P. Avner

840 total citations
16 papers, 542 citations indexed

About

P. Avner is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, P. Avner has authored 16 papers receiving a total of 542 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 5 papers in Molecular Biology and 2 papers in Genetics. Recurrent topics in P. Avner's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (3 papers) and CRISPR and Genetic Engineering (2 papers). P. Avner is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (9 papers), Genetics and Neurodevelopmental Disorders (3 papers) and CRISPR and Genetic Engineering (2 papers). P. Avner collaborates with scholars based in France, United Kingdom and United States. P. Avner's co-authors include Claire Rougeulle, B.M. Cattanach, C. Rasberry, Marie‐Christine Simmler, Yves Maulet, Heinrich Betz, Jean Louis Guénet, Laurence Amar, D. Arnaud and Édith Heard and has published in prestigious journals such as Nature, Proceedings of the National Academy of Sciences and Journal of Biological Chemistry.

In The Last Decade

P. Avner

16 papers receiving 529 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
P. Avner France	11	389	254	122	39	36	16	542
D. Arnaud France	8	328 0.8×	228 0.9×	42 0.3×	37 0.9×	43 1.2×	14	434
Fernando J. Sallés United States	8	633 1.6×	65 0.3×	75 0.6×	20 0.5×	44 1.2×	10	797
Laurie K. Sorge United States	10	409 1.1×	96 0.4×	94 0.8×	21 0.5×	44 1.2×	15	534
Hidehiko Sugino Japan	13	349 0.9×	87 0.3×	102 0.8×	15 0.4×	43 1.2×	23	547
L. Frati Italy	8	207 0.5×	185 0.7×	83 0.7×	31 0.8×	11 0.3×	16	426
Mathew P. Dixon Australia	11	726 1.9×	214 0.8×	55 0.5×	86 2.2×	21 0.6×	14	864
Kanako Oda Japan	10	249 0.6×	113 0.4×	126 1.0×	80 2.1×	26 0.7×	17	440
Rui-Ting Zong United States	9	368 0.9×	194 0.8×	42 0.3×	84 2.2×	11 0.3×	9	492
NG Copeland United States	6	244 0.6×	69 0.3×	146 1.2×	35 0.9×	7 0.2×	7	464
Hilger H. Ropers Germany	6	372 1.0×	209 0.8×	73 0.6×	14 0.4×	15 0.4×	7	521

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-authorship network of co-authors of P. Avner

This figure shows the co-authorship network connecting the top 25 collaborators of P. Avner. A scholar is included among the top collaborators of P. Avner 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 P. Avner. P. Avner is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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16 of 16 papers shown

Hierholzer, Andreas, Andrea Cerase, & P. Avner. (2023). Reply to Rafael Galupa: Discussing the role of Lppnx in the complexity of the X controlling element, Xce. Proceedings of the National Academy of Sciences. 120(7). e2219685120–e2219685120. 2 indexed citations

Hierholzer, Andreas, Corinne Chureau, Nerea Ruiz, et al.. (2022). A long noncoding RNA influences the choice of the X chromosome to be inactivated. Proceedings of the National Academy of Sciences. 119(28). e2118182119–e2118182119. 9 indexed citations

Rheault, Michelle N., Stefan M. Kren, Melanie M. Wall, et al.. (2009). X-inactivation modifies disease severity in female carriers of murine X-linked Alport syndrome. Nephrology Dialysis Transplantation. 25(3). 764–769. 37 indexed citations

Heard, Édith & P. Avner. (2000). Trans-Siberian X press report. Trends in Genetics. 16(2). 64–65. 2 indexed citations

Rougeulle, Claire & P. Avner. (1996). Identification of an S19 pseudogene lying close to the Xist sequence in the mouse. Mammalian Genome. 7(8). 606–607. 6 indexed citations

Rougeulle, Claire & P. Avner. (1996). Cloning and Characterization of a Murine Brain Specific Gene Bpx and Its Human Homologue Lying within the Xic Candidate Region. Human Molecular Genetics. 5(1). 41–49. 35 indexed citations

Maulet, Yves, et al.. (1994). Structural analysis of mouse glycine receptor alpha subunit genes. Identification and chromosomal localization of a novel variant.. Journal of Biological Chemistry. 269(4). 2607–2612. 116 indexed citations

Heard, Édith & P. Avner. (1994). Role play in X-inactivation [published erratum appears in Hum Mol Genet 1994 Nov;3(11):2092]. Human Molecular Genetics. 3(suppl_1). 1481–1485. 27 indexed citations

Simmler, Marie‐Christine, B.M. Cattanach, C. Rasberry, Claire Rougeulle, & P. Avner. (1993). Mapping the murine Xce locus with (CA)n repeats. Mammalian Genome. 4(9). 523–530. 91 indexed citations

10.

Brown, S.D.M., P. Avner, Yvonne Boyd, et al.. (1993). Mouse X chromosome. Mammalian Genome. 4(S1). S269–S281. 11 indexed citations

11.

Brown, S.D.M., P. Avner, & Gail E. Herman. (1992). Mouse X Chromosome. Mammalian Genome. 3(S1). S274–S288. 12 indexed citations

12.

Cattanach, B.M., C. Rasberry, E.P. Evans, et al.. (1991). Genetic and molecular evidence of an X-chromosome deletion spanning the tabby (<i>Ta</i>) and testicular feminization (<i>Tfm</i>) loci in the mouse. Cytogenetic and Genome Research. 56(3-4). 137–143. 25 indexed citations

13.

Avner, P., et al.. (1987). Characterization of a panel of somatic cell hybrids for regional mapping of the mouse X chromosome.. Proceedings of the National Academy of Sciences. 84(15). 5330–5334. 23 indexed citations

14.

Dautigny, A., Marie‐Geneviève Mattéi, D. Morello, et al.. (1986). The structural gene coding for myelin-associated proteolipid protein is mutated in jimpy mice. Nature. 321(6073). 867–869. 128 indexed citations

15.

Avner, P., D. Arnaud, Sultan Y, Patrick Maisonneuve, & C. Jeanneau. (1984). Monoclonal antibodies against the human factor VIII von Willebrand molecule: characterization and potential for screening of von Willebrand patients.. PubMed. 57. 69–76. 1 indexed citations

16.

Sola, Brigitte, P. Avner, Y Sultan, C. Jeanneau, & Patrick Maisonneuve. (1982). Monoclonal antibodies against human factor VIII molecular neutralize antihemophilic factor and ristocetin cofactor activities.. Proceedings of the National Academy of Sciences. 79(1). 183–187. 17 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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