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Silvana Penco
Silvana Penco
Medical Genetics - Laboratory Department - Niguarda Ca' Granda Hospital - Milan - Italy
Verified email at ospedaleniguarda.it - Homepage
Title
Cited by
Cited by
Year
Genome-wide association analyses identify new risk variants and the genetic architecture of amyotrophic lateral sclerosis
W Van Rheenen, A Shatunov, AM Dekker, RL McLaughlin, FP Diekstra, ...
Nature genetics 48 (9), 1043-1048, 2016
5882016
Genome-wide analyses identify KIF5A as a novel ALS gene
A Nicolas, KP Kenna, AE Renton, N Ticozzi, F Faghri, R Chia, ...
Neuron 97 (6), 1268-1283. e6, 2018
5762018
RAR‐specific agonist/antagonists which dissociate transactivation and AP1 transrepression inhibit anchorage‐independent cell proliferation.
JY Chen, S Penco, J Ostrowski, P Balaguer, M Pons, JE Starrett, ...
The EMBO journal 14 (6), 1187-1197, 1995
3331995
Cerebral Autosomal Dominant Arteriopathy with Subcortical Infarcts and Leukoencephalopathy (CADASIL) as a model of small vessel disease: update on clinical, diagnostic, and …
I Di Donato, S Bianchi, N De Stefano, M Dichgans, MT Dotti, M Duering, ...
BMC medicine 15, 1-12, 2017
2692017
Risk of venous thromboembolism associated with single and combined effects of Factor V Leiden, Prothrombin 20210A and Methylenetethraydrofolate reductase C677T: a meta-analysis …
B Simone, V De Stefano, E Leoncini, J Zacho, I Martinelli, J Emmerich, ...
European journal of epidemiology 28, 621-647, 2013
2382013
Clinical characteristics of patients with familial amyotrophic lateral sclerosis carrying the pathogenic GGGGCC hexanucleotide repeat expansion of C9ORF72
A Chiò, G Borghero, G Restagno, G Mora, C Drepper, BJ Traynor, ...
Brain 135 (3), 784-793, 2012
2302012
Mutations of FUS gene in sporadic amyotrophic lateral sclerosis
L Corrado, R Del Bo, B Castellotti, A Ratti, C Cereda, S Penco, G Sorarù, ...
Journal of medical genetics 47 (3), 190-194, 2010
2152010
Shared polygenic risk and causal inferences in amyotrophic lateral sclerosis
S Bandres‐Ciga, AJ Noyce, G Hemani, A Nicolas, A Calvo, G Mora, ...
Annals of neurology 85 (4), 470-481, 2019
1602019
Genetic counselling in ALS: facts, uncertainties and clinical suggestions
A Chiò, S Battistini, A Calvo, C Caponnetto, FL Conforti, M Corbo, ...
Journal of Neurology, Neurosurgery & Psychiatry 85 (5), 478-485, 2014
1522014
SOD1 mutations in amyotrophic lateral sclerosis: results from a multicenter Italian study
S Battistini, F Giannini, G Greco, G Bibbò, L Ferrera, V Marini, ...
Journal of neurology 252, 782-788, 2005
1432005
A genome-wide association meta-analysis identifies a novel locus at 17q11. 2 associated with sporadic amyotrophic lateral sclerosis
I Fogh, A Ratti, C Gellera, K Lin, C Tiloca, V Moskvina, L Corrado, ...
Human molecular genetics 23 (8), 2220-2231, 2014
1382014
Genetic correlation between amyotrophic lateral sclerosis and schizophrenia
RL McLaughlin, D Schijven, W Van Rheenen, KR Van Eijk, M O’brien, ...
Nature communications 8 (1), 14774, 2017
1352017
Clues to detect tumor necrosis factor receptor-associated periodic syndrome (TRAPS) among patients with idiopathic recurrent acute pericarditis: results of a multicentre study
L Cantarini, OM Lucherini, A Brucato, L Barone, D Cumetti, F Iacoponi, ...
Clinical Research in Cardiology 101, 525-531, 2012
1202012
The genetic and clinical spectrum of a large cohort of patients with distal renal tubular acidosis
V Palazzo, A Provenzano, F Becherucci, G Sansavini, B Mazzinghi, ...
Kidney international 91 (5), 1243-1255, 2017
1092017
C9ORF72 hexanucleotide repeat expansions in the Italian sporadic ALS population
M Sabatelli, FL Conforti, M Zollino, G Mora, MR Monsurrò, P Volanti, ...
Neurobiology of aging 33 (8), 1848. e15-1848. e20, 2012
1012012
Identification of an import signal for, and the nuclear localization of, human lactoferrin
S Penco, S Scarfi, M Giovine, G Damonte, E Millo, B Villaggio, ...
Biotechnology and applied biochemistry 34 (3), 151-159, 2001
902001
Recurrent pericarditis: autoimmune or autoinflammatory?
S Maestroni, PR Di Corato, D Cumetti, S Ghidoni, L Prisacaru, L Cantarini, ...
Autoimmunity reviews 12 (1), 60-65, 2012
842012
Factors affecting formation and rupture of intracranial saccular aneurysms
S Bacigaluppi, M Piccinelli, L Antiga, A Veneziani, T Passerini, P Rampini, ...
Neurosurgical review 37, 1-14, 2014
752014
Chronic hypercalcaemia from inactivating mutations of vitamin D 24-hydroxylase (CYP24A1): implications for mineral metabolism changes in chronic renal failure
G Colussi, L Ganon, S Penco, ME De Ferrari, F Ravera, M Querques, ...
Nephrology Dialysis Transplantation 29 (3), 636-643, 2014
702014
Acquired lecithin: cholesterol acyltransferase deficiency as a major factor in lowering plasma HDL levels in chronic kidney disease
L Calabresi, S Simonelli, P Conca, G Busnach, M Cabibbe, L Gesualdo, ...
Journal of internal medicine 277 (5), 552-561, 2015
682015
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