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Biology and Biochemistry

D-Index
77
Citations
37222
World Ranking
4677
National Ranking
346

Overview

Manfred Schmidt is affiliated with the German Cancer Research Center in Germany. Their research spans medicine and biochemistry, genetics, and molecular biology, with a focus on several specialized subfields. These include genetics, molecular biology, oncology, pulmonary and respiratory medicine, and radiology, nuclear medicine, and imaging.

Schmidt's work addresses main topics such as virus-based gene therapy research, hemoglobinopathies and related disorders, CRISPR and genetic engineering, RNA interference and gene delivery, CAR-T cell therapy research, prenatal screening and diagnostics, and parvovirus B19 infection studies.

Among their recent publications are:

  • Betibeglogene Autotemcel Gene Therapy for Non-β 00 Genotype β-Thalassemia, 2021, New England Journal of Medicine
  • Autologous Ex Vivo Lentiviral Gene Therapy for Adenosine Deaminase Deficiency, 2021, New England Journal of Medicine
  • Myelodysplastic syndrome unrelated to lentiviral vector in a patient treated with gene therapy for sickle cell disease, 2020, Blood Advances
  • Interleukin-10 receptor signaling promotes the maintenance of a PD-1int TCF-1+ CD8+ T cell population that sustains anti-tumor immunity, 2021, Immunity
  • Long-term outcomes of lentiviral gene therapy for the β-hemoglobinopathies: the HGB-205 trial, 2022, Nature Medicine

Frequent co-authors collaborating with Schmidt include Alexis A. Thompson, Mark C. Walters, Janet L. Kwiatkowski, Julie Kanter, and John F. Tisdale.

Schmidt's research has been published in several key venues, with multiple contributions to Leukemia and Transplantation and Cellular Therapy, each hosting four publications. They have also published extensively in Nature Communications, Cancers, and the International Journal of Hyperthermia.

Best Publications

  • LMO2-associated clonal T cell proliferation in two patients after gene therapy for SCID-X1.

    S. Hacein-Bey-Abina;C. Von Kalle;C. Von Kalle;M. Schmidt;M. P. McCormack

  • A Serious Adverse Event after Successful Gene Therapy for X-Linked Severe Combined Immunodeficiency

    Salima Hacein-Bey-Abina;Christof Von Kalle;Manfred Schmidt;Françoise Le Deist

  • Hematopoietic Stem Cell Gene Therapy with a Lentiviral Vector in X-Linked Adrenoleukodystrophy

    Nathalie Cartier;Salima Hacein-Bey-Abina;Cynthia C. Bartholomae;Gabor Veres

  • Insertional mutagenesis combined with acquired somatic mutations causes leukemogenesis following gene therapy of SCID-X1 patients

    Steven J. Howe;Marc R. Mansour;Kerstin Schwarzwaelder;Cynthia Bartholomae

  • Lentiviral hematopoietic stem cell gene therapy benefits metachromatic leukodystrophy.

    Alessandra Biffi;Eugenio Montini;Laura Lorioli;Martina Cesani

  • Correction of X-linked chronic granulomatous disease by gene therapy, augmented by insertional activation of MDS1-EVI1, PRDM16 or SETBP1.

    Marion G Ott;Manfred Schmidt;Kerstin Schwarzwaelder;Stefan Stein

  • Lentiviral Hematopoietic Stem Cell Gene Therapy in Patients with Wiskott-Aldrich Syndrome

    Alessandro Aiuti;Luca Biasco;Samantha Scaramuzza;Francesca Ferrua

  • Dissecting the genomic complexity underlying medulloblastoma

    David T. W. Jones;Natalie Jäger;Marcel Kool;Thomas Zichner

  • Genomic instability and myelodysplasia with monosomy 7 consequent to EVI1 activation after gene therapy for chronic granulomatous disease

    Stefan Stein;Marion G. Ott;Stephan Schultze-Strasser;Anna Jauch

  • Hematopoietic stem cell gene transfer in a tumor-prone mouse model uncovers low genotoxicity of lentiviral vector integration

    Eugenio Montini;Daniela Cesana;Manfred Schmidt;Francesca Sanvito

  • Gene therapy of X-linked severe combined immunodeficiency by use of a pseudotyped gammaretroviral vector

    H Bobby Gaspar;Kathryn L Parsley;Steven Howe;Doug King

  • Murine leukemia induced by retroviral gene marking.

    Zhixiong Li;Zhixiong Li;Jochen Düllmann;Bernd Schiedlmeier;Manfred Schmidt

  • An unbiased genome-wide analysis of zinc-finger nuclease specificity

    Richard Gabriel;Angelo Lombardo;Anne Arens;Jeffrey C Miller

  • The genotoxic potential of retroviral vectors is strongly modulated by vector design and integration site selection in a mouse model of HSC gene therapy.

    Eugenio Montini;Daniela Cesana;Manfred Schmidt;Francesca Sanvito

  • Stem-Cell Gene Therapy for the Wiskott–Aldrich Syndrome

    Kaan Boztug;Manfred Schmidt;Adrian Schwarzer;Pinaki P. Banerjee

  • Gene Therapy for Wiskott-Aldrich Syndrome—Long-Term Efficacy and Genotoxicity

    Christian Jörg Braun;Kaan Boztug;Anna Paruzynski;Maximilian Witzel

  • Effective gene therapy with nonintegrating lentiviral vectors

    Rafael J Yáñez-Muñoz;Rafael J Yáñez-Muñoz;Rafael J Yáñez-Muñoz;Kamaljit S Balaggan;Angus MacNeil;Steven J Howe

  • High-resolution insertion-site analysis by linear amplification-mediated PCR (LAM-PCR).

    Manfred Schmidt;Kerstin Schwarzwaelder;Cynthia Bartholomae;Karim Zaoui

  • Integrative Genomic Analyses Reveal an Androgen-Driven Somatic Alteration Landscape in Early-Onset Prostate Cancer

    Joachim Weischenfeldt;Ronald Simon;Lars Feuerbach;Karin Schlangen

  • Distinct types of tumor-initiating cells form human colon cancer tumors and metastases

    Sebastian M. Dieter;Claudia R. Ball;Christopher M. Hoffmann;Ali Nowrouzi

Frequent Co-Authors

Christof von Kalle
Christof von Kalle Charité - University Medicine Berlin
Hanno Glimm
Hanno Glimm TU Dresden
Adrian J. Thrasher
Adrian J. Thrasher University College London
Alessandro Aiuti
Alessandro Aiuti Vita-Salute San Raffaele University
Philippe Leboulch
Philippe Leboulch Brigham and Women's Hospital
Luigi Naldini
Luigi Naldini Vita-Salute San Raffaele University
Claudio Bordignon
Claudio Bordignon MolMed (Italy)
Jakub Tolar
Jakub Tolar University of Minnesota
Marina Cavazzana-Calvo
Marina Cavazzana-Calvo Necker-Enfants Malades Hospital
Eugenio Montini
Eugenio Montini IRCCS Ospedale San Raffaele

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