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Items: 1 to 50 of 134

1.

Chromoanagenesis: cataclysms behind complex chromosomal rearrangements.

Pellestor F.

Mol Cytogenet. 2019 Feb 11;12:6. doi: 10.1186/s13039-019-0415-7. eCollection 2019. Review.

2.

Chromoanasynthesis: another way for the formation of complex chromosomal abnormalities in human reproduction.

Pellestor F, Gatinois V.

Hum Reprod. 2018 Aug 1;33(8):1381-1387. doi: 10.1093/humrep/dey231.

PMID:
30325427
3.

Chromothripsis, a credible chromosomal mechanism in evolutionary process.

Pellestor F, Gatinois V.

Chromosoma. 2019 Mar;128(1):1-6. doi: 10.1007/s00412-018-0679-4. Epub 2018 Aug 7. Review.

PMID:
30088093
4.

Looking for Broken TAD Boundaries and Changes on DNA Interactions: Clinical Guide to 3D Chromatin Change Analysis in Complex Chromosomal Rearrangements and Chromothripsis.

Yauy K, Gatinois V, Guignard T, Sati S, Puechberty J, Gaillard JB, Schneider A, Pellestor F.

Methods Mol Biol. 2018;1769:353-361. doi: 10.1007/978-1-4939-7780-2_22.

PMID:
29564835
5.

Chromothripsis and the Macroevolution Theory.

Pellestor F.

Methods Mol Biol. 2018;1769:43-49. doi: 10.1007/978-1-4939-7780-2_4. Review.

PMID:
29564817
6.

Potential Role of Chromothripsis in the Genesis of Complex Chromosomal Rearrangements in Human Gametes and Preimplantation Embryo.

Pellestor F, Gatinois V.

Methods Mol Biol. 2018;1769:35-41. doi: 10.1007/978-1-4939-7780-2_3. Review.

PMID:
29564816
7.

The Genomic Characteristics and Origin of Chromothripsis.

Marcozzi A, Pellestor F, Kloosterman WP.

Methods Mol Biol. 2018;1769:3-19. doi: 10.1007/978-1-4939-7780-2_1. Review.

PMID:
29564814
8.

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.

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.

Am J Med Genet A. 2015 Dec;167A(12):3031-7. doi: 10.1002/ajmg.a.37350. Epub 2015 Sep 3.

PMID:
26333717
9.

Chromothripsis: potential origin in gametogenesis and preimplantation cell divisions. A review.

Pellestor F, Gatinois V, Puechberty J, Geneviève D, Lefort G.

Fertil Steril. 2014 Dec;102(6):1785-96. doi: 10.1016/j.fertnstert.2014.09.006. Epub 2014 Oct 18. Review.

PMID:
25439810
10.

Discordant sex in monozygotic XXY/XX twins: a case report.

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.

Hum Reprod. 2014 Dec;29(12):2814-20. doi: 10.1093/humrep/deu275. Epub 2014 Oct 21.

PMID:
25336706
11.

Temporal analysis of genome alterations induced by single-cell passaging in human embryonic stem cells.

Bai Q, Ramirez JM, Becker F, Pantesco V, Lavabre-Bertrand T, Hovatta O, Lemaître JM, Pellestor F, De Vos J.

Stem Cells Dev. 2015 Mar 1;24(5):653-62. doi: 10.1089/scd.2014.0292. Epub 2014 Nov 25.

12.

[Chromothripsis, an unexpected novel form of complexity for chromosomal rearrangements].

Pellestor F, Gatinois V, Puechberty J, Geneviève D, Lefort G.

Med Sci (Paris). 2014 Mar;30(3):266-73. doi: 10.1051/medsci/20143003014. Epub 2014 Mar 31. Review. French.

13.

[Complex chromosomal rearrangements: a paradigm for the study of chromosomal instability].

Gatinois V, Puechberty J, Lefort G, Geneviève D, Pellestor F.

