Genes Chromosomes Cancer

ISSN	1098-2264
ISSN-L	1045-2257
IUID	701d86b6f1a84fbd8215601181bc038b
Modified	2020-11-27T13:14:01.385Z
Created	2017-05-09T09:12:11.225Z

Year 2024

DOI Crossref

Characterization of Pediatric Acute Myeloid Leukemia With t(7;12)(q36;p13)

Östlund A, Waraky A, Staffas A, ..., Abrahamsson J, Palmqvist L

Genes Chromosomes Cancer 63 (11) - [2024-11-00; online 2024-11-07]

NGI Short read [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]

PubMed DOI Crossref

Precision Diagnostics in Myeloid Malignancies: Development and Validation of a National Capture-Based Gene Panel.

Orsmark-Pietras C, Lyander A, Ladenvall C, ..., Fioretos T, SciLifeLab Clinical Genomics Platform and Genomic Medicine Sweden

Genes Chromosomes Cancer 63 (7) e23257 [2024-07-00; online 2024-07-20]

Clinical Genomics Lund [Service] Clinical Genomics Stockholm [Service] Clinical Genomics Uppsala [Technology development]

Year 2023

PubMed DOI Crossref

Increased MYB alternative promoter usage is associated with relapse in acute lymphoblastic leukemia.

Fehr A, Arvidsson G, Nordlund J, ..., Stenman G, Andersson MK

Genes Chromosomes Cancer 62 (10) 597-606 [2023-10-00; online 2023-05-23]

NGI SNP genotyping [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]

PubMed DOI Crossref

Inactivation of RB1, CDKN2A, and TP53 have distinct effects on genomic stability at side-by-side comparison in karyotypically normal cells.

Andersson N, Saba KH, Magnusson L, ..., Nord KH, Gisselsson D

Genes Chromosomes Cancer 62 (2) 93-100 [2023-02-00; online 2022-09-30]

Clinical Genomics Lund [Service]

Year 2022

PubMed DOI Crossref

Amplification of ERBB2 (HER2) in embryonal rhabdomyosarcoma: A potential treatment target in rare cases?

Mitra S, Sydow S, Magnusson L, ..., Gisselsson D, Mertens F

Genes Chromosomes Cancer 61 (1) 5-9 [2022-01-00; online 2021-09-01]

Clinical Genomics Lund [Service]

PubMed DOI Crossref

Transcriptome sequencing of archived lymphoma specimens is feasible and clinically relevant using exome capture technology.

Skaftason A, Qu Y, Abdulla M, ..., Rosenquist R, Mansouri L

Genes Chromosomes Cancer 61 (1) 27-36 [2022-01-00; online 2021-10-23]

Clinical Genomics Uppsala [Service] NGI Short read [Technology development] NGI Uppsala (SNP&SEQ Technology Platform) [Technology development] National Genomics Infrastructure [Technology development]

Year 2021

PubMed DOI Crossref

Genomic and transcriptomic characterization of desmoplastic small round cell tumors.

Sydow S, Versleijen-Jonkers YMH, Hansson M, ..., Flucke UE, Mertens F

Genes Chromosomes Cancer 60 (9) 595-603 [2021-09-00; online 2021-05-17]

Bioinformatics Support for Computational Resources [Service] Clinical Genomics Lund [Service]

PubMed DOI Crossref

Single‐cell sequencing in translational cancer research and challenges to meet clinical diagnostic needs

Pfisterer U, Bräunig J, Brattås P, ..., Karlsson G, Fioretos T

Genes Chromosomes Cancer 60 (7) 504-524 [2021-07-00; online 2021-03-15]

Clinical Genomics Lund [Service]

Year 2020

PubMed DOI Crossref

Deep sequencing of myxoinflammatory fibroblastic sarcoma.

Arbajian E, Hofvander J, Magnusson L, Mertens F

Genes Chromosomes Cancer 59 (5) 309-317 [2020-05-00; online 2020-01-31]

Clinical Genomics Lund [Service]

Year 2019

PubMed DOI Crossref

Genetic analyses supporting colorectal, gastric, and prostate cancer syndromes.

