Aditional Information about PGD
The articles showed in this page, provied importante aditional information about Preimplantational Genetic Diagnosis.
Munne S, Ary J, Zouves C, Escudero T, Barnes F, Cinioglu C, Ary B, Cohen J (2006) Wide range of chromosome abnormalities in the embryos of young egg donors. Reproductive Biomed Online, 12:340-346
Munne S (2006) Chromosome abnormalities and their relationship to morphology and development of human embryos. Reproductive Biomedicine Online 12:234-253
Munne S, Fischer J, Warner A, Chen S, Zouves C, Cohen J, And referring centers PGD group (2006) Preimplantation Genetic Diagnosis Significantly Reduces Pregnancy Loss in Infertile Couples: A Multi-Center Study. Fertil Steril 85:326-332
Munne S (2005) Analysis of the segregation of chromosomes during preimplantation genetic diagnosis in both male and female translocation heterozygotes. Cytogenetics and Genomic Res 305-309
Munne S, Velilla E, Colls P, Garcia-Bermudez M, Vemuri MC, Steuerwald N, Garrisi J, Cohen J (2005) Self correction of chromosomally abnormal embryos in culture and implications for stem cell production. Fertil Steril, 84:331-335Stachecki J, Cohen J, Munne S (2005) Cryopreservation of biopsied cleavage stage biopsied embryos. Reproductive Biomed online 6:711-715
Chen SH, Escudero T, Cekleniak NA, Sable DB, Garrisi MG, Cohen J, Munne S (2005) Maternal balanced translocation is a risk factor for poor response to ovarian stimulation. Fertil Steril 83:1504-1509
Munne S, Chen S, Fischer J, Colls P, Zheng X, Stevens J, Escudero T, Oter M, Schoolcraft W, Simpson JL, Cohen J (2005) Preimplantation genetic diagnosis reduces pregnancy loss in women 35 and older with a history of recurrent miscarriages. Fertil Steril 84:331-335
Gutirrez-Mateo C, Gadea L, Benet J, Wells D, Munne S, Navarro J (2005) Aneuploidy 12 in a Robertsonian (13;14) carrier: Case Report. Human Reprod 20:1256-1260Weier HUG, Weier JF, Oter Renom M, Zheng X, Colls P, Nureddin A, Pham CD, Chu LW, Racowsky C, Munne S (2005) Fluorescence in situ hybridization and spectral imaging analysis of human oocytes and first polar bodies. J Histochem Cytochem 53:269-272
Munne S, Escudero T, Fischer J, Chen S, Hill J, Stelling JR, Estop E (2005) Negligible interchromosomal effect in embryos of Robertsonian translocation carriers. Reprod Biomed Online 10:363-369
Munne S, Escudero T, Pere C, Xuezhong Z, Oter M, Garrisi M, Barnes F, Zouves C, Werlin L, Magli C, Cohen J (2004) Predictability of Preimplantation Genetic Diagnosis of Aneuploidy and Translocations on Prospective Attempts. Reprod Biomed Online 9:645-651
Munne S, Sandalinas M, Alikani M, Cohen J (2004) Chromosome abnormalities in human embryos. In: Textbook of Assisted Reproductive Technology. Laboratory and Clinical Perspectives. David K Gardner, Weissman A, Howles CM, Shoham Z, Dunitz M Eds. Chapter 28, 355-377Munne S, Cohen J (2004) The situation of Preimplantation Genetic Diagnosis in Japan: a criticism. Reprod Biomed Online 9:258-259
Stachecki J, Munne S, Cohen J (2004) Spindle organization after cryopreservation of mouse, human, and bovine oocytes. Reprod Biomed Online 8:664-672
Gutirrez CM, Wells D, Benet J, Snchez-Garca JF, Bermdez MG, Belil I, Egozcue J, Munne S, Navarro J (2004) Reliability of Comparative Genomic Hybridization to detect chromosome abnormalities in first polar bodies and metaphase II oocytes. Human Reprod 19:2118-2125
