List of works - Svetlana Rechitsky

Accuracy of preimplantation diagnosis of single-gene disorders by polar body analysis of oocytes

scientific article

Allele dropout in polar bodies and blastomeres.

scientific article

Allele dropout in sequential PCR and FISH analysis of single cells (cell recycling).

scientific article published in February 1996

Before the beginning: the genetic risk of a couple aiming to conceive

scientific article published on 01 October 2019

Birth of a healthy girl after preimplantation gender determination using a combination of polymerase chain reaction and fluorescent in situ hybridization analysis. Preimplantation Genetics Group.

scientific article published in February 1996

Birth of healthy children after preimplantation diagnosis of thalassemias.

scientific article

Construction and sequence analysis of subtraction complementary DNA libraries from human preimplantation embryos

scholarly article

Continuing to deliver: the evidence base for pre-implantation genetic screening

scientific article published on 14 February 2017

Cytogenetic analysis of human somatic cell haploidization.

scientific article published in February 2005

Designer babies - are they a reality yet? Case report: simultaneous preimplantation genetic diagnosis for Fanconi anaemia and HLA typing for cord blood transplantation

scientific article published on 01 January 2000

Expression of homebox-containing genes in human preimplantation development and in embryos with chromosomal aneuploidies

scientific article

First experience of hematopoietic stem cell transplantation treatment of Shwachman-Diamond syndrome using unaffected HLA-matched sibling donor produced through preimplantation HLA typing.

scientific article published on 27 March 2017

First systematic experience of preimplantation genetic diagnosis for de-novo mutations

scientific article published on 20 January 2011

First systematic experience of preimplantation genetic diagnosis for single-gene disorders, and/or preimplantation human leukocyte antigen typing, combined with 24-chromosome aneuploidy testing

scientific article published on 13 December 2014

Fusion as the etiology of chimerism in monochorionic dizygotic twins

scientific article published on 01 January 2005

Homeobox gene expression in human oocytes and preembryos

scientific article

Human embryonic stem cell lines with genetic disorders

scientific article

Improving assisted reproductive technology pregnancy rates: excluding aneuploid and interrogating euploid embryos

scientific article published on 29 June 2015

Isolation of cDNA libraries from individual human preimplantation embryos

scientific article

Next-generation sequencing for preimplantation genetic diagnosis

scientific article published on 13 February 2013

Nonisotopic identification of two point mutations in the CYP21 gene responsible for nonclassic 21-hydroxylase deficiency

scientific article published on 01 August 1994

Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future Direction

scientific article published on 01 January 2019

PGD for all cystic fibrosis carrier couples: novel strategy for preventive medicine and cost analysis

scientific article published on 4 June 2010

PGD for cystic fibrosis patients and couples at risk of an additional genetic disorder combined with 24-chromosome aneuploidy testing.

scientific article published on 29 January 2013

PGD for inherited cardiac diseases.

scientific article

Polar body-based preimplantation diagnosis for X-linked disorders.

scientific article published in January 2002

Polar body-based preimplantation genetic diagnosis for Mendelian disorders.

scientific article

Pre-embryonic diagnosis for Sandhoff disease

scientific article

Preconception and preimplantation diagnosis for cystic fibrosis

scientific article published on February 1, 1992

Preembryonic diagnosis for sickle cell disease.

scientific article

Preimplantation HLA testing

scientific article published on 01 May 2004

Preimplantation HLA typing with aneuploidy testing

scientific article published on 01 January 2006

Preimplantation diagnosis and HLA typing for haemoglobin disorders

scientific article published on 01 September 2005

Preimplantation diagnosis and other modern methods for prenatal diagnosis

scientific article published on 21 April 2016

Preimplantation diagnosis for Fanconi anemia combined with HLA matching

scientific article (publication date: 27 June 2001)

Preimplantation diagnosis for early-onset Alzheimer disease caused by V717L mutation

scientific article published in February 2002

Preimplantation diagnosis for homeobox gene HLXB9 mutation causing Currarino syndrome

scientific article published on 01 April 2005

Preimplantation diagnosis for immunodeficiencies

scientific article published on 01 February 2007

Preimplantation diagnosis for long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

scientific article published in January 2001

Preimplantation diagnosis for neurofibromatosis.

scientific article published in May 2002

Preimplantation diagnosis for ornithine transcarbamylase deficiency.

