Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation

Search Page

Filters

My Custom Filters

Publication date

Text availability

Article attribute

Article type

Additional filters

Article Language

Species

Sex

Age

Other

Search Results

14 results

Filters applied: . Clear all
Results are displayed in a computed author sort order. The Publication Date timeline is not available.
Page 1
High frequency of pathogenic germline variants within homologous recombination repair in patients with advanced cancer.
Bertelsen B, Tuxen IV, Yde CW, Gabrielaite M, Torp MH, Kinalis S, Oestrup O, Rohrberg K, Spangaard I, Santoni-Rugiu E, Wadt K, Mau-Sorensen M, Lassen U, Nielsen FC. Bertelsen B, et al. Among authors: kinalis s. NPJ Genom Med. 2019 Jun 21;4:13. doi: 10.1038/s41525-019-0087-6. eCollection 2019. NPJ Genom Med. 2019. PMID: 31263571 Free PMC article.
Genomic profiling of newly diagnosed glioblastoma patients and its potential for clinical utility - a prospective, translational study.
Nørøxe DS, Yde CW, Østrup O, Michaelsen SR, Schmidt AY, Kinalis S, Torp MH, Skjøth-Rasmussen J, Brennum J, Hamerlik P, Poulsen HS, Nielsen FC, Lassen U. Nørøxe DS, et al. Among authors: kinalis s. Mol Oncol. 2020 Nov;14(11):2727-2743. doi: 10.1002/1878-0261.12790. Epub 2020 Sep 18. Mol Oncol. 2020. PMID: 32885540 Free PMC article.
A Comparison of Tools for Copy-Number Variation Detection in Germline Whole Exome and Whole Genome Sequencing Data.
Gabrielaite M, Torp MH, Rasmussen MS, Andreu-Sánchez S, Vieira FG, Pedersen CB, Kinalis S, Madsen MB, Kodama M, Demircan GS, Simonyan A, Yde CW, Olsen LR, Marvig RL, Østrup O, Rossing M, Nielsen FC, Winther O, Bagger FO. Gabrielaite M, et al. Among authors: kinalis s. Cancers (Basel). 2021 Dec 14;13(24):6283. doi: 10.3390/cancers13246283. Cancers (Basel). 2021. PMID: 34944901 Free PMC article.
The Number of Signaling Pathways Altered by Driver Mutations in Chronic Lymphocytic Leukemia Impacts Disease Outcome.
Brieghel C, da Cunha-Bang C, Yde CW, Schmidt AY, Kinalis S, Nadeu F, Andersen MA, Jacobsen LO, Andersen MK, Pedersen LB, Delgado J, Baumann T, Mattsson M, Mansouri L, Rosenquist R, Campo E, Nielsen FC, Niemann CU. Brieghel C, et al. Among authors: kinalis s. Clin Cancer Res. 2020 Mar 15;26(6):1507-1515. doi: 10.1158/1078-0432.CCR-18-4158. Epub 2020 Jan 9. Clin Cancer Res. 2020. PMID: 31919133
A catalog of curated breast cancer genes.
Bose M, Benada J, Thatte JV, Kinalis S, Ejlertsen B, Nielsen FC, Sørensen CS, Rossing M. Bose M, et al. Among authors: kinalis s. Breast Cancer Res Treat. 2022 Jan;191(2):431-441. doi: 10.1007/s10549-021-06441-y. Epub 2021 Nov 10. Breast Cancer Res Treat. 2022. PMID: 34755241 Free PMC article.
Application of whole-exome sequencing to direct the specific functional testing and diagnosis of rare inherited bleeding disorders in patients from the Öresund Region, Scandinavia.
Leinøe E, Zetterberg E, Kinalis S, Østrup O, Kampmann P, Norström E, Andersson N, Klintman J, Qvortrup K, Nielsen FC, Rossing M. Leinøe E, et al. Among authors: kinalis s. Br J Haematol. 2017 Oct;179(2):308-322. doi: 10.1111/bjh.14863. Epub 2017 Jul 27. Br J Haematol. 2017. PMID: 28748566 Free PMC article. Clinical Trial.
14 results