Gutirrez-Mateo C, Benet J, Wells D, Colls P, Bermdez MG, Snchez-Garca JF, Egozcue J, Navarro J, Munne S (2004) Aneuploidy study of human oocytes first polar body comparative genomic hybridization and metaphase II fluorescence in situ hybridization analysis. Human Reprod 19:2859-2868
Munne S, Sandalinas M, Magli M, Gianaroli L, Cohen J, Warburton D (2004) Increased rate of aneuploid embryos in young women with previous aneuploid conceptions. Prenat Diagn. 24:638-647
Weier HUG, Weier JF, Oter Renom M, Zheng X, Colls P, Nureddin A, Pham CD, Chu LW, Racowsky C, Munne S (2004) Fluorescence in situ hybridization and spectral image analysis of human oocytes and first polar bodies. J Histochem Cytochem 52:1-4
Colls P, Sandalinas M, Pagidas K, Munne S (2004) PGD analysis for aneuploidy in a patient heterozygous for a polymorphism of chromosome 16 (16qh-). Prenat Diagn 24:741-744
Verlinsky, Y, Cohen J, Munne S, Gianaroli L, Simpson JL, Ferraretti AP, Kuliev A (2004) Over a decade of preimplantation genetic diagnosis experience – a multicenter report . Fertil Steril. 82:292-294Bermdez MG, Wells D, Malter H, Munne S, Cohen J, Steuerwald NM (2004) Expression Profiles of Individual Human Oocytes using Microarray Technology. Reproductive Biomedicine Online. Online 8:325-337
Santiago Munne, Muhterem Bahe, Mireia Sandalinas, Toms Escudero, Carmen Mrquez, Esther Velilla, Pere Colls, Maria Oter, Mina Alikani, Jacques Cohen (2004) Differences in chromosome susceptibility to aneuploidy and survival to first trimester. Reproductive Biomedicine Online, 8:81-90
Munne S (2003) Preimplantation Genetic Diagnosis and Human implantation – A review. Placenta 24: S70-76Werlin L, Rodi I, DeCherney A, Marello E, Hill D, Munne S (2003) Preimplantation genetic diagnosis (PGD) as both a therapeutic and diagnostic tool in assisted reproductive technology. Fertil Steril, 80 :467-468
Munne S, Sandalinas M, Escudero T, Velilla E, Walmsley R, Sadowy S, Cohen J, Sable D (2003) Improved implantation after preimplantation genetic diagnosis of aneuploidy. Reprod Biomed Online, 7:91-97
Escudero T, Abdelhadi I, Sandalinas M, Munne S (2003) Predictive value of sperm chromosome analysis on the outcome of PGD for translocations. Fertil Steril 79:1528-1534
AbdelhadiI I, Colls P, Sandalinas M, Escudero T, Munne S. Preimplantation genetic diagnosis of numerical abnormalities for 13 chromosomes. Reprod Biomed online, 2003: 6:226-231
Silber S, Escudero T, Lenahan K, Sadowy S, Abdelhadi I, Kilani Z, Munn S (2003) Chromosomal abnormalities in embryos derived from TESE. Fertil Steril, 30-38
Wells D, Escudero T, Levy B, Hirschhorn K, Delhanty JDA, Munne S (2002) First clinical application of comparative genome hybridization (CGH) and polar body testing for Preimplantation genetic diagnosis (PGD) of aneuploidy. Fertil Steril 78, 543-549
Munne S, Cohen J, Sable D (2002) Preimplantation Genetic Diagnosis for advanced maternal age and other indications. Fertil Steril 78:234-236
Munne S, Wells D (2002) Preimplantation genetic diagnosis. Current Opinion Obstet Gynecol 14: 239-244
Velilla E, Escudero T, Munne S (2002)Blastomere fixation techniques and risk of misdiagnosis for PGD of Aneuploidy. Reprod Biomed Online, 4:210-217
Munne S, Sandalinas M, Escudero T, Marquez C, Cohen J (2002)Chromosome mosaicism in cleavage stage human embryos: evidence of a maternal age effect. Reprod Biomed Online 4:223-232
