Jelena Martinović

7.4k citations

107 papers · 2.7k indexed · h-index 27

Obstetrics and Gynecology top 2%
Pediatrics, Perinatology and Child Health top 2%
- Prenatal Screening and Diagnostics 16
- Fetal and Pediatric Neurological Disorders 14
Genetics top 2%
- Genomic variations and chromosomal abnormalities 11
- Genetic and Kidney Cyst Diseases 8
Urology top 5%
Pulmonary and Respiratory Medicine top 5%
- Neonatal Respiratory Health Research 11
Surgery
- Congenital Diaphragmatic Hernia Studies 19
- Congenital Anomalies and Fetal Surgery 15
Molecular Biology
- Renal and related cancers 7

Co-authors: Alexandra Benachi Tania Attié‐Bitach Yves Dumez Arnold Münnich Martine Le Merrer Marc Dommergues Anne‐Lise Delezoide Rodrigo Ruano
Cited by: Obstetrics and Gynecology Pediatrics, Perinatology and Child Health Genetics
Journals: Proceedings of the National Academy of Sciences (1 paper)SHILAP Revista de lepidopterología (1 paper)PLoS ONE (1 paper)
Partner nations: France Canada United States

In The Last Decade

Jelena Martinović

103 papers receiving 2.6k citations

Peers

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

The 25 scholars most cited alongside Jelena Martinović, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Jelena Martinović Line = papers co-authored together Jelena Martinović links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Macrophages Are Enriched Pre- and Postnatally in Hypoplastic Lungs from Patients with Congenital Diaphragmatic Hernia American Journal of Respiratory and Critical Care Medicine ·Jan Riedel,Katinka Sturm,Christopher D. Pascoe,Nicole Peukert,Ophelia Aubert,Grit Gesine Ruth Hiller,Xingbin Ai,Michael Böttcher,Jan-Hendrik Gosemann,Martin Lacher,Jelena Martinović,Alexandra Benachi,Richard Wagner	2025	0
2	Management of copy number variants associated with incomplete penetrance and variable expressivity—Results of a French survey Clinical Genetics ·Floriane Lejamtel,Cécile Oheix,Elisa Morales,Jelena Martinović,Philippe Labrune,François Petit,Aline Receveur,Nelly Frydman,Alexandra Benachi,Chloé Puisney‐Dakhli,Alexandre Vivanti	2022	1
3	Bi-allelic MYH3 loss-of-function variants cause a lethal form of contractures, pterygia, and spondylocarpotarsal fusion syndrome 1B Neuromuscular Disorders ·Benjamin Kamien,Joshua S. Clayton,Han‐Shin Lee,Disna Abeysuriya,Elyshia McNamara,Jelena Martinović,Marie Gonzalès,Judith Melki,Gianina Ravenscroft	2022	3
4	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 ·Chloé Puisney‐Dakhli,F. Gubana,François Petit,Hanane Bouchghoul,Valérie Gautier,Jelena Martinović,Gérard Tachdjian,Aline Receveur	2021	2
5	Chronic histiocytic intervillositis: manifestation of placental alloantibody-mediated rejection American Journal of Obstetrics and Gynecology ·Alexandra Benachi,Marion Rabant,Jelena Martinović,Hanane Bouchghoul,Alexandre Vivanti,Juliette Léon,Anne Grünenwald,Lubka T. Roumenina,J.L. Celton,Bettina Bessières,Jean‐Luc Taupin,Julien Zuber	2021	22
6	A retrospective study on the efficacy of prenatal diagnosis for pregnancies at risk of mitochondrial DNA disorders Genetics in Medicine ·Julie Steffann,Sophie Monnot,Maryse Magen,Zahra Assouline,Nadine Gigarel,Y. Ville,Laurent Salomon,Bettina Bessière,Jelena Martinović,Agnès Rötig,Joana Bengoa,Roxana Borghèse,Arnold Münnich,Giulia Barcia,Jean‐Paul Bonnefont	2020	9
7	Fetal phenotype of Rubinstein‐Taybi syndrome caused by CREBBP mutations Clinical Genetics ·Julien Van‐Gils,Sophie Naudion,Jérôme Toutain,Gwenaëlle Lancelot,Tania Attié‐Bitach,Sophie Blesson,Bénédicte Demeer,Bérénice Doray,Marie Gonzalès,Jelena Martinović,Sandra Whalen,Laurence Taine,Benoı̂t Arveiler,Didier Lacombe,Patricia Fergelot	2019	8
8	SALL4 and NFATC2: Two major actors of interstitial 20q13.2 duplication European Journal of Medical Genetics ·Audrey Briand‐Suleau,Jelena Martinović,Lucie Tosca,Bassim Tou,Sophie Brisset,Jérôme Bouligand,V. Delattre,Irina Giurgea,J. Bachir,P. Folliot,Carole Goumy,Christine Francannet,Anne Guiochon‐Mantel,Alexandra Benachi,Joris Vermeesch,Gérard Tachdjian,Philippe Vago,Michel Goossens,Corinne Métay	2014	2
9	Antenatal ultrasound prediction of pulmonary hypoplasia in congenital diaphragmatic hernia: correlation with pathology Ultrasound in Obstetrics and Gynecology ·Jacques Jani,Anne‐Gaël Cordier,Jelena Martinović,Cleisson Fábio Andrioli Peralta,Marie‐Victoire Sénat,Veerle Segers,Alexandra Benachi	2011	21
10	RET and GDNF mutations are rare in fetuses with renal agenesis or other severe kidney development defects Journal of Medical Genetics ·Marc Jeanpierre,G. Macé,Mélanie Parisot,Vincent Morinière,A. Pawtowsky,Max E. Benabou,Jelena Martinović,Jeanne Amiel,Tania Attié‐Bitach,Anne‐Lise Delezoide,Philippe Loget,Patricia Blanchet,Dominique Gaillard,M. Gonzalés,Wassila Carpentier,Patrick Nitschké,Frédéric Torès,Laurence Heidet,Corinne Antignac,Rémi Salomon,(unknown)	2011	37
