-
1
-
-
0030034519
-
Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum
-
Bianchi DW, Zickwolf GK, Weil GJ, Sylvester S, De Maria MA. Male fetal progenitor cells persist in maternal blood for as long as 27 years postpartum. Proc Natl Acad Sci USA 1996; 93:705-8.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 705-708
-
-
Bianchi, D.W.1
Zickwolf, G.K.2
Weil, G.J.3
Sylvester, S.4
de Maria, M.A.5
-
2
-
-
0029957667
-
Two-way cell traffic between mother and fetus: Biologic and clinical implications
-
Lo YM, Lo ES, Watson N, Noakes L, Sargent IL, Thilaganathan B, Wainscoat JS. Two-way cell traffic between mother and fetus: biologic and clinical implications. Blood 1996; 88:4390-5.
-
(1996)
Blood
, vol.88
, pp. 4390-4395
-
-
Lo, Y.M.1
Lo, E.S.2
Watson, N.3
Noakes, L.4
Sargent, I.L.5
Thilaganathan, B.6
Wainscoat, J.S.7
-
3
-
-
0033804933
-
Fetal cells in the mother: From genetic diagnosis to diseases associated with fetal cell microchimerism
-
Bianchi DW. Fetal cells in the mother: from genetic diagnosis to diseases associated with fetal cell microchimerism. Eur J Obstet Gynecol Reprod Biol 2000; 92:103-8.
-
(2000)
Eur J Obstet Gynecol Reprod Biol
, vol.92
, pp. 103-108
-
-
Bianchi, D.W.1
-
4
-
-
0033559750
-
Long-term fetal microchimerism in peripheral blood mononuclear cell subsets in healthy women and women with scleroderma
-
Evans PC, Lambert N, Maloney S, Furst DE, Moore JM, Nelson JL. Long-term fetal microchimerism in peripheral blood mononuclear cell subsets in healthy women and women with scleroderma. Blood 1999; 93:2033-7.
-
(1999)
Blood
, vol.93
, pp. 2033-2037
-
-
Evans, P.C.1
Lambert, N.2
Maloney, S.3
Furst, D.E.4
Moore, J.M.5
Nelson, J.L.6
-
5
-
-
0032717523
-
Microchimerism of maternal origin persists into adult life
-
Maloney S, Smith A, Furst DE, Myerson D, Rupert K, Evans PC, Nelson JL. Microchimerism of maternal origin persists into adult life. J Clin Invest 1999; 104:41-7.
-
(1999)
J Clin Invest
, vol.104
, pp. 41-47
-
-
Maloney, S.1
Smith, A.2
Furst, D.E.3
Myerson, D.4
Rupert, K.5
Evans, P.C.6
Nelson, J.L.7
-
6
-
-
0032796001
-
Microchimerism: Implications for autoimmune disease
-
Nelson JL. Microchimerism: implications for autoimmune disease. Lupus 1999; 8:370-4.
-
(1999)
Lupus
, vol.8
, pp. 370-374
-
-
Nelson, J.L.1
-
7
-
-
0036918548
-
Feto-maternal microchimerism in connective tissue diseases
-
Gannage M, Amoura Z, Lantz O, Piette JC, Caillat-Zucman S. Feto-maternal microchimerism in connective tissue diseases. Eur J Immunol 2002; 32:3405-13.
-
(2002)
Eur J Immunol
, vol.32
, pp. 3405-3413
-
-
Gannage, M.1
Amoura, Z.2
Lantz, O.3
Piette, J.C.4
Caillat-Zucman, S.5
-
8
-
-
0141819038
-
Microchimerism in autoimmune disease: More questions than answers?
-
Lambert N, Nelson JL. Microchimerism in autoimmune disease: more questions than answers? Autoimmun Rev 2003; 2:133-9.
-
(2003)
Autoimmun Rev
, vol.2
, pp. 133-139
-
-
Lambert, N.1
Nelson, J.L.2
-
9
-
-
0025364769
-
Isolation of fetal DNA from nucleated erythrocytes in maternal blood
-
Bianchi DW, Flint AF, Pizzimenti MF, Knoll JH, Latt SA. Isolation of fetal DNA from nucleated erythrocytes in maternal blood. Proc Natl Acad Sci USA 1990; 87:3279-83.
-
(1990)
Proc Natl Acad Sci USA
, vol.87
, pp. 3279-3283
-
-
Bianchi, D.W.1
Flint, A.F.2
Pizzimenti, M.F.3
Knoll, J.H.4
Latt, S.A.5
-
10
-
-
0029589896
-
Prenatal diagnosis by analysis of fetal cells in maternal blood
-
Bianchi DW. Prenatal diagnosis by analysis of fetal cells in maternal blood. J Pediatr 1995; 127:847-56.
-
(1995)
J Pediatr
, vol.127
, pp. 847-856
-
-
Bianchi, D.W.1
-
11
-
-
0031725469
-
Fetal cells in maternal blood as a second non-invasive step for fetal Down syndrome screening
-
Farina A, Bianchi DW. Fetal cells in maternal blood as a second non-invasive step for fetal Down syndrome screening. Prenat Diagn 1998; 18:983-4.
-
(1998)
Prenat Diagn
, vol.18
, pp. 983-984
-
-
Farina, A.1
Bianchi, D.W.2
-
12
-
-
0030293185
-
Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood
-
Cheung MC, Goldberg JD, Kan YW. Prenatal diagnosis of sickle cell anaemia and thalassaemia by analysis of fetal cells in maternal blood. Nat Genet 1996; 14:264-8.
-
(1996)
Nat Genet
, vol.14
, pp. 264-268
-
-
Cheung, M.C.1
Goldberg, J.D.2
Kan, Y.W.3
-
14
-
-
0342618532
-
Presence of fetal DNA in maternal plasma and serum
-
Lo YM, Corbetta N, Chamberlain PF, Rai V, Sargent IL, Redman CW, Wainscoat JS. Presence of fetal DNA in maternal plasma and serum. Lancet 1997; 350:485-7.
-
(1997)
Lancet
, vol.350
, 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
-
15
-
-
0030776456
-
PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies
-
Bianchi DW, Williams JM, Sullivan LM, Hanson FW, Klinger KW, Shuber AP. PCR quantitation of fetal cells in maternal blood in normal and aneuploid pregnancies. Am J Hum Genet 1997; 61:822-9.
-
(1997)
Am J Hum Genet
, vol.61
, pp. 822-829
-
-
Bianchi, D.W.1
Williams, J.M.2
Sullivan, L.M.3
Hanson, F.W.4
Klinger, K.W.5
Shuber, A.P.6
-
16
-
-
0347898005
-
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, et al. Quantitative analysis of fetal DNA in maternal plasma and serum: implications for noninvasive prenatal diagnosis. Am J Hum Genet 1998; 62:768-75.
