List of works - Santiago Munné

A greater number of euploid blastocysts in a given cohort predicts excellent outcomes in single embryo transfer cycles

scientific article

Analysis of chromosome segregation during preimplantation genetic diagnosis in both male and female translocation heterozygotes.

scientific article

Aneuploidies of chromosomes 1, 4, and 6 are not compatible with human embryos' implantation.

scientific article published in February 2010

Aneuploidy 12 in a Robertsonian (13;14) carrier: Case report.

scientific article published on 3 February 2005

Aneuploidy study of human oocytes first polar body comparative genomic hybridization and metaphase II fluorescence in situ hybridization analysis.

scientific article published in November 2004

Array CGH analysis shows that aneuploidy is not related to the number of embryos generated

scientific article published on 25 February 2012

Assessment of numeric abnormalities of X, Y, 18, and 16 chromosomes in preimplantation human embryos before transfer

scientific article published in April 1995

Biomarkers for infertility and recurrent pregnancy loss

article

Carrier-specific breakpoint-spanning DNA probes: an approach to preimplantation genetic diagnosis in interphase cells.

scientific article published on September 1997

Chromosomal abnormalities in embryos derived from testicular sperm extraction

scientific article published on 01 January 2003

Chromosome abnormalities in embryos obtained after conventional in vitro fertilization and intracytoplasmic sperm injection

scientific article published in May 1998

Clinical application of comprehensive chromosomal screening at the blastocyst stage

article

Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation

scientific article

Comment 2 on Staessen et al. (2004). Two-cell biopsy and PGD pregnancy outcome

scientific article published on 01 August 2005

Comparative genomic hybridization of oocytes and first polar bodies from young donors

scientific article published in August 2009

Comprehensive chromosome screening of polar bodies and blastocysts from couples experiencing repeated implantation failure

scientific article published on 21 June 2009

Culture-induced chromosome abnormalities: the canary in the mine

article

Diminished effect of maternal age on implantation after preimplantation genetic diagnosis with array comparative genomic hybridization.

scientific article

Double locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy ⬇️

scientific article published on December 1, 2001

Dynamic blastomere behaviour reflects human embryo ploidy by the four-cell stage

scientific article

Effect of infertility, maternal age, and number of previous miscarriages on the outcome of preimplantation genetic diagnosis for idiopathic recurrent pregnancy loss.

scientific article published on 9 August 2008

First Pregnancies After Preconception Diagnosis of Translocations of Maternal Origin ⬇️

scientific article published on April 1, 1998

First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy

scientific article published in September 2002

Fluorescence in situ hybridization and spectral imaging analysis of human oocytes and first polar bodies

scientific article published in March 2005

Formation of male pronuclei in partitioned human oocytes

scientific article published in July 1995

Idiopathic recurrent miscarriage is caused mostly by aneuploid embryos ⬇️

scientific article published on June 7, 2012

Improved detection of aneuploid blastocysts using a new 12-chromosome FISH test.

scientific article

In Vitro Fertilization with Preimplantation Genetic Screening

scientific article published on 01 October 2007

Incidence of chromosomal abnormalities from a morphologically normal cohort of embryos in poor-prognosis patients

scientific article

Increased efficiency of preimplantation genetic diagnosis for aneuploidy by testing 12 chromosomes

scientific article published on 01 October 2009

Increased efficiency of preimplantation genetic diagnosis for infertility using “no result rescue”

article

Increased rate of aneuploid embryos in young women with previous aneuploid conceptions

article

Intra-age, intercenter, and intercycle differences in chromosome abnormalities in oocytes

scientific article published on 11 February 2012

Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies

Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique.

scientific article published on 26 August 2005

Lack of association between polycystic ovary syndrome and embryonic aneuploidy

scientific article published on 16 April 2007

Male and Female Genomes Associated in a Single Pronucleus in Human Zygotes

scientific article published on 01 March 1995

Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis

scientific article published in January 1998

Mitochondrial DNA deletion in human oocytes and embryos

scientific article published in September 1998

Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)

article

Ooplasmic transfer in mature human oocytes

scientific article published in March 1998

Origin of single pronucleated human zygotes

scientific article published on 01 May 1993

Over a decade of experience with preimplantation genetic diagnosis

scientific article published on 01 August 2004

Over a decade of experience with preimplantation genetic diagnosis: a multicenter report

scientific article published in August 2004

PGD analysis for aneuploidy in a patient heterozygous for a polymorphism of chromosome 16(16qh−)

article

PGD and aneuploidy screening for 24 chromosomes: advantages and disadvantages of competing platforms ⬇️

scientific article published on June 17, 2011

Patterns of ovarian response to gonadotropin stimulation in female carriers of balanced translocation

article

Positive outcome after preimplantation diagnosis of aneuploidy in human embryos.

scientific article

Predictive value of sperm fluorescence in situ hybridization analysis on the outcome of preimplantation genetic diagnosis for translocations

scientific article

Pregnancy after polar body biopsy and freezing and thawing of human embryos

scientific article published in March 2000

Pregnancy complicated by triploidy: a comparison of the three karyotypes.

