-
1
-
-
84894904513
-
The evolving role of genetics in reproductive medicine
-
Brezina PR, Kearns WG. The evolving role of genetics in reproductive medicine. Obstet Gynecol Clin N Am. 2014;41:41–55.
-
(2014)
Obstet Gynecol Clin N Am
, vol.41
, pp. 41-55
-
-
Brezina, P.R.1
Kearns, W.G.2
-
2
-
-
84923869716
-
Clinical applications of preimplantation genetic testing
-
Brezina PR, Kutteh WH. Clinical applications of preimplantation genetic testing. BMJ (Clin Res Ed). 2015;350:g7611.
-
(2015)
BMJ (Clin Res Ed)
, vol.350
, pp. g7611
-
-
Brezina, P.R.1
Kutteh, W.H.2
-
4
-
-
0019198839
-
A cytogenetic study of 1000 spontaneous abortions
-
COI: 1:STN:280:DyaL38%2FovFyrtA%3D%3D, PID: 7316468
-
Hassold T, Chen N, Funkhouser J, et al. A cytogenetic study of 1000 spontaneous abortions. Ann Hum Genet. 1980;44:151–78.
-
(1980)
Ann Hum Genet
, vol.44
, pp. 151-178
-
-
Hassold, T.1
Chen, N.2
Funkhouser, J.3
-
6
-
-
0027366474
-
Early spontaneous abortion: morphologic and karyotypic findings in 3,912 cases
-
COI: 1:STN:280:DyaK2c7gvVWjtw%3D%3D, PID: 8280893
-
Kalousek DK, Pantzar T, Tsai M, Paradice B. Early spontaneous abortion: morphologic and karyotypic findings in 3,912 cases. Birth Defects Orig Artic Ser. 1993;29:53–61.
-
(1993)
Birth Defects Orig Artic Ser
, vol.29
, pp. 53-61
-
-
Kalousek, D.K.1
Pantzar, T.2
Tsai, M.3
Paradice, B.4
-
7
-
-
0025307919
-
Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification
-
COI: 1:STN:280:DyaK3c3jtFCisQ%3D%3D, PID: 2330030
-
Handyside AH, Kontogianni EH, Hardy K, Winston RM. Pregnancies from biopsied human preimplantation embryos sexed by Y-specific DNA amplification. Nature. 1990;344:768–70.
-
(1990)
Nature
, vol.344
, pp. 768-770
-
-
Handyside, A.H.1
Kontogianni, E.H.2
Hardy, K.3
Winston, R.M.4
-
8
-
-
0036099646
-
Multiplex interphase FISH as a screen for common aneuploidies in spontaneous abortions
-
COI: 1:CAS:528:DC%2BD38Xks1Sqtrs%3D
-
Jobanputra V, Sobrino A, Kinney A, Kline J, Warburton D. Multiplex interphase FISH as a screen for common aneuploidies in spontaneous abortions. Hum Reprod (Oxford, England). 2002;17:1166–70.
-
(2002)
Hum Reprod (Oxford, England)
, vol.17
, pp. 1166-1170
-
-
Jobanputra, V.1
Sobrino, A.2
Kinney, A.3
Kline, J.4
Warburton, D.5
-
10
-
-
79958734907
-
Preimplantation genetic screening: a systematic review and meta-analysis of RCTs
-
COI: 1:STN:280:DC%2BC3MrnvFKqug%3D%3D, PID: 21531751
-
Mastenbroek S, Twisk M, van der Veen F, Repping S. Preimplantation genetic screening: a systematic review and meta-analysis of RCTs. Hum Reprod Update. 2011;17:454–66.
-
(2011)
Hum Reprod Update
, vol.17
, pp. 454-466
-
-
Mastenbroek, S.1
Twisk, M.2
van der Veen, F.3
Repping, S.4
-
11
-
-
34347375082
-
In vitro fertilization with preimplantation genetic screening
-
COI: 1:CAS:528:DC%2BD2sXnsVygu70%3D, PID: 17611204
-
Mastenbroek S, Twisk M, van Echten-Arends J, et al. In vitro fertilization with preimplantation genetic screening. N Engl J Med. 2007;357:9–17.
