日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

Two distinct fetal-type signatures characterize juvenile myelomonocytic leukemia

幼年型骨髓单核细胞白血病具有两种不同的胎儿型特征。

Strullu, Marion; Arfeuille, Chloé; Caye-Eude, Aurélie; Maillard, Loïc; Lainey, Elodie; Piques, Florian; Cassinat, Bruno; Guimiot, Fabien; Dalle, Jean-Hugues; Baruchel, André; Chomienne, Christine; Bonnet, Dominique; Souyri, Michèle; Cavé, Hélène

Mapping the developmental profile of ventricular zone-derived neurons in the human cerebellum

绘制人类小脑室区衍生神经元的发育图谱

Erickson, Anders W; Tan, Henry; Hendrikse, Liam D; Millman, Jake; Thomson, Zachary; Golser, Joseph; Khan, Omar; He, Guanyi; Bach, Kathleen; Mishra, Arpit Suresh; Kopic, Janja; Krsnik, Zeljka; Encha-Razavi, Ferechte; Petrilli, Giulia; Guimiot, Fabien; Silvestri, Evelina; Aldinger, Kimberly A; Taylor, Michael D; Millen, Kathleen J; Haldipur, Parthiv

Radial Microbrain (Micrencephaly) Is Caused by a Recurrent Variant in the RTTN Gene

放射状小脑畸形(小脑畸形)是由RTTN基因的复发性变异引起的。

Gins, Clarisse; Guimiot, Fabien; Drunat, Séverine; Prévost, Clemence; Rosenblatt, Jonathan; Capri, Yline; Letard, Pascaline; Khung-Savatovsky, Suonavy; Mahi Henni, Mohamed Amine; Elalaoui, Siham Chafai; Alison, Marianne; Guilmin Crepon, Sophie; Gressens, Pierre; Verloes, Alain; Basto, Renata; El Ghouzzi, Vincent; Passemard, Sandrine

MPDZ Pathogenic Variants Cause Obstructive Ventriculomegaly Related to Diencephalosynapsis and Third Ventricle Atresia

MPDZ致病变异导致梗阻性脑室扩大,与间脑融合和第三脑室闭锁相关

Cabet, Sara; Ghersi-Egea, Jean-François; Khung-Savatovsky, Suonavy; Guimiot, Fabien; Putoux, Audrey; Sabatier, Isabelle; Fernandez, Carla; Raymond, Laure; Mortreux, Jérémie; Laurichesse Delmas, Hélène; Cuillier, Fabrice Eric; Ho, Fabien; Lesca, Gaetan; Alessandri, Jean-Luc; Guibaud, Laurent

Immunologic aspects of preeclampsia

先兆子痫的免疫学方面

Boulanger, Henri; Bounan, Stéphane; Mahdhi, Amel; Drouin, Dominique; Ahriz-Saksi, Salima; Guimiot, Fabien; Rouas-Freiss, Nathalie

Reply to Pubpeer anonymous contributors: incomplete penetrance and phenotypic variability of 6q16 deletions including SIM1

回复 Pubpeer 匿名贡献者:6q16 缺失(包括 SIM1)的不完全外显率和表型变异性

El Khattabi, Laila; Guimiot, Fabien; Delahaye-Duriez, Andrée

Phenotypic spectrum and genomics of undiagnosed arthrogryposis multiplex congenita

