| Year |
Citation |
Score |
| 2021 |
Pellestor F, Gaillard JB, Schneider A, Puechberty J, Gatinois V. Chromoanagenesis, the mechanisms of a genomic chaos. Seminars in Cell & Developmental Biology. PMID 33608210 DOI: 10.1016/j.semcdb.2021.01.004 |
0.408 |
|
| 2020 |
Vaché C, Puechberty J, Faugère V, Darmaisin F, Liquori A, Baux D, Blanchet C, Garcia-Garcia G, Meunier I, Pellestor F, Koenig M, Roux AF. A 4.6 Mb Inversion Leading to - and - Fusion Transcripts as a New Pathogenic Mechanism Implicated in Usher Syndrome Type 1. Frontiers in Genetics. 11: 623. PMID 32714370 DOI: 10.3389/Fgene.2020.00623 |
0.375 |
|
| 2020 |
Pellestor F, Gatinois V. Chromoanagenesis: a piece of the macroevolution scenario. Molecular Cytogenetics. 13: 3. PMID 32010222 DOI: 10.1186/S13039-020-0470-0 |
0.418 |
|
| 2019 |
Erkilic N, Gatinois V, Torriano S, Bouret P, Sanjurjo-Soriano C, Luca V, Damodar K, Cereso N, Puechberty J, Sanchez-Alcudia R, Hamel CP, Ayuso C, Meunier I, Pellestor F, Kalatzis V. A Novel Chromosomal Translocation Identified due to Complex Genetic Instability in iPSC Generated for Choroideremia. Cells. 8. PMID 31514470 DOI: 10.3390/Cells8091068 |
0.476 |
|
| 2019 |
Zenagui R, Bernicot I, Ranisavljevic N, Haquet E, Ferrieres-Hoa A, Pellestor F, Anahory T. Inheritance of imbalances in recurrent chromosomal translocation t(11;22): clarification by PGT-SR and sperm-FISH analysis. Reproductive Biomedicine Online. PMID 31097322 DOI: 10.1016/J.Rbmo.2019.02.010 |
0.483 |
|
| 2019 |
Pellestor F. Chromoanagenesis: cataclysms behind complex chromosomal rearrangements. Molecular Cytogenetics. 12: 6. PMID 30805029 DOI: 10.1186/S13039-019-0415-7 |
0.526 |
|
| 2018 |
Pellestor F, Gatinois V. Chromoanasynthesis: another way for the formation of complex chromosomal abnormalities in human reproduction. Human Reproduction (Oxford, England). 33: 1381-1387. PMID 30325427 DOI: 10.1093/Humrep/Dey231 |
0.558 |
|
| 2018 |
Pellestor F, Gatinois V. Chromothripsis, a credible chromosomal mechanism in evolutionary process. Chromosoma. PMID 30088093 DOI: 10.1007/S00412-018-0679-4 |
0.492 |
|
| 2018 |
Yauy K, Gatinois V, Guignard T, Sati S, Puechberty J, Gaillard JB, Schneider A, Pellestor F. Looking for Broken TAD Boundaries and Changes on DNA Interactions: Clinical Guide to 3D Chromatin Change Analysis in Complex Chromosomal Rearrangements and Chromothripsis. Methods in Molecular Biology (Clifton, N.J.). 1769: 353-361. PMID 29564835 DOI: 10.1007/978-1-4939-7780-2_22 |
0.452 |
|
| 2018 |
Pellestor F. Chromothripsis and the Macroevolution Theory. Methods in Molecular Biology (Clifton, N.J.). 1769: 43-49. PMID 29564817 DOI: 10.1007/978-1-4939-7780-2_4 |
0.464 |
|
| 2018 |
Pellestor F, Gatinois V. Potential Role of Chromothripsis in the Genesis of Complex Chromosomal Rearrangements in Human Gametes and Preimplantation Embryo. Methods in Molecular Biology (Clifton, N.J.). 1769: 35-41. PMID 29564816 DOI: 10.1007/978-1-4939-7780-2_3 |
0.519 |
|
| 2018 |
Marcozzi A, Pellestor F, Kloosterman WP. The Genomic Characteristics and Origin of Chromothripsis. Methods in Molecular Biology (Clifton, N.J.). 1769: 3-19. PMID 29564814 DOI: 10.1007/978-1-4939-7780-2_1 |
0.453 |
|
| 2015 |
Schneider A, Puechberty J, Ng BL, Coubes C, Gatinois V, Tournaire M, Girard M, Dumont B, Bouret P, Magnetto J, Baghdadli A, Pellestor F, Geneviève D. Identification of disrupted AUTS2 and EPHA6 genes by array painting in a patient carrying a de novo balanced translocation t(3;7) with intellectual disability and neurodevelopment disorder. American Journal of Medical Genetics. Part A. PMID 26333717 DOI: 10.1002/Ajmg.A.37350 |
0.427 |
|
| 2015 |
Bai Q, Ramirez JM, Becker F, Pantesco V, Lavabre-Bertrand T, Hovatta O, Lemaître JM, Pellestor F, De Vos J. Temporal analysis of genome alterations induced by single-cell passaging in human embryonic stem cells. Stem Cells and Development. 24: 653-62. PMID 25254421 DOI: 10.1089/Scd.2014.0292 |
0.307 |
|
| 2014 |
Tachon G, Lefort G, Puechberty J, Schneider A, Jeandel C, Boulot P, Prodhomme O, Meyer P, Taviaux S, Touitou I, Pellestor F, Geneviève D, Gatinois V. Discordant sex in monozygotic XXY/XX twins: a case report. Human Reproduction (Oxford, England). 29: 2814-20. PMID 25336706 DOI: 10.1093/Humrep/Deu275 |
