Hélène Cave (H Cavé, Helene Cavé, Hélène Cavé)

ORCID

Publication Activity (10 Years)

Years Active: 2017-2024
Publications (10 Years): 33

Top Venues

Leukemia

European journal of human genetics : EJHG

EMBO reports

Journal of the European Academy of Dermatology and Venereology : JEADV

Robert Debré hospital and Paris Diderot university

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

Affiliation History

Robert Debré hospital and Paris Diderot university Nov 01 2009

France

PUPH, Head of the molecular Genetics unit :: Genetics

Publications

Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Didier Bessis, Anne-Claire Bursztejn, Fanny Morice-Picard, Yline Capri, Sébastien Barbarot, Hélène Aubert, Damien Bodet, Emmanuelle Bourrat, Christine Chiaverini, Laura Poujade, Marjolaine Willems, Jacques Rouanet, Anne Dompmartin-Blanchère, David Geneviève, Marion Gerard, Emmanuelle Ginglinger, Smail Hadj Rabia, Ludovic Martin, Juliette Mazereeuw-Hautier, Nathalie Bibas, Nicolas Molinari, Fanchon Herman, Alice Phan, Julien Rod, Hugues Roger, Sabine Sigaudy, Alban Ziegler, Yoann Vial, Alain Verloes, Hélène Cave, Didier Lacombe
Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients. Journal of the European Academy of Dermatology and Venereology : JEADV (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Nicolas Lecornec, Mony Fahd, Paola De Lorenzo, Maria Grazia Valsecchi, Concetta Micalizzi, Paulina Diaz, Carla Pennella, Franco Locatelli, Luciana Vinti, Hélène Cave, Aurélie Caye-Eude, Jan Stary, Rob Pieters, André Baruchel, Benoit Brethon
Outcomes of infants with very late relapse of acute lymphoblastic leukaemia initially treated in Interfant-06. British journal of haematology (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG 32 (8) (2024)
Marion Droin-Mollard, Sandrine De Montgolfier, Anne-Paule Gimenez-Roqueplo, Cécile Flahault, Arnaud Petit, Franck Bourdeaut, Sophie Julia, Emmanuelle Rial-Sebbag, Isabelle Coupier, Fatoumata Simaga, Laurence Brugières, Léa Guerrini-Rousseau, Béatrice Claret, Hélène Cave, Marion Strullu, Lucile Hervouet, Khadija Lahlou-Laforêt
Psychological and ethical issues raised by genomic in paediatric care pathway, a qualitative analysis with parents and childhood cancer patients. European journal of human genetics : EJHG (2024)
Marion Droin-Mollard, Sandrine De Montgolfier, Anne-Paule Gimenez-Roqueplo, Cécile Flahault, Arnaud Petit, Franck Bourdeaut, Sophie Julia, Emmanuelle Rial-Sebbag, Isabelle Coupier, Fatoumata Simaga, Laurence Brugières, Léa Guerrini-Rousseau, Béatrice Claret, Hélène Cave, Marion Strullu, Lucile Hervouet, Khadija Lahlou-Laforêt
Psychological and ethical issues raised by genomic in paediatric care pathway, a qualitative analysis with parents and childhood cancer patients. European journal of human genetics : EJHG (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG 32 (8) (2024)
Yoann Vial, Jeannette Nardelli, Adeline A Bonnard, Justine Rousselot, Michèle Souyri, Pierre Gressens, Hélène Cave, Séverine Drunat
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis. EMBO reports 25 (5) (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG 32 (8) (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG (2024)
