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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

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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