0.405 |
|
| 2014 |
Gatinois V, Puechberty J, Lefort G, Geneviève D, Pellestor F. [Complex chromosomal rearrangements: a paradigm for the study of chromosomal instability]. Medecine Sciences : M/S. 30: 55-63. PMID 24472460 DOI: 10.1051/Medsci/20143001014 |
0.509 |
|
| 2014 |
Pellestor F. Chromothripsis: how does such a catastrophic event impact human reproduction? Human Reproduction (Oxford, England). 29: 388-93. PMID 24452388 DOI: 10.1093/Humrep/Deu003 |
0.566 |
|
| 2014 |
Bhatt SS, Manvelyan M, Moradkhani K, Hunstig F, Mrasek K, Puechberty J, Lefort G, Sarda P, Weise A, Liehr T, Pellestor F. Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis. Cytogenetic and Genome Research. 142: 145-9. PMID 24217531 DOI: 10.1159/000356142 |
0.753 |
|
| 2013 |
Gatinois V, Lefort G, Coubes C, Puechberty J, Schneider A, Taviaux T, Tournaire M, Di Nicola M, Girard M, Sarda P, Pellestor F. P-58 When transmission modifies the complexity of familial chromosome rearrangements Reproductive Biomedicine Online. 26: S49. DOI: 10.1016/S1472-6483(13)60121-2 |
0.308 |
|
| 2012 |
Bernicot I, Schneider A, Mace A, Hamamah S, Hedon B, Pellestor F, Anahory T. Analysis using fish of sperm and embryos from two carriers of rare rob(13;21) and rob(15;22) robertsonian translocation undergoing PGD European Journal of Medical Genetics. 55: 245-251. PMID 22406402 DOI: 10.1016/J.Ejmg.2012.02.003 |
0.54 |
|
| 2011 |
Nili HA, Mozdarani H, Pellestor F. Impact of DNA damage on the frequency of sperm chromosomal aneuploidy in normal and subfertile men. Iranian Biomedical Journal. 15: 122-9. PMID 22395136 DOI: 10.6091/Ibj.990.2012 |
0.367 |
|
| 2011 |
Delhanty JD, Pellestor F. Aneuploidy. Preface. Cytogenetic and Genome Research. 133: 89-90. PMID 21487226 DOI: 10.1159/000324234 |
0.395 |
|
| 2011 |
Pellestor F, Anahory T, Lefort G, Puechberty J, Liehr T, Hédon B, Sarda P. Complex chromosomal rearrangements: origin and meiotic behavior Human Reproduction Update. 17: 476-494. PMID 21486858 DOI: 10.1093/Humupd/Dmr010 |
0.411 |
|
| 2011 |
Pellestor F, Puechberty J, Weise A, Lefort G, Anahory T, Liehr T, Sarda P. Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier. Fertility and Sterility. 95: 2433.e17-22. PMID 21367411 DOI: 10.1016/J.Fertnstert.2011.01.159 |
0.343 |
|
| 2010 |
Pellestor F, Monzo C, Hamamah S. PNA-FISH on human sperm. Methods in Molecular Biology (Clifton, N.J.). 659: 283-9. PMID 20809320 DOI: 10.1007/978-1-60761-789-1_21 |
0.413 |
|
| 2010 |
Brugnon F, Janny L, Communal Y, Darcha C, Szczepaniak C, Pellestor F, Vago P, Pons-Rejraji H, Artonne C, Grizard G. Apoptosis and meiotic segregation in ejaculated sperm from Robertsonian translocation carrier patients Human Reproduction. 25: 1631-1642. PMID 20472914 DOI: 10.1093/Humrep/Deq113 |
0.326 |
|
| 2010 |
Bernicot I, Dechanet C, MacE A, Hedon B, Hamamah S, Pellestor F, Anahory T. Predictive value of sperm-FISH analysis on the outcome of preimplantation genetic diagnosis (PGD) for a pericentric inversion inv5(p15.3q11.2) carrier Human Reproduction. 25: 1818-1823. PMID 20406738 DOI: 10.1093/humrep/deq101 |
0.472 |
|
| 2010 |
Loup V, Bernicot I, Janssens P, Hedon B, Hamamah S, Pellestor F, Anahory T. Combined FISH and PRINS sperm analysis of complex chromosome rearrangement t(1;19;13): an approach facilitating PGD Molecular Human Reproduction. 16: 111-116. PMID 20019162 DOI: 10.1093/Molehr/Gap105 |
0.596 |
|
| 2009 |
Ferrières A, Reyftmann L, Pellestor F, Hédon B, Decaud H, Hamamah S. Oocyte recovery post human follicular fluid centrifugation in modified natural cycle and achieving embryo. Reproductive Biomedicine Online. 18: 671-3. PMID 19549446 DOI: 10.1016/S1472-6483(10)60012-0 |
0.329 |
|
| 2009 |
Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Manvelyan M, Hunstig F, Lefort G, Weise A, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F. Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions. European Journal of Human Genetics : Ejhg. 17: 44-50. PMID 18685557 DOI: 10.1038/Ejhg.2008.144 |
0.838 |
|
| 2009 |
Pellestor F, Monzo C, Nadal L, Vos JD, Hamamah S. Occurrence of chromosomal imbalance in human embryonic stem cell lines Fertility and Sterility. 92. DOI: 10.1016/J.Fertnstert.2009.07.1338 |
