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H

Hélène Cavé

université paris cité

77H指数
408论文数
2.0W被引数
收录论文 147
发表时间
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Identification of favorable subgroups of pediatric high-hyperdiploid acute lymphoblastic leukemia—A retrospective multinational study识别儿童高超二倍体急性淋巴细胞白血病有利亚组——一项多国回顾性研究
errHemaSphere
IF14.6
err2026-09-18
err0
errOAAI
errAndishe Attarbaschi; Amir Enshaei; Saskia Sonnenberg; Chloé Arfeuille; Draga Barbaric; Lena Behrman; Anke Bergmann; Nicole Bodmer; Judith M. Boer; Myriam Campbell; Gunnar Cario; Hélène Cavé; Lydia Champezou; Sarah Elitzur; Gabriele Escherich; Hester A. de Groot-Kruseman; Monique L. den Boer; Csongor Kiss; Jelena Lazic; Anja Möricke; Hannah Muhle; Karin Nebral; Rob Pieters; Pierre Rohrlich; Martin Schrappe; Lucie Srámková; Ajay Vora; Emese Zsigrai; Arndt Borkhardt; Martin Zimmermann; Anthony V. Moorman; International Berlin-Frankfurt-Münster (i-BFM) Study Group
err分享
err收藏
Genomic fusion breakpoints for DNA-based measurable residual disease monitoring in pediatric acute lymphoblastic leukemia用于儿童急性淋巴细胞白血病中基于DNA的可测量残留疾病监测的基因组融合断点
errLeukemia
IF13.4
err2026-04-21
err0
errOAAI
errArno H. Houtman; Chloé Arfeuille; Marion Strullu; André Baruchel; Hélène Cavé; Aurélie Caye-Eude
err分享
err收藏
Biological and clinical characteristics of ETV6::RUNX1-like ALLETV6::RUNX1样急性淋巴细胞白血病的生物学和临床特征
errHemaSphere
IF14.6
err2026-04-17
err0
errOAAI
errMarketa Zaliova; Dagmar Schinnerl; Judith M. Boer; Aurélie Caye-Eude; Jacqueline Rehn; Claire Schwab; Chloé Arfeuille; Andishe Attarbaschi; Anke Katharina Bergmann; Karel Fiser; Hester A. de Groot-Kruseman; Sabrina Haslinger; Andrea Inthal; Iveta Janotova; Lennart Lenk; Margarita Maurer-Granofszky; Karin Nebral; Fiona Poyer; Lucie Sramkova; Jan Stary; Marion Strullu; Jan Stuchly; Rosemary Sutton; Martina Vaskova; Lucie Winkowska; Gunnar Cario; Hélène Cavé; Monique L. den Boer; Christine Harrison; Sabine Strehl; Deborah White; Jan Trka; Jan Zuna
err分享
err收藏
Maturity Onset Diabetes of the Young (MODY): French National Diagnosis and Care Protocol (PNDS, Protocole National de Diagnostic et de Soins)青年成熟期发病糖尿病（MODY）：法国国家诊断与治疗方案（PNDS，Protocole National de Diagnostic et de Soins）
errOrphanet Journal of Rare Diseases
IF3.5
err2026-03-31
err0
errOAAI
errDanièle Dubois-Laforgue; Bruno Donadille; Cécile Ciangura ; Chloé Amouyal; Jean-Baptiste Arnoux; Pascal Barat; Sabine Baron; Jacques Beltrand; Elise Bismuth; Clara Bouché; Jean-Claude Carel; Hélène Cavé; Sophie Christin-Maitre; Delphine Collin-Chavagnac; Christiane Damgé; Brigitte Delemer; Pierre Gourdy ; Sophie Jacqueminet; Sonja Janmaat ; Marc de Kerdanet; Laurence Kessler; Dominique Langin ; Jean-Charles Nault; Jacky Nizard; Michel Polak ; Rachel Reynaud; Cécile Saint-Martin; Igor Tauveron; René Valéro; Anne Vambergue; Marie-Christine Vantyghem; Camille Vatier; Marc Nicolino; Christine Bellanné-Chantelot; Corinne Vigouroux
err分享
err收藏
Interpreting the functional impact of genetic variants: The need for context qualifiers解读基因变异的功能影响：需要背景限定因素
errThe American Journal of Human Genetics