-
(2007)
N Engl J Med
, vol.357
, pp. 9-17
-
-
Mastenbroek, S.1
Twisk, M.2
van Echten-Arends, J.3
-
12
-
-
55449087440
-
-
Preimplantation genetic testing: a Practice Committee opinion. Fertility and sterility 2008;90:S136-43.
-
Preimplantation genetic testing: a Practice Committee opinion. Fertility and sterility 2008;90:S136-43.
-
-
-
-
13
-
-
77949964522
-
What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium Steering Committee
-
Harper J, Coonen E, De Rycke M, et al. What next for preimplantation genetic screening (PGS)? A position statement from the ESHRE PGD Consortium Steering Committee. Hum Reprod (Oxford, England). 2010;25:821–3.
-
(2010)
Hum Reprod (Oxford, England)
, vol.25
, pp. 821-823
-
-
Harper, J.1
Coonen, E.2
De Rycke, M.3
-
14
-
-
64249151388
-
430: preimplantation genetic screening for aneuploidy
-
Committee Opinion No ACOG. 430: preimplantation genetic screening for aneuploidy. Obstet Gynecol. 2009;113:766–7.
-
(2009)
Obstet Gynecol
, vol.113
, pp. 766-767
-
-
Committee Opinion No, A.C.O.G.1
-
15
-
-
80052271116
-
Live birth outcome with trophectoderm biopsy, blastocyst vitrification, and single-nucleotide polymorphism microarray-based comprehensive chromosome screening in infertile patients
-
PID: 21782169
-
Schoolcraft WB, Treff NR, Stevens JM, Ferry K, Katz-Jaffe M, Scott Jr RT. Live birth outcome with trophectoderm biopsy, blastocyst vitrification, and single-nucleotide polymorphism microarray-based comprehensive chromosome screening in infertile patients. Fertil Steril. 2011;96:638–40.
-
(2011)
Fertil Steril
, vol.96
, pp. 638-640
-
-
Schoolcraft, W.B.1
Treff, N.R.2
Stevens, J.M.3
Ferry, K.4
Katz-Jaffe, M.5
Scott, R.T.6
-
16
-
-
84859155553
-
Comprehensive chromosome screening is highly predictive of the reproductive potential of human embryos: a prospective, blinded, nonselection study
-
PID: 22305103
-
Scott Jr RT, Ferry K, Su J, Tao X, Scott K, Treff NR. Comprehensive chromosome screening is highly predictive of the reproductive potential of human embryos: a prospective, blinded, nonselection study. Fertil Steril. 2012;97:870–5.
-
(2012)
Fertil Steril
, vol.97
, pp. 870-875
-
-
Scott, R.T.1
Ferry, K.2
Su, J.3
Tao, X.4
Scott, K.5
Treff, N.R.6
-
17
-
-
84883453649
-
Blastocyst biopsy with comprehensive chromosome screening and fresh embryo transfer significantly increases in vitro fertilization implantation and delivery rates: a randomized controlled trial
-
PID: 23731996
-
Scott Jr RT, Upham KM, Forman EJ, et al. Blastocyst biopsy with comprehensive chromosome screening and fresh embryo transfer significantly increases in vitro fertilization implantation and delivery rates: a randomized controlled trial. Fertil Steril. 2013;100:697–703.
-
(2013)
Fertil Steril
, vol.100
, pp. 697-703
-
-
Scott, R.T.1
Upham, K.M.2
Forman, E.J.3
-
18
-
-
85027539003
-
The use of next-generation sequencing (NGS) for preimplantation genetic screening (PGS) and diagnosis (PGD)
-
Tobler KJ, Ross R, Benner AT, Du L, Brezina PR, Kearns WG. The use of next-generation sequencing (NGS) for preimplantation genetic screening (PGS) and diagnosis (PGD). Fertil Steril. 2014;102:e184–5.
