Jorge Martin
Overview
Explore the profile of Jorge Martin including associated specialties, affiliations and a list of published articles.
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Snapshot
Articles
28
Citations
365
Followers
0
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Recent Articles
1.
Romero R, Pavia J, Martin J, Romero G
J Appl Stat
. 2022 Jun;
47(13-15):2711-2736.
PMID: 35707414
Inferring electoral individual behaviour from aggregated data is a very active research area, with ramifications in sociology and political science. A new approach based on linear programming is proposed to...
2.
Bosakova M, Abraham S, Nita A, Hruba E, Buchtova M, Paige Taylor S, et al.
EMBO Mol Med
. 2020 Nov;
12(11):e11739.
PMID: 33200460
Mutations in genes affecting primary cilia cause ciliopathies, a diverse group of disorders often affecting skeletal development. This includes Jeune syndrome or asphyxiating thoracic dystrophy (ATD), an autosomal recessive skeletal...
3.
Balasubramanian K, Weis M, Eyre D, Martin J, Ortiz-Sanchez J, Duran I, et al.
Am J Med Genet A
. 2019 Jun;
179(8):1672-1677.
PMID: 31161720
No abstract available.
4.
Duran I, Paige Taylor S, Zhang W, Martin J, Qureshi F, Jacques S, et al.
Cilia
. 2017 Apr;
6:7.
PMID: 28400947
Background: Skeletal ciliopathies comprise a spectrum of ciliary malfunction disorders that have a profound effect on the skeleton. Most common among these disorders is short rib polydactyly syndrome (SRPS), a...
5.
Marques F, Tenney J, Duran I, Martin J, Nevarez L, Pogue R, et al.
PLoS Genet
. 2016 Dec;
12(12):e1006502.
PMID: 27935951
[This corrects the article DOI: 10.1371/journal.pgen.1006307.].
6.
Duran I, Paige Taylor S, Zhang W, Martin J, Forlenza K, Spiro R, et al.
Sci Rep
. 2016 Sep;
6:34232.
PMID: 27666822
Short-rib polydactyly syndromes (SRPS) and Asphyxiating thoracic dystrophy (ATD) or Jeune Syndrome are recessively inherited skeletal ciliopathies characterized by profound skeletal abnormalities and are frequently associated with polydactyly and multiorgan...
7.
Marques F, Tenney J, Duran I, Martin J, Nevarez L, Pogue R, et al.
PLoS Genet
. 2016 Sep;
12(9):e1006307.
PMID: 27622494
The acrofacial dysostoses (AFD) are a genetically heterogeneous group of inherited disorders with craniofacial and limb abnormalities. Rodriguez syndrome is a severe, usually perinatal lethal AFD, characterized by severe retrognathia,...
8.
Valdes I, Gil L, Lazo L, Marcos E, Martin J, Suzarte E, et al.
Arch Virol
. 2015 Nov;
161(2):465-70.
PMID: 26590068
There are several dengue vaccine candidates at advanced stages of development, but none of them are licensed. Despite the reactogenicity and immunogenicity profile in humans of the tetravalent ChimeriVax™ dengue...
9.
Buchtova M, Chaloupkova R, Zakrzewska M, Vesela I, Cela P, Barathova J, et al.
Cell Mol Life Sci
. 2015 Apr;
72(12):2445-59.
PMID: 25854632
Fibroblast growth factors (FGFs) deliver extracellular signals that govern many developmental and regenerative processes, but the mechanisms regulating FGF signaling remain incompletely understood. Here, we explored the relationship between intrinsic...
10.
Xue Y, Sun A, Mekikian P, Martin J, Rimoin D, Lachman R, et al.
Mol Genet Genomic Med
. 2015 Jan;
2(6):497-503.
PMID: 25614871
Fibroblast growth factor receptor 3 (FGFR3) is the only gene known to cause achondroplasia (ACH), hypochondroplasia (HCH), and thanatophoric dysplasia types I and II (TD I and TD II). A...