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S

Stephan Lobitz

University of London
H指数:22
被引数:2,072

个人简介

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教育背景

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工作经历

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荣誉奖项

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Gene therapy in transfusion-dependent non- (3 0 / (3 0 genotype (3-thalassemia: fi rst real-world experience of beti-cel

输血依赖性非β0/β0基因型β-地中海贫血的基因治疗：Beti-cel的首个真实世界经验

BLOOD ADVANCES
IF7.1
2024-12-261
OA
Mirza, Adil; Ritsert, Mona-Lisa; Tao, Gloria; Thakar, Himal; Lobitz, Stephan; Heine, Sabine; Koscher, Leila; Duerken, Matthias; Schmitt, Anita; Schmitt, Michael; Pavel, Petra; Laier, Sascha; Jakoby, Donate; Greil, Johann; Kunz, Joachim; Kulozik, Andreas
Exagamglogene Autotemcel for Severe Sickle Cell Disease
NEW ENGLAND JOURNAL OF MEDICINE
IF78.5
2024-05-0954
PRE
Frangoul, H.; Locatelli, F.; Sharma, A.; Bhatia, M.; Mapara, M.; Molinari, L.; Wall, D.; Liem, R. I.; Telfer, P.; Shah, A. J.; Cavazzana, M.; Corbacioglu, S.; Rondelli, D.; Meisel, R.; Dedeken, L.; Lobitz, S.; de Montalembert, M.; Steinberg, M. H.; Walters, M. C.; Eckrich, M. J.; Imren, S.; Bower, L.; Simard, C.; Zhou, W.; Xuan, F.; Morrow, P. K.; Hobbs, W. E.; Grupp, S. A.
Sickle cell disease landscape and challenges in the EU the ERN-EuroBloodNet perspective

