Association of Socioeconomic Factors and Sedentary Lifestyle in Belgrade’s Suburb, Working Class Community

Tekijä KONEVIC, Slavica, MARTINOVIC, Jelena, DJONOVIC, Nela
Julkaisussa Iran J Public Health (2015)

Role of Ectonucleotidases in Synapse Formation During Brain Development: Physiological and Pathological Implications

Tekijä Grković, Ivana, Drakulić, Dunja, Martinović, Jelena, Mitrović, Nataša
Julkaisussa Curr Neuropharmacol (2019)

Evidence for and against vertical transmission for severe acute respiratory syndrome coronavirus 2

Tekijä Lamouroux, Audrey, Attie-Bitach, Tania, Martinovic, Jelena, Leruez-Ville, Marianne, Ville, Yves
Julkaisussa Am J Obstet Gynecol (2020)

Umbilical vein thrombosis: to deliver or not to deliver at the time of diagnosis?

Tekijä Dussaux, Chloé, Picone, Olivier, Chambon, Guillemette, Tassin, Mikael, Martinovic, Jelena, Benachi, Alexandra, Cordier, Anne-Gaël
Julkaisussa Clin Case Rep (2014)

Teratogen-Induced, Dietary and Genetic Models of Congenital Diaphragmatic Hernia Share a Common Mechanism of Pathogenesis

Tekijä Clugston, Robin D., Klattig, Jürgen, Englert, Chistoph, Clagett-Dame, Margaret, Martinovic, Jelena, Benachi, Alexandra, Greer, John J.
Julkaistu 2006

Surfactant Maturation Is Not Delayed in Human Fetuses with Diaphragmatic Hernia

Tekijä Boucherat, Olivier, Benachi, Alexandra, Chailley-Heu, Bernadette, Franco-Montoya, Marie-Laure, Elie, Caroline, Martinovic, Jelena, Bourbon, Jacques R
Julkaistu 2007

Analysis of human samples reveals impaired SHH-dependent cerebellar development in Joubert syndrome/Meckel syndrome

Tekijä Aguilar, Andrea, Meunier, Alice, Strehl, Laetitia, Martinovic, Jelena, Bonniere, Maryse, Attie-Bitach, Tania, Encha-Razavi, Féréchté, Spassky, Nathalie
Julkaistu 2012

Prenatal Diagnosis of a 2.5 Mb De Novo 17q24.1q24.2 Deletion Encompassing KPNA2 and PSMD12 Genes in a Fetus with Craniofacial Dysmorphism, Equinovarus Feet, and Syndactyly

Tekijä Naud, Marie-Emmanuelle, Tosca, Lucie, Martinovic, Jelena, Saada, Julien, Métay, Corinne, Drévillon, Loïc, Benoit, Virginie, Brisset, Sophie, Tachdjian, Gérard
Julkaisussa Case Rep Genet (2017)

Evaluation of different formulas for LDL-C calculation

Tekijä Vujovic, Ana, Kotur-Stevuljevic, Jelena, Spasic, Slavica, Bujisic, Nada, Martinovic, Jelena, Vujovic, Milica, Spasojevic-Kalimanovska, Vesna, Zeljkovic, Aleksandra, Pajic, Dragoljub
Julkaistu 2010

Defective angiogenesis in hypoplastic human fetal lungs correlates with nitric oxide synthase deficiency that occurs despite enhanced angiopoietin-2 and VEGF

Tekijä Boucherat, Olivier, Franco-Montoya, Marie-Laure, Delacourt, Christophe, Martinovic, Jelena, Masse, Virginie, Elie, Caroline, Thebaud, Bernard, Benachi, Alexandra, Bourbon, Jacques R.
Julkaistu 2010

New Insight on FGFR3-Related Chondrodysplasias Molecular Physiopathology Revealed by Human Chondrocyte Gene Expression Profiling

Tekijä Schibler, Laurent, Gibbs, Linda, Benoist-Lasselin, Catherine, Decraene, Charles, Martinovic, Jelena, Loget, Philippe, Delezoide, Anne-Lise, Gonzales, Marie, Munnich, Arnold, Jais, Jean-Philippe, Legeai-Mallet, Laurence
Julkaistu 2009

Fgf9 and FGF20 maintain the stemness of nephron progenitors in mice and man

Tekijä Barak, Hila, Huh, Sung-Ho, Chen, Shuang, Jeanpierre, Cécile, Martinovic, Jelena, Parisot, Mélanie, Bole-Feysot, Christine, Nitschké, Patrick, Salomon, Rémi, Antignac, Corinne, Ornitz, David M., Kopan, Raphael
Julkaistu 2012

Segregation of mtDNA Throughout Human Embryofetal Development: m.3243A > G as a Model System

Tekijä Monnot, Sophie, Gigarel, Nadine, Samuels, David C, Burlet, Philippe, Hesters, Laetitia, Frydman, Nelly, Frydman, René, Kerbrat, Violaine, Funalot, Benoit, Martinovic, Jelena, Benachi, Alexandra, Feingold, Josué, Munnich, Arnold, Bonnefont, Jean-Paul, Steffann, Julie
Julkaistu 2011

DYNC2H1 Mutations Cause Asphyxiating Thoracic Dystrophy and Short Rib-Polydactyly Syndrome, Type III

