Yline Capri

2.9k total citations
33 papers, 381 citations indexed

About

Yline Capri is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Yline Capri has authored 33 papers receiving a total of 381 indexed citations (citations by other indexed papers that have themselves been cited), including 21 papers in Genetics, 20 papers in Molecular Biology and 4 papers in Cell Biology. Recurrent topics in Yline Capri's work include Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Protein Tyrosine Phosphatases (5 papers). Yline Capri is often cited by papers focused on Genetics and Neurodevelopmental Disorders (7 papers), Genomic variations and chromosomal abnormalities (6 papers) and Protein Tyrosine Phosphatases (5 papers). Yline Capri collaborates with scholars based in France, United States and Belgium. Yline Capri's co-authors include Alain Verloès, Clarisse Baumann, Anne‐Claude Tabet, Céline Dupont, Azzedine Aboura, Séverine Drunat, Laurence Perrin, Catherine Delanöe, Essam Al Ageeli and Stéphane Auvin and has published in prestigious journals such as Journal of Bone and Mineral Research, Journal of Medical Genetics and European Journal of Endocrinology.

In The Last Decade

Yline Capri

29 papers receiving 349 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Yline Capri France 12 222 181 62 56 36 33 381
Kit San Yeung Hong Kong 13 252 1.1× 245 1.4× 43 0.7× 65 1.2× 32 0.9× 29 529
Siren Berland Norway 11 360 1.6× 207 1.1× 20 0.3× 51 0.9× 11 0.3× 28 478
Arivudainambi Ramalingam United States 9 219 1.0× 128 0.7× 29 0.5× 29 0.5× 75 2.1× 13 361
Emmanuelle Ranza Switzerland 12 137 0.6× 103 0.6× 56 0.9× 20 0.4× 18 0.5× 22 295
Kemal O. Yariz United States 8 212 1.0× 90 0.5× 32 0.5× 12 0.2× 27 0.8× 9 346
Tadeusz Mazurczak Poland 17 299 1.3× 444 2.5× 25 0.4× 102 1.8× 70 1.9× 57 763
Sietske H. Kevelam Netherlands 10 283 1.3× 83 0.5× 35 0.6× 19 0.3× 10 0.3× 11 473
Nara Sobreira United States 10 325 1.5× 323 1.8× 42 0.7× 20 0.4× 17 0.5× 27 550
Dominique J. Verlaan Canada 12 224 1.0× 122 0.7× 38 0.6× 16 0.3× 16 0.4× 13 655
Michèle Mathieu France 9 341 1.5× 310 1.7× 12 0.2× 64 1.1× 36 1.0× 18 622