Didier Bessis, Anne-Claire Bursztejn, Fanny Morice-Picard, Yline Capri, Sébastien Barbarot, Hélène Aubert, Damien Bodet, Emmanuelle Bourrat, Christine Chiaverini, Laura Poujade, Marjolaine Willems, Jacques Rouanet, Anne Dompmartin-Blanchère, David Geneviève, Marion Gerard, Emmanuelle Ginglinger, Smail Hadj Rabia, Ludovic Martin, Juliette Mazereeuw-Hautier, Nathalie Bibas, Nicolas Molinari, Fanchon Herman, Alice Phan, Julien Rod, Hugues Roger, Sabine Sigaudy, Alban Ziegler, Yoann Vial, Alain Verloes, Hélène Cave, Didier Lacombe
Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients. Journal of the European Academy of Dermatology and Venereology : JEADV 38 (9) (2024)
Didier Bessis, Anne-Claire Bursztejn, Fanny Morice-Picard, Yline Capri, Sébastien Barbarot, Hélène Aubert, Damien Bodet, Emmanuelle Bourrat, Christine Chiaverini, Laura Poujade, Marjolaine Willems, Jacques Rouanet, Anne Dompmartin-Blanchère, David Geneviève, Marion Gerard, Emmanuelle Ginglinger, Smail Hadj Rabia, Ludovic Martin, Juliette Mazereeuw-Hautier, Nathalie Bibas, Nicolas Molinari, Fanchon Herman, Alice Phan, Julien Rod, Hugues Roger, Sabine Sigaudy, Alban Ziegler, Yoann Vial, Alain Verloes, Hélène Cave, Didier Lacombe
Dermatological manifestations in Costello syndrome: A prospective multicentric study of 31 HRAS-positive variant patients. Journal of the European Academy of Dermatology and Venereology : JEADV 38 (9) (2024)
Maria Lisa Dentici, Marcello Niceta, Francesca Romana Lepri, Cecilia Mancini, Manuela Priolo, Adeline Alice Bonnard, Camilla Cappelletti, Chiara Leoni, Andrea Ciolfi, Simone Pizzi, Viviana Cordeddu, Cesare Rossi, Marco Ferilli, Mafalda Mucciolo, Vito Luigi Colona, Christine Fauth, Melissa Bellini, Giacomo Biasucci, Lorenzo Sinibaldi, Silvana Briuglia, Andrea Gazzin, Diana Carli, Luigi Memo, Eva Trevisson, Concetta Schiavariello, Maria Luca, Antonio Novelli, Caroline Michot, Anne Sweertvaegher, David Germanaud, Emanuela Scarano, Alessandro De Luca, Giuseppe Zampino, Martin Zenker, Alessandro Mussa, Bruno Dallapiccola, Hélène Cave, Maria Cristina Digilio, Tartaglia Marco
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis. European journal of human genetics : EJHG 32 (8) (2024)
M Tarek Elghetany, Hélène Cave, Rita De Vito, Mirinal S Patnaik, Eric Solary, Joseph D Khoury
Juvenile myelomonocytic leukemia; moving forward. Leukemia 37 (3) (2023)
C Meyer, P Larghero, Bruno A Lopes, Thomas Burmeister, D Gröger, Rosemary Sutton, N C Venn, G Cazzaniga, L Corral Abascal, G Tsaur, L Fechina, Mariana Emerenciano, Maria S Pombo-de-Oliveira, T Lund-Aho, T Lundán, M Montonen, V Juvonen, Jan Zuna, J Trka, P Ballerini, H Lapillonne, Vincent H J van der Velden, E Sonneveld, E Delabesse, Roberto R Capela de Matos, Maria Luiza Macedo Silva, Simon Bomken, K Katsibardi, M Keernik, N Grardel, J Mason, R Price, J Kim, C Eckert, L Lo Nigro, C Bueno, P Menendez, U Zur Stadt, P Gameiro, L Sedék, T Szczepański, Audrey Bidet, V Marcu, K Shichrur, S Izraeli, H O Madsen, Beat W Schäfer, S Kubetzko, Rathana Kim, E Clappier, Heiko Trautmann, M Brüggemann, P Archer, J Hancock, J Alten, A Möricke, Martin Stanulla, J Lentes, A K Bergmann, Sabine Strehl, S Köhrer, K Nebral, M N Dworzak, Oskar A Haas, C Arfeuille, Aurélie Caye-Eude, Hélène Cave, Rolf Marschalek
The KMT2A recombinome of acute leukemias in 2023. Leukemia (2023)
