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Andreas E. Kulozik

Andreas E. Kulozik

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Genetics
Germany
2024

D-Index & Metrics

Genetics

D-Index
90
Citations
39918
World Ranking
1063
National Ranking
88

Medicine

D-Index
92
Citations
41494
World Ranking
11122
National Ranking
603

Research.com Recognitions

  • 2024 - Research.com Genetics in Germany Leader Award
  • 2023 - Research.com Genetics in Germany Leader Award
  • 2011 - German National Academy of Sciences Leopoldina - Deutsche Akademie der Naturforscher Leopoldina – Nationale Akademie der Wissenschaften Human Genetics and Molecular Medicine
  • Member of the European Molecular Biology Organization (EMBO)
  • Member of the European Molecular Biology Organization (EMBO)
  • Member of the European Molecular Biology Organization (EMBO)
  • Member of the European Molecular Biology Organization (EMBO)

Overview

Andreas E. Kulozik is affiliated with Heidelberg University in Germany. Their research spans several fields with a focus on genetics, molecular biology, hematology, public health, environmental and occupational health, and oncology. The primary areas of study include hemoglobinopathies and related disorders, acute lymphoblastic leukemia research, iron metabolism and disorders, CAR-T cell therapy, sarcoma diagnosis and treatment, neonatal health and biochemistry, and immune cell function and interaction.

Their scholarly output includes significant contributions published in renowned journals such as Blood, Transplantation and Cellular Therapy, HemaSphere, bioRxiv (Cold Spring Harbor Laboratory), and Nature Communications. These venues reflect the scope and interdisciplinary nature of their work.

Recent papers authored or coauthored by Andreas E. Kulozik include:

  • "Sarcoma classification by DNA methylation profiling," 2021, Nature Communications
  • "The Pediatric Precision Oncology INFORM Registry: Clinical Outcome and Benefit for Patients with Very High-Evidence Targets," 2021, Cancer Discovery
  • "Recommendations for diagnosis and treatment of methemoglobinemia," 2021, American Journal of Hematology
  • "The evaluation of iron deficiency and iron overload," 2021, Deutsches Ärzteblatt international
  • "2,6-Diaminopurine as a highly potent corrector of UGA nonsense mutations," 2020, Nature Communications

Frequent coauthors working alongside Andreas E. Kulozik include:

  • Joachim B. Kunz
  • Mark C. Walters
  • Suradej Hongeng
  • Martin G. Sauer
  • Adrian J. Thrasher

Their research topics cover a broad spectrum within molecular medicine and clinical hematology, specifically focusing on:

  • Hemoglobinopathies and Related Disorders
  • Acute Lymphoblastic Leukemia research
  • Iron Metabolism and Disorders
  • CAR-T cell therapy research
  • Sarcoma Diagnosis and Treatment
  • Neonatal Health and Biochemistry
  • Immune Cell Function and Interaction

Throughout their career, Andreas E. Kulozik has been recognized by scientific organizations, including the German National Academy of Sciences Leopoldina, where they were inducted in 2011 with a citation in Human Genetics and Molecular Medicine. They are also a member of the European Molecular Biology Organization (EMBO).

Best Publications

  • DNA methylation-based classification of central nervous system tumours

    David Capper;David Capper;David Capper;David T. W. Jones;Martin Sill;Volker Hovestadt

  • Driver mutations in histone H3.3 and chromatin remodelling genes in paediatric glioblastoma

    Jeremy Schwartzentruber;Andrey Korshunov;Xiao Yang Liu;David T.W. Jones

  • Hotspot mutations in H3F3A and IDH1 define distinct epigenetic and biological subgroups of glioblastoma.

