Laure Raymond

1.6k total citations
22 papers, 355 citations indexed

About

Laure Raymond is a scholar working on Genetics, Molecular Biology and Nephrology. According to data from OpenAlex, Laure Raymond has authored 22 papers receiving a total of 355 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Molecular Biology and 4 papers in Nephrology. Recurrent topics in Laure Raymond's work include Renal Diseases and Glomerulopathies (4 papers), Genomics and Rare Diseases (3 papers) and Renal and related cancers (3 papers). Laure Raymond is often cited by papers focused on Renal Diseases and Glomerulopathies (4 papers), Genomics and Rare Diseases (3 papers) and Renal and related cancers (3 papers). Laure Raymond collaborates with scholars based in France, Morocco and Germany. Laure Raymond's co-authors include Manuel Bardiès, Jean‐Pierre Pouget, Pierre‐Olivier Kotzki, D. Azria, Caroline Mollévi, André Pèlegrin, Nicolas Chouin, Éric Vivès, Hélèna Huguet and Lore Santoro and has published in prestigious journals such as Journal of the American Society of Nephrology, The American Journal of Human Genetics and Gene.

In The Last Decade

Laure Raymond

19 papers receiving 349 citations

Peers

Laure Raymond
Kemal O. Yariz United States
Elizabeth Asch United States
P Sedlaczek Poland
Andreas Turzynski Germany
Mary Lin United States
Duncan Forster United Kingdom
Raj Nayan Sewduth Belgium
Rosita Winkler Belgium
Kemal O. Yariz United States
Laure Raymond
Citations per year, relative to Laure Raymond Laure Raymond (= 1×) peers Kemal O. Yariz

Countries citing papers authored by Laure Raymond

Since Specialization
Citations

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

Fields of papers citing papers by Laure Raymond

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laure Raymond

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

All Works

20 of 20 papers shown
1.
Robert, Thomas, et al.. (2025). Kidney Cysts in Alport Syndrome: Illustrative Cases, but Misleading Conclusions. American Journal of Kidney Diseases. 87(1). 134–135.
2.
Launay, Manon, Laure Raymond, Jérôme Guitton, et al.. (2024). Can we identify patients carrying targeted deleterious DPYD variants with plasma uracil and dihydrouracil? A GPCO-RNPGx retrospective analysis. Clinical Chemistry and Laboratory Medicine (CCLM). 62(12). 2415–2424.
3.
Robert, Thomas, et al.. (2024). Systematic Screening of Autosomal Dominant Tubulointerstitial Kidney Disease–MUC1 27dupC Pathogenic Variant through Exome Sequencing. Journal of the American Society of Nephrology. 36(2). 256–263. 3 indexed citations
4.
Verstuyft, Céline, Olivier Blin, Laurent Mesnard, et al.. (2024). How to facilitate the wider use of pharmacogenetic tests?. Therapies. 80(1). 103–112.
5.
Raymond, Laure, et al.. (2024). Diagnostic Yield of Exome Sequencing in Early-Onset Hypertensive Nephropathy in Adults. American Journal of Nephrology. 55(4). 468–471. 1 indexed citations
6.
Mesnard, Laurent, et al.. (2023). #6812 ON THE TOP PHARMACOGENETICS STUDY EXTRACTED FROM EXOME SEQUENCING DONE FOR CHRONIC KIDNEY DISEASES OF UNKNOW ORIGIN. Nephrology Dialysis Transplantation. 38(Supplement_1). 1 indexed citations
7.
8.
Raymond, Laure, et al.. (2023). Role of the I416L Variant of Complement Factor I in Thrombotic Microangiopathy Among Patients of African Ancestry. Kidney International Reports. 8(10). 2136–2140. 1 indexed citations
9.
Robert, Thomas, Laure Raymond, Noémie Jourde‐Chiche, et al.. (2023). Diagnosis of Kidney Diseases of Unknown Etiology Through Biopsy-Genetic Analysis. Kidney International Reports. 8(10). 2077–2087. 7 indexed citations
10.
Mattioli, Francesca, Lina Worpenberg, Shagufta Naz, et al.. (2023). Biallelic variants in NSUN6 cause an autosomal recessive neurodevelopmental disorder. Genetics in Medicine. 25(9). 100900–100900. 12 indexed citations
11.
Robert, Thomas, Laure Raymond, Noémie Jourde‐Chiche, et al.. (2023). Beyond the kidney biopsy: genomic approach to undetermined kidney diseases. Clinical Kidney Journal. 17(1). sfad099–sfad099. 10 indexed citations
12.
Kherraf, Zine‐Eddine, Caroline Cazin, Sélima Fourati Ben Mustapha, et al.. (2022). Whole-exome sequencing improves the diagnosis and care of men with non-obstructive azoospermia. The American Journal of Human Genetics. 109(3). 508–517. 74 indexed citations
13.
Letavernier, Emmanuel, Marine Livrozet, Laure Raymond, et al.. (2021). Atypical Clinical Presentation of Autosomal Recessive Polycystic Kidney Mimicking Medullary Sponge Kidney Disease. Kidney International Reports. 7(4). 916–919. 4 indexed citations
14.
Elalaoui, Siham Chafai, et al.. (2020). Exome sequencing revealed a novel homozygous METTL23 gene mutation leading to familial mild intellectual disability with dysmorphic features. European Journal of Medical Genetics. 63(7). 103951–103951. 9 indexed citations
15.
Jaouad, Imane Cherkaoui, et al.. (2018). A novel non sense mutation in WDR62 causes autosomal recessive primary microcephaly: a case report. BMC Medical Genetics. 19(1). 118–118. 6 indexed citations
16.
17.
Lyahyai, Jaber, et al.. (2017). Next Generation Sequencing identifies mutations in GNPTG gene as a cause of familial form of scleroderma-like disease. Pediatric Rheumatology. 15(1). 72–72. 2 indexed citations
18.
Raymond, Laure, Bruno Francou, François Petit, et al.. (2015). Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts. European Journal of Medical Genetics. 58(11). 591–596. 3 indexed citations
19.
Raymond, Laure, Hélène Maurey, Valérie Drouin‐Garraud, et al.. (2012). Validation of high-resolution DNA melting analysis for mutation scanning of the CDKL5 gene: Identification of novel mutations. Gene. 512(1). 70–75. 8 indexed citations
20.
Pouget, Jean‐Pierre, Lore Santoro, Laure Raymond, et al.. (2008). Cell Membrane is a More Sensitive Target than Cytoplasm to Dense Ionization Produced by Auger Electrons. Radiation Research. 170(2). 192–200. 102 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.

Explore authors with similar magnitude of impact

Breakdown of academic impact, for papers by Kemal O. Yariz Breakdown of academic impact, for papers by Elizabeth Asch Breakdown of academic impact, for papers by P Sedlaczek Breakdown of academic impact, for papers by Andreas Turzynski Breakdown of academic impact, for papers by Mary Lin Breakdown of academic impact, for papers by Duncan Forster Breakdown of academic impact, for papers by Raj Nayan Sewduth Breakdown of academic impact, for papers by Rosita Winkler
Rankless by CCL
2026