| Increased sensitivity of the neuronal nicotinic receptor α2 subunit causes familial epilepsy with nocturnal wandering and ictal fear P Aridon, C Marini, C Di Resta, E Brilli, M De Fusco, F Politi, E Parrini, ... The American Journal of Human Genetics 79 (2), 342-350, 2006 | 290 | 2006 |
| Next-generation sequencing approach for the diagnosis of human diseases: open challenges and new opportunities C Di Resta, S Galbiati, P Carrera, M Ferrari Ejifcc 29 (1), 4, 2018 | 170 | 2018 |
| Development, evaluation, and validation of machine learning models for COVID-19 detection based on routine blood tests F Cabitza, A Campagner, D Ferrari, C Di Resta, D Ceriotti, E Sabetta, ... Clinical Chemistry and Laboratory Medicine (CCLM) 59 (2), 421-431, 2021 | 162 | 2021 |
| Brugada syndrome genetics is associated with phenotype severity G Ciconte, MM Monasky, V Santinelli, E Micaglio, G Vicedomini, ... European heart journal 42 (11), 1082-1090, 2021 | 82 | 2021 |
| A Brugada syndrome mutation (p. S216L) and its modulation by p. H558R polymorphism: standard and dynamic characterization S Marangoni, C Di Resta, M Rocchetti, L Barile, R Rizzetto, A Summa, ... Cardiovascular research 91 (4), 606-616, 2011 | 68 | 2011 |
| The gender impact assessment among healthcare workers in the SARS-CoV-2 vaccination—an analysis of serological response and side effects C Di Resta, D Ferrari, M Viganò, M Moro, E Sabetta, M Minerva, ... Vaccines 9 (5), 522, 2021 | 66 | 2021 |
| Genetics can contribute to the prognosis of Brugada syndrome: a pilot model for risk stratification E Sommariva, C Pappone, F Martinelli Boneschi, C Di Resta, ... European Journal of Human Genetics 21 (9), 911-917, 2013 | 63 | 2013 |
| Pharmacogenomics education in medical and pharmacy schools: conclusions of a global survey N Karas Kuželički, I Prodan Žitnik, D Gurwitz, A Llerena, I Cascorbi, ... Pharmacogenomics 20 (9), 643-657, 2019 | 62 | 2019 |
| Exome sequencing and pathway analysis for identification of genetic variability relevant for bronchopulmonary dysplasia (BPD) in preterm newborns: a pilot study P Carrera, C Di Resta, C Volonteri, E Castiglioni, S Bonfiglio, D Lazarevic, ... Clinica chimica acta 451, 39-45, 2015 | 56 | 2015 |
| Next generation sequencing: from research area to clinical practice C Di Resta, M Ferrari Ejifcc 29 (3), 215, 2018 | 45 | 2018 |
| Updated clinical overview on cardiac laminopathies: an electrical and mechanical disease G Peretto, S Sala, S Benedetti, C Di Resta, L Gigli, M Ferrari, P Della Bella Nucleus 9 (1), 380-391, 2018 | 43 | 2018 |
| Personalized laboratory medicine: a patient-centered future approach I Prodan Žitnik, D Černe, I Mancini, L Simi, M Pazzagli, C Di Resta, ... Clinical Chemistry and Laboratory Medicine (CCLM) 56 (12), 1981-1991, 2018 | 40 | 2018 |
| High-throughput genetic characterization of a cohort of Brugada syndrome patients C Di Resta, A Pietrelli, S Sala, P Della Bella, G De Bellis, M Ferrari, ... Human molecular genetics 24 (20), 5828-5835, 2015 | 40 | 2015 |
| Cardiac and Neuromuscular Features of Patients With LMNA-Related Cardiomyopathy G Peretto, C Di Resta, J Perversi, C Forleo, L Maggi, L Politano, A Barison, ... Annals of Internal Medicine 171 (7), 458-463, 2019 | 39 | 2019 |
| Effect of carbamazepine and oxcarbazepine on wild-type and mutant neuronal nicotinic acetylcholine receptors linked to nocturnal frontal lobe epilepsy C Di Resta, P Ambrosi, G Curia, A Becchetti European journal of pharmacology 643 (1), 13-20, 2010 | 37 | 2010 |
| Impaired turnover of hyperfused mitochondria in severe axonal neuropathy due to a novel DRP1 mutation F Longo, S Benedetti, AA Zambon, MGN Sora, C Di Resta, D De Ritis, ... Human Molecular Genetics 29 (2), 177-188, 2020 | 35 | 2020 |
| New molecular approaches to Alzheimer's disease C Di Resta, M Ferrari Clinical biochemistry 72, 81-86, 2019 | 30 | 2019 |
| Harmonization of six quantitative SARS-CoV-2 serological assays using sera of vaccinated subjects D Ferrari, N Clementi, SM Spanò, S Albitar-Nehme, S Ranno, ... Clinica Chimica Acta 522, 144-151, 2021 | 29 | 2021 |
| Introduction to ion channels C Di Resta, A Becchetti Integrins and Ion Channels: Molecular Complexes and Signaling, 9-21, 2010 | 29 | 2010 |
| SETBP1 accumulation induces P53 inhibition and genotoxic stress in neural progenitors underlying neurodegeneration in Schinzel-Giedion syndrome F Banfi, A Rubio, M Zaghi, L Massimino, G Fagnocchi, E Bellini, M Luoni, ... Nature communications 12 (1), 4050, 2021 | 28 | 2021 |