-
(2014)
Fertil Steril
, vol.102
, pp. e184-e185
-
-
Tobler, K.J.1
Ross, R.2
Benner, A.T.3
Du, L.4
Brezina, P.R.5
Kearns, W.G.6
-
19
-
-
84923921673
-
23-chromosome single nucleotide polymorphism (SNP) microarray preimplantation genetic screening (PGS) for recurrent pregnancy loss (RPL) in 687 in vitro fertilization (IVF) cycles and 5871 embryos
-
Tobler KJ, Brezina PR, Benner AT, Du L, Boyd B, Kearns WG. 23-chromosome single nucleotide polymorphism (SNP) microarray preimplantation genetic screening (PGS) for recurrent pregnancy loss (RPL) in 687 in vitro fertilization (IVF) cycles and 5871 embryos. Fertil Steril. 2012;98:S54.
-
(2012)
Fertil Steril
, vol.98
, pp. S54
-
-
Tobler, K.J.1
Brezina, P.R.2
Benner, A.T.3
Du, L.4
Boyd, B.5
Kearns, W.G.6
-
20
-
-
84866630166
-
Evaluation of 571 in vitro fertilization (IVF) cycles and 4,873 embryos using 23-chromosome single nucleotide polymorphism (SNP) microarray preimplantation genetic screening (PGS)
-
Brezina P, Tobler K, Benner A, Du L, Boyd B, Kearns W. Evaluation of 571 in vitro fertilization (IVF) cycles and 4,873 embryos using 23-chromosome single nucleotide polymorphism (SNP) microarray preimplantation genetic screening (PGS). Fertil Steril. 2012;97:S23–4.
-
(2012)
Fertil Steril
, vol.97
, pp. S23-S24
-
-
Brezina, P.1
Tobler, K.2
Benner, A.3
Du, L.4
Boyd, B.5
Kearns, W.6
-
21
-
-
84977463395
-
-
Technology PCotASfRMatSfAR. ASRM practice committee brief communication on pre-implantation genetic screening for aneuploidy: a committee opinion. 2016: En Press.
-
Technology PCotASfRMatSfAR. ASRM practice committee brief communication on pre-implantation genetic screening for aneuploidy: a committee opinion. 2016: En Press.
-
-
-
-
22
-
-
77955126785
-
SNP microarray-based 24 chromosome aneuploidy screening demonstrates that cleavage-stage FISH poorly predicts aneuploidy in embryos that develop to morphologically normal blastocysts
-
COI: 1:CAS:528:DC%2BC3cXptlegt7c%3D, PID: 20479065
-
Northrop LE, Treff NR, Levy B, Scott Jr RT. SNP microarray-based 24 chromosome aneuploidy screening demonstrates that cleavage-stage FISH poorly predicts aneuploidy in embryos that develop to morphologically normal blastocysts. Mol Hum Reprod. 2010;16:590–600.
-
(2010)
Mol Hum Reprod
, vol.16
, pp. 590-600
-
-
Northrop, L.E.1
Treff, N.R.2
Levy, B.3
Scott, R.T.4
-
23
-
-
84894899969
-
All 23 chromosomes have significant levels of aneuploidy in recurrent pregnancy loss couples
-
Brezina PR, Tobler K, Benner AT, Du L, Xu X, Kearns WG. All 23 chromosomes have significant levels of aneuploidy in recurrent pregnancy loss couples. Fertil Steril. 2012;97:S7.
-
(2012)
Fertil Steril
, vol.97
, pp. S7
-
-
Brezina, P.R.1
Tobler, K.2
Benner, A.T.3
Du, L.4
Xu, X.5
Kearns, W.G.6
-
24
-
-
78649281579
-
Comprehensive analysis of karyotypic mosaicism between trophectoderm and inner cell mass
-
COI: 1:STN:280:DC%2BC3cbot1SgsA%3D%3D, PID: 20643877
-
Johnson DS, Cinnioglu C, Ross R, et al. Comprehensive analysis of karyotypic mosaicism between trophectoderm and inner cell mass. Mol Hum Reprod. 2010;16:944–9.