IF0
err2025-12-01
err0
PREAI
errSimone Martinelli; Hélène Cavé; Alessandro De Luca; Marina DiStefano; Rachel Karchin; Ana Clara Lugones; Anne O’Donnell-Luria; Deborah I. Ritter; David Tamborero; Michael Y. Tolstorukov; Paulo Vidal Campregher; Marco Tartaglia; Dmitriy Sonkin
err分享
err收藏
THE WATCH-AND-WAIT APPROACH IN PATIENTS WITH JUVENILE MYELOMONOCYTIC LEUKEMIA: RESULTS OF THE FRENCH COHORT
errEJC Paediatric Oncology
IF0
err2025-11-01
err0
errOAAI
errNeven, Quentin; Arfeuille, Chloe; Caye-Eude, Aurelie; Durand, Pauline; Lainey, Elodie; Nelken, Brigitte; Nola, Marie; Sterin, Arthur; Thomas, Caroline; Khouri, Celine; Dourthe, Marie-Emilie; Fahd, Mony; Millot, Frederic; Neven, Benedicte; Petit, Arnaud; Dalle, Jean-Hugues; Baruchel, Andre; Cave, Helene; Strullu, Marion
err分享
err收藏
The watch-and-wait approach for patients with juvenile myelomonocytic leukemia: results of the French cohort对于儿童骨髓单核细胞白血病患者采取的观察等待策略：法国队列研究的结果
errBlood
IF23.1
err2025-09-22
err0
PREAI
errQuentin Neven; Chloé Arfeuille; Aurélie Caye-Eude; Pauline Durand; Elodie Lainey; Odile Fenneteau; Brigitte Nelken; Marie Nolla; Arthur Sterin; Audrey Grain; Céline Khouri; Mathieu Simonin; Marie-Emilie Dourthe; Mony Fahd; Frédéric Millot; Bénédicte Neven; Arnaud Petit; Sylvie Chevret; Jean-Hugues Dalle; André Baruchel; Hélène Cavé; Marion Strullu
err分享
err收藏
Neurofibromatosis-Noonan syndrome: a prospective monocentric study of 26 patients and literature review神经纤维瘤病-Noonan综合征：一项前瞻性单中心研究（纳入26例患者）及文献综述
errORPHANET JOURNAL OF RARE DISEASES
IF3.5
err2025-04-27
err0
errOAAI
errBessis, Didier; Vidaud, Dominique; Meyer, Pierre; Pacot, Laurence; Villeon, de La G.; Bonnard, Adeline Alice; Capri, Yline; Coubes, Christine; Herman, Fanchon; Lacombe, Didier; Molinari, Nicolas; Poujade, Laura; Roubertie, Agathe; Van Gils, Julien; Verloes, Alain; Genevieve, David; Cave, Helene; Willems, Marjolaine
err分享
err收藏
Two distinct fetal-type signatures characterize juvenile myelomonocytic leukemia两种不同的胎儿型特征谱可表征幼年型髓单核细胞白血病
errHEMASPHERE
IF14.6
err2025-03-25
err0
errOAAI
errStrullu, Marion; Arfeuille, Chloe; Caye-Eude, Aurelie; Maillard, Loic; Lainey, Elodie; Piques, Florian; Cassinat, Bruno; Guimiot, Fabien; Dalle, Jean-Hugues; Baruchel, Andre; Chomienne, Christine; Bonnet, Dominique; Souyri, Michele; Cave, Helene
err分享
err收藏
Overt and covert genetic causes of pediatric acute lymphoblastic leukemia儿童急性淋巴细胞白血病的显性及隐性遗传病因
errLEUKEMIA
IF13.4
err2025-03-24
err0
PREAI
errStoltze, Ulrik; Junk, Stefanie V.; Byrjalsen, Anna; Cave, Helene; Cazzaniga, Giovanni; Elitzur, Sarah; Fronkova, Eva; Hjalgrim, Lisa Lyngsie; Kuiper, Roland P.; Lundgren, Louise; Mescher, Melina; Mikkelsen, Theis; Pastorczak, Agata; Strullu, Marion; Trka, Jan; Wadt, Karin; Izraeli, Shai; Borkhardt, Arndt; Schmiegelow, Kjeld
err分享
err收藏
PAX5::AUTS2 childhood B-ALL: a relapse-prone genetic subtype with frequent central nervous system involvement and a poor outcome: ACUTE LYMPHOBLASTIC LEUKEMIA
errLEUKEMIA
IF13.4
err2024-12-19
err0
errOAAI
