World's Best Scientists 2026 revealed!

D-Index & Metrics

Genetics

D-Index
90
Citations
28219
World Ranking
1074
National Ranking
11

Medicine

D-Index
93
Citations
30015
World Ranking
10937
National Ranking
206

Catharina Larsson 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 Catharina Larsson 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: 399 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.

Catharina Larsson 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 Catharina Larsson 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: 90 D-Index — 76th percentile

76% of scientists in this discipline score the same or lower.

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

Overview

Catharina Larsson is affiliated with Karolinska University Hospital in Sweden. Their research primarily spans medicine and biochemistry, genetics, and molecular biology, with a substantial focus on endocrinology, diabetes, metabolism, molecular biology, surgery, cancer research, and oncology.

Their work addresses a variety of specific scientific topics including:

  • Cancer, Hypoxia, and Metabolism
  • Adrenal and Paraganglionic Tumors
  • Thyroid Cancer Diagnosis and Treatment
  • Neuroblastoma Research and Treatments
  • Hormonal Regulation and Hypertension
  • Pituitary Gland Disorders and Treatments
  • Genetic factors in colorectal cancer

Catharina Larsson has contributed publications to several frequently appearing venues such as:

  • Endocrine Related Cancer
  • Endocrine Pathology
  • International Journal of Molecular Sciences
  • Cancers
  • Nature Metabolism

Among the recent published papers associated with Larsson's research are:

  • Single-nuclei transcriptomes from human adrenal gland reveal distinct cellular identities of low and high-risk neuroblastoma tumors (2021, Nature Communications)
  • Maternal and fetal outcomes in phaeochromocytoma and pregnancy: a multicentre retrospective cohort study and systematic review of literature (2020, The Lancet Diabetes & Endocrinology)
  • GABPA-dependent down-regulation of DICER1 in follicular thyroid tumours (2020, Endocrine Related Cancer)
  • Downregulation and Hypermethylation of GABPB1 Is Associated with Aggressive Thyroid Cancer Features (2022, Cancers)
  • PLEKHS1 Over-Expression is Associated with Metastases and Poor Outcomes in Papillary Thyroid Carcinoma (2020, Cancers)

The scientist has collaborated frequently with several co-authors, including:

  • C. Christofer Juhlin
  • Jan Zedenius
  • Adam Stenman
  • Weng-Onn Lui
  • L. Samuel Hellgren

Best Publications

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

    Catharina Larsson;Britt Skogseid;Kjell Öberg;Yusuke Nakamura

  • Human mitochondrial DNA deletions associated with mutations in the gene encoding Twinkle, a phage T7 gene 4-like protein localized in mitochondria.

    Johannes N. Spelbrink;Fang Yuan Li;Valeria Tiranti;Kaisu Nikali

  • Identification of the Multiple Endocrine Neoplasia Type 1 (MEN1) Gene. The European Consortium on MEN1

    Irma Lemmens;Wim J. M. Van de Ven;Koen Kas;Chang X. Zhang

  • HRPT2, encoding parafibromin, is mutated in hyperparathyroidism–jaw tumor syndrome

    J.D. Carpten;C.M. Robbins;A. Villablanca;L. Forsberg

  • Somatic and Germ-Line Mutations of the HRPT2 Gene in Sporadic Parathyroid Carcinoma

    Trisha M. Shattuck;Stiina Välimäki;Takao Obara;Randall D. Gaz

  • BRCA2 mutations in primary breast and ovarian cancers

    Johnathan M. Lancaster;Richard Wooster;Jonathon Mangion;Catherine M. Phelan;Catherine M. Phelan;Catherine M. Phelan

  • Loss-of-heterozygosity analysis of small-cell lung carcinomas using single-nucleotide polymorphism arrays.

    Kerstin Lindblad-Toh;David M. Tanenbaum;Mark J. Daly;Ellen Winchester

  • 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

  • Mechanisms underlying the activation of TERT transcription and telomerase activity in human cancer: old actors and new players

    Xiaotian Yuan;Xiaotian Yuan;Catharina Larsson;Dawei Xu

  • Somatic deletions and mutations in the Cowden disease gene, PTEN, in sporadic thyroid tumors

    Patricia L M Dahia;Debbie J. Marsh;Zimu Zheng;Jan Zedenius

  • Characterization of the mutational landscape of anaplastic thyroid cancer via whole exome sequencing

    John W. Kunstman;C. Christofer Juhlin;Gerald Goh;Taylor C. Brown

  • LUMA (LUminometric Methylation Assay)--a high throughput method to the analysis of genomic DNA methylation.

    Mohsen Karimi;Sofia Johansson;Dirk Stach;Martin Corcoran

  • Mutation analysis of the BRCA2 gene in 49 site–specific breast cancer families

    C M Phelan;J M Lancaster;P Tonin;C Gumbs

  • MicroRNA Expression Profiles Associated with Mutational Status and Survival in Malignant Melanoma

    Stefano Caramuta;Suzanne Egyházi;Monica Rodolfo;Daniela Witten

  • Ovarian cancer risk in BRCA1 carriers is modified by the HRAS1 variable number of tandem repeat (VNTR) locus

    Catherine M. Phelan;Catherine M. Phelan;Timothy R. Rebbeck;Barbara L. Weber;Peter Devilee

  • The age- and shorter telomere-dependent TERT promoter mutation in follicular thyroid cell-derived carcinomas.

    T Liu;N Wang;J Cao;A Sofiadis

  • Genetic Aberrations in Adrenocortical Tumors Detected Using Comparative Genomic Hybridization Correlate with Tumor Size and Malignancy

    Magnus Kjellman;Olli-P. Kallioniemi;Ritva Karhu;Anders Höög

  • Involvement of the PAX8/peroxisome proliferator-activated receptor γ rearrangement in follicular thyroid tumors

    Trisha Dwight;Srinivasan R. Thoppe;Theodoros Foukakis;Weng O. Lui

  • Clustered inactivating mutations and benign polymorphisms of the calcium receptor gene in familial benign hypocalciuric hypercalcemia suggest receptor functional domains.

    Hunter Heath;Shannon Odelberg;Charles E. Jackson;Bin Tean Teh

  • Thymic carcinoids in multiple endocrine neoplasia type 1

    Bin Tean Teh;Jan Zedenius;Soili Kytölä;Britt Skogseid

Frequent Co-Authors

Bin Tean Teh
Bin Tean Teh National University of Singapore
Magnus Nordenskjöld
Magnus Nordenskjöld Karolinska Institute
Tomas J. Ekström
Tomas J. Ekström Karolinska Institute
Catherine M. Phelan
Catherine M. Phelan University of South Florida
Bruce G. Robinson
Bruce G. Robinson University of Sydney
Fredrik Piehl
Fredrik Piehl Karolinska Institute
Annika Lindblom
Annika Lindblom Karolinska Institute
Janne Lehtiö
Janne Lehtiö Karolinska Institute
Steven A. Narod
Steven A. Narod University of Toronto
Juha Kere
Juha Kere Karolinska Institute

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