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Nils Mandahl

Nils Mandahl

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Genetics
Sweden
2026
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Genetics and Molecular Biology
Sweden
2024

D-Index & Metrics

Genetics

D-Index
106
Citations
34629
World Ranking
609
National Ranking
6

Medicine

D-Index
106
Citations
34960
World Ranking
6609
National Ranking
135

Research.com Recognitions

  • 2026 - Research.com Genetics in Sweden Leader Award
  • 2025 - Research.com Genetics in Sweden Leader Award
  • 2024 - Research.com Genetics in Sweden Leader Award
  • 2024 - Research.com Genetics and Molecular Biology in Sweden Leader Award
  • 2023 - Research.com Genetics in Sweden Leader Award
  • 2022 - Research.com Genetics and Molecular Biology in Sweden Leader Award

Overview

Nils Mandahl is a researcher affiliated with Lund University in Sweden. Their work primarily spans the fields of Medicine, and Biochemistry, Genetics and Molecular Biology, with specific focus on several subfields including Neurology, Molecular Biology, Cancer Research, Genetics, and Oncology.

The main topics addressed in their research encompass:

  • Neuroblastoma Research and Treatments
  • Cancer Genomics and Diagnostics
  • Neurofibromatosis and Schwannoma Cases
  • Genomic variations and chromosomal abnormalities
  • Genomics and Chromatin Dynamics
  • Pancreatic and Hepatic Oncology Research
  • Sarcoma Diagnosis and Treatment

Mandahl's publications appear in multiple scientific venues, with frequent contributions to the following journals:

  • Genes Chromosomes and Cancer
  • EBioMedicine
  • SSRN Electronic Journal
  • International Journal of Cancer

Notable recent publications include:

  • "Transcriptomic subtyping of malignant peripheral nerve sheath tumours highlights immune signatures, genomic profiles, patient survival and therapeutic targets," 2023, EBioMedicine
  • "Giemsa-negative chromosome bands preferentially recombine in cancer-associated translocations and gene fusions," 2022, Genes Chromosomes and Cancer
  • "Gene amplification in neoplasia: A cytogenetic survey of 80,131 cases," 2023, Genes Chromosomes and Cancer
  • "Transcriptomic Subtyping of Malignant Peripheral Nerve Sheath Tumours Highlights Immune Signatures, Genomic Profiles, Patient Survival and Therapeutic Targets," 2023, SSRN Electronic Journal
  • "Aneuploidy in neoplasia: Single-cell data on 83,862 tumors," 2024, International Journal of Cancer

Frequent collaborators in their research include:

  • Fredrik Mertens
  • Felix Mitelman
  • Maren Høland
  • Kaja C. G. Berg
  • Ina A. Eilertsen

Best Publications

  • TERT promoter mutations occur frequently in gliomas and a subset of tumors derived from cells with low rates of self-renewal

    Patrick J. Killela;Zachary J. Reitman;Yuchen Jiao;Chetan Bettegowda

  • Fusion of CHOP to a novel RNA-binding protein in human myxoid liposarcoma.

    Anne Crozat;Pierre Åman;Nils Mandahl;David Ron

  • The der(17)t(x;17)(p11;q25) of human alveolar soft part sarcoma fuses the TFE3 transcription factor gene to ASPL, a novel gene at 17q25

    Marc Ladanyi;Man Yee Lui;Cristina R Antonescu;Amber Krause-Boehm

  • Deregulation of the platelet-derived growth factor B-chain gene via fusion with collagen gene COL1A1 in dermatofibrosarcoma protuberans and giant-cell fibroblastoma

    Marie Pierre Simon;Florence Pedeutour;Nicolas Sirvent;Josiane Grosgeorge

  • Telomere dysfunction triggers extensive DNA fragmentation and evolution of complex chromosome abnormalities in human malignant tumors

    David Gisselsson;Tord Jonson;Åsa Petersén;Bodil Strömbeck

  • Chromosomal breakage-fusion-bridge events cause genetic intratumor heterogeneity

    David Gisselsson;Louise Pettersson;Mattias Höglund;Markus Heidenblad

  • TERT PROMOTER MUTATIONS OCCUR FREQUENTLY IN GLIOMAS AND A SUBSET OF TUMORS DERIVED FROM CELLS WITH LOW RATES OF SELF-RENEWAL

    Hai Yan;P.J. Killela;Z.J. Reitman;Y. Jiao

  • Correlation between clinicopathological features and karyotype in lipomatous tumors. A report of 178 cases from the Chromosomes and Morphology (CHAMP) Collaborative Study Group.

