Pierre F. Ray

9.9k total citations · 2 hit papers
121 papers, 4.9k citations indexed

About

Pierre F. Ray is a scholar working on Reproductive Medicine, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, Pierre F. Ray has authored 121 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 56 papers in Reproductive Medicine, 55 papers in Genetics and 48 papers in Public Health, Environmental and Occupational Health. Recurrent topics in Pierre F. Ray's work include Sperm and Testicular Function (50 papers), Reproductive Biology and Fertility (45 papers) and Prenatal Screening and Diagnostics (36 papers). Pierre F. Ray is often cited by papers focused on Sperm and Testicular Function (50 papers), Reproductive Biology and Fertility (45 papers) and Prenatal Screening and Diagnostics (36 papers). Pierre F. Ray collaborates with scholars based in France, United Kingdom and United States. Pierre F. Ray's co-authors include Christophe Arnoult, Charles Coutton, Guillaume Martinez, Aminata Touré, Alan H. Handyside, Jessica Escoffier, Sylviane Hennebicq, Robert Winston, Raoudha Zouari and Zine‐Eddine Kherraf and has published in prestigious journals such as Science, The Lancet and Journal of Biological Chemistry.

In The Last Decade

Pierre F. Ray

116 papers receiving 4.8k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Polyalanine expansion and frameshift mutations of the paired-like homeobox gene PHOX2B in congenital central hypoventilation syndrome

2003 619 citations Pierre F. Ray et al. profile →
Understanding the genetics of human infertility

2023 63 citations Pierre F. Ray et al. profile →

Peers

Countries citing papers authored by Pierre F. Ray

Since Specialization

Citations

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

Fields of papers citing papers by Pierre F. Ray

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Pierre F. Ray. 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 Pierre F. Ray. The network helps show where Pierre F. Ray may publish in the future.

Co-authorship network of co-authors of Pierre F. Ray

This figure shows the co-authorship network connecting the top 25 collaborators of Pierre F. Ray. A scholar is included among the top collaborators of Pierre F. Ray 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 Pierre F. Ray. Pierre F. Ray 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