0.449 |
|
| 2008 |
Gasca S, Reyftmann L, Pellestor F, Rème T, Assou S, Anahory T, Dechaud H, Klein B, De Vos J, Hamamah S. Total fertilization failure and molecular abnormalities in metaphase II oocytes. Reproductive Biomedicine Online. 17: 772-81. PMID 19079960 DOI: 10.1016/S1472-6483(10)60404-X |
0.31 |
|
| 2008 |
Manvelyan M, Hunstig F, Bhatt S, Mrasek K, Pellestor F, Weise A, Simonyan I, Aroutiounian R, Liehr T. Chromosome distribution in human sperm - a 3D multicolor banding-study. Molecular Cytogenetics. 1: 25. PMID 19014589 DOI: 10.1186/1755-8166-1-25 |
0.761 |
|
| 2008 |
Pellestor F, Paulasova P, Hamamah S. Peptide nucleic acids (PNAs) as diagnostic devices for genetic and cytogenetic analysis. Current Pharmaceutical Design. 14: 2439-44. PMID 18781993 DOI: 10.2174/138161208785777405 |
0.476 |
|
| 2008 |
Vialard F, Pellestor F. [Benefit of human gamete cytogenetics: results and perspectives]. Pathologie-Biologie. 56: 388-99. PMID 18534785 DOI: 10.1016/j.patbio.2008.04.012 |
0.451 |
|
| 2008 |
Manvelyan M, Riegel M, Santos M, Fuster C, Pellestor F, Mazaurik ML, Schulze B, Polityko A, Tittelbach H, Reising-Ackermann G, Belitz B, Hehr U, Kelbova C, Volleth M, Gödde E, et al. Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature. International Journal of Molecular Medicine. 21: 705-14. PMID 18506363 DOI: 10.3892/Ijmm.21.6.705 |
0.522 |
|
| 2008 |
Manvelyan M, Hunstig F, Mrasek K, Bhatt S, Pellestor F, Weise A, Liehr T. Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon. Molecular Cytogenetics. 1: 9. PMID 18471270 DOI: 10.1186/1755-8166-1-9 |
0.765 |
|
| 2008 |
Loup V, Bernicot T, Janssens P, Pellestor F, Lefort G, Hamamah S, Anahory T. 6.001 Sperm FISH analysis of a familial complex chromosome rearrangement: predictive value on the outcome of PGD Reproductive Biomedicine Online. 16. DOI: 10.1016/S1472-6483(10)61396-X |
0.422 |
|
| 2008 |
Pellestor F, Bhatt S, Puechberty J, Lefort G, Liehr T, Sarda P, Hamamah S. The meiotic segregation of paracentric inversions: how breakpoint mapping can make the difference Reproductive Biomedicine Online. 16. DOI: 10.1016/S1472-6483(10)61357-0 |
0.666 |
|
| 2008 |
Loup V, Bernicot I, Janssens P, Pellestor F, Hamamah S, Anahory T. Complex chromosome rearrangement (CCR): first sperm fish analysis of a t(1;19;13) and predictive value on the outcome of preimplantation genetic diagnosis (PGD) Fertility and Sterility. 90: S298-S299. DOI: 10.1016/J.FERTNSTERT.2008.07.993 |
0.32 |
|
| 2008 |
Bhatt S, Liehr T, Lefort G, Sarda P, Hamamah S, Pellestor F. Segregation analysis of paracentric inversions in human sperm: inverted segment size, low copy repeats (LCRs) and recombination hot spots have a story to tell Fertility and Sterility. 90. DOI: 10.1016/J.Fertnstert.2008.07.1678 |
0.695 |
|
| 2007 |
Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Lefort G, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F. Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm. Molecular Human Reproduction. 13: 751-756. PMID 17913851 DOI: 10.1093/Molehr/Gam048 |
0.841 |
|
| 2007 |
Yurov YB, Iourov IY, Vorsanova SG, Liehr T, Kolotii AD, Kutsev SI, Pellestor F, Beresheva AK, Demidova IA, Kravets VS, Monakhov VV, Soloviev IV. Aneuploidy and confined chromosomal mosaicism in the developing human brain. Plos One. 2: e558. PMID 17593959 DOI: 10.1371/Journal.Pone.0000558 |
0.347 |
|
| 2007 |
Gasca S, Pellestor F, Assou S, Loup V, Anahory T, Dechaud H, De Vos J, Hamamah S. Identifying new human oocyte marker genes: a microarray approach. Reproductive Biomedicine Online. 14: 175-83. PMID 17298719 DOI: 10.1016/S1472-6483(10)60785-7 |
0.305 |
|
| 2007 |
Bhatt S, Puechberty J, Thomas L, Sarda P, Hamamah S, Pellestor F. Segregation analysis of two paracentric inversions using a new approach of breakpoint characterization Fertility and Sterility. 88. DOI: 10.1016/J.Fertnstert.2007.07.1143 |
0.636 |
|
| 2006 |
Pellestor F, Paulasova P, Andréo B, Lefort G, Hamamah S. Multicolor PRINS and multicolor PNA. Cytogenetic and Genome Research. 114: 263-9. PMID 16954664 DOI: 10.1159/000094211 |
0.424 |
|
| 2006 |
