Santiago Munné

Santiago Munné's AcademicInfluence.com Rankings

Santiago Munné

Biology

#8163

World Rank

#11199

Historical Rank

Genetics

#808

World Rank

#900

Historical Rank

Molecular Biology

#1009

World Rank

#1033

Historical Rank

Biochemistry

#1167

World Rank

#1285

Historical Rank

biology Degrees

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Biology

Santiago Munné's Degrees

PhD Genetics University of California, San Francisco
Masters Molecular Biology Stanford University

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Santiago Munné's Published Works

Number of citations in a given year to any of this author's works

Total number of citations to an author for the works they published in a given year. This highlights publication of the most important work(s) by the author

Published Works

The Istanbul consensus workshop on embryo assessment: proceedings of an expert meeting. (2011) (1235)
Embryo morphology, developmental rates, and maternal age are correlated with chromosome abnormalities. (1995) (715)
Diagnosis of major chromosome aneuploidies in human preimplantation embryos. (1993) (498)
Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with a poor prognosis: identification of the categories for which it should be proposed. (1999) (441)
Positive outcome after preimplantation diagnosis of aneuploidy in human embryos. (1999) (380)
Ooplasmic transfer in mature human oocytes. (1998) (335)
Developmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage. (2001) (334)
Clinical application of comprehensive chromosomal screening at the blastocyst stage. (2010) (332)
Improved implantation after preimplantation genetic diagnosis of aneuploidy. (2003) (329)
Validation of microarray comparative genomic hybridization for comprehensive chromosome analysis of embryos. (2011) (304)
Chromosome mosaicism in human embryos. (1994) (278)
Preimplantation genetic testing for aneuploidy versus morphology as selection criteria for single frozen-thawed embryo transfer in good-prognosis patients: a multicenter randomized clinical trial. (2019) (276)
Preimplantation genetic testing for aneuploidy versus morphology as selection criteria for single frozen-thawed embryo transfer in good-prognosis patients: a multicenter randomized clinical trial. (2019) (276)
Chromosome abnormalities in human embryos. (1998) (269)
Outcome of preimplantation genetic diagnosis of translocations. (2000) (258)
Dynamic blastomere behaviour reflects human embryo ploidy by the four-cell stage (2012) (252)
Treatment-related chromosome abnormalities in human embryos. (1997) (249)
Altered Levels of Mitochondrial DNA Are Associated with Female Age, Aneuploidy, and Provide an Independent Measure of Embryonic Implantation Potential (2015) (245)
Maternal age, morphology, development and chromosome abnormalities in over 6000 cleavage-stage embryos. (2007) (244)
Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13, 14, 15, 16, 18, 21, 22 (1998) (236)
Diminished effect of maternal age on implantation after preimplantation genetic diagnosis with array comparative genomic hybridization. (2013) (231)
Association between nondisjunction and maternal age in meiosis-II human oocytes. (1996) (228)
Chromosome abnormalities and their relationship to morphology and development of human embryos. (2006) (228)
Preimplantation genetic diagnosis reduces pregnancy loss in women aged 35 years and older with a history of recurrent miscarriages. (2005) (227)
ESHRE preimplantation genetic diagnosis consortium: Data collection III (May 2001) (2002) (223)
Chromosome abnormalities in 1255 cleavage-stage human embryos. (2000) (217)
The human zygote inherits its mitotic potential from the male gamete. (1994) (216)
Detailed investigation into the cytogenetic constitution and pregnancy outcome of replacing mosaic blastocysts detected with the use of high-resolution next-generation sequencing. (2017) (208)
Live birth derived from oocyte spindle transfer to prevent mitochondrial disease. (2017) (208)
Removal of 2 cells from cleavage stage embryos is likely to reduce the efficacy of chromosomal tests that are used to enhance implantation rates. (2007) (206)
First clinical application of comparative genomic hybridization and polar body testing for preimplantation genetic diagnosis of aneuploidy. (2002) (203)
Over a decade of experience with preimplantation genetic diagnosis: a multicenter report. (2004) (202)
Chromosome mosaicism in cleavage-stage human embryos: evidence of a maternal age effect. (2002) (201)
Clinical utilisation of a rapid low-pass whole genome sequencing technique for the diagnosis of aneuploidy in human embryos prior to implantation (2014) (188)
Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities. (2002) (188)
Maternal age-related differential global expression profiles observed in human oocytes. (2007) (185)
The human sex ratio from conception to birth (2015) (181)
The presence of multinucleated blastomeres in human embryos is correlated with chromosomal abnormalities. (1996) (181)
Chromosome abnormalities in human arrested preimplantation embryos: a multiple-probe FISH study. (1994) (180)
Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos. (1997) (179)
Idiopathic recurrent miscarriage is caused mostly by aneuploid embryos. (2012) (167)
Array CGH analysis shows that aneuploidy is not related to the number of embryos generated. (2012) (167)
Self-correction of chromosomally abnormal embryos in culture and implications for stem cell production. (2005) (166)
Forty years of IVF. (2018) (165)
The use of first polar bodies for preimplantation diagnosis of aneuploidy. (1995) (159)
Comprehensive chromosome screening of polar bodies and blastocysts from couples experiencing repeated implantation failure. (2010) (158)
Preimplantation aneuploidy testing for infertile patients of advanced maternal age: a randomized prospective trial. (2009) (149)
Assessment of numeric abnormalities of X, Y, 18, and 16 chromosomes in preimplantation human embryos before transfer. (1995) (147)
Chromosomal abnormalities in embryos derived from testicular sperm extraction. (2003) (147)
Preimplantation genetic diagnosis significantly reduces pregnancy loss in infertile couples: a multicenter study. (2006) (144)
Why do euploid embryos miscarry? A case-control study comparing the rate of aneuploidy within presumed euploid embryos that resulted in miscarriage or live birth using next-generation sequencing. (2016) (142)
Differences in chromosome susceptibility to aneuploidy and survival to first trimester. (2004) (141)
Diagnosing and preventing inherited disease: The use of first polar bodies for preimplantation diagnosis of aneuploidy (1995) (141)
Meiotic products of a Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis. (1998) (138)
Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X, Y, 13, 16, 18 and 21. (1998) (138)
Increased efficiency of preimplantation genetic diagnosis for infertility using "no result rescue". (2007) (132)
Spectral karyotyping of fresh, non-inseminated oocytes. (2002) (129)
First pregnancies after preconception diagnosis of translocations of maternal origin. (1998) (126)
Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro (2014) (125)
Detection of mosaicism at blastocyst stage with the use of high-resolution next-generation sequencing. (2017) (124)
Possible interchromosomal effect in embryos generated by gametes from translocation carriers. (2002) (123)
Preimplantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses. (2010) (122)
