Olivier Gribouval

8.4k total citations · 1 hit paper
47 papers, 3.9k citations indexed

About

Olivier Gribouval is a scholar working on Molecular Biology, Nephrology and Genetics. According to data from OpenAlex, Olivier Gribouval has authored 47 papers receiving a total of 3.9k indexed citations (citations by other indexed papers that have themselves been cited), including 31 papers in Molecular Biology, 27 papers in Nephrology and 10 papers in Genetics. Recurrent topics in Olivier Gribouval's work include Renal Diseases and Glomerulopathies (27 papers), Renal and related cancers (16 papers) and Ion Transport and Channel Regulation (11 papers). Olivier Gribouval is often cited by papers focused on Renal Diseases and Glomerulopathies (27 papers), Renal and related cancers (16 papers) and Ion Transport and Channel Regulation (11 papers). Olivier Gribouval collaborates with scholars based in France, United Kingdom and Switzerland. Olivier Gribouval's co-authors include Corinne Antignac, Marie-Claire Gübler, Patrick Niaudet, Séverine Roselli, Nicolas Boute, France Benessy, Arno Fuchshuber, Hyun Joo Lee, Karin Dahan and M. Broyer and has published in prestigious journals such as New England Journal of Medicine, Nature Genetics and PLoS ONE.

In The Last Decade

Olivier Gribouval

44 papers receiving 3.9k citations

Hit Papers

NPHS2, encoding the glomerular protein podocin, is mutate... 2000 2026 2008 2017 2000 250 500 750 1000
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.

  1. NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome
    2000 1.1k citations Nicolas Boute, Olivier Gribouval et al. Nature Genetics profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Olivier Gribouval France 25 2.4k 1.9k 906 871 523 47 3.9k
Constantinos Deltas Cyprus 31 1.1k 0.5× 2.4k 1.3× 531 0.6× 2.0k 2.3× 301 0.6× 104 4.3k
Sandra Merscher United States 26 1.6k 0.7× 1.2k 0.6× 423 0.5× 314 0.4× 67 0.1× 56 2.9k
Vesa Ruotsalainen Finland 22 3.4k 1.4× 2.1k 1.1× 603 0.7× 868 1.0× 118 0.2× 26 4.4k
Lorenz Sellin Germany 28 1.0k 0.4× 1.5k 0.8× 488 0.5× 739 0.8× 93 0.2× 59 2.8k
Emily Farrow United States 28 1.1k 0.5× 951 0.5× 332 0.4× 1.3k 1.4× 113 0.2× 73 2.5k
Friedhelm Hildebrandt United States 22 971 0.4× 958 0.5× 264 0.3× 618 0.7× 209 0.4× 44 1.9k
Nina Jones Canada 30 940 0.4× 2.1k 1.1× 206 0.2× 391 0.4× 29 0.1× 59 3.3k
Anne S. Olsen United States 12 1.5k 0.6× 1.1k 0.6× 279 0.3× 462 0.5× 63 0.1× 16 2.2k
Séverine Roselli Australia 16 1.4k 0.6× 1.0k 0.5× 266 0.3× 389 0.4× 54 0.1× 23 2.4k
Laura Giardino Italy 15 1.0k 0.4× 654 0.3× 198 0.2× 242 0.3× 56 0.1× 19 1.6k