-
(2010)
Mol Hum Reprod
, vol.16
, pp. 944-949
-
-
Johnson, D.S.1
Cinnioglu, C.2
Ross, R.3
-
25
-
-
0028031007
-
Chromosome mosaicism in human embryos
-
COI: 1:STN:280:DyaK2M7gtFymsw%3D%3D, PID: 7803609
-
Munne S, Weier HU, Grifo J, Cohen J. Chromosome mosaicism in human embryos. Biol Reprod. 1994;51:373–9.
-
(1994)
Biol Reprod
, vol.51
, pp. 373-379
-
-
Munne, S.1
Weier, H.U.2
Grifo, J.3
Cohen, J.4
-
26
-
-
84895924699
-
The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts
-
PID: 24581286
-
Novik V, Moulton EB, Sisson ME, et al. The accuracy of chromosomal microarray testing for identification of embryonic mosaicism in human blastocysts. Mol Cytogenet. 2014;7:18.
-
(2014)
Mol Cytogenet
, vol.7
, pp. 18
-
-
Novik, V.1
Moulton, E.B.2
Sisson, M.E.3
-
27
-
-
0027531981
-
Mosaicism in chorionic villus sampling: an analysis of incidence and chromosomes involved in 2612 consecutive cases
-
COI: 1:STN:280:DyaK3s3otFGjug%3D%3D, PID: 8506219
-
Wang BB, Rubin CH, Williams 3rd J. Mosaicism in chorionic villus sampling: an analysis of incidence and chromosomes involved in 2612 consecutive cases. Prenat Diagn. 1993;13:179–90.
-
(1993)
Prenat Diagn
, vol.13
, pp. 179-190
-
-
Wang, B.B.1
Rubin, C.H.2
Williams, J.3
-
28
-
-
84923861272
-
Genetic normalization of differentiating aneuploid cleavage stage embryos
-
Brezina PR, Ross R, Kaufmann R, Anchan R, Zhao Y, Kearns WG. Genetic normalization of differentiating aneuploid cleavage stage embryos. Fertil Steril. 2013;100:S69.
-
(2013)
Fertil Steril
, vol.100
, pp. S69
-
-
Brezina, P.R.1
Ross, R.2
Kaufmann, R.3
Anchan, R.4
Zhao, Y.5
Kearns, W.G.6
-
29
-
-
84947968568
-
Preimplantation genetic screening (PGS) is an excellent tool, but not perfect: a guide to counseling patients considering PGS
-
PID: 26493116
-
Brezina PR, Kutteh WH, Bailey AP, Ke RW. Preimplantation genetic screening (PGS) is an excellent tool, but not perfect: a guide to counseling patients considering PGS. Fertil Steril. 2016;105:49–50.
-
(2016)
Fertil Steril
, vol.105
, pp. 49-50
-
-
Brezina, P.R.1
Kutteh, W.H.2
Bailey, A.P.3
Ke, R.W.4
-
30
-
-
84880566187
-
FISH reanalysis of inner cell mass and trophectoderm samples of previously array-CGH screened blastocysts shows high accuracy of diagnosis and no major diagnostic impact of mosaicism at the blastocyst stage
-
COI: 1:CAS:528:DC%2BC3sXhtFOgtrrI
-
Capalbo A, Wright G, Elliott T, Ubaldi FM, Rienzi L, Nagy ZP. FISH reanalysis of inner cell mass and trophectoderm samples of previously array-CGH screened blastocysts shows high accuracy of diagnosis and no major diagnostic impact of mosaicism at the blastocyst stage. Hum Reprod (Oxford, England). 2013;28:2298–307.
-
(2013)
Hum Reprod (Oxford, England)
, vol.28
, pp. 2298-2307
-
-
Capalbo, A.1
Wright, G.2
Elliott, T.3
Ubaldi, F.M.4
Rienzi, L.5
Nagy, Z.P.6
-
31
-
-
70350487415
-
Impact of cleavage-stage embryo biopsy in view of PGD on human blastocyst implantation: a prospective cohort of single embryo transfers
-
De Vos A, Staessen C, De Rycke M, et al. Impact of cleavage-stage embryo biopsy in view of PGD on human blastocyst implantation: a prospective cohort of single embryo transfers. Hum Reprod (Oxford, England). 2009;24:2988–96.