-
(1998)
Am J Hum Genet
, vol.62
, 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
-
17
-
-
0033364339
-
Rapid clearance of fetal DNA from maternal plasma
-
Lo YM, Zhang J, Leung TN, Lau TK, Chang AM, Hjelm NM. Rapid clearance of fetal DNA from maternal plasma. Am J Hum Genet 1999; 64:218-24.
-
(1999)
Am J Hum Genet
, vol.64
, pp. 218-224
-
-
Lo, Y.M.1
Zhang, J.2
Leung, T.N.3
Lau, T.K.4
Chang, A.M.5
Hjelm, N.M.6
-
18
-
-
0033639168
-
Fetal DNA in maternal plasma: Biology and diagnostic applications
-
Lo YM. Fetal DNA in maternal plasma: biology and diagnostic applications. Clin Chem 2000; 46:1903-6.
-
(2000)
Clin Chem
, vol.46
, pp. 1903-1906
-
-
Lo, Y.M.1
-
19
-
-
0032506669
-
Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma
-
Lo YM, Hjelm NM, Fidler C, Sargent IL, Murphy MF, Chamberlain PF, et al. Prenatal diagnosis of fetal RhD status by molecular analysis of maternal plasma. N Engl J Med 1998; 339:1734-8.
-
(1998)
N Engl J Med
, vol.339
, pp. 1734-1738
-
-
Lo, Y.M.1
Hjelm, N.M.2
Fidler, C.3
Sargent, I.L.4
Murphy, M.F.5
Chamberlain, P.F.6
-
20
-
-
0032505654
-
Detection of fetal RHDspecific sequences in maternal plasma
-
Faas BH, Beuling EA, Christiaens GC, von dem Borne AE, van der Schoot CE. Detection of fetal RHDspecific sequences in maternal plasma. Lancet 1998; 352:1196.
-
(1998)
Lancet
, vol.352
, pp. 1196
-
-
Faas, B.H.1
Beuling, E.A.2
Christiaens, G.C.3
von dem Borne, A.E.4
van der Schoot, C.E.5
-
21
-
-
0036692036
-
Prediction of fetal D status from maternal plasma: Introduction of a new noninvasive fetal RHD genotyping service
-
Finning KM, Martin PG, Soothill PW, Avent ND. Prediction of fetal D status from maternal plasma: introduction of a new noninvasive fetal RHD genotyping service. Transfusion 2002; 42:1079-85.
-
(2002)
Transfusion
, vol.42
, pp. 1079-1085
-
-
Finning, K.M.1
Martin, P.G.2
Soothill, P.W.3
Avent, N.D.4
-
22
-
-
0037046654
-
New strategy for prenatal diagnosis of X-linked disorders
-
Costa JM, Benachi A, Gautier E. New strategy for prenatal diagnosis of X-linked disorders. N Engl J Med 2002; 346:1502.
-
(2002)
N Engl J Med
, vol.346
, pp. 1502
-
-
Costa, J.M.1
Benachi, A.2
Gautier, E.3
-
23
-
-
0037190608
-
Prenatal exclusion of beta thalassaemia major by examination of maternal plasma
-
Chiu RW, Lau TK, Leung TN, Chow KC, Chui DH, Lo YM. Prenatal exclusion of beta thalassaemia major by examination of maternal plasma. Lancet 2002; 360:998-1000.
-
(2002)
Lancet
, vol.360
, pp. 998-1000
-
-
Chiu, R.W.1
Lau, T.K.2
Leung, T.N.3
Chow, K.C.4
Chui, D.H.5
Lo, Y.M.6
-
24
-
-
3242703837
-
MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis
-
Ding C, Chiu RW, Lau TK, Leung TN, Chan LC, Chan AY, et al. MS analysis of single-nucleotide differences in circulating nucleic acids: Application to noninvasive prenatal diagnosis. Proc Natl Acad Sci USA 2004; 101:10762-7.
-
(2004)
Proc Natl Acad Sci USA
, vol.101
, pp. 10762-10767
-
-
Ding, C.1
Chiu, R.W.2
Lau, T.K.3
Leung, T.N.4
Chan, L.C.5
Chan, A.Y.6
-
25
-
-
13844269123
-
Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma
-
Li Y, Di Naro E, Vitucci A, Zimmermann B, Holzgreve W, Hahn S. Detection of paternally inherited fetal point mutations for beta-thalassemia using size-fractionated cell-free DNA in maternal plasma. JAMA 2005; 293:843-9.
-
(2005)
JAMA
, vol.293
, pp. 843-849
-
-
Li, Y.1
di Naro, E.2
Vitucci, A.3
Zimmermann, B.4
Holzgreve, W.5
Hahn, S.6
-
26
-
-
0033968645
-
Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma
-
Amicucci P, Gennarelli M, Novelli G, Dallapiccola B. Prenatal diagnosis of myotonic dystrophy using fetal DNA obtained from maternal plasma. Clin Chem 2000; 46:301-2.
-
(2000)
Clin Chem
, vol.46
, pp. 301-302
-
-
Amicucci, P.1
Gennarelli, M.2
Novelli, G.3
Dallapiccola, B.4
-
27
-
-
0036231537
-
Noninvasive prenatal exclusion of congenital adrenal hyperplasia by maternal plasma analysis: A feasibility study
-
Chiu RW, Lau TK, Cheung PT, Gong ZQ, Leung TN, Lo YM. Noninvasive prenatal exclusion of congenital adrenal hyperplasia by maternal plasma analysis: a feasibility study. Clin Chem 2002; 48:778-80.
-
(2002)
Clin Chem
, vol.48
, pp. 778-780
-
-
Chiu, R.W.1
Lau, T.K.2
Cheung, P.T.3
Gong, Z.Q.4
Leung, T.N.5
Lo, Y.M.6
-
28
-
-
0032992867
-
Quantitative abnormalities of fetal DNA in maternal serum in preeclampsia
-
Lo YM, Leung TN, Tein MS, Sargent IL, Zhang J, Lau TK, et al. Quantitative abnormalities of fetal DNA in maternal serum in preeclampsia. Clin Chem 1999; 45:184-8.
-
(1999)
Clin Chem
, vol.45
, pp. 184-188
-
-
Lo, Y.M.1
Leung, T.N.2
Tein, M.S.3
Sargent, I.L.4
Zhang, J.5
Lau, T.K.6
-
29
-
-
1642423713
-
Two-stage elevation of cell-free fetal DNA in maternal sera before onset of preeclampsia
-
Levine RJ, Qian C, Le shane ES, Yu KF, England LJ, Schisterman EF, et al. Two-stage elevation of cell-free fetal DNA in maternal sera before onset of preeclampsia. Am J Obstet Gynecol 2004; 190:707-13.