Preimplantation genetic analysis of translocations: case-specific probes for interphase cell analysis (1998) (122)
Incidence of Chromosomal Abnormalities from a Morphologically Normal Cohort of Embryos in Poor-Prognosis Patients (1998) (121)
Will preimplantation genetic diagnosis assist patients with a poor prognosis to achieve pregnancy? (1997) (118)
Optimal euploid embryo transfer strategy, fresh versus frozen, after preimplantation genetic screening with next generation sequencing: a randomized controlled trial. (2017) (117)
Blastomere fixation techniques and risk of misdiagnosis for preimplantation genetic diagnosis of aneuploidy. (2002) (117)
Aneuploidy 16 in human embryos increases significantly with maternal age. (1996) (110)
Preimplantation genetic diagnosis significantly improves the pregnancy outcome of translocation carriers with a history of recurrent miscarriage and unsuccessful pregnancies. (2006) (110)
Increased rate of aneuploid embryos in young women with previous aneuploid conceptions (2004) (109)
The why, the how and the when of PGS 2.0: current practices and expert opinions of fertility specialists, molecular biologists, and embryologists. (2016) (109)
Predicting the likelihood of live birth for elective oocyte cryopreservation: a counseling tool for physicians and patients (2016) (108)
Spontaneous Abortions Are Reduced After Preconception Diagnosis of Translocations (1998) (106)
Substandard application of preimplantation genetic screening may interfere with its clinical success. (2007) (105)
Rapid visualization of metaphase chromosomes in single human blastomeres after fusion with in-vitro matured bovine eggs. (1999) (105)
Predictive value of sperm fluorescence in situ hybridization analysis on the outcome of preimplantation genetic diagnosis for translocations. (2003) (102)
Wide range of chromosome abnormalities in the embryos of young egg donors. (2006) (101)
Simultaneous enumeration of chromosomes 13, 18, 21, X, and Y in interphase cells for preimplantation genetic diagnosis of aneuploidy. (1996) (101)
Mitochondrial DNA deletion in human oocytes and embryos. (1998) (100)
Preimplantation genetic diagnosis as both a therapeutic and diagnostic tool in assisted reproductive technology. (2003) (99)
Validation of next-generation sequencing for comprehensive chromosome screening of embryos. (2015) (99)
Aneuploidy study of human oocytes first polar body comparative genomic hybridization and metaphase II fluorescence in situ hybridization analysis. (2004) (98)
Chromosome identification in human oocytes and polar bodies by spectral karyotyping (1998) (98)
Chromosome abnormalities in embryos obtained after conventional in vitro fertilization and intracytoplasmic sperm injection. (1998) (97)
Impact of blastomere biopsy and cryopreservation techniques on human embryo viability. (1999) (97)
Unsuitability of multinucleated human blastomeres for preimplantation genetic diagnosis. (1993) (93)
Chromosomal status of uni-pronuclear human zygotes following in-vitro fertilization and intracytoplasmic sperm injection. (1995) (93)
Mosaicism: "survival of the fittest" versus "no embryo left behind". (2016) (92)
Technology requirements for preimplantation genetic diagnosis to improve assisted reproduction outcomes. (2010) (92)
Mitochondrial DNA quantification as a tool for embryo viability assessment: retrospective analysis of data from single euploid blastocyst transfers (2017) (90)
Euploidy rates in donor egg cycles significantly differ between fertility centers (2017) (88)
Preimplantation genetic diagnosis for advanced maternal age and other indications. (2002) (88)
Next generation sequencing for preimplantation genetic screening improves pregnancy outcomes compared with array comparative genomic hybridization in single thawed euploid embryo transfer cycles. (2018) (87)
Impaired development of zygotes with uneven pronuclear size (1998) (87)
PGDIS Position Statement on the Transfer of Mosaic Embryos 2019. (2019) (85)
Preimplantation Genetic Diagnosis for Aneuploidy and Translocations Using Array Comparative Genomic Hybridization (2012) (83)
Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers (2000) (83)
Analysis of chromosome segregation during preimplantation genetic diagnosis in both male and female translocation heterozygotes (2005) (83)
Reliability of comparative genomic hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes. (2004) (82)
Validation of array comparative genome hybridization for diagnosis of translocations in preimplantation human embryos. (2012) (81)
Clinical implications of mitochondrial DNA quantification on pregnancy outcomes: a blinded prospective non-selection study (2017) (79)
Expression profiles of individual human oocytes using microarray technology. (2004) (77)
Spindle organization after cryopreservation of mouse, human, and bovine oocytes. (2004) (76)
Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies (2000) (72)
Healthy deliveries from biopsied human embryos. (1994) (72)
Effect of infertility, maternal age, and number of previous miscarriages on the outcome of preimplantation genetic diagnosis for idiopathic recurrent pregnancy loss. (2009) (71)
Preimplantation genetic diagnosis of single-gene disorders: experience with more than 200 cycles conducted by a reference laboratory in the United States. (2009) (69)
Male and female genomes associated in a single pronucleus in human zygotes. (1995) (68)
The cytogenetic constitution of human blastocysts: insights from comprehensive chromosome screening strategies (2018) (67)
Lack of association between polycystic ovary syndrome and embryonic aneuploidy. (2007) (67)
A fast and efficient method for simultaneous X and Y in situ hybridization of human blastomeres (2005) (66)
Comparative genomic hybridization of oocytes and first polar bodies from young donors. (2009) (63)
Monospermic polyploidy and atypical embryo morphology. (1994) (63)
Over a decade of experience with preimplantation genetic diagnosis. (2004) (63)
Preimplantation Genetic Diagnosis of Aneuploidy: Were We Looking at the Wrong Chromosomes? (1999) (62)
The effect of timing of embryonic progression on chromosomal abnormality. (2012) (61)
Development of a new comprehensive and reliable endometrial receptivity map (ER Map/ER Grade) based on RT-qPCR gene expression analysis (2018) (61)
Gamete segregation in female carriers of Robertsonian translocations (2000) (60)
Live births following Karyomapping of human blastocysts: experience from clinical application of the method. (2015) (59)
Clinical outcomes after the transfer of blastocysts characterized as mosaic by high resolution Next Generation Sequencing- further insights. (2020) (58)
Carrier-specific breakpoint-spanning DNA probes: an approach to preimplantation genetic diagnosis in interphase cells. (1997) (58)
Status of preimplantation genetic testing and embryo selection. (2018) (56)
Double locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy (2001) (55)
First live birth using human oocytes reconstituted by spindle nuclear transfer for mitochondrial DNA mutation causing Leigh syndrome (2016) (54)
Reduction in signal overlap results in increased FISH efficiency: Implications for preimplantation genetic diagnosis (1996) (52)
Improved detection of aneuploid blastocysts using a new 12-chromosome FISH test. (2010) (52)
Sex determination of human embryos using the polymerase chain reaction and confirmation by fluorescence in situ hybridization (1994) (51)
