Paul Kuentz

8.3k total citations
32 papers, 323 citations indexed

About

Paul Kuentz is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Paul Kuentz has authored 32 papers receiving a total of 323 indexed citations (citations by other indexed papers that have themselves been cited), including 18 papers in Genetics, 16 papers in Molecular Biology and 4 papers in Surgery. Recurrent topics in Paul Kuentz's work include Genomics and Rare Diseases (6 papers), Genetic and rare skin diseases. (5 papers) and Hedgehog Signaling Pathway Studies (4 papers). Paul Kuentz is often cited by papers focused on Genomics and Rare Diseases (6 papers), Genetic and rare skin diseases. (5 papers) and Hedgehog Signaling Pathway Studies (4 papers). Paul Kuentz collaborates with scholars based in France, United States and Netherlands. Paul Kuentz's co-authors include Laurence Faivre, Julien Thévenon, Stéphane Viville, Naeem Iqbal, Petra De Sutter, F. Carré‐Pigeon, Zaid Kilani, Elias Elinati, Mohammad Hossein Nasr‐Esfahani and Timur Gürgan and has published in prestigious journals such as Nature Communications, The EMBO Journal and Human Molecular Genetics.

In The Last Decade

Paul Kuentz

31 papers receiving 320 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Paul Kuentz France 11 189 157 53 48 35 32 323
Glen R. Monroe Netherlands 12 216 1.1× 313 2.0× 23 0.4× 54 1.1× 44 1.3× 20 524
Rachel D. Mullen United States 11 220 1.2× 159 1.0× 79 1.5× 73 1.5× 16 0.5× 15 396
Marija Volk Slovenia 14 155 0.8× 115 0.7× 69 1.3× 54 1.1× 76 2.2× 36 378
Özge Özalp Yüreğir Türkiye 8 137 0.7× 133 0.8× 25 0.5× 19 0.4× 58 1.7× 20 288
N. A. Skryabin Russia 10 184 1.0× 157 1.0× 46 0.9× 10 0.2× 121 3.5× 46 371
Akiko Iizuka‐Kogo Japan 11 297 1.6× 106 0.7× 27 0.5× 26 0.5× 21 0.6× 21 419
Henrik Jörnvall Sweden 8 473 2.5× 76 0.5× 39 0.7× 11 0.2× 22 0.6× 20 581
Cassandra R. Farthing United Kingdom 6 497 2.6× 118 0.8× 36 0.7× 17 0.4× 64 1.8× 7 571
Ruth Kläver Germany 5 161 0.9× 56 0.4× 50 0.9× 81 1.7× 50 1.4× 6 278
Irén Haltrich Hungary 9 103 0.5× 93 0.6× 36 0.7× 10 0.2× 22 0.6× 33 239