-
(2004)
Am J Obstet Gynecol
, vol.190
, pp. 707-713
-
-
Levine, R.J.1
Qian, C.2
le shane, E.S.3
Yu, K.F.4
England, L.J.5
Schisterman, E.F.6
-
30
-
-
22144459608
-
High levels of fetal cell-free DNA in maternal serum: A risk factor for spontaneous preterm delivery
-
Farina A, LeShane ES, Romero R, Gomez R, Chaiworapongsa T, Rizzo N, Bianchi DW. High levels of fetal cell-free DNA in maternal serum: a risk factor for spontaneous preterm delivery. Am J Obstet Gynecol 2005; 193:421-5.
-
(2005)
Am J Obstet Gynecol
, vol.193
, pp. 421-425
-
-
Farina, A.1
LeShane, E.S.2
Romero, R.3
Gomez, R.4
Chaiworapongsa, T.5
Rizzo, N.6
Bianchi, D.W.7
-
31
-
-
0032512311
-
Maternal plasma fetal DNA as a marker for preterm labour
-
Leung TN, Zhang J, Lau TK, Hjelm NM, Lo YM. Maternal plasma fetal DNA as a marker for preterm labour. Lancet 1998; 352:1904-5.
-
(1998)
Lancet
, vol.352
, pp. 1904-1905
-
-
Leung, T.N.1
Zhang, J.2
Lau, T.K.3
Hjelm, N.M.4
Lo, Y.M.5
-
32
-
-
0032855554
-
Increased fetal DNA concentrations in the plasma of pregnant women carrying fetuses with trisomy 21
-
Lo YM, Lau TK, Zhang J, Leung TN, Chang AM, Hjelm NM, et al. Increased fetal DNA concentrations in the plasma of pregnant women carrying fetuses with trisomy 21. Clin Chem 1999; 45:1747-51.
-
(1999)
Clin Chem
, vol.45
, pp. 1747-1751
-
-
Lo, Y.M.1
Lau, T.K.2
Zhang, J.3
Leung, T.N.4
Chang, A.M.5
Hjelm, N.M.6
-
33
-
-
0033751975
-
Fetal DNA in maternal plasma is elevated in pregnancies with aneuploid fetuses
-
Zhong XY, Burk MR, Troeger C, Jackson LR, Holzgreve W, Hahn S. Fetal DNA in maternal plasma is elevated in pregnancies with aneuploid fetuses. Prenat Diagn 2000; 20:795-8.
-
(2000)
Prenat Diagn
, vol.20
, pp. 795-798
-
-
Zhong, X.Y.1
Burk, M.R.2
Troeger, C.3
Jackson, L.R.4
Holzgreve, W.5
Hahn, S.6
-
34
-
-
0035201589
-
Cell-free fetal DNA is increased in plasma of women with hyperemesis gravidarum
-
Sekizawa A, Sugito Y, Iwasaki M, Watanabe A, Jimbo M, Hoshi S, et al. Cell-free fetal DNA is increased in plasma of women with hyperemesis gravidarum. Clin Chem 2001; 47:2164-5.
-
(2001)
Clin Chem
, vol.47
, pp. 2164-2165
-
-
Sekizawa, A.1
Sugito, Y.2
Iwasaki, M.3
Watanabe, A.4
Jimbo, M.5
Hoshi, S.6
-
35
-
-
0141838946
-
Relationship between severity of hyperemesis gravidarum and fetal DNA concentration in maternal plasma
-
Sugito Y, Sekizawa A, Farina A, Yukimoto Y, Saito H, Iwasaki M, et al. Relationship between severity of hyperemesis gravidarum and fetal DNA concentration in maternal plasma. Clin Chem 2003; 49:1667-9.
-
(2003)
Clin Chem
, vol.49
, pp. 1667-1669
-
-
Sugito, Y.1
Sekizawa, A.2
Farina, A.3
Yukimoto, Y.4
Saito, H.5
Iwasaki, M.6
-
36
-
-
0036156063
-
Increased cell-free fetal DNA in plasma of two women with invasive placenta
-
Sekizawa A, Jimbo M, Saito H, Iwasaki M, Sugito Y, Yukimoto Y, et al. Increased cell-free fetal DNA in plasma of two women with invasive placenta. Clin Chem 2002; 48:353-4.
-
(2002)
Clin Chem
, vol.48
, pp. 353-354
-
-
Sekizawa, A.1
Jimbo, M.2
Saito, H.3
Iwasaki, M.4
Sugito, Y.5
Yukimoto, Y.6
-
37
-
-
54049132561
-
Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma
-
Lun FM, Chiu RW, Allen Chan KC, Yeung Leung T, Kin Lau T, Dennis Lo YM. Microfluidics digital PCR reveals a higher than expected fraction of fetal DNA in maternal plasma. Clin Chem 2008; 54:1664-72.
-
(2008)
Clin Chem
, vol.54
, pp. 1664-1672
-
-
Lun, F.M.1
Chiu, R.W.2
Allen Chan, K.C.3
Yeung Leung, T.4
Kin Lau, T.5
Dennis Lo, Y.M.6
-
38
-
-
0033833793
-
Cellfree fetal deoxyribonucleic acid in maternal circulation as a marker of fetal-maternal hemorrhage in patients undergoing external cephalic version near term
-
Lau TK, Lo KW, Chan LY, Leung TY, Lo YM. Cellfree fetal deoxyribonucleic acid in maternal circulation as a marker of fetal-maternal hemorrhage in patients undergoing external cephalic version near term. Am J Obstet Gynecol 2000; 183:712-6.
-
(2000)
Am J Obstet Gynecol
, vol.183
, pp. 712-716
-
-
Lau, T.K.1
Lo, K.W.2
Chan, L.Y.3
Leung, T.Y.4
Lo, Y.M.5
-
39
-
-
0034734711
-
Prenatal DNA diagnosis of a single-gene disorder from maternal plasma
-
Saito H, Sekizawa A, Morimoto T, Suzuki M, Yanaihara T. Prenatal DNA diagnosis of a single-gene disorder from maternal plasma. Lancet 2000; 356:1170.
-
(2000)
Lancet
, vol.356
, pp. 1170
-
-
Saito, H.1
Sekizawa, A.2
Morimoto, T.3
Suzuki, M.4
Yanaihara, T.5
-
40
-
-
0032754195
-
Detection of fetal-derived paternally inherited X-chromosome polymorphisms in maternal plasma
-
Tang NL, Leung TN, Zhang J, Lau TK, Lo YM. Detection of fetal-derived paternally inherited X-chromosome polymorphisms in maternal plasma. Clin Chem 1999; 45:2033-5.