The impact of LH-containing gonadotropins on diploidy rates in preimplantation embryos: long protocol stimulation. (2008) (51)
Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing (2015) (51)
Using outcome data from one thousand mosaic embryo transfers to formulate an embryo ranking system for clinical use. (2021) (49)
Preimplantation genetic diagnosis of numerical abnormalities for 13 chromosomes. (2003) (49)
Improvements of preimplantation diagnosis of aneuploidy by using microwave hybridization, cell recycling and monocolour labelling of probes. (2000) (48)
Diminished effect of maternal age on implantation after preimplantation genetic diagnosis with array comparative genomic hybridization (2014) (48)
Increased efficiency of preimplantation genetic diagnosis for aneuploidy by testing 12 chromosomes. (2009) (48)
An analysis of human sperm chromosome aneuploidy. (1996) (44)
Preimplantation genetic diagnosis and human implantation--a review. (2003) (43)
An analysis of human sperm chromosome breakpoints. (1995) (43)
Multicolor fluorescence in situ hybridization analysis of the spermatozoa of a male heterozygous for a reciprocal translocation t(11;22)(q23;q11) (1999) (43)
Genetics of abnormal human fertilization. (1995) (41)
Cryopreservation of unfertilized human oocytes. (2006) (41)
Advantages of Day 4 Embryo Transfer in Patients Undergoing Preimplantation Genetic Diagnosis of Aneuploidy (1999) (40)
Preimplantation genetic diagnosis (PGD), a collaborative activity of clinical genetic departments and IVF centres (2001) (38)
Sperm quality may adversely affect the chromosome constitution of embryos that result from intracytoplasmic sperm injection. (1999) (37)
Preimplantation genetic diagnosis (2002) (37)
Preimplantation genetic diagnosis for complex chromosome rearrangements (2008) (37)
Preimplantation genetic diagnosis of structural abnormalities (2001) (36)
Reprint of: Embryo morphology, developmental rates, and maternal age are correlated with chromosome abnormalities. (2019) (36)
PGD and aneuploidy screening for 24 chromosomes: advantages and disadvantages of competing platforms. (2011) (35)
Case report: chromatid exchange and predivision of chromatids as other sources of abnormal oocytes detected by preimplantation genetic diagnosis of translocations (1998) (34)
Studies on sperm chromatin structure alterations and cytogenetic damage of mouse sperm following in vitro incubation. Studies on in vitro-incubated mouse sperm. (1993) (31)
Negligible interchromosomal effect in embryos of Robertsonian translocation carriers. (2005) (31)
The role of preimplantation genetic diagnosis in diagnosing embryo aneuploidy (2009) (31)
Chromosome analysis of human spermatozoa stored in vitro. (1993) (31)
Patient-Specific Probes for Preimplantation Genetic Diagnosis of Structural and Numerical Aberrations in Interphase Cells (1999) (30)
Preimplantation diagnosis of genetic and chromosomal disorders (1994) (30)
Pregnancies from single normal embryo transfer in women older than 40 years. (2001) (30)
First PGT-A using human in vivo blastocysts recovered by uterine lavage: comparison with matched IVF embryo controls† (2019) (30)
Discrepant diagnosis rate of array comparative genomic hybridization in thawed euploid blastocysts (2016) (29)
Selection of the most common chromosome abnormalities in oocytes prior to ICSI (2000) (29)
Preimplantation genetic diagnosis of pericentric inversions (2001) (28)
The impact of LH-containing gonadotropin stimulation on euploidy rates in preimplantation embryos: antagonist cycles. (2009) (28)
PGDIS position statement on the transfer of mosaic embryos 2021. (2022) (28)
Selection of embryos by morphology is less effective than by a combination of aneuploidy testing and morphology observations. (2009) (28)
The effect of in-vitro ageing on mouse sperm chromosomes. (1991) (27)
Predictability of preimplantation genetic diagnosis of aneuploidy and translocations on prospective attempts. (2004) (27)
Patterns of ovarian response to gonadotropin stimulation in female carriers of balanced translocation. (2005) (26)
Derivation of human embryonic stem cells in xeno-free conditions. (2007) (26)
Global multicenter randomized controlled trial comparing single embryo transfer with embryo selected by preimplantation genetic screening using next-generation sequencing versus morphologic assessment (2017) (26)
Cryopreservation of biopsied cleavage stage human embryos. (2005) (26)
Questions concerning the suitability of comparative genomic hybridization for preimplantation genetic diagnosis. (2003) (25)
Intra-age, intercenter, and intercycle differences in chromosome abnormalities in oocytes. (2012) (25)
Genetic testing of embryos: a critical need for data. (2005) (25)
Differences in pregnancy outcomes in donor egg frozen embryo transfer (FET) cycles following preimplantation genetic screening (PGS): a single center retrospective study (2016) (25)
Pregnancy complicated by triploidy: a comparison of the three karyotypes. (2009) (24)
Karyotyping of human oocytes by cenM-FISH, a new 24-colour centromere-specific technique. (2005) (24)
Comment 2 on Staessen et al. (2004). Two-cell biopsy and PGD pregnancy outcome. (2005) (23)
DNA Probe Pooling for Rapid Delineation of Chromosomal Breakpoints (2009) (23)
Flow cytometry separation of X and Y spermatozoa could be detrimental for human embryos. (1994) (23)
Origin of single pronucleated human zygotes (1993) (23)
The number of biopsied trophectoderm cells may affect pregnancy outcomes (2018) (23)
PGD analysis for aneuploidy in a patient heterozygous for a polymorphism of chromosome 16 (16qh−) (2004) (21)
Human Oocytes (2007) (21)
Current status of preimplantation diagnosis (1997) (21)
Towards a full karyotype screening of interphase cells: ‘FISH and chip’ technology (2001) (20)
Preimplantation genetic diagnosis of aneuploidy and male infertility. (1997) (20)
Pregnancy after polar body biopsy and freezing and thawing of human embryos. (2000) (20)
Cytogenetic studies in human sperm (1991) (19)
Detection of chromosome translocation products in single interphase cell nuclei. (2001) (19)
Micromanipulation in clinical management of fertility disorders (1994) (18)
Preimplantation genetic diagnosis for gender selection in the USA. (2009) (18)
Aneuploidy 12 in a Robertsonian (13;14) carrier: Case report. (2005) (18)
Advanced maternal age patients benefit from preimplantation genetic diagnosis of aneuploidy. (2017) (17)
Female gamete segregation in two carriers of translocations involving 2q and 14q (2000) (17)
The cost of a euploid embryo identified from preimplantation genetic testing for aneuploidy (PGT-A): a counseling tool (2018) (17)
High pregnancy rate after comprehensive chromosomal screening of blastocysts (2008) (16)
Discordance among serial biopsies of mosaic embryos (2016) (16)
Clinical error rates of next generation sequencing and array comparative genomic hybridization with single thawed euploid embryo transfer. (2020) (15)
The parental origin of the distal pronucleus in dispermic human zygotes (1994) (15)
Nonviable human pre-implantation embryos as a source of stem cells for research and potential therapy (2005) (15)
Fluorescence In Situ Hybridization and Spectral Imaging Analysis of Human Oocytes and First Polar Bodies (2005) (15)
Formation of male pronuclei in partitioned human oocytes. (1995) (14)
The rate of mosaic embryos from donor egg as detected by next generation sequencing (NGS) varies by IVF laboratory (2016) (14)