errCaye-Eude, Aurelie; Fazio, Grazia; Pastorczak, Agata; Boer, Judith M.; Steinemann, Doris; Ganguli, Debdutta; Sonneveld, Edwin; Haslinger, Sabrina; D'Andrea, Lucia; Bradtke, Jutta; Lopes, Bruno A.; Zaliova, Marketa; Escherich, Gabriele; Koenig, Margit; Fortschegger, Klaus; Inthal, Andrea; Stasevich, Irina; Emerenciano, Mariana; Trka, Jan; Castillo, Luis; Parihar, Mayur; Moorman, Anthony V.; Bergmann, Anke K.; den Boer, Monique L.; Mlynarski, Wojciech; Cazzaniga, Giovanni; Cave, Helene; Nebral, Karin; Schinnerl, Dagmar; Strehl, Sabine
err分享
err收藏
Results of the prospective EORTC Children Leukemia Group study 58081 in precursor B- and T-cell acute lymphoblastic leukemia
errHEMASPHERE
IF14.6
err2024-11-13
err0
errOAAI
errDomenech, Carine; Kicinski, Michal; De Moerloose, Barbara; Piette, Caroline; Chahla, Wadih A.; Kornreich, Laure; Pasquet, Marlene; Uyttebroeck, Anne; Theron, Alexandre; Poiree, Marilyne; Arfeuille, Chloe; Bakkus, Marleen; Grardel, Nathalie; Paillard, Catherine; Freycon, Claire; Millot, Frederic; Simon, Pauline; Philippet, Pierre; Pluchart, Claire; Suciu, Stefan; Rohrlich, Pierre; Ferster, Alina; Bertrand, Yves; Cave, Helene
err分享
err收藏
How to Administer Pegaspargase during Induction Treatment of Acute Lymphoblastic Leukemia in Children and Adolescents? Results of the Caall-F01, a Multicentre Randomized Clinical Trial from the French Pediatric Cancer Society (SFCE)如何在儿童和青少年急性淋巴细胞白血病的诱导治疗期间使用Pegaspargase？Caall-F01研究结果，一项来自法国儿科肿瘤学会（SFCE）的多中心随机临床试验。
errBLOOD
IF23.1
err2024-11-05
err0
PREAI
errStrullu, Marion; Petit, Arnaud; Halfon-Domenech, Carine; Ray-Lunven, Anne-France; Saultier, Paul; Abou Chahla, Wadih; Ducassou, Stephane; Pasquet, Marlene; Thomas, Caroline; Pochon, Cecile; Gandemer, Virginie; Paillard, Catherine; Theron, Alexandre; Pluchart, Claire; Schneider, Pascale; Bodet, Damien; Pellier, Isabelle; Rohrlich, Pierre Simon; Jourdain, Anne-France; Simon, Pauline; Millot, Frederic; Carausu, Liana; Alla, Corinne Armari; Leglise, Camille; Kanold, Justyna; Desplantes, Claire; Thouvenin, Sandrine; Piguet, Christophe; Boissel, Nicolas; Cuccuini, Wendy; Asnafi, Vahid; Caye-Eude, Aurelie; Cave, Helene; Leverger, Guy; Benoist, Jean-Francois; Bertrand, Yves; Chevret, Sylvie; Baruchel, Andre
err分享
err收藏
CD36 cell surface expression as a surrogate marker to identify ABL/JAK-class kinase fusions in pediatric BCP-ALL
errLEUKEMIA
IF13.4
err2024-10-17
err0
PREAI
errStrullu, Marion; Caye-Eude, Aurelie; Robert, Elie; Renard, Jean-Marie; Chaye, Amandine; Galimand, Julie; Fenneteau, Odile; Arfeuille, Chloe; Cuccuini, Wendy; Theron, Alexandre; Thouvenin, Sandrine; Paillard, Catherine; Petit, Arnaud; Rohrlich, Pierre-Simon; Cave, Helene; Baruchel, Andre; Lainey, Elodie
err分享
err收藏
Psychological and ethical issues raised by genomic in paediatric care pathway, a qualitative analysis with parents and childhood cancer patients
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-07-13
err4
errOAAI
errDroin-Mollard, Marion; de Montgolfier, Sandrine; Gimenez-Roqueplo, Anne-Paule; Flahault, Cecile; Petit, Arnaud; Bourdeaut, Franck; Julia, Sophie; Rial-Sebbag, Emmanuelle; Coupier, Isabelle; Simaga, Fatoumata; Brugieres, Laurence; Guerrini-Rousseau, Lea; Claret, Beatrice; Cave, Helene; Strullu, Marion; Hervouet, Lucile; Lahlou-Laforet, Khadija
