Jelena Martinovic

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 7

Top Topics

Inferior Vena Cava

Transcatheter Aortic Valve Replacement

Preterm Infants

Top Venues

Prenatal diagnosis

Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society

American journal of medical genetics. Part A

Genetics in medicine : official journal of the American College of Medical Genetics

This page only lists publications with an associated author ORCID identifier.

Publications

Nicoleta-Andreea Bobric, Julie Grevoul-Fesquet, Luc Rigonnot, Detlef Trost, Aïcha Boughalem, Jelena Martinovic
The First Fetal Case of Shwachman-Diamond Syndrome Mimicking Vascular Growth Restriction. Pediatric and developmental pathology : the official journal of the Society for Pediatric Pathology and the Paediatric Pathology Society (2024)
Floriane Lejamtel, Cécile Oheix, Elisa Morales, Jelena Martinovic, Philippe Labrune, François Mickaël Petit, Aline Receveur, Nelly Achour-Frydman, Alexandra Benachi, Chloé Puisney-Dakhli, Alexandre Joseph Vivanti
Management of copy number variants associated with incomplete penetrance and variable expressivity-Results of a French survey. Clinical genetics (2022)
Marie Boisson, Anne-Gael Cordier, Jelena Martinovic, Aline Receveur, Aurélie Mouka, Romain Diot, Catherine Egoroff, Geoffroy Esnault, Loïc Drévillon, Alexandra Benachi, Gérard Tachdjian, Lucie Tosca
Copy number variations analysis in a cohort of 47 fetuses and newborns with congenital diaphragmatic hernia. Prenatal diagnosis (2022)
Chloé Puisney-Dakhli, Francesca Gubana, François Mickaël Petit, Hanane Bouchghoul, Valérie Gautier, Jelena Martinovic, Gérard Tachdjian, Aline Receveur
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) (2021)
Hanane Bouchghoul, Chloé Quelin, Philippe Loget, Féréchté Encha-Razavi, Marie-Victoire Senat, Lorraine Maheut, Julie Galimand, Sophie Collardeau-Frachon, Lydie Da Costa, Jelena Martinovic
Fetal cerebral hemorrhage due to X-linked GATA1 gene mutation. Prenatal diagnosis 38 (10) (2018)
Hanane Bouchghoul, Oriane Marty, Virginie Fouquet, Anne-Gaël Cordier, Marie-Victoire Senat, Julien Saada, Mostafa Mokhtari, Nolwenn Le Sache, Jelena Martinovic, Alexandra Benachi
Congenital diaphragmatic hernia has a better prognosis when associated with a hernia sac. Prenatal diagnosis 38 (9) (2018)
Paul Kuentz, Judith St-Onge, Yannis Duffourd, Jean-Benoît Courcet, Virginie Carmignac, Thibaud Jouan, Arthur Sorlin, Claire Abasq-Thomas, Juliette Albuisson, Jeanne Amiel, Daniel Amram, Stéphanie Arpin, Tania Attie-Bitach, Nadia Bahi-Buisson, Sébastien Barbarot, Geneviève Baujat, Didier Bessis, Olivia Boccara, Maryse Bonnière, Odile Boute, Anne-Claire Bursztejn, Christine Chiaverini, Valerie Cormier-Daire, Christine Coubes, Bruno Delobel, Patrick Edery, Salima El Chehadeh, Christine Francannet, David Genevieve, Alice Goldenberg, Damien Haye, Bertrand Isidor, Marie-Line Jacquemont, Philippe Khau Van Kien, Didier Lacombe, Ludovic Martin, Jelena Martinovic, Annabel Maruani, Michèle Mathieu-Dramard, Juliette Mazereeuw-Hautier, Caroline Michot, Mignot Cyril, Juliette Miquel, Fanny Morice-Picard, Florence Petit, Alice Phan, Massimiliano Rossi, Renaud Touraine, Alain Verloes, Marie Vincent, Catherine Vincent-Delorme, Sandra Whalen, Marjolaine Willems, Nathalie Marle, Daphne Lehalle, Julien Thevenon, Christel Thauvin-Robinet, Christel Thauvin-Robinet, Laurence Faivre, Pierre Vabres, Jean-Baptiste Rivière
Molecular diagnosis of PIK3CA-related overgrowth spectrum (PROS) in 162 patients and recommendations for genetic testing. Genetics in medicine : official journal of the American College of Medical Genetics 19 (9) (2017)