Moradkhani K, Puechberty J, Bhatt S, Lespinasse J, Vago P, Lefort G, Sarda P, Hamamah S, Pellestor F. Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: A Case Report Human Reproduction. 21: 3193-3198. PMID 16917122 DOI: 10.1093/Humrep/Del314 |
0.81 |
|
| 2006 |
Pellestor F. Development and adaptation of the PRINS technology: an overview. Methods in Molecular Biology (Clifton, N.J.). 334: 211-20. PMID 16861766 DOI: 10.1385/1-59745-068-5:211 |
0.518 |
|
| 2006 |
Pellestor F, Andréo B, Anahory T, Hamamah S. PRINS as an efficient tool for aneuploidy assessment in human oocytes and preimplantation embryos. Methods in Molecular Biology (Clifton, N.J.). 334: 151-60. PMID 16861761 DOI: 10.1385/1-59745-068-5:151 |
0.452 |
|
| 2006 |
Iourov IY, Vorsanova SG, Pellestor F, Yurov YB. Brain tissue preparations for chromosomal PRINS labeling. Methods in Molecular Biology (Clifton, N.J.). 334: 123-32. PMID 16861758 DOI: 10.1385/1-59745-068-5:123 |
0.405 |
|
| 2006 |
Pellestor F, Andréo B, Puechberty J, Lefort G, Sarda P. Analysis of sperm aneuploidy by PRINS. Methods in Molecular Biology (Clifton, N.J.). 334: 49-59. PMID 16861752 DOI: 10.1385/1-59745-068-5:49 |
0.479 |
|
| 2006 |
Pellestor F, Paulasova P. PRINS combined with peptide nucleic acid labeling. Methods in Molecular Biology (Clifton, N.J.). 334: 15-22. PMID 16861748 DOI: 10.1385/1-59745-068-5:15 |
0.379 |
|
| 2006 |
Pellestor F. In situ aneuploidy assessment in human sperm: the use of primed in situ and peptide nucleic acid-fluorescence in situ hybridization techniques. Asian Journal of Andrology. 8: 387-92. PMID 16763713 DOI: 10.1111/J.1745-7262.2006.00137.X |
0.473 |
|
| 2006 |
Pellestor F, Andréo B, Anahory T, Hamamah S. The occurrence of aneuploidy in human: lessons from the cytogenetic studies of human oocytes. European Journal of Medical Genetics. 49: 103-16. PMID 16530707 DOI: 10.1016/J.Ejmg.2005.08.001 |
0.52 |
|
| 2006 |
Moradkhani K, Puechberty J, Bhatt S, Vago P, Janny L, Lefort G, Hamamah S, Sarda P, Pellestor F. Meiotic segregation of rare Robertsonian translocations: sperm analysis of three t(14q;22q) cases Human Reproduction. 21: 1166-1171. PMID 16439506 DOI: 10.1093/Humrep/Dei477 |
0.828 |
|
| 2006 |
Moradkhani K, Puechberty J, Lefort G, Sarda P, Hamamah S, Pellestor F. P-975: Location of chromosome breakpoints and meiotic segregation in rare Robertsonian translocations Fertility and Sterility. 86. DOI: 10.1016/J.Fertnstert.2006.07.1372 |
0.767 |
|
| 2005 |
Pellestor F, Anahory T, Hamamah S. Effect of maternal age on the frequency of cytogenetic abnormalities in human oocytes. Cytogenetic and Genome Research. 111: 206-212. PMID 16192696 DOI: 10.1159/000086891 |
0.484 |
|
| 2005 |
Pellestor F, Paulasova P, Macek M, Hamamah S. [The peptide nucleic acids (PNAs): "high-tech" probes for genetic and molecular cytogenetic investigations]. Medecine Sciences : M/S. 21: 753-8. PMID 16115462 DOI: 10.1051/Medsci/2005218-9753 |
0.485 |
|
| 2005 |
Pinton A, Faraut T, Yerle M, Gruand J, Pellestor F, Ducos A. Comparison of male and female meiotic segregation patterns in translocation heterozygotes: a case study in an animal model (Sus scrofa domestica L.). Human Reproduction (Oxford, England). 20: 2476-82. PMID 15878917 DOI: 10.1093/HUMREP/DEI067 |
0.333 |
|
| 2005 |
Anahory T, Hamamah S, Andréo B, Hédon B, Claustres M, Sarda P, Pellestor F. Sperm segregation analysis of a (13;22) Robertsonian translocation carrier by FISH: a comparison of locus-specific probe and whole chromosome painting Human Reproduction. 20: 1850-1854. PMID 15845597 DOI: 10.1093/Humrep/Deh886 |
0.614 |
|
| 2005 |
Pellestor F, Paulasova P, Macek M, Hamamah S. The use of peptide nucleic acids for in situ identification of human chromosomes. The Journal of Histochemistry and Cytochemistry : Official Journal of the Histochemistry Society. 53: 395-400. PMID 15750028 DOI: 10.1369/Jhc.4R6399.2005 |
0.516 |
|
| 2005 |
Pellestor F, Anahory T, Hamamah S. The chromosomal analysis of human oocytes. An overview of established procedures Human Reproduction Update. 11: 15-32. PMID 15569701 DOI: 10.1093/Humupd/Dmh051 |
0.572 |
|
| 2005 |
Pellestor F, Moradkani K, Puechberty J, Lefort G, Anahory T, Sarda P, Hamamah S. O▪48 Rare Robertsonian translocations: sperm analysis of meiotic segregation Reproductive Biomedicine Online. 10: 16. DOI: 10.1016/S1472-6483(11)60269-1 |