    C. D. M. Fletcher;M. Akerman;P. Dal Cin;I. De Wever

  • Rearrangement of the transcription factor gene CHOP in myxoid liposarcomas with t(12;16)(q13;p11).

    Pierre Åman;David Ron;Nils Mandahl;Thoas Fioretos

  • Three major cytogenetic subgroups can be identified among chromosomally abnormal solitary lipomas.

    Nils Mandahl;Sverre Heim;Kristina Arheden;Anders Rydholm

  • Fusion of the EWS and CHOP genes in myxoid liposarcoma.

    Ioannis Panagopoulos;M Höglund;Fredrik Mertens;Nils Mandahl

  • Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor

    Arezoo Mohajeri;Johnbosco Tayebwa;Anna Collin;Jenny Nilsson

  • Clinicopathologic and molecular genetic characterization of low-grade fibromyxoid sarcoma, and cloning of a novel FUS/CREB3L1 fusion gene.

    Fredrik Mertens;Christopher D M Fletcher;Cristina R Antonescu;Jean-Michel Coindre

  • Chromosome analysis of 97 primary breast carcinomas: identification of eight karyotypic subgroups.

    Nikos Pandis;Nikos Pandis;Yuesheng Jin;Yuesheng Jin;Ludmila Gorunova;Catarina Petersson

  • LPP, the preferred fusion partner gene of HMGIC in lipomas, is a novel member of the LIM protein gene family.

    Marleen M.R. Petit;Raf Mols;Eric F.P.M. Schoenmakers;Nils Mandahl

  • The chimeric FUS/CREB3l2 gene is specific for low‐grade fibromyxoid sarcoma

    Ioannis Panagopoulos;Clelia Tiziana Storlazzi;Clelia Tiziana Storlazzi;Christopher D.M. Fletcher;Jonathan A. Fletcher

  • Combined morphologic and karyotypic study of 59 atypical lipomatous tumors. Evaluation of their relationship and differential diagnosis with other adipose tissue tumors (a report of the CHAMP Study Group).

    J. Rosai;M. Akerman;P. Dal Cin;I. Dewever

  • Abnormal nuclear shape in solid tumors reflects mitotic instability

    David Gisselsson;Jonas Björk;Mattias Höglund;Fredrik Mertens

  • Various regions within the alpha-helical domain of the COL1A1 gene are fused to the second exon of the PDGFB gene in dermatofibrosarcomas and giant-cell fibroblastomas

    Kevin P. O'Brien;Eyal Seroussi;Paola Dal Cin;Raf Sciot

  • Recurrent t(16;17)(q22;p13) in aneurysmal bone cysts.

    Giorgos Panoutsakopoulos;Nikos Pandis;Ioannis Kyriazoglou;Pelle Gustafson

Frequent Co-Authors

Felix Mitelman
Felix Mitelman Lund University
Fredrik Mertens
Fredrik Mertens Lund University
Sverre Heim
Sverre Heim Oslo University Hospital
Anders Rydholm
Anders Rydholm Lund University
Ioannis Panagopoulos
Ioannis Panagopoulos Oslo University Hospital
Bertil Johansson
Bertil Johansson Lund University
Mattias Höglund
Mattias Höglund Lund University
David Gisselsson
David Gisselsson Lund University
Paola Dal Cin
Paola Dal Cin Harvard Medical School
Christopher D.M. Fletcher
Christopher D.M. Fletcher Brigham and Women's Hospital

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