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Andrea Ciolfi
Andrea Ciolfi
Staff Scientist, Bambino Gesu' Children's Hospital
在 opbg.net 的电子邮件经过验证 - 首页
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引用次数
引用次数
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A dynamic balance between gene activation and repression regulates the shade avoidance response in Arabidopsis
G Sessa, M Carabelli, M Sassi, A Ciolfi, M Possenti, F Mittempergher, ...
Genes & development 19 (23), 2811-2815, 2005
2842005
ACE2 gene variants may underlie interindividual variability and susceptibility to COVID-19 in the Italian population
E Benetti, R Tita, O Spiga, A Ciolfi, G Birolo, A Bruselles, G Doddato, ...
European Journal of Human Genetics 28 (11), 1602-1614, 2020
2752020
Canopy shade causes a rapid and transient arrest in leaf development through auxin-induced cytokinin oxidase activity
M Carabelli, M Possenti, G Sessa, A Ciolfi, M Sassi, G Morelli, I Ruberti
Genes & development 21 (15), 1863-1868, 2007
2392007
Plant adaptation to dynamically changing environment: the shade avoidance response
I Ruberti, G Sessa, A Ciolfi, M Possenti, M Carabelli, G Morelli
Biotechnology advances 30 (5), 1047-1058, 2012
2382012
Evaluation of DNA methylation episignatures for diagnosis and phenotype correlations in 42 Mendelian neurodevelopmental disorders
E Aref-Eshghi, J Kerkhof, VP Pedro, M Barat-Houari, N Ruiz-Pallares, ...
The American Journal of Human Genetics 106 (3), 356-370, 2020
2142020
Mutations in KCNH1 and ATP6V1B2 cause Zimmermann-Laband syndrome
F Kortüm, V Caputo, CK Bauer, L Stella, A Ciolfi, M Alawi, G Bocchinfuso, ...
Nature genetics 47 (6), 661-667, 2015
2062015
A novel disorder involving dyshematopoiesis, inflammation, and HLH due to aberrant CDC42 function
MT Lam, S Coppola, OHF Krumbach, G Prencipe, A Insalaco, C Cifaldi, ...
Journal of Experimental Medicine 216 (12), 2778-2799, 2019
1712019
The Arabidopsis homeodomain-leucine zipper II gene family: diversity and redundancy
AR Ciarbelli, A Ciolfi, S Salvucci, V Ruzza, M Possenti, M Carabelli, ...
Plant molecular biology 68, 465-478, 2008
1562008
Organoids as a new model for improving regenerative medicine and cancer personalized therapy in renal diseases
L Grassi, R Alfonsi, F Francescangeli, M Signore, ML De Angelis, ...
Cell death & disease 10 (3), 201, 2019
1322019
Modeling medulloblastoma in vivo and with human cerebellar organoids
C Ballabio, M Anderle, M Gianesello, C Lago, E Miele, M Cardano, ...
Nature communications 11 (1), 583, 2020
1312020
Mutations impairing GSK3-mediated MAF phosphorylation cause cataract, deafness, intellectual disability, seizures, and a down syndrome-like facies
M Niceta, E Stellacci, KW Gripp, G Zampino, M Kousi, M Anselmi, ...
The American Journal of Human Genetics 96 (5), 816-825, 2015
1282015
Novel diagnostic DNA methylation episignatures expand and refine the epigenetic landscapes of Mendelian disorders
MA Levy, H McConkey, J Kerkhof, M Barat-Houari, S Bargiacchi, ...
Human Genetics and Genomics Advances 3 (1), 2022
1152022
Integrin α7 is a functional marker and potential therapeutic target in glioblastoma
TL Haas, MR Sciuto, L Brunetto, C Valvo, M Signore, ME Fiori, ...
Cell stem cell 21 (1), 35-50. e9, 2017
1142017
Dynamics of the shade-avoidance response in Arabidopsis
A Ciolfi, G Sessa, M Sassi, M Possenti, S Salvucci, M Carabelli, G Morelli, ...
Plant physiology 163 (1), 331-353, 2013
1132013
Mutations in ZBTB20 cause Primrose syndrome
V Cordeddu, B Redeker, E Stellacci, A Jongejan, A Fragale, TEJ Bradley, ...
Nature genetics 46 (8), 815-817, 2014
1032014
Mutations in KCNK4 that affect gating cause a recognizable neurodevelopmental syndrome
CK Bauer, P Calligari, FC Radio, V Caputo, ML Dentici, N Falah, F High, ...
The American Journal of Human Genetics 103 (4), 621-630, 2018
932018
A Restricted Spectrum of Mutations in the SMAD4 Tumor-Suppressor Gene Underlies Myhre Syndrome.
V Caputo, L Cianetti, M Niceta, C Carta, A Ciolfi, G Bocchinfuso, E Carrani, ...
American journal of human genetics 90 (1), 161, 2012
932012
Activating mutations affecting the Dbl homology domain of SOS2 cause Noonan syndrome
V Cordeddu, JC Yin, C Gunnarsson, C Virtanen, S Drunat, F Lepri, ...
Human mutation 36 (11), 1080-1087, 2015
892015
Biallelic mutations in TBCD, encoding the tubulin folding cofactor D, perturb microtubule dynamics and cause early-onset encephalopathy
E Flex, M Niceta, S Cecchetti, I Thiffault, MG Au, A Capuano, E Piermarini, ...
The American Journal of Human Genetics 99 (4), 962-973, 2016
792016
Solve-RD: systematic pan-European data sharing and collaborative analysis to solve rare diseases
B Zurek, K Ellwanger, LELM Vissers, R Schüle, M Synofzik, A Töpf, ...
European Journal of Human Genetics 29 (9), 1325-1331, 2021
742021
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