P. Avner

841 citations
16 papers · 552 · h-index 10

Impact in

  • Genetics top 10%
    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
    • Genetics and Neurodevelopmental Disorders
    • Animal Genetics and Reproduction

Papers in

    • Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 8
    • Genetics and Neurodevelopmental Disorders 3
    • Animal Genetics and Reproduction 2
    • Estrogen and related hormone effects 1
    • Coagulation, Bradykinin, Polyphosphates, and Angioedema 1
    • CRISPR and Genetic Engineering 2
    • Nicotinic Acetylcholine Receptors Study 1

P. Avner

16 papers receiving 530 citations

Peers

P. Avner
Comparison fields: 5 of 62
  • Developmental Neuroscience 44
  • Genetics 240
  • Cellular and Molecular Neuroscience 134
  • Immunology and Allergy 34
  • Molecular Biology 389
Replace NG Copeland with:
NG Copeland United States
Kanako Oda Japan
NA Jenkins United States
D. Arnaud France
Rui-Ting Zong United States
L. Frati Italy
Laurie K. Sorge United States
Sara Corbetta Italy
Hidehiko Sugino Japan
A. Kume-Iwaki United States
P. Avner relative to NG Copeland United States NG Copeland's profile →
Citations per field
00.5×3.6×
NG Copeland · 1×
Citations per year

Countries citing papers authored by P. Avner

Since Specialization
Citations

This map shows the geographic impact of P. Avner'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 P. Avner with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites P. Avner more than expected).

Fields of papers citing papers by P. Avner

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by P. Avner. 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 P. Avner. The network helps show where P. Avner may publish in the future.

Co-authors

The 25 scholars most cited alongside P. Avner, 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 P. Avner Line = papers co-authored together P. Avner links everyone, so they are left out of the graph.

All Works

16 of 16 papers shown
#Work
1 1986146
2 1994121
3 199394
4 200941
5 199635
6 199429
7 198723
8 198218
9 199212
10 199311
11 20229
12 19966
13 20082
14 20002
15 20232
16
Monoclonal antibodies against the human factor VIII von Willebrand molecule: characterization and potential for screening of von Willebrand patients.
19841

About P. Avner

P. Avner is a scholar working on Genetics, Molecular Biology, Genetics, Hematology and Cellular and Molecular Neuroscience, having authored 16 papers that have together received 552 indexed citations. Recurring topics across this work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Genetics and Neurodevelopmental Disorders (3 papers), Animal Genetics and Reproduction (2 papers), CRISPR and Genetic Engineering (2 papers), Platelet Disorders and Treatments (2 papers), Estrogen and related hormone effects (1 paper), Coagulation, Bradykinin, Polyphosphates, and Angioedema (1 paper) and Nicotinic Acetylcholine Receptors Study (1 paper). The work is most often cited by research in Developmental Neuroscience (44 citations), Genetics (240 citations), Cellular and Molecular Neuroscience (134 citations), Immunology and Allergy (34 citations) and Molecular Biology (389 citations). P. Avner has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Claire Rougeulle, B.M. Cattanach, C. Rasberry, Marie‐Christine Simmler, Yves Maulet, Jean Louis Guénet, Heinrich Betz, D. Arnaud, Laurence Amar and Édith Heard. Their work appears in journals such as Mammalian Genome, Proceedings of the National Academy of Sciences, Human Molecular Genetics, Trends in Genetics and Nature.

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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