-
1
-
-
0034075712
-
Outcome of preimplantation genetic diagnosis of translocations
-
Munné S, Sandalinas M, Escudero T, et al. Outcome of preimplantation genetic diagnosis of translocations. Fertil Steril 2000;73:1209-18.
-
(2000)
Fertil Steril
, vol.73
, pp. 1209-1218
-
-
Munné, S.1
Sandalinas, M.2
Escudero, T.3
-
2
-
-
23144438542
-
Preimplantation testing for chromosomal disorders improves reproductive outcome of poor-prognosis patients
-
Verlinsky Y, Tur-Kaspa I, Cieslak J, et al. Preimplantation testing for chromosomal disorders improves reproductive outcome of poor-prognosis patients. Reprod Biomed Online 2005;11:219-25.
-
(2005)
Reprod Biomed Online
, vol.11
, pp. 219-225
-
-
Verlinsky, Y.1
Tur-Kaspa, I.2
Cieslak, J.3
-
3
-
-
0032425535
-
Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis
-
Scriven PN, Handyside AH, Ogilvie CM. Chromosome translocations: segregation modes and strategies for preimplantation genetic diagnosis. Prenat Diagn 1998;18:1437-49.
-
(1998)
Prenat Diagn
, vol.18
, pp. 1437-1449
-
-
Scriven, P.N.1
Handyside, A.H.2
Ogilvie, C.M.3
-
4
-
-
77952551870
-
Preimplantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses
-
Fischer J, Colls P, Escudero T, et al. Preimplantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses. Fertil Steril 2010;94:283-9.
-
(2010)
Fertil Steril
, vol.94
, pp. 283-289
-
-
Fischer, J.1
Colls, P.2
Escudero, T.3
-
5
-
-
0031977265
-
First pregnancies after preconception diagnosis of translocations of maternal origin
-
Munné S, Scott R, Sable D, et al. First pregnancies after preconception diagnosis of translocations of maternal origin. Fertil Steril 1998;69:675-81.
-
(1998)
Fertil Steril
, vol.69
, pp. 675-681
-
-
Munné, S.1
Scott, R.2
Sable, D.3
-
6
-
-
0031879163
-
Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysis
-
Munné S, Fung J, Cassel MJ, et al. Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysis. Hum Genet 1998;102:663-74.
-
(1998)
Hum Genet
, vol.102
, pp. 663-674
-
-
Munné, S.1
Fung, J.2
Cassel, M.J.3
-
7
-
-
0031922774
-
Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions
-
Conn CM, Harper JC, Winston RML, et al. Infertile couples with Robertsonian translocations: preimplantation genetic analysis of embryos reveals chaotic cleavage divisions. Hum Genet 1998;102:117-23.
-
(1998)
Hum Genet
, vol.102
, pp. 117-123
-
-
Conn, C.M.1
Harper, J.C.2
Winston, R.M.L.3
-
8
-
-
0032902635
-
Karyotyping of human oocytes by chromosomal analysis of the second polar body
-
Verlinsky Y, Evsikov S. Karyotyping of human oocytes by chromosomal analysis of the second polar body. Mol Hum Reprod 1999;5:89-95.
-
(1999)
Mol Hum Reprod
, vol.5
, pp. 89-95
-
-
Verlinsky, Y.1
Evsikov, S.2
-
9
-
-
77958120314
-
ESHRE PGD Consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008
-
Harper JC, Coonen E, De Rycke M, et al. ESHRE PGD Consortium data collection X: cycles from January to December 2007 with pregnancy follow-up to October 2008. Hum Reprod 2010;25:2685-707.
-
(2010)
Hum Reprod
, vol.25
, pp. 2685-2707
-
-
Harper, J.C.1
Coonen, E.2
De Rycke, M.3
-
10
-
-
0036490364
-
Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities
-
Munné S. Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities. Reprod Biomed Online 2002;4:183-96.
-
(2002)
Reprod Biomed Online
, vol.4
, pp. 183-196
-
-
Munné, S.1
-
11
-
-
0038624559
-
Blastomere fixation techniques and risk of misdiagnosis for preimplantation genetic diagnosis of aneuploidy
-
Velilla E, Escudero T, Munné S. Blastomere fixation techniques and risk of misdiagnosis for preimplantation genetic diagnosis of aneuploidy. Reprod Biomed Online 2002;4:210-7.
-
(2002)
Reprod Biomed Online
, vol.4
, pp. 210-217
-
-
Velilla, E.1
Escudero, T.2
Munné, S.3
-
12
-
-
52949149666
-
Accuracy of FISH analysis in predicting chromosomal status in patients undergoing preimplantation genetic diagnosis
-
De Ugarte M, Li M, Surrey M, et al. Accuracy of FISH analysis in predicting chromosomal status in patients undergoing preimplantation genetic diagnosis. Fertil Steril 2008;90:1049-54.
