B. Sele

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Homozygous mutation of AURKC yields large-headed polyploid spermatozoa and causes male infertility

Klaus Dieterich, Pierre-Simon Jouk, Sophie Rousseaux, 2007, Nature Genetics.

No Long-Term Increase in Sperm Aneuploidy Rates after Anticancer Therapy

C. Cans, S. Rousseaux, S. Hennebicq, 2004, Clinical Cancer Research.

[Effects of trichlorethylene and its metabolites on the rate of sister-chromatid exchange. In vivo and in vitro study on the human lymphocytes. (author's transl)].

B. Sele, Z. Gu, C. Marka, 1981, Annales de genetique.

Meiotic behaviour of sex chromosomes investigated by three-colour FISH on 35 142 sperm nuclei from two 47,XYY males

Y. Usson, S. Rousseaux, B. Sele, 1997, Human Genetics.

Misregulation of histone acetylation in Sertoli cell-only syndrome and testicular cancer.

M. Péoc'h, S. Khochbin, S. Rousseaux, 2003, Molecular human reproduction.

Regulated hyperacetylation of core histones during mouse spermatogenesis: involvement of histone deacetylases.

Y. Usson, S. Khochbin, S. Rousseaux, 2000, European journal of cell biology.

Increased incidence of hyperhaploid 24,XY spermatozoa detected by three-colour FISH in a 46,XY/47,XXY male

Y. Usson, S. Rousseaux, B. Sele, 1996, Human Genetics.

Reciprocal translocations: A way to predict the mode of imbalanced segregation by pachytene-diagram drawing

B. Sele, P. Jalbert, H. Jalbert, 1980, Human Genetics.

Meiotic segregation in males heterozygote for reciprocal translocations: analysis of sperm nuclei by two and three colour fluorescence in situ hybridization.

S. Rousseaux, J. Lespinasse, B. Sele, 1995, Cytogenetics and cell genetics.

Meiotic segregation of the X and Y chromosomes and chromosome 1 analyzed by three-color FISH in human interphase spermatozoa.

S. Rousseaux, B. Sele, M. Monteil, 1995, Cytogenetics and cell genetics.

A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.

P. Jouk, S. Viville, F. Abada, 2011, American journal of human genetics.

Polyploidy in large-headed sperm: FISH study of three cases.

C. Metzler-Guillemain, S. Rousseaux, M. Guichaoua, 2002, Human reproduction.

Relationship between sexual abstinence of men and chromosomally abnormal spermatozoa.

F. Pellestor, B. Sele, 1991, Journal of reproduction and fertility.

Disomy rates for chromosomes 14 and 21 studied by fluorescent in-situ hybridization in spermatozoa from three men over 60 years of age.

Y. Usson, S. Rousseaux, B. Sele, 1998, Molecular human reproduction.

Sperm nuclei analysis of a Robertsonian t(14q21q) carrier, by FISH, using three plasmids and two YAC probes

S. Rousseaux, B. Sele, M. Monteil, 1995, Human Genetics.

Direct segregation analysis of reciprocal translocations: a study of 283 sperm karyotypes from four carriers.

F. Pellestor, B. Sele, P. Jalbert, 1989, American journal of human genetics.

Chromosome analysis of spermatozoa from a male heterozygous for a 13;14 Robertsonian translocation

F. Pellestor, B. Sele, H. Jalbert, 1987, Human Genetics.

Achievement of meiosis in XXY germ cells: study of 543 sperm karyotypes from an XY/XXY mosaic patient

S. Rousseaux, B. Sele, E. Chevret, 2004, Human Genetics.

Male meiotic segregation of gonosomes analysed by two colour FISH in human interphase spermatozoa

S. Rousseaux, B. Sele, M. Monteil, 1994, Human Genetics.

Factors predisposing to adjacent 2 and 3:1 disjunctions: study of 161 human reciprocal translocations.

B. Sele, P. Jalbert, 1979, Journal of medical genetics.

Segregation of sex chromosomes in a klinefelter patient (47,xxy)

S. Rousseaux, B. Sele, S. Hennebicq, 2000 .

Genome organization in the human sperm nucleus studied by FISH and confocal microscopy

Y. Usson, C. Vourc’h, F. Mongelard, 2000, Molecular reproduction and development.

Increased aneuploid frequency in spermatozoa from a Hodgkin's disease patient after chemotherapy and radiotherapy.

S. Rousseaux, B. Sele, M. Monteil, 1997, Cytogenetics and cell genetics.

Immediate rearrangements of human sperm chromosomes following in-vivo irradiation.

S. Rousseaux, B. Sele, E. Chevret, 1993, Human reproduction.

Comparison of acrocentric associations in male and female cells. Relationship to the active nucleolar organizers

L. Hens, B. Sele, H. Galperin-Lemaître, 2004, Human Genetics.

Assessment of aneuploidy in the human female by using cytogenetics of IVF failures.

F. Pellestor, B. Sele, 1988, American journal of human genetics.

Partial trisomy for the long arms of chromosome no. 5 due to insertion and further 'aneusomie de recombinaison'.

B. Sele, C. Mouriquand, P. Jalbert, 1975, Journal of medical genetics.

[Ring 6-chromosome: a nonspecific clinical picture].

B. Sele, A. Joannard, P. Jalbert, 1977, Annales de genetique.

Distribution of human chromosomes on the metaphase plate using banding techniques

B. Cutsem, B. Sele, C. Mouriquand, 1977, Human Genetics.

[Mechanism of duplication formation relating to a case of 10q22 to q25 duplication].

B. Sele, D. Pasquier, P. Jalbert, 1982, Annales de genetique.

[Ring-20 chromosome: a new syndrome].

B. Sele, M. Bost, P. Jalbert, 1977, Annales de genetique.

The Aurora Kinase C c.144delC mutation causes meiosis I arrest in men and is frequent in the North African population.

P. Jouk, S. Viville, P. Ray, 2009, Human molecular genetics.

[Cytogenetic analysis of the Bloom syndrome. A study of the exchange-break relationship].

D. Leroux, B. Sele, P. Jalbert, 1983, Annales de genetique.

A recurrent deletion of DPY19L2 causes infertility in man by blocking sperm head elongation and acrosome formation.

P. Jouk, S. Viville, F. Abada, 2011, American journal of human genetics.