Michal Kicinski, Chloé Arfeuille, Nathalie Grardel, Marleen Bakkus, Aurélie Caye-Eude, Geneviève Plat, Alina Ferster, Anne Uyttebroeck, Barbara De Moerloose, Pierre Rohrlich, Stefan Suciu, Yves Bertrand, Hélène Cave
The prognostic value of IKZF1 plus in B-cell progenitor acute lymphoblastic leukemia: Results from the EORTC 58951 trial. Pediatric blood & cancer (2023)
M Tarek Elghetany, Hélène Cave, Rita De Vito, Mirinal S Patnaik, Eric Solary, Joseph D Khoury
Juvenile myelomonocytic leukemia; moving forward. Leukemia (2023)
M Tarek Elghetany, Hélène Cave, Rita De Vito, Mirinal S Patnaik, Eric Solary, Joseph D Khoury
Juvenile myelomonocytic leukemia; moving forward. Leukemia 37 (3) (2023)
M Tarek Elghetany, Hélène Cave, Rita De Vito, Mirinal S Patnaik, Eric Solary, Joseph D Khoury
Juvenile myelomonocytic leukemia; moving forward. Leukemia 37 (3) (2023)
Marius Külp, Patrizia Larghero, Julia Alten, Gunnar Cario, Cornelia Eckert, Aurélie Caye-Eude, Hélène Cave, Tessa Schmachtel, Michela Bardini, Giovanni Cazzaniga, Paola De Lorenzo, Maria Grazia Valsecchi, Halvard Bonig, Claus Meyer, Michael A Rieger, Rolf Marschalek
The EGR3 regulome of infant KMT2A-r acute lymphoblastic leukemia identifies differential expression of B-lineage genes predictive for outcome. Leukemia (2023)
Marius Külp, Patrizia Larghero, Julia Alten, Gunnar Cario, Cornelia Eckert, Aurélie Caye-Eude, Hélène Cave, Tessa Schmachtel, Michela Bardini, Giovanni Cazzaniga, Paola De Lorenzo, Maria Grazia Valsecchi, Halvard Bonig, Claus Meyer, Michael A Rieger, Rolf Marschalek
The EGR3 regulome of infant KMT2A-r acute lymphoblastic leukemia identifies differential expression of B-lineage genes predictive for outcome. Leukemia (2023)
Maja Solman, Sasja Blokzijl-Franke, Florian Piques, Chuan Yan, Qiqi Yang, Marion Strullu, Sarah M Kamel, Pakize Ak, Jeroen Bakkers, David M Langenau, Hélène Cave, Jeroen den Hertog
Inflammatory response in hematopoietic stem and progenitor cells triggered by activating SHP2 mutations evokes blood defects. eLife 11 (2022)
Kentaro Ohki, Ellie R Butler, Nobutaka Kiyokawa, Shinsuke Hirabayashi, Anke K Bergmann, Anja Möricke, Judith M Boer, Hélène Cave, Giovanni Cazzaniga, Allen Eng Juh Yeoh, Masashi Sanada, Toshihiko Imamura, Hiroto Inaba, Charles G Mullighan, Mignon L Loh, Ulrika Norén-Nyström, Lee-Yung Shih, Marketa Zaliova, Ching-Hong Pui, Oskar A Haas, Christine J Harrison, Anthony V Moorman, Atsushi Manabe
Clinical characteristics and outcomes of B-cell precursor ALL with MEF2D rearrangements: a retrospective study by the Ponte di Legno Childhood ALL Working Group. Leukemia (2022)
Shinsuke Hirabayashi, Ellie R Butler, Kentaro Ohki, Nobutaka Kiyokawa, Anke K Bergmann, Anja Möricke, Judith M Boer, Hélène Cave, Giovanni Cazzaniga, Allen Eng-Juh Yeoh, Masashi Sanada, Toshihiko Imamura, Hiroto Inaba, Charles G Mullighan, Mignon L Loh, Ulrika Norén-Nyström, Agata Pastorczak, Lee-Yung Shih, Marketa Zaliova, Ching-Hong Pui, Oskar A Haas, Christine J Harrison, Anthony V Moorman, Atsushi Manabe
Clinical characteristics and outcomes of B-ALL with ZNF384 rearrangements: a retrospective analysis by the Ponte di Legno Childhood ALL Working Group. Leukemia 35 (11) (2021)