-
(2009)
Hum Reprod (Oxford, England)
, vol.24
, pp. 2988-2996
-
-
De Vos, A.1
Staessen, C.2
De Rycke, M.3
-
32
-
-
84894904638
-
Classic and cutting-edge strategies for the management of early pregnancy loss
-
Brezina PR, Kutteh WH. Classic and cutting-edge strategies for the management of early pregnancy loss. Obstet Gynecol Clin N Am. 2014;41:1–18.
-
(2014)
Obstet Gynecol Clin N Am
, vol.41
, pp. 1-18
-
-
Brezina, P.R.1
Kutteh, W.H.2
-
34
-
-
85040956381
-
Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study
-
PID: 22551456
-
Yang Z, Liu J, Collins GS, et al. Selection of single blastocysts for fresh transfer via standard morphology assessment alone and with array CGH for good prognosis IVF patients: results from a randomized pilot study. Mol Cytogenet. 2012;5:24.
-
(2012)
Mol Cytogenet
, vol.5
, pp. 24
-
-
Yang, Z.1
Liu, J.2
Collins, G.S.3
-
35
-
-
84923933730
-
Deletions and duplications identified by 23 chromosome single nucleotide polymorphism (SNP) microarray are associated with aneuploidy
-
Chipko C, Brezina PR, Benner AT, Du L, Christianson MS, Kearns WG. Deletions and duplications identified by 23 chromosome single nucleotide polymorphism (SNP) microarray are associated with aneuploidy. Fertil Steril. 2011;96:S21.
-
(2011)
Fertil Steril
, vol.96
, pp. S21
-
-
Chipko, C.1
Brezina, P.R.2
Benner, A.T.3
Du, L.4
Christianson, M.S.5
Kearns, W.G.6
-
36
-
-
84923911494
-
Chromosomal duplications (≥200 KILOBASES (KB)) are more common than deletions ≥200 KB in developing human embryos as identified by 23 chromosome single nucleotide polymorphism (SNP) microarray
-
Christianson MS, Brezina PR, Benner AT, Du L, Siegel A, Kearns WG. Chromosomal duplications (≥200 KILOBASES (KB)) are more common than deletions ≥200 KB in developing human embryos as identified by 23 chromosome single nucleotide polymorphism (SNP) microarray. Fertil Steril. 2011;96:S21–2.
-
(2011)
Fertil Steril
, vol.96
, pp. S21-S22
-
-
Christianson, M.S.1
Brezina, P.R.2
Benner, A.T.3
Du, L.4
Siegel, A.5
Kearns, W.G.6
-
37
-
-
84977445322
-
-
Ion Personal Genome Machine® (PGM™) System. (Accessed March 31, 2016, at.)
-
Ion Personal Genome Machine® (PGM™) System. (Accessed March 31, 2016, at https://www.thermofisher.com/order/catalog/product/4462921.)
-
-
-
-
38
-
-
84977465797
-
-
MiSeq® System. 2016. at.
-
MiSeq® System. 2016. at http://www.illumina.com/content/dam/illumina-marketing/documents/products/datasheets/datasheet_miseq.pdf.)
-
-
-
-
39
-
-
33847347259
-
High resolution array-CGH analysis of single cells
-
PID: 17178751
-
Fiegler H, Geigl JB, Langer S, et al. High resolution array-CGH analysis of single cells. Nucleic Acids Res. 2007;35:e15.