Countries citing papers authored by Olivier Gribouval

Since Specialization
Citations

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

Fields of papers citing papers by Olivier Gribouval

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olivier Gribouval

This figure shows the co-authorship network connecting the top 25 collaborators of Olivier Gribouval. A scholar is included among the top collaborators of Olivier Gribouval 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 Olivier Gribouval. Olivier Gribouval 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.
Gribouval, Olivier, Christelle Arrondel, Olivia Boyer, et al.. (2023). Overcoming the challenges associated with identification of deep intronic variants by whole genome sequencing. Clinical Genetics. 103(6). 693–698. 3 indexed citations
2.
Dorval, Guillaume, Olivier Gribouval, Gavin I. Welsh, et al.. (2019). TBC1D8B Loss-of-Function Mutations Lead to X-Linked Nephrotic Syndrome via Defective Trafficking Pathways. The American Journal of Human Genetics. 104(2). 348–355. 33 indexed citations
3.
Servais, Aude, Olivier Gribouval, F. Gaillard, & Corinne Antignac. (2019). APOL1 risk genotype in Europe: Data in patients with focal segmental glomerulosclerosis and after renal transplantation. Néphrologie & Thérapeutique. 15. S85–S89. 3 indexed citations
4.
Gribouval, Olivier, Olivia Boyer, Aurélie Hummel, et al.. (2018). Identification of genetic causes for sporadic steroid-resistant nephrotic syndrome in adults. Kidney International. 94(5). 1013–1022. 41 indexed citations
5.
Michaud, Annie, K. Ravi Acharya, Geoffrey Masuyer, et al.. (2013). Absence of cell surface expression of human ACE leads to perinatal death. Human Molecular Genetics. 23(6). 1479–1491. 14 indexed citations
6.
Schreiber, Ruth, Marie-Claire Gübler, Olivier Gribouval, Hanna Shalev, & Daniel Landau. (2010). Inherited renal tubular dysgenesis may not be universally fatal. Pediatric Nephrology. 25(12). 2531–2534. 19 indexed citations
7.
Danilov, Sergei M., Sergey Kalinin, Zhenlong Chen, et al.. (2010). Angiotensin I-Converting Enzyme Gln1069Arg Mutation Impairs Trafficking to the Cell Surface Resulting in Selective Denaturation of the C-Domain. PLoS ONE. 5(5). e10438–e10438. 28 indexed citations
8.
Machuca, Eduardo, Geneviève Benoît, Fabien Névo, et al.. (2010). Genotype–Phenotype Correlations in Non-Finnish Congenital Nephrotic Syndrome. Journal of the American Society of Nephrology. 21(7). 1209–1217. 92 indexed citations
9.
Benoît, Geneviève, Eduardo Machuca, Fabien Névo, et al.. (2009). Analysis of recessive CD2AP and ACTN4 mutations in steroid-resistant nephrotic syndrome. Pediatric Nephrology. 25(3). 445–451. 25 indexed citations
10.
Bacchetta, Justine, Pierre Corvol, Annie Michaud, et al.. (2007). Inherited renal tubular dysgenesis: the first patients surviving the neonatal period. European Journal of Pediatrics. 167(3). 311–316. 27 indexed citations
11.
Plaisier, Emmanuelle, Olivier Gribouval, Sonia Alamowitch, et al.. (2007). COL4A1 Mutations and Hereditary Angiopathy, Nephropathy, Aneurysms, and Muscle Cramps. New England Journal of Medicine. 357(26). 2687–2695. 226 indexed citations
12.
Gribouval, Olivier, Corinne Antignac, & Marie-Claire Gübler. (2006). Mutations des gènes du système rénine-angiotensine et dysgénésie tubulaire rénale. médecine/sciences. 22(3). 246–248. 1 indexed citations
13.
Plaisier, Emmanuelle, Sonia Alamowitch, Olivier Gribouval, et al.. (2005). Autosomal-dominant familial hematuria with retinal arteriolar tortuosity and contractures: A novel syndrome. Kidney International. 67(6). 2354–2360. 28 indexed citations
14.
Zhang, Shaoyu, Arnaud Marlier, Olivier Gribouval, et al.. (2004). In vivo expression of podocyte slit diaphragm-associated proteins in nephrotic patients with NPHS2 mutation. Kidney International. 66(3). 945–954. 37 indexed citations
15.
Özer, Esra Arun, Nejat Aksu, Hakan Erdoğan, et al.. (2004). A novel NPHS2 gene mutation in Turkish children with familial steroid‐resistant nephrotic syndrome. Nephrology. 9(5). 310–312. 4 indexed citations
16.
Roselli, Séverine, Olivier Gribouval, Nicolas Boute, et al.. (2002). Podocin Localizes in the Kidney to the Slit Diaphragm Area. American Journal Of Pathology. 160(1). 131–139. 264 indexed citations
17.
Boute, Nicolas, Olivier Gribouval, Séverine Roselli, et al.. (2000). NPHS2, encoding the glomerular protein podocin, is mutated in autosomal recessive steroid-resistant nephrotic syndrome. Nature Genetics. 24(4). 349–354. 1074 indexed citations breakdown →
18.
Town, Margaret, G Jean, Stéphanie Cherqui, et al.. (1998). A novel gene encoding an integral membrane protein is mutated in nephropathic cystinosis. Nature Genetics. 18(4). 319–324. 447 indexed citations
19.
Fuchshuber, Arno, Olivier Gribouval, G Jean, et al.. (1996). Congenital nephrotic syndrome of the Finnish type: linkage to the locus in a non-Finnish population. Pediatric Nephrology. 10(2). 135–138. 29 indexed citations
20.
Fuchshuber, Arno, G Jean, Olivier Gribouval, et al.. (1995). Mapping a gene (SRN1) to chromosome 1q25-q31 in idiopathic nephrotic syndrome confirms a distinct entity of autosomal recessive nephrosis. Human Molecular Genetics. 4(11). 2155–2158. 92 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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