Network


Latest external collaboration on country level. Dive into details by clicking on the dots.

Hotspot


Dive into the research topics where L. Du is active.

Publication


Featured researches published by L. Du.


Fertility and Sterility | 2015

Blastocoel fluid from differentiated blastocysts harbors embryonic genomic material capable of a whole-genome deoxyribonucleic acid amplification and comprehensive chromosome microarray analysis

Kyle J. Tobler; Yulian Zhao; R. Ross; Andy T. Benner; X. Xu; L. Du; Kathleen Broman; Kim Thrift; P.R. Brezina; W.G. Kearns

OBJECTIVE To obtain embryonic molecular karyotypes from genomic DNA (deoxyribonucleic acid) isolated from blastocoel fluid (BF) and to compare these karyotypes with the karyotypes from the remaining inner cell mass (ICM) and trophectoderm (TE) of the blastocyst. DESIGN Prospective cohort study. SETTING Academic center and preimplantation genetics laboratory. PATIENT(S) Ninety-six donated cryopreserved embryos. INTERVENTION(S) Embryo biopsy, BF aspiration, DNA analysis using a comparative genomic hybridization microarray (aCGH). MAIN OUTCOME MEASURE(S) The aCGH of a single blastomere, BF-DNA, and ICM-TE. RESULT(S) The BF-DNA samples resulted in a successful aCGH in 63% of cases. Discordance in karyotypes was found between the BF-DNA and the ICM-TE in 52% of cases. A total of 70% of aneusomic (mosaicism), cleavage-stage embryos differentiated into euploid blastocysts. Probabilities for diagnostic accuracy were calculated and demonstrated the following: sensitivity of 0.88 (95% confidence interval [CI]: 0.62-0.98); specificity of 0.55 (95% CI: 0.39-0.70); positive predictive value of 0.41 (95% CI: 0.25-0.60); negative predictive value of 0.92 (95% CI: 0.75-0.99). CONCLUSION(S) Genomic DNA from the BF can be amplified and characterized by comprehensive chromosome microarrays. The results demonstrated that aneusomic cleavage-stage embryos differentiated into euploid blastocysts, possibly using a mechanism that marginalizes aneuploid nuclei into the blastocoel cavity. In addition, owing to the high discordance between the karyotypes obtained from the BF-DNA and the ICM-TE, using BF-DNA for preimplantation genetic testing is not yet advised.


Journal of Assisted Reproduction and Genetics | 2014

Two different microarray technologies for preimplantation genetic diagnosis and screening, due to reciprocal translocation imbalances, demonstrate equivalent euploidy and clinical pregnancy rates.

K.J. Tobler; P.R. Brezina; A.T. Benner; L. Du; X. Xu; W.G. Kearns


Fertility and Sterility | 2012

All 23 Chromosomes have Significant Levels of Aneuploidy in Recurrent Pregnancy Loss Couples

P.R. Brezina; K.J. Tobler; A.T. Benner; L. Du; X. Xu; W.G. Kearns


Fertility and Sterility | 2011

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

L. Du; P.R. Brezina; A.T. Benner; B.B. Swelstad; M. Gunn; W.G. Kearns


Fertility and Sterility | 2014

The potential use of blastocoel fluid (BF) from expanded blastocysts as a less invasive form of embryo biopsy for preimplantation genetic testing

K.J. Tobler; Y. Zhao; R. Ross; A.T. Benner; X. Xu; L. Du; K. Broman; K. Thrift; P.R. Brezina; W.G. Kearns


Fertility and Sterility | 2011

Deletions and duplications identified by 23 chromosome single nucleotide polymorphism (SNP) microarray are associated with aneuploidy

C. Chipko; P.R. Brezina; A.T. Benner; L. Du; Mindy S. Christianson; W.G. Kearns


Fertility and Sterility | 2011

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

Mindy S. Christianson; P.R. Brezina; A.T. Benner; L. Du; A. Siegel; W.G. Kearns


Fertility and Sterility | 2014

Blastocoel fluid (BF) harbors embryonic DNA that may result from the marginalization of aneuploid cells during embryogenesis

K.J. Tobler; Y. Zhao; R. Ross; A.T. Benner; X. Xu; L. Du; K. Broman; K. Thrift; P.R. Brezina; W.G. Kearns


Fertility and Sterility | 2012

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

K.J. Tobler; P.R. Brezina; A.T. Benner; L. Du; B. Boyd; W.G. Kearns


Fertility and Sterility | 2011

23-chromosome single nucleotide polymorphism (SNP) microarray preimplantation genetic screening (PGS) on blastocysts, versus day-3 embryos, results in significantly higher clinical pregnancy rates

A.T. Benner; P.R. Brezina; L. Du; C. Chipko; M. Gunn; W.G. Kearns

Collaboration


Dive into the L. Du's collaboration.

Top Co-Authors

Avatar
Top Co-Authors

Avatar

A.T. Benner

National Institutes of Health

View shared research outputs
Top Co-Authors

Avatar

W.G. Kearns

Johns Hopkins University

View shared research outputs
Top Co-Authors

Avatar

K.J. Tobler

Johns Hopkins University

View shared research outputs
Top Co-Authors

Avatar

B. Boyd

Johns Hopkins University

View shared research outputs
Top Co-Authors

Avatar

W.G. Kearns

Johns Hopkins University

View shared research outputs
Top Co-Authors

Avatar

R. Ross

National Institutes of Health

View shared research outputs
Top Co-Authors

Avatar

K. Broman

Johns Hopkins University

View shared research outputs
Top Co-Authors

Avatar

K. Thrift

Johns Hopkins University

View shared research outputs
Top Co-Authors

Avatar

Y. Zhao

Johns Hopkins University

View shared research outputs
Researchain Logo
Decentralizing Knowledge