-
(2007)
Nucleic Acids Res
, vol.35
, pp. e15
-
-
Fiegler, H.1
Geigl, J.B.2
Langer, S.3
-
40
-
-
58249096083
-
Use of comprehensive chromosomal screening for embryo assessment: microarrays and CGH
-
COI: 1:CAS:528:DC%2BD1MXltV2gtA%3D%3D, PID: 18957518
-
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
-
41
-
-
84894906269
-
The rate of de novo and inherited aneuploidy as determined by 23-chromosome single nucleotide polymorphism microarray (SNP) in embryos generated from parents with known chromosomal translocations
-
Du L, Brezina P, Benner A, Swelstad B, Gunn M, Kearns W. The rate of de novo and inherited aneuploidy as determined by 23-chromosome single nucleotide polymorphism microarray (SNP) in embryos generated from parents with known chromosomal translocations. Fertil Steril. 2011;96:S221.
-
(2011)
Fertil Steril
, vol.96
, pp. S221
-
-
Du, L.1
Brezina, P.2
Benner, A.3
Swelstad, B.4
Gunn, M.5
Kearns, W.6
-
42
-
-
77955123936
-
SNP microarray-based 24 chromosome aneuploidy screening is significantly more consistent than FISH
-
COI: 1:CAS:528:DC%2BC3cXptlegtL4%3D, PID: 20484246
-
Treff NR, Levy B, Su J, Northrop LE, Tao X, Scott Jr RT. SNP microarray-based 24 chromosome aneuploidy screening is significantly more consistent than FISH. Mol Hum Reprod. 2010;16:583–9.
-
(2010)
Mol Hum Reprod
, vol.16
, pp. 583-589
-
-
Treff, N.R.1
Levy, B.2
Su, J.3
Northrop, L.E.4
Tao, X.5
Scott, R.T.6
-
43
-
-
82855175112
-
PGD and aneuploidy screening for 24 chromosomes by genome-wide SNP analysis: seeing the wood and the trees
-
COI: 1:CAS:528:DC%2BC38XmtlGns70%3D, PID: 22033395
-
Handyside AH. PGD and aneuploidy screening for 24 chromosomes by genome-wide SNP analysis: seeing the wood and the trees. Reprod Biomed Online. 2011;23:686–91.
-
(2011)
Reprod Biomed Online
, vol.23
, pp. 686-691
-
-
Handyside, A.H.1
-
44
-
-
85027539098
-
23-chromosome single nucleotide polymorphism (SNP) microarray detects genomic aberrations that may be missed by comparative genomic hybridization (CGH) arrays in preimplantation genetic screening (PGS)
-
Siegel A, Brezina PR, Benner AT, Du L, Gunn M, Kearns WG. 23-chromosome single nucleotide polymorphism (SNP) microarray detects genomic aberrations that may be missed by comparative genomic hybridization (CGH) arrays in preimplantation genetic screening (PGS). Fertil Steril. 2011;96:S224.
-
(2011)
Fertil Steril
, vol.96
, pp. S224
-
-
Siegel, A.1
Brezina, P.R.2
Benner, A.T.3
Du, L.4
Gunn, M.5
Kearns, W.G.6
-
45
-
-
84930865705
-
Comparison of array comparative genomic hybridization and quantitative real-time PCR-based aneuploidy screening of blastocyst biopsies
-
COI: 1:CAS:528:DC%2BC2cXhvVGisb%2FE, PID: 25351780
-
Capalbo A, Treff NR, Cimadomo D, et al. Comparison of array comparative genomic hybridization and quantitative real-time PCR-based aneuploidy screening of blastocyst biopsies. Eur J Hum Genet: EJHG. 2015;23:901–6.
-
(2015)
Eur J Hum Genet: EJHG
, vol.23
, pp. 901-906
-
-
Capalbo, A.1
Treff, N.R.2
Cimadomo, D.3
-
46
-
-
84977464371
-
-
Validation report for next generation sequencing for chromosomes (Ploidy) as compared to CGH microarrays. 2015.
-
Validation report for next generation sequencing for chromosomes (Ploidy) as compared to CGH microarrays. 2015.
-
-
-
-
47
-
-
84858380925
-
Development and validation of an accurate quantitative real-time polymerase chain reaction-based assay for human blastocyst comprehensive chromosomal aneuploidy screening
-
COI: 1:CAS:528:DC%2BC38XkvFyktbo%3D, PID: 22342859
-
Treff NR, Tao X, Ferry KM, Su J, Taylor D, Scott Jr RT. Development and validation of an accurate quantitative real-time polymerase chain reaction-based assay for human blastocyst comprehensive chromosomal aneuploidy screening. Fertil Steril. 2012;97:819–24.
