Pascale Hilbert

2.9k total citations
36 papers, 1.6k citations indexed

About

Pascale Hilbert is a scholar working on Molecular Biology, Genetics and Physiology. According to data from OpenAlex, Pascale Hilbert has authored 36 papers receiving a total of 1.6k indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Molecular Biology, 14 papers in Genetics and 6 papers in Physiology. Recurrent topics in Pascale Hilbert's work include Renal and related cancers (7 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers) and Nuclear Structure and Function (4 papers). Pascale Hilbert is often cited by papers focused on Renal and related cancers (7 papers), Genetic Mapping and Diversity in Plants and Animals (4 papers) and Nuclear Structure and Function (4 papers). Pascale Hilbert collaborates with scholars based in Belgium, France and United Kingdom. Pascale Hilbert's co-authors include G.M. Lathrop, Christopher Dubay, T. Serikawa, Michel Georges, J. Beckmann, Detlev Ganten, D Ganten, Cécile Julier, Klaus Lindpaintner and Florent Soubrier and has published in prestigious journals such as Nature, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Pascale Hilbert

34 papers receiving 1.5k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Pascale Hilbert Belgium 17 736 656 328 323 285 36 1.6k
Michiko Hayasaka Japan 14 1.6k 2.1× 421 0.6× 106 0.3× 69 0.2× 172 0.6× 22 2.0k
Ellen S. Pentz United States 23 1.1k 1.5× 156 0.2× 510 1.6× 259 0.8× 91 0.3× 34 1.5k
Juliette Hadchouel France 29 2.3k 3.1× 337 0.5× 226 0.7× 330 1.0× 175 0.6× 55 2.7k
Josef G. Heuer United States 20 818 1.1× 137 0.2× 357 1.1× 242 0.7× 108 0.4× 34 1.7k
Yasunobu Uchijima Japan 22 1.3k 1.7× 259 0.4× 76 0.2× 180 0.6× 176 0.6× 41 1.9k
Emil Karaulanov Germany 17 1.3k 1.8× 176 0.3× 176 0.5× 132 0.4× 80 0.3× 25 1.7k
Avinash Abhyankar United States 20 959 1.3× 650 1.0× 124 0.4× 39 0.1× 116 0.4× 30 1.9k
Ana C.P. Thirone Brazil 17 630 0.9× 101 0.2× 84 0.3× 354 1.1× 264 0.9× 21 1.3k
Diana Escalante‐Alcalde Mexico 21 2.3k 3.2× 263 0.4× 105 0.3× 42 0.1× 236 0.8× 38 2.8k
Masao Katoh Japan 20 564 0.8× 187 0.3× 43 0.1× 215 0.7× 262 0.9× 36 1.3k

Countries citing papers authored by Pascale Hilbert

Since Specialization
Citations

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

Fields of papers citing papers by Pascale Hilbert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pascale Hilbert

