-
1
-
-
83255189758
-
The International Stem Cell Initiative. (2011).Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage
-
Amps K., et al. The International Stem Cell Initiative. (2011).Screening ethnically diverse human embryonic stem cells identifies a chromosome 20 minimal amplicon conferring growth advantage. Nat. Biotechnol. 2011, 29:1132-1144.
-
(2011)
Nat. Biotechnol.
, vol.29
, pp. 1132-1144
-
-
Amps, K.1
-
2
-
-
63449086972
-
The impact of copy number variation on local gene expression in mouse hematopoietic stem and progenitor cells
-
Cahan P., Li Y., Izumi M., Graubert T.A. The impact of copy number variation on local gene expression in mouse hematopoietic stem and progenitor cells. Nat. Genet. 2009, 41:430-437.
-
(2009)
Nat. Genet.
, vol.41
, pp. 430-437
-
-
Cahan, P.1
Li, Y.2
Izumi, M.3
Graubert, T.A.4
-
3
-
-
54149087448
-
Human ESCs predisposition to karyotypic instability: is a matter of culture adaptation or differential vulnerability among hESC lines due to inherent properties?
-
Catalina P., et al. Human ESCs predisposition to karyotypic instability: is a matter of culture adaptation or differential vulnerability among hESC lines due to inherent properties?. Mol. Cancer 2008, 7:76.
-
(2008)
Mol. Cancer
, vol.7
, pp. 76
-
-
Catalina, P.1
-
4
-
-
72849134550
-
Genomic profiling of plasmablastic lymphoma using array comparative genomic hybridization (aCGH): revealing significant overlapping genomic lesions with diffuse large B-cell lymphoma
-
Chang C.C., et al. Genomic profiling of plasmablastic lymphoma using array comparative genomic hybridization (aCGH): revealing significant overlapping genomic lesions with diffuse large B-cell lymphoma. J. Hematol. Oncol. 2009, 2:47.
-
(2009)
J. Hematol. Oncol.
, vol.2
, pp. 47
-
-
Chang, C.C.1
-
5
-
-
76349093158
-
The impact of human copy number variation on a new era of genetic testing
-
Choy K.W., Setlur S.R., Lee C., Lau T.K. The impact of human copy number variation on a new era of genetic testing. BJOG 2010, 117:391-398.
-
(2010)
BJOG
, vol.117
, pp. 391-398
-
-
Choy, K.W.1
Setlur, S.R.2
Lee, C.3
Lau, T.K.4
-
6
-
-
54049144653
-
Copy-number variations associated with neuropsychiatric conditions
-
Cook E.H., Scherer S.W. Copy-number variations associated with neuropsychiatric conditions. Nature 2008, 455:919-923.
-
(2008)
Nature
, vol.455
, pp. 919-923
-
-
Cook, E.H.1
Scherer, S.W.2
-
7
-
-
61449505236
-
Genetic and epigenetic instability of human bone marrow mesenchymal stem cells expanded in autologous serum or fetal bovine serum
-
Dahl J.A., et al. Genetic and epigenetic instability of human bone marrow mesenchymal stem cells expanded in autologous serum or fetal bovine serum. Int. J. Dev. Biol. 2008, 52:1033-1042.
-
(2008)
Int. J. Dev. Biol.
, vol.52
, pp. 1033-1042
-
-
Dahl, J.A.1
-
8
-
-
47249136157
-
CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation
-
De Temmerman N., et al. CTG repeat instability in a human embryonic stem cell line carrying the myotonic dystrophy type 1 mutation. Mol. Hum. Reprod. 2008, 14:405-412.
-
(2008)
Mol. Hum. Reprod.
, vol.14
, pp. 405-412
-
-
De Temmerman, N.1
-
9
-
-
80052185338
-
Studies of genomic copy number changes in human cancers reveal signatures of DNA replication stress
-
Dereli-Öz A., Versini G., Halazonetis T.D. Studies of genomic copy number changes in human cancers reveal signatures of DNA replication stress. Mol. Oncol. 2011, 5:308-314.
-
(2011)
Mol. Oncol.
, vol.5
, pp. 308-314
-
-
Dereli-Öz, A.1
Versini, G.2
Halazonetis, T.D.3
-
10
-
-
77958085268
-
High resolution array-CGH characterization of human stem cells using a stem cell focused microarray
-
Elliott A.M., Elliott K.A., Kammesheidt A. High resolution array-CGH characterization of human stem cells using a stem cell focused microarray. Mol. Biotechnol. 2010, 46:234-342.
-
(2010)
Mol. Biotechnol.