-
(2012)
Fertil Steril
, vol.97
, pp. 819-824
-
-
Treff, N.R.1
Tao, X.2
Ferry, K.M.3
Su, J.4
Taylor, D.5
Scott, R.T.6
-
48
-
-
84876409196
-
Four-hour quantitative real-time polymerase chain reaction-based comprehensive chromosome screening and accumulating evidence of accuracy, safety, predictive value, and clinical efficacy
-
COI: 1:CAS:528:DC%2BC38XhslynsbzL, PID: 23206734
-
Treff NR, Scott Jr RT. Four-hour quantitative real-time polymerase chain reaction-based comprehensive chromosome screening and accumulating evidence of accuracy, safety, predictive value, and clinical efficacy. Fertil Steril. 2013;99:1049–53.
-
(2013)
Fertil Steril
, vol.99
, pp. 1049-1053
-
-
Treff, N.R.1
Scott, R.T.2
-
49
-
-
84935848930
-
Application of next-generation sequencing for 24-chromosome aneuploidy screening of human preimplantation embryos
-
PID: 26085841
-
Zheng H, Jin H, Liu L, Liu J, Wang WH. Application of next-generation sequencing for 24-chromosome aneuploidy screening of human preimplantation embryos. Mol Cytogenet. 2015;8:38.
-
(2015)
Mol Cytogenet
, vol.8
, pp. 38
-
-
Zheng, H.1
Jin, H.2
Liu, L.3
Liu, J.4
Wang, W.H.5
-
50
-
-
84899932270
-
Development and validation of a next-generation sequencing-based protocol for 24-chromosome aneuploidy screening of embryos
-
COI: 1:CAS:528:DC%2BC2cXjvFSltbw%3D, PID: 24613537
-
Fiorentino F, Biricik A, Bono S, et al. Development and validation of a next-generation sequencing-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
-
51
-
-
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 (Oxford, England). 2014;29:2802–13.
-
(2014)
Hum Reprod (Oxford, England)
, vol.29
, pp. 2802-2813
-
-
Fiorentino, F.1
Bono, S.2
Biricik, A.3
-
52
-
-
84875700912
-
Evaluation of targeted next-generation sequencing–based preimplantation genetic diagnosis of monogenic disease
-
COI: 1:CAS:528:DC%2BC3sXnslegug%3D%3D, PID: 23312231, e6
-
Treff NR, Fedick A, Tao X, Devkota B, Taylor D, Scott RT. Evaluation of targeted next-generation sequencing–based preimplantation genetic diagnosis of monogenic disease. Fertil Steril. 2013;99:1377–84. e6.
-
(2013)
Fertil Steril
, vol.99
, pp. 1377-1384
-
-
Treff, N.R.1
Fedick, A.2
Tao, X.3
Devkota, B.4
Taylor, D.5
Scott, R.T.6
-
53
-
-
84897109315
-
Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis
-
COI: 1:CAS:528:DC%2BC2cXltFWns7w%3D, PID: 24306492
-
Damerla RR, Chatterjee B, Li Y, Francis RJ, Fatakia SN, Lo CW. Ion Torrent sequencing for conducting genome-wide scans for mutation mapping analysis. Mamm Genome. 2014;25:120–8.
-
(2014)
Mamm Genome
, vol.25
, pp. 120-128
-
-
Damerla, R.R.1
Chatterjee, B.2
Li, Y.3
Francis, R.J.4
Fatakia, S.N.5
Lo, C.W.6
-
54
-
-
84977462004
-
-
Wherever testing can show the way forward, Good Start Genetics offers an option. 2016. at
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Wherever testing can show the way forward, Good Start Genetics offers an option. 2016. at https://www.goodstartgenetics.com/clinicians/genetic-testing-services-portfolio/.)
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