scientific article published in January 2000

Preimplantation diagnosis for p53 tumour suppressor gene mutations

scientific article published in January 2001

Preimplantation diagnosis for sonic hedgehog mutation causing familial holoprosencephaly.

scientific article

Preimplantation diagnosis of autosomal dominant retinitis pigmentosum using two simultaneous single cell assays for a point mutation in the rhodopsin gene.

scientific article published in April 1998

Preimplantation diagnosis of single disorders.

scientific article

Preimplantation diagnosis of single gene disorders by two-step oocyte genetic analysis using first and second polar body

scientific article

Preimplantation diagnosis of thalassemias

scientific article

Preimplantation genetic diagnosis (PGD) for genetic prion disorder due to F198S mutation in the PRNP gene

scientific article

Preimplantation genetic diagnosis for Pelizaeus-Merzbacher disease with testing for age-related aneuploidies.

scientific article published in January 2006

Preimplantation genetic diagnosis for cancer predisposition

scientific article published in September 2002

Preimplantation genetic diagnosis for early-onset torsion dystonia

scientific article published in February 2004

Preimplantation genetic diagnosis for familial dysautonomia

scientific article published in June 2003

Preimplantation genetic diagnosis for hemoglobinopathies

scientific article published on 12 September 2011

Preimplantation genetic diagnosis for polycystic kidney disease.

scientific article published in October 2004

Preimplantation genetic diagnosis for the Kell genotype

scientific article published on 01 October 2003

Preimplantation genetic diagnosis with HLA matching

scientific article published in August 2004

Preimplantation genetic testing to reduce preterm births in assisted reproductive technology

scientific article published on 01 July 2020

Preimplantation genetic testing: current challenges and future prospects

scientific article published on 17 October 2017

Preimplantation genetics: Improving access to stem cell therapy.

scientific article

Preimplantation testing for phenylketonuria.

scientific article published in August 2001

Prenatal genetic testing and treatment for congenital adrenal hyperplasia

scientific article published on 01 January 2019

Prenatal paternity testing with deoxyribonucleic acid techniques.

scientific article published in June 1996

Prepregnancy testing for single-gene disorders by polar body analysis.

scientific article published in January 1999

Reliability of gender determination using the polymerase chain reaction (PCR) for single cells

scientific article published in August 1991

Reliability of polymerase chain reaction (PCR) analysis of single cells for preimplantation genetic diagnosis

scientific article published on 01 February 1994

Reliability of preimplantation diagnosis for single gene disorders

scientific article

Repository of human embryonic stem cell lines and development of individual specific lines using stembrid technology

scientific article published on October 2006

Sequence analysis of libraries from individual human blastocysts

scientific article

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

scientific article published on 18 November 2019

Single-gene testing combined with single nucleotide polymorphism microarray preimplantation genetic diagnosis for aneuploidy: a novel approach in optimizing pregnancy outcome

scientific article published on 08 December 2010

Three births after preimplantation genetic diagnosis for cystic fibrosis with sequential first and second polar body analysis.

scientific article published in June 1998

Use of nested PCR to identify charred human remains and minute amounts of blood.

scientific article published in May 1998

List of works by Svetlana Rechitsky

Accuracy of preimplantation diagnosis of single-gene disorders by polar body analysis of oocytes

Allele dropout in polar bodies and blastomeres.

Allele dropout in sequential PCR and FISH analysis of single cells (cell recycling).

Before the beginning: the genetic risk of a couple aiming to conceive

Birth of a healthy girl after preimplantation gender determination using a combination of polymerase chain reaction and fluorescent in situ hybridization analysis. Preimplantation Genetics Group.

Birth of healthy children after preimplantation diagnosis of thalassemias.

Construction and sequence analysis of subtraction complementary DNA libraries from human preimplantation embryos

Continuing to deliver: the evidence base for pre-implantation genetic screening

Cytogenetic analysis of human somatic cell haploidization.

Designer babies - are they a reality yet? Case report: simultaneous preimplantation genetic diagnosis for Fanconi anaemia and HLA typing for cord blood transplantation

Expression of homebox-containing genes in human preimplantation development and in embryos with chromosomal aneuploidies

First experience of hematopoietic stem cell transplantation treatment of Shwachman-Diamond syndrome using unaffected HLA-matched sibling donor produced through preimplantation HLA typing.

