Pall Melsted
Overview
Explore the profile of Pall Melsted including associated specialties, affiliations and a list of published articles.
Author names and details appear as published. Due to indexing inconsistencies, multiple individuals may share a name, and a single author may have variations. MedLuna displays this data as publicly available, without modification or verification
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Articles
62
Citations
9971
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Recent Articles
11.
Hjorleifsson Eldjarn G, Ferkingstad E, Lund S, Helgason H, Magnusson O, Gunnarsdottir K, et al.
Nature
. 2024 May;
630(8015):E3.
PMID: 38778117
No abstract available.
12.
Rich J, Moses L, Einarsson P, Jackson K, Luebbert L, Booeshaghi A, et al.
bioRxiv
. 2024 Apr;
PMID: 38617255
Standard single-cell RNA-sequencing analysis (scRNA-seq) workflows consist of converting raw read data into cell-gene count matrices through sequence alignment, followed by analyses including filtering, highly variable gene selection, dimensionality reduction,...
13.
Sullivan D, Min K, Hjorleifsson K, Luebbert L, Holley G, Moses L, et al.
bioRxiv
. 2023 Dec;
PMID: 38045414
The term "RNA-seq" refers to a collection of assays based on sequencing experiments that involve quantifying RNA species from bulk tissue, from single cells, or from single nuclei. The kallisto,...
14.
Stacey S, Zink F, Halldorsson G, Stefansdottir L, Gudjonsson S, Einarsson G, et al.
Nat Genet
. 2023 Nov;
55(12):2149-2159.
PMID: 37932435
Clonal hematopoiesis (CH) arises when a substantial proportion of mature blood cells is derived from a single hematopoietic stem cell lineage. Using whole-genome sequencing of 45,510 Icelandic and 130,709 UK...
15.
Bjornsdottir G, Chalmer M, Stefansdottir L, Skuladottir A, Einarsson G, Andresdottir M, et al.
Nat Genet
. 2023 Oct;
55(11):1843-1853.
PMID: 37884687
Migraine is a complex neurovascular disease with a range of severity and symptoms, yet mostly studied as one phenotype in genome-wide association studies (GWAS). Here we combine large GWAS datasets...
16.
Hjorleifsson Eldjarn G, Ferkingstad E, Lund S, Helgason H, Magnusson O, Gunnarsdottir K, et al.
Nature
. 2023 Oct;
622(7982):348-358.
PMID: 37794188
High-throughput proteomics platforms measuring thousands of proteins in plasma combined with genomic and phenotypic information have the power to bridge the gap between the genome and diseases. Here we performed...
17.
Moses L, Einarsson P, Jackson K, Luebbert L, Booeshaghi A, Antonsson S, et al.
bioRxiv
. 2023 Aug;
PMID: 37645732
Exploratory spatial data analysis (ESDA) can be a powerful approach to understanding single-cell genomics datasets, but it is not yet part of standard data analysis workflows. In particular, geospatial analyses,...
18.
Kristjansson R, Oskarsson G, Skuladottir A, Oddsson A, Rognvaldsson S, Sveinbjornsson G, et al.
Commun Biol
. 2023 Jul;
6(1):703.
PMID: 37430141
Urticaria is a skin disorder characterized by outbreaks of raised pruritic wheals. In order to identify sequence variants associated with urticaria, we performed a meta-analysis of genome-wide association studies for...
19.
Oddsson A, Sulem P, Sveinbjornsson G, Arnadottir G, Steinthorsdottir V, Halldorsson G, et al.
Nat Commun
. 2023 Jul;
14(1):3923.
PMID: 37400429
No abstract available.
20.
Oddsson A, Sulem P, Sveinbjornsson G, Arnadottir G, Steinthorsdottir V, Halldorsson G, et al.
Nat Commun
. 2023 Jun;
14(1):3453.
PMID: 37301908
Genotypes causing pregnancy loss and perinatal mortality are depleted among living individuals and are therefore difficult to find. To explore genetic causes of recessive lethality, we searched for sequence variants...