Zobrazeno 1 - 7
of 7
pro vyhledávání: '"Aleksandra Köhler"'
Autor:
Chiara Campo, Aleksandra Köhler, Gisella Figlioli, Rossella Elisei, Cristina Romei, Monica Cipollini, Franco Bambi, Kari Hemminki, Federica Gemignani, Stefano Landi, Asta Försti
Publikováno v:
PLoS ONE, Vol 13, Iss 8, p e0202208 (2018)
[This corrects the article DOI: 10.1371/journal.pone.0174995.].
Externí odkaz:
https://doaj.org/article/644414e2de4245bebb82010748856d8d
Autor:
Chiara Campo, Aleksandra Köhler, Gisella Figlioli, Rossella Elisei, Cristina Romei, Monica Cipollini, Franco Bambi, Kari Hemminki, Federica Gemignani, Stefano Landi, Asta Försti
Publikováno v:
PLoS ONE, Vol 12, Iss 4, p e0174995 (2017)
BACKGROUND:Tumour suppressor genes when mutated in the germline cause various cancers, but they can also be somatically mutated in sporadic tumours. We hypothesized that there may also be cancer-related germline variants in the genes commonly mutated
Externí odkaz:
https://doaj.org/article/5c2acb27505f4b7693b787ae8ad48ff7
Autor:
Stefano Landi, Asta Försti, Federica Gemignani, Kari Hemminki, Alfonso Cristaudo, Aleksandra Köhler, Bowang Chen, Franco Bambi, Monica Cipollini, Ombretta Melaiu, Cristina Romei, Rossella Elisei, Gisella Figlioli
Table S1. Comparison between results from literature and results from the present GWAS for all the SNPs extracted from literature. Table S2. Data published in literature where only one genetic model (either dominant or recessive) was reported in the
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::04e7049897df9292350a566105932ac7
https://doi.org/10.1158/1055-9965.22437037
https://doi.org/10.1158/1055-9965.22437037
Autor:
Stefano Landi, Asta Försti, Federica Gemignani, Kari Hemminki, Alfonso Cristaudo, Aleksandra Köhler, Bowang Chen, Franco Bambi, Monica Cipollini, Ombretta Melaiu, Cristina Romei, Rossella Elisei, Gisella Figlioli
Background: Linkage analyses and association studies suggested that inherited genetic variations play a role in the development of differentiated thyroid carcinoma (DTC).Methods: We combined the results from a genome-wide association study (GWAS) per
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::7ad7ee144117656cc93c3a1a13446120
https://doi.org/10.1158/1055-9965.c.6515689
https://doi.org/10.1158/1055-9965.c.6515689
Autor:
Aleksandra Köhler, Gisella Figlioli, Rossella Elisei, Cristina Romei, Franco Bambi, Monica Cipollini, Chiara Campo, Stefano Landi, Kari Hemminki, Federica Gemignani, Asta Försti
Publikováno v:
PLoS ONE
PLoS ONE, Vol 12, Iss 4, p e0174995 (2017)
PLoS ONE, Vol 12, Iss 4, p e0174995 (2017)
Background Tumour suppressor genes when mutated in the germline cause various cancers, but they can also be somatically mutated in sporadic tumours. We hypothesized that there may also be cancer-related germline variants in the genes commonly mutated
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::c39dfa7cd558cb4ca79e4b985249d0d3
http://europepmc.org/articles/PMC5391920
http://europepmc.org/articles/PMC5391920
Autor:
Ricard Marcos, Michał Kalemba, Aleksandra Köhler, Stefan Herms, Rossella Elisei, Franco Bambi, Monica Cipollini, Susana Pastor, Cristina Romei, Gisella Figlioli, Barbara Jarząb, Kari Hemminki, Dorota Kula, Elisa Paolicchi, Alfonso Cristaudo, Stefano Landi, Antonia Velázquez, Per Hoffmann, Asta Försti, Federica Gemignani, Bowang Chen
Publikováno v:
The Journal of Clinical Endocrinology & Metabolism. 99:E2084-E2092
Genome-wide association studies (GWASs) on differentiated thyroid cancer (DTC) have identified robust associations with single nucleotide polymorphisms (SNPs) at 9q22.33 (FOXE1), 14q13.3 (NKX2-1), and 2q35 (DIRC3). Our recently published GWAS suggest
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4dc1e2c1b78c81a119aa947af4dbf2aa
https://doi.org/10.1210/jc.2014-1734
https://doi.org/10.1210/jc.2014-1734
Autor:
Cristina Romei, Stefan Herms, Alfonso Cristaudo, Susana Pastor, Federica Gemignani, Dorota Kula, Monica Cipollini, Antonia Velázquez, Kari Hemminki, Gisella Figlioli, Richard S. Houlston, Per Hoffmann, Stefano Landi, Barbara Jarzab, Peter Broderick, Rossella Elisei, Franco Bambi, Asta Försti, Bowang Chen, Shelley Harris, Aleksandra Köhler, Ricard Marcos, Michał Kalemba
Context: Genome-wide association studies (GWASs) of differentiated thyroid cancer (DTC) have identified associations with polymorphisms at 2q35 (DIRC3), 8p12 (NRG1), 9q22.33 (FOXE1), and 14q13.2 (NKX2-1). However, most of the inherited genetic risk f
Externí odkaz:
https://explore.openaire.eu/search/publication?articleId=doi_dedup___::851f2e7e91dfa04d316edf9a84c6573d
http://hdl.handle.net/11568/685064
http://hdl.handle.net/11568/685064