D. Leigh

发表

Blastocyst trophectoderm biopsy and preimplantation genetic diagnosis for familial monogenic disorders and chromosomal translocations

R. Jansen, S. McArthur, D. Leigh, 2008, Prenatal diagnosis.

Activated Ki‐ras proto‐oncogene in spontaneously transformed and chemical tumor‐derived cell lines related to the mouse lung alveologenic carcinoma

G. Smith, J. Bentel, D. Leigh, 1990, Molecular carcinogenesis.

What next for preimplantation genetic screening (PGS)? Experience with blastocyst biopsy and testing for aneuploidy.

R. Jansen, S. McArthur, D. Leigh, 2008, Human reproduction.

Pregnancies and live births after trophectoderm biopsy and preimplantation genetic testing of human blastocysts.

R. Jansen, S. McArthur, D. Leigh, 2005, Fertility and sterility.

Array CGH and Partial Genome Sequencing for Rapidly Karyotyping IVF Blastocysts Before Single Transfer

R. Jansen, S. McArthur, P. Barahona, 2015 .

Molecular screening for fragile X syndrome among Indonesian children with developmental disability.

S. Faradz, M. Buckley, D. Leigh, 1999, American journal of medical genetics.

Allelic losses in carcinoma in situ and testicular germ cell tumours of adolescents and adults: evidence suggestive of the linear progression model

L. Looijenga, M. Friedlander, H. Roelofs, 2000, British Journal of Cancer.

Identification of X‐linked severe combined immunodeficiency by mutation analysis of blood and hair roots

J. Ziegler, R. Lindeman, D. Leigh, 1999, British journal of haematology.

PGT‐A: The biology and hidden failures of randomized control trials

D. Cram, Xiaohong Wang, S. Quan, 2022, Prenatal diagnosis.

Flow Cytometric Sorting of Fresh and Frozen‐Thawed Spermatozoa in the Western Lowland Gorilla (Gorilla gorilla gorilla)

K. M. Evans, E. G. Crichton, G. Evans, 2005, American journal of primatology.

A small molecule harpagoside inhibits IL-1beta-induced expression of IL-6 by blocking the expression of C-FOS in primary human osteoarthritis chondrocytes

D. Leigh, A. Haseeb, T. Haqqi, 2015 .

A molecular strategy for routine preimplantation genetic diagnosis in both reciprocal and Robertsonian translocation carriers.

M. Traversa, L. Carey, D. Leigh, 2010, Molecular human reproduction.

Uniparental disomy 15 resulting from "correction" of an initial trisomy 15.

S. Purvis-Smith, D. Leigh, M. Yip, 1992, American journal of human genetics.

Prenatal diagnosis of chromosomal mosaicism in over 1600 cases using array comparative genomic hybridization as a first line test

F. Scott, K. Murphy, L. Carey, 2014, Prenatal diagnosis.

Direct PCR sequencing of dystrophin polymorphic CACA alleles after purification to remove shadow bands.

B. Neilan, V. Murray, D. Leigh, 1992, DNA and cell biology.

Embryo Biopsy for PGD: Current Perspective

M. Traversa, S. McArthur, D. Leigh, 2019, In Vitro Fertilization.

Embryo Biopsy for PGD: Current Perspective

R. Jansen, M. Traversa, S. McArthur, 2012 .

Variant haplophasing by long-read sequencing: a new approach to preimplantation genetic testing workups.

D. Cram, Wenling Zhang, Yuanqing Yao, 2021, Fertility and sterility.

Preferential selection and transfer of euploid noncarrier embryos in preimplantation genetic diagnosis cycles for reciprocal translocations.

A. Trounson, D. Cram, Jiayin Liu, 2017, Fertility and sterility.

Mitochondrial DNA Levels are not a simple indicator for preselection of Euploid Embrios with higher developmental potential

A. Kuliev, D. Cram, Yuanqing Yao, 2019, Reproductive BioMedicine Online.

Moving to blastocyst biopsy for preimplantation genetic diagnosis and single embryo transfer at Sydney IVF.

R. Jansen, S. McArthur, D. Leigh, 2004, Fertility and sterility.

The role of preimplantation genetic diagnosis in the management of severe rhesus alloimmunization: first unaffected pregnancy: case report.

J. Morris, S. Seeho, D. Leigh, 2005, Human reproduction.

Clinical application of single‐molecule optical mapping to a multigeneration FSHD1 pedigree

Y. Liu, D. Cram, Xueqin Xu, 2019, Molecular genetics & genomic medicine.

Investigation of a unique male and female sibship with Kallmann's syndrome and 46,XX gonadal dysgenesis with short stature.

I. Fraser, D. Leigh, P. Taylor, 1999, Human reproduction.

Genetic diversity at the FMR1 locus in the Indonesian population

J. Leggo, S. Faradz, M. Buckley, 2000, Annals of human genetics.

Carrier detection in X-linked retinitis pigmentosa.

D. Leigh, A. Gurvitz, F. Halliday, 1994, Australian and New Zealand journal of ophthalmology.

IVF embryo choices and pregnancy outcomes

D. Cram, Xiaohong Wang, S. Quan, 2021, Prenatal diagnosis.

EGF-receptor and extracellular matrix changes in mouse pulmonary carcinogenesis.

G. C. Rhodes, D. Leigh, Angelina Wong, 1991, Experimental lung research.

Single Molecule Sequencing A New Approach for Preimplantation Testing and Noninvasive Prenatal Diagnosis Confirmation of Fetal Genotype.

S. Rechitsky, A. Kuliev, D. Cram, 2019, The Journal of molecular diagnostics : JMD.

Microsatellite genome screening: rapid non-denaturing, non-isotopic dinucleotide repeat analysis.

B. Neilan, D. Leigh, E. Rapley, 1994, BioTechniques.

Third-generation sequencing: any future opportunities for PGT?

D. Cram, Yuanqing Yao, D. Leigh, 2020, Journal of Assisted Reproduction and Genetics.

Counselling risk figures for fragile X carrier females of varying band sizes for use in predicting the likelihood of retardation in their offspring.

G. Turner, S. Laing, A. Turner, 1994, American journal of medical genetics.

The application of a molecular strategy using STR for routine PGD in both reciprocal and Robertsonian translocation carriers

M. Traversa, D. Leigh, 2009 .

Universal amplification of DNA isolated from small regions of paraffin-embedded, formalin-fixed tissue.

D. Leigh, S. Faulkner, Stefan W. Faulkner, 1998, BioTechniques.

The rapid analysis of dystrophin gene deletions shows variable electrophoretic mobility.

B. Neilan, D. Leigh, B. McDonald, 1993, Journal of medical genetics.

Detection of polymorphisms using thermal cycling with a single oligonucleotide on a DNA sequencing gel

M. Cairns, P. England, V. Murray, 1993, Human mutation.

Rapid preparation of limited biological samples for small-volume PCR.

B. Neilan, D. Leigh, A. Gurvitz, 1993, PCR methods and applications.