Atypical activation and fertilization patterns in humans (1995) (14)
Why do array-CGH (ACGH) euploid embryos miscarry? Reanalysis by NGS reveals undetected abnormalities which would have prevented 56% of the miscarriages (2015) (13)
Case report: unusually high rates of aneuploid embryos in a 28-year old woman with incontinentia pigmenti. (1996) (13)
Culture-induced chromosome abnormalities: the canary in the mine. (2011) (12)
Reply: Mitochondrial DNA Quantification-the devil in the detail. (2017) (12)
Aneuploidies of chromosomes 1, 4, and 6 are not compatible with human embryos' implantation. (2010) (12)
A greater number of euploid blastocysts in a given cohort predicts excellent outcomes in single embryo transfer cycles (2014) (12)
Preimplantation diagnosis in older patients--but of course! (1997) (12)
Continuing to deliver: the evidence base for pre-implantation genetic screening (2017) (12)
Chromosomal status of human embryos (2007) (11)
The genetic risks of in vitro fertilization techniques: The use of an animal model (1992) (11)
Update in preimplantation genetic diagnosis: successes, advances, and problems. (1996) (11)
Molecular cloning of translocation breakpoints in a case of constitutional translocation t(11;22)(q23;q11) and preparation of probes for preimplantation genetic diagnosis. (1999) (11)
Microinjection of FITC-dextran into mouse blastomeres to assess topical effects of zona photoablation (1993) (11)
Rapid mapping of chromosomal breakpoints: from blood to BAC in 20 days. (2010) (11)
Preimplantation genetic diagnosis for translocations. (2006) (10)
Preimplantation genetic diagnosis using array CGH significantly increases ongoing pregnancy rates per transfer (2010) (10)
Controlled ovarian hyperstimulation (COH) parameters associated with euploidy rates in donor oocytes. (2019) (10)
Sex distribution in arrested precompacted human embryos (1993) (10)
O-28. Blastomere fixation techniques and risk of misdiagnosis in PGD of aneuploidy (2002) (10)
Live Birth Derived From Oocyte Spindle Transfer to Prevent Mitochondrial Disease (2017) (9)
Follicle size indicates oocyte maturity and blastocyst formation but not blastocyst euploidy following controlled ovarian hyperstimulation of oocyte donors. (2020) (9)
O-21. Some mosaic types increase with maternal age (2002) (9)
Validation and first clinical application of karyomapping for preimplantation diagnosis (PGD) of Gaucher disease combined with 24 chromosome screening (2010) (9)
Aneuploidy and recombination in the human preimplantation embryo. Copy number variation analysis and genome-wide polymorphism genotyping. (2019) (8)
Chromosomal abnormalities in embryos derived from TESE in Y-deleted and non-Y-deleted men (2002) (8)
'Chromosomal Rainbows' Detect Oncogenic Rearrangements of Signaling Molecules in Thyroid Tumors. (2010) (8)
Significant decrease in miscarriages after preimplantation genetic diagnosis (PGD) for recurrent pregnancy loss using array comparative genome hybridization (Array CGH) (2011) (8)
Origins of mosaicism and criteria for the transfer of mosaic embryos. (2018) (8)
Case-specific, breakpoint-spanning DNA probes for analysis of single interphase cells. (2000) (7)
NEW INSIGHTS FROM ONE THOUSAND MOSAIC EMBRYO TRANSFERS: FEATURES OF MOSAICISM DICTATING RATES OF IMPLANTATION, SPONTANEOUS ABORTION, AND NEONATE HEALTH (2020) (7)
Highly significant improvement in embryo implantation and increased live birth rate achieved after comprehensive chromosomal screening: implications for single embryo transfer (2009) (7)
Preimplantation genetic diagnosis (PGD) effectively reduces idiopathic recurrent pregnancy loss (RPL) among patients with up to five previous miscarriages after natural conception (2007) (7)
The status of preimplantation genetic diagnosis in Japan: a criticism. (2004) (6)
Genetically identical analyzable sperm-derived nuclei produced in enucleated mammalian eggs (2002) (6)
The high rate of abnormal embryos in donor cycles is reflected in donor oocyte pregnancy outcomes (2016) (6)
Predictive value of sperm chromosome analysis on the outcome of PGD for translocations. (2001) (6)
Increased embryo implantation and high birth rates following comprehensive chromosomal screening of in-vitro fertilized embryos (2009) (6)
Reduced spontaneous abortion and increased live birth rate after PGD for advanced maternal age (2007) (6)
Comprehensive aneuploidy screening in single cells using microarray comparative genomic hybridization methods implications for preimplantation genetic diagnosis (2007) (6)
Corrigendum. Mitochondrial DNA quantification as a tool for embryo viability assessment: retrospective analysis of data from single euploid blastocyst transfers. (2019) (5)
Preimplantation genetic screening for recurrent pregnancy loss (2008) (5)
Egg donor aneuploidy rates significantly differ between fertility centers (2014) (5)
Developmental morphology and continuous time-lapse microscopy (TLM) of human embryos: can we predict euploidy? (2012) (5)
Factors affecting embryonic mosaicism (2017) (4)
O-37. Obstetric outcome of 100 cycles of PGD of translocations and other structural abnormalities (2002) (4)
Reply: PGD and aneuploidy screening for 24 chromosomes by genome-wide SNP analysis: a responsible path towards greater utility. (2012) (4)
SELECTED ORAL COMMUNICATION SESSION, SESSION 48: REPRODUCTIVE GENETICS, Tuesday 5 July 2011 15:15 – 16:30 (2011) (4)
Live Birth from Previously Vitrified Oocytes, After Trophectoderm Biopsy, Revitrification, and Transfer of a Euploid Blastocyst (2013) (4)
Does laser assisted biopsy introduce mosaic or chaotic changes to biopsied cells (2017) (4)
25 historic papers: an ASRM 75th birthday gift from Fertility and Sterility. (2019) (4)
Preimplantation genetic diagnosis (PGD) as both a diagnostic and therapeutic tool in women with advanced maternal age (AMA) undergoing IVF (2002) (4)
Use of single nucleotide polymorphism (SNP) arrays and next generation sequencing (NGS) to study the incidence, type and origin of aneuploidy in the human preimplantation embryo (2016) (4)
Corrigendum to 'Live birth derived from oocyte spindle transfer to prevent mitochondrial disease' [Reproductive BioMedicine Online 34 (2017) 361-368]. (2017) (4)
Preimplantation Genetic Diagnosis: Preimplantation genetic diagnosis for infertility (PGS) (2009) (4)
Clinical error rates of next generation sequencing (NGS) compared to array comparative genomic hybridization (ACGH) in euploid blastocysts (2017) (4)
Deliveries from trophectoderm biopsied, fresh and vitrified blastocysts derived from polar body biopsied, vitrified oocytes. (2015) (4)
Next generation sequencing (NGS) for preimplantation genetic screening (PGS) discovers mosaicism is independent of age (2016) (4)
Causes and estimated incidences of sex-chromosome misdiagnosis in preimplantation genetic diagnosis of aneuploidy. (2016) (4)
PREGNANCY OUTCOME FOLLOWING COMPREHENSIVE CHROMOSOME ANALYSIS AT THE CLEAVAGE AND BLASTOCYST STAGES. (2010) (3)
Validation of microarray CGH for PGD by FISH reanalysis (2009) (3)
Dissociation between embyro morphology and euploidy in IVF patients with poor prognosis (2002) (3)
Frequency and clinical relevance of mosaic segmental aneuploidy in blastocyst stage human embryos (2017) (3)
P-242 Sperm morphology and chromosome aneuploidy in men with infertility as determined by fluorescence in situ hybridization (FISH) (1997) (3)
Preimplantation genetic diagnosis (PGD) as both a diagnostic and therapeutic tool in assisted reproductive technology (ART) (2002) (3)
