu G, Proc Natl Acad Sci U S A 2001 98 9 5116 5121 10.1073/pnas.091062498 11309499
-
(2001)
Proc Natl Acad Sci U S A
, vol.98
, Issue.9
, pp. 5116-5121
-
-
Tusher, V.G.1
Tibshirani, R.2
Chu, G.3
-
19
-
-
0030825309
-
COBRA: A sensitive and quantitative DNA methylation assay
-
10.1093/nar/25.12.2532 9171110
-
COBRA: a sensitive and quantitative DNA methylation assay. Xiong Z, Laird PW, Nucleic Acids Res 1997 25 12 2532 2534 10.1093/nar/25.12.2532 9171110
-
(1997)
Nucleic Acids Res
, vol.25
, Issue.12
, pp. 2532-2534
-
-
Xiong, Z.1
Laird, P.W.2
-
20
-
-
55049097760
-
Cryptic chromosomal abnormalities identified in children with congenital heart disease
-
10.1203/PDR.0b013e31818095d0 18535492
-
Cryptic chromosomal abnormalities identified in children with congenital heart disease. Richards AA, Santos LJ, Nichols HA, Crider BP, Elder FF, Hauser NS, Zinn AR, Garg V, Pediatr Res 2008 64 4 358 363 10.1203/PDR.0b013e31818095d0 18535492
-
(2008)
Pediatr Res
, vol.64
, Issue.4
, pp. 358-363
-
-
Richards, A.A.1
Santos, L.J.2
Nichols, H.A.3
Crider, B.P.4
Elder, F.F.5
Hauser, N.S.6
Zinn, A.R.7
Garg, V.8
-
21
-
-
81155160840
-
Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype
-
10.1002/uog.8988 21400624
-
Identification of submicroscopic chromosomal aberrations in fetuses with increased nuchal translucency and apparently normal karyotype. Leung TY, Vogel I, Lau TK, Chong W, Hyett JA, Petersen OB, Choy KW, Ultrasound Obstet Gynecol 2011 38 3 314 319 10.1002/uog.8988 21400624
-
(2011)
Ultrasound Obstet Gynecol
, vol.38
, Issue.3
, pp. 314-319
-
-
Leung, T.Y.1
Vogel, I.2
Lau, T.K.3
Chong, W.4
Hyett, J.A.5
Petersen, O.B.6
Choy, K.W.7
-
22
-
-
79952060606
-
Aberrant methylation frequency of TNFRSF10C promoter in pancreatic cancer cell lines
-
10.1016/S1499-3872(11)60014-3 21269942
-
Aberrant methylation frequency of TNFRSF10C promoter in pancreatic cancer cell lines. Cai HH, Sun YM, Miao Y, Gao WT, Peng Q, Yao J, Zhao HL, Hepatobiliary Pancreat Dis Int 2011 10 1 95 100 10.1016/S1499-3872(11)60014-3 21269942
-
(2011)
Hepatobiliary Pancreat Dis Int
, vol.10
, Issue.1
, pp. 95-100
-
-
Cai, H.H.1
Sun, Y.M.2
Miao, Y.3
Gao, W.T.4
Peng, Q.5
Yao, J.6
Zhao, H.L.7
-
23
-
-
77956432698
-
MGMT gene promoter methylation correlates with tolerance of temozolomide treatment in melanoma but not with clinical outcome
-
10.1038/sj.bjc.6605796 20736948
-
MGMT gene promoter methylation correlates with tolerance of temozolomide treatment in melanoma but not with clinical outcome. Hassel JC, Sucker A, Edler L, Kurzen H, Moll I, Stresemann C, Spieth K, Mauch C, Rass K, Dummer R, et al. Br J Cancer 2010 103 6 820 826 10.1038/sj.bjc.6605796 20736948
-
(2010)
Br J Cancer
, vol.103
, Issue.6
, pp. 820-826
-
-
Hassel, J.C.1
Sucker, A.2
Edler, L.3
Kurzen, H.4
Moll, I.5
Stresemann, C.6
Spieth, K.7
Mauch, C.8
Rass, K.9
Dummer, R.10
-
24
-
-
84856080822
-
Gene expression and epigenetic changes by furan in rat liver
-
22079235
-
Gene expression and epigenetic changes by furan in rat liver. Chen T, Williams TD, Mally A, Hamberger C, Mirbahai L, Hickling K, Chipman JK, Toxicology 2012 292 2-3 63 70 22079235
-
(2012)
Toxicology
, vol.292
, Issue.2-3
, pp. 63-70
-
-
Chen, T.1
Williams, T.D.2
Mally, A.3
Hamberger, C.4
Mirbahai, L.5
Hickling, K.6
Chipman, J.K.7
-
25
-
-
77950813610
-
CpG island hypermethylation in human astrocytomas
-
10.1158/0008-5472.CAN-09-3631 20233874
-
CpG island hypermethylation in human astrocytomas. Wu X, Rauch TA, Zhong X, Bennett WP, Latif F, Krex D, Pfeifer GP, Cancer Res 2010 70 7 2718 2727 10.1158/0008-5472.CAN-09-3631 20233874
-
(2010)
Cancer Res
, vol.70
, Issue.7
, pp. 2718-2727
-
-
Wu, X.1
Rauch, T.A.2
Zhong, X.3
Bennett, W.P.4
Latif, F.5
Krex, D.6
Pfeifer, G.P.7
-
26
-
-
0347898005
-
Quantitative analysis of fetal DNA in maternal plasma and serum: Implications for noninvasive prenatal diagnosis
-
10.1086/301800 9529358
-
Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. Lo YM, Tein MS, Lau TK, Haines CJ, Leung TN, Poon PM, Wainscoat JS, Johnson PJ, Chang AM, Hjelm NM, Am J Hum Genet 1998 62 4 768 775 10.1086/301800 9529358
-
(1998)
Am J Hum Genet
, vol.62
, Issue.4
, pp. 768-775
-
-
Lo, Y.M.1
Tein, M.S.2
Lau, T.K.3
Haines, C.J.4
Leung, T.N.5
Poon, P.M.6
Wainscoat, J.S.7
Johnson, P.J.8
Chang, A.M.9
Hjelm, N.M.10
-
27
-
-
0036403788
-
Prenatal diagnosis using fetal cells and cell-free fetal DNA in maternal blood: What is currently feasible?
