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Magnus Nordenskjöld

Magnus Nordenskjöld

D-Index & Metrics

Discipline name D-Index World Ranking Current World Ranking National Ranking Current National Ranking Publications Citations
Medicine 90 12219 11496 231 223 349 29207
Genetics 89 1124 1064 13 13 318 28052

Magnus Nordenskjöld publications per year

The chart shows the history of publications by Magnus Nordenskjöld between 1977 and 2026, highlighting the no. of papers published in each year and offering an overview of the publication velocity of this scholar. Magnus Nordenskjöld published across 50 years, from 1977 to 2026, averaging 7.8 papers a year. Output peaked at 36 publications in 2024. 4 of the 391 publications appeared in the last two years.

No. of publications
10 20 30
Bar chart. Horizontal axis: year, 1977 to 2026. Vertical axis: number of publications, 0 to 36. Peak 36 publications in 2024. 1977: 1 publication 1978: 1 publication 1979: 1 publication 1980: 0 publications 1981: 1 publication 1982: 2 publications 1983: 5 publications 1984: 6 publications 1985: 2 publications 1986: 2 publications 1987: 4 publications 1988: 3 publications 1989: 1 publication 1990: 7 publications 1991: 8 publications 1992: 5 publications 1993: 14 publications 1994: 20 publications 1995: 11 publications 1996: 11 publications 1997: 7 publications 1998: 7 publications 1999: 9 publications 2000: 8 publications 2001: 11 publications 2002: 12 publications 2003: 8 publications 2004: 7 publications 2005: 11 publications 2006: 9 publications 2007: 14 publications 2008: 11 publications 2009: 15 publications 2010: 10 publications 2011: 13 publications 2012: 8 publications 2013: 8 publications 2014: 11 publications 2015: 11 publications 2016: 9 publications 2017: 7 publications 2018: 7 publications 2019: 12 publications 2020: 6 publications 2021: 6 publications 2022: 4 publications 2023: 5 publications 2024: 36 publications 2025: 3 publications 2026: 1 publication
1977 2026

391 publications in total across all disciplines

View publications per year as a table
Magnus Nordenskjöld: publications per year, 1977 to 2026
Year Publications
1977 1
1978 1
1979 1
1980 0
1981 1
1982 2
1983 5
1984 6
1985 2
1986 2
1987 4
1988 3
1989 1
1990 7
1991 8
1992 5
1993 14
1994 20
1995 11
1996 11
1997 7
1998 7
1999 9
2000 8
2001 11
2002 12
2003 8
2004 7
2005 11
2006 9
2007 14
2008 11
2009 15
2010 10
2011 13
2012 8
2013 8
2014 11
2015 11
2016 9
2017 7
2018 7
2019 12
2020 6
2021 6
2022 4
2023 5
2024 36
2025 3
2026 1
Total 391
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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.

No. of scientists
50 100 150 200
Bar chart with 67 bars. Horizontal axis: publications, 45–54 to 703+. Vertical axis: number of scientists, 0 to 217. Most scientists, 217, have 125–134 publications. The last bar groups every scientist with 703 publications or more. The highlighted bar, 315–324 publications, is where this scientist sits. 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
45–54 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.

View publications distribution as a table
Number of Genetics scientists by publication count, Research.com 2026 ranking edition. Based on 4,342 ranked scientists.
Publications Scientists This scientist
45–54 6
55–64 10
65–74 35
75–84 84
85–94 102
95–104 151
105–114 175
115–124 203
125–134 217
135–144 205
145–154 193
155–164 188
165–174 170
175–184 178
185–194 164
195–204 173
205–214 159
215–224 134
225–234 143
235–244 105
245–254 114
255–264 92
265–274 88
275–284 87
285–294 80
295–304 62
305–314 75
315–324 67 318
325–334 60
335–344 52
345–354 40
355–364 48
365–374 47
375–384 46
385–394 31
395–404 27
405–414 40
415–424 30
425–434 43
435–444 29
445–454 14
455–464 28
465–474 21
475–484 21
485–494 22
495–504 17
505–514 12
515–524 11
525–534 8
535–544 8
545–554 14
555–564 4
565–574 11
575–584 5
585–594 11
595–604 12
605–614 7
615–624 6
625–634 10
635–644 9
645–654 10
655–664 6
665–674 6
675–684 6
685–694 4
695–702 6
703+ 100
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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.

No. of scientists
50 100 150
Bar chart with 61 bars. Horizontal axis: D-Index, 40–41 to 160+. Vertical axis: number of scientists, 0 to 191. Most scientists, 191, have 62–63 D-Index. The last bar groups every scientist with 160 D-Index or more. The highlighted bar, 88–89 D-Index, is where this scientist sits. 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
40–41 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.

View D-Index distribution as a table
Number of Genetics scientists by D-index, Research.com 2026 ranking edition. Based on 4,342 ranked scientists.
D-Index Scientists This scientist
40–41 24
42–43 52
44–45 84
46–47 112
48–49 118
50–51 141
52–53 143
54–55 145
56–57 179
58–59 162
60–61 175
62–63 191
64–65 172
66–67 184
68–69 164
70–71 158
72–73 150
74–75 136
76–77 127
78–79 127
80–81 111
82–83 110
84–85 110
86–87 84
88–89 102 89
90–91 66
92–93 72
94–95 70
96–97 54
98–99 60
100–101 49
102–103 55
104–105 45
106–107 42
108–109 28
110–111 39
112–113 25
114–115 31
116–117 29
118–119 34
120–121 29
122–123 29
124–125 18
126–127 27
128–129 22
130–131 16
132–133 11
134–135 17
136–137 12
138–139 21
140–141 4
142–143 9
144–145 14
146–147 6
148–149 10
150–151 7
152–153 9
154–155 8
156–157 8
158–159 9
160+ 96
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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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