未确诊先天性多发性关节挛缩症的表型谱和基因组学

Laquerriere, Annie; Jaber, Dana; Abiusi, Emanuela; Maluenda, Jérome; Mejlachowicz, Dan; Vivanti, Alexandre; Dieterich, Klaus; Stoeva, Radka; Quevarec, Loic; Nolent, Flora; Biancalana, Valerie; Latour, Philippe; Sternberg, Damien; Capri, Yline; Verloes, Alain; Bessieres, Bettina; Loeuillet, Laurence; Attie-Bitach, Tania; Martinovic, Jelena; Blesson, Sophie; Petit, Florence; Beneteau, Claire; Whalen, Sandra; Marguet, Florent; Bouligand, Jerome; Héron, Delphine; Viot, Géraldine; Amiel, Jeanne; Amram, Daniel; Bellesme, Céline; Bucourt, Martine; Faivre, Laurence; Jouk, Pierre-Simon; Khung, Suonavy; Sigaudy, Sabine; Delezoide, Anne-Lise; Goldenberg, Alice; Jacquemont, Marie-Line; Lambert, Laetitia; Layet, Valérie; Lyonnet, Stanislas; Munnich, Arnold; Van Maldergem, Lionel; Piard, Juliette; Guimiot, Fabien; Landrieu, Pierre; Letard, Pascaline; Pelluard, Fanny; Perrin, Laurence; Saint-Frison, Marie-Hélène; Topaloglu, Haluk; Trestard, Laetitia; Vincent-Delorme, Catherine; Amthor, Helge; Barnerias, Christine; Benachi, Alexandra; Bieth, Eric; Boucher, Elise; Cormier-Daire, Valerie; Delahaye-Duriez, Andrée; Desguerre, Isabelle; Eymard, Bruno; Francannet, Christine; Grotto, Sarah; Lacombe, Didier; Laffargue, Fanny; Legendre, Marine; Martin-Coignard, Dominique; Mégarbané, André; Mercier, Sandra; Nizon, Mathilde; Rigonnot, Luc; Prieur, Fabienne; Quélin, Chloé; Ranjatoelina-Randrianaivo, Hanitra; Resta, Nicoletta; Toutain, Annick; Verhelst, Helene; Vincent, Marie; Colin, Estelle; Fallet-Bianco, Catherine; Granier, Michèle; Grigorescu, Romulus; Saada, Julien; Gonzales, Marie; Guiochon-Mantel, Anne; Bessereau, Jean-Louis; Tawk, Marcel; Gut, Ivo; Gitiaux, Cyril; Melki, Judith

Extracellular LGALS3BP regulates neural progenitor position and relates to human cortical complexity

细胞外LGALS3BP调控神经祖细胞的位置,并与人类皮层复杂性相关。

Christina Kyrousi ,Adam C O'Neill ,Agnieska Brazovskaja ,Zhisong He ,Pavel Kielkowski ,Laure Coquand ,Rossella Di Giaimo ,Pierpaolo D' Andrea ,Alexander Belka ,Andrea Forero Echeverry ,Davide Mei ,Matteo Lenge ,Cristiana Cruceanu ,Isabel Y Buchsbaum ,Shahryar Khattak ,Guimiot Fabien ,Elisabeth Binder ,Frances Elmslie ,Renzo Guerrini ,Alexandre D Baffet ,Stephan A Sieber ,Barbara Treutlein ,Stephen P Robertson ,Silvia Cappello

CD117(hi) expression identifies a human fetal hematopoietic stem cell population with high proliferation and self-renewal potential

CD117(hi)表达可识别具有高增殖和自我更新能力的人类胎儿造血干细胞群。

Maillard, Loïc; Sanfilippo, Sandra; Domenech, Carine; Kasmi, Nassima; Petit, Laurence; Jacques, Sébastien; Delezoide, Anne-Lise; Guimiot, Fabien; Eladak, Soria; Moison, Delphine; Nicolas, Nour; Rouiller-Fabre, Virginie; Pozzi-Godin, Stéphanie; Mennesson, Benoit; Brival, Marie-Laure; Letourneur, Franck; Jaffredo, Thierry; Chomienne, Christine; Souyri, Michèle

Spatiotemporal expansion of primary progenitor zones in the developing human cerebellum

人类小脑发育过程中初级祖细胞区的时空扩张

Haldipur, Parthiv; Aldinger, Kimberly A; Bernardo, Silvia; Deng, Mei; Timms, Andrew E; Overman, Lynne M; Winter, Conrad; Lisgo, Steven N; Razavi, Ferechte; Silvestri, Evelina; Manganaro, Lucia; Adle-Biassette, Homa; Guimiot, Fabien; Russo, Rosa; Kidron, Debora; Hof, Patrick R; Gerrelli, Dianne; Lindsay, Susan J; Dobyns, William B; Glass, Ian A; Alexandre, Paula; Millen, Kathleen J