| Listening to silence and understanding nonsense: exonic mutations that affect splicing L Cartegni, SL Chew, AR Krainer Nature reviews genetics 3 (4), 285-298, 2002 | 2784 | 2002 |
| ESEfinder: a web resource to identify exonic splicing enhancers L Cartegni, J Wang, Z Zhu, MQ Zhang, AR Krainer Nucleic acids research 31 (13), 3568-3571, 2003 | 1886 | 2003 |
| Disruption of an SF2/ASF-dependent exonic splicing enhancer in SMN2 causes spinal muscular atrophy in the absence of SMN1 L Cartegni, