-
1
-
-
38549086464
-
Defining 'chromosomal instability'
-
Geigl, J.B., Obenauf, A.C., Schwarzbraun, T. & Speicher, M.R. Defining 'chromosomal instability'. Trends Genet. 24, 64-69 (2008).
-
(2008)
Trends Genet
, vol.24
, pp. 64-69
-
-
Geigl, J.B.1
Obenauf, A.C.2
Schwarzbraun, T.3
Speicher, M.R.4
-
2
-
-
0031004175
-
Genetic instability in colorectal cancers
-
Lengauer, C., Kinzler, K.W. & Vogelstein, B. Genetic instability in colorectal cancers. Nature 386, 623-627 (1997).
-
(1997)
Nature
, vol.386
, pp. 623-627
-
-
Lengauer, C.1
Kinzler, K.W.2
Vogelstein, B.3
-
3
-
-
34547433234
-
Chromosome instability, chromosome transcriptome, and clonal evolution of tumor cell populations
-
Gao, C. et al. Chromosome instability, chromosome transcriptome, and clonal evolution of tumor cell populations. Proc. Natl. Acad. Sci. USA 104, 8995-9000 (2007).
-
(2007)
Proc. Natl. Acad. Sci. USA
, vol.104
, pp. 8995-9000
-
-
Gao, C.1
-
4
-
-
9244263076
-
Aneuploidy and cancer
-
Rajagopalan, H. & Lengauer, C. Aneuploidy and cancer. Nature 432, 338-341 (2004).
-
(2004)
Nature
, vol.432
, pp. 338-341
-
-
Rajagopalan, H.1
Lengauer, C.2
-
5
-
-
26244455545
-
Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis
-
Delhanty, J.D. Mechanisms of aneuploidy induction in human oogenesis and early embryogenesis. Cytogenet. Genome Res. 111, 237-244 (2005).
-
(2005)
Cytogenet. Genome Res
, vol.111
, pp. 237-244
-
-
Delhanty, J.D.1
-
6
-
-
0034064674
-
Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization
-
Voullaire, L., Slater, H., Williamson, R. & Wilton, L. Chromosome analysis of blastomeres from human embryos by using comparative genomic hybridization. Hum. Genet. 106, 210-217 (2000).
-
(2000)
Hum. Genet
, vol.106
, pp. 210-217
-
-
Voullaire, L.1
Slater, H.2
Williamson, R.3
Wilton, L.4
-
7
-
-
0033679573
-
Comprehensive chromosomal analysis of human preimplan-tation embryos using whole genome amplification and single cell comparative genomic hybridization
-
Wells, D. & Delhanty, J.D. Comprehensive chromosomal analysis of human preimplan-tation embryos using whole genome amplification and single cell comparative genomic hybridization. Mol. Hum. Reprod. 6, 1055-1062 (2000).
-
(2000)
Mol. Hum. Reprod
, vol.6
, pp. 1055-1062
-
-
Wells, D.1
Delhanty, J.D.2
-
8
-
-
40049088129
-
Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH
-
Daphnis, D.D. et al. Analysis of the evolution of chromosome abnormalities in human embryos from Day 3 to 5 using CGH and FISH. Mol. Hum. Reprod. 14, 117-125 (2008).
-
(2008)
Mol. Hum. Reprod
, vol.14
, pp. 117-125
-
-
Daphnis, D.D.1
-
9
-
-
40749093284
-
What next for preimplantation genetic screening?
-
Harper, J. et al. What next for preimplantation genetic screening? Hum. Reprod. 23, 478-480 (2008).
-
(2008)
Hum. Reprod
, vol.23
, pp. 478-480
-
-
Harper, J.1
-
10
-
-
33646916059
-
Single-cell chromosomal imbalances detection by array CGH. ucleic
-
Le Caignec, C. et al. Single-cell chromosomal imbalances detection by array CGH. ucleic Acids Res. 34, e68 (2006).
-
(2006)
Acids Res
, vol.34
-
-
Le Caignec, C.1
-
11
-
-
33847347259
-
High resolution array-CGH analysis of single cells
-
Fiegler, H. et al. High resolution array-CGH analysis of single cells. Nucleic Acids Res. 35, e15 (2007).
-
(2007)
Nucleic Acids Res
, vol.35
-
-
Fiegler, H.1
-
12
-
-
44949125672
-
Detection of chromosomal structural alterations in single cells by SNP arrays: A systematic survey of amplification bias and optimized workflow
-
Iwamoto, K. et al. Detection of chromosomal structural alterations in single cells by SNP arrays: a systematic survey of amplification bias and optimized workflow. PLoS One 2, e1306 (2007).
-
(2007)
PLoS One
, vol.2
-
-
Iwamoto, K.1
-
13
-
-
0042232610
-
Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions
-
Ballif, B.C., Yu, W., Shaw, C.A., Kashork, C.D. & Shaffer, L.G. Monosomy 1p36 breakpoint junctions suggest pre-meiotic breakage-fusion-bridge cycles are involved in generating terminal deletions. Hum. Mol. Genet. 12, 2153-2165 (2003).
-
(2003)
Hum. Mol. Genet
, vol.12
, pp. 2153-2165
-
-
Ballif, B.C.1
Yu, W.2
Shaw, C.A.3
Kashork, C.D.4
Shaffer, L.G.5
-
14
-
-
40649085830
-
Duplications in addition to terminal deletions are present in a proportion of ring chromosomes. Clues to the mechanisms of formation
-
Rossi, E. et al. Duplications in addition to terminal deletions are present in a proportion of ring chromosomes. Clues to the mechanisms of formation. J. Med. Genet. 45, 147-154 (2008).
-
(2008)
J. Med. Genet
, vol.45
, pp. 147-154
-
-
Rossi, E.1
-
15
-
-
40749092486
-
Neocentromeres: New insights into centromere structure, disease development, and karyotype evolution
-
Marshall, O.J., Chueh, A.C., Wong, L.H. & Choo, K.H. Neocentromeres: new insights into centromere structure, disease development, and karyotype evolution. Am. J. Hum. Genet. 82, 261-282 (2008).
-
(2008)
Am. J. Hum. Genet
, vol.82
, pp. 261-282
-
-
Marshall, O.J.1
Chueh, A.C.2
Wong, L.H.3
Choo, K.H.4
-
16
-
-
33646046176
-
Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization
-
Ballif, B.C. et al. Detecting sex chromosome anomalies and common triploidies in products of conception by array-based comparative genomic hybridization. Prenat. Diagn. 26, 333-339 (2006).
-
(2006)
Prenat. Diagn
, vol.26
, pp. 333-339
-
-
Ballif, B.C.1
-
17
-
-
0033613977
-
Abnormal phenotypes in uniparental disomy (UPD): Fundamental aspects and a critical review with bibliography of UPD other than 15
-
Kotzot, D. Abnormal phenotypes in uniparental disomy (UPD): fundamental aspects and a critical review with bibliography of UPD other than 15. Am. J. Med. Genet. 82, 265-274 (1999).
-
(1999)
Am. J. Med. Genet
, vol.82
, pp. 265-274
-
-
Kotzot, D.1
-
18
-
-
0034890364
-
Complex and segmental uniparental disomy (UPD): Review and lessons from rare chromosomal complements
-
Kotzot, D. Complex and segmental uniparental disomy (UPD): review and lessons from rare chromosomal complements. J. Med. Genet. 38, 497-507 (2001).
-
(2001)
J. Med. Genet
, vol.38
, pp. 497-507
-
-
Kotzot, D.1
-
19
-
-
14044258836
-
Centric fission - simple and complex mechanisms
-
Perry, J., Slater, H.R. & Choo, K.H. Centric fission - simple and complex mechanisms. Chromosome Res. 12, 627-640 (2004).
-
(2004)
Chromosome Res
, vol.12
, pp. 627-640
-
-
Perry, J.1
Slater, H.R.2
Choo, K.H.3
-
20
-
-
0032472367
-
Interstitial deletions and intrachromosomal amplification initiated from a double-strand break targeted to a mammalian chromosome
-
Pipiras, E., Coquelle, A., Bieth, A. & Debatisse, M. Interstitial deletions and intrachromosomal amplification initiated from a double-strand break targeted to a mammalian chromosome. EMBO J. 17, 325-333 (1998).
-
(1998)
EMBO J
, vol.17
, pp. 325-333
-
-
Pipiras, E.1
Coquelle, A.2
Bieth, A.3
Debatisse, M.4
-
21
-
-
0034632717
-
Telomere dysfunction promotes non-reciprocal translocations and epithelial cancers in mice
-
Artandi, S.E. et al. Telomere dysfunction promotes non-reciprocal translocations and epithelial cancers in mice. Nature 406, 641-645 (2000).
-
(2000)
Nature
, vol.406
, pp. 641-645
-
-
Artandi, S.E.1
-
22
-
-
34548441098
-
Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution
-
Bignell, G.R. et al. Architectures of somatic genomic rearrangement in human cancer amplicons at sequence-level resolution. Genome Res. 17, 1296-1303 (2007).
-
(2007)
Genome Res
, vol.17
, pp. 1296-1303
-
-
Bignell, G.R.1
-
23
-
-
0030955751
-
Treatment-related chromosome abnormalities in human embryos
-
Munné, S. et al. Treatment-related chromosome abnormalities in human embryos. Hum. Reprod. 12, 780-784 (1997).
-
(1997)
Hum. Reprod
, vol.12
, pp. 780-784
-
-
Munné, S.1
-
24
-
-
40749118090
-
The impact of LH-containing gonadotropins on diploidy rates in preimplantation embryos: Long protocol stimulation
-
Weghofer, A. et al. The impact of LH-containing gonadotropins on diploidy rates in preimplantation embryos: long protocol stimulation. Hum. Reprod. 23, 499-503 (2008).
-
(2008)
Hum. Reprod
, vol.23
, pp. 499-503
-
-
Weghofer, A.1
-
25
-
-
43249131029
-
ESHRE PGD consortium data collection VII: Cycles from January to December 2004 with pregnancy follow-up to October 2005
-
Harper, J.C. et al. ESHRE PGD consortium data collection VII: cycles from January to December 2004 with pregnancy follow-up to October 2005. Hum. Reprod. 23, 741-755 (2008).
-
(2008)
Hum. Reprod
, vol.23
, pp. 741-755
-
-
Harper, J.C.1
-
26
-
-
0037248093
-
Chromosomal abnormalities and embryo development in recurrent miscarriage couples
-
Rubio, C. et al. Chromosomal abnormalities and embryo development in recurrent miscarriage couples. Hum. Reprod. 18, 182-188 (2003).
-
(2003)
Hum. Reprod
, vol.18
, pp. 182-188
-
-
Rubio, C.1
-
27
-
-
4243089454
-
Increased rate of aneuploid embryos in young women with previous aneuploid conceptions
-
Munne, S. et al. Increased rate of aneuploid embryos in young women with previous aneuploid conceptions. Prenat. Diagn. 24, 638-643 (2004).
-
(2004)
Prenat. Diagn
, vol.24
, pp. 638-643
-
-
Munne, S.1
-
28
-
-
29144482655
-
Preimplantation genetic screening reveals a high incidence of aneuploidy and mosaicism in embryos from young women undergoing IVF
-
Baart, E.B. et al. Preimplantation genetic screening reveals a high incidence of aneuploidy and mosaicism in embryos from young women undergoing IVF. Hum. Reprod. 21, 223-233 (2006).
-
(2006)
Hum. Reprod
, vol.21
, pp. 223-233
-
-
Baart, E.B.1
-
29
-
-
0023874053
-
Human gene expression first occurs between the four- and eight-cell stages of preimplantation development
-
Braude, P., Bolton, V. & Moore, S. Human gene expression first occurs between the four- and eight-cell stages of preimplantation development. Nature 332, 459-461 (1988).