-
(1999)
Clin Chem
, vol.45
, pp. 2033-2035
-
-
Tang, N.L.1
Leung, T.N.2
Zhang, J.3
Lau, T.K.4
Lo, Y.M.5
-
41
-
-
42249108710
-
Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: Prospective feasibility study
-
Finning K, Martin P, Summers J, Massey E, Poole G, Daniels G. Effect of high throughput RHD typing of fetal DNA in maternal plasma on use of anti-RhD immunoglobulin in RhD negative pregnant women: prospective feasibility study. BMJ 2008; 336:816-8.
-
(2008)
BMJ
, vol.336
, pp. 816-818
-
-
Finning, K.1
Martin, P.2
Summers, J.3
Massey, E.4
Poole, G.5
Daniels, G.6
-
42
-
-
0010377117
-
From genomics to epigenomics: A loftier view of life
-
Beck S, Olek A, Walter J. From genomics to epigenomics: a loftier view of life. Nat Biotechnol 1999; 17:1144.
-
(1999)
Nat Biotechnol
, vol.17
, pp. 1144
-
-
Beck, S.1
Olek, A.2
Walter, J.3
-
43
-
-
33746407333
-
The emerging science of epigenomics
-
Callinan PA, Feinberg AP. The emerging science of epigenomics. Hum Mol Genet 2006; 151:95-101.
-
(2006)
Hum Mol Genet
, vol.151
, pp. 95-101
-
-
Callinan, P.A.1
Feinberg, A.P.2
-
44
-
-
17444417521
-
Cancer epigenetics
-
Laird PW. Cancer epigenetics. Hum Mol Genet 2005; 14:65-76.
-
(2005)
Hum Mol Genet
, vol.14
, pp. 65-76
-
-
Laird, P.W.1
-
45
-
-
0037068353
-
DNA methylation in cancer: Too much, but also too little
-
Ehrlich M. DNA methylation in cancer: too much, but also too little. Oncogene 2002; 21:5400-13.
-
(2002)
Oncogene
, vol.21
, pp. 5400-5413
-
-
Ehrlich, M.1
-
46
-
-
33847065486
-
The epigenomics of cancer
-
Jones PA, Baylin SB. The epigenomics of cancer. Cell 2007; 128:683-92.
-
(2007)
Cell
, vol.128
, pp. 683-692
-
-
Jones, P.A.1
Baylin, S.B.2
-
47
-
-
0033566692
-
Quantitative analysis of aberrant p16 methylation using real-time quantitative methylation-specific polymerase chain reaction
-
Lo YM, Wong IH, Zhang J, Tein MS, Ng MH, Hjelm NM. Quantitative analysis of aberrant p16 methylation using real-time quantitative methylation-specific polymerase chain reaction. Cancer Res 1999; 59:3899-903.
-
(1999)
Cancer Res
, vol.59
, pp. 3899-3903
-
-
Lo, Y.M.1
Wong, I.H.2
Zhang, J.3
Tein, M.S.4
Ng, M.H.5
Hjelm, N.M.6
-
48
-
-
0032893755
-
Detection of aberrant p16 methylation in the plasma and serum of liver cancer patients
-
Wong IH, Lo YM, Zhang J, Liew CT, Ng MH, Wong N, et al. Detection of aberrant p16 methylation in the plasma and serum of liver cancer patients. Cancer Res 1999; 59:71-3.
-
(1999)
Cancer Res
, vol.59
, pp. 71-73
-
-
Wong, I.H.1
Lo, Y.M.2
Zhang, J.3
Liew, C.T.4
Ng, M.H.5
Wong, N.6
-
49
-
-
0032894125
-
Detection of aberrant promoter hypermethylation of tumor suppressor genes in serum DNA from non-small cell lung cancer patients
-
Esteller M, Sanchez-Cespedes M, Rosell R, Sidransky D, Baylin SB, Herman JG. Detection of aberrant promoter hypermethylation of tumor suppressor genes in serum DNA from non-small cell lung cancer patients. Cancer Res 1999; 59:67-70.
-
(1999)
Cancer Res
, vol.59
, pp. 67-70
-
-
Esteller, M.1
Sanchez-Cespedes, M.2
Rosell, R.3
Sidransky, D.4
Baylin, S.B.5
Herman, J.G.6
-
50
-
-
0036140193
-
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. Differential DNA methylation between fetus and mother as a strategy for detecting fetal DNA in maternal plasma. Clin Chem 2002; 48:35-41.
-
(2002)
Clin Chem
, vol.48
, pp. 35-41
-
-
Poon, L.L.1
Leung, T.N.2
Lau, T.K.3
Chow, K.C.4
Lo, Y.M.5
-
51
-
-
26844478953
-
Detection of the placental epigenetic signature of the maspin gene in maternal plasma
-
Chim SS, Tong YK, Chiu RW, Lau TK, Leung TN, Chan LY, et al. Detection of the placental epigenetic signature of the maspin gene in maternal plasma. Proc Natl Acad Sci USA 2005; 102:14753-8.
-
(2005)
Proc Natl Acad Sci USA
, vol.102
, pp. 14753-14758
-
-
Chim, S.S.1
Tong, Y.K.2
Chiu, R.W.3
Lau, T.K.4
Leung, T.N.5
Chan, L.Y.6
-
52
-
-
33845512998
-
Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis
-
Chan KC, Ding C, Gerovassili A, Yeung SW, Chiu RW, Leung TN, et al. Hypermethylated RASSF1A in maternal plasma: A universal fetal DNA marker that improves the reliability of noninvasive prenatal diagnosis. Clin Chem 2006; 52:2211-8.
-
(2006)
Clin Chem
, vol.52
, pp. 2211-2218
-
-
Chan, K.C.1
Ding, C.2
Gerovassili, A.3
Yeung, S.W.4
Chiu, R.W.5
Leung, T.N.6
-
53
-
-
0027378582
-
Role for DNA methylation in genomic imprinting
-
Li E, Beard C, Jaenisch R. Role for DNA methylation in genomic imprinting. Nature 1993; 366:362-5.
-
(1993)
Nature
, vol.366
, pp. 362-365
-
-
Li, E.1
Beard, C.2
Jaenisch, R.3
-
54
-
-
0026700732
-
A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes
-
Driscoll DJ, Waters MF, Williams CA, Zori RT, Glenn CC, Avidano KM, Nicholls RD. A DNA methylation imprint, determined by the sex of the parent, distinguishes the Angelman and Prader-Willi syndromes. Genomics 1992; 13:917-24.
-
(1992)
Genomics
, vol.13
, pp. 917-924
-
-
Driscoll, D.J.1
Waters, M.F.2
Williams, C.A.3
Zori, R.T.4
Glenn, C.C.5
Avidano, K.M.6
Nicholls, R.D.7
-
55
-
-
0021145377
-
Role of paternal and maternal genomes in mouse development
-
Barton SC, Surani MA, Norris ML. Role of paternal and maternal genomes in mouse development. Nature 1984; 311:374-6.