Embryologist agreement when assessing blastocyst implantation probability: is data-driven prediction the solution to embryo assessment subjectivity? (2022) (3)
Session 16: Innovations in reproductive genetics (2013) (3)
Day 3 Blastomere Biopsy Does Not Affect Subsequent Blastocyst Development or Implantation Rate (2000) (3)
How well do morphokinetic (MK) parameters and time-lapse microscopy (TLM) predict euploidy? a pilot study of TLM with trophectoderm (TE) biopsy with array comparative genomic hybridization (aCGH) (2013) (3)
Preimplantation Genetic Diagnosis (PGD) as a Beneficial Tool in Women With Recurrent Pregnancy Loss (RPL) and Advanced Maternal Age (AMA) (2004) (3)
Retracted: Validation of a multiplex genotyping platform using a novel genomic database approach (2015) (3)
Is there an interchromosomal effect in reciprocal translocation carriers? Sperm FISH studies (2000) (3)
Improving pregnancy outcome for IVF patients with preimplantation genetic screening (2008) (3)
Maternal balanced translocation is a risk factor for poor response to ovarian stimulation (2002) (3)
O-122 ICSI in a box: development of a successful automated sperm injection robot with external supervision and minimal manual intervention (2021) (2)
ER Map allow the reliable determination of the window of implantation in infertile women (2016) (2)
Corrigendum to 'Live birth derived from oocyte spindle transfer to prevent mitochondrial disease': [Reproductive BioMedicine Online 34 (2017) 361-368]. (2017) (2)
Comprehensive cytogenetic analysis of the human blastocyst stage (2008) (2)
Spectral Karyotyping of Unfertilized and Noninseminated Oocytes (2000) (2)
A NOVEL NON-INVASIVE METABOLOMICS APPROACH TO SCREEN EMBRYOS FOR ANEUPLOIDY (2020) (2)
Response: how PGS/PGT-a laboratories succeeded in losing all credibility. (2018) (2)
Implantation and Miscarriage Rates Following Array CGH Analysis at the Cleavage and Blastocyst Stages (2011) (2)
In vitro fertilization with preimplantation genetic screening. (2007) (2)
Mosaic embryos - a comprehensive and powered analysis of clinical outcomes (2019) (2)
O4 First clinical application of karyomapping for PGD of Gaucher disease combined with 24 chromosome screening (2010) (2)
O-137: The quantitative and qualitative impact of gonadotropin stimulation on human preimplantation embryos: A preliminary study (2006) (2)
Overview of preimplantation genetic diagnosis (2010) (2)
PGS analysis of over 33,000 blastocysts using high resolution Next Generation Sequencing (HRNGS) of over 33,000 blastocysts using high resolution Next Generation Sequencing (HRNGS) (2016) (2)
Biomarkers for infertility and recurrent pregnancy loss. (2014) (2)
Microarrays and CGH for PGD of Chromosome Abnormalities and Gene Defects (2012) (2)
PGD of aneuploidy to reduce multiple gestations and maintain high pregnancy rates in women 35 and older. M. Oter, M. Sandalinas, P. (2004) (2)
The biological and clinical impact of mitochondrial genome variation in human embryos (2015) (2)
O-138: Preimplantation genetic diagnosis (PGD) is indicated for recurrent miscarriage even in cycles producing five or fewer embryos (2006) (2)
Large Intra-Age Group Variation in Chromosome Abnormalities in Human Blastocysts (2021) (1)
Some Chromosomal Abnormalities in Early Embryos Preclude Blastocyst Formation in Vitro (2000) (1)
What patients can expect for percentage of embryos biopsied and normal embryos available for fresh blastocyst transfer when undergoing trophectoderm biopsy with 24-chromosome genetic analysis (2013) (1)
Recurrent abortion and live birth rate per patient. (2006) (1)
O▪37 Results of PGD for infertility in 3597 cycles (2005) (1)
The availability of normal embryos for transfer is difficult to predict in PGD cycles. (2001) (1)
Chromosome abnormalities found in >60,000 blastocysts tested via array CGH (2015) (1)
P-064 Mitochondrial DNA deletions in human oocytes and embryos (1997) (1)
High performance analysis of single interphase cells with custom DNA probes spanning translocation breakpoints : Advanced Techniques in Analytical Cytology (1999) (1)
Reporting of Mosaics as High-level and Low level mosaics makes more number of embryos available as alternatives for transfer when no euploid embryos are available (2019) (1)
Subject Index Vol. 90, 2000 (2000) (1)
WHOLE-GENOME SEQUENCING TECHNOLOGY FOR THE ASSESSMENT OF EMBRYO GENETICS AND VIABILITY. (2013) (1)
PGD improves pregnancy outcome for translocation carriers with a history of recurrent losses (2009) (1)
O-11. Comprehensive aneuploidy screening in human IVF embryos using CGH: protocol development and clinical application (2002) (1)
The timing of onset of mosaicism in human blastocysts impacts the utility of next generation sequencing (NGS) (2016) (1)
Current and Novel Methods for Chromosome Testing (2019) (1)
Abstracts of the 12th European Colloquium on Cytogenetics of Domestic Animals (1996) (1)
Implantation and ongoing pregnancy rate with euploid embryo transfer is independent of maternal age (2013) (1)
High-performance analysis of single interphase cells with custom DNA probes spanning translocation break points (1999) (1)
O-201 Prenatal and postnatal outcome of mosaic embryo transfers: multicentric study of one thousand mosaic embryos diagnosed by preimplantation genetic testing with trophectoderm biopsy (2021) (1)
Human sperm sex selection (1994) (1)
Human leukocyte antigen (HLA) matching of preimplantation embryos using a polymerase chain reaction (PCR) based methodology and karyomapping (2015) (1)
Corrigendum. First PGT-A using human in vivo blastocysts recovered by uterine lavage: comparison with matched IVF embryo controls (2021) (1)
Increased incidence of mosaicism among biopsied trophectoderm cells analyzed by Next Generation Sequencing (2015) (1)
Session 31: PGD/PGS (2013) (1)
Preimplantation genetic diagnosis for reciprocal translocations—the Japanese experience (2008) (1)
P39 Clinical results of array CGH for PGS (2010) (1)
O▪8 Embryonic chromosome abnormalities (2005) (1)
Miscarriage rate comparison of PGS cycles performed with array comparative genome hybridization (aCGH) and next generation sequencing (NGS) (2016) (1)
The in vitro development of human zygote reconstructed by pronuclear transfer (2015) (1)
Blastocyst formation rate in chromosomally normal versus abnormal embryos. (2001) (1)
Response to comment on: Gleicher N et al., 2016. Reprod biol endocrinol Sep 5;14(1):54 (2017) (1)
SELECTED ORAL COMMUNICATION SESSION, SESSION 63: PREIMPLANTATION GENETICS Wednesday 6 July 2011 10:00 – 11:45 (2011) (1)
VALIDATION OF AN OOCYTE VITRIFICATION USING DAVITRI, A NOVEL AUTOMATED MICROFLUIDICS DEVICE (2021) (1)
Laser Biopsy of Day 3 Embryos Yields Higher Implantation Rate Than Biopsy With Acidic Tyrodes (2005) (1)
O-219. High implantation rate in ‘poor prognosis’ patients following the transfer of embryos analysed by FISH (1997) (1)
First Attempt at Complete Sequencing of Blastocyst Biopsies for Use in PGD (2011) (1)
Genetic carrier screening in an egg donor program (2015) (1)
Aneuploidy in spermatozoa using fluorescence in situ hybridization (1993) (1)
ADVANCES IN IN-VIVO FERTILIZED AND MATURED HUMAN EMBRYOS AND CHARACTERIZATION BY PRE-IMPLANTATION GENETIC TESTING (PGT-A) (2019) (1)
Differences between blastomere and blastocyst biopsies for preimplantation genetic diagnosis (PGD) using array comparative genomic hybridization (aCGH) (2013) (1)
PGD VIA array comparative genome hybridization (aCGH) can be used for any translocation to simultaneously detect unbalanced embryos and aneuploidy (2011) (1)
