N Ayraud

1.1k citations
56 papers · 808 · h-index 14

Impact in

Papers in

    • Genomic variations and chromosomal abnormalities 12
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 4
    • Genomics and Rare Diseases 3

N Ayraud

54 papers receiving 761 citations

Peers

N Ayraud
Comparison fields: 5 of 80
  • Hematology 137
  • Reproductive Medicine 72
  • Developmental Biology 20
  • Genetics 208
  • Genetics 68
Replace W. M. COURT-BROWN with:
W. M. COURT-BROWN United Kingdom
Darrell J. Tomkins Canada
KarinE. Buckton United Kingdom
Valerié Schumacher Germany
Margaret A. Strong United States
Heinz-Ulrich Weier United States
Aki Ishikawa Japan
Susi Scappaticci Italy
T Sonoda Japan
Jane Yui Canada
N Ayraud relative to W. M. COURT-BROWN United Kingdom W. M. COURT-BROWN's profile →
Citations per field
00.5×10×14×
W. M. COURT-BROWN · 1×
Citations per year

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-authors

The 25 scholars most cited alongside N Ayraud, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with N Ayraud Line = papers co-authored together N Ayraud links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 56 papers — load more, or switch the sort, to bring in the rest.

#Work
1 1982108
2 199176
3 199667
4 200063
5 200862
6 199458
7 198149
8 198344
9 199627
10
[Interstitial deletion of the long arm of chromosome 7 in a female child with leprechaunism].
197620
11
Identification par dénaturation thermique ménagée des anomalies chromosomiques observées dans six tumeurs métastatiques humaines
197520
12
Délétion interstitielle du bras long d'un chromosome 7 chez une enfant lepréchaune
197617
13
[Identification by means of heat denaturation of chromosome aberrations in 6 human metastatic tumors].
197517
14 198213
15
[Trisomy 11 q (q23.1 - qter) through maternal translocation t(11;22) (q23.1;q11.1). A new case].
197613
16
[Comparative cytogenetic study of 7 types of mammary cancer].
197712
17
Recurrent cytogenetic abnormalities observed in complete remission of acute myeloid leukemia do not necessarily mark preleukemic cells.
199412
18 198510
19 19817
20 19797

About N Ayraud

N Ayraud is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Hematology and Pulmonary and Respiratory Medicine, having authored 56 papers that have together received 808 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (12 papers), Acute Myeloid Leukemia Research (7 papers), Prenatal Screening and Diagnostics (6 papers), Chronic Myeloid Leukemia Treatments (5 papers), Sarcoma Diagnosis and Treatment (5 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (4 papers), Congenital limb and hand anomalies (4 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Hematology (137 citations), Reproductive Medicine (72 citations), Developmental Biology (20 citations), Genetics (208 citations) and Genetics (68 citations). N Ayraud has collaborated with scholars based in France, United States and Italy. Frequent co-authors include M Donzeau, Florence Pédeutour, Claude Turc‐Carel, I Dvorăcková, Sophie Raynaud, D Farahifar, Bae‐Li Hsi, Patrick Fénichel, Jean‐Charles Lambert and Gabriella Sozzi. Their work appears in journals such as Human Genetics, Blood, Journal of Medical Genetics, Marine Biology and Fertility and Sterility.

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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