, vol.46
, pp. 234-342
-
-
Elliott, A.M.1
Elliott, K.A.2
Kammesheidt, A.3
-
11
-
-
79955816862
-
Establishment of a Brazilian line of human embryonic stem cells in defined medium: implications for cell therapy in an ethnically diverse population
-
Fraga A.M., et al. Establishment of a Brazilian line of human embryonic stem cells in defined medium: implications for cell therapy in an ethnically diverse population. Cell Transplant. 2011, 20:431-440.
-
(2011)
Cell Transplant.
, vol.20
, pp. 431-440
-
-
Fraga, A.M.1
-
12
-
-
0033989262
-
Centrosome amplification and instability occurs exclusively in aneuploid, but not in diploid colorectal cancer cell lines, and correlates with numerical chromosomal aberrations
-
Ghadimi B.M., et al. Centrosome amplification and instability occurs exclusively in aneuploid, but not in diploid colorectal cancer cell lines, and correlates with numerical chromosomal aberrations. Genes Chromosomes Cancer 2000, 27:183-190.
-
(2000)
Genes Chromosomes Cancer
, vol.27
, pp. 183-190
-
-
Ghadimi, B.M.1
-
13
-
-
79952258224
-
Somatic coding mutations in human induced pluripotent stem cells
-
Gore A., et al. Somatic coding mutations in human induced pluripotent stem cells. Nature 2011, 471:63-67.
-
(2011)
Nature
, vol.471
, pp. 63-67
-
-
Gore, A.1
-
14
-
-
84857236931
-
Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia
-
Grozeva D., et al. Independent estimation of the frequency of rare CNVs in the UK population confirms their role in schizophrenia. Schizophr. Res. 2012, 135:1-7.
-
(2012)
Schizophr. Res.
, vol.135
, pp. 1-7
-
-
Grozeva, D.1
-
15
-
-
79952126043
-
Copy number variation and selection during reprogramming to pluripotency
-
Hussein S.M., et al. Copy number variation and selection during reprogramming to pluripotency. Nature 2011, 471:58-62.
-
(2011)
Nature
, vol.471
, pp. 58-62
-
-
Hussein, S.M.1
-
16
-
-
33744975168
-
In vitro culture conditions favoring selection of chromosomal abnormalities in human ES cells
-
Imreh M.P., et al. In vitro culture conditions favoring selection of chromosomal abnormalities in human ES cells. J. Cell. Biochem. 2006, 99:508-516.
-
(2006)
J. Cell. Biochem.
, vol.99
, pp. 508-516
-
-
Imreh, M.P.1
-
17
-
-
2642530148
-
Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long-term cultivation
-
Inzunza J., et al. Comparative genomic hybridization and karyotyping of human embryonic stem cells reveals the occurrence of an isodicentric X chromosome after long-term cultivation. Mol. Hum. Reprod. 2004, 10:461-466.
-
(2004)
Mol. Hum. Reprod.
, vol.10
, pp. 461-466
-
-
Inzunza, J.1
-
18
-
-
84856225986
-
De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia
-
Kirov G., et al. De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia. Mol. Psychiatry 2012, 17:142-153.
-
(2012)
Mol. Psychiatry
, vol.17
, pp. 142-153
-
-
Kirov, G.1
-
19
-
-
78650971216
-
Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture
-
Laurent L.C., et al. Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture. Cell Stem Cell 2011, 8:106-180.
-
(2011)
Cell Stem Cell
, vol.8
, pp. 106-180
-
-
Laurent, L.C.1
-
20
-
-
56249134560
-
Extensive genomic copy number variation in embryonic stem cells
-
Liang Q., Conte N., Skarnes W.C., Bradley A. Extensive genomic copy number variation in embryonic stem cells. Proc. Natl. Acad. Sci. U. S. A. 2008, 105:17453-17456.
-
(2008)
Proc. Natl. Acad. Sci. U. S. A.
, vol.105
, pp. 17453-17456
-
-
Liang, Q.1
Conte, N.2
Skarnes, W.C.3
Bradley, A.4
-
21
-
-
84855390254
-
Concise review: genomic stability of human induced pluripotent stem cells
-
Martins-Taylor K., Xu R.H. Concise review: genomic stability of human induced pluripotent stem cells. Stem Cells 2012, 30:22-27.
-
(2012)
Stem Cells
, vol.30
, pp. 22-27
-
-
Martins-Taylor, K.1
Xu, R.H.2
-
22
-
-
79958109873
-
Recurrent copy number variations in human induced pluripotent stem cells
-
Martins-Taylor K., et al. Recurrent copy number variations in human induced pluripotent stem cells. Nat. Biotechnol. 2011, 29:488-491.
-
(2011)
Nat. Biotechnol.
, vol.29
, pp. 488-491
-
-
Martins-Taylor, K.1
-
23
-
-
78650002534
-
The human genome puzzle-the role of copy number variation in somatic mosaicism
-
Mkrtchyan H., et al. The human genome puzzle-the role of copy number variation in somatic mosaicism. Curr. Genomics 2010, 11:426-431.