Comprehensive cytogenetic analysis of human blastocysts (2009) (1)
Implantation rate improvement after preimplantation genetic diagnosis (PGD) of aneuploidy depends on the maternal age of the patient. (2001) (1)
Predictive value of sperm fish analysis on the outcome of PGD for translocations (2002) (1)
PGD : a model to evaluate efficacy? Authors' reply (2006) (1)
The use of next generation sequencing to determine the developmental potential of mosaic blastocysts (2016) (1)
Estimation of mosaicism in a blastocyst cohort (2017) (1)
Genetic Selection of the Human Embryos: From FISH to NGS, Past and Future (2018) (1)
Types of abnormalities in complex abnormal embryos (2016) (1)
CLINICAL EXPERIENCE WITH KARYOMAPPING FOR PREIMPLANTATION GENETIC DIAGNOSIS (PGD) OF SINGLE GENE DISORDERS. (2014) (1)
Planning for the future: how many eggs do patients need to harvest to achieve their fertility goals? (2016) (0)
Micromanipulation of gametes and embryos: Biopsy of a blastomere from an 8-cell human embryo. (1997) (0)
PGS analysis of over 100,000 blastocysts using high resolution next generation sequencing (2017) (0)
No diagnosis after day 3 biopsy: indicative of embryo prognosis or biopsy error (2016) (0)
AUTOMATED OOCYTE AND ZYGOTE DENUDATION USING A NOVEL MICROFLUIDIC DEVICE (2020) (0)
Contents Vol. 111, 2005 (2005) (0)
Derivation of Human Embryonic Stem (hES) Cells From Chromosomally Abnormal Embryos That Exhibit Self Correction in Culture (2005) (0)
Prevention of Mitochondrial Disease Caused by mtDNA Mutation through Mitochondrial Replacement Therapy (MRT) (2016) (0)
Are partial aneuploidies linked with chromosomal structural abnormalities (2014) (0)
Is one cycle of PGS predictive of the next? evidence from embryo banking (2014) (0)
Results and follow-up: preimplantation genetic diagnosis (PGD) for structural chromosomal aberrations (2008) (0)
O▪39 Chromosome abnormalities in embryos and spermatozoa of TESE patients compared with controls (2005) (0)
Chromosomal abnormalities in embryos from non-obstructive azoospermic patients (2004) (0)
The effect of the biopsy procedure and the removal of a single blastomere from day 3 human embryos on their implantation potential. (2001) (0)
Embryo cohort size does not affect euploidy (2011) (0)
Single Cell Cytogenetics (2009) (0)
I12 Next generation sequencing (2013) (0)
Corrigendum. Clinical implications of mitochondrial DNA quantification on pregnancy outcomes: a blinded prospective non-selection study. (2019) (0)
Predictive value of preimplantation genetic diagnosis of aneuploidy and translocations (2004) (0)
VALIDATION OF A NON-INVASIVE METABOLOMICS METHOD TO PREDICT EMBRYO IMPLANTATION (2021) (0)
SELECTED ORAL COMMUNICATION SESSION, SESSION 22: FERTILITY PRESERVATION – BASIC, Monday 4 July 2011 15:15 – 16:30 (2011) (0)
Three-Fold Increase in Embryo Implantation Rates After Preimplantation Genetic Diagnosis (PGD) of Advanced Maternal Age (2005) (0)
Next generation sequencing (NGS) and the rate of partial aneuploidy in preimplantation genetic screening (PGS) (2016) (0)
Pregnancy outcomes following transfer of embryos diagnosed as chromosomally mosaic by next-generation sequencing (NGS) (2017) (0)
Preimplantation genetic diagnosis (PGD) reduces pregnancy loss in patients with previous recurrent miscarriages (RM) (2004) (0)
Preimplantation genetic diagnosis of single gene disorders: outcome from over 200 cases (2008) (0)
O▪61 Restrictive assisted reproduction laws and PGD (2005) (0)
In vitro fertilization and development of human oocytes reconstituted by spindle nuclear transfer to replace mutated mitochondrial DNA (2016) (0)
Comparison of next generation sequencing (NGS) and aCGH for PGS (2014) (0)
Exogenous gondotropin use not associated with increase in aneuploidy of in vivo recovered blastocysts (2019) (0)
Aneuploidy Screening in Human Preimplantation Embryos Via Array Comparative Genomic Hybridization (ACGH) – Can Extraneous Sperm Affect Diagnosis? (2015) (0)
Simultaneous analysis of preimplantation genetic diagnosis (PGD) for fragile X syndrome (FXS) and array CGH (aCGH): advantages of selecting a PGD strategy with comprehensive diagnosis (2016) (0)
A genome-wide study of recombination events in human preimplantation embryos (2014) (0)
PGT as Quality Control for ART methods (2019) (0)
Aneuploidy Patterns in 3143 day-3 Embryos Analyzed by Array CGH (2011) (0)
Incidence and causes of gender misdiagnosis in preimplantation genetic screening (2013) (0)
Effect of karyotype and cell number on blastocyst development following day 3 biopsy (2003) (0)
High rate of survival after cryopreservation of biopsied human embryos (2002) (0)
P-540 Preimplantation genetic diagnosis cycle outcome in carriers of balanced reciprocal translocations (2004) (0)
The number of available embryos for biopsy is predictive for the outcome of PGD cycles (2002) (0)
Conception after transfer of blastocysts diagnosed on day 3 as monosomic following preimplantation genetic screening (PGS) (2008) (0)
Embryonic stem cell lines from abnormal human embryos: rationale and feasibility (2008) (0)
Reproductive (epi)genetics (2012) (0)
O▪29 Microarray technology to assess gene expression profiles of human oocytes and embryos (2005) (0)
Preimplantation genetic diagnosis for gender selection in the United States (2009) (0)
Preimplantation genetic diagnosis for recurrent pregnancy loss also reduces miscarriage risk for young women (2010) (0)
Preimplantation genetic diagnosis (PGD) for chromosomal rearrangements (CR) using aCGH. risk assessment depending on the type of CR, the maternal age and the sex of the carrier (2012) (0)
The impact of human oocyte reconstruction using meiosis II spindle transfer on the pre-implantation embryonic development (2015) (0)
Letter to the editorReply of the Authors (2011) (0)
Whole exome sequencing of embryo biopsies reveals clinically-significant de novo mutations (2014) (0)
C14 Preimplantation aneuploidy testing outcome (2010) (0)
Expanded carrier screening reveals insights into enrichment of specific disorders within a reproductive genomic space (2017) (0)
Could Morphokinetic Parameters Predict Ongoing Pregnancy or Miscarriage? (2022) (0)
Significant differences in miscarriage rates between centers after replacement of euploid blastocysts tested by array comparitive genome hybridization (2017) (0)
Pooling for Rapid Delineation of Chromosomal Breakpoints * (2009) (0)
Idiopathic recurrent pregnancy loss is mostly caused by aneuploid embryos (2012) (0)
O▪80 Embryo cohort size does not affect the rate of chromosome abnormalities (2005) (0)
Center specific variations of triploid embryos (2016) (0)
O▪38 Maternal age is the most important parameter predicting aneuploidy, yet it is an unpredictable indicator of chromosome abnormalities (2005) (0)
Screening of 24 chromosomes in single cells using microarray comparative genomic hybridization methods: implications for preimplantation genetic diagnosis (2008) (0)
Estimated number of mature oocytes needed for fertility preservation patients based on the number of euploid blastocysts diagnosed following preimplantation genetic screening (PGS) (2013) (0)
Preconception screening and preimplantation genetic diagnosis (PGD): for what are you really getting tested? (2010) (0)
Preimplantation genetic testing for aneuploidy: a pragmatic, multicenter randomized clinical trial of single frozen euploid embryo transfer versus selection by morphology alone (2019) (0)