0.467 |
|
| 2004 |
Paulasova P, Pellestor F. The peptide nucleic acids (PNAs): a new generation of probes for genetic and cytogenetic analyses. Annales De Genetique. 47: 349-58. PMID 15581832 DOI: 10.1016/J.Anngen.2004.07.001 |
0.355 |
|
| 2004 |
Pellestor F, Anahory T, Andréo B, Régnier-Vigouroux G, Soulié JP, Baudouin M, Demaille J. Fluorescence in situ hybridization analysis of human oocytes: advantages of a double-labeling procedure. Fertility and Sterility. 82: 919-22. PMID 15482769 DOI: 10.1016/J.Fertnstert.2004.03.050 |
0.497 |
|
| 2004 |
Pellestor F. [Maternal age and chromosomal abnormalities in human oocytes]. Medecine Sciences : M/S. 20: 691-6. PMID 15329821 DOI: 10.1051/Medsci/2004206-7691 |
0.458 |
|
| 2004 |
Pellestor F, Paulasova P, Macek M, Hamamah S. The peptide nucleic acids: a new way for chromosomal investigation on isolated cells? Human Reproduction. 19: 1946-1951. PMID 15229198 DOI: 10.1093/Humrep/Deh386 |
0.463 |
|
| 2004 |
Pellestor F, Paulasova P. The peptide nucleic acids (PNAs), powerful tools for molecular genetics and cytogenetics. European Journal of Human Genetics : Ejhg. 12: 694-700. PMID 15213706 DOI: 10.1038/Sj.Ejhg.5201226 |
0.346 |
|
| 2004 |
Pellestor F, Paulasova P. The peptide nucleic acids (PNAs): introduction to a new class of probes for chromosomal investigation. Chromosoma. 112: 375-80. PMID 15156326 DOI: 10.1007/S00412-004-0282-8 |
0.392 |
|
| 2004 |
Krabchi K, Lavoie J, Coullin P, Bronsard M, Pellestor F, Yan J, Drouin R. [From the conception of the PRINS to its coronation]. MéDecine Sciences : M/S. 20: 465-73. PMID 15124121 DOI: 10.1051/Medsci/2004204465 |
0.376 |
|
| 2004 |
Paulasova P, Andréo B, Diblik J, Macek M, Pellestor F. The peptide nucleic acids as probes for chromosomal analysis: application to human oocytes, polar bodies and preimplantation embryos. Molecular Human Reproduction. 10: 467-472. PMID 15100384 DOI: 10.1093/Molehr/Gah061 |
0.554 |
|
| 2004 |
Pellestor F, Paulasova P. The peptide nucleic acids, efficient tools for molecular diagnosis (Review). International Journal of Molecular Medicine. 13: 521-5. PMID 15010851 DOI: 10.3892/Ijmm.13.4.521 |
0.362 |
|
| 2004 |
Pellestor F, Anahory T, Andréo B, Régnier-Vigouroux G, Soulié JP, Baudouin M, Demaille J. Fast multicolor primed in situ protocol for chromosome identification in isolated cells may be used for human oocytes and polar bodies. Fertility and Sterility. 81: 408-15. PMID 14967382 DOI: 10.1016/J.Fertnstert.2003.08.014 |
0.438 |
|
| 2004 |
Pellestor F, Anahory T, Andréo B, Hédon B, Hamamah S. Maternal aging and aneuploidy: Lessons from human oocytes Fertility and Sterility. 82. DOI: 10.1016/J.Fertnstert.2004.07.755 |
0.302 |
|
| 2004 |
Pellestor F, Anahory T, Andréo B, Hédon B, Hamamah S. The topological organization of chromosomes in the human male pronucleus during fertilization Fertility and Sterility. 82. DOI: 10.1016/J.Fertnstert.2004.07.754 |
0.509 |
|
| 2004 |
Anahory T, Andréo B, Hamamah S, Déchaud H, Pellestor F. Sequential multiple probe fluorescence in situ hybridization (FISH) analysis of human oocytes and polar bodies Fertility and Sterility. 82. DOI: 10.1016/J.Fertnstert.2004.07.696 |
0.387 |
|
| 2004 |
Pellestor F, Paulasova P, Anahory T, Andréo B, Macek M, Hamamah S. The peptide nucleic acids (PNAs) as probes for chromosomal analysis of human oocytes and preimplantation embryos Fertility and Sterility. 82: S29. DOI: 10.1016/J.FERTNSTERT.2004.07.079 |
0.388 |
|
| 2003 |
Anahory T, Andréo B, Régnier‐Vigouroux G, Soulie JP, Baudouin M, Demaille J, Pellestor F. Sequential multiple probe fluorescence in-situ hybridization analysis of human oocytes and polar bodies by combining centromeric labelling and whole chromosome painting. Molecular Human Reproduction. 9: 577-585. PMID 12970395 DOI: 10.1093/Molehr/Gag075 |
0.609 |
|
| 2003 |
Pellestor F, Andréo B, Taneja K, Williams B. PNA on human sperm: a new approach for in situ aneuploidy estimation. European Journal of Human Genetics : Ejhg. 11: 337-41. PMID 12700607 DOI: 10.1038/Sj.Ejhg.5200958 |
0.468 |
|
| 2003 |
Lefort G, Blanchet P, Belgrade N, Rivier F, Chaze AM, Sarda P, Demaille J, Pellestor F. Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion. American Journal of Medical Genetics. Part A. 118: 333-8. PMID 12698965 |
