T. Escudero

发表

CACROMOS: A Computer Program to Reconstruct the Position of Chromosomes on the Metaphase Plate

C. Cuadras, C. Arenas, T. Escudero, 2004 .

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

S. Munné, T. Escudero, Serena H. Chen, 2005, Fertility and sterility.

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

K. Hirschhorn, B. Levy, D. Wells, 2002 .

Blastomere fixation techniques and risk of misdiagnosis for preimplantation genetic diagnosis of aneuploidy.

S. Munné, T. Escudero, E. Velilla, 2002, Reproductive biomedicine online.

Chromosome mosaicism in cleavage-stage human embryos: evidence of a maternal age effect.

Jacques Cohen, C. Márquez, S. Munné, 2002, Reproductive biomedicine online.

Differences in chromosome susceptibility to aneuploidy and survival to first trimester.

Jacques Cohen, C. Márquez, M. Alikani, 2004, Reproductive biomedicine online.

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

Jacques Cohen, J. Simpson, P. Colls, 2005, Fertility and sterility.

Wide range of chromosome abnormalities in the embryos of young egg donors.

J. Cohen, S. Munné, T. Escudero, 2006, Reproductive biomedicine online.

Increased efficiency of preimplantation genetic diagnosis for infertility using "no result rescue".

Jacques Cohen, P. Colls, S. Munné, 2007, Fertility and sterility.

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

K. Hirschhorn, B. Levy, D. Wells, 2002, Fertility and sterility.

DNA Probe Pooling for Rapid Delineation of Chromosomal Breakpoints

H. Zitzelsberger, H. Weier, J. Weier, 2009, Journal of Histochemistry and Cytochemistry.

Rapid mapping of chromosomal breakpoints: from blood to BAC in 20 days.

H. Weier, J. Weier, S. Munné, 2010, Folia histochemica et cytobiologica.

Improvements of preimplantation diagnosis of aneuploidy by using microwave hybridization, cell recycling and monocolour labelling of probes.

L. Morrison, M. Legator, S. Munné, 2000, Molecular human reproduction.

Outcome of preimplantation genetic diagnosis of translocations.

L. Gianaroli, J. Cohen, S. Munné, 2000, Fertility and sterility.

Causes and estimated incidences of sex-chromosome misdiagnosis in preimplantation genetic diagnosis of aneuploidy.

Jacques Cohen, D. Wells, Xuezhong Zheng, 2016, Reproductive biomedicine online.

Preimplantation genetic diagnosis for gender selection in the United States

J. Weier, P. Colls, S. Munné, 2009 .

Preimplantation genetic diagnosis for gender selection in the USA.

J. Weier, P. Colls, S. Munné, 2009, Reproductive biomedicine online.

A case with 47,XXY,del(15)(q11;q13) karyotype associated with Prader-Willi phenotype.

M. D. Coll, T. Escudero, R. García-mayor, 1997, Hormone Research.

Chromosomal abnormalities in embryos derived from testicular sperm extraction.

Santiago Munné, S. Munné, S. Silber, 2003, Fertility and sterility.

PGDIS Position Statement on the Transfer of Mosaic Embryos 2019.

C. Rubio, S. Kahraman, C. Strom, 2019, Reproductive biomedicine online.

Analysis of chromosome abnormalities in sperm and embryos from two 45,XY,t(13;14)(q10;q10) carriers

S. Munné, T. Escudero, J. Blanco, 2000, Prenatal diagnosis.

Preimplantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses.

P. Colls, S. Munné, T. Escudero, 2010, Fertility and sterility.

Running Headline: BAC POOLS FOR FISH

H. Zitzelsberger, H. Weier, J. Weier, 2009 .

Negligible interchromosomal effect in embryos of Robertsonian translocation carriers.

S. Munné, T. Escudero, Serena H. Chen, 2005, Reproductive biomedicine online.

Possible interchromosomal effect in embryos generated by gametes from translocation carriers.

L. Gianaroli, A. Ferraretti, S. Munné, 2002, Human reproduction.

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

S. Munné, T. Escudero, M. Sandalinas, 2003, Fertility and sterility.

Preimplantation genetic diagnosis for complex chromosome rearrangements

S. Munné, T. Escudero, J. Fischer, 2008, American journal of medical genetics. Part A.

Predictability of preimplantation genetic diagnosis of aneuploidy and translocations on prospective attempts.

J. Cohen, P. Colls, S. Munné, 2004, Reproductive biomedicine online.

Female gamete segregation in two carriers of translocations involving 2q and 14q

S. Munné, T. Escudero, M. Sandalinas, 2000, Prenatal diagnosis.

Gamete segregation in female carriers of Robertsonian translocations

J. Cohen, S. Munné, T. Escudero, 2000, Cytogenetic and Genome Research.

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

J. Grifo, A. Hershlag, P. Colls, 2012, Reproductive biomedicine online.

Preimplantation genetic diagnosis significantly improves the pregnancy outcome of translocation carriers with a history of recurrent miscarriage and unsuccessful pregnancies.

P. Colls, S. Munné, T. Escudero, 2006, Reproductive biomedicine online.

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

Santiago Munné, D. Wells, Dagan Wells, 2011, Fertility and sterility.

Recurrent First-trimester Pregnancy Loss: Is Preimplantation Genetic Diagnosis the Answer?

T. Escudero, D. Sable, S. Chen, 2002 .

Improved implantation after preimplantation genetic diagnosis of aneuploidy.

Jacques Cohen, S. Munné, T. Escudero, 2003, Reproductive biomedicine online.

Preimplantation genetic diagnosis of numerical abnormalities for 13 chromosomes.

P. Colls, S. Munné, T. Escudero, 2003, Reproductive biomedicine online.

Preimplantation genetic diagnosis (PGD) as both a diagnostic and therapeutic tool in women with advanced maternal age (AMA) undergoing IVF

S. Munné, T. Escudero, T. Nass, 2002 .

Follow-up of chimerism in children with hematological diseases after allogeneic hematopoietic progenitor cell transplants

M. Caballín, T. Escudero, T. Olivé, 1999, Bone Marrow Transplantation.

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

L. Morrison, L. Gianaroli, A. Ferraretti, 2001, Prenatal diagnosis.

Preimplantation genetic diagnosis of pericentric inversions

S. Munné, T. Escudero, J. Stevens, 2001, Prenatal diagnosis.

SELECTED ORAL COMMUNICATION SESSION, SESSION 48: REPRODUCTIVE GENETICS, Tuesday 5 July 2011 15:15 – 16:30

C. Giménez, C. Arjona, G. Liumbruno, 2011 .

Association between spindle assembly checkpoint expression and maternal age in human oocytes.

N. Steuerwald, D. Wells, J. Cohen, 2000, Molecular human reproduction.

Rapid mapping of chromosomal breakpoints: from blood to BAC in 20 days.

H. Weier, J. Weier, S. Munné, 2010, Folia histochemica et cytobiologica.