Sandalinas M, Mrquez M, Munne S (2002) Spectral karyotyping of unfertilized and non-inseminated oocytes. Molec Human Reprod, 8:580-585
Munne S (2002) Preimplantation genetic diagnosis of numerical and structural chromosome abnormalities. Reprod Biomed Online 4:183-196
Magli MC, Sandalinas M, Escudero T, Morrison L, Ferraretti AP, Gianaroli L, Munne S (2001) Double locus analysis of chromosome 21 for preimplantation genetic diagnosis of aneuploidy. Prenatal diagnosis 21:1080-1085
Munne S (2001) Preimplantation genetic diagnosis of Structural abnormalities. Molec Cell endocrinol 183: S55-S58
Weier HUG, Munne S, Lersch RA, Hsieh HB, Smida J, Chen XN, Korenberg JR, Pedersen RA, Fung J (2001) Towards a full karyotype screening of interphase cells: 'FISH and chip' technology. Molec Cell Endocrinol. 183: S41-S45
Escudero T, Lee M, Stevens J, Sandalinas M, Munne S (2001) Preimplantation Genetic diagnosis of pericentric inversions. Prenatal Diagnosis 21:760-766
Sandalinas M, Sadowy S, Alikani M, Calderon G, Cohen J, Munne S. (2001) Developmental ability of chromosomally abnormal human embryos to develop to the blastocyst stage. Human Reprod, 16:1954-1958
Obasaju M, Kadam A, Biancardi T, Sultan K, Fateh M, Munne S (2001) Pregnancy rate from the transfer of a single normal embryo in women over 40 years of age undergoing PGD for chromosomal abnormalities. Reproductive Biomedicine Online 2:98-101
Munne S, Escudero T, Sandalinas M, Sable D, Cohen J (2000) Gamete segregation in female carriers of Robertsonian translocations. Cytogenet Cell Genet 90:303-308
Mrquez C, Sandalinas M, Bahe M, Alikani M, Munne S (2000) Chromosome abnormalities in 1255 cleavage-stage human embryos. Reproductive Biomedicine Online 1:17-27
Bahe M, Escudero T, Sandalinas M, Morrison L, Legator M, Munne S (2000) Improvements of preimplantation diagnosis of aneuploidy by using microwave-hybridization, cell recycling and monocolor labeling of probes. Molec Human Reprod 9:849-854
Munne S, Sepulveda S, Balmaceda J, Fernandez E, Fabres C, Mackenna A, Lopez T, Crosby JA, Zegers-Hochschild F (2000) Selection of the most common chromosome abnormalities in oocytes prior to ICSI. Prerat Diagn 20:582-586
Escudero T, Lee L, Carrel D, Blanco J, Munne S (2000) Analysis Of Chromosome Abnormalities In Sperm And Embryos From Two 45,XY,t(13;14)(q10;q10) Carriers. Prenat Diagn 20:599-602
Munne S, Sandalinas M, Escudero T, Fung J, Gianaroli L, Cohen J (2000) Outcome of preimplantation genetic diagnosis of translocations. Fertil Steril. 73:1209-1218
Lee M, Munne S (2000) Pregnancy after polar body biopsy and freezing and thawing of human embryos. Fertil Steril 73:645-647
Escudero T, Lee Michael L, Sandalinas S, Munne S (2000) Female gamete segregation in two carriers of translocations involving 2q and 14q. Prenat Diagn, 20:235-237
Obasaju M, Kadam A, Sultan K, Fateh M, Munne S (1999) Evidence that sperm quality may adversely affect the chromosome constitution of embryos resulting from ICSI. Fertil. Steril. 1113-1115
Gianaroli L, Magli MC, Ferraretti AP, Munne S (1999) Preimplantation diagnosis for aneuploidies in patients undergoing in vitro fertilization with poor prognosis: identification of the categories to which it should be proposed. Fertil. Steril. 72:837-844