This figure shows the co-authorship network connecting the top 25 collaborators of Pascale Hilbert. A scholar is included among the top collaborators of Pascale Hilbert 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 Pascale Hilbert. Pascale Hilbert 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.. (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
2.
Wérion, Alexis, Claire Beguin, J. A. Bernards, et al.. (2023). Epidemiology, Outcomes, and Complement Gene Variants in Secondary Thrombotic Microangiopathies. Clinical Journal of the American Society of Nephrology. 18(7). 881–891. 12 indexed citations
3.
4.
Pace, Nikolai Paul, et al.. (2019). Two novel GJA1 variants in oculodentodigital dysplasia. Molecular Genetics & Genomic Medicine. 7(9). e882–e882. 6 indexed citations
5.
Gillion, Valentine, Karin Dahan, Jean‐Pierre Cosyns, et al.. (2018). Genotype and Outcome After Kidney Transplantation in Alport Syndrome. Kidney International Reports. 3(3). 652–660. 20 indexed citations
6.
Savige, Judy, Helen Storey, Hae Il Cheong, et al.. (2016). X-Linked and Autosomal Recessive Alport Syndrome: Pathogenic Variant Features and Further Genotype-Phenotype Correlations. PLoS ONE. 11(9). e0161802–e0161802. 63 indexed citations
7.
Rostami, Parastoo, et al.. (2013). AGPAT2 gene mutation in a child with Berardinelli-Seip congenital lipodystrophy syndrome. Annales d Endocrinologie. 74(1). 59–61. 5 indexed citations
8.
Oliveira, Jorge, Márcia E. Oliveira, Wolfram Kreß, et al.. (2012). Expanding the MTM1 mutational spectrum: novel variants including the first multi-exonic duplication and development of a locus-specific database. European Journal of Human Genetics. 21(5). 540–549. 20 indexed citations
9.
Terryn, Wim, Wouter Meersseman, Wim Van Biesen, et al.. (2012). Prevalence of Fabry disease in a predominantly hypertensive population with left ventricular hypertrophy. International Journal of Cardiology. 167(6). 2555–2560. 43 indexed citations
10.
Fríguls, Bibiana, et al.. (2008). Severe cardiac phenotype of Berardinelli-Seip congenital lipodystrophy in an infant with homozygous E189X BSCL2 mutation. European Journal of Medical Genetics. 52(1). 14–16. 25 indexed citations
11.
Cotton, Richard G.H., Arleen D. Auerbach, A. F. Brown, et al.. (2007). A structured simple form for ordering genetic tests is needed to ensure coupling of clinical detail (phenotype) with DNA variants (genotype) to ensure utility in publication and databases. Human Mutation. 28(10). 931–932. 9 indexed citations
12.
Houinato, Dismand Stéphan, et al.. (2007). Hypokalaemic periodic paralysis due to the CACNA1S R1239H mutation in a large African family. Neuromuscular Disorders. 17(5). 419–422. 8 indexed citations
13.
Hilbert, Pascale, et al.. (2006). Clinical findings and PDS mutations in 15 patients with hearing loss and dilatation of the vestibular aqueduct. The Journal of Laryngology & Otology. 121(4). 312–317. 8 indexed citations
14.
Dargent, Jean‐Louis, Candice Roufosse, Jean‐Pierre Delville, et al.. (1998). Subcutaneous panniculitis‐like T‐cell lymphoma: further evidence for a distinct neoplasm originating from large granular lymphocytes of T/NK phenotype. Journal of Cutaneous Pathology. 25(7). 394–400. 26 indexed citations
15.
Dan, Bernard, et al.. (1997). Institutionalised Adults with Angelman Syndrome. European Journal of Paediatric Neurology. 1(4). 2 indexed citations
16.
Lindpaintner, Klaus, Pascale Hilbert, Detlev Ganten, et al.. (1993). Molecular genetics of the SA-gene: cosegregation with hypertension and mapping to rat chromosome 1. Journal of Hypertension. 11(1). 19–23. 84 indexed citations
17.
Serikawa, T., Takashi Kuramoto, Pascale Hilbert, et al.. (1992). Rat gene mapping using PCR-analyzed microsatellites.. Genetics. 131(3). 701–721. 304 indexed citations
18.
Hilbert, Pascale, Klaus Lindpaintner, J. Beckmann, et al.. (1991). Chromosomal mapping of two genetic loci associated with blood-pressure regulation in hereditary hypertensive rats. Nature. 353(6344). 521–529. 495 indexed citations
19.
Georges, Michel, M Lathrop, Pascale Hilbert, et al.. (1990). Linkage relationships among 20 genetic markers in cattle Evidence for linkage between two pairs of blood group systems: B‐Z and S‐F/V respectively. Animal Genetics. 21(2). 95–105. 18 indexed citations
20.
Georges, Michel, et al.. (1988). Use of DNA bar codes to resolve a canine paternity dispute. Journal of the American Veterinary Medical Association. 193(9). 1095–1098. 1 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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