Med Sci (Paris). 2014 Jan;30(1):55-63. doi: 10.1051/medsci/20143001014. Epub 2014 Jan 24. Review. French.

14.

Chromothripsis: how does such a catastrophic event impact human reproduction?

Pellestor F.

Hum Reprod. 2014 Mar;29(3):388-93. doi: 10.1093/humrep/deu003. Epub 2014 Jan 21.

PMID:
24452388
15.

Inverted segment size and the presence of recombination hot spot clusters matter in sperm segregation analysis.

Bhatt SS, Manvelyan M, Moradkhani K, Hunstig F, Mrasek K, Puechberty J, Lefort G, Sarda P, Weise A, Liehr T, Pellestor F.

Cytogenet Genome Res. 2014;142(2):145-9. doi: 10.1159/000356142. Epub 2013 Nov 6. No abstract available.

PMID:
24217531
16.

Analysis using fish of sperm and embryos from two carriers of rare rob(13;21) and rob(15;22) robertsonian translocation undergoing PGD.

Bernicot I, Schneider A, Mace A, Hamamah S, Hedon B, Pellestor F, Anahory T.

Eur J Med Genet. 2012 Apr;55(4):245-51. doi: 10.1016/j.ejmg.2012.02.003. Epub 2012 Feb 22.

PMID:
22406402
17.
18.

Genes with a spike expression are clustered in chromosome (sub)bands and spike (sub)bands have a powerful prognostic value in patients with multiple myeloma.

Kassambara A, Hose D, Moreaux J, Walker BA, Protopopov A, Reme T, Pellestor F, Pantesco V, Jauch A, Morgan G, Goldschmidt H, Klein B.

Haematologica. 2012 Apr;97(4):622-30. doi: 10.3324/haematol.2011.046821. Epub 2011 Nov 18.

19.

Rejuvenating senescent and centenarian human cells by reprogramming through the pluripotent state.

Lapasset L, Milhavet O, Prieur A, Besnard E, Babled A, Aït-Hamou N, Leschik J, Pellestor F, Ramirez JM, De Vos J, Lehmann S, Lemaitre JM.

Genes Dev. 2011 Nov 1;25(21):2248-53. doi: 10.1101/gad.173922.111.

20.

Aneuploidy. Preface.

Delhanty JD, Pellestor F.

Cytogenet Genome Res. 2011;133(2-4):89-90. doi: 10.1159/000324234. Epub 2011 Apr 7. No abstract available.

21.

Complex chromosomal rearrangements: origin and meiotic behavior.

Pellestor F, Anahory T, Lefort G, Puechberty J, Liehr T, Hédon B, Sarda P.

Hum Reprod Update. 2011 Jul-Aug;17(4):476-94. doi: 10.1093/humupd/dmr010. Epub 2011 Apr 11. Review.

PMID:
21486858
22.

Meiotic segregation of complex reciprocal translocations: direct analysis of the spermatozoa of a t(5;13;14) carrier.

Pellestor F, Puechberty J, Weise A, Lefort G, Anahory T, Liehr T, Sarda P.

Fertil Steril. 2011 Jun;95(7):2433.e17-22. doi: 10.1016/j.fertnstert.2011.01.159. Epub 2011 Mar 2.

PMID:
21367411
23.

PNA-FISH on human sperm.

Pellestor F, Monzo C, Hamamah S.

Methods Mol Biol. 2010;659:283-9. doi: 10.1007/978-1-60761-789-1_21.

PMID:
20809320
24.

Apoptosis and meiotic segregation in ejaculated sperm from Robertsonian translocation carrier patients.

Brugnon F, Janny L, Communal Y, Darcha C, Szczepaniak C, Pellestor F, Vago P, Pons-Rejraji H, Artonne C, Grizard G.

Hum Reprod. 2010 Jul;25(7):1631-42. doi: 10.1093/humrep/deq113. Epub 2010 May 15.

PMID:
20472914
25.