Countries citing papers authored by Paul Kuentz

Since Specialization
Citations

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

Fields of papers citing papers by Paul Kuentz

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Paul Kuentz

This figure shows the co-authorship network connecting the top 25 collaborators of Paul Kuentz. A scholar is included among the top collaborators of Paul Kuentz 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 Paul Kuentz. Paul Kuentz 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.
Bonniaud, B., Maxime Luu, Catherine Cormier, et al.. (2025). Lack of behavioural improvement with sirolimus in a patient with MTOR-related macrocephaly with pigmentary mosaicism: A new case report. European Journal of Medical Genetics. 75. 105012–105012.
2.
Kuentz, Paul, Rachida Tacine, Marie Vincent, et al.. (2025). A postzygotic GNA13 variant upregulates the RHOA/ROCK pathway and alters melanocyte function in a mosaic skin hypopigmentation syndrome. Nature Communications. 16(1). 1751–1751. 2 indexed citations
3.
Hirsch, Théo Z., Dominique Vidaud, Véronique Laithier, et al.. (2025). Hepatoblastoma in a patient with neurofibromatosis type 1: A case report. Cancer Genetics. 292-293. 35–37. 1 indexed citations
4.
Chevarin, Martin, Juliette Piard, Quentin Thomas, et al.. (2024). Allelic heterogeneity in a patient with postzygotic MTOR ‐related hypomelanosis of Ito with neurodevelopmental abnormalities. Clinical Genetics. 105(5). 581–583. 2 indexed citations
5.
Bupp, Caleb, Dorothy K. Grange, Geoffroy Delplancq, et al.. (2023). TELO2‐related syndrome (You‐Hoover‐Fong syndrome): Description of 14 new affected individuals and review of the literature. American Journal of Medical Genetics Part A. 191(5). 1261–1272. 7 indexed citations
6.
Douzgou, Sofia, Eulàlia Baselga, Moise Danielpour, et al.. (2021). A standard of care for individuals with PIK3CA ‐related disorders: An international expert consensus statement. Clinical Genetics. 101(1). 32–47. 20 indexed citations
7.
Ravel, Jean‐Marie, Natacha Dreumont, Desirée E.C. Smith, et al.. (2021). A bi‐allelic loss‐of‐function SARS1 variant in children with neurodevelopmental delay, deafness, cardiomyopathy, and decompensation during fever. Human Mutation. 42(12). 1576–1583. 6 indexed citations
8.
Theiler, Martin, Lisa Weibel, Stéphanie Christen‐Zaech, et al.. (2021). Cerebriform sebaceous nevus: a subtype of organoid nevus due to specific postzygotic FGFR2 mutations. Journal of the European Academy of Dermatology and Venereology. 35(10). 2085–2090. 4 indexed citations
9.
Carmignac, Virginie, Arthur Sorlin, Yannis Duffourd, et al.. (2021). Clinical and molecular data in cases of prenatal localized overgrowth disorder: major implication of genetic variants in PI3K‐AKT‐mTOR signaling pathway. Ultrasound in Obstetrics and Gynecology. 59(4). 532–542. 7 indexed citations
10.
Besnard, Thomas, Mathilde Nizon, Christel Thauvin‐Robinet, et al.. (2021). Loss‐of‐function variants in ARHGEF9 are associated with an X‐linked intellectual disability dominant disorder. Human Mutation. 42(5). 498–505. 2 indexed citations
11.
Assoum, Mirna, Ange‐Line Bruel, Melissa Crenshaw, et al.. (2020). NovelKIAA1033/WASHC4mutations in three patients with syndromic intellectual disability and a review of the literature. American Journal of Medical Genetics Part A. 182(4). 792–797. 10 indexed citations
12.
Delplancq, Geoffroy, Antonio Vitobello, Sophie Nambot, et al.. (2020). Cardiomyopathy due to PRDM16 mutation: First description of a fetal presentation, with possible modifier genes. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 184(1). 129–135. 15 indexed citations
13.
Renosi, Florian, et al.. (2020). Post-Essential Thrombocythemia Myelofibrosis and Multiple Isodicentric Y Chromosomes: A Unique Case among a Rare Association. Cytogenetic and Genome Research. 160(1). 18–21. 1 indexed citations
14.
Ramond, Francis, Marlène Rio, Bénédicte Héron, et al.. (2020). AICA‐ribosiduria due to ATIC deficiency: Delineation of the phenotype with three novel cases, and long‐term update on the first case. Journal of Inherited Metabolic Disease. 43(6). 1254–1264. 26 indexed citations
15.
Thévenon, Julien, Yannis Duffourd, Sophie Nambot, et al.. (2018). TBL1XR1 mutations in Pierpont syndrome are not restricted to the recurrent p.Tyr446Cys mutation. American Journal of Medical Genetics Part A. 176(12). 2813–2818. 12 indexed citations
16.
Kuentz, Paul, Yannis Duffourd, Laurence Faivre, et al.. (2018). Severe gynaecological involvement in Proteus Syndrome. European Journal of Medical Genetics. 62(4). 270–272. 2 indexed citations
17.
Falcon‐Eicher, Sylvie, Gabriel Laurent, E Villain, et al.. (2016). Incomplete Timothy syndrome secondary to a mosaic mutation of the CACNA1C gene diagnosed using next‐generation sequencing. American Journal of Medical Genetics Part A. 173(2). 531–536. 8 indexed citations
18.
Chevrier, Véronique, Ange‐Line Bruel, Teunis J. P. van Dam, et al.. (2015). OFIP/KIAA0753 forms a complex with OFD1 and FOR20 at pericentriolar satellites and centrosomes and is mutated in one individual with oral-facial-digital syndrome. Human Molecular Genetics. 25(3). 497–513. 35 indexed citations
19.
Kuentz, Paul, Frauke Vanden Meerschaut, Elias Elinati, et al.. (2013). Assisted oocyte activation overcomes fertilization failure in globozoospermic patients regardless of the DPY19L2 status. Human Reproduction. 28(4). 1054–1061. 59 indexed citations
20.
Kuentz, Paul, et al.. (2011). Child with Beckwith-Wiedemann syndrome born after assisted reproductive techniques to an human immunodeficiency virus serodiscordant couple. Fertility and Sterility. 96(1). e35–e38. 4 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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