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Umeå University
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Kristina Cederquist

Contact

E-mail
kristina.cederquist@umu.se
Phone

Works at

Affiliation
Affiliated as other position at Department of Medical Biosciences Section: Pathology
Location
By 6M, Sjukhusområdet Umeå universitet, 901 85 Umeå
A geographically matched control population efficiently limits the number of candidate disease-causing variants in an unbiased whole-genome analysis
PLOS ONE, Public Library of Science 2019, Vol. 14, (3)
Rentoft, Matilda; Svensson, Daniel; Sjödin, Andreas; et al.
Genetic screening in sudden cardiac death in the young can save future lives
International journal of legal medicine, Vol. 130, (1) : 59-66
Stattin, Eva-Lena; Westin, Ida Maria; Cederquist, Kristina; et al.
Germline rearrangements in families with strong family history of glioma and malignant melanoma, colon, and breast cancer
Neuro-Oncology, Oxford University Press 2014, Vol. 16, (10) : 1333-1340
Andersson, Ulrika; Wibom, Carl; Cederquist, Kristina; et al.
Frequency of the transthyretin Val30Met mutation in the northern Swedish population
Amyloid: Journal of Protein Folding Disorders, Vol. 21, (1) : 18-20
Olsson, Malin; Jonasson, Jenni; Cederquist, Kristina; et al.
Founder mutations characterise the mutation panorama in 200 Swedish index cases referred for Long QT syndrome genetic testing
BMC Cardiovascular Disorders, BioMed Central 2012, Vol. 12 : 95-
Stattin, Eva-Lena; Boström, Ida Maria; Winbo, Annika; et al.
A possible role for miRNA silencing in disease phenotype variation in Swedish transthyretin V30M carriers
BMC Medical Genetics, Vol. 11 : 130-
Olsson, Malin; Norgren, Nina; Obayashi, Konen; et al.
Retained immunohistochemical staining in a large Swedish HNPCC family with a pathogenic MLH1 missense mutation
Cederquist, Kristina; Palmqvist, Richard; Emanuelsson, Monica; et al.
View publications in DiVA