Jelena Martinović

7.4k total citations
107 papers, 2.7k citations indexed

About

Jelena Martinović is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Jelena Martinović has authored 107 papers receiving a total of 2.7k indexed citations (citations by other indexed papers that have themselves been cited), including 38 papers in Genetics, 37 papers in Molecular Biology and 36 papers in Surgery. Recurrent topics in Jelena Martinović's work include Congenital Diaphragmatic Hernia Studies (19 papers), Prenatal Screening and Diagnostics (16 papers) and Congenital Anomalies and Fetal Surgery (15 papers). Jelena Martinović is often cited by papers focused on Congenital Diaphragmatic Hernia Studies (19 papers), Prenatal Screening and Diagnostics (16 papers) and Congenital Anomalies and Fetal Surgery (15 papers). Jelena Martinović collaborates with scholars based in France, Canada and United States. Jelena Martinović's co-authors include Alexandra Benachi, Tania Attié‐Bitach, Yves Dumez, Arnold Münnich, Martine Le Merrer, Marc Dommergues, Anne‐Lise Delezoide, Rodrigo Ruano, Marie-Claire Gübler and Y. Ville and has published in prestigious journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

In The Last Decade

Jelena Martinović

103 papers receiving 2.6k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Jelena Martinović France 27 1.1k 848 730 630 620 107 2.7k
Heiko Reutter Germany 27 909 0.8× 1.1k 1.3× 607 0.8× 445 0.7× 637 1.0× 178 2.7k
Christina Engel Hoei‐Hansen Denmark 27 1.5k 1.4× 1.3k 1.6× 600 0.8× 228 0.4× 265 0.4× 87 2.7k
Christine Francannet France 23 751 0.7× 552 0.7× 737 1.0× 440 0.7× 241 0.4× 77 2.0k
Tom H. Lindner Germany 21 1.1k 1.0× 634 0.7× 694 1.0× 92 0.1× 409 0.7× 49 2.2k
David D. Weaver United States 33 1.3k 1.2× 970 1.1× 1.6k 2.2× 262 0.4× 699 1.1× 117 3.3k
Mahin Golabi United States 26 1.3k 1.2× 470 0.6× 1.2k 1.6× 146 0.2× 386 0.6× 59 2.4k
Michelle Wei United States 11 1.2k 1.1× 251 0.3× 349 0.5× 396 0.6× 291 0.5× 17 1.9k
Luisa De Sanctis Italy 26 973 0.9× 301 0.4× 896 1.2× 334 0.5× 316 0.5× 126 2.3k
Dianne Abuelo United States 23 757 0.7× 699 0.8× 768 1.1× 199 0.3× 298 0.5× 52 1.9k
Katja P. Wolffenbuttel Netherlands 30 2.2k 1.9× 1.3k 1.5× 1.2k 1.6× 263 0.4× 395 0.6× 85 3.2k