Predictive value of sperm-FISH analysis on the outcome of preimplantation genetic diagnosis (PGD) for a pericentric inversion inv5(p15.3q11.2) carrier.

Bernicot I, Dechanet C, Mace A, Hedon B, Hamamah S, Pellestor F, Anahory T.

Hum Reprod. 2010 Jul;25(7):1818-23. doi: 10.1093/humrep/deq101. Epub 2010 Apr 20.

PMID:
20406738
26.

Combined FISH and PRINS sperm analysis of complex chromosome rearrangement t(1;19;13): an approach facilitating PGD.

Loup V, Bernicot I, Janssens P, Hedon B, Hamamah S, Pellestor F, Anahory T.

Mol Hum Reprod. 2010 Feb;16(2):111-6. doi: 10.1093/molehr/gap105. Epub 2009 Dec 17.

PMID:
20019162
27.

Oocyte recovery post human follicular fluid centrifugation in modified natural cycle and achieving embryo.

Ferrières A, Reyftmann L, Pellestor F, Hédon B, Decaud H, Hamamah S.

Reprod Biomed Online. 2009 May;18(5):671-3.

PMID:
19549446
28.

Total fertilization failure and molecular abnormalities in metaphase II oocytes.

Gasca S, Reyftmann L, Pellestor F, Rème T, Assou S, Anahory T, Dechaud H, Klein B, De Vos J, Hamamah S.

Reprod Biomed Online. 2008 Dec;17(6):772-81.

PMID:
19079960
29.

Chromosome distribution in human sperm - a 3D multicolor banding-study.

Manvelyan M, Hunstig F, Bhatt S, Mrasek K, Pellestor F, Weise A, Simonyan I, Aroutiounian R, Liehr T.

Mol Cytogenet. 2008 Nov 14;1:25. doi: 10.1186/1755-8166-1-25.

30.

Peptide nucleic acids (PNAs) as diagnostic devices for genetic and cytogenetic analysis.

Pellestor F, Paulasova P, Hamamah S.

Curr Pharm Des. 2008;14(24):2439-44. Review.

PMID:
18781993
31.

Breakpoint mapping and complete analysis of meiotic segregation patterns in three men heterozygous for paracentric inversions.

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.

Eur J Hum Genet. 2009 Jan;17(1):44-50. doi: 10.1038/ejhg.2008.144. Epub 2008 Aug 6.

32.

[Could apoptotic markers help the exploration of male infertility?].

Haouzi D, Fourar M, Pellestor F, Déchaud H, De Vos J, Klein B, Hamamah S.

Gynecol Obstet Fertil. 2008 Jul-Aug;36(7-8):721-9. doi: 10.1016/j.gyobfe.2008.02.027. Epub 2008 Jul 1. Review. French.

PMID:
18595760
33.

[Benefit of human gamete cytogenetics: results and perspectives].

Vialard F, Pellestor F.

Pathol Biol (Paris). 2008 Sep;56(6):388-99. doi: 10.1016/j.patbio.2008.04.012. Epub 2008 Jun 4. Review. French.

PMID:
18534785
34.

Thirty-two new cases with small supernumerary marker chromosomes detected in connection with fertility problems: detailed molecular cytogenetic characterization and review of the literature.

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, Anderson J, Küpferling P, Köhler S, Duba HC, Dufke A, Aktas D, Martin T, Schreyer I, Ewers E, Reich D, Mrasek K, Weise A, Liehr T.

Int J Mol Med. 2008 Jun;21(6):705-14.

35.

Position of chromosomes 18, 19, 21 and 22 in 3D-preserved interphase nuclei of human and gorilla and white hand gibbon.

Manvelyan M, Hunstig F, Mrasek K, Bhatt S, Pellestor F, Weise A, Liehr T.

Mol Cytogenet. 2008 Apr 29;1:9. doi: 10.1186/1755-8166-1-9.

36.