Countries citing papers authored by Yline Capri

Since Specialization
Citations

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

Fields of papers citing papers by Yline Capri

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Yline Capri

This figure shows the co-authorship network connecting the top 25 collaborators of Yline Capri. A scholar is included among the top collaborators of Yline Capri 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 Yline Capri. Yline Capri 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.
2.
Capri, Yline, Thérèsa Kwon, Olivia Boyer, et al.. (2023). Biallelic NPR1 loss of function variants are responsible for neonatal systemic hypertension. Journal of Medical Genetics. 60(10). 993–998.
3.
Capri, Yline, Céline Dupont, Fabien Guimiot, et al.. (2023). DST variants are responsible for neurogenic arthrogryposis multiplex congenita enlarging the spectrum of type VI hereditary sensory autonomic neuropathy. Clinical Genetics. 104(5). 587–592. 2 indexed citations
4.
Breton, Sylvain, Marie‐Liesse Piketty, Alexandra Afenjar, et al.. (2022). SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients. Orphanet Journal of Rare Diseases. 17(1). 100–100. 10 indexed citations
5.
Baer, Sarah, Cathy Obringer, Sophie Julia, et al.. (2020). Early‐onset nucleotide excision repair disorders with neurological impairment: Clues for early diagnosis and prognostic counseling. Clinical Genetics. 98(3). 251–260. 11 indexed citations
6.
Lévy, Jonathan, Yline Capri, Céline Dupont, et al.. (2020). LEF1 haploinsufficiency causes ectodermal dysplasia. Clinical Genetics. 97(4). 595–600. 12 indexed citations
7.
Pennamen, Perrine, Angèle Tingaud‐Sequeira, Vincent Michaud, et al.. (2020). Novel variants in the BLOC1S3 gene in patients presenting a mild form of Hermansky–Pudlak syndrome. Pigment Cell & Melanoma Research. 34(1). 132–135. 7 indexed citations
8.
Michot, Caroline, Geneviève Baujat, S. Baron, et al.. (2019). Pycnodysostosis: Natural history and management guidelines from 27 French cases and a literature review. Clinical Genetics. 96(4). 309–316. 31 indexed citations
9.
Capri, Yline, Catherine Pienkowski, Benoît Lepage, et al.. (2019). Gonadal Function of Female Patients with Noonan Syndrome. 92. 1 indexed citations
10.
Jacquinet, Adeline, Yline Capri, Didier Martin, et al.. (2019). Oligo-astrocytoma in LZTR1-related Noonan syndrome. European Journal of Medical Genetics. 63(1). 103617–103617. 19 indexed citations
11.
Bruel, Ange‐Line, Jonathan Lévy, Narcisse Elenga, et al.. (2018). INTU‐related oral‐facial‐digital syndrome type VI: A confirmatory report. Clinical Genetics. 93(6). 1205–1209. 6 indexed citations
12.
Lévy, Jonathan, Aurélie Coussement, Céline Dupont, et al.. (2017). Molecular and clinical delineation of 2p15p16.1 microdeletion syndrome. American Journal of Medical Genetics Part A. 173(8). 2081–2087. 15 indexed citations
13.
Saugier-Véber, Pascale, Florent Marguet, François Lecoquierre, et al.. (2017). Hydrocephalus due to multiple ependymal malformations is caused by mutations in the MPDZ gene. Acta Neuropathologica Communications. 5(1). 36–36. 23 indexed citations
14.
Capri, Yline, et al.. (2017). Pachydermoperiostosis: The value of molecular diagnosis. Annales de Dermatologie et de Vénéréologie. 144(12). 799–803. 1 indexed citations
15.
Ehlinger, Virginie, Catherine Arnaud, Armelle Yart, et al.. (2016). Growth patterns of patients with Noonan syndrome: correlation with age and genotype. European Journal of Endocrinology. 174(5). 641–650. 37 indexed citations
16.
Bouchereau, Juliette, Thierry Dupré, Stuart Moore, et al.. (2016). Abnormal Glycosylation Profile and High Alpha-Fetoprotein in a Patient with Twinkle Variants. JIMD Reports. 29. 109–113. 5 indexed citations
17.
Brisset, Sophie, Yline Capri, Audrey Briand‐Suleau, et al.. (2015). Inherited 1q21.1q21.2 duplication and 16p11.2 deletion: A two-hit case with more severe clinical manifestations. European Journal of Medical Genetics. 58(9). 497–501. 19 indexed citations
18.
Ageeli, Essam Al, Séverine Drunat, Catherine Delanöe, et al.. (2013). Duplication of the 15q11-q13 region: Clinical and genetic study of 30 new cases. European Journal of Medical Genetics. 57(1). 5–14. 67 indexed citations
19.
Rambaud, Jérôme, Isabelle Marey, Céline Dupont, et al.. (2012). Nail and phalangeal agenesis in a patient with 4pter and 9pter duplication. American Journal of Medical Genetics Part A. 158A(9). 2277–2282. 2 indexed citations
20.
Debost‐Legrand, Anne, Yline Capri, Laëtitia Gouas, et al.. (2010). De novo unbalanced translocation 2;4 characterized by metaphase CGH and array CGH in a child with mental retardation and dysmorphic features. Pathologie Biologie. 59(6). 309–313.

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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