World's Best Scientists 2026 revealed!
Fredrik Mertens

Fredrik Mertens

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Genetics
Sweden
2026

D-Index & Metrics

Genetics

D-Index
101
Citations
43480
World Ranking
721
National Ranking
10

Medicine

D-Index
104
Citations
48410
World Ranking
6964
National Ranking
143

Fredrik Mertens publication distribution in Genetics in 2026

The chart shows the distribution of publications by all Research.com ranked scientists in the field of Genetics in 2026. The highlighted bar marks where Fredrik Mertens sits on this spectrum.

45–54 publications: 6 scientists 55–64 publications: 10 scientists 65–74 publications: 35 scientists 75–84 publications: 84 scientists 85–94 publications: 102 scientists 95–104 publications: 151 scientists 105–114 publications: 175 scientists 115–124 publications: 203 scientists 125–134 publications: 217 scientists 135–144 publications: 205 scientists 145–154 publications: 193 scientists 155–164 publications: 188 scientists 165–174 publications: 170 scientists 175–184 publications: 178 scientists 185–194 publications: 164 scientists 195–204 publications: 173 scientists 205–214 publications: 159 scientists 215–224 publications: 134 scientists 225–234 publications: 143 scientists 235–244 publications: 105 scientists 245–254 publications: 114 scientists 255–264 publications: 92 scientists 265–274 publications: 88 scientists 275–284 publications: 87 scientists 285–294 publications: 80 scientists 295–304 publications: 62 scientists 305–314 publications: 75 scientists 315–324 publications: 67 scientists 325–334 publications: 60 scientists 335–344 publications: 52 scientists 345–354 publications: 40 scientists 355–364 publications: 48 scientists 365–374 publications: 47 scientists 375–384 publications: 46 scientists 385–394 publications: 31 scientists 395–404 publications: 27 scientists 405–414 publications: 40 scientists 415–424 publications: 30 scientists 425–434 publications: 43 scientists 435–444 publications: 29 scientists 445–454 publications: 14 scientists 455–464 publications: 28 scientists 465–474 publications: 21 scientists 475–484 publications: 21 scientists 485–494 publications: 22 scientists 495–504 publications: 17 scientists 505–514 publications: 12 scientists 515–524 publications: 11 scientists 525–534 publications: 8 scientists 535–544 publications: 8 scientists 545–554 publications: 14 scientists 555–564 publications: 4 scientists 565–574 publications: 11 scientists 575–584 publications: 5 scientists 585–594 publications: 11 scientists 595–604 publications: 12 scientists 605–614 publications: 7 scientists 615–624 publications: 6 scientists 625–634 publications: 10 scientists 635–644 publications: 9 scientists 645–654 publications: 10 scientists 655–664 publications: 6 scientists 665–674 publications: 6 scientists 675–684 publications: 6 scientists 685–694 publications: 4 scientists 695–702 publications: 6 scientists 703+ publications: 100 scientists
45 publications 703+

This scientist: 409 publications — 88th percentile

88% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 703 publications or more.

Fredrik Mertens D-index placement in Genetics in 2026

The chart shows the D-index (discipline H-index) distribution of Genetics scientists ranked by Research.com in 2026. The highlighted bar marks where Fredrik Mertens sits on this spectrum.

40–41 D-Index: 24 scientists 42–43 D-Index: 52 scientists 44–45 D-Index: 84 scientists 46–47 D-Index: 112 scientists 48–49 D-Index: 118 scientists 50–51 D-Index: 141 scientists 52–53 D-Index: 143 scientists 54–55 D-Index: 145 scientists 56–57 D-Index: 179 scientists 58–59 D-Index: 162 scientists 60–61 D-Index: 175 scientists 62–63 D-Index: 191 scientists 64–65 D-Index: 172 scientists 66–67 D-Index: 184 scientists 68–69 D-Index: 164 scientists 70–71 D-Index: 158 scientists 72–73 D-Index: 150 scientists 74–75 D-Index: 136 scientists 76–77 D-Index: 127 scientists 78–79 D-Index: 127 scientists 80–81 D-Index: 111 scientists 82–83 D-Index: 110 scientists 84–85 D-Index: 110 scientists 86–87 D-Index: 84 scientists 88–89 D-Index: 102 scientists 90–91 D-Index: 66 scientists 92–93 D-Index: 72 scientists 94–95 D-Index: 70 scientists 96–97 D-Index: 54 scientists 98–99 D-Index: 60 scientists 100–101 D-Index: 49 scientists 102–103 D-Index: 55 scientists 104–105 D-Index: 45 scientists 106–107 D-Index: 42 scientists 108–109 D-Index: 28 scientists 110–111 D-Index: 39 scientists 112–113 D-Index: 25 scientists 114–115 D-Index: 31 scientists 116–117 D-Index: 29 scientists 118–119 D-Index: 34 scientists 120–121 D-Index: 29 scientists 122–123 D-Index: 29 scientists 124–125 D-Index: 18 scientists 126–127 D-Index: 27 scientists 128–129 D-Index: 22 scientists 130–131 D-Index: 16 scientists 132–133 D-Index: 11 scientists 134–135 D-Index: 17 scientists 136–137 D-Index: 12 scientists 138–139 D-Index: 21 scientists 140–141 D-Index: 4 scientists 142–143 D-Index: 9 scientists 144–145 D-Index: 14 scientists 146–147 D-Index: 6 scientists 148–149 D-Index: 10 scientists 150–151 D-Index: 7 scientists 152–153 D-Index: 9 scientists 154–155 D-Index: 8 scientists 156–157 D-Index: 8 scientists 158–159 D-Index: 9 scientists 160+ D-Index: 96 scientists
40 D-Index 160+

This scientist: 101 D-Index — 84th percentile

84% of scientists in this discipline score the same or lower.

