David Salgado
Overview
Explore the profile of David Salgado including associated specialties, affiliations and a list of published articles.
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51
Citations
1918
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Recent Articles
1.
Salgado D, Kang J, Costa A
Curr Probl Diagn Radiol
. 2024 Dec;
PMID: 39701879
Interpreting imaging examinations of the pancreas can be a challenge. Several different entities can mimic or mask pancreatic neoplasms, including normal anatomic variants, non-pancreatic lesions, and both acute and chronic...
2.
Gurbuz O, Aldrete R, Salgado D, Gurbuz T
Transp Res Rec
. 2024 Apr;
2677(4):826-838.
PMID: 38602941
More than a year after COVID-19 was declared a pandemic by the World Health Organization, the U.S.A. and Mexico rank first and fourth, respectively, with regard to the number of...
3.
Neves A, Cuesta I, Hjerde E, Klemetsen T, Salgado D, van Helden J, et al.
Front Public Health
. 2023 Dec;
11:1289945.
PMID: 38074768
The COVID-19 pandemic has exemplified the importance of interoperable and equitable data sharing for global surveillance and to support research. While many challenges could be overcome, at least in some...
4.
Protein domains provide a new layer of information for classifying human variations in rare diseases
Corcuff M, Garibal M, Desvignes J, Guien C, Grattepanche C, Collod-Beroud G, et al.
Front Bioinform
. 2023 Mar;
3:1127341.
PMID: 36896423
Using the ACMG-AMP guidelines for the interpretation of sequence variants, it remains difficult to meet the criterion associated with the protein domain, PM1, which is assigned in only about 10%...
5.
Laurie S, Piscia D, Matalonga L, Corvo A, Fernandez-Callejo M, Garcia-Linares C, et al.
Hum Mutat
. 2022 Feb;
43(6):717-733.
PMID: 35178824
Rare disease patients are more likely to receive a rapid molecular diagnosis nowadays thanks to the wide adoption of next-generation sequencing. However, many cases remain undiagnosed even after exome or...
6.
Koeppel F, Muller E, Harle A, Guien C, Sujobert P, Trabelsi Grati O, et al.
Eur J Cancer
. 2021 Oct;
159:1-15.
PMID: 34700215
Background: The difficulty in interpreting somatic alterations is correlated with the increase in sequencing panel size. To correctly guide the clinical management of patients with cancer, there needs to be...
7.
Salgado D, Armean I, Baudis M, Beltran S, Capella-Gutierrez S, Carvalho-Silva D, et al.
F1000Res
. 2021 Aug;
9.
PMID: 34367618
Copy number variations (CNVs) are major causative contributors both in the genesis of genetic diseases and human neoplasias. While "High-Throughput" sequencing technologies are increasingly becoming the primary choice for genomic...
8.
Gargaun E, Falcone S, Sole G, Durigneux J, Urtizberea A, Cuisset J, et al.
Biomedicines
. 2021 Mar;
9(2).
PMID: 33672764
In skeletal muscle, long noncoding RNAs (lncRNAs) are involved in dystrophin protein stabilization but also in the regulation of myocytes proliferation and differentiation. Hence, they could represent promising therapeutic targets...
9.
Melendez J, Sieiro D, Salgado D, Morin V, Dejardin M, Zhou C, et al.
Nat Commun
. 2021 Feb;
12(1):749.
PMID: 33531476
Fusion of nascent myoblasts to pre-existing myofibres is critical for skeletal muscle growth and repair. The vast majority of molecules known to regulate myoblast fusion are necessary in this process....
10.
MacGrogan D, Martinez-Poveda B, Desvignes J, Fernandez-Friera L, Gomez M, Gil Vilarino E, et al.
Physiol Genomics
. 2020 Oct;
52(12):563-574.
PMID: 33044885
Calcific aortic valve disease (CAVD) is a significant cause of illness and death worldwide. Identification of early predictive markers could help optimize patient management. RNA-sequencing was carried out on human...