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N. Ayraud · SciRah

Researcher profile · Semantic Scholar

N. Ayraud

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N. Ayraud — researcher profile on SciRah

h-index: 11
Works: 75
Citations: 639

Most-cited papers

Translocation, t(17;22)(q22;q13), in dermatofibrosarcoma protuberans: a new tumor-associated chromosome rearrangement.
Florence Pedeutour, M. Simon, F. Minoletti, G. Barcelo +5 more
1996Cytogenetics and Cell Genetics194 citations
Semantic Scholar
Dynamics of human sperm acrosome reaction: relation with in vitro fertilization.
Patrick Fénichel, Michèle Donzeau, Dariush Farahifar, Bernard Basteris +2 more
1991Fertility and Sterility94 citations Open access
Semantic Scholar
Characterization of centromere alterations in liposarcomas
Nicolas Sirvent, A. Forus, Willy Lescaut, Fanny Burel +9 more
2000Genes, Chromosomes and Cancer75 citations
Semantic Scholar
Evidence for aflatoxin B1 in two cases of lung cancer in man
I. Dvořáčková, C. Stora, N. Ayraud
2004Journal of Cancer Research and Clinical Oncology46 citations Open access
Semantic Scholar
Another case of t(17;22)(q22;q13) in an infantile dermatofibrosarcoma protuberans.
F. Pedeutour, J. Lacour, C. Perrin, K. Huffermann +3 more
1996Cancer Genetics and Cytogenetics38 citations
Semantic Scholar
Variant translocation t(8;21;15) in an acute myeloblastic leukemia with phenotypic differential evolution.
N. Ayraud, S. Raynaud, J. Bayle, P. Dujardin
1985Cancer Genetics and Cytogenetics18 citations
Semantic Scholar
Transfer, tissue localization and proliferation of fetal cells in pregnant mice.
P. Philip, N. Ayraud, René Masseyeff
1982Immunology Letters15 citations
Semantic Scholar
[Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].
N. Ayraud, J. Rovinski, J. Lambert, A. Galiana
1976Annales de Genetique15 citations
Semantic Scholar
[Identification by means of heat denaturation of chromosome aberrations in 6 human metastatic tumors].
N. Ayraud
1975Biomedicine / [publiee pour l'A.A.I.C.I.G.]14 citations
Semantic Scholar
[Comparative cytogenetic study of 7 types of mammary cancer].
N. Ayraud, J. Lambert, K. Hufferman-Tribollet, B. Basteris
1977Annales de Genetique13 citations
Semantic Scholar
[Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].
N. Ayraud, A. Galiana, M. Llyod, M. Deswarte
1976Annales de Genetique12 citations
Semantic Scholar
Characterization of aflatoxin BI (AFB) in human liver cancer.
C. Stora, I. Dvořáčková, N. Ayraud
1981Research communications in chemical pathology and pharmacology8 citations
Semantic Scholar
[18p- syndrome. A further case].
N. Ayraud, G. Darcourt, M. D'oelsnitz, J. Poujol +2 more
1969Annales de Genetique8 citations
Semantic Scholar
Antibody Transfer Mechanisms From Mother to Fetus Across Rat Yolk Sac Endoderm *
F. Laliberté, Alain Mucchielli, N. Ayraud, René Masseyeff
19817 citations
Semantic Scholar
Correspondence and Requests for Reprints to Dr Triploidy with Cyclopia and Identical Hla Alleles in the Parents
Van Dyke, Dl, W. L., L. M +8 more
7 citations
Semantic Scholar
Aflatoxin and Reye's syndrome.
C. Stora, I. Dvořáčková, N. Ayraud
1983Journal of medicine5 citations
Semantic Scholar
[A recent case of partial deletion of short arm of chromosome 18].
J. Vaillaud, J. Martin, N. Ayraud
1970Annales de Genetique5 citations
