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1.
The current status of cell-free human papillomavirus DNA as a biomarker in cervical cancer and other HPV-associated tumors: A review.
Int J Cancer
; 152(11): 2232-2242, 2023 06 01.
Article
in English
| MEDLINE | ID: mdl-36274628
2.
Whole-body MRI surveillance in TP53 carriers is perceived as beneficial with no increase in cancer worry regardless of previous cancer: Data from the Swedish TP53 Study.
Cancer
; 129(6): 946-955, 2023 03 15.
Article
in English
| MEDLINE | ID: mdl-36601958
3.
Extended genetic analysis and tumor characteristics in over 4600 women with suspected hereditary breast and ovarian cancer.
BMC Cancer
; 23(1): 738, 2023 Aug 10.
Article
in English
| MEDLINE | ID: mdl-37563628
4.
Patient-specific targeted analysis of circulating tumour DNA in plasma is feasible and may be a potential biomarker in UTUC.
World J Urol
; 41(12): 3421-3427, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37721600
5.
Consultation on UTUC II Stockholm 2022: diagnostic and prognostic methods-what's around the corner?
World J Urol
; 41(12): 3405-3411, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37725130
6.
Prevalence of human papillomavirus (HPV) types 16 and 18 in cervical cancer in Stockholm, Sweden during 2019-2023 compared to 2003-2008.
Acta Oncol
; 62(12): 1649-1652, 2023 Dec.
Article
in English
| MEDLINE | ID: mdl-37793801
7.
Genome sequencing is a sensitive first-line test to diagnose individuals with intellectual disability.
Genet Med
; 24(11): 2296-2307, 2022 11.
Article
in English
| MEDLINE | ID: mdl-36066546
8.
Circulating cell-free tumor human papillomavirus DNA is a promising biomarker in cervical cancer.
Gynecol Oncol
; 167(1): 107-114, 2022 10.
Article
in English
| MEDLINE | ID: mdl-35918201
9.
Genomic profile - a possible diagnostic and prognostic marker in upper tract urothelial carcinoma.
BJU Int
; 130(1): 92-101, 2022 07.
Article
in English
| MEDLINE | ID: mdl-34375486
10.
TUBB3 Arg262His causes a recognizable syndrome including CFEOM3, facial palsy, joint contractures, and early-onset peripheral neuropathy.
Hum Genet
; 140(12): 1709-1731, 2021 Dec.
Article
in English
| MEDLINE | ID: mdl-34652576
11.
A Recurrent De Novo Heterozygous COG4 Substitution Leads to Saul-Wilson Syndrome, Disrupted Vesicular Trafficking, and Altered Proteoglycan Glycosylation.
Am J Hum Genet
; 103(4): 553-567, 2018 10 04.
Article
in English
| MEDLINE | ID: mdl-30290151
12.
Whole-genome sequencing of synchronous thyroid carcinomas identifies aberrant DNA repair in thyroid cancer dedifferentiation.
J Pathol
; 250(2): 183-194, 2020 02.
Article
in English
| MEDLINE | ID: mdl-31621921
13.
Massive parallel sequencing in individuals with multiple primary tumours reveals the benefit of re-analysis.
Hered Cancer Clin Pract
; 19(1): 46, 2021 Oct 28.
Article
in English
| MEDLINE | ID: mdl-34711244
14.
pyCancerSig: subclassifying human cancer with comprehensive single nucleotide, structural and microsatellite mutational signature deconstruction from whole genome sequencing.
BMC Bioinformatics
; 21(1): 128, 2020 Apr 03.
Article
in English
| MEDLINE | ID: mdl-32245405
15.
Defining the clinical phenotype of Saul-Wilson syndrome.
Genet Med
; 22(5): 857-866, 2020 05.
Article
in English
| MEDLINE | ID: mdl-31949312
16.
Public support for healthcare-mediated disclosure of hereditary cancer risk information: Results from a population-based survey in Sweden.
Hered Cancer Clin Pract
; 18: 18, 2020.
Article
in English
| MEDLINE | ID: mdl-32944097
17.
Whole-body MRI within a surveillance program for carriers with clinically actionable germline TP53 variants - the Swedish constitutional TP53 study SWEP53.
Hered Cancer Clin Pract
; 18: 1, 2020.
Article
in English
| MEDLINE | ID: mdl-31956380
18.
Parafibromin immunostainings of parathyroid tumors in clinical routine: a near-decade experience from a tertiary center.
Mod Pathol
; 32(8): 1082-1094, 2019 07.
Article
in English
| MEDLINE | ID: mdl-30923346
19.
Functional characterization of novel germline TP53 variants in Swedish families.
Clin Genet
; 96(3): 216-225, 2019 09.
Article
in English
| MEDLINE | ID: mdl-31081129
20.
Alu-Alu mediated intragenic duplications in IFT81 and MATN3 are associated with skeletal dysplasias.
Hum Mutat
; 39(10): 1456-1467, 2018 10.
Article
in English
| MEDLINE | ID: mdl-30080953