-
(1984)
Nature
, vol.311
, pp. 374-376
-
-
Barton, S.C.1
Surani, M.A.2
Norris, M.L.3
-
56
-
-
0027231511
-
Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome
-
Schneid H, Seurin D, Vazquez MP, Gourmelen M, Cabrol S, Le Bouc Y. Parental allele specific methylation of the human insulin-like growth factor II gene and Beckwith-Wiedemann syndrome. J Med Genet 1993; 30:353-62.
-
(1993)
J Med Genet
, vol.30
, pp. 353-362
-
-
Schneid, H.1
Seurin, D.2
Vazquez, M.P.3
Gourmelen, M.4
Cabrol, S.5
le Bouc, Y.6
-
57
-
-
0020522019
-
Tissue-specific differences in DNA methylation in various mammals
-
Gama-Sosa MA, Midgett RM, Slagel VA, Githens S, Kuo KC, Gehrke CW, Ehrlich M. Tissue-specific differences in DNA methylation in various mammals. Biochim Biophys Acta 1983; 740:212-9.
-
(1983)
Biochim Biophys Acta
, vol.740
, pp. 212-219
-
-
Gama-Sosa, M.A.1
Midgett, R.M.2
Slagel, V.A.3
Githens, S.4
Kuo, K.C.5
Gehrke, C.W.6
Ehrlich, M.7
-
58
-
-
4444375474
-
Age related changes in 5-methylcytosine content in human peripheral leukocytes and placentas: An HPLC-based study
-
Fuke C, Shimabukuro M, Petronis A, Sugimoto J, Oda T, Miura K, et al. Age related changes in 5-methylcytosine content in human peripheral leukocytes and placentas: an HPLC-based study. Ann Hum Genet 2004; 68:196-204.
-
(2004)
Ann Hum Genet
, vol.68
, pp. 196-204
-
-
Fuke, C.1
Shimabukuro, M.2
Petronis, A.3
Sugimoto, J.4
Oda, T.5
Miura, K.6
-
59
-
-
34247843101
-
Hypermethylation of RASSF1A in human and rhesus placentas
-
Chiu RW, Chim SS, Wong IH, Wong CS, Lee WS, To KF, et al. Hypermethylation of RASSF1A in human and rhesus placentas. Am J Pathol 2007; 170:941-50.
-
(2007)
Am J Pathol
, vol.170
, pp. 941-950
-
-
Chiu, R.W.1
Chim, S.S.2
Wong, I.H.3
Wong, C.S.4
Lee, W.S.5
To, K.F.6
-
60
-
-
53049098239
-
Specific tumour-associated methylation in normal human term placenta and firsttrimester cytotrophoblasts
-
Novakovic B, Rakyan V, Ng HK, Manuelpillai U, Dewi C, Wong NC, et al. Specific tumour-associated methylation in normal human term placenta and firsttrimester cytotrophoblasts. Mol Hum Reprod 2008; 14:547-54.
-
(2008)
Mol Hum Reprod
, vol.14
, pp. 547-554
-
-
Novakovic, B.1
Rakyan, V.2
Ng, H.K.3
Manuelpillai, U.4
Dewi, C.5
Wong, N.C.6
-
61
-
-
67649344487
-
Placenta-specific methylation of the vitamin D 24-hydroxylase gene: Implications for feedback autoregulation of active vitamin D levels at the fetomaternal interface
-
Novakovic B, Sibson M, Ng HK, Manuelpillai U, Rakyan V, Down T, et al. Placenta-specific methylation of the vitamin D 24-hydroxylase gene: implications for feedback autoregulation of active vitamin D levels at the fetomaternal interface. J Biol Chem 2009; 284:14838-48.
-
(2009)
J Biol Chem
, vol.284
, pp. 14838-14848
-
-
Novakovic, B.1
Sibson, M.2
Ng, H.K.3
Manuelpillai, U.4
Rakyan, V.5
Down, T.6
-
63
-
-
77950368485
-
DNA methylation-mediated downregulation of DNA methyltransferase-1 (DNMT1) is coincident with, but not essential for, global hypomethylation in human placenta
-
Novakovic B, Wong NC, Sibson M, Ng HK, Morley R, Manuelpillai U, et al. DNA methylation-mediated downregulation of DNA methyltransferase-1 (DNMT1) is coincident with, but not essential for, global hypomethylation in human placenta. J Biol Chem 2010; 285:9583-93.
-
(2010)
J Biol Chem
, vol.285
, pp. 9583-9593
-
-
Novakovic, B.1
Wong, N.C.2
Sibson, M.3
Ng, H.K.4
Morley, R.5
Manuelpillai, U.6
-
64
-
-
0031946988
-
Fetal DNA in maternal plasma: The plot thickens and the placental barrier thins
-
Bianchi DW. Fetal DNA in maternal plasma: the plot thickens and the placental barrier thins. Am J Hum Genet 1998; 62:763-4.
-
(1998)
Am J Hum Genet
, vol.62
, pp. 763-764
-
-
Bianchi, D.W.1
-
65
-
-
0037447089
-
mRNA of placental origin is readily detectable in maternal plasma
-
Ng EK, Tsui NB, Lau TK, Leung TN, Chiu RW, Panesar NS, et al. mRNA of placental origin is readily detectable in maternal plasma. Proc Natl Acad Sci USA 2003; 100:4748-53.
-
(2003)
Proc Natl Acad Sci USA
, vol.100
, 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
-
66
-
-
1542501831
-
Circulating cell-free fetal DNA in maternal serum appears to originate from cyto- and syncytio-trophoblastic cells. Case report
-
Flori E, Doray B, Gautier E, Kohler M, Ernault P, Flori J, Costa JM. Circulating cell-free fetal DNA in maternal serum appears to originate from cyto- and syncytio-trophoblastic cells. Case report. Hum Reprod 2004; 19:723-4.
-
(2004)
Hum Reprod
, vol.19
, pp. 723-724
-
-
Flori, E.1
Doray, B.2
Gautier, E.3
Kohler, M.4
Ernault, P.5
Flori, J.6
Costa, J.M.7
-
67
-
-
1942501800
-
Detection of cell free placental DNA in maternal plasma: Direct evidence from three cases of confined placental mosaicism
-
Masuzaki H, Miura K, Yoshiura KI, Yoshimura S, Niikawa N, Ishimaru T. Detection of cell free placental DNA in maternal plasma: direct evidence from three cases of confined placental mosaicism. J Med Genet 2004; 41:289-92.
-
(2004)
J Med Genet
, vol.41
, pp. 289-292
-
-
Masuzaki, H.1
Miura, K.2
Yoshiura, K.I.3
Yoshimura, S.4
Niikawa, N.5
Ishimaru, T.6
-
68
-
-
0036177799
-
Predominant hematopoietic origin of cell-free DNA in plasma and serum after sex-mismatched bone marrow transplantation
-
Lui YY, Chik KW, Chiu RW, Ho CY, Lam CW, Lo YM. Predominant hematopoietic origin of cell-free DNA in plasma and serum after sex-mismatched bone marrow transplantation. Clin Chem 2002; 48:421-7.
