Joanne J van der Vis
Overview
Explore the profile of Joanne J van der Vis 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
Snapshot
Snapshot
Articles
40
Citations
543
Followers
0
Related Specialties
Related Specialties
Top 10 Co-Authors
Top 10 Co-Authors
Published In
Published In
Affiliations
Affiliations
Soon will be listed here.
Recent Articles
11.
Groen K, van der Vis J, van Batenburg A, Kazemier K, Grutters J, van Moorsel C
Int J Mol Sci
. 2023 Feb;
24(3).
PMID: 36769106
In only around 40% of families with pulmonary fibrosis (PF) a suspected genetic cause can be found. Genetic overlap analysis of Whole Exome Sequencing (WES) data may be a powerful...
12.
Maus M, Groen K, van der Vis J, Grutters J, van Moorsel C
J Clin Med
. 2023 Jan;
12(2).
PMID: 36675603
: Familial pulmonary fibrosis (FPF) can be defined as pulmonary fibrosis in two or more first-degree family members. The first-degree family members of FPF patients are at high risk of...
13.
van der Vis J, Prasse A, Renzoni E, Stock C, Caliskan C, Maher T, et al.
Respirology
. 2022 Dec;
28(5):455-464.
PMID: 36571111
Background And Objective: The minor T-allele of the MUC5B promoter polymorphism rs35705950 is strongly associated with idiopathic pulmonary fibrosis (IPF). However, conflicting results have been reported on the relationship between...
14.
Klay D, Grutters J, van der Vis J, Platenburg M, Kelder J, Tromp E, et al.
Chest
. 2022 Nov;
163(4):870-880.
PMID: 36370864
Background: In some patients with progressive fibrosing interstitial lung disease (ILD), disease is caused by carriage of a mutation in a surfactant-related gene (SRG) such as SFTPC, SFTPA2, or ABCA3....
15.
Groen K, Huitema M, van der Vis J, Post M, Grutters J, Baughman R, et al.
Diagnostics (Basel)
. 2022 Oct;
12(10).
PMID: 36292254
Background: Pulmonary hypertension (PH) is a severe complication of sarcoidosis in a minority of patients. Several genetic defects are known to cause hereditary or sporadic PH, but whether variants in...
16.
Karakaya B, van der Vis J, Veltkamp M, Biesma D, Grutters J, van Moorsel C
Cells
. 2022 May;
11(9).
PMID: 35563867
Sarcoidosis is an immune mediated granulomatous disease commonly affecting the lungs. Genome wide association studies identified many genomic regions that are shared among multiple immune mediated diseases. However, gene polymorphism...
17.
Kelich J, Aramburu T, van der Vis J, Showe L, Kossenkov A, van der Smagt J, et al.
J Exp Med
. 2022 Apr;
219(5).
PMID: 35420632
Exonic sequencing identified a family with idiopathic pulmonary fibrosis (IPF) containing a previously unreported heterozygous mutation in POT1 p.(L259S). The family displays short telomeres and genetic anticipation. We found that...
18.
Hoffman T, van der Vis J, Biesma D, Grutters J, van Moorsel C
Respirology
. 2022 Apr;
27(11):959-965.
PMID: 35419815
Background And Objective: Idiopathic pulmonary fibrosis (IPF) is a heterogenous disease with a median survival of 3-4 years. Patients with mutations in telomere-related genes exhibit extrapulmonary signs and symptoms. These...
19.
Farre X, Espin R, Baiges A, Blommaert E, Kim W, Giannikou K, et al.
ERJ Open Res
. 2022 Jan;
8(1).
PMID: 35083324
Introduction: Lymphangioleiomyomatosis (LAM) is a rare low-grade metastasising disease characterised by cystic lung destruction. The genetic basis of LAM remains incompletely determined, and the disease cell-of-origin is uncertain. We analysed...
20.
van Moorsel C, van der Vis J, Duckworth A, Scotton C, Benschop C, Ellinghaus D, et al.
Front Med (Lausanne)
. 2021 Dec;
8:668024.
PMID: 34888316
Diversity in response on exposure to severe acute respiratory syndrome coronavirus 2 may be related to the innate immune response in the elderly. The mucin MUC5B is an important component...