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Ladenvall C
JSON
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Family name
Ladenvall
Given name
Claes
Initials
C
ORCID
ORCID
0000-0002-7501-6598
Affiliations
Department of Clinical Sciences, Diabetes & Endocrinology, Lund University Diabetes Center, Malmö, Sweden (C.L., L.G.).
6 publications
DOI
Crossref
Single cell sequencing reveals shared clonal signatures in non-malignant B- and tumor cells in T-prolymphocytic leukemia
Hesselager C, Thörn I, Marincevic M, ...,
Baliakas P
,
Amini RM
Blood Neoplasia
-
(-) 100076 [2025-02-00; online 2025-02-00]
Clinical Genomics [Collaborative]
Clinical Genomics Uppsala [Collaborative]
PubMed
DOI
Crossref
Visualization using NIPTviewer support the clinical interpretation of noninvasive prenatal testing results.
Smeds P, Baranowska Körberg I,
Melin M
,
Ladenvall C
BMC Med Genomics
18
(1) 15 [2025-01-20; online 2025-01-20]
Clinical Genomics [Technology development]
Clinical Genomics Uppsala [Technology development]
PubMed
DOI
Crossref
From SARS-CoV-2 to Global Preparedness: A Graphical Interface for Standardised High-Throughput Bioinformatics Analysis in Pandemic Scenarios and Surveillance of Drug Resistance.
Cumlin T,
Karlsson I
,
Haars J
, ...,
Ladenvall C
,
Kaden R
Int J Mol Sci
25
(12) - [2024-06-17; online 2024-06-17]
Clinical Genomics [Technology development]
Clinical Genomics Uppsala [Technology development]
PubMed
DOI
Crossref
Genetic insights into resting heart rate and its role in cardiovascular disease.
van de Vegte YJ
, Eppinga RN, van der Ende MY, ..., Verweij N, van der Harst P
Nat Commun
14
(1) 4646 [2023-08-02; online 2023-08-02]
Clinical Genomics [Collaborative]
Clinical Genomics Gothenburg [Collaborative]
NGI SNP genotyping [Service]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Somatic Exonic Deletions in RUNX1 Constitutes a Novel Recurrent Genomic Abnormality in Acute Myeloid Leukemia.
Eriksson A
,
Engvall M
,
Mathot L
, ...,
Ladenvall C
,
Baliakas P
Clin. Cancer Res.
29
(15) 2826-2834 [2023-08-01; online 2023-04-07]
Bioinformatics Support for Computational Resources [Service]
Clinical Genomics [Collaborative]
Clinical Genomics Uppsala [Collaborative]
NGI Short read [Service]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
PubMed
DOI
Crossref
Genetic Predisposition to Coronary Artery Disease in Type 2 Diabetes Mellitus.
van Zuydam NR
,
Ladenvall C
,
Voight BF
, ...,
Palmer CNA
, SUMMIT Steering Committee; CARDIOGRAMplusC4D Steering Committee*
Circ Genom Precis Med
13
(6) e002769 [2020-12-00; online 2020-08-13]
NGI Uppsala (SNP&SEQ Technology Platform) [Service]
National Genomics Infrastructure [Service]
SciLifeLab Data Centre
Publications
9.5.1