-
(1988)
Nature
, vol.332
, pp. 459-461
-
-
Braude, P.1
Bolton, V.2
Moore, S.3
-
30
-
-
0036629078
-
Conception to ongoing pregnancy: The 'black box' of early pregnancy loss
-
Macklon, N.S., Geraedts, J.P. & Fauser, B.C. Conception to ongoing pregnancy: the 'black box' of early pregnancy loss. Hum. Reprod. Update 8, 333-343 (2002).
-
(2002)
Hum. Reprod. Update
, vol.8
, pp. 333-343
-
-
Macklon, N.S.1
Geraedts, J.P.2
Fauser, B.C.3
-
31
-
-
0002697449
-
Cytogenetics of spontaneous abortion
-
eds. Gersen, S. & Keagle, M, Humana Press, New Jersey
-
Pflueger, S. Cytogenetics of spontaneous abortion. in The Principles of Clinical Cytogenetics (eds. Gersen, S. & Keagle, M.) 317-343 (Humana Press, New Jersey, 1999).
-
(1999)
The Principles of Clinical Cytogenetics
, pp. 317-343
-
-
Pflueger, S.1
-
32
-
-
17844397183
-
Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH) - re-evaluation of chromosome aberration rates in early spontaneous abortions
-
Fritz, B. et al. Cytogenetic analyses of culture failures by comparative genomic hybridisation (CGH) - re-evaluation of chromosome aberration rates in early spontaneous abortions. Eur. J. Hum. Genet. 9, 539-547 (2001).
-
(2001)
Eur. J. Hum. Genet
, vol.9
, pp. 539-547
-
-
Fritz, B.1
-
33
-
-
27144547761
-
Array comparative genomic hybridization profiling of firsttrimester spontaneous abortions that fail to grow in vitro
-
Benkhalifa, M. et al. Array comparative genomic hybridization profiling of firsttrimester spontaneous abortions that fail to grow in vitro. Prenat. Diagn. 25, 894-900 (2005).
-
(2005)
Prenat. Diagn
, vol.25
, pp. 894-900
-
-
Benkhalifa, M.1
-
35
-
-
11144305136
-
Comparison of blastocyst transfer with or without preimplantation genetic diagnosis for aneuploidy screening in couples with advanced maternal age: A prospective randomized controlled trial
-
Staessen, C. et al. Comparison of blastocyst transfer with or without preimplantation genetic diagnosis for aneuploidy screening in couples with advanced maternal age: a prospective randomized controlled trial. Hum. Reprod. 19, 2849-2858 (2004).
-
(2004)
Hum. Reprod
, vol.19
, pp. 2849-2858
-
-
Staessen, C.1
-
36
-
-
27644521166
-
Fluorescence in situ hybridization reanalysis of day-6 human blastocysts diagnosed with aneuploidy on day 3
-
Li, M. et al. Fluorescence in situ hybridization reanalysis of day-6 human blastocysts diagnosed with aneuploidy on day 3. Fertil. Steril. 84, 1395-1400 (2005).
-
(2005)
Fertil. Steril
, vol.84
, pp. 1395-1400
-
-
Li, M.1
-
37
-
-
27644495027
-
Self-correction of chromosomally abnormal embryos in culture and implications for stem cell production
-
Munne, S. et al. Self-correction of chromosomally abnormal embryos in culture and implications for stem cell production. Fertil. Steril. 84, 1328-1334 (2005).
-
(2005)
Fertil. Steril
, vol.84
, pp. 1328-1334
-
-
Munne, S.1
-
38
-
-
37049012350
-
Aneuploidy and confined chromosomal mosaicism in the developing human brain
-
Yurov, YB. et al. Aneuploidy and confined chromosomal mosaicism in the developing human brain. PLoS One 2, e558 (2007).
-
(2007)
PLoS One
, vol.2
-
-
Yurov, Y.B.1
|