Wallander K, Liu W, von Holst S, ..., Lindblom A, Lagerstedt-Robinson K

Genes Chromosomes Cancer - (-) - [2019-07-23; online 2019-07-23]

Bioinformatics Support for Computational Resources [Service] NGI Stockholm (Genomics Applications) [Service] NGI Stockholm (Genomics Production) [Service] NGI Uppsala (SNP&SEQ Technology Platform) [Service] National Genomics Infrastructure [Service]

Year 2016

PubMed DOI Crossref

The role of germline alterations in the DNA damage response genes BRIP1 and BRCA2 in melanoma susceptibility.

Tuominen R, Engström PG, Helgadottir H, ..., Hansson J, Höiom V

Genes Chromosomes Cancer 55 (7) 601-611 [2016-07-00; online 2016-04-14]

Bioinformatics Long-term Support WABI [Collaborative] Bioinformatics Support, Infrastructure and Training [Collaborative] NGI Stockholm (Genomics Applications) [Service] NGI Stockholm (Genomics Production) [Service] National Genomics Infrastructure [Service]

PubMed DOI Crossref

GREM1 and POLE variants in hereditary colorectal cancer syndromes.

Rohlin A, Eiengård F, Lundstam U, ..., Björk J, Nordling M

Genes Chromosomes Cancer 55 (1) 95-106 [2016-01-00; online 2015-10-23]

Swedish NMR Centre (SNC) [Collaborative]

PubMed DOI Crossref

Genetic heterogeneity in rhabdomyosarcoma revealed by SNP array analysis.

Walther C, Mayrhofer M, Nilsson J, ..., Gisselsson D, Mertens F

Genes Chromosomes Cancer 55 (1) 3-15 [2016-01-00; online 2015-10-20]

Array and Analysis Facility [Collaborative]

Year 2015

PubMed DOI Crossref

Cooperative genetic changes in pediatric B-cell precursor acute lymphoblastic leukemia with deletions or mutations of IKZF1.

Olsson L, Albitar F, Castor A, ..., Paulsson K, Johansson B

Genes Chromosomes Cancer 54 (5) 315-325 [2015-05-00; online 2015-03-03]

NGI Uppsala (SNP&SEQ Technology Platform) National Genomics Infrastructure

Year 2013

PubMed DOI Crossref

Comprehensive genetic analysis identifies a pathognomonic NAB2/STAT6 fusion gene, nonrandom secondary genomic imbalances, and a characteristic gene expression profile in solitary fibrous tumor.

Mohajeri A, Tayebwa J, Collin A, ..., Nord KH, Mertens F

Genes Chromosomes Cancer 52 (10) 873-886 [2013-10-00; online 2013-06-14]

NGI Stockholm (Genomics Applications) NGI Stockholm (Genomics Production) National Genomics Infrastructure

PubMed DOI Crossref

Hereditary uveal melanoma: a report of a germline mutation in BAP1.

Höiom V, Edsgärd D, Helgadottir H, ..., Emanuelsson O, Hansson J

Genes Chromosomes Cancer 52 (4) 378-384 [2013-04-00; online 2013-01-23]

NGI Stockholm (Genomics Applications) NGI Stockholm (Genomics Production) National Genomics Infrastructure

Year 2011

PubMed DOI Crossref

Common pathogenetic mechanism involving human chromosome 18 in familial and sporadic ileal carcinoid tumors.

Cunningham JL, Díaz de Ståhl T, Sjöblom T, ..., Dumanski JP, Janson ET

Genes Chromosomes Cancer 50 (2) 82-94 [2011-02-00; online 2010-11-26]

NGI Uppsala (SNP&SEQ Technology Platform) National Genomics Infrastructure

PubMed DOI Crossref

High-resolution genomic screening in mantle cell lymphoma--specific changes correlate with genomic complexity, the proliferation signature and survival.

Halldórsdóttir AM, Sander B, Göransson H, ..., Rosenquist R, Ehrencrona H

Genes Chromosomes Cancer 50 (2) 113-121 [2011-02-00; online 2010-12-01]

Array and Analysis Facility NGI Stockholm (Genomics Applications) NGI Stockholm (Genomics Production) National Genomics Infrastructure