11	Mutation in IFT80 in a fetus with the phenotype of Verma-Naumoff provides molecular evidence for Jeune-Verma-Naumoff dysplasia spectrum Journal of Medical Genetics ·Denise Pontes Cavalcanti,Céline Huber,Kim‐Hanh Le Quan Sang,Geneviève Baujat,Felicity Collins,Anne‐Lise Delezoide,Nathalie Dagoneau,Martine Le Merrer,Jelena Martinović,M. F. S. Mello,Michel Vekemans,Arnold Munnich,Valérie Cormier‐Daire	2009	53
12	Thanatophoric dysplasia caused by double missense FGFR3 mutations American Journal of Medical Genetics Part A ·Stéphanie Pannier,Jelena Martinović,S. Heuertz,Anne‐Lise Delezoide,Arnold Münnich,Laurent Schibler,Valérie Serre,Laurence Legeai‐Mallet	2009	16
13	Refining the clinicopathological pattern of cerebral proliferative glomeruloid vasculopathy (Fowler syndrome): Report of 16 fetal cases European Journal of Medical Genetics ·B. Bessières-Grattagliano,B. Foliguet,Louise Devisme,Laurence Lœuillet,Pascale Marcorelles,Maryse Bonnière,A. Laquérrière,Catherine Fallet‐Bianco,Jelena Martinović,S. Zrelli,N. Léticée,Véronique Cayol,Heather Etchevers,Michel Vekemans,Tania Attié‐Bitach,Férechté Encha‐Razavi	2009	11
14	Surfactant Maturation Is Not Delayed in Human Fetuses with Diaphragmatic Hernia PLoS Medicine ·Olivier Boucherat,Alexandra Benachi,Bernadette Chailley‐Heu,Marie‐Laure Franco‐Montoya,Caroline Elie,Jelena Martinović,Jacques R. Bourbon	2007	61
15	Decreased Lung Fibroblast Growth Factor 18 and Elastin in Human Congenital Diaphragmatic Hernia and Animal Models American Journal of Respiratory and Critical Care Medicine ·Olivier Boucherat,Alexandra Benachi,Anne‐Marie Barlier‐Mur,Marie‐Laure Franco‐Montoya,Jelena Martinović,Bernard Thébaud,Bernadette Chailley‐Heu,Jacques R. Bourbon	2007	41
16	Teratogen-Induced, Dietary and Genetic Models of Congenital Diaphragmatic Hernia Share a Common Mechanism of Pathogenesis American Journal Of Pathology ·Robin D. Clugston,Jürgen Klattig,Christoph Englert,Margaret Clagett‐Dame,Jelena Martinović,Alexandra Benachi,John J. Greer	2006	93
17	Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome The American Journal of Human Genetics ·Nathalie Dagoneau,Déborah Scheffer,Céline Huber,L.I. Al-Gazali,Maja Di Rocco,Anne Godard,Jelena Martinović,Annick Raas‐Rothschild,Sabine Sigaudy,Sheila Unger,Sophie Nicole,Bertrand Fontaine,Jean‐Luc Taupin,Jean-François Moreau,Andrea Superti‐Furga,Martine Le Merrer,Jacky Bonaventure,Arnold Münnich,Laurence Legeai‐Mallet,Valérie Cormier‐Daire	2004	136
18	Systemic arteriovenous fistula leads to pulmonary artery remodeling and abnormal vasoreactivity in the fetal lamb American Journal of Physiology-Lung Cellular and Molecular Physiology ·Jean-Marie Jouannic,Régine Roussin,Alison A. Hislop,Sophie Lanone,Jelena Martinović,Jorge Boczkowski,Yves Dumez,Anh Tuan Dinh‐Xuan	2003	13
19	Neocortical neuronal arrangement in LIS1 and DCX lissencephaly may be different American Journal of Medical Genetics Part A ·Géraldine Viot,Pascale Sonigo,Isabelle Simon,Brigitte Simon‐Bouy,Frédéric Chadeyron,Chérif Beldjord,Julia Tantau,Jelena Martinović,Chantal Esculpavit,Françis Brunelle,Arnold Münnich,Michel Vekemans,Férechté Encha‐Razavi	2003	23
20	The effect of a systemic arteriovenous fistula on the pulmonary arterial blood pressure in the fetal sheep Prenatal Diagnosis ·Jean‐Marie Jouannic,Jelena Martinović,Régine Roussin,F Laborde,Yves Dumez,Anh Tuan Dinh‐Xuan	2002	6

About Jelena Martinović

Jelena Martinović is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Urology, having authored 107 papers that have together received 2.7k indexed citations. Recurring topics across this work include Congenital Diaphragmatic Hernia Studies (19 papers), Prenatal Screening and Diagnostics (16 papers), Congenital Anomalies and Fetal Surgery (15 papers), Fetal and Pediatric Neurological Disorders (14 papers), Neonatal Respiratory Health Research (11 papers), Genomic variations and chromosomal abnormalities (11 papers), Genetic and Kidney Cyst Diseases (8 papers) and Renal and related cancers (7 papers). The work is most often cited by research in Obstetrics and Gynecology (275 citations), Pediatrics, Perinatology and Child Health (620 citations) and Genetics (730 citations). Jelena Martinović has collaborated with scholars based in France, Canada and United States. Frequent 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. Their work appears in journals such as Proceedings of the National Academy of Sciences, SHILAP Revista de lepidopterología and PLoS ONE.

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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