Guy Longepied

1.2k total citations
17 papers, 807 citations indexed

About

Guy Longepied is a scholar working on Molecular Biology, Genetics and Reproductive Medicine. According to data from OpenAlex, Guy Longepied has authored 17 papers receiving a total of 807 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Molecular Biology, 10 papers in Genetics and 4 papers in Reproductive Medicine. Recurrent topics in Guy Longepied's work include Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Genomics and Chromatin Dynamics (6 papers) and Nuclear Structure and Function (5 papers). Guy Longepied is often cited by papers focused on Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (8 papers), Genomics and Chromatin Dynamics (6 papers) and Nuclear Structure and Function (5 papers). Guy Longepied collaborates with scholars based in France, United Kingdom and United States. Guy Longepied's co-authors include Michael Mitchell, Catherine Metzler‐Guillemain, Carole A. Sargent, Nicolas Lévy, Noémie Saut, R. A. Furlong, T. B. Hargreave, Michael H. Jones, Robert P. Erickson and Nabeel A. Affara and has published in prestigious journals such as PLoS ONE, Current Biology and The American Journal of Human Genetics.

In The Last Decade

Guy Longepied

17 papers receiving 779 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Guy Longepied France	14	606	525	387	123	99	17	807
Barbara Arredi Italy	9	633 1.0×	356 0.7×	373 1.0×	136 1.1×	55 0.6×	11	840
Katrien Stouffs Belgium	21	649 1.1×	618 1.2×	534 1.4×	187 1.5×	78 0.8×	47	1.0k
Anna Mielnik United States	15	715 1.2×	632 1.2×	681 1.8×	187 1.5×	66 0.7×	34	990
Jonah Cool United States	8	410 0.7×	565 1.1×	291 0.8×	133 1.1×	29 0.3×	9	764
M Fellous France	11	663 1.1×	617 1.2×	294 0.8×	52 0.4×	57 0.6×	16	779
Kun Ma United Kingdom	8	671 1.1×	543 1.0×	433 1.1×	67 0.5×	176 1.8×	9	798
A. Muallem United States	6	698 1.2×	621 1.2×	644 1.7×	124 1.0×	96 1.0×	7	899
Cindy M. Korver Netherlands	17	1.1k 1.7×	907 1.7×	765 2.0×	292 2.4×	330 3.3×	21	1.5k
Christopher Tilmann United States	8	661 1.1×	675 1.3×	435 1.1×	171 1.4×	9 0.1×	8	943
Esther Sleddens–Linkels Netherlands	11	250 0.4×	495 0.9×	94 0.2×	99 0.8×	126 1.3×	15	633

Countries citing papers authored by Guy Longepied

Since Specialization

Citations

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

Fields of papers citing papers by Guy Longepied

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Guy Longepied

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

All Works

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17 of 17 papers shown

Longepied, Guy, et al.. (2023). Spermatozoa in mice lacking the nucleoporin NUP210L show defects in head shape and motility but not in nuclear compaction or histone replacement. Clinical Genetics. 105(4). 364–375. 2 indexed citations

Paci, Marine, Guy Longepied, Patrice Bourgeois, et al.. (2018). The involvement of the nuclear lamina in human and rodent spermiogenesis: a systematic review. Basic and Clinical Andrology. 28(1). 7–7. 4 indexed citations

Delague, Valérie, Jean‐Pierre Desvignes, Guy Longepied, et al.. (2018). Loss of Calmodulin- and Radial-Spoke-Associated Complex Protein CFAP251 Leads to Immotile Spermatozoa Lacking Mitochondria and Infertility in Men. The American Journal of Human Genetics. 103(3). 413–420. 67 indexed citations

Paci, Marine, Guy Longepied, Sylviane Hennebicq, et al.. (2017). Abnormal retention of nuclear lamina and disorganization of chromatin-related proteins in spermatozoa from DPY19L2-deleted globozoospermic patients. Reproductive BioMedicine Online. 35(5). 562–570. 9 indexed citations

