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Julian Nevado
Julian Nevado
FEA, Responsable de Genómica, INGEMM. Hospital Universitario La Paz
Verified email at salud.madrid.org
Title
Cited by
Cited by
Year
Endothelial dysfunction in aged humans is related with oxidative stress and vascular inflammation
L Rodríguez‐Mañas, M El‐Assar, S Vallejo, P López‐Dóriga, J Solís, ...
Aging cell 8 (3), 226-238, 2009
2672009
Extracellular PBEF/NAMPT/visfatin activates pro-inflammatory signalling in human vascular smooth muscle cells through nicotinamide phosphoribosyltransferase activity
T Romacho, V Azcutia, M Vazquez-Bella, N Matesanz, E Cercas, ...
Diabetologia 52, 2455-2463, 2009
2062009
The anticancer drug cisplatin induces an intrinsic apoptotic pathway inside the inner ear
JR Garcia‐Berrocal, J Nevado, R Ramirez‐Camacho, R Sanz, ...
British journal of pharmacology 152 (7), 1012-1020, 2007
1372007
New microdeletion and microduplication syndromes: A comprehensive review
J Nevado, R Mergener, M Palomares-Bralo, KR Souza, E Vallespín, ...
Genetics and molecular biology 37, 210-219, 2014
1242014
Clinical utility of chromosomal microarray analysis in invasive prenatal diagnosis
L Armengol, J Nevado, C Serra-Juhé, A Plaja, C Mediano, ...
Human genetics 131, 513-523, 2012
1142012
Microhomology-Mediated Mechanisms Underlie Non-Recurrent Disease-Causing Microdeletions of the FOXL2 Gene or Its Regulatory Domain
H Verdin, B D'haene, D Beysen, Y Novikova, B Menten, T Sante, ...
PLoS genetics 9 (3), e1003358, 2013
1032013
Pathogenetics of alveolar capillary dysplasia with misalignment of pulmonary veins
P Szafranski, T Gambin, AV Dharmadhikari, KC Akdemir, SN Jhangiani, ...
Human genetics 135, 569-586, 2016
972016
Simpson-Golabi-Behmel syndrome types I and II
J Tenorio, P Arias, V Martínez-Glez, F Santos, S García-Miñaur, J Nevado, ...
Orphanet Journal of Rare Diseases 9, 1-8, 2014
902014
Highly glycated oxyhaemoglobin impairs nitric oxide relaxations in human mesenteric microvessels
S Vallejo, J Angulo, C Peiro, J Nevado, A Sanchez-Ferrer, R Petidier, ...
Diabetologia 43, 83-90, 2000
902000
A founder EIF2AK4 mutation causes an aggressive form of pulmonary arterial hypertension in Iberian Gypsies
J Tenorio, P Navas, E Barrios, L Fernández, J Nevado, CA Quezada, ...
Clinical Genetics 88 (6), 579-583, 2015
762015
A deletion and a duplication in distal 22q11. 2 deletion syndrome region. Clinical implications and review
L Fernández, J Nevado, F Santos, D Heine-Suñer, V Martinez-Glez, ...
BMC Medical Genetics 10, 1-13, 2009
712009
Transcriptional activation by artificial recruitment in yeast is influenced by promoter architecture and downstream sequences
L Gaudreau, M Keaveney, J Nevado, Z Zaman, GO Bryant, K Struhl, ...
Proceedings of the National Academy of Sciences 96 (6), 2668-2673, 1999
711999
CLAPO syndrome: identification of somatic activating PIK3CA mutations and delineation of the natural history and phenotype
L Rodriguez-Laguna, K Ibañez, G Gordo, S Garcia-Minaur, ...
Genetics in Medicine 20 (8), 882-889, 2018
692018
GLI1 inactivation is associated with developmental phenotypes overlapping with Ellis–van Creveld syndrome
A Palencia-Campos, A Ullah, J Nevado, R Yıldırım, E Unal, M Ciorraga, ...
Human molecular genetics 26 (23), 4556-4571, 2017
632017
Specific variants in WDR35 cause a distinctive form of Ellis-van Creveld syndrome by disrupting the recruitment of the EvC complex and SMO into the cilium
JA Caparrós-Martín, A De Luca, F Cartault, M Aglan, S Temtamy, ...
Human molecular genetics 24 (14), 4126-4137, 2015
592015
Prenatal molecular testing for Beckwith–Wiedemann and Silver–Russell syndromes: a challenge for molecular analysis and genetic counseling
T Eggermann, F Brioude, S Russo, MP Lombardi, J Bliek, ER Maher, ...
European Journal of Human Genetics 24 (6), 784-793, 2016
582016
Prevention of endothelial dysfunction in streptozotocin-induced diabetic rats by gliclazide treatment
S Vallejo, J Angulo, C Peiró, A Sánchez-Ferrer, E Cercas, JL Llergo, ...
Journal of Diabetes and its Complications 14 (4), 224-233, 2000
572000
Beckwith–Wiedemann syndrome and uniparental disomy 11p: fine mapping of the recombination breakpoints and evaluation of several techniques
V Romanelli, HNM Meneses, L Fernández, V Martínez-Glez, ...
European journal of human genetics 19 (4), 416-421, 2011
552011
Transcriptional activation by artificial recruitment in mammalian cells
J Nevado, L Gaudreau, M Adam, M Ptashne
Proceedings of the National Academy of Sciences 96 (6), 2674-2677, 1999
551999
Epigenetic age acceleration changes 2 years after antiretroviral therapy initiation in adults with HIV: a substudy of the NEAT001/ANRS143 randomised trial
A Esteban-Cantos, J Rodríguez-Centeno, P Barruz, B Alejos, ...
The lancet HIV 8 (4), e197-e205, 2021
542021
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