Semantic Scholar
[Cytogenetic effects of anticonvulsants. Apropos of an observation of abnormalities transmitted during intra-uterine life].
N. Ayraud, J. Kermarec, J. Martinón
1968Annales de Genetique5 citations
Semantic Scholar
Immunolocalization of alpha-fetoprotein in the ovary and hypophysis of immature female rats
D. Castelli, C. Aussel, M. Lafaurie, N. Ayraud +1 more
1982The Histochemical Journal4 citations
Semantic Scholar
Familial occurrence of a syndrome with branchial dysplasia, mental deficiency, club feet, and inguinal herniae
J. Lambert, N. Ayraud, J. Martin, R. Mariani +2 more
1982Journal of Medical Genetics4 citations Open access
Semantic Scholar
18q- Syndrome resulting from a tdic(14p;18q)
J. Lambert, M. Ferrari, C. Bergondi, Alena Galliana +1 more
1979Human Genetics4 citations
Semantic Scholar
Action des médicaments anticonvulsivants sur les chromosomes de lymphocytes humains
N. Ayraud, C. Cantrelle, G. Darcourt
19744 citations
Semantic Scholar
[45,X-46,XX-47,XXX karyotype and tumor of the nervous system. 2 cases].
N. Ayraud, J. Duplay, P. Grellier, A. Bezon +1 more
1972La Nouvelle presse medicale4 citations
Semantic Scholar
HLA in families with Down's syndrome children.
P. Soubiran, S. Benzaken, J. Piereschi, M. Ferrari +2 more
2008Tissue Antigens3 citations
Semantic Scholar
Letter to the editor: Translocation t(4;11) and morphologically burkitt-like blasts
S. Raynaud, P. Philip, N. Ayraud, J. Bayle +1 more
19883 citations
Semantic Scholar
Distribution of neutral maltase activity in mononuclear cells from different human lymphoid organs.
J. Giudicelli, P. Philip, Pascale Delque, N. Ayraud +1 more
1983Clinica chimica acta; international journal of clinical chemistry3 citations
Semantic Scholar
Role of alpha-fetoprotein (AFP) in the regulation of ovarian activity during hepatocarcinogenesis and post-natal development.
C. Aussel, D. Castelli, M. Lafaurie, B. Krebs +3 more
1982Oncodevelopmental biology and medicine : the journal of the International Society for Oncodevelopmental Biology and Medicine3 citations
Semantic Scholar
Arthrogryposis-like signs in trisomy 18
J. Lambert, M. Ferrari, M. Donzeau, N. Ayraud +2 more
2004Human Genetics2 citations
Semantic Scholar
Neutral maltase: a marker of cell differentiation in human myeloid leukaemias?
P. Philip, J. Giudicelli, Pascale Delque, J. Cassuto +2 more
1982British Journal of Haematology2 citations
Semantic Scholar
[Monosomy 7qter (author's transl)].
J. Lambert, R. Mariani, M. Donzeau, M. Ferrari +2 more
1981Archives francaises de pediatrie2 citations
Semantic Scholar
[Pure ovarian dysgenesis with translocation t (X;3) (q21;q12) (author's transl)].
R. Mariani, J. Lambert, B. Krebs, G. Depaz +1 more
1980Annales de pediatrie2 citations
Semantic Scholar
[4p monosomy with paternal t(13;14) (p11;p11) translocation].
J. Lambert, J. Rovinski, J. Mattéi, M. Carvi +3 more
1979Pediatrie2 citations
Semantic Scholar
[A small supernumerary metacentric chromosome: interprétation test (author's transl)].
N. Ayraud, B. Noel, M. Llyod, J. Letourneau +1 more
1976Journal de genetique humaine2 citations
Semantic Scholar
[Cornelia de Lange's syndrome. 4 neonatal cases].
M. D'oelsnitz, N. Ayraud, J. Vaillant, M. Deswarte
1971Annales de pediatrie2 citations
Semantic Scholar
[Karyotype 46,XY-47,XXY-48,XXXY in 2 cases of Klinefelter's syndrome].