Munne S, Magli C, Cohen J, Morton P, Sadowy S, Gianaroli L, Tucker M, Mrquez C, Sable D, Ferraretti AP, Massey JB, Scott R (1999) Positive outcome after preimplantation diagnosis of aneuploidy in human embryos. Human Reprod, 14:2191-2199
Gianaroli L, Magli MC, Munne S, Fortini D, Ferraretti AP (1999) Advantages of day four embryo transfer in patients undergoing preimplantation genetic diagnosis of aneuploidy. J. Assisted Reprod Genet 16:170-175
Weier HUG, Munne S, Fung J (1999) patient-specific probes for Preimplantion genetic diagnosis (PGD) of structural and numerical aberrations in interphase cells. J. Assisted Reprod Genet 16:182-191
Bahe M, Cohen J, Munne S (1999) PGD of aneuploidy: were we looking at the wrong chromosomes? J. Assisted Reprod Genet. 16: 176-181
Magli MC, Gianaroli L, Ferraretti AP, Fortini D, Munne S (1999) Impact of blastomere biopsy and cryopreservation techniques on human embryo viability. Human Reprod. 14:770-773
Willadsen S, Levron J, Munne S, Schimmel T, Mrquez C, Scott R, Cohen J (1999) Rapid Visualization of Metaphase Chromosomes in Single Human Blastomeres After Fusion with In Vitro Matured Bovine Eggs. Human Reprod 14:470-475
Munne S and Cohen J (1998) Chromosome abnormalities in human embryos. Human Reprod Update. 4: 842-855
Munne S, Magli C, Bahe M, Fung J, Legator M, Morrison L, Cohen J, Gianaroli L (1998) Preimplantation diagnosis of the aneuploidies most commonly found in spontaneous abortions and live births: XY, 13, 14, 15, 16, 18, 21, 22. Prenat Diagn. 18:1459-1466
Cohen J, Scott R, Alikani M. Schimmel T, Munne S, Levron J, Wu L, Brenner C, Warner C, Willadsen S (1998) Ooplasmic transfer in mature human oocytes. Molec Human Reprod 4: 269-280
Munne S, Marquez C, Magli C, Morton P, Morrison (1998) Scoring criteria for preimplantation genetic diagnosis of numerical abnormalities for chromosomes X, Y, 13, 16, 18 and 21. Human Molec Reprod 9:863-870
Marquez C, Cohen J, Munne S (1998) Chromosome identification on human oocytes and polar bodies by spectral karyotyping. Cytogenet Cell Genet 81:254-258
Munne S, Fung J, Cassel MJ, Marquez C, Weier HUG (1998) Preimplantation Genetic Analysis of Translocations: Case-Specific Probes for Interphase Cell Analysis. Human Genet, 102:663-674
Magli MC, Gianaroli L, Munne S, Ferraretti AP (1998) Incidence of chromosomal abnormalities from a morphologically normal cohort of embryos in poor-prognosis patients. J Assist Reprod Genet 15:297-301
Munne S, Morrison L, Fung J, Marquez C, Weier U, Bahe M, Sable D, Grundfelt L, Schoolcraft, Scott R, Cohen J (1998). Spontaneous abortions are reduced after pre-conception diagnosis of translocations. J Assist Reprod Genet 290-296
Munne S, Marquez C, Reing A, Garrisi J, Alikani M (1998) Chromosome abnormalities in embryos obtained following conventional IVF and ICSI. Fertil Steril 69:904-908
Estop AM, Munne S, Cieply KM, Vandermark KK, Lamb AN, Fisch H (1998) Meiotic products of Klinefelter 47,XXY male as determined by sperm fluorescence in-situ hybridization analysis. Human Reprod. 13: 124-127
Munne S, Scott R, Sable D, Cohen J (1998) First pregnancies after pre-conception diagnosis of translocations of maternal origin. Fertil Steril 69:675-681
Gianaroli L, Munne S, Magli MC, Ferraretti AP (1997) Preimplantation genetic diagnosis of aneuploidy and male infertility. Int.J.Androl. 20:Suppl.3:31-34
