Daniel Nilsson
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Explore the profile of Daniel Nilsson including associated specialties, affiliations and a list of published articles.
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161
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3900
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Recent Articles
31.
Nilsson D, Ohlsson B
Front Med (Lausanne)
. 2021 Sep;
8:646658.
PMID: 34540857
The influence of daily life exposure on the gastrointestinal tract is not fully understood. This study aimed to examine associations between functional gastrointestinal symptoms and sociodemographic status and lifestyle habits...
32.
Samuelsson J, Sunila M, Rentzos A, Nilsson D
Neuroradiol J
. 2021 Aug;
35(2):213-219.
PMID: 34350797
Objectives: Cerebral vasospasm is a known complication to aneurysmal subarachnoid haemorrhage, which can lead to severe morbidity. Intra-arterial vasodilation therapy is widely used as a last resort treatment in patients...
33.
Nilsson D, Irback A
J Chem Phys
. 2021 Jul;
154(23):235101.
PMID: 34241264
Computer simulation can provide valuable insight into the forces driving biomolecular liquid-liquid phase separation. However, the simulated systems have a limited size, which makes it important to minimize and control...
34.
Hammarsjo A, Pettersson M, Chitayat D, Handa A, Anderlid B, Bartocci M, et al.
J Hum Genet
. 2021 Apr;
66(10):995-1008.
PMID: 33875766
Skeletal ciliopathies are a heterogenous group of disorders with overlapping clinical and radiographic features including bone dysplasia and internal abnormalities. To date, pathogenic variants in at least 30 genes, coding...
35.
Samuelsson J, Jakobsson H, Rentzos A, Jakola A, Nilsson D
World Neurosurg
. 2021 Apr;
151:e122-e127.
PMID: 33831611
Objective: Long-term data on neurological and radiological outcome after aneurysmal subarachnoid hemorrhage (aSAH) are scarce. The aim of this study was to report neurological and radiological outcome >15 years after...
36.
Stranneheim H, Lagerstedt-Robinson K, Magnusson M, Kvarnung M, Nilsson D, Lesko N, et al.
Genome Med
. 2021 Mar;
13(1):40.
PMID: 33726816
Background: We report the findings from 4437 individuals (3219 patients and 1218 relatives) who have been analyzed by whole genome sequencing (WGS) at the Genomic Medicine Center Karolinska-Rare Diseases (GMCK-RD)...
37.
Paucar M, Agren R, Li T, Lissmats S, Bergendal A, Weinberg J, et al.
Neurol Genet
. 2021 Feb;
7(1):e546.
PMID: 33575485
Objective: Ataxia channelopathies share common features such as slow motor progression and variable degrees of cognitive dysfunction. Mutations in potassium voltage-gated channel subfamily D member 3 (), encoding the K+...
38.
Wallander K, Eisfeldt J, Lindblad M, Nilsson D, Billiau K, Foroughi H, et al.
PLoS One
. 2021 Feb;
16(2):e0245488.
PMID: 33539436
Background: Analysis of cell-free tumour DNA, a liquid biopsy, is a promising biomarker for cancer. We have performed a proof-of principle study to test the applicability in the clinical setting,...
39.
Mereaux J, Firanescu C, Coarelli G, Kvarnung M, Rodrigues R, Pegoraro E, et al.
Neurogenetics
. 2021 Jan;
22(1):71-79.
PMID: 33486633
Spastic ataxias are rare neurogenetic disorders involving spinocerebellar and pyramidal tracts. Many genes are involved. Among them, CAPN1, when mutated, is responsible for a complex inherited form of spastic paraplegia...
40.
Eisfeldt J, Pettersson M, Petri A, Nilsson D, Feuk L, Lindstrand A
Hum Genet
. 2020 Dec;
140(5):775-790.
PMID: 33315133
Chromoanagenesis is a genomic event responsible for the formation of complex structural chromosomal rearrangements (CCRs). Germline chromoanagenesis is rare and the majority of reported cases are associated with an affected...