-
(2002)
Clin Chem
, vol.48
, pp. 421-427
-
-
Lui, Y.Y.1
Chik, K.W.2
Chiu, R.W.3
Ho, C.Y.4
Lam, C.W.5
Lo, Y.M.6
-
69
-
-
73449106855
-
Noninvasive prenatal detection of trisomy 21 by an epigenetic-genetic chromosome-dosage approach
-
Tong YK, Jin S, Chiu RW, Ding C, Chan KC, Leung TY, et al. Noninvasive prenatal detection of trisomy 21 by an epigenetic-genetic chromosome-dosage approach. Clin Chem 2010; 56:90-8.
-
(2010)
Clin Chem
, vol.56
, pp. 90-98
-
-
Tong, Y.K.1
Jin, S.2
Chiu, R.W.3
Ding, C.4
Chan, K.C.5
Leung, T.Y.6
-
70
-
-
43749098985
-
DNA methylation landscapes: Provocative insights from epigenomics
-
Suzuki MM, Bird A. DNA methylation landscapes: provocative insights from epigenomics. Nat Rev Genet 2008; 9:465-76.
-
(2008)
Nat Rev Genet
, vol.9
, pp. 465-476
-
-
Suzuki, M.M.1
Bird, A.2
-
71
-
-
0026546877
-
A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands
-
Frommer M, McDonald LE, Millar DS, Collis CM, Watt F, Grigg GW, et al. A genomic sequencing protocol that yields a positive display of 5-methylcytosine residues in individual DNA strands. Proc Natl Acad Sci USA 1992; 89:1827-31.
-
(1992)
Proc Natl Acad Sci USA
, vol.89
, pp. 1827-1831
-
-
Frommer, M.1
McDonald, L.E.2
Millar, D.S.3
Collis, C.M.4
Watt, F.5
Grigg, G.W.6
-
72
-
-
0029843950
-
Methylation-specific PCR: A novel PCR assay for methylation status of CpG islands
-
Herman JG, Graff JR, Myohanen S, Nelkin BD, Baylin SB. Methylation-specific PCR: a novel PCR assay for methylation status of CpG islands. Proc Natl Acad Sci USA 1996; 93:9821-6.
-
(1996)
Proc Natl Acad Sci USA
, vol.93
, pp. 9821-9826
-
-
Herman, J.G.1
Graff, J.R.2
Myohanen, S.3
Nelkin, B.D.4
Baylin, S.B.5
-
74
-
-
49249091385
-
DNA methylation analysis by digital bisulfite genomic sequencing and digital MethyLight
-
Weisenberger DJ, Trinh BN, Campan M, Sharma S, Long TI, Ananthnarayan S, et al. DNA methylation analysis by digital bisulfite genomic sequencing and digital MethyLight. Nucleic Acids Res 2008; 36:4689-98.
-
(2008)
Nucleic Acids Res
, vol.36
, pp. 4689-4698
-
-
Weisenberger, D.J.1
Trinh, B.N.2
Campan, M.3
Sharma, S.4
Long, T.I.5
Ananthnarayan, S.6
-
75
-
-
70249147655
-
Sensitive digital quantification of DNA methylation in clinical samples
-
Li M, Chen WD, Papadopoulos N, Goodman SN, Bjerregaard NC, Laurberg S, et al. Sensitive digital quantification of DNA methylation in clinical samples. Nat Biotechnol 2009; 27:858-63.
-
(2009)
Nat Biotechnol
, vol.27
, pp. 858-863
-
-
Li, M.1
Chen, W.D.2
Papadopoulos, N.3
Goodman, S.N.4
Bjerregaard, N.C.5
Laurberg, S.6
-
76
-
-
0035407651
-
Bisulfite genomic sequencing: Systematic investigation of critical experimental parameters
-
65-65
-
Grunau C, Clark SJ, Rosenthal A. Bisulfite genomic sequencing: systematic investigation of critical experimental parameters. Nucleic Acids Res 2001; 29:65-5.
-
(2001)
Nucleic Acids Res
, vol.29
-
-
Grunau, C.1
Clark, S.J.2
Rosenthal, A.3
-
77
-
-
0028060576
-
Effect of sitespecific modification on restriction endonucleases and DNA modification methyltransferases
-
McClelland M, Nelson M, Raschke E. Effect of sitespecific modification on restriction endonucleases and DNA modification methyltransferases. Nucleic Acids Res 1994; 22:3640-59.
-
(1994)
Nucleic Acids Res
, vol.22
, pp. 3640-3659
-
-
McClelland, M.1
Nelson, M.2
Raschke, E.3
-
78
-
-
35648987069
-
Detection of restriction enzymedigested 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. Detection of restriction enzymedigested target DNA by PCR amplification using a stem-loop primer: application to the detection of hypomethylated fetal DNA in maternal plasma. Clin Chem 2007; 53:1906-14.
-
(2007)
Clin Chem
, vol.53
, 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
-
79
-
-
29144470346
-
Real-time quantification of microRNAs by stem-loop RT-PCR
-
Chen C, Ridzon DA, Broomer AJ, Zhou Z, Lee DH, Nguyen JT, Barbisin M, et al. Real-time quantification of microRNAs by stem-loop RT-PCR. Nucleic Acids Res 2005; 33:179.
-
(2005)
Nucleic Acids Res
, vol.33
, pp. 179
-
-
Chen, C.1
Ridzon, D.A.2
Broomer, A.J.3
Zhou, Z.4
Lee, D.H.5
Nguyen, J.T.6
Barbisin, M.7
-
80
-
-
40449109999
-
Systematic search for placental DNA-methylation markers on chromosome 21: Toward a maternal plasmabased epigenetic test for fetal trisomy 21
-
Chim SS, Jin S, Lee TY, Lun FM, Lee WS, Chan LY, et al. Systematic search for placental DNA-methylation markers on chromosome 21: toward a maternal plasmabased epigenetic test for fetal trisomy 21. Clin Chem 2008; 54:500-11.
-
(2008)
Clin Chem
, vol.54
, 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
-
81
-
-
33845522324
-
Noninvasive prenatal detection of fetal trisomy 18 by epigenetic allelic ratio analysis in maternal plasma: Theoretical and empirical considerations
-
Tong YK, Ding C, Chiu RW, Gerovassili A, Chim SS, Leung TY, et al. Noninvasive prenatal detection of fetal trisomy 18 by epigenetic allelic ratio analysis in maternal plasma: Theoretical and empirical considerations. Clin Chem 2006; 52:2194-202.