Tekijä Dagoneau, Nathalie, Goulet, Marie, Geneviève, David, Sznajer, Yves, Martinovic, Jelena, Smithson, Sarah, Huber, Céline, Baujat, Geneviève, Flori, Elisabeth, Tecco, Laura, Cavalcanti, Denise, Delezoide, Anne-Lise, Serre, Valérie, Le Merrer, Martine, Munnich, Arnold, Cormier-Daire, Valérie
Julkaistu 2009

Severe Prenatal Renal Anomalies Associated with Mutations in HNF1B or PAX2 Genes

Tekijä Madariaga, Leire, Morinière, Vincent, Jeanpierre, Cécile, Bouvier, Raymonde, Loget, Philippe, Martinovic, Jelena, Dechelotte, Pierre, Leporrier, Nathalie, Thauvin-Robinet, Christel, Jensen, Uffe Birk, Gaillard, Dominique, Mathieu, Michele, Turlin, Bruno, Attie-Bitach, Tania, Salomon, Rémi, Gübler, Marie-Claire, Antignac, Corinne, Heidet, Laurence
Julkaistu 2013

Null Leukemia Inhibitory Factor Receptor (LIFR) Mutations in Stüve-Wiedemann/Schwartz-Jampel Type 2 Syndrome

Tekijä Dagoneau, Nathalie, Scheffer, Deborah, Huber, Céline, Al-Gazali, Lihadh I., Di Rocco, Maja, Godard, Anne, Martinovic, Jelena, Raas-Rothschild, Annick, Sigaudy, Sabine, Unger, Sheila, Nicole, Sophie, Fontaine, Bertrand, Taupin, Jean-Luc, Moreau, Jean-François, Superti-Furga, Andrea, Le Merrer, Martine, Bonaventure, Jacky, Munnich, Arnold, Legeai-Mallet, Laurence, Cormier-Daire, Valérie
Julkaistu 2004

Targeted Exome Sequencing Identifies PBX1 as Involved in Monogenic Congenital Anomalies of the Kidney and Urinary Tract

Tekijä Heidet, Laurence, Morinière, Vincent, Henry, Charline, De Tomasi, Lara, Reilly, Madeline Louise, Humbert, Camille, Alibeu, Olivier, Fourrage, Cécile, Bole-Feysot, Christine, Nitschké, Patrick, Tores, Frédéric, Bras, Marc, Jeanpierre, Marc, Pietrement, Christine, Gaillard, Dominique, Gonzales, Marie, Novo, Robert, Schaefer, Elise, Roume, Joëlle, Martinovic, Jelena, Malan, Valérie, Salomon, Rémi, Saunier, Sophie, Antignac, Corinne, Jeanpierre, Cécile
Julkaisussa J Am Soc Nephrol (2017)

Loss-of-function mutations in KIF14 cause severe microcephaly and kidney development defects in humans and zebrafish

Tekijä Reilly, Madeline Louise, Stokman, Marijn F, Magry, Virginie, Jeanpierre, Cecile, Alves, Marine, Paydar, Mohammadjavad, Hellinga, Jacqueline, Delous, Marion, Pouly, Daniel, Failler, Marion, Martinovic, Jelena, Loeuillet, Laurence, Leroy, Brigitte, Tantau, Julia, Roume, Joelle, Gregory-Evans, Cheryl Y, Shan, Xianghong, Filges, Isabel, Allingham, John S, Kwok, Benjamin H, Saunier, Sophie, Giles, Rachel H, Benmerah, Alexandre
Julkaisussa Hum Mol Genet (2019)

Antenatal Presentation of Bardet-Biedl Syndrome May Mimic Meckel Syndrome

Tekijä Karmous-Benailly, Houda, Martinovic, Jelena, Gubler, Marie-Claire, Sirot, Yoann, Clech, Laure, Ozilou, Catherine, Augé, Joëlle, Brahimi, Nora, Etchevers, Heather, Detrait, Eric, Esculpavit, Chantal, Audollent, Sophie, Goudefroye, Géraldine, Gonzales, Marie, Tantau, Julia, Loget, Philippe, Joubert, Madeleine, Gaillard, Dominique, Jeanne-Pasquier, Corinne, Delezoide, Anne-Lise, Peter, Marie-Odile, Plessis, Ghislaine, Simon-Bouy, Brigitte, Dollfus, Hélène, Le Merrer, Martine, Munnich, Arnold, Encha-Razavi, Férechté, Vekemans, Michel, Attié-Bitach, Tania
Julkaistu 2005

CC2D2A mutations in Meckel and Joubert syndromes indicate a genotype-phenotype correlation

Tekijä Mougou-Zerelli, Soumaya, Thomas, Sophie, Szenker, Emmanuelle, Audollent, Sophie, Elkhartoufi, Nadia, Babarit, Candice, Romano, Stéphane, Salomon, Rémi, Amiel, Jeanne, Esculpavit, Chantal, Gonzales, Marie, Escudier, Estelle, Leheup, Bruno, Loget, Philippe, Odent, Sylvie, Roume, Joëlle, Gérard, Marion, Delezoide, Anne-Lise, Khung, Suonavy, Patrier, Sophie, Cordier, Marie-Pierre, Bouvier, Raymonde, Martinovic, Jéléna, Gubler, Marie-Claire, Boddaert, Nathalie, Munnich, Arnold, Encha-Razavi, Férechté, Valente, Enza Maria, Saad, Ali, Saunier, Sophie, Vekemans, Michel, Attié-Bitach, Tania
Julkaistu 2009