World's Best Scientists 2026 revealed!
Magnus Nordenskjöld

Magnus Nordenskjöld

D-Index & Metrics

Genetics

D-Index
89
Citations
28052
World Ranking
1124
National Ranking
13

Medicine

D-Index
90
Citations
29207
World Ranking
12220
National Ranking
231

Magnus Nordenskjöld 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 Magnus Nordenskjöld 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: 318 publications — 79th percentile

79% of scientists in this discipline score the same or lower.

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

Magnus Nordenskjöld 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 Magnus Nordenskjöld 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: 89 D-Index — 75th percentile

75% of scientists in this discipline score the same or lower.

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

Overview

Magnus Nordenskjöld is affiliated with the Karolinska Institute in Sweden and has produced a substantial body of research in the fields of Medicine and Biochemistry, Genetics and Molecular Biology. Their work concentrates on Genetics, Cancer Research, Molecular Biology, Immunology, and Pathology and Forensic Medicine.

Their recent publications include:

  • Integration of whole genome sequencing into a healthcare setting: high diagnostic rates across multiple clinical entities in 3219 rare disease patients, 2021, Genome Medicine
  • Rare deleterious mutations of HNRNP genes result in shared neurodevelopmental disorders, 2021, Genome Medicine
  • An integrative proteomics method identifies a regulator of translation during stem cell maintenance and differentiation, 2021, Nature Communications
  • Chromatin interactions in differentiating keratinocytes reveal novel atopic dermatitis- and psoriasis-associated genes, 2020, Journal of Allergy and Clinical Immunology
  • Circulating cell-free tumor human papillomavirus DNA is a promising biomarker in cervical cancer, 2022, Gynecologic Oncology

The topics covered in their research include:

  • Cancer Genomics and Diagnostics
  • Genomics and Rare Diseases
  • Genetic factors in colorectal cancer
  • Genomic variations and chromosomal abnormalities
  • Dermatology and Skin Diseases
  • Immunodeficiency and Autoimmune Disorders
  • Cervical Cancer and HPV Research

Magnus Nordenskjöld frequently collaborates with the following co-authors:

  • Emma Tham
  • Jesper Eisfeldt
  • Kristina Lagerstedt-Robinson
  • Ann Nordgren
  • Cecilia Arthur

Their research appears regularly in the following publication venues:

  • Genome Medicine
  • PLoS ONE
  • Cancers
  • Nature Communications
  • Nature Genetics

Best Publications

  • Human estrogen receptor beta-gene structure, chromosomal localization, and expression pattern.

    Eva Enmark;Markku Pelto-Huikko;Markku Pelto-Huikko;Kaj Grandien;Svetlana Lagercrantz

  • The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.

    Charis Eng;Charis Eng;David Clayton;Isabelle Schuffenecker;Gilbert Lenoir

  • Multiple endocrine neoplasia type 1 gene maps to chromosome 11 and is lost in insulinoma

    Catharina Larsson;Britt Skogseid;Kjell Öberg;Yusuke Nakamura

  • Cytogenetic analysis by chromosome painting using dop-pcr amplified flow-sorted chromosomes

    H Telenius;A H Pelmear;A Tunnacliffe;N P Carter

  • Clonal Genomic Alterations in Glioma Malignancy Stages

    James Cd;Carlbom E;Dumanski Jp;Hansen M

  • Birt-Hogg-Dubé syndrome: diagnosis and management

    Fred H Menko;Maurice Am van Steensel;Sophie Giraud;Lennart Friis-Hansen

  • Evidence for the complete inactivation of the NF2 gene in the majority of sporadic meningiomas

    M H Ruttledge;J Sarrazin;S Rangaratnam;C M Phelan

  • Genetic mapping of a second locus predisposing to hereditary non–polyposis colon cancer

    Annika Lindblom;Pia Tannergård;Barbro Werelius;Magnus Nordenskjöld

  • Targeted sequencing identifies 91 neurodevelopmental-disorder risk genes with autism and developmental-disability biases

    Holly A.F. Stessman;Bo Xiong;Bo Xiong;Bradley P. Coe;Tianyun Wang

  • Genetic origin of mutations predisposing to retinoblastoma.

    Webster K. Cavenee;Marc F. Hansen;Magnus Nordenskjold;Eric Kock

  • Localization of the MEN1 gene to a small region within chromosome 11q13 by deletion mapping in tumors

    Camilla Bystrom;Catharina Larsson;Carl Blomberg;Kerstin Sandelin

  • Defective cytotoxic lymphocyte degranulation in syntaxin-11 deficient familial hemophagocytic lymphohistiocytosis 4 (FHL4) patients.

    Yenan T. Bryceson;Yenan T. Bryceson;Eva Rudd;Chengyun Y. Zheng;Josefine Edner

  • Spectrum of perforin gene mutations in familial hemophagocytic lymphohistiocytosis

    Kim Göransdotter Ericson;Bengt Fadeel;Sofie Nilsson-Ardnor;Cilla Söderhäll

  • Clonal culturing of human embryonic stem cells on laminin-521/E-cadherin matrix in defined and xeno-free environment

    Sergey Rodin;Liselotte Antonsson;Colin Niaudet;Oscar E. Simonson

  • Detection of chromosomal imbalances in children with idiopathic mental retardation by array based comparative genomic hybridisation (array-CGH)

    Schoumans J;Ruivenkamp C;Holmberg E;Kyllerman M

  • Prediction of the risk of hereditary retinoblastoma, using DNA polymorphisms within the retinoblastoma gene.

    Janey Wiggs;Magnus Nordenskjöld;David Yandell;Joyce Rapaport

  • Loss of heterozygosity in human ductal breast tumors indicates a recessive mutation on chromosome 13.

    Catharina Lundberg;Lambert Skoog;Webster K. Cavenee;Magnus Nordenskjold

  • Increased frequency of sister chromatid exchanges in cigarette smokers.

    Bo Lambert;Annette Lindblad;Magnus Nordenskjöld;Barbro Werelius

  • Deletion mapping of a locus on human chromosome 22 involved in the oncogenesis of meningioma.

    J P Dumanski;E Carlbom;V P Collins;M Nordenskjöld

  • Microdeletions within 22q11 associated with sporadic and familial DiGeorge syndrome

    Peter J. Scambler;Alisoun H. Carey;Richard K.H. Wyse;Sherry Roach

Frequent Co-Authors

Ann Nordgren
Ann Nordgren Karolinska University Hospital
Jan-Inge Henter
Jan-Inge Henter Karolinska University Hospital
Elisabeth Blennow
Elisabeth Blennow Karolinska Institute
Bengt Fadeel
Bengt Fadeel Karolinska Institute
Yenan T. Bryceson
Yenan T. Bryceson Karolinska Institute
Catharina Larsson
Catharina Larsson Karolinska University Hospital
Jan P. Dumanski
Jan P. Dumanski Uppsala University
Annika Lindblom
Annika Lindblom Karolinska Institute
Bin Tean Teh
Bin Tean Teh National University of Singapore
Jozef Gecz
Jozef Gecz University of Adelaide

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