    Dominik Sturm;Hendrik Witt;Hendrik Witt;Volker Hovestadt;Dong Anh Khuong-Quang

  • The landscape of genomic alterations across childhood cancers

    Susanne N. Gröbner;Barbara C. Worst;Joachim Weischenfeldt;Joachim Weischenfeldt;Ivo Buchhalter

  • Molecular Classification of Ependymal Tumors across All CNS Compartments, Histopathological Grades, and Age Groups

    Kristian W. Pajtler;Kristian W. Pajtler;Hendrik Witt;Martin Sill;David T.W. Jones

  • A perfect message : RNA surveillance and nonsense-mediated decay

    Matthias W Hentze;Andreas E Kulozik

  • Dissecting the genomic complexity underlying medulloblastoma

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

  • Genome Sequencing of Pediatric Medulloblastoma Links Catastrophic DNA Rearrangements with TP53 Mutations

    Tobias Rausch;David T.W. Jones;Marc Zapatka;Adrian M. Stütz

  • Recurrent somatic alterations of FGFR1 and NTRK2 in pilocytic astrocytoma

    David T W Jones;Barbara Hutter;Natalie Jäger;Andrey Korshunov;Andrey Korshunov

  • Genome Sequencing of SHH Medulloblastoma Predicts Genotype-Related Response to Smoothened Inhibition

    Marcel Kool;David T.W. Jones;Natalie Jäger;Paul A. Northcott

  • Nonsense-mediated decay approaches the clinic

    Jill A Holbrook;Gabriele Neu-Yilik;Gabriele Neu-Yilik;Matthias W Hentze;Andreas E Kulozik;Andreas E Kulozik

  • Enhancer hijacking activates GFI1 family oncogenes in medulloblastoma

    Paul A. Northcott;Catherine Lee;Catherine Lee;Thomas Zichner;Adrian M. Stütz

  • Epigenomic alterations define lethal CIMP-positive ependymomas of infancy

    S. C. Mack;H. Witt;R. M. Piro;L. Gu

  • A sensitive array for microRNA expression profiling (miChip) based on locked nucleic acids (LNA).

    Mirco Castoldi;Sabine Schmidt;Vladimir Benes;Mikkel Noerholm

  • Delineation of Two Clinically and Molecularly Distinct Subgroups of Posterior Fossa Ependymoma

    Hendrik Witt;Stephen C. Mack;Marina Ryzhova;Sebastian Bender;Sebastian Bender

  • BRAF gene duplication constitutes a mechanism of MAPK pathway activation in low-grade astrocytomas

    Stefan Pfister;Wibke G. Janzarik;Marc Remke;Aurélie Ernst

  • Atypical Teratoid/Rhabdoid Tumors Are Comprised of Three Epigenetic Subgroups with Distinct Enhancer Landscapes

    Pascal D. Johann;Pascal D. Johann;Serap Erkek;Marc Zapatka;Kornelius Kerl

  • BINARY SPECIFICATION OF NONSENSE CODONS BY SPLICING AND CYTOPLASMIC TRANSLATION

    Rolf Thermann;Gabriele Neu‐Yilik;Andrea Deters;Ute Frede

  • Gain-of-function mutations in interleukin-7 receptor-α (IL7R) in childhood acute lymphoblastic leukemias

    Chen Shochat;Noa Tal;Noa Tal;Obul R. Bandapalli;Obul R. Bandapalli;Chiara Palmi

  • 3′ end mRNA processing: molecular mechanisms and implications for health and disease

    Sven Danckwardt;Matthias W Hentze;Andreas E Kulozik;Andreas E Kulozik

Frequent Co-Authors

Stefan M. Pfister
Stefan M. Pfister German Cancer Research Center
Andrey Korshunov
Andrey Korshunov German Cancer Research Center
Matthias W. Hentze
Matthias W. Hentze European Molecular Biology Laboratory
Andreas von Deimling
Andreas von Deimling Heidelberg University
Martina U. Muckenthaler
Martina U. Muckenthaler Heidelberg University
Peter Lichter
Peter Lichter German Cancer Research Center
Marc Remke
Marc Remke German Cancer Research Center
Jan O. Korbel
Jan O. Korbel European Molecular Biology Laboratory
David T. W. Jones
David T. W. Jones German Cancer Research Center
Martin Schrappe
Martin Schrappe Kiel University

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