scientific article published on 23 April 2009

Preimplantation aneuploidy testing for infertile patients of advanced maternal age: a randomized prospective trial

scientific article

Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: identification of the categories for which it should be proposed.

scientific article

Preimplantation diagnosis of genetic and chromosomal disorders.

scientific article

Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13, 14, 15, 16, 18, 21, 22

scientific article published on 01 December 1998

Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysis

article

Preimplantation genetic diagnosis

scientific article published on 01 June 2002

Preimplantation genetic diagnosis and human implantation--a review.

scientific article published on October 2003

Preimplantation genetic diagnosis as both a therapeutic and diagnostic tool in assisted reproductive technology

scientific article published on 01 August 2003

Preimplantation genetic diagnosis for advanced maternal age and other indications.

scientific article

Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization.

scientific article

Preimplantation genetic diagnosis for complex chromosome rearrangements

scientific article published on 01 July 2008

Preimplantation genetic diagnosis for gender selection in the USA.

scientific article published in January 2009

Preimplantation genetic diagnosis for translocations

scientific article published on 01 March 2006

Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos

scientific article published in December 1997

Preimplantation genetic diagnosis of pericentric inversions

scientific article published on 01 September 2001

Preimplantation genetic diagnosis of single-gene disorders: experience with more than 200 cycles conducted by a reference laboratory in the United States.

scientific article published on 19 October 2008

Preimplantation genetic diagnosis of structural abnormalities.

scientific article

Preimplantation genetic diagnosis reduces pregnancy loss in women aged 35 years and older with a history of recurrent miscarriages.

scientific article

Preimplantation genetic diagnosis significantly reduces pregnancy loss in infertile couples: a multicenter study

article

Questions concerning the suitability of comparative genomic hybridization for preimplantation genetic diagnosis

scientific article published on 01 October 2003

Recurrent abortion and live birth rate per patient.

scientific article

Reduction in signal overlap results in increased FISH efficiency: implications for preimplantation genetic diagnosis

scientific article published in February 1996

Reliability of comparative genomic hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes

scientific article published on 22 July 2004

Removal of 2 cells from cleavage stage embryos is likely to reduce the efficacy of chromosomal tests that are used to enhance implantation rates

scientific article published on 04 December 2006

Reply: PGD and aneuploidy screening for 24 chromosomes by genome-wide SNP analysis: a responsible path towards greater utility

scientific article published on 16 November 2011

Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X, Y, 13, 16, 18 and 21

scientific article published on 01 September 1998

Selection of embryos by morphology is less effective than by a combination of aneuploidy testing and morphology observations

scientific article published on 10 October 2007

Selection of the most common chromosome abnormalities in oocytes prior to ICSI.

scientific article published in July 2000

Self-correction of chromosomally abnormal embryos in culture and implications for stem cell production.

scientific article

Sperm quality may adversely affect the chromosome constitution of embryos that result from intracytoplasmic sperm injection

scientific article published on 01 December 1999

Spontaneous abortions are reduced after preconception diagnosis of translocations

scientific article

Substandard application of preimplantation genetic screening may interfere with its clinical success

scientific article published on 01 October 2007

Technology requirements for preimplantation genetic diagnosis to improve assisted reproduction outcomes.

scientific article published on 05 May 2009

The effect of timing of embryonic progression on chromosomal abnormality.

scientific article published on 11 July 2012

The genetic risks of in vitro fertilization techniques: the use of an animal model

scientific article published in October 1992

The impact of LH-containing gonadotropin stimulation on euploidy rates in preimplantation embryos: antagonist cycles

scientific article

The impact of LH-containing gonadotropins on diploidy rates in preimplantation embryos: long protocol stimulation

scientific article published on 7 January 2008

Treatment-related chromosome abnormalities in human embryos

scientific article published on 01 April 1997

Validation of array comparative genome hybridization for diagnosis of translocations in preimplantation human embryos

scientific article published on 22 February 2012

Validation of microarray comparative genomic hybridization for comprehensive chromosome analysis of embryos

scientific article published on 25 October 2010

Video. Micromanipulation of gametes and embryos: biopsy of a blastomere from an 8-cell human embryo

scientific article published on 01 September 1997

Will preimplantation genetic diagnosis assist patients with a poor prognosis to achieve pregnancy?

scientific article published on 01 August 1997

List of works by Santiago Munné

A greater number of euploid blastocysts in a given cohort predicts excellent outcomes in single embryo transfer cycles

Analysis of chromosome segregation during preimplantation genetic diagnosis in both male and female translocation heterozygotes.

Aneuploidies of chromosomes 1, 4, and 6 are not compatible with human embryos' implantation.

Aneuploidy 12 in a Robertsonian (13;14) carrier: Case report.

Aneuploidy study of human oocytes first polar body comparative genomic hybridization and metaphase II fluorescence in situ hybridization analysis.

Array CGH analysis shows that aneuploidy is not related to the number of embryos generated

Assessment of numeric abnormalities of X, Y, 18, and 16 chromosomes in preimplantation human embryos before transfer

Biomarkers for infertility and recurrent pregnancy loss

Carrier-specific breakpoint-spanning DNA probes: an approach to preimplantation genetic diagnosis in interphase cells.