Prognostic value of preimplantation genetic screening (PGS) for patients with altered results in sperm fish (fluorescent in situ hybridisation) analysis (2014) (0)
Pregnancy outcomes per transfer after PGS via array CGH is constant through maternal age (2015) (0)
A paradigm of maximum efficiency in the utilization of cryopreserved embryos (2013) (0)
Results of PGD for Translocations in 539 Cycles (2005) (0)
QUANTITATIVE DETECTION OF BIOLOGICALLY RELEVANT ANTI-MULLERIAN HORMONE (AMH) AND PROGESTERONE IN HUMAN HAIR SAMPLES (2020) (0)
Altered levels of mitochondrial DNA are associated with female age, aneuploidy, and reveal the implantation potential of chromosomally normal embryos (2014) (0)
To test or not to test? variable spectrum mutations (VSMS) in high impact diseases identified in 3,208 clinical samples screened via an expanded carrier screening platform (2014) (0)
O4 Preimplantation Genetic Diagnosis (PGD) for chromosomal rearrangements (CR) using arrays of comparative genome hybridization (aCGH). Risk assessment depending on the type of CR, the maternal age and the sex of the carrier (2012) (0)
Pregnancy rates following fresh day 6, fresh day 7 or frozen embryo transfer (FET) of euploid blastocysts after micro-array comparative genomic hybridization (aCGH) analysis (2013) (0)
O-35. PGD of aneuploidy for good responder IVF patients (2002) (0)
Frozen Embryo Transfer Outcomes Following Preimplantation Genetic Screening: Is it Better to Biopsy Pre-Vitrification or Can We Biopsy Post-Warming? (2015) (0)
Are euploidy rates different in blastocysts from donor oocytes and those from young infertile patients (2014) (0)
New recommendations for male factor and repeated pregnancy loss patients who are considering IVF and are at risk of having translocations (2007) (0)
Subject Index, Vol. 75, 1996 (1996) (0)
Preimplantation Genetic Testing for Aneuploidy Versus Morphology as Selection Criteria for Single Frozen-Thawed Embryo Transfer in Good-Prognosis Patients: A Multicenter Randomized Clinical Trial (2020) (0)
CCS improves pregnancy outcomes in egg donor FET cycles (2015) (0)
Human Uterine Lavage: First Live Births from In Vivo Conceived Genetically Screened Blastocysts. (2023) (0)
Infertility and Assisted Reproduction: PGD for Chromosomal Anomalies (2008) (0)
An analysis of comprehensive carrier screening results for 1000 clinical samples: the importance of transparent disease classification & criteria for selection (2013) (0)
Validation of blastocyst biopsy and next generation sequencing (NGS) for the purpose of preimplantation genetic screening (PGS) (2014) (0)
Using a single trophectoderm biopsy to carry out PGD for single gene disorders in combination with next generation sequencing for aneuploidy screening (2016) (0)
Icsi vs. Insemination for Trophectoderm Biopsy PGS Cycles: Is There Any Difference in Chromosomal Abnormalities or Pregnancy Rates? (2015) (0)
Outcomes from 9822 array comparative genomic hybridization (aCGH) cycles for preimplantation genetic screening (PGS) (2016) (0)
Reanalysis of Monosomic Embryos at the Blastocyst Stage Following Day 3 Biopsy and Array Comparative Genomic Hybridization (aCGH) (2011) (0)
Preimplantation genetic diagnosis for chromosome abnormalities (2005) (0)
Comparison of embryo aneuploidy rates and patterns between brca mutation carriers and infertile women (2018) (0)
Segmental chromosome imbalance in human oocytes and preimplantation embryos: incidence, origin and clinical relevance (2011) (0)
O15 Extended culture is a poor tool for selecting chromosomally normal embryos: Comparison of day-3 and day-5 embryos analyzed using comprehensive chromosome screening methods (2010) (0)
The increase in the aneuploidy rate in embryos is mostly due to an absolute decrease in the number of euploid embryos (2018) (0)
S7 Blastocyst biopsy for aneuploidy screening (2012) (0)
Blastocysts needed to transfer at least one euploid embryo: data from 10,852 pre-implantation genetic screening (PGS) cycles (2015) (0)
Incidence, origin and type of aneuploidy seen in human preimplantation blastocysts: concurrent analysis using single nucleotide polymorphism (SNP) arrays and next generation sequencing (NGS) (2016) (0)
A comprehensive genetic assessment of male and female infertility using next-generation sequencing (2017) (0)
Pregnancy outcome of 345 cycles of preimplantation genetic diagnosis (PGD) for chromosomal structural aberrations (2004) (0)
O-020 Aneuploidy and mosaicism in human embryos: How correct detection may improve IVF clinical outcomes (2021) (0)
Mitochondrial levels concordant over multiple trophectoderm biopsies from the same embryo (2017) (0)
The chromosome 11 olfactory receptor gene cluster is a candidate reproductive partner-specific compatibility locus (2017) (0)
Comparison of sperm chromosomal abnormalities and preimplantation genetic diagnosis outcome in patients with extreme male factor (2007) (0)
Pregnancy outcome after te biopsy with fresh transfer or vitrification (2012) (0)
Reply: Possible impact of LH-containing gonadotrophins on diploidy rates in preimplantation embryos (2009) (0)
Analysis of human blastomere chromosomes following nuclear injection into mature mouse oocytes. (2001) (0)
P▪52 PGD for complex cases of structural chromosome aberrations (2005) (0)
Selection of chromosomally normal embryos improves egg donor frozen transfer pregnancy rates (2014) (0)
Translocation Testing Prior to Embryo Transfer (2000) (0)
Follicle diameter predicts oocyte maturity but not formation of blastocysts or ploidy of blastocysts arising from mature oocytes of donors (2019) (0)
Preimplantation Genetic Diagnosis (PGD) for Complex Cases of Structural Chromosome Aberrations (2005) (0)
O-40. Predictive value of sperm FISH analysis on the outcome of PGD for translocations (2002) (0)
P-941: Reduced miscarriage and increased delivery rates when comparing natural conception and IVF/PGD (2006) (0)
101 Babies Born after Embryo Biopsy and Aneuploidy Testing (2000) (0)
I18 Reproductive outcome of aneuploidy testing depending on biopsy procedure and microarray technology application (2013) (0)
23. SCORING METHOD TO ESTIMATE CLINICAL PREGNANCY USING ARTIFICIAL INTELLIGENCE MODEL (2019) (0)
Analysis of 4795 day-3 embryos by array comparative genome hybridization (aCGH): aneuploidy patterns (2011) (0)
P–171 Automated oocyte and zygote denudation using a novel microfluidic device supervised by a computer vision algorithm (2021) (0)
Does polar body biopsy (PBB) predict the outcome of vitrified oocytes (OV): preliminary results of PBB, OV, thaw, trophectoderm biopsy (TEBX) and embryo transfer (ET) with ongoing pregnancies (2013) (0)
P-930: Ploidy of day 5 and 6 embryos reaching blastocyst and classified as chromosomally abnormal after single cell biopsy and PGD on day 3 (2006) (0)
Outcome of PGD for the indication of previous trisomic conception (2009) (0)
O▪84 The importance of a full chromosome count (2005) (0)
Genetic influences on endocrine signaling in women (2015) (0)
Preimplantation genetic screening to improve embryo selection (2008) (0)
Should egg donors be screened for X-linked disease? (2015) (0)
High variability in chromosome abnormality rates in embryos from young infertile women (2016) (0)
O▪41 Full karyotype interphase cell analysis (2005) (0)
Intracytoplasmic Sperm Injection Compared With Insemination in Trophectoderm Biopsy Preimplantation Genetic Screening Cycles: An Effect on Aneuploidy or Pregnancy Rates? [352] (2015) (0)