Judith M Boer, Maria Grazia Valsecchi, Femke M Hormann, Željko Antić, Marketa Zaliova, Claire Schwab, Giovanni Cazzaniga, Chloé Arfeuille, Hélène Cave, Andishe Attarbaschi, Sabine Strehl, Gabriele Escherich, Toshihiko Imamura, Kentaro Ohki, Tanja A Grüber, Rosemary Sutton, Agata Pastorczak, Tim Lammens, Frédéric Lambert, Chi-Kong Li, Enrique Carrillo de Santa Pau, Steve Hoffmann, Anja Möricke, Christine J Harrison, Monique L Den Boer, Paola De Lorenzo, Ronald W Stam, Anke K Bergmann, Rob Pieters
Favorable outcome of NUTM1-rearranged infant and pediatric B cell precursor acute lymphoblastic leukemia in a collaborative international study. Leukemia 35 (10) (2021)
Marie-Emilie Dourthe, Florence Rabian, Karima Yakouben, Florian Chevillon, Aurélie Cabannes-Hamy, Françoise Méchinaud, Audrey Grain, Delphine Chaillou, Ilhem Rahal, Sophie Caillat-Zucman, Emmanuelle Lesprit, Jérôme Naudin, Julie Roupret-Serzec, Nathalie Parquet, Anne Brignier, Valérie Guérin-El Khourouj, Elodie Lainey, Aurélie Caye-Eude, Hélène Cave, Emmanuelle Clappier, Stéphanie Mathis, Elie Azoulay, Jean Hugues Dalle, Nathalie Dhédin, Isabelle Madelaine, Jérôme Larghero, Nicolas Boissel, Andre Baruchel
Determinants of CD19-positive vs CD19-negative relapse after tisagenlecleucel for B-cell acute lymphoblastic leukemia. Leukemia 35 (12) (2021)
Christina Lissewski, Valérie Chune, Francesca Pantaleoni, Alessandro De Luca, Yline Capri, Julia Brinkmann, Francesca Lepri, Paola Daniele, Erika Leenders, Laura Mazzanti, Emanuela Scarano, Francesca Clementina Radio, Kerstin Kutsche, Alma Kuechler, Marion Gérard, Kara Ranguin, Marine Legendre, Yoann Vial, Ineke van der Burgt, Tuula Rinne, Elena Andreucci, Gioia Mastromoro, Maria Cristina Digilio, Hélène Cave, Tartaglia Marco, Martin Zenker
Variants of SOS2 are a rare cause of Noonan syndrome with particular predisposition for lymphatic complications. European journal of human genetics : EJHG 29 (1) (2020)
Julia Brinkmann, Christina Lissewski, Valentina Pinna, Yoann Vial, Francesca Pantaleoni, Francesca Lepri, Paola Daniele, Birute Burnyte, Goran Cuturilo, Christine Fauth, Alper Gezdirici, Dieter Kotzot, Elif Yılmaz Güleç, Violeta Iotova, Denny Schanze, Francis Ramond, Markéta Havlovicová, Gulen Eda Utine, Pelin Ozlem Simsek-Kiper, Milena Stoyanova, Alain Verloes, Alessandro De Luca, Tartaglia Marco, Hélène Cave, Martin Zenker
The clinical significance of A2ML1 variants in Noonan syndrome has to be reconsidered. European journal of human genetics : EJHG 29 (3) (2020)
Claire Schwab, Karin Nebral, Lucy Chilton, Cristina Leschi, Esmé Waanders, Judith M Boer, Markéta Žaliová, Rosemary Sutton, Ingegerd Ivanov Öfverholm, Kentaro Ohki, Yuka Yamashita, Stefanie Groeneveld-Krentz, Eva Froňková, Marleen Bakkus, Joelle Tchinda, Thayana da Conceição Barbosa, Grazia Fazio, Wojciech Mlynarski, Agata Pastorczak, Giovanni Cazzaniga, Maria S Pombo-de-Oliveira, Jan Trka, Renate Kirschner-Schwabe, Toshihiko Imamura, Gisela Barbany, Martin Stanulla, Andishe Attarbaschi, Renate Panzer-Grümayer, Roland P Kuiper, Monique L den Boer, Hélène Cave, Anthony V Moorman, Christine J Harrison, Sabine Strehl
Intragenic amplification of PAX5: a novel subgroup in B-cell precursor acute lymphoblastic leukemia? Blood advances 1 (19) (2017)

Hélène Cave.css-eqlu8i{font-size:small;padding-left:4px;} (H Cavé, Helene Cavé, Hélène Cavé)

Publication Activity (10 Years)

Top Topics

Top Venues

Hélène Cave (H Cavé, Helene Cavé, Hélène Cavé)