欧盟的镰状细胞病景观和挑战ern-eurobloodnet观点

LANCET HAEMATOLOGY
IF17.7
2023-08-0111
PRE
Pereira, Maria del Mar Manu; Colombatti, Raffaella; Alvarez, Federico; Bartolucci, Pablo; Bento, Celeste; Brunetta, Angelo Loris; Cela, Elena; Christou, Soteroula; Collado, Anna; de Montalembert, Mariane; Dedeken, Laurence; Fenaux, Pierre; Galacteros, Frederic; Glenthoj, Andreas; Valle, Victoria Gutierrez; Kattamis, Antonis; Kunz, Joachim; Lobitz, Stephan; McMahon, Corrina; Pellegrini, Mariangela; Reidel, Sara; Russo, Giovanna; Freire, Miriam Santos; van Beers, Eduard; Kountouris, Petros; Gulbis, Beatrice
Constitutional Microsatellite Instability, Genotype, and Phenotype Correlations in Constitutional Mismatch Repair Deficiency
GASTROENTEROLOGY
IF25.1
2023-04-0118
OA
Gallon, Richard; Phelps, Rachel; Hayes, Christine; Brugieres, Laurence; Guerrini-Rousseau, Lea; Colas, Chrystelle; Muleris, Martine; Ryan, Neil A. J.; Evans, D. Gareth; Grice, Hannah; Jessop, Emily; Kunzemann-Martinez, Annabel; Marshall, Lilla; Schamschula, Esther; Oberhuber, Klaus; Azizi, Amedeo A.; Feldman, Hagit Baris; Beilken, Andreas; Brauer, Nina; Brozou, Triantafyllia; Dahan, Karin; Demirsoy, Ugur; Florkin, Benoit; Foulkes, William; Januszkiewicz-Lewandowska, Danuta; Jones, Kristi J.; Kratz, Christian P.; Lobitz, Stephan; Meade, Julia; Nathrath, Michaela; Pander, Hans-Jurgen; Perne, Claudia; Ragab, Iman; Ripperger, Tim; Rosenbaum, Thorsten; Rueda, Daniel; Sarosiek, Tomasz; Sehested, Astrid; Spier, Isabel; Suerink, Manon; Zimmermann, Stefanie-Yvonne; Zschocke, Johannes; Borthwick, Gillian M.; Wimmer, Katharina; Burn, John; Jackson, Michael S.; Santibanez-Koref, Mauro
High-sensitivity microsatellite instability assessment for the detection of mismatch repair defects in normal tissue of biallelic germline mismatch repair mutation carriers
JOURNAL OF MEDICAL GENETICS
IF3.7
2019-09-0729
OAAI
Gonzalez-Acosta, Maribel; Marin, Fatima; Puliafito, Benjamin; Bonifaci, Nuria; Fernandez, Anna; Navarro, Matilde; Salvador, Hector; Balaguer, Francesc; Iglesias, Silvia; Velasco, Angela; Garces, Elia Grau; Moreno, Victor; Gonzalez-Granado, Luis Ignacio; Guerra-Garcia, Pilar; Ayala, Rosa; Florkin, Benoit; Kratz, Christian; Ripperger, Tim; Rosenbaum, Thorsten; Januszkiewicz-Lewandowska, Danuta; Azizi, Amedeo A.; Ragab, Iman; Nathrath, Michaela; Pander, Hans-Juergen; Lobitz, Stephan; Suerink, Manon; Dahan, Karin; Imschweiler, Thomas; Demirsoy, Ugur; Brunet, Joan; Lazaro, Conxi; Rueda, Daniel; Wimmer, Katharina; Capella, Gabriel; Pineda, Marta
A sensitive and scalable microsatellite instability assay to diagnose constitutional mismatch repair deficiency by sequencing of peripheral blood leukocytes
HUMAN MUTATION
IF3.7
2019-03-0641
OAAI
Gallon, Richard; Muehlegger, Barbara; Wenzel, Soeren-Sebastian; Sheth, Harsh; Hayes, Christine; Aretz, Stefan; Dahan, Karin; Foulkes, William; Kratz, Christian P.; Ripperger, Tim; Azizi, Amedeo A.; Feldman, Hagit Baris; Chong, Anne-Laure; Demirsoy, Ugur; Florkin, Benoit; Imschweiler, Thomas; Januszkiewicz-Lewandowska, Danuta; Lobitz, Stephan; Nathrath, Michaela; Pander, Hans-Juergen; Perez-Alonso, Vanesa; Perne, Claudia; Ragab, Iman; Rosenbaum, Thorsten; Rueda, Daniel; Seidel, Markus G.; Suerink, Manon; Taeubner, Julia; Zimmermann, Stefanie-Yvonne; Zschocke, Johannes; Borthwick, Gillian M.; Burn, John; Jackson, Michael S.; Santibanez-Koref, Mauro; Wimmer, Katharina
A comprehensive strategy for the subtyping of patients with Fanconi anaemia:: conclusions from the Spanish Fanconi Anemia Research Network
JOURNAL OF MEDICAL GENETICS
IF3.7
2007-04-0144
OAAI
Casado, Jose Antonio; Callen, Elsa; Jacome, Ariana; Rio, Paula; Castella, Maria; Lobitz, Stephan; Ferro, Teresa; Munoz, Arturo; Sevilla, Julian; Cantalejo, Angeles; Cela, Elena; Cervera, Jose; Sanchez-Calero, Jesus; Badell, Isabel; Estella, Jesus; Dasi, Angeles; Olive, Teresa; Ortega, Juan Jose; Rodriguez-Villa, Antonia; Tapia, Maria; Molines, Antonio; Madero, Luis; Segovia, Jose C.; Neveling, Kornelia; Kalb, Reinhard; Schindler, Detlev; Hanenberg, Helmut; Surralles, Jordi; Bueren, Juan A.

研究方向

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J
Joachim B. Kunz
H 指数:31论文数:154被引数:4,094
A
Andreas E. Kulozik
H 指数:80论文数:524被引数:3.6万
C
Christian P. Kratz
H 指数:60论文数:365被引数:2.1万
A
Amedeo A. Azizi
H 指数:32论文数:244被引数:4,420
O
Oliver Blankenstein
H 指数:35论文数:187被引数:3,672
K
Katharina Wimmer
H 指数:43论文数:168被引数:7,260
M
Michaela Nathrath
H 指数:36论文数:207被引数:6,983
D
Daniel Rueda
H 指数:25论文数:96被引数:3,166
K
Karin Dahan
H 指数:39论文数:141被引数:6,808
D
Danuta Januszkiewicz‐Lewandowska
H 指数:21论文数:155被引数:1,453