Chromosomal abnormalities in embryos derived from testicular sperm extraction

Chromosome abnormalities in embryos obtained after conventional in vitro fertilization and intracytoplasmic sperm injection

Clinical application of comprehensive chromosomal screening at the blastocyst stage

Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation

Comment 2 on Staessen et al. (2004). Two-cell biopsy and PGD pregnancy outcome

Comparative genomic hybridization of oocytes and first polar bodies from young donors

Comprehensive chromosome screening of polar bodies and blastocysts from couples experiencing repeated implantation failure

Culture-induced chromosome abnormalities: the canary in the mine

Diminished effect of maternal age on implantation after preimplantation genetic diagnosis with array comparative genomic hybridization.

Double locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy ⬇️

Dynamic blastomere behaviour reflects human embryo ploidy by the four-cell stage

Effect of infertility, maternal age, and number of previous miscarriages on the outcome of preimplantation genetic diagnosis for idiopathic recurrent pregnancy loss.

First Pregnancies After Preconception Diagnosis of Translocations of Maternal Origin ⬇️

First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy

Fluorescence in situ hybridization and spectral imaging analysis of human oocytes and first polar bodies

Formation of male pronuclei in partitioned human oocytes

Idiopathic recurrent miscarriage is caused mostly by aneuploid embryos ⬇️

Improved detection of aneuploid blastocysts using a new 12-chromosome FISH test.

In Vitro Fertilization with Preimplantation Genetic Screening

Incidence of chromosomal abnormalities from a morphologically normal cohort of embryos in poor-prognosis patients

Increased efficiency of preimplantation genetic diagnosis for aneuploidy by testing 12 chromosomes

Increased efficiency of preimplantation genetic diagnosis for infertility using “no result rescue”

Increased rate of aneuploid embryos in young women with previous aneuploid conceptions

Intra-age, intercenter, and intercycle differences in chromosome abnormalities in oocytes

Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies

Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique.

Lack of association between polycystic ovary syndrome and embryonic aneuploidy

Male and Female Genomes Associated in a Single Pronucleus in Human Zygotes

Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis

Mitochondrial DNA deletion in human oocytes and embryos

Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11)

Ooplasmic transfer in mature human oocytes

Origin of single pronucleated human zygotes

Over a decade of experience with preimplantation genetic diagnosis

Over a decade of experience with preimplantation genetic diagnosis: a multicenter report

PGD analysis for aneuploidy in a patient heterozygous for a polymorphism of chromosome 16(16qh−)

PGD and aneuploidy screening for 24 chromosomes: advantages and disadvantages of competing platforms ⬇️

Patterns of ovarian response to gonadotropin stimulation in female carriers of balanced translocation

Positive outcome after preimplantation diagnosis of aneuploidy in human embryos.

Predictive value of sperm fluorescence in situ hybridization analysis on the outcome of preimplantation genetic diagnosis for translocations

Pregnancy after polar body biopsy and freezing and thawing of human embryos

Pregnancy complicated by triploidy: a comparison of the three karyotypes.

Preimplantation aneuploidy testing for infertile patients of advanced maternal age: a randomized prospective trial

Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: identification of the categories for which it should be proposed.

Preimplantation diagnosis of genetic and chromosomal disorders.

Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13, 14, 15, 16, 18, 21, 22

Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysis

Preimplantation genetic diagnosis

Preimplantation genetic diagnosis and human implantation--a review.

Preimplantation genetic diagnosis as both a therapeutic and diagnostic tool in assisted reproductive technology

Preimplantation genetic diagnosis for advanced maternal age and other indications.

Preimplantation genetic diagnosis for aneuploidy and translocations using array comparative genomic hybridization.

Preimplantation genetic diagnosis for complex chromosome rearrangements

Preimplantation genetic diagnosis for gender selection in the USA.

Preimplantation genetic diagnosis for translocations

Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos

Preimplantation genetic diagnosis of pericentric inversions

Preimplantation genetic diagnosis of single-gene disorders: experience with more than 200 cycles conducted by a reference laboratory in the United States.

Preimplantation genetic diagnosis of structural abnormalities.

Preimplantation genetic diagnosis reduces pregnancy loss in women aged 35 years and older with a history of recurrent miscarriages.

Preimplantation genetic diagnosis significantly reduces pregnancy loss in infertile couples: a multicenter study

Questions concerning the suitability of comparative genomic hybridization for preimplantation genetic diagnosis

Recurrent abortion and live birth rate per patient.

Reduction in signal overlap results in increased FISH efficiency: implications for preimplantation genetic diagnosis

Reliability of comparative genomic hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes

Removal of 2 cells from cleavage stage embryos is likely to reduce the efficacy of chromosomal tests that are used to enhance implantation rates

Reply: PGD and aneuploidy screening for 24 chromosomes by genome-wide SNP analysis: a responsible path towards greater utility

Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X, Y, 13, 16, 18 and 21

Selection of embryos by morphology is less effective than by a combination of aneuploidy testing and morphology observations

Selection of the most common chromosome abnormalities in oocytes prior to ICSI.