#	Work	Indexed citations
1	Ovarian response in preimplantation genetic testing for myotonic dystrophy type 1 2024 ·Journal of Assisted Reproduction and Genetics ·Charlotte Sonigo, Noémie Ranisavljevic, (unknown), T. Anahory, Anne Mayeur, Céline Moutou, C Rongières, Arnaud Reignier, (unknown), (unknown), Anne Girardet, Pierre F. Ray, Julie Steffann, (unknown), Michaël Grynberg	0
2	A splice donor variant of GAS8 induces structural disorganization of the axoneme in sperm flagella and leads to nonsyndromic male infertility 2023 ·Clinical Genetics ·Zine‐Eddine Kherraf, Anne‐Laure Barbotin, Guillaume Martinez, (unknown), Caroline Cazin, Charles Coutton, Christophe Arnoult, Nicolas Thierry‐Mieg, Nathalie Rives, Aurélie Rives‐Feraille, Pierre F. Ray	4
3	Identification of IQCH as a calmodulin-associated protein required for sperm motility in humans 2023 ·iScience ·(unknown), Camille Sayou, Patrick Lorès, Caroline Cazin, Laurence Stouvenel, Elma El Khouri, Charles Coutton, Zine‐Eddine Kherraf, Catherine Patrat, Jérôme Govin, Nicolas Thierry‐Mieg, Marjorie Whitfield, Pierre F. Ray, Emmanuel Dulioust, Aminata Touré	2
4	CCDC65 , encoding a component of the axonemal Nexin‐Dynein regulatory complex, is required for sperm flagellum structure in humans 2023 ·Clinical Genetics ·(unknown), (unknown), Amir Amiri‐Yekta, Caroline Cazin, (unknown), Elma El Khouri, Catherine Patrat, Nicolas Thierry‐Mieg, Pierre F. Ray, Emmanuel Dulioust, Marjorie Whitfield, Aminata Touré	11
5	Results and perinatal outcomes from 189 ICSI cycles of couples with asthenozoospermic men and flagellar defects assessed by transmission electron microscopy 2023 ·Reproductive BioMedicine Online ·(unknown), (unknown), Valérie Mitchell, Anne Loyens, Nathalie Rives, Alexandre Moerman, Lucie Thomas, Estelle Escudier, Aminata Touré, Marjorie Whitfield, Charles Coutton, Guillaume Martinez, Pierre F. Ray, Zine‐Eddine Kherraf, Stéphane Viville, Marie Legendre, Thomas Smol, Geoffroy Robin, Anne‐Laure Barbotin	4
6	A recurrent ZP1 variant is responsible for oocyte maturation defect with degenerated oocytes in infertile females 2022 ·Clinical Genetics ·Corinne Loeuillet, (unknown), Caroline Cazin, Zine‐Eddine Kherraf, Sélima Fourati Ben Mustapha, Raoudha Zouari, Nicolas Thierry‐Mieg, Christophe Arnoult, Pierre F. Ray	8
7	Identification and Characterization of the Most Common Genetic Variant Responsible for Acephalic Spermatozoa Syndrome in Men Originating from North Africa 2021 ·International Journal of Molecular Sciences ·Caroline Cazin, (unknown), Guillaume Martinez, Sélima Fourati Ben Mustapha, Marjorie Whitfield, Charles Coutton, Nicolas Thierry‐Mieg, (unknown), Nathalie Rives, Christophe Arnoult, Aminata Touré, Pierre F. Ray, Raoudha Zouari, C. Sifer, Zine‐Eddine Kherraf	6
8	Genetic diagnosis, sperm phenotype and ICSI outcome in case of severe asthenozoospermia with multiple morphological abnormalities of the flagellum 2021 ·Human Reproduction ·Lucile Ferreux, Mathilde Bourdon, (unknown), Alain Schmitt, Laurence Stouvenel, Patrick Lorès, Pierre F. Ray, (unknown), Khaled Pocate-Cheriet, Piétro Santulli, Emmanuel Dulioust, Aminata Touré, Catherine Patrat	25
9	A missense mutation in IFT74, encoding for an essential component for intraflagellar transport of Tubulin, causes asthenozoospermia and male infertility without clinical signs of Bardet–Biedl syndrome 2021 ·Human Genetics ·Patrick Lorès, Zine‐Eddine Kherraf, Amir Amiri‐Yekta, Marjorie Whitfield, Abbas Daneshipour, Laurence Stouvenel, Caroline Cazin, (unknown), Charles Coutton, (unknown), Christophe Arnoult, Nicolas Thierry‐Mieg, Lucile Ferreux, Catherine Patrat, (unknown), Sélima Fourati Ben Mustapha, Raoudha Zouari, Emmanuel Dulioust, Pierre F. Ray, Aminata Touré	20