Breakpoint characterization: a new approach for segregation analysis of paracentric inversion in human sperm.

Bhatt S, Moradkhani K, Mrasek K, Puechberty J, Lefort G, Lespinasse J, Sarda P, Liehr T, Hamamah S, Pellestor F.

Mol Hum Reprod. 2007 Oct;13(10):751-6. Epub 2007 Oct 3.

PMID:
17913851
37.

Aneuploidy and confined chromosomal mosaicism in the developing human brain.

Yurov YB, Iourov IY, Vorsanova SG, Liehr T, Kolotii AD, Kutsev SI, Pellestor F, Beresheva AK, Demidova IA, Kravets VS, Monakhov VV, Soloviev IV.

PLoS One. 2007 Jun 27;2(6):e558.

38.

Identifying new human oocyte marker genes: a microarray approach.

Gasca S, Pellestor F, Assou S, Loup V, Anahory T, Dechaud H, De Vos J, Hamamah S.

Reprod Biomed Online. 2007 Feb;14(2):175-83.

39.

Multicolor PRINS and multicolor PNA.

Pellestor F, Paulasova P, Andréo B, Lefort G, Hamamah S.

Cytogenet Genome Res. 2006;114(3-4):263-9.

PMID:
16954664
40.

Rare Robertsonian translocations and meiotic behaviour: sperm FISH analysis of t(13;15) and t(14;15) translocations: a case report.

Moradkhani K, Puechberty J, Bhatt S, Lespinasse J, Vago P, Lefort G, Sarda P, Hamamah S, Pellestor F.

Hum Reprod. 2006 Dec;21(12):3193-8. Epub 2006 Aug 17.

PMID:
16917122
41.

Development and adaptation of the PRINS technology: an overview.

Pellestor F.

Methods Mol Biol. 2006;334:211-20. Review.

PMID:
16861766
42.

PRINS as an efficient tool for aneuploidy assessment in human oocytes and preimplantation embryos.

Pellestor F, Andréo B, Anahory T, Hamamah S.

Methods Mol Biol. 2006;334:151-60.

PMID:
16861761
43.

Brain tissue preparations for chromosomal PRINS labeling.

Iourov IY, Vorsanova SG, Pellestor F, Yurov YB.

Methods Mol Biol. 2006;334:123-32.

PMID:
16861758
44.

Analysis of sperm aneuploidy by PRINS.

Pellestor F, Andréo B, Puechberty J, Lefort G, Sarda P.

Methods Mol Biol. 2006;334:49-59.

PMID:
16861752
45.

PRINS combined with peptide nucleic acid labeling.

Pellestor F, Paulasova P.

Methods Mol Biol. 2006;334:15-22.

PMID:
16861748
47.

The human cumulus--oocyte complex gene-expression profile.

Assou S, Anahory T, Pantesco V, Le Carrour T, Pellestor F, Klein B, Reyftmann L, Dechaud H, De Vos J, Hamamah S.

Hum Reprod. 2006 Jul;21(7):1705-19. Epub 2006 Mar 29.

48.

The occurrence of aneuploidy in human: lessons from the cytogenetic studies of human oocytes.

Pellestor F, Andréo B, Anahory T, Hamamah S.

Eur J Med Genet. 2006 Mar-Apr;49(2):103-16. Epub 2005 Sep 26. Review.

PMID:
16530707
49.

Meiotic segregation of rare Robertsonian translocations: sperm analysis of three t(14q;22q) cases.

Moradkhani K, Puechberty J, Bhatt S, Vago P, Janny L, Lefort G, Hamamah S, Sarda P, Pellestor F.

Hum Reprod. 2006 May;21(5):1166-71. Epub 2006 Jan 26.

PMID:
16439506
50.

Effect of maternal age on the frequency of cytogenetic abnormalities in human oocytes.

Pellestor F, Anahory T, Hamamah S.

Cytogenet Genome Res. 2005;111(3-4):206-12. Review.

PMID:
16192696

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