0.497 |
|
| 2003 |
Pellestor F, Andréo B, Arnal F, Humeau C, Demaille J. Maternal aging and chromosomal abnormalities: new data drawn from in vitro unfertilized human oocytes. Human Genetics. 112: 195-203. PMID 12522562 DOI: 10.1007/S00439-002-0852-X |
0.463 |
|
| 2002 |
Lefort G, Blanchet P, Belgrade N, Rivier F, Chaze AM, Sarda P, Demaille J, Pellestor F. Stable dicentric duplication-deficiency chromosome 14 resulting from crossing-over within a maternal paracentric inversion. American Journal of Medical Genetics. 113: 333-8. PMID 12457404 DOI: 10.1002/Ajmg.B.10720 |
0.579 |
|
| 2002 |
Pellestor F, Malki S, Andréo B, Lefort G. Ultra-rapid multicolor PRINS protocol for chromosome detection in human sperm. Chromosome Research. 10: 359-367. PMID 12296518 DOI: 10.1023/A:1016845517798 |
0.563 |
|
| 2002 |
Pellestor F, Andréo B, Arnal F, Humeau C, Demaille J. Mechanisms of non-disjunction in human female meiosis: the co-existence of two modes of malsegregation evidenced by the karyotyping of 1397 in-vitro unfertilized oocytes. Human Reproduction (Oxford, England). 17: 2134-45. PMID 12151449 DOI: 10.1093/Humrep/17.8.2134 |
0.474 |
|
| 2002 |
Coullin P, Roy L, Pellestor F, Candelier JJ, Bed-Hom B, Guillier-Gencik Z, Bernheim A. PRINS, the other in situ DNA labeling method useful in cellular biology. American Journal of Medical Genetics. 107: 127-35. PMID 11807887 DOI: 10.1002/Ajmg.10103 |
0.367 |
|
| 2002 |
Pellestor F, Imbert I, Andréo B. Rapid chromosome detection by PRINS in human sperm. American Journal of Medical Genetics. 107: 109-14. PMID 11807883 DOI: 10.1002/Ajmg.10101 |
0.603 |
|
| 2001 |
Imbert I, Coignet LJA, Pellestor F. 6p abnormalities and TNF-α over-expression in retinoblastoma cell line Cancer Genetics and Cytogenetics. 128: 141-147. PMID 11463453 DOI: 10.1016/S0165-4608(01)00402-2 |
0.474 |
|
| 2001 |
Pellestor F, Imbert I, Andréo B, Lefort G. Study of the occurrence of interchromosomal effect in spermatozoa of chromosomal rearrangement carriers by fluorescence in-situ hybridization and primed in-situ labelling techniques. Human Reproduction (Oxford, England). 16: 1155-64. PMID 11387286 DOI: 10.1093/Humrep/16.6.1155 |
0.599 |
|
| 2001 |
Lefort G, Blanchet P, Chaze AM, Girardet A, Sarda P, Demaille J, Pellestor F. Cytogenetic and molecular study of a jumping translocation in a baby with Dandy-Walker malformation Journal of Medical Genetics. 38: 67-73. PMID 11334011 DOI: 10.1136/Jmg.38.1.67 |
0.773 |
|
| 2000 |
Catalan J, Auffray JC, Pellestor F, Britton-Davidian J. Spontaneous occurrence of a Robertsonian fusion involving chromosome 19 by single whole-arm reciprocal translocation (WART) in wild-derived house mice. Chromosome Research : An International Journal On the Molecular, Supramolecular and Evolutionary Aspects of Chromosome Biology. 8: 593-601. PMID 11117355 DOI: 10.1023/A:1009281823488 |
0.558 |
|
| 2000 |
Girardet A, McPeek MS, Leeflang EP, Munier F, Arnheim N, Claustres M, Pellestor F. Meiotic segregation analysis of RB1 alleles in retinoblastoma pedigrees by use of single-sperm typing. American Journal of Human Genetics. 66: 167-75. PMID 10631148 DOI: 10.1086/302715 |
0.717 |
|
| 2000 |
Imbert I, Coignet LJA, Pellestor F. Molecular analysis of chromosome 6p rearrangement in retinoblastoma Genetics in Medicine. 2: 105-105. DOI: 10.1097/00125817-200001000-00198 |
0.404 |
|
| 1999 |
Pellestor F, Andréo B, Coullin P. Interphasic Analysis of Aneuploidy in Cancer Cell Lines Using Primed In Situ Labeling Cancer Genetics and Cytogenetics. 111: 111-118. PMID 10347546 DOI: 10.1016/S0165-4608(98)00224-6 |
0.508 |
|
| 1999 |
Girardet A, Lien S, Leeflang EP, Beaufrère L, Tuffery S, Munier F, Arnheim N, Claustres M, Pellestor F. Direct estimation of the recombination frequency between the RB1 gene and two closely linked microsatellites using sperm typing European Journal of Human Genetics. 7: 239-242. PMID 10196709 DOI: 10.1038/Sj.Ejhg.5200250 |
0.688 |
|
| 1999 |
Girardet A, Pellestor F, Claustres M. Mise au point des conditions d'amplification de l'ADN unicellulaire. M S-Medecine Sciences. 15: 86-89. DOI: 10.4267/10608/1203 |
0.624 |
|
| 1998 |