N. Ayraud, M. Namer, R. Pastorello, M. Abbes
1970Annales de Genetique2 citations
Semantic Scholar
[Embryonic sarcoma and ring D chromosome].
N. Ayraud, G. Szepetowski, R. Garés, J. Vaillaud
1970Annales de Genetique2 citations
Semantic Scholar
Inversion (14)(q11q32) in a case of acute myeloid leukemia expressing lymphoid-associated antigens.
S. Raynaud, Benedicte Brunet, N. Ayraud, F. Monpoux +2 more
1993Cancer Genetics and Cytogenetics1 citations
Semantic Scholar
T PROLYMPHOCYTOID LEUKAEMIC TRANSFORMATION OF A T CHRONIC LYMPHOID LEUKAEMIA CHARACTERIZED BY SURFACE MARKERS AS HELPER T CELLS FOR B CELL IMMUNOGLOBULIN SYNTHESIS
P. Philip, Isabelle Sudaka, N. Gratecos, J. Bayle +1 more
1988British Journal of Haematology1 citations
Semantic Scholar
Neutral maltase: the first human B-cell enzymatic marker reflecting terminal differentiation of mature B cells into plasma cells.
P. Philip, J. Giudicelli, Pascale Delque, J. Cassuto +2 more
1983Blood1 citations Open access
Semantic Scholar
Ultrastructural localization of alpha-fetoprotein in the immature rat uterus with use of the immunoperoxidase technique.
F. Laliberté, B. Basteris, C. Aussel, N. Ayraud +1 more
1981Journal of Steroid Biochemistry1 citations
Semantic Scholar
On the synthesis of alpha-fetoprotein during liver carcinogenesis by N-2-fluorenylacetamide and its relationships with the intracellular localization of the carcinogen.
Claude Stora, C. Aussel, M. Lafaurie, B. Krebs +1 more
1981Oncology1 citations
Semantic Scholar
[Partial trisomy 13 (13q14 leads to 13qter) in mosaic (author's transl)].
J. Lambert, A. Galiana, M. Donzeau, M. Ferrari +1 more
1978Journal de genetique humaine1 citations
Semantic Scholar
[Cat eye syndrome: chromosome study and genetic counseling].
B. Noël, N. Ayraud, M. Lévy, D. Cau
1976Journal de genetique humaine1 citations
Semantic Scholar
[Distribution of chromosome breakage point induced by arabinosylcytosine on in-vitro human lymphocytes].
N. Ayraud, C. Cantrelle, M. Lloyd
1976Annales de Genetique1 citations
Semantic Scholar
[Letter: Acute lymphoblastic leukemia with Philadelphia chromosome. Probable role of a 14-22 translocation].
N. Ayraud, P. Dujardin, P. Audoly
1975La Nouvelle presse medicale1 citations
Semantic Scholar
[Phl chromosome and B 12 hypervitaminemia without patent symptoms of chronic myeloid leukemia: proof of their early appearance or autonomous syndrome?].
P. Cassuto, N. Ayraud, P. Dujardin, P. Audoly
1972Marseille medical1 citations
Semantic Scholar
[A case of deletion of short arm of chromosome 18].
M. D'oelsnitz, N. Ayraud, M. Deswarte, J. Vaillant +1 more
1970Pediatrie1 citations
Semantic Scholar
[Embryonal sarcoma. Karyotype study of 7 cases].
C. Nezelof, M. Laurent, M. F. Rousseau, N. Ayraud +1 more
1967Bulletin du Cancer1 citations
Semantic Scholar
myelodysplastic syndromes in recurring chromosomal abnormality involving the TEL gene (ETV6) Fluorescence in situ hybridization analysis of t(3; 12)(q26; p13): a
B. Taillan, N. Ayraud, P. Marynen, M. Baens +4 more
20110 citations
Semantic Scholar
Translocation t(17;22)(q21;q13) in dermatofibrosarcoma protuberans: A new tumour-associated rearrangement
F. Pedeutour, M. Simon, F. Minoletti, G. Sozzi +3 more
19960 citations
Semantic Scholar

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