-
discussion 730-642 10.1097/00003081-200209000-00008 12370604
-
Prenatal diagnosis using fetal cells and cell-free fetal DNA in maternal blood: what is currently feasible? Hahn S, Holzgreve W, Clin Obstet Gynecol 2002 45 3 649 656 discussion 730-642 10.1097/00003081-200209000-00008 12370604
-
(2002)
Clin Obstet Gynecol
, vol.45
, Issue.3
, pp. 649-656
-
-
Hahn, S.1
Holzgreve, W.2
-
28
-
-
40449109999
-
Systematic search for placental DNA-methylation markers on chromosome 21: Toward a maternal plasma-based epigenetic test for fetal trisomy 21
-
10.1373/clinchem.2007.098731 18202156
-
Systematic search for placental DNA-methylation markers on chromosome 21: toward a maternal plasma-based epigenetic test for fetal trisomy 21. Chim SS, Jin S, Lee TY, Lun FM, Lee WS, Chan LY, Jin Y, Yang N, Tong YK, Leung TY, et al. Clin Chem 2008 54 3 500 511 10.1373/clinchem.2007.098731 18202156
-
(2008)
Clin Chem
, vol.54
, Issue.3
, pp. 500-511
-
-
Chim, S.S.1
Jin, S.2
Lee, T.Y.3
Lun, F.M.4
Lee, W.S.5
Chan, L.Y.6
Jin, Y.7
Yang, N.8
Tong, Y.K.9
Leung, T.Y.10
-
29
-
-
84856474843
-
Intragenic DNA methylation: Implications of this epigenetic mechanism for cancer research
-
10.1038/bjc.2011.550 22166804
-
Intragenic DNA methylation: implications of this epigenetic mechanism for cancer research. Shenker N, Flanagan JM, Br J Cancer 2012 106 2 248 253 10.1038/bjc.2011.550 22166804
-
(2012)
Br J Cancer
, vol.106
, Issue.2
, pp. 248-253
-
-
Shenker, N.1
Flanagan, J.M.2
-
30
-
-
3242694973
-
Fetal cell-free nucleic acids in the maternal circulation: New clinical applications
-
10.1196/annals.1318.015 15251945
-
Fetal cell-free nucleic acids in the maternal circulation: new clinical applications. Wataganara T, Bianchi DW, Ann N Y Acad Sci 2004 1022 90 99 10.1196/annals.1318.015 15251945
-
(2004)
Ann N y Acad Sci
, vol.1022
, pp. 90-99
-
-
Wataganara, T.1
Bianchi, D.W.2
-
31
-
-
33645512300
-
An unusual class of PITX2 mutations in Axenfeld-Rieger syndrome
-
10.1002/bdra.20226 16498627
-
An unusual class of PITX2 mutations in Axenfeld-Rieger syndrome. Saadi I, Toro R, Kuburas A, Semina E, Murray JC, Russo AF, Birth Defects Res A Clin Mol Teratol 2006 76 3 175 181 10.1002/bdra.20226 16498627
-
(2006)
Birth Defects Res A Clin Mol Teratol
, vol.76
, Issue.3
, pp. 175-181
-
-
Saadi, I.1
Toro, R.2
Kuburas, A.3
Semina, E.4
Murray, J.C.5
Russo, A.F.6
-
32
-
-
33845637974
-
Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome
-
17167399
-
Identification of four new PITX2 gene mutations in patients with Axenfeld-Rieger syndrome. Vieira V, David G, Roche O, de la Houssaye G, Boutboul S, Arbogast L, Kobetz A, Orssaud C, Camand O, Schorderet DF, et al. Mol Vis 2006 12 1448 1460 17167399
-
(2006)
Mol Vis
, vol.12
, pp. 1448-1460
-
-
Vieira, V.1
David, G.2
Roche, O.3
De La Houssaye, G.4
Boutboul, S.5
Arbogast, L.6
Kobetz, A.7
Orssaud, C.8
Camand, O.9
Schorderet, D.F.10
|