Gianaroli L, Magli MC, Ferraretti AP, Fiorentino A, garrisi J, Munne S (1997) Preimplantation genetic diagnosis increases the implantation rate in human in vitro fertilization by avoiding the transfer of chromosomally abnormal embryos. Fertil.Steril. 68:1128-1131
Cassel MJ, Munne S, Fung J, Weier HUG (1997) Carrier-specific breakpoint-spanning DNA probes: an approach to preimplantation genetic diagnosis in interphase cells. Human Reprod 2019-2027
Gianaroli L, Magli MC, Munne S, Fiorentino A, Montanaro N, Ferraretti AP (1997) Will preimplantation genetic diagnosis assist patients with a poor prognosis to achieve pregnancy? Hum Reprod 12:1762-1767
Munne S, Magli C, Adler A, Wright G, de Boer K, Mortimer D, Tucker M, Cohen J, Gianaroli L (1997) Treatment-related chromosome abnormalities in human embryos. Human Reprod, 12:780-784
Munne S, Weier, U (1996) Simultaneous enumeration of chromosomes 13, 18, 21, X and Y in interphase cells for preimplantation genetic diagnosis of aneuploidy. Cytogenet. Cell. Genet 75:263-270
Templado C, Marquez C, Munne S, Colls P, Martorell MR, Cieply K, Benet J, Van Kirk V, Navarro J, Estop AM (1996) An analysis of human sperm chromosome aneuploidy. Cytogenet Cell Genet 74:194-200
Dailey T, Dale B, Cohen J and Munne S (1996) Association between non-disjunction and maternal age in meiosis-II human oocytes detected by FISH analysis. Am.J.Hum.Genet, 59:176-184
Kligman I, Benadiva C, Alikani M, Munne S (1996) The presence of multinucleated blastomeres in human embryos correlates with chromosomal abnormalities. Human Reprod, 11:1492-1498.
Benadiva C, Kligman I, Grifo J, Munne S (1996) Aneuploidy 16 in human embryos increases significantly with maternal age. Fertil. Steril. 66:248-255
Munne S, Dailey T, Finkelstein M, Weier HUG (1996) Reduction in signal overlap results in increased FISH efficiency: implications for preimplantation genetic diagnosis. J. Assisted Reprod. Genet. 13:149-156.
Munne S, Alonso ML, Grifo J (1996) case report: unusually high rates of aneuploid embryos in a 28-year old woman with incontinentia pigmenti. Cytogenet. Cell Genet., 72:43-45
Munne S, Alikani M, Tomkin G, Grifo J, Cohen J (1995) Embryo morphology, developmental rates and maternal age are correlated with chromosome abnormalities. Fertil.Steril., 64:382-391
Munne S, Dailey T, Sultan KM, Grifo J, Cohen J.(1995) The use of first polar bodies for preimplantation diagnosis of aneuploidy. Human Reprod. 10:1015-1021
Munne S, Sultan KM, Weier HUG, Grifo J, Cohen J, Rosenwaks Z (1995) Assessment of numerical abnormalities of X, Y, 18 and 16-chromosomes in preimplantation human embryos prior transfer. Am. J. Obs. Gyn 172:1191-1201
Grifo JA, Tang YX, Munne S, Alikani M, Cohen J , Rosenwaks Z (1994) Healthy deliveries from biopsied human embryos. Hum.Reprod. 9:912-916
Palermo G, Munne S and Cohen J (1994) The human zygote inherits its mitotic potential from the male gamete. Hum.Reprod. 9:1220-1225.
Munne S, Weier HUG, Grifo J, Cohen J (1994) Chromosome mosaicism in human embryos. Biol. Reprod. 51:373-379Munne S, Grifo J, Cohen J, Weier HUG (1994) Chromosome abnormalities in Arrested Human Preimplantation Embryos: A Multiple Probe Fluorescence In Situ Hybridization (FISH) Study. Am.J.Hum.Genet. 55,1:150-159.
Munne S, Lee A, Rosenwaks Z, Grifo J, Cohen J (1993) diagnosis of major chromosome aneuploidies in human preimplantation embryos. Hum Reprod 8:2185-2191