Countries citing papers authored by Jelena Martinović

Since Specialization
Citations

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

Fields of papers citing papers by Jelena Martinović

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Jelena Martinović

This figure shows the co-authorship network connecting the top 25 collaborators of Jelena Martinović. A scholar is included among the top collaborators of Jelena Martinović 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 Jelena Martinović. Jelena Martinović 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.
Martinović, Jelena, Sophie Patrier, Briac Thierry, et al.. (2025). Evaluation of Intrinsic Fetal Airway Obstruction (CHAOS): Correlations Between Ultrasound, Fetoscopic, and Pathological Findings. Prenatal Diagnosis. 45(3). 433–438. 1 indexed citations
2.
Riedel, Jan, Christopher D. Pascoe, Grit Gesine Ruth Hiller, et al.. (2025). Macrophages Are Enriched Pre- and Postnatally in Hypoplastic Lungs from Patients with Congenital Diaphragmatic Hernia. American Journal of Respiratory and Critical Care Medicine. 211(11). 2130–2133.
3.
Buffin‐Meyer, Bénédicte, Julie Klein, Jacqueline Aziza, et al.. (2024). Improved prenatal assessment of kidney disease using multiple ultrasound features. Nephrology Dialysis Transplantation. 40(2). 341–351. 1 indexed citations
4.
Rigonnot, Luc, et al.. (2024). The First Fetal Case of Shwachman-Diamond Syndrome Mimicking Vascular Growth Restriction. Pediatric and Developmental Pathology. 27(6). 603–607. 1 indexed citations
5.
Bruel, Ange‐Line, Lenka Nosková, Irene Valenzuela, et al.. (2023). Pathogenic RAB34 variants impair primary cilium assembly and cause a novel oral-facial-digital syndrome. Human Molecular Genetics. 32(18). 2822–2831. 8 indexed citations
6.
Morales, Elisa, Jelena Martinović, Philippe Labrune, et al.. (2022). Management of copy number variants associated with incomplete penetrance and variable expressivity—Results of a French survey. Clinical Genetics. 103(3). 335–340. 1 indexed citations
7.
Kamien, Benjamin, Joshua S. Clayton, Elyshia McNamara, et al.. (2022). Bi-allelic MYH3 loss-of-function variants cause a lethal form of contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B. Neuromuscular Disorders. 32(5). 445–449. 3 indexed citations
8.
Petit, François, et al.. (2021). Early prenatal diagnosis of alveolar capillary dysplasia with misalignment of pulmonary veins due to a 16q24.1 deletion. American Journal of Medical Genetics Part A. 185(5). 1494–1497. 2 indexed citations
9.
Marguet, Florent, Fabien Guimiot, Jelena Martinović, et al.. (2021). Human neuropathology confirms projection neuron and interneuron defects and delayed oligodendrocyte production and maturation in FOXG1 syndrome. European Journal of Medical Genetics. 64(9). 104282–104282. 7 indexed citations
10.
Cordier, Anne‐Gaël, Jelena Martinović, Anne Couturier‐Tarrade, et al.. (2020). Preserved efficiency of sickle cell disease placentas despite altered morphology and function. Placenta. 100. 81–88. 4 indexed citations
11.
Van‐Gils, Julien, Sophie Naudion, Jérôme Toutain, et al.. (2019). Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations. Clinical Genetics. 95(3). 420–426. 8 indexed citations
12.
Martinović, Jelena. (2019). A Brief History of Death and American Psychiatry. Harvard Review of Psychiatry. 27(4). 260–267.
13.
Bouchghoul, Hanane, Chloé Quēlin, Philippe Loget, et al.. (2018). Fetal cerebral hemorrhage due to X‐linkedGATA1gene mutation. Prenatal Diagnosis. 38(10). 772–778. 7 indexed citations
14.
Timoh, Krystel Nyangoh, Thomas Bessède, C. Lebâcle, et al.. (2016). Levator ani muscle innervation: Anatomical study in human fetus. Neurourology and Urodynamics. 36(6). 1464–1471. 19 indexed citations
15.
Raymond, Laure, Bruno Francou, François Petit, et al.. (2015). Complex translocation t(1;12;14)(q42;q14;q32) and HMGA2 deletion in a fetus presenting growth delay and bilateral cataracts. European Journal of Medical Genetics. 58(11). 591–596. 3 indexed citations
16.
Briand‐Suleau, Audrey, Jelena Martinović, Lucie Tosca, et al.. (2014). SALL4 and NFATC2: Two major actors of interstitial 20q13.2 duplication. European Journal of Medical Genetics. 57(4). 174–180. 2 indexed citations
17.
Boucherat, Olivier, Alexandra Benachi, Anne‐Marie Barlier‐Mur, et al.. (2007). Decreased Lung Fibroblast Growth Factor 18 and Elastin in Human Congenital Diaphragmatic Hernia and Animal Models. American Journal of Respiratory and Critical Care Medicine. 175(10). 1066–1077. 41 indexed citations
18.
Boucherat, Olivier, Alexandra Benachi, Bernadette Chailley‐Heu, et al.. (2007). Surfactant Maturation Is Not Delayed in Human Fetuses with Diaphragmatic Hernia. PLoS Medicine. 4(7). e237–e237. 61 indexed citations
19.
Clugston, Robin D., Christoph Englert, Margaret Clagett‐Dame, et al.. (2006). Teratogen-Induced, Dietary and Genetic Models of Congenital Diaphragmatic Hernia Share a Common Mechanism of Pathogenesis. American Journal Of Pathology. 169(5). 1541–1549. 93 indexed citations
20.
Ruano, Rodrigo, Olivier Picone, Alexandra Benachi, et al.. (2003). First‐trimester diagnosis of osteogenesis imperfecta associated with encephalocele by conventional and three‐dimensional ultrasound. Prenatal Diagnosis. 23(7). 539–542. 13 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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