First systematic experience of preimplantation genetic diagnosis for de-novo mutations

First systematic experience of preimplantation genetic diagnosis for single-gene disorders, and/or preimplantation human leukocyte antigen typing, combined with 24-chromosome aneuploidy testing

Fusion as the etiology of chimerism in monochorionic dizygotic twins

Homeobox gene expression in human oocytes and preembryos

Human embryonic stem cell lines with genetic disorders

Improving assisted reproductive technology pregnancy rates: excluding aneuploid and interrogating euploid embryos

Isolation of cDNA libraries from individual human preimplantation embryos

Next-generation sequencing for preimplantation genetic diagnosis

Nonisotopic identification of two point mutations in the CYP21 gene responsible for nonclassic 21-hydroxylase deficiency

Overview of Preimplantation Genetic Diagnosis (PGD): Historical Perspective and Future Direction

PGD for all cystic fibrosis carrier couples: novel strategy for preventive medicine and cost analysis

PGD for cystic fibrosis patients and couples at risk of an additional genetic disorder combined with 24-chromosome aneuploidy testing.

PGD for inherited cardiac diseases.

Polar body-based preimplantation diagnosis for X-linked disorders.

Polar body-based preimplantation genetic diagnosis for Mendelian disorders.

Pre-embryonic diagnosis for Sandhoff disease

Preconception and preimplantation diagnosis for cystic fibrosis

Preembryonic diagnosis for sickle cell disease.

Preimplantation HLA testing

Preimplantation HLA typing with aneuploidy testing

Preimplantation diagnosis and HLA typing for haemoglobin disorders

Preimplantation diagnosis and other modern methods for prenatal diagnosis

Preimplantation diagnosis for Fanconi anemia combined with HLA matching

Preimplantation diagnosis for early-onset Alzheimer disease caused by V717L mutation

Preimplantation diagnosis for homeobox gene HLXB9 mutation causing Currarino syndrome

Preimplantation diagnosis for immunodeficiencies

Preimplantation diagnosis for long-chain 3-hydroxyacyl-CoA dehydrogenase deficiency.

Preimplantation diagnosis for neurofibromatosis.

Preimplantation diagnosis for ornithine transcarbamylase deficiency.

Preimplantation diagnosis for p53 tumour suppressor gene mutations

Preimplantation diagnosis for sonic hedgehog mutation causing familial holoprosencephaly.

Preimplantation diagnosis of autosomal dominant retinitis pigmentosum using two simultaneous single cell assays for a point mutation in the rhodopsin gene.

Preimplantation diagnosis of single disorders.

Preimplantation diagnosis of single gene disorders by two-step oocyte genetic analysis using first and second polar body

Preimplantation diagnosis of thalassemias

Preimplantation genetic diagnosis (PGD) for genetic prion disorder due to F198S mutation in the PRNP gene

Preimplantation genetic diagnosis for Pelizaeus-Merzbacher disease with testing for age-related aneuploidies.

Preimplantation genetic diagnosis for cancer predisposition

Preimplantation genetic diagnosis for early-onset torsion dystonia

Preimplantation genetic diagnosis for familial dysautonomia

Preimplantation genetic diagnosis for hemoglobinopathies

Preimplantation genetic diagnosis for polycystic kidney disease.

Preimplantation genetic diagnosis for the Kell genotype

Preimplantation genetic diagnosis with HLA matching

Preimplantation genetic testing to reduce preterm births in assisted reproductive technology

Preimplantation genetic testing: current challenges and future prospects

Preimplantation genetics: Improving access to stem cell therapy.

Preimplantation testing for phenylketonuria.

Prenatal genetic testing and treatment for congenital adrenal hyperplasia

Prenatal paternity testing with deoxyribonucleic acid techniques.

Prepregnancy testing for single-gene disorders by polar body analysis.

Reliability of gender determination using the polymerase chain reaction (PCR) for single cells

Reliability of polymerase chain reaction (PCR) analysis of single cells for preimplantation genetic diagnosis

Reliability of preimplantation diagnosis for single gene disorders

Repository of human embryonic stem cell lines and development of individual specific lines using stembrid technology

Sequence analysis of libraries from individual human blastocysts

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

Single-gene testing combined with single nucleotide polymorphism microarray preimplantation genetic diagnosis for aneuploidy: a novel approach in optimizing pregnancy outcome

Three births after preimplantation genetic diagnosis for cystic fibrosis with sequential first and second polar body analysis.

Use of nested PCR to identify charred human remains and minute amounts of blood.