-
(2008)
Fertil Steril
, vol.90
, pp. 1049-1054
-
-
De Ugarte, M.1
Li, M.2
Surrey, M.3
-
13
-
-
78049282793
-
Polymerase chain reaction-based detection of chromosomal imbalances on embryos: the evolution of preimplantation genetic diagnosis for chromosomal translocations
-
Fiorentino F, Kokkali G, Biricik A, et al. Polymerase chain reaction-based detection of chromosomal imbalances on embryos: the evolution of preimplantation genetic diagnosis for chromosomal translocations. Fertil Steril 2010;94:2001-11.
-
(2010)
Fertil Steril
, vol.94
, pp. 2001-2011
-
-
Fiorentino, F.1
Kokkali, G.2
Biricik, A.3
-
14
-
-
77952046831
-
A molecular strategy for routine preimplantation genetic diagnosis in both reciprocal and Robertsonian translocation carriers
-
Traversa MV, Carey L, Leigh D. A molecular strategy for routine preimplantation genetic diagnosis in both reciprocal and Robertsonian translocation carriers. Mol Hum Reprod 2010;16:329-37.
-
(2010)
Mol Hum Reprod
, vol.16
, pp. 329-337
-
-
Traversa, M.V.1
Carey, L.2
Leigh, D.3
-
15
-
-
77955162240
-
Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays
-
Treff NR, Su J, Tao X, et al. Accurate single cell 24 chromosome aneuploidy screening using whole genome amplification and single nucleotide polymorphism microarrays. Fertil Steril 2010;94:2017-21.
-
(2010)
Fertil Steril
, vol.94
, pp. 2017-2021
-
-
Treff, N.R.1
Su, J.2
Tao, X.3
-
16
-
-
79951956230
-
Validation of microarray comparative genomic hybridization for comprehensive chromosome analysis of embryos
-
Gutiérrez-Mateo C, Colls P, Sánchez-García J, et al. Validation of microarray comparative genomic hybridization for comprehensive chromosome analysis of embryos. Fertil Steril 2011;95:953-8.
-
(2011)
Fertil Steril
, vol.95
, pp. 953-958
-
-
Gutiérrez-Mateo, C.1
Colls, P.2
Sánchez-García, J.3
-
17
-
-
58249096083
-
Use of comprehensive chromosomal screening for embryo assessment: microarrays and CGH
-
Wells D, Alfarawati S, Fragouli E. Use of comprehensive chromosomal screening for embryo assessment: microarrays and CGH. Mol Hum Reprod 2008;14:703-10.
-
(2008)
Mol Hum Reprod
, vol.14
, pp. 703-710
-
-
Wells, D.1
Alfarawati, S.2
Fragouli, E.3
-
18
-
-
79957478276
-
First births after preimplantation genetic diagnosis of structural chromosome abnormalities using comparative genomic hybridization and microarray analysis
-
Alfarawati S, Fragouli E, Colls P, et al. First births after preimplantation genetic diagnosis of structural chromosome abnormalities using comparative genomic hybridization and microarray analysis. Hum Reprod 2011;26:1560-74.
-
(2011)
Hum Reprod
, vol.26
, pp. 1560-1574
-
-
Alfarawati, S.1
Fragouli, E.2
Colls, P.3
-
19
-
-
79959426439
-
PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization
-
Fiorentino F, Spizzichino L, Bono S, et al. PGD for reciprocal and Robertsonian translocations using array comparative genomic hybridization. Hum Reprod 2011;26:1925-35.
-
(2011)
Hum Reprod
, vol.26
, pp. 1925-1935
-
-
Fiorentino, F.1
Spizzichino, L.2
Bono, S.3
-
20
-
-
79952987085
-
Single nucleotide polymorphism microarray-based concurrent screening of 24-chromosome aneuploidy and unbalanced translocations in preimplantation human embryos
-
1606-12e1-2
-
Treff NR, Northrop LE, Kasabwala K, et al. Single nucleotide polymorphism microarray-based concurrent screening of 24-chromosome aneuploidy and unbalanced translocations in preimplantation human embryos. Fertil Steril 2011;95:1606-12.e1-2.
-
(2011)
Fertil Steril
, vol.95
-
-
Treff, N.R.1
Northrop, L.E.2
Kasabwala, K.3
-
21
-
-
84904381760
-
Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates
-
Tobler KJ, Brezina PR, Benner AT, et al. Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates. J Assist Reprod Genet 2014;31:843-50.