-
(2006)
Clin Chem
, vol.52
, pp. 2194-2202
-
-
Tong, Y.K.1
Ding, C.2
Chiu, R.W.3
Gerovassili, A.4
Chim, S.S.5
Leung, T.Y.6
-
82
-
-
58149401202
-
Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma
-
Lun FM, Tsui NB, Chan KC, Leung TY, Lau TK, Charoenkwan P, et al. Noninvasive prenatal diagnosis of monogenic diseases by digital size selection and relative mutation dosage on DNA in maternal plasma. Proc Natl Acad Sci USA 2008; 105:19920-5.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 19920-19925
-
-
Lun, F.M.1
Tsui, N.B.2
Chan, K.C.3
Leung, T.Y.4
Lau, T.K.5
Charoenkwan, P.6
-
83
-
-
55849124028
-
Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood
-
Fan HC, Blumenfeld YJ, Chitkara U, Hudgins L, Quake SR. Noninvasive diagnosis of fetal aneuploidy by shotgun sequencing DNA from maternal blood. Proc Natl Acad Sci USA 2008; 105:16266-71.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 16266-16271
-
-
Fan, H.C.1
Blumenfeld, Y.J.2
Chitkara, U.3
Hudgins, L.4
Quake, S.R.5
-
84
-
-
58149490683
-
Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma
-
Chiu RW, Chan KC, Gao Y, Lau VY, Zheng W, Leung TY, et al. Noninvasive prenatal diagnosis of fetal chromosomal aneuploidy by massively parallel genomic sequencing of DNA in maternal plasma. Proc Natl Acad Sci USA 2008; 105:20458-63.
-
(2008)
Proc Natl Acad Sci USA
, vol.105
, pp. 20458-20463
-
-
Chiu, R.W.1
Chan, K.C.2
Gao, Y.3
Lau, V.Y.4
Zheng, W.5
Leung, T.Y.6
-
85
-
-
77649208031
-
Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of trisomy 21
-
Chiu RW, Sun H, Akolekar R, Clouser C, Lee C, McKernan K, et al. Maternal plasma DNA analysis with massively parallel sequencing by ligation for noninvasive prenatal diagnosis of trisomy 21. Clin Chem 2010; 56:459-63.
-
(2010)
Clin Chem
, vol.56
, pp. 459-463
-
-
Chiu, R.W.1
Sun, H.2
Akolekar, R.3
Clouser, C.4
Lee, C.5
McKernan, K.6
-
86
-
-
37349014758
-
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, et al. Quantitative aberrations of hypermethylated RASSF1A gene sequences in maternal plasma in pre-eclampsia. Prenat Diagn 2007; 27:1212-8.
-
(2007)
Prenat Diagn
, vol.27
, 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
-
87
-
-
67149115401
-
Clinical practice. Prenatal screening for aneuploidy
-
Driscoll DA, Gross S. Clinical practice. Prenatal screening for aneuploidy. N Engl J Med 2009; 360:2556-62.
-
(2009)
N Engl J Med
, vol.360
, pp. 2556-2562
-
-
Driscoll, D.A.1
Gross, S.2
-
88
-
-
34547962325
-
Candidate epigenetic biomarkers for non-invasive prenatal diagnosis of Down syndrome
-
Old RW, Crea F, Puszyk W, Hulten MA. Candidate epigenetic biomarkers for non-invasive prenatal diagnosis of Down syndrome. Reprod Biomed Online 2007; 15:227-35.
-
(2007)
Reprod Biomed Online
, vol.15
, pp. 227-235
-
-
Old, R.W.1
Crea, F.2
Puszyk, W.3
Hulten, M.A.4
-
89
-
-
10744233914
-
A tiling resolution DNA microarray with complete coverage of the human genome
-
Ishkanian AS, Malloff CA, Watson SK, De Leeuw RJ, Chi B, Coe BP, et al. A tiling resolution DNA microarray with complete coverage of the human genome. Nat Genet 2004; 36:299-303.
-
(2004)
Nat Genet
, vol.36
, pp. 299-303
-
-
Ishkanian, A.S.1
Malloff, C.A.2
Watson, S.K.3
de Leeuw, R.J.4
Chi, B.5
Coe, B.P.6
-
90
-
-
37749031255
-
Next-generation sequencing transforms today's biology
-
Schuster SC. Next-generation sequencing transforms today's biology. Nat Methods 2008; 5:16-8.
-
(2008)
Nat Methods
, vol.5
, pp. 16-18
-
-
Schuster, S.C.1
-
91
-
-
23044514626
-
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. Chromosome-wide and promoter-specific analyses identify sites of differential DNA methylation in normal and transformed human cells. Nat Genet 2005; 37:853-62.
-
(2005)
Nat Genet
, vol.37
, 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
-
92
-
-
0034640130
-
Methylspecific DNA binding by McrBC, a modificationdependent restriction enzyme
-
Stewart FJ, Panne D, Bickle TA, Raleigh EA. Methylspecific DNA binding by McrBC, a modificationdependent restriction enzyme. J Mol Biol 2000; 298:611-22.
-
(2000)
J Mol Biol
, vol.298
, pp. 611-622
-
-
Stewart, F.J.1
Panne, D.2
Bickle, T.A.3
Raleigh, E.A.4
-
93
-
-
33646870108
-
Genome-wide profiling of promoter methylation in human
-
Hatada I, Fukasawa M, Kimura M, Morita S, Yamada K, Yoshikawa T, et al. Genome-wide profiling of promoter methylation in human. Oncogene 2006; 25:3059-64.
-
(2006)
Oncogene
, vol.25
, pp. 3059-3064
-
-
Hatada, I.1
Fukasawa, M.2
Kimura, M.3
Morita, S.4
Yamada, K.5
Yoshikawa, T.6
-
94
-
-
33746756014
-
Comparative isoschizomer profiling of cytosine methylation: The HELP assay
-
Khulan B, Thompson RF, Ye K, Fazzari MJ, Suzuki M, Stasiek E, et al. Comparative isoschizomer profiling of cytosine methylation: the HELP assay. Genome Res 2006; 16:1046-55.
-
(2006)
Genome Res
, vol.16
, pp. 1046-1055
-
-
Khulan, B.1
Thompson, R.F.2
Ye, K.3
Fazzari, M.J.4
Suzuki, M.5
Stasiek, E.6
-
95
-
-
23744484912
-
Profiling DNA methylation patterns using genomic tiling microarrays
-
Lippman Z, Gendrel AV, Colot V, Martienssen R. Profiling DNA methylation patterns using genomic tiling microarrays. Nat Methods 2005; 2:219-24.
