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Genetics
Germany
2024
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Genetics and Molecular Biology
Germany
2024

D-Index & Metrics

Genetics

D-Index
93
Citations
31316
World Ranking
975
National Ranking
82

Medicine

D-Index
95
Citations
32223
World Ranking
10093
National Ranking
555

Research.com Recognitions

  • 2024 - Research.com Genetics in Germany Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in Germany Leader Award
  • 2023 - Research.com Genetics in Germany Leader Award

Overview

Norbert Hubner is affiliated with the Max Delbrück Center for Molecular Medicine in Germany. Their research spans biochemistry, genetics, molecular biology, and medicine, with particular focus on molecular biology and cardiology. They have contributed extensively to subfields such as molecular biology, cardiology and cardiovascular medicine, immunology, cancer research, and physiology.

Hubner's main topics of research include RNA and protein synthesis mechanisms, RNA research and splicing, RNA modifications and cancer, cancer-related molecular mechanisms, single-cell and spatial transcriptomics, congenital heart defects research, and adipose tissue and metabolism.

The scientist has a record of notable publications published primarily in high-impact journals. Key recent papers include:

  • Cells of the adult human heart, 2020, Nature
  • Myocarditis and inflammatory cardiomyopathy: current evidence and future directions, 2020, Nature Reviews Cardiology
  • Spatially resolved multiomics of human cardiac niches, 2023, Nature
  • Standardized annotation of translated open reading frames, 2022, Nature Biotechnology
  • Pathogenic variants damage cell composition and single cell transcription in cardiomyopathies, 2022, Science

They have coauthored many papers with several researchers, including Sebastiaan van Heesch, Jorge Ruiz-Orera, Eric L. Lindberg, Giannino Patone, and Henrike Maatz. These frequent collaborations emphasize the multidisciplinary and collaborative nature of Hubner's research activities.

Their work has been published in multiple journals and venues, with the largest number of papers appearing in bioRxiv (Cold Spring Harbor Laboratory), Nature, Nature Communications, Cardiovascular Research, and Molecular Cell. The distribution across these venues highlights a commitment to both preprint and peer-reviewed scientific communication.

Best Publications

  • Genome sequence of the Brown Norway rat yields insights into mammalian evolution

    Richard A. Gibbs;George M. Weinstock;Michael L. Metzker;Donna M. Muzny

  • Cells of the adult human heart.

    Monika Litviňuková;Monika Litviňuková;Carlos Talavera-López;Carlos Talavera-López;Henrike Maatz;Daniel Reichart;Daniel Reichart

  • Myocarditis and inflammatory cardiomyopathy: current evidence and future directions.

    Carsten Tschöpe;Enrico Ammirati;Biykem Bozkurt;Biykem Bozkurt;Alida L.P. Caforio

  • Mutations in the gene encoding the 3'-5' DNA exonuclease TREX1 are associated with systemic lupus erythematosus.

    Min Ae Lee-Kirsch;Maolian Gong;Dipanjan Chowdhury;Lydia Senenko

  • Genetics and Beyond – The Transcriptome of Human Monocytes and Disease Susceptibility

    Tanja Zeller;Philipp Wild;Silke Szymczak;Maxime Rotival

  • Multi-ancestry genome-wide association study of 21,000 cases and 95,000 controls identifies new risk loci for atopic dermatitis

    Lavinia Paternoster;Marie Standl;Johannes Waage;Hansjoerg Baurecht

  • Integrated transcriptional profiling and linkage analysis for identification of genes underlying disease

    Norbert Hubner;Caroline A Wallace;Heike Zimdahl;Enrico Petretto

  • Titin mutations in iPS cells define sarcomere insufficiency as a cause of dilated cardiomyopathy

    John Travis Hinson;Anant Chopra;N. Nafissi;William Polacheck;William Polacheck

  • RBM20, a gene for hereditary cardiomyopathy, regulates titin splicing

    Wei Guo;Sebastian Schafer;Marion L Greaser;Michael H Radke

  • Conditional mutation of the ErbB2(HER2) receptor in cardiomyocytes leads to dilated cardiomyopathy.

    Cemil Özcelik;Bettina Erdmann;Bernhard Pilz;Nina Wettschureck

  • Shared genetic origin of asthma, hay fever and eczema elucidates allergic disease biology

    Manuel A. Ferreira;Judith M. Vonk;Hansjörg Baurecht;Ingo Marenholz;Ingo Marenholz

  • IL-11 is a crucial determinant of cardiovascular fibrosis

    Sebastian Schafer;Sivakumar Viswanathan;Anissa A Widjaja;Wei-Wen Lim

  • Role of endocytosis in cellular uptake of sex steroids.

    Annette Hammes;Thomas K. Andreassen;Robert Spoelgen;Jens Raila

  • The Translational Landscape of the Human Heart

    Sebastiaan van Heesch;Franziska Witte;Valentin Schneider-Lunitz;Jana F. Schulz

  • Integrated allelic, transcriptional, and phenomic dissection of the cardiac effects of titin truncations in health and disease

    Angharad M. Roberts;Angharad M. Roberts;James S. Ware;Daniel S. Herman;Daniel S. Herman;Daniel S. Herman;Sebastian Schafer

  • Cerebrovascular dysfunction and microcirculation rarefaction precede white matter lesions in a mouse genetic model of cerebral ischemic small vessel disease

    Anne Joutel;Marie Monet-Leprêtre;Claudia Gosele;Céline Baron-Menguy

  • Functional improvement and maturation of rat and human engineered heart tissue by chronic electrical stimulation.

    Marc N. Hirt;Jasper Boeddinghaus;Alice Mitchell;Sebastian Schaaf

  • A common variant on chromosome 11q13 is associated with atopic dermatitis

    Jorge Esparza-Gordillo;Stephan Weidinger;Regina Fölster-Holst;Anja Bauerfeind

  • Progress and prospects in rat genetics: a community view.

    Timothy J Aitman;John K Critser;Edwin Cuppen;Anna Dominiczak

  • A trans-acting locus regulates an anti-viral expression network and type 1 diabetes risk

    Matthias Heinig;Enrico Petretto;Chris Wallace;Leonardo Bottolo

Frequent Co-Authors

Herbert Schulz
Herbert Schulz University of Cologne
Stuart A. Cook
Stuart A. Cook Duke NUS Graduate Medical School
Michal Pravenec
Michal Pravenec Czech Academy of Sciences
Kathrin Saar
Kathrin Saar Max Delbrück Center for Molecular Medicine
Enrico Petretto
Enrico Petretto Duke NUS Graduate Medical School
Franz Rüschendorf
Franz Rüschendorf Max Delbrück Center for Molecular Medicine
Timothy J. Aitman
Timothy J. Aitman University of Edinburgh
Christine E. Seidman
Christine E. Seidman Harvard University
Detlev Ganten
Detlev Ganten Max Delbrück Center for Molecular Medicine
Friedrich C. Luft
Friedrich C. Luft Charité - University Medicine Berlin

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