-
(2014)
J Assist Reprod Genet
, vol.31
, pp. 843-850
-
-
Tobler, K.J.1
Brezina, P.R.2
Benner, A.T.3
-
22
-
-
84861797808
-
Validation of array comparative genome hybridization for diagnosis of translocations in preimplantation human embryos
-
Colls P, Escudero T, Fischer J, et al. Validation of array comparative genome hybridization for diagnosis of translocations in preimplantation human embryos. Reprod Biomed Online 2012;24:621-9.
-
(2012)
Reprod Biomed Online
, vol.24
, pp. 621-629
-
-
Colls, P.1
Escudero, T.2
Fischer, J.3
-
23
-
-
84875700912
-
Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease
-
Treff NR, Fedick A, Tao X, et al. Evaluation of targeted next-generation sequencing-based preimplantation genetic diagnosis of monogenic disease. Fertil Steril 2013;99:1377-84.
-
(2013)
Fertil Steril
, vol.99
, pp. 1377-1384
-
-
Treff, N.R.1
Fedick, A.2
Tao, X.3
-
24
-
-
84883364133
-
24-Chromosome copy number analysis: a comparison of available technologies
-
Handyside AH. 24-Chromosome copy number analysis: a comparison of available technologies. Fertil Steril 2013;100:595-602.
-
(2013)
Fertil Steril
, vol.100
, pp. 595-602
-
-
Handyside, A.H.1
-
25
-
-
84899932270
-
Development and validation of a next-generation sequencing (NGS)-based protocol for 24-chromosome aneuploidy screening of embryos
-
Fiorentino F, Biricik A, Bono S, et al. Development and validation of a next-generation sequencing (NGS)-based protocol for 24-chromosome aneuploidy screening of embryos. Fertil Steril 2014;101:1375-82.
-
(2014)
Fertil Steril
, vol.101
, pp. 1375-1382
-
-
Fiorentino, F.1
Biricik, A.2
Bono, S.3
-
26
-
-
84928973006
-
Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles
-
Fiorentino F, Bono S, Biricik A, et al. Application of next-generation sequencing technology for comprehensive aneuploidy screening of blastocysts in clinical preimplantation genetic screening cycles. Hum Reprod 2014;29:2802-13.
-
(2014)
Hum Reprod
, vol.29
, pp. 2802-2813
-
-
Fiorentino, F.1
Bono, S.2
Biricik, A.3
-
27
-
-
84876350157
-
The impact of next-generation sequencing technology on preimplantation genetic diagnosis and screening
-
Martín J, Cervero A, Mir P, et al. The impact of next-generation sequencing technology on preimplantation genetic diagnosis and screening. Fertil Steril 2013;99:1054-61.
-
(2013)
Fertil Steril
, vol.99
, pp. 1054-1061
-
-
Martín, J.1
Cervero, A.2
Mir, P.3
-
28
-
-
84899935997
-
Next-generation sequencing: challenges in reproductive genetics
-
Rubio C. Next-generation sequencing: challenges in reproductive genetics. Fertil Steril 2014;101:1252-3.
-
(2014)
Fertil Steril
, vol.101
, pp. 1252-1253
-
-
Rubio, C.1
-
29
-
-
84905487367
-
Clinical utilization of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation
-
Wells D, Kaur K, Grifo J, et al. Clinical utilization of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation. J Med Genet 2014;51:553-62.
-
(2014)
J Med Genet
, vol.51
, pp. 553-562
-
-
Wells, D.1
Kaur, K.2
Grifo, J.3
-
31
-
-
33646916059
-
Single-cell chromosomal imbalances detection by array CGH
-
e68.
-
Le Caignec C, Spits C, Sermon K, et al. Single-cell chromosomal imbalances detection by array CGH. Nucleic Acids Res 2006;34:e68.
-
(2006)
Nucleic Acids Res
, vol.34
-
-
Le Caignec, C.1
Spits, C.2
Sermon, K.3
-
32
-
-
84930795257
-
Routine use of next-generation sequencing for preimplantation genetic diagnosis of blastomeres obtained from embryos on day 3 in fresh in vitro fertilization cycles
-
Łukaszuk K, Pukszta S, Wells D, et al. Routine use of next-generation sequencing for preimplantation genetic diagnosis of blastomeres obtained from embryos on day 3 in fresh in vitro fertilization cycles. Fertil Steril 2015;103:1031-6.
-
(2015)
Fertil Steril
, vol.103
, pp. 1031-1036
-
-
Łukaszuk, K.1
Pukszta, S.2
Wells, D.3
-
33
-
-
84856305295
-
Generating barcoded libraries for multiplex high-throughput sequencing
-
Knapp M, Stiller M, Meyer M. Generating barcoded libraries for multiplex high-throughput sequencing. Methods Mol Biol 2012;840:155-70.
-
(2012)
Methods Mol Biol
, vol.840
, pp. 155-170
-
-
Knapp, M.1
Stiller, M.2
Meyer, M.3
|