10	The sodium/proton exchanger SLC9C1 ( sNHE ) is essential for human sperm motility and fertility 2021 ·Clinical Genetics ·(unknown), Marjorie Whitfield, (unknown), Laurence Stouvenel, Patrick Lorès, Charles Coutton, Christophe Arnoult, Piétro Santulli, Catherine Patrat, Nicolas Thierry‐Mieg, Pierre F. Ray, Emmanuel Dulioust, Aminata Touré	33
11	CFAP61 is required for sperm flagellum formation and male fertility in human and mouse 2021 ·Development ·Siyu Liu, Jintao Zhang, Zine‐Eddine Kherraf, Shuya Sun, Xin Zhang, Caroline Cazin, Charles Coutton, Raoudha Zouari, Shuqin Zhao, Fan Hu, Sélima Fourati Ben Mustapha, Christophe Arnoult, Pierre F. Ray, Mingxi Liu	37
12	Combined Use of Whole Exome Sequencing and CRISPR/Cas9 to Study the Etiology of Non-Obstructive Azoospermia: Demonstration of the Dispensable Role of the Testis-Specific Genes C1orf185 and CCT6B 2021 ·Cells ·Caroline Cazin, Yasmine Neirijnck, Corinne Loeuillet, (unknown), Françoise Kühne, (unknown), Sélima Fourati Ben Mustapha, (unknown), Raoudha Zouari, Nicolas Thierry‐Mieg, Serge Nef, Christophe Arnoult, Pierre F. Ray, Zine‐Eddine Kherraf	1
13	Leucine zipper transcription factor-like 1 (LZTFL1), an intraflagellar transporter protein 27 (IFT27) associated protein, is required for normal sperm function and male fertility 2021 ·Developmental Biology ·Qian Huang, Wei Li, Qi Zhou, Parirokh Awasthi, Caroline Cazin, (unknown), (unknown), Bo Hu, Pancharatnam Jeyasuria, Ling Zhang, James G. Granneman, Rex A. Hess, Pierre F. Ray, Zine‐Eddine Kherraf, Ven Natarajan, Zhibing Zhang	8
14	The sperm-associated antigen 6 interactome and its role in spermatogenesis 2019 ·Reproduction ·Yunhao Liu, Ling Zhang, Wei Li, Qian Huang, Shuo Yuan, Yuhong Li, (unknown), Shiyang Zhang, (unknown), Shizhen Song, Pierre F. Ray, Christophe Arnoult, Chunghee Cho, (unknown), Uwe Knippschild, Jerome F. Strauss, Zhibing Zhang	28
15	Slo3 K+ channel blocker clofilium extends bull and mouse sperm-fertilizing competence 2018 ·Reproduction ·(unknown), Guillaume Martinez, (unknown), (unknown), (unknown), (unknown), Pierre F. Ray, Jessica Escoffier, Éric Schmitt, Christophe Arnoult	7
16	Missense Mutations in SLC26A8, Encoding a Sperm-Specific Activator of CFTR, Are Associated with Human Asthenozoospermia 2013 ·The American Journal of Human Genetics ·Thassadite Dirami, Baptiste Rode, (unknown), Nathalie Da Silva, Denise Escalier, (unknown), Caroline Norez, Pierre Tufféry, Jean‐Philippe Wolf, Frédéric Becq, Pierre F. Ray, Emmanuel Dulioust, Gérard Gâcon, Thierry Bienvenu, Aminata Touré	94
17	MLPA and sequence analysis of DPY19L2 reveals point mutations causing globozoospermia 2012 ·Human Reproduction ·Charles Coutton, Raoudha Zouari, (unknown), Mariem Ben Khelifa, Ghaya Merdassi, Chahnez Triki, Denise Escalier, Laëtitia Hesters, Valérie Mitchell, Rachel Lévy, Nathalie Sermondade, Florence Boitrelle, François Vialard, Véronique Satre, Sylviane Hennebicq, Pierre‐Simon Jouk, Christophe Arnoult, Joël Lunardi, Pierre F. Ray	52
18	DPY19L2 Deletion as a Major Cause of Globozoospermia 2011 ·The American Journal of Human Genetics ·Isabelle Koscinski, Elias Elinati, (unknown), Claire Redin, Jean Muller, (unknown), Françoise Schmitt, Mariem Ben Khelifa, Pierre F. Ray, Zaid Kilani, Christopher L. R. Barratt, Stéphane Viville	149
19	ESHRE preimplantation genetic diagnosis consortium: Data collection III (May 2001) 2002 ·Human Reproduction ·Karen Sermon, Joyce Harper, Joep Geraedts, (unknown), Alan H. Handyside, Damian J. Hussey, M.C. Magli, S. Munné, Pierre F. Ray, Josep Santaló, C. Staessen, Alan R. Thornhill, Stéphane Viville, L. Wilton	172
20	Paternal transcripts for glucose-6-phosphate dehydrogenase and adenosine deaminase are first detectable in the human preimplantation embryo at the Three- to Four-Cell stage 1997 ·Molecular Reproduction and Development ·Deborah M. Taylor, Pierre F. Ray, Asangla Ao, Robert Winston, Alan H. Handyside	53

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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