err分享
err收藏
Loss-of-function variants in ERF are associated with a Noonan syndrome-like phenotype with or without craniosynostosis
errEUROPEAN JOURNAL OF HUMAN GENETICS
IF4.6
err2024-06-01
err3
PREAI
errDentici, Maria Lisa; Niceta, Marcello; Lepri, Francesca Romana; Mancini, Cecilia; Priolo, Manuela; Bonnard, Adeline Alice; Cappelletti, Camilla; Leoni, Chiara; Ciolfi, Andrea; Pizzi, Simone; Cordeddu, Viviana; Rossi, Cesare; Ferilli, Marco; Mucciolo, Mafalda; Colona, Vito Luigi; Fauth, Christine; Bellini, Melissa; Biasucci, Giacomo; Sinibaldi, Lorenzo; Briuglia, Silvana; Gazzin, Andrea; Carli, Diana; Memo, Luigi; Trevisson, Eva; Schiavariello, Concetta; Luca, Maria; Novelli, Antonio; Michot, Caroline; Sweertvaegher, Anne; Germanaud, David; Scarano, Emanuela; De Luca, Alessandro; Zampino, Giuseppe; Zenker, Martin; Mussa, Alessandro; Dallapiccola, Bruno; Cave, Helene; Digilio, Maria Cristina; Tartaglia, Marco
err分享
err收藏
Analysis of measurable residual disease by IG/TR gene rearrangements: quality assurance and updated EuroMRD guidelines
errLEUKEMIA
IF13.4
err2024-05-14
err5
errOAAI
errvan der Velden, Vincent H. J.; Dombrink, Isabel; Alten, Julia; Cazzaniga, Giovanni; Clappier, Emmanuelle; Drandi, Daniela; Eckert, Cornelia; Fronkova, Eva; Hancock, Jeremy; Kotrova, Michaela; Kraemer, Rebekka; Montonen, Mirkka; Pfeifer, Heike; Pott, Christiane; Raff, Thorsten; Trautmann, Heiko; Cave, Helene; Schaefer, Beat W.; van Dongen, Jacques J. M.; Trka, Jan; Brueggemann, Monika; van der Velden, Vincent H. J.; Raff, Thorsten; van Dongen, Jacques J. M.
err分享
err收藏
Investigation of genetic predisposition to acute lymphoblastic Leukemia in 25 French families
errCLINICA CHIMICA ACTA
IF2.9
err2024-05-01
err0
PREAI
errBenboubker, T.; Caye, A.; Cave, H.; Vial, Y.
err分享
err收藏
Differential activation of basal and IL-7-induced PI3K/Akt/ mTOR and JAK/STAT5 signaling distinguishes pediatric from adult acute lymphoblastic leukemia
errHAEMATOLOGICA
IF7.9
err2024-04-24
err0
errOAAI
errFernandes, Marta B.; Gomes, A. Margarida; Oliveira, Mariana L.; Caldas, Joana; Lucio, Paulo; Kim, Rathana; Caye-Eude, Aurelie; Pereira, Filomena; de Sousa, Aida B.; De Stefano, Alessia; Follo, Matilde Y.; Soares, Maria, V; Lacerda, Joao F.; Desterro, Joana; Cave, Helene; Clappier, Emmanuelle; Duarte, Ximo; Ribeiro, Patricia; Barata, Joao T.
err分享
err收藏
Mcph1, mutated in primary microcephaly, is also crucial for erythropoiesis
errEMBO REPORTS
IF6.2
err2024-04-11
err0
errOAAI
errVial, Yoann; Nardelli, Jeannette; Bonnard, Adeline A.; Rousselot, Justine; Souyri, Michele; Gressens, Pierre; Cave, Helene; Drunat, Severine
err分享
err收藏

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Stefan Schreiber
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Todd R. Golub
H 指数: 176 · 论文数: 749
P
Philippe Froguel
H 指数: 163 · 论文数: 1.2K
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Pier Paolo Pandolfi
H 指数: 160 · 论文数: 818
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