Ludmila Jornéa

1.2k total citations
14 papers, 316 citations indexed

About

Ludmila Jornéa is a scholar working on Obstetrics and Gynecology, Reproductive Medicine and Neurology. According to data from OpenAlex, Ludmila Jornéa has authored 14 papers receiving a total of 316 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Obstetrics and Gynecology, 7 papers in Reproductive Medicine and 6 papers in Neurology. Recurrent topics in Ludmila Jornéa's work include Endometriosis Research and Treatment (7 papers), Endometrial and Cervical Cancer Treatments (6 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Ludmila Jornéa is often cited by papers focused on Endometriosis Research and Treatment (7 papers), Endometrial and Cervical Cancer Treatments (6 papers) and Amyotrophic Lateral Sclerosis Research (6 papers). Ludmila Jornéa collaborates with scholars based in France, United Kingdom and Italy. Ludmila Jornéa's co-authors include Sofiane Bendifallah, Cyril Touboul, Yohann Dabi, Anne Puchar, Stéphane Suisse, Delphine Bouteiller, Émile Daraï, François Golfier, Philippe Descamps and Léa Delbos and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and The American Journal of Human Genetics.

In The Last Decade

Ludmila Jornéa

14 papers receiving 311 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Ludmila Jornéa France	10	128	116	103	85	73	14	316
W Halliday Canada	6	28 0.2×	29 0.3×	89 0.9×	210 2.5×	18 0.2×	6	358
Jennifer Hague United Kingdom	6	22 0.2×	10 0.1×	12 0.1×	146 1.7×	8 0.1×	7	252
Elena Fineberg United Kingdom	6	6 0.0×	40 0.3×	180 1.7×	144 1.7×	18 0.2×	6	396
Yinghui Fu China	9	8 0.1×	10 0.1×	12 0.1×	211 2.5×	41 0.6×	13	328
Erika Della Mina Italy	8	30 0.2×	2 0.0×	25 0.2×	124 1.5×	11 0.2×	16	263
Jiajing Wu China	9	5 0.0×	7 0.1×	45 0.4×	139 1.6×	42 0.6×	19	261
Bei Jun Chen Australia	12	5 0.0×	12 0.1×	17 0.2×	407 4.8×	14 0.2×	21	469
David Nonis Germany	10	11 0.1×	3 0.0×	95 0.9×	257 3.0×	5 0.1×	12	371
Mohammed Omedul Islam Japan	9	2 0.0×	22 0.2×	13 0.1×	149 1.8×	7 0.1×	10	305
Christopher Terranova United States	11	26 0.2×	2 0.0×	5 0.0×	257 3.0×	12 0.2×	17	367

Countries citing papers authored by Ludmila Jornéa

Since Specialization

Citations

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

Fields of papers citing papers by Ludmila Jornéa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Ludmila Jornéa

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

All Works

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14 of 14 papers shown

Bendifallah, Sofiane, Yohann Dabi, Stéphane Suisse, et al.. (2024). Saliva-based microRNA diagnostic signature for the superficial peritoneal endometriosis phenotype. European Journal of Obstetrics & Gynecology and Reproductive Biology. 297. 187–196. 7 indexed citations

Kacher, Radhia, François‐Xavier Lejeune, Giulia Coarelli, et al.. (2024). CAG repeat mosaicism is gene specific in spinocerebellar ataxias. The American Journal of Human Genetics. 111(5). 913–926. 9 indexed citations

Dabi, Yohann, Stéphane Suisse, Yannick Marie, et al.. (2023). New class of RNA biomarker for endometriosis diagnosis: The potential of salivary piRNA expression. European Journal of Obstetrics & Gynecology and Reproductive Biology. 291. 88–95. 10 indexed citations

Bendifallah, Sofiane, Stéphane Suisse, Anne Puchar, et al.. (2022). Salivary MicroRNA Signature for Diagnosis of Endometriosis. Journal of Clinical Medicine. 11(3). 612–612. 76 indexed citations

Dabi, Yohann, Stéphane Suisse, Anne Puchar, et al.. (2022). Endometriosis-associated infertility diagnosis based on saliva microRNA signatures. Reproductive BioMedicine Online. 46(1). 138–149. 20 indexed citations

Bendifallah, Sofiane, Yohann Dabi, Stéphane Suisse, et al.. (2022). MicroRNome analysis generates a blood-based signature for endometriosis. Scientific Reports. 12(1). 4051–4051. 31 indexed citations

Bendifallah, Sofiane, Yohann Dabi, Stéphane Suisse, et al.. (2022). A Bioinformatics Approach to MicroRNA-Sequencing Analysis Based on Human Saliva Samples of Patients with Endometriosis. International Journal of Molecular Sciences. 23(14). 8045–8045. 14 indexed citations

Bendifallah, Sofiane, Yohann Dabi, Stéphane Suisse, et al.. (2022). Endometriosis Associated-miRNome Analysis of Blood Samples: A Prospective Study. Diagnostics. 12(5). 1150–1150. 5 indexed citations

Anquetil, Vincent, Dario Saracino, Daisy Rinaldi, et al.. (2020). Plasma microRNA signature in presymptomatic and symptomatic subjects with C9orf72-associated frontotemporal dementia and amyotrophic lateral sclerosis. Journal of Neurology Neurosurgery & Psychiatry. 92(5). 485–493. 32 indexed citations

10.

Saracino, Dario, Leila Sellami, Fabienne Clot, et al.. (2019). The missense p.Trp7Arg mutation in GRN gene leads to progranulin haploinsufficiency. Neurobiology of Aging. 85. 154.e9–154.e11. 4 indexed citations

11.

Caroppo, Paola, Agnès Camuzat, Anne de Septenville, et al.. (2015). Semantic and nonfluent aphasic variants, secondarily associated with amyotrophic lateral sclerosis, are predominant frontotemporal lobar degeneration phenotypes in TBK1 carriers. Alzheimer s & Dementia Diagnosis Assessment & Disease Monitoring. 1(4). 481–486. 30 indexed citations

12.

Clot, Fabienne, Anne Rovelet‐Lecrux, Foudil Lamari, et al.. (2014). Partial deletions of the GRN gene are a cause of frontotemporal lobar degeneration. Neurogenetics. 15(2). 95–100. 7 indexed citations

13.

Ber, Isabelle Le, Gaël Nicolas, Agnès Camuzat, et al.. (2013). hnRNPA2B1 and hnRNPA1 mutations are rare in patients with “multisystem proteinopathy” and frontotemporal lobar degeneration phenotypes. Neurobiology of Aging. 35(4). 934.e5–934.e6. 51 indexed citations

14.

Guillot‐Noël, Léna, Florence Pasquier, Ludmila Jornéa, et al.. (2010). CHMP2B mutations are rare in French families with frontotemporal lobar degeneration. Journal of Neurology. 257(12). 2032–2036. 20 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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