The last bar groups every scientist with 160 D-Index or more.

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
  • 2023 - Research.com Genetics in Sweden Leader Award

Overview

Fredrik Mertens is affiliated with Lund University in Sweden and conducts research primarily in the fields of Medicine and Biochemistry, Genetics and Molecular Biology. Their work spans several subfields including Pulmonary and Respiratory Medicine, Cancer Research, Oncology, Genetics, and Rheumatology.

Mertens has contributed extensively to topics such as Sarcoma Diagnosis and Treatment, Cancer Genomics and Diagnostics, Histiocytic Disorders and Treatments, Genomic Variations and Chromosomal Abnormalities, Genomics and Rare Diseases, Hippo Pathway Signaling and YAP/TAZ, and Urologic and Reproductive Health Conditions.

Recent publications by Mertens include:

  • "Signatures of copy number alterations in human cancer," 2022, Nature
  • "HUGO Gene Nomenclature Committee (HGNC) recommendations for the designation of gene fusions," 2021, Leukemia
  • "Recurrent Fusions Between YAP1 and KMT2A in Morphologically Distinct Neoplasms Within the Spectrum of Low-grade Fibromyxoid Sarcoma and Sclerosing Epithelioid Fibrosarcoma," 2020, The American Journal of Surgical Pathology
  • "Signatures of copy number alterations in human cancer," 2021, bioRxiv (Cold Spring Harbor Laboratory)
  • "'Inflammatory Leiomyosarcoma' and 'Histiocyte-rich Rhabdomyoblastic Tumor': a clinicopathological, immunohistochemical and genetic study of 13 cases, with a proposal for reclassification as 'Inflammatory Rhabdomyoblastic Tumor'," 2020, Modern Pathology

Mertens frequently publishes in several scientific journals, including:

  • Genes Chromosomes and Cancer
  • The American Journal of Surgical Pathology
  • Modern Pathology
  • bioRxiv (Cold Spring Harbor Laboratory)
  • Nature

The scientist collaborates regularly with a number of co-authors, including:

  • Linda Magnusson
  • Saskia Sydow
  • Paul Piccinelli
  • Florian Puls
  • Nischalan Pillay

Best Publications

  • World Health Organization Classification of Tumours. Pathology and Genetics of Tumours of Soft Tissue and Bone

    Christopher D.M. Fletcher;Krisjnan Unni;Fredrik Mertens

  • WHO Classification of Tumours of Soft Tissue and Bone: WHO Classification of Tumours, vol. 5

    Christopher Fletcher;JA Bridge;Pcw Hogendoorn

  • Pathology and genetics of tumours of soft tissue and bone

    Christopher D. M. Fletcher;K. Krishnan Unni;Fredrik Mertens

  • The impact of translocations and gene fusions on cancer causation

    Felix Mitelman;Bertil Johansson;Fredrik Mertens

  • 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

  • A breakpoint map of recurrent chromosomal rearrangements in human neoplasia.

    Felix Mitelman;Fredrik Mertens;Bertil Johansson

  • Nuclear expression of STAT6 distinguishes solitary fibrous tumor from histologic mimics

    Leona A. Doyle;Marina Vivero;Christopher D. M. Fletcher;Fredrik Mertens

  • The emerging complexity of gene fusions in cancer

    Fredrik Mertens;Bertil Johansson;Thoas Fioretos;Felix Mitelman

  • 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

  • Chromosomal Imbalance Maps of Malignant Solid Tumors: A Cytogenetic Survey of 3185 Neoplasms

    Fredrik Mertens;Bertil Johansson;Mattias Höglund;Felix Mitelman

  • 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

  • Tumor-Infiltrating Macrophages Are Associated with Metastasis Suppression in High-Grade Osteosarcoma: A Rationale for Treatment with Macrophage Activating Agents

    Emilie P. Buddingh;Marieke L. Kuijjer;Ronald A J Duim;Horst Bürger

  • 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

  • Fusion genes and rearranged genes as a linear function of chromosome aberrations in cancer.

    Felix Mitelman;Bertil Johansson;Fredrik Mertens

  • Mitelman database of chromosome aberrations and gene fusions in cancer

    F Mitelman;B Johansson;F Mertens

  • MUC4 is a highly sensitive and specific marker for low-grade fibromyxoid sarcoma.

    Leona A Doyle;Emely Möller;Paola Dal Cin;Christopher D M Fletcher

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

    Ioannis Panagopoulos;M Höglund;Fredrik Mertens;Nils Mandahl

  • Identification of a novel, recurrent HEY1-NCOA2 fusion in mesenchymal chondrosarcoma based on a genome-wide screen of exon-level expression data

    Lu Wang;Toru Motoi;Raya Khanin;Adam Olshen

Frequent Co-Authors

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

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