-
(2010)
Curr. Genomics
, vol.11
, pp. 426-431
-
-
Mkrtchyan, H.1
-
24
-
-
77949725632
-
Early embryonic chromosome instability results in stable mosaic pattern in human tissues
-
Mkrtchyan H., et al. Early embryonic chromosome instability results in stable mosaic pattern in human tissues. PLoS One 2010, 95:e9591.
-
(2010)
PLoS One
, vol.95
-
-
Mkrtchyan, H.1
-
25
-
-
77950651133
-
High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity
-
Närvä E., et al. High-resolution DNA analysis of human embryonic stem cell lines reveals culture-induced copy number changes and loss of heterozygosity. Nat. Biotechnol. 2010, 28:371-377.
-
(2010)
Nat. Biotechnol.
, vol.28
, pp. 371-377
-
-
Närvä, E.1
-
26
-
-
84889737022
-
-
Altered oxygen metabolism associated to neurogenesis of induced pluripotent stem cells derived from a schizophrenic patient. Cell Transplant.
-
Paulsen, B.D., et al., (in press). Altered oxygen metabolism associated to neurogenesis of induced pluripotent stem cells derived from a schizophrenic patient. Cell Transplant.
-
-
-
Paulsen, B.D.1
-
27
-
-
58149389526
-
High-resolution genomic profiling of adenomas and carcinomas of the salivary glands reveals amplification, rearrangement, and fusion of HMGA2
-
Persson F., et al. High-resolution genomic profiling of adenomas and carcinomas of the salivary glands reveals amplification, rearrangement, and fusion of HMGA2. Genes Chromosomes Cancer 2009, 48:69-82.
-
(2009)
Genes Chromosomes Cancer
, vol.48
, pp. 69-82
-
-
Persson, F.1
-
28
-
-
51549095601
-
Somatic mosaicism for copy number variation in differentiated human tissues
-
Piotrowski A., et al. Somatic mosaicism for copy number variation in differentiated human tissues. Hum. Mutat. 2008, 29:1118-1124.
-
(2008)
Hum. Mutat.
, vol.29
, pp. 1118-1124
-
-
Piotrowski, A.1
-
29
-
-
33751329250
-
Global variation in copy number in the human genome
-
Redon R., et al. Global variation in copy number in the human genome. Nature 2006, 444:444-454.
-
(2006)
Nature
, vol.444
, pp. 444-454
-
-
Redon, R.1
-
30
-
-
34347348166
-
Challenges and standards in integrating surveys of structural variation
-
Scherer S.W., et al. Challenges and standards in integrating surveys of structural variation. Nat. Genet. 2007, 39:S7-S15.
-
(2007)
Nat. Genet.
, vol.39
-
-
Scherer, S.W.1
-
31
-
-
57449090630
-
Recurrent chromosomal abnormalities in human embryonic stem cells
-
Spits C., et al. Recurrent chromosomal abnormalities in human embryonic stem cells. Nat. Biotechnol. 2008, 26:1361-1363.
-
(2008)
Nat. Biotechnol.
, vol.26
, pp. 1361-1363
-
-
Spits, C.1
-
32
-
-
79953854769
-
Karotypic abnormalities in human induced pluripotent stem cells and embryonic stem cells
-
Taapken S.M., et al. Karotypic abnormalities in human induced pluripotent stem cells and embryonic stem cells. Nat. Biotechnol. 2011, 29:313-314.
-
(2011)
Nat. Biotechnol.
, vol.29
, pp. 313-314
-
-
Taapken, S.M.1
-
34
-
-
0031890165
-
Neural differentiation of rhesus embryonic stem cells
-
Thomson J.A., Marshall V.S., Trojanowski J.Q. Neural differentiation of rhesus embryonic stem cells. APMIS 1998, 106:149-156.
-
(1998)
APMIS
, vol.106
, pp. 149-156
-
-
Thomson, J.A.1
Marshall, V.S.2
Trojanowski, J.Q.3
-
35
-
-
77954344374
-
Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies
-
van der Veken L.T., et al. Low grade mosaic for a complex supernumerary ring chromosome 18 in an adult patient with multiple congenital anomalies. Mol. Cytogenet. 2010, 3:13.
-
(2010)
Mol. Cytogenet.
, vol.3
, pp. 13
-
-
van der Veken, L.T.1
-
36
-
-
84862312747
-
Microdeletion and microduplication syndromes
-
Weise A., et al. Microdeletion and microduplication syndromes. J. Histochem. Cytochem. 2012, 60:346-358.
-
(2012)
J. Histochem. Cytochem.
, vol.60
, pp. 346-358
-
-
Weise, A.1
|