Zobrazeno 1 - 10
of 41
pro vyhledávání: '"Anna M. Dahlin"'
Autor:
Adam Rosenbaum, Anna M. Dahlin, Ulrika Andersson, Benny Björkblom, Wendy Yi-Ying Wu, Håkan Hedman, Carl Wibom, Beatrice Melin
Publikováno v:
Scientific Reports, Vol 13, Iss 1, Pp 1-9 (2023)
Abstract Genome-wide association studies (GWAS) have contributed to our understanding of glioma susceptibility. To date, 25 risk loci for development of any of the glioma subtypes are known. However, GWAS studies reveal little about the molecular pro
Externí odkaz:
https://doaj.org/article/fd0f3a703d9e4e7c89cbe908bd914f26
Autor:
Wendy Yi‐Ying Wu, Florentin Späth, Carl Wibom, Benny Björkblom, Anna M. Dahlin, Beatrice Melin
Publikováno v:
Cancer Medicine, Vol 11, Iss 4, Pp 1016-1025 (2022)
Abstract No strong aetiological factors have been established for glioma aside from genetic mutations and variants, ionising radiation and an inverse relationship with asthmas and allergies. Our aim was to investigate the association between pre‐di
Externí odkaz:
https://doaj.org/article/96b7b1bce85a4b789d8e6dbb8f515c86
Autor:
Daniel Svensson, Matilda Rentoft, Anna M. Dahlin, Emma Lundholm, Pall I. Olason, Andreas Sjödin, Carin Nylander, Beatrice S. Melin, Johan Trygg, Erik Johansson, Ludmila Prokunina-Olsson
Publikováno v:
PLoS ONE, Vol 15, Iss 9 (2020)
The number of national reference populations that are whole-genome sequenced are rapidly increasing. Partly driving this development is the fact that genetic disease studies benefit from knowing the genetic variation typical for the geographical area
Externí odkaz:
https://doaj.org/article/6257811d142944b5a93dbe0a8ce0be79
Autor:
Bethany R. Van Guelpen, Åke Öberg, Jörgen Rutegård, Vincy Eklöf, Maria Jacobsson, Maria L. Henriksson, Richard Palmqvist, Anna M. Dahlin
Purpose: The aim of this study was to relate the CpG island methylator phenotype (CIMP; characterized by extensive promoter hypermethylation) to cancer-specific survival in colorectal cancer, taking into consideration relevant clinicopathologic facto
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0223d333af0cb1fdae1335e1c3d5a905
https://doi.org/10.1158/1078-0432.c.6519197.v1
https://doi.org/10.1158/1078-0432.c.6519197.v1
Autor:
Bethany R. Van Guelpen, Åke Öberg, Jörgen Rutegård, Vincy Eklöf, Maria Jacobsson, Maria L. Henriksson, Richard Palmqvist, Anna M. Dahlin
Supplementary Data from The Role of the CpG Island Methylator Phenotype in Colorectal Cancer Prognosis Depends on Microsatellite Instability Screening Status
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::0d26b3617d82fef311c51589d1c994a1
https://doi.org/10.1158/1078-0432.22442480.v1
https://doi.org/10.1158/1078-0432.22442480.v1
Autor:
Beatrice Melin, Ulrika Andersson, Tom Børge Johannesen, Preetha Rajaraman, Eivind Hovig, Hilde Langseth, Anna M. Dahlin, Florentin Späth, Carl Wibom
Supplementary Tables 1-7 Supplementary Table 1. PCR primers and conditions Supplementary Table 2. List of included diagnoses in each histological subgroup Supplementary Table 3. Associations between published genetic risk variants and risk of disease
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7599ed08db3c1e370c210c8789413fdb
https://doi.org/10.1158/1055-9965.22436310
https://doi.org/10.1158/1055-9965.22436310
Autor:
Beatrice Melin, Ulrika Andersson, Tom Børge Johannesen, Preetha Rajaraman, Eivind Hovig, Hilde Langseth, Anna M. Dahlin, Florentin Späth, Carl Wibom
Background: Although glioma etiology is poorly understood in general, growing evidence indicates a genetic component. Four large genome-wide association studies (GWAS) have linked common genetic variants with an increased glioma risk. However, to dat
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::3b7d0b848dbcb1728b5d74c99fec45d9
https://doi.org/10.1158/1055-9965.c.6515328
https://doi.org/10.1158/1055-9965.c.6515328
Autor:
Jon Foss-Skiftesvik, Shaobo Li, Adam Rosenbaum, Christian Munch Hagen, Ulrik Kristoffer Stoltze, Sally Ljungqvist, Ulf Hjalmars, Kjeld Schmiegelow, Libby Morimoto, Adam J de Smith, René Mathiasen, Catherine Metayer, David Hougaard, Beatrice Melin, Kyle M Walsh, Jonas Bybjerg-Grauholm, Anna M Dahlin, Joseph L Wiemels
Publikováno v:
Neuro-Oncology.
Background Although recent sequencing studies have revealed that 10% of childhood gliomas are caused by rare germline mutations, the role of common variants is undetermined and no genome-wide significant risk loci for pediatric central nervous system
Publikováno v:
Neuro-oncology advances. 4(Suppl 2)
Background Understanding the trajectory and development of disease is important and the knowledge can be used to find novel targets for therapy and new diagnostic tools for early diagnosis. Methods Large cohorts from different parts of the world are
Autor:
Ingvar Syk, Beatrice Melin, Barbro Numan Hellquist, Gustav Silander, Anna M. Dahlin, Olle Sjöström
Publikováno v:
PLoS ONE
PLoS ONE, Vol 15, Iss 8, p e0236799 (2020)
PLoS ONE, Vol 15, Iss 8, p e0236799 (2020)
IntroductionNumerous prior studies, even from countries with free access to care, have associated long travel time to care with poor survival in patients with colorectal cancer.MethodsThis is a data-linkage study of all 3718 patients with colorectal