Preimplantation genetic diagnosis (PGD), a collaborative activity of clinical genetic departments and IVF centres. Prenatal Diagnosis 21(12) 2001, 1086–1092 (2002) (0)
Are we introducing variables that iatrogenically increase the rate of aneuploidy in women with advanced maternal age (AMA) undergoing in vitro fertilization (IVF) (2010) (0)
Similar pregnancy and implantation rates following day 6 embryo transfer or frozen embryo transfer (FET) after blastocyst biopsy for preimplantation genetic screening (PGS) (2013) (0)
The weight of the interchromosomal effect in reciprocal translocation carriers (2016) (0)
Going beyond the guidelines: a call for expanded carrier screen based on an analysis of 3,208 clinical samples (2014) (0)
Strategy for euploid embryo banking (2013) (0)
The incidental finding of microdeletions and microduplications during preimplantation genetic diagnosis (PGD) - test implication and clinical correlation (2016) (0)
Don’t wait to freeze your eggs: as age increases significantly more eggs are needed to generate a normal embryo (2014) (0)
Contents Vol. 90, 2000 (2000) (0)
ASSISTED REPRODUCTION TECHNOLOGIES Differences in pregnancy outcomes in donor egg frozen embryo transfer ( FET ) cycles following preimplantation genetic screening ( PGS ) : a single center retrospective study (2016) (0)
The peptide nucleic acids (PNAs) as probes for chromosomal analysis of human oocytes and preimplantation embryos. F. Pellestor, P. Paulasova, (2004) (0)
Does preimplantation genetic diagnosis (PGD) need a new name? (2000) (0)
Erratum to: Comment on: Gleicher N et al.,2016. Reprod biol endocrinol Sep 5;14(1):54 (2017) (0)
O-140 : Preimplantation genetic diagnosis of single gene disorders: Conclusions from the application of novel methodologies to more than 100 cases (2006) (0)
Aneuploidy rates in embryos produced by fertile couples (2015) (0)
First Clinical Pregnancies with an ICSI Robot (2022) (0)
Relationship between cohort size, hormonal stimulation, and chromosome abnormalities detected by preimplantation genetic diagnosis (PGD) (2009) (0)
PGD via ACGH for translocations: a review of cycle outcomes (2015) (0)
Comparison of clinical outcomes in programmed frozen embryo transfer cycles (FET) with and without blastocyst biopsy and aneuploidy screening (2013) (0)
Comparison between microarray comparative genomic hybridization (aCGH) and fluorescence in-situ hybridization (FISH) for preimplantation genetic diagnosis (PGD) in translocations carriers (2013) (0)
Array-CGH analysis of products of conception (POC) from naturally or IVF conceived pregnancies (2013) (0)
Mosaicism per chromosomes per age (2017) (0)
Appropriate culture conditions for preimplantation genetic diagnosis of aneuploidy (2003) (0)
Controlled ovarian hyperstimulation (COH) parameters associated with donor euploidy rates (2017) (0)
How indicative is the trophectoderm biopsy of the ICM in human embryos? (2018) (0)
The frequency of X-linked disorders in preimplantation genetic diagnosis (PGD): a call for wider screening (2016) (0)
Asynchronous division in human embryos is associated with complex chromosome abnormalities but this association is absent in euploid embryos and those with single or double chromosome gain or loss (2011) (0)
Quantitative relationship between mitochondrial DNA (MTDNA) amounts and implantation can help improve pregnancy outcomes (2016) (0)
The role of aneuploidy in repeated implantation failure: implications for patient counseling and preimplantation genetic screening (2008) (0)
FIRST PRE-CLINICAL AND CLINICAL VALIDATION OF AN AUTOMATED SPERM INJECTION ROBOT (ICSI-A) IN HUMAN OOCYTES (2022) (0)
Biology of chromosome abnormalities as learned from embryo biopsy and PGD (2009) (0)
HUMAN UTERINE LAVAGE: EMBRYO SAFETY AND FIRST LIVE BIRTHS FROM IN VIVO CONCEIVED GENETICALLY SCREENED BLASTOCYSTS (2020) (0)
P-210 Development of a new device for automatic vitrification of oocytes (2022) (0)
Investigating the efficacy of non-invasive pre-implantation genetic testing for aneuploidy (NI-PGT-A) using spent culture media as a source of embryonic DNA (2018) (0)
Diagnostic and clinical outcomes of 694 cycles using karyomapping for preimplantation genetic diagnosis (PGD) of single gene disorders (2016) (0)
Contents, Vol. 75, 1996 (1996) (0)
P-173. Preimplantation genetic diagnosis and IVF as an alternative for achieving pregnancies in patients with an altered karyotype (1997) (0)
Intention to treat: how many initiated PGS cycles produce blastocysts for biopsy as maternal age increases? (2014) (0)
Chromosomal abnormalities demonstrated by in-vivo conceived& cultured human embryos (2018) (0)
From carrier screening to single gene PGD: an analysis of 762 couples screened via an expanded carrier screening platform (2014) (0)
O▪12 Comprehensive aneuploidy diagnosis in single cells (2005) (0)
Identification of patients presenting for preimplantation genetic diagnosis: trends in risk ascertainment for single gene testing and impact of expanded carrier screening (2017) (0)
Single embryo transfer (SET) vs. double embryo transfer (DET) in preimplantation genetic screening (PGS) cycles: does size of euploid embryo cohort matter? (2013) (0)
Mosaicism and error rates in PGD (2008) (0)
A novel method for single cell dissection and sequencing of human blastocysts (2017) (0)
AUTOMATED VITRIFICATION AND WARMING OF OOCYTES MEDIATED BY A NOVEL MICROFLUIDICS DEVICE (2020) (0)
Transfer fresh or vitrify after blastocyst biopsy? results of an RCT (2016) (0)
O▪81 PGD for chromosome structural aberrations: outcome and comparison (2005) (0)
Comprehensive aneuploidy screening of oocytes: scientific data and clinical application (2008) (0)
PostersReproductive Genetics (PGD/PGS) (2010) (0)
Variant detection by NGS from embryo biopsies (2018) (0)
O-125. Effect of one cell biopsy on embryo development (1999) (0)
PCO and High Responders Have Higher Rates of Aneuploidy by PGD (2005) (0)
Transfer of blastocysts with lower mitochondrial DNA (MTDNA) quantities improves IVF outcomes (2016) (0)
Pre-implantation diagnosis of aneuploidy by polar body and blastomere FISH analysis (1994) (0)
Monosomy rescue in preimplantation genetic diagnosis of aneuploidy (2008) (0)
Development of a comprehensive, cost effective microarray-based genetic test for 216 of the most highly penetrant monogenic diseases (2012) (0)
P-203. Embryo development and chromosomal abnormalities after ICSI with frozen-thawed non-ejaculated spermatozoa (1999) (0)
Are specific types of aneuploidy more common in high-risk patients undergoing preimplantation genetic diagnosis (PGD)? (2004) (0)
Blastulation and implantation rates of microarray CGH-defined normal embryos compared to abnormal and non-biopsied embryos (2012) (0)
Design, validation and clinical application of a novel next-generation sequencing protocol for detection of mitochondrial disease and simultaneous aneuploidy screening in preimplantation embryos (2016) (0)
What is the Likelihood of Success for Biopsied Day 5 Embryos That Have Not Achieved Blastocyst Formation (2005) (0)
Reply: PGD—a model to evaluate efficacy? (2006) (0)
Clinical application of mitochondrial DNA quantification for embryo viability assessment: a blinded prospective non-selection study (2016) (0)
Does preimplantation genetic screening (PGS) in frozen embryo transfer (FET) cycles improve pregnancy rates when compared to fresh PGS cycles (2009) (0)
Validation and preliminary clinical results of array CGH for PGS (2010) (0)

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