Munier FL, Thonney F, Girardet A, Balmer A, Claustre M, Pellestor F, Senn A, Pescia G, Schorderet DF. Evidence of Somatic and Germinal Mosaicism in Pseudo–Low-Penetrant Hereditary Retinoblastoma, by Constitutional and Single-Sperm Mutation Analysis American Journal of Human Genetics. 63: 1903-1907. PMID 9837842 DOI: 10.1086/302138 |
0.599 |
|
| 1998 |
Orsetti B, Lefort G, Boulot P, Andreo B, Pellestor F. Fetal cells in maternal blood: the use of primed in situ (PRINS) labelling technique for fetal cell detection and sex assessment Prenatal Diagnosis. 18: 1014-1022. PMID 9826893 DOI: 10.1002/(Sici)1097-0223(1998100)18:10<1014::Aid-Pd382>3.0.Co;2-Z |
0.376 |
|
| 1998 |
Pellestor F, Girardet A, Andréo B. Efficiency of Primed In Situ Labeling (PRINS) Method for Interphasic Chromosomal Screening: a Review Acta Histochemica Et Cytochemica. 31: 369-374. DOI: 10.1267/Ahc.31.369 |
0.779 |
|
| 1997 |
Pellestor F, Girardet A, Coignet L, Andréo B, Lefort G, Charlieu JP. Cytogenetic analysis of meiotic segregation in sperm from two males heterozygous for reciprocal translocations using PRINS and humster techniques. Cytogenetic and Genome Research. 78: 202-208. PMID 9465888 DOI: 10.1159/000134657 |
0.728 |
|
| 1997 |
Coullin P, Pellestor F. Rapid characterization of human chromosomes in hybrid cell lines by primed in situ (PRINS) labeling Somatic Cell and Molecular Genetics. 23: 159-163. PMID 9330644 DOI: 10.1007/Bf02679975 |
0.565 |
|
| 1997 |
Coullin P, Andréo B, Charlieu JP, Candelier J, Pellestor F. Primed in situ (PRINS) Labelling with Alu and Satellite Primers for Rapid Characterization of Human Chromosomes in Hybrid Cell Lines Chromosome Research. 5: 307-312. PMID 9292235 DOI: 10.1023/B:Chro.0000038761.15856.4D |
0.564 |
|
| 1997 |
Pellestor F, Girardet A, Andréo B, Lefort G, Charlieu JP. Incidence of chromosome 1 disomy in human sperm estimated by the primed in situ (PRINS) labeling technique Cytogenetic and Genome Research. 76: 192-195. PMID 9186522 DOI: 10.1159/000134547 |
0.77 |
|
| 1997 |
Girardet A, Pellestor F, Tuffery S, Claustres M, Munier F, Duperray C. Amplification of the RB1.20 polymorphism in single spermatozoa Journal of Assisted Reproduction and Genetics. 14: 176-179. PMID 9090563 DOI: 10.1007/Bf02766137 |
0.632 |
|
| 1997 |
Charlieu JP, Pellestor F. Chromosome-specific PRINS. Methods in Molecular Biology (Clifton, N.J.). 71: 7-12. PMID 8959684 DOI: 10.1385/0-89603-395-3:7 |
0.492 |
|
| 1996 |
Pellestor F, Girardet A, Andréo B, Lefort G, Charlieu JP. The PRINS technique: potential use for rapid preimplantation embryo chromosome screening Molecular Human Reproduction. 2: 135-138. PMID 9238671 DOI: 10.1093/Molehr/2.2.135 |
0.795 |
|
| 1996 |
Pellestor F, Girardet A, Lefort G, Andréo B, Charlieu JP. Rapid chromosome detection in human gametes, zygotes, and preimplantation embryos using the PRINS technique. Journal of Assisted Reproduction and Genetics. 13: 675-680. PMID 8897129 DOI: 10.1007/Bf02069648 |
0.788 |
|
| 1996 |
Pellestor F, Girardet A, Andréo B, Lefort G, Charlieu JP. Preimplantation embryo chromosome analysis by primed in situ labeling method Fertility and Sterility. 66: 781-786. PMID 8893685 DOI: 10.1016/S0015-0282(16)58636-1 |
0.749 |
|
| 1996 |
Girardet A, Coignet L, Andréo B, Lefort G, Charlieu JP, Pellestor F. Aneuploidy detection in human sperm nuclei using PRINS technique. American Journal of Medical Genetics. 64: 488-492. PMID 8862627 DOI: 10.1002/(Sici)1096-8628(19960823)64:3<488::Aid-Ajmg8>3.0.Co;2-L |
0.768 |
|
| 1996 |
Coignet L, Girardet A, Andréo B, Charlieu JP, Pellestor F. Double and triple in situ chromosomal labeling of human spermatozoa by PRINS. Cytogenetic and Genome Research. 73: 300-303. PMID 8751381 DOI: 10.1159/000134361 |
0.773 |
|
| 1996 |
Pellestor F, Quenesson I, Coignet L, Girardet A, Andréo B, Lefort G, Charlieu JP. FISH and PRINS, a strategy for rapid chromosome screening: application to the assessment of aneuploidy in human sperm. Cytogenetic and Genome Research. 72: 34-36. PMID 8565628 DOI: 10.1159/000134155 |
0.794 |
|
| 1996 |
Pellestor F, Quennesson I, Coignet L, Girardet A, Andréo B, Charlieu JP. Direct detection of disomy in human sperm by the PRINS technique. Human Genetics. 97: 21-25. PMID 8557255 DOI: 10.1007/Bf00218827 |
