N Ayraud

1.1k total citations
56 papers, 886 citations indexed

About

N Ayraud is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, N Ayraud has authored 56 papers receiving a total of 886 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 12 papers in Molecular Biology and 11 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in N Ayraud's work include Genomic variations and chromosomal abnormalities (12 papers), Acute Myeloid Leukemia Research (7 papers) and Prenatal Screening and Diagnostics (6 papers). N Ayraud is often cited by papers focused on Genomic variations and chromosomal abnormalities (12 papers), Acute Myeloid Leukemia Research (7 papers) and Prenatal Screening and Diagnostics (6 papers). N Ayraud collaborates with scholars based in France, United States and Italy. N Ayraud's co-authors include Claude Turc‐Carel, Florence Pédeutour, M Donzeau, Gabriella Sozzi, Marie‐Pierre Simon, I Dvorăcková, Fabiola Minoletti, P. Combemale, Marie‐José Terrier‐Lacombe and Sophie Raynaud and has published in prestigious journals such as Blood, Fertility and Sterility and British Journal of Haematology.

In The Last Decade

N Ayraud

54 papers receiving 837 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
N Ayraud France	14	266	238	218	162	144	56	886
Jan Steffen Poland	19	190 0.7×	656 2.8×	235 1.1×	101 0.6×	16 0.1×	38	1.3k
Öztürk Özdemir Türkiye	16	82 0.3×	284 1.2×	98 0.4×	26 0.2×	170 1.2×	102	910
T. Abe Japan	17	101 0.4×	349 1.5×	121 0.6×	68 0.4×	453 3.1×	43	1.0k
Jane Yui Canada	12	82 0.3×	610 2.6×	119 0.5×	140 0.9×	85 0.6×	13	1.7k
Sang In Shim South Korea	16	103 0.4×	189 0.8×	56 0.3×	166 1.0×	45 0.3×	59	622
M Nose Japan	21	72 0.3×	447 1.9×	113 0.5×	114 0.7×	130 0.9×	57	1.4k
Valerié Schumacher Germany	24	284 1.1×	1.4k 6.0×	276 1.3×	28 0.2×	43 0.3×	36	1.8k
Angshumoy Roy United States	23	406 1.5×	639 2.7×	510 2.3×	115 0.7×	49 0.3×	68	2.0k
Gönül Oğur Türkiye	13	71 0.3×	468 2.0×	210 1.0×	40 0.2×	42 0.3×	51	700
T Sonoda Japan	14	111 0.4×	279 1.2×	198 0.9×	26 0.2×	21 0.1×	82	808

Countries citing papers authored by N Ayraud

Since Specialization

Citations

This map shows the geographic impact of N Ayraud's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by N Ayraud with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites N Ayraud more than expected).

Fields of papers citing papers by N Ayraud

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by N Ayraud. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by N Ayraud. The network helps show where N Ayraud may publish in the future.

Co-authorship network of co-authors of N Ayraud

This figure shows the co-authorship network connecting the top 25 collaborators of N Ayraud. A scholar is included among the top collaborators of N Ayraud based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with N Ayraud. N Ayraud is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

Sirvent, Nicolas, Anne Forus, W. Lescaut, et al.. (2000). Characterization of centromere alterations in liposarcomas. Genes Chromosomes and Cancer. 29(2). 117–129. 63 indexed citations

Pédeutour, Florence, J.‐P. Lacour, C Perrin, et al.. (1996). Another case of t(17;22)(q22;q13) in an infantile dermatofibrosarcoma protuberans. Cancer Genetics and Cytogenetics. 89(2). 175–176. 27 indexed citations

Pédeutour, Florence, Marie‐Pierre Simon, Fabiola Minoletti, et al.. (1996). Translocation, t(17;22)(q22;q13), in dermatofibrosarcoma protuberans: a new tumor-associated chromosome rearrangement. Cytogenetic and Genome Research. 72(2-3). 171–174. 140 indexed citations

Pédeutour, Florence, Jean‐Michel Coindre, Gabriella Sozzi, et al.. (1994). Supernumerary ring chromosomes containing chromosome 17 sequences. Cancer Genetics and Cytogenetics. 76(1). 1–9. 58 indexed citations

Fénichel, Patrick, et al.. (1991). Dynamics of human sperm acrosome reaction: relation with in vitro fertilization. Fertility and Sterility. 55(5). 994–999. 76 indexed citations

Fénichel, Patrick, et al.. (1991). Le ionophore A23187. Andrologie. 1(1). 15–16.

Lambert, Jean‐Charles, et al.. (1981). [Monosomy 7qter (author's transl)].. PubMed. 38(3). 177–80. 1 indexed citations

Ferrari, Marcella De, et al.. (1978). [Partial trisomy 13 (13q14 leads to 13qter) in mosaic (author's transl)].. PubMed. 26(2). 161–71. 2 indexed citations

Ayraud, N, et al.. (1977). [Comparative cytogenetic study of 7 types of mammary cancer].. PubMed. 20(3). 171–7. 12 indexed citations

10.

Ayraud, N, et al.. (1976). [Distribution of chromosome breakage point induced by arabinosylcytosine on in-vitro human lymphocytes].. PubMed. 19(1). 29–35. 2 indexed citations

11.

Ayraud, N, et al.. (1976). [Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].. PubMed. 19(4). 265–8. 20 indexed citations

12.

Ayraud, N, et al.. (1976). Délétion interstitielle du bras long d'un chromosome 7 chez une enfant lepréchaune. Annales de Génétique. 19(4). 17 indexed citations

13.

Ayraud, N, et al.. (1976). [Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].. PubMed. 19(1). 65–8. 13 indexed citations

14.

Ayraud, N. (1975). [Identification by means of heat denaturation of chromosome aberrations in 6 human metastatic tumors].. PubMed. 23(10). 423–30. 17 indexed citations

15.

Ayraud, N. (1975). Identification par dénaturation thermique ménagée des anomalies chromosomiques observées dans six tumeurs métastatiques humaines. 23(10). 20 indexed citations

16.

Ayraud, N, et al.. (1970). Caryotype 46,XY-47,XXY-48,XXXY dans deux observations de syndrome de Klinefelter.. Annales de Génétique. 13(2). 1 indexed citations

17.

Ayraud, N, et al.. (1970). Un cas de délétion du bras court du chromosome 18.. 25(2). 2 indexed citations

18.

Ayraud, N, et al.. (1969). Un cas de chromosome D en anneau.. Annales de Génétique. 12(4). 4 indexed citations

19.

Ayraud, N, et al.. (1969). [A case of D ring chromosome].. PubMed. 12(4). 259–61. 3 indexed citations

20.

Ayraud, N, et al.. (1968). Effets cytogénétique des médicaments anticonvulsants. A propos d'une observation d'anomalies transmises pendant la vie intra-utérine.. Annales de Génétique. 11(4). 2 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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