Paci, Marine, Guy Longepied, J. Saïas‐Magnan, et al.. (2017). Homozygous deletion of SUN5 in three men with decapitated spermatozoa. Human Molecular Genetics. 26(16). 3167–3171. 51 indexed citations

Paci, Marine, R. Boissier, Guy Longepied, et al.. (2017). LEM-domain proteins are lost during human spermiogenesis but BAF and BAF-L persist. Reproduction. 154(4). 387–401. 16 indexed citations

Vernet, Nadège, Shantha K. Mahadevaiah, Guy Longepied, et al.. (2016). Mouse Y-Encoded Transcription Factor Zfy2 Is Essential for Sperm Head Remodelling and Sperm Tail Development. PLoS ONE. 11(1). e0145398–e0145398. 19 indexed citations

Longepied, Guy, Marine Paci, Vincent Achard, et al.. (2014). Nuclear envelope remodelling during human spermiogenesis involves somatic B-type lamins and a spermatid-specific B3 lamin isoform. Molecular Human Reproduction. 21(3). 225–236. 22 indexed citations

Vernet, Nadège, Shantha K. Mahadevaiah, Guy Longepied, et al.. (2012). Human and mouse ZFY genes produce a conserved testis-specific transcript encoding a zinc finger protein with a short acidic domain and modified transactivation potential. Human Molecular Genetics. 21(12). 2631–2645. 32 indexed citations

10.

Vernet, Nadège, Shantha K. Mahadevaiah, Obah A. Ojarikre, et al.. (2011). The Y-Encoded Gene Zfy2 Acts to Remove Cells with Unpaired Chromosomes at the First Meiotic Metaphase in Male Mice. Current Biology. 21(9). 787–793. 47 indexed citations

11.

Ducourneau, Axel, Gilles Boëtsch, Guy Longepied, et al.. (2010). Genetic diversity on the Comoros Islands shows early seafaring as major determinant of human biocultural evolution in the Western Indian Ocean. European Journal of Human Genetics. 19(1). 89–94. 32 indexed citations

12.

Longepied, Guy, Noémie Saut, Isabelle Aknin‐Seifer, et al.. (2010). Complete deletion of the AZFb interval from the Y chromosome in an oligozoospermic man. Human Reproduction. 25(10). 2655–2663. 38 indexed citations

13.

Saut, Noémie, Guy Longepied, P. Terriou, et al.. (2004). Sequence family variant loss from the AZFc interval of the human Y chromosome, but not gene copy loss, is strongly associated with male infertility. Journal of Medical Genetics. 41(11). 814–825. 118 indexed citations

14.

Delbridge, Margaret L., Guy Longepied, D. Depétris, et al.. (2004). TSPY, the Candidate Gonadoblastoma Gene on the Human Y Chromosome, has a Widely Expressed Homologue on the X - Implications for Y Chromosome Evolution. Chromosome Research. 12(4). 345–356. 57 indexed citations

15.

Agulnik, Alexander I., et al.. (1999). Mouse H-Y encoding Smcy gene and its X Chromosomal homolog Smcx. Mammalian Genome. 10(9). 926–929. 37 indexed citations

16.

Furlong, R. A., Carole A. Sargent, Robert P. Erickson, et al.. (1998). Characterisation of the coding sequence and fine mapping of the human DFFRY gene and comparative expression analysis and mapping to the Sxrb interval of the mouse Y chromosome of the Dffry gene. Human Molecular Genetics. 7(1). 97–107. 166 indexed citations

17.

Saut, Noémie, Carole A. Sargent, Sean M. Grimmond, et al.. (1998). The Mouse Y Chromosome Interval Necessary for Spermatogonial Proliferation is Gene Dense with Syntenic Homology to the Human AZFa Region. Human Molecular Genetics. 7(11). 1713–1724. 90 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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