0.789 |
|
| 1996 |
Girardet A, Claustres M, Pellestor F. Typage génique des spermatozoïdes : application à l'étude du génome M S-Medecine Sciences. 12: 1389-1393. DOI: 10.4267/10608/681 |
0.604 |
|
| 1996 |
Spurr NK, Naylor S, Zatsepina OV, Schöfer C, Weipoltshammer K, Mosgoeller W, Almeder M, Stefanova VN, Jordan EG, Wachtler F, Raabe M, Seedorf U, Hameister H, Ellinghaus P, Assmann G, ... ... Pellestor F, et al. Subject Index, Vol. 73, 1996 Cytogenetic and Genome Research. 73: 348-348. DOI: 10.1159/000134374 |
0.569 |
|
| 1996 |
Spurr NK, Naylor S, Zatsepina OV, Schöfer C, Weipoltshammer K, Mosgoeller W, Almeder M, Stefanova VN, Jordan EG, Wachtler F, Raabe M, Seedorf U, Hameister H, Ellinghaus P, Assmann G, ... ... Pellestor F, et al. Contents, Vol. 73, 1996 Cytogenetic and Genome Research. 73. DOI: 10.1159/000134351 |
0.559 |
|
| 1995 |
Pellestor F. The cytogenetic analysis of human zygotes and preimplantation embryos Human Reproduction Update. 1: 581-585. PMID 9079398 DOI: 10.1093/Humupd/1.6.581 |
0.508 |
|
| 1995 |
Pellestor F, Girardet A, Lefort G, Andréo B, Charlieu JP. Use of the primed in situ labelling (PRINS) technique for a rapid detection of chromosomes 13, 16, 18, 21, X and Y Human Genetics. 95: 12-17. PMID 7814017 DOI: 10.1007/Bf00225066 |
0.782 |
|
| 1995 |
Pellestor F, Girardet A, Lefort G, Andréo B, Charlieu JP. PRINS as a method for rapid chromosomal labeling on human spermatozoa Molecular Reproduction and Development. 40: 333-337. PMID 7772343 DOI: 10.1002/Mrd.1080400309 |
0.75 |
|
| 1995 |
Pellestor F, Girardet A, Lefort G, Andréo B, Charlieu JP. Selection of chromosome-specific primers and their use in simple and double PRINS techniques for rapid in situ identification of human chromosomes. Cytogenetic and Genome Research. 70: 138-142. PMID 7736779 DOI: 10.1159/000134079 |
0.785 |
|
| 1995 |
Pellestor F, Girardet A, Lefort G, Andréo B, Charlieu JP. Rapid in situ detection of chromosome 21 by PRINS technique American Journal of Medical Genetics. 56: 393-397. PMID 7604848 DOI: 10.1002/Ajmg.1320560409 |
0.783 |
|
| 1994 |
Pellestor F, Dufour MC, Arnal F, Humeau C. Direct assessment of the rate of chromosomal abnormalities in grade IV human embryos produced by in-vitro fertilization procedure. Human Reproduction (Oxford, England). 9: 293-302. PMID 8027286 DOI: 10.1093/Oxfordjournals.Humrep.A138497 |
0.497 |
|
| 1994 |
Pellestor F, Girardet A, Andréo B, Charlieu J. A polymorphic alpha satellite sequence specific for human chromosome 13 detected by oligonucleotide primed in situ labelling (PRINS). Human Genetics. 94: 346-348. PMID 7927326 DOI: 10.1007/Bf00201590 |
0.76 |
|
| 1994 |
Pellestor F, Girardet A, AndréO B, Arnal F, Humeau C. Relationship between morphology and chromosomal constitution in human preimplantation embryo. Molecular Reproduction and Development. 39: 141-146. PMID 7826614 DOI: 10.1002/Mrd.1080390204 |
0.758 |
|
| 1993 |
Pellestor F, Dufour MC, Arnal F, Humeau C. A simplified method for R banding of human oocyte chromosomes. Human Reproduction (Oxford, England). 8: 604-8. PMID 8501193 DOI: 10.1093/Oxfordjournals.Humrep.A138104 |
0.517 |
|
| 1992 |
Pellestor F. Differential distribution of aneuploidy in human gametes according to their sex. Human Reproduction (Oxford, England). 6: 1252-8. PMID 1752927 DOI: 10.1093/OXFORDJOURNALS.HUMREP.A137522 |
0.466 |
|
| 1991 |
Pellestor F. Frequency and distribution of aneuploidy in human female gametes. Human Genetics. 86: 283-288. PMID 1997383 DOI: 10.1007/Bf00202410 |
0.572 |
|
| 1991 |
Pellestor F, Sèle B. Relationship between sexual abstinence of men and chromosomally abnormal spermatozoa. Journal of Reproduction and Fertility. 91: 65-71. PMID 1995863 DOI: 10.1530/JRF.0.0910065 |
0.387 |
|
| 1990 |
Pellestor F. Analysis of meiotic segregation in a man heterozygous for a 13;15 Robertsonian translocation and a review of the literature. Human Genetics. 85: 49-54. PMID 2358303 DOI: 10.1007/Bf00276325 |
0.499 |
|
| 1987 |
Pellestor F, Sele B, Jalbert H. Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation Human Genetics. 76: 116-120. PMID 3475245 DOI: 10.1007/Bf00284905 |
0.524 |
|
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