-
(2005)
Nat Methods
, vol.2
, pp. 219-224
-
-
Lippman, Z.1
Gendrel, A.V.2
Colot, V.3
Martienssen, R.4
-
96
-
-
43149098062
-
Comprehensive high-throughput arrays for relative methylation (CHARM)
-
Irizarry RA, Ladd-Acosta C, Carvalho B, Wu H, Brandenburg SA, Jeddeloh JA, et al. Comprehensive high-throughput arrays for relative methylation (CHARM). Genome Res 2008; 18:780-90.
-
(2008)
Genome Res
, vol.18
, pp. 780-790
-
-
Irizarry, R.A.1
Ladd-Acosta, C.2
Carvalho, B.3
Wu, H.4
Brandenburg, S.A.5
Jeddeloh, J.A.6
-
97
-
-
46949098742
-
A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis
-
Down TA, Rakyan VK, Turner DJ, Flicek P, Li H, Kulesha E, et al. A Bayesian deconvolution strategy for immunoprecipitation-based DNA methylome analysis. Nat Biotechnol 2008; 26:779-85.
-
(2008)
Nat Biotechnol
, vol.26
, pp. 779-785
-
-
Down, T.A.1
Rakyan, V.K.2
Turner, D.J.3
Flicek, P.4
Li, H.5
Kulesha, E.6
-
98
-
-
74949087173
-
Methylated DNA immunoprecipitation and microarray-based analysis: Detection of DNA methylation in breast cancer cell lines
-
Weng YI, Huang TH, Yan PS. Methylated DNA immunoprecipitation and microarray-based analysis: detection of DNA methylation in breast cancer cell lines. Methods Mol Biol 2009; 590:165-76.
-
(2009)
Methods Mol Biol
, vol.590
, pp. 165-176
-
-
Weng, Y.I.1
Huang, T.H.2
Yan, P.S.3
-
99
-
-
77950409567
-
Genome-wide analysis of aberrant methylation in human breast cancer cells using methyl-DNA immunoprecipitation combined with high-throughput sequencing
-
Ruike Y, Imanaka Y, Sato F, Shimizu K, Tsujimoto G. Genome-wide analysis of aberrant methylation in human breast cancer cells using methyl-DNA immunoprecipitation combined with high-throughput sequencing. BMC Genomics 2010; 11:137.
-
(2010)
BMC Genomics
, vol.11
, pp. 137
-
-
Ruike, Y.1
Imanaka, Y.2
Sato, F.3
Shimizu, K.4
Tsujimoto, G.5
-
100
-
-
33747587864
-
Model-based analysis of tilingarrays for ChIP-chip
-
Johnson WE, Li W, Meyer CA, Gottardo R, Carroll JS, Brown M, Liu XS. Model-based analysis of tilingarrays for ChIP-chip. Proc Natl Acad Sci USA 2006; 103:12457-62.
-
(2006)
Proc Natl Acad Sci USA
, vol.103
, pp. 12457-12462
-
-
Johnson, W.E.1
Li, W.2
Meyer, C.A.3
Gottardo, R.4
Carroll, J.S.5
Brown, M.6
Liu, X.S.7
-
101
-
-
53549104134
-
MEDME: An experimental and analytical methodology for the estimation of DNA methylation levels based on microarray derived MeDIP-enrichment
-
Pelizzola M, Koga Y, Urban AE, Krauthammer M, Weissman S, Halaban R, Molinaro AM. MEDME: an experimental and analytical methodology for the estimation of DNA methylation levels based on microarray derived MeDIP-enrichment. Genome Res 2008; 18:1652-9.
-
(2008)
Genome Res
, vol.18
, pp. 1652-1659
-
-
Pelizzola, M.1
Koga, Y.2
Urban, A.E.3
Krauthammer, M.4
Weissman, S.5
Halaban, R.6
Molinaro, A.M.7
-
102
-
-
70350440343
-
A microarray-based approach for the identification of epigenetic biomarkers for the noninvasive diagnosis of fetal disease
-
Chu T, Burke B, Bunce K, Surti U, Allen Hogge W, Peters DG. A microarray-based approach for the identification of epigenetic biomarkers for the noninvasive diagnosis of fetal disease. Prenat Diagn 2009; 29:1020-30.
-
(2009)
Prenat Diagn
, vol.29
, pp. 1020-1030
-
-
Chu, T.1
Burke, B.2
Bunce, K.3
Surti, U.4
Allen Hogge, W.5
Peters, D.G.6
-
103
-
-
65649095218
-
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, et al. Sites of differential DNA methylation between placenta and peripheral blood: molecular markers for noninvasive prenatal diagnosis of aneuploidies. Am J Pathol 2009; 174:1609-18.
-
(2009)
Am J Pathol
, vol.174
, pp. 1609-1618
-
-
Papageorgiou, E.A.1
Fiegler, H.2
Rakyan, V.3
Beck, S.4
Hulten, M.5
Lamnissou, K.6
-
104
-
-
34548727890
-
Digital PCR for the molecular detection of fetal chromosomal aneuploidy
-
Lo YM, Lun FM, Chan KC, Tsui NB, Chong KC, Lau TK, et al. Digital PCR for the molecular detection of fetal chromosomal aneuploidy. Proc Natl Acad Sci USA 2007; 104:13116-21.
-
(2007)
Proc Natl Acad Sci USA
, vol.104
, pp. 13116-13121
-
-
Lo, Y.M.1
Lun, F.M.2
Chan, K.C.3
Tsui, N.B.4
Chong, K.C.5
Lau, T.K.6
-
105
-
-
67649958254
-
Non-invasive prenatal diagnosis by single molecule counting technologies
-
Chiu RW, Cantor CR, Lo YM. Non-invasive prenatal diagnosis by single molecule counting technologies. Trends Genet 2009; 25:324-31.
-
(2009)
Trends Genet
, vol.25
, pp. 324-331
-
-
Chiu, R.W.1
Cantor, C.R.2
Lo, Y.M.3
-
106
-
-
57449085114
-
Noninvasive prenatal detection of fetal chromosomal aneuploidies by maternal plasma nucleic acid analysis: A review of the current state of the art
-
Lo YM. Noninvasive prenatal detection of fetal chromosomal aneuploidies by maternal plasma nucleic acid analysis: a review of the current state of the art. BJOG 2009; 116:152-7.
-
(2009)
BJOG
, vol.116
, pp. 152-157
-
-
Lo, Y.M.1
-
107
-
-
33846903851
-
Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection
-
Lo YM, Tsui NB, Chiu RW, Lau TK, Leung TN, Heung MM, et al. Plasma placental RNA allelic ratio permits noninvasive prenatal chromosomal aneuploidy detection. Nat Med 2007; 13:218-23.
-
(2007)
Nat Med
, vol.13
, pp. 218-223
-
-
Lo, Y.M.1
Tsui, N.B.2
Chiu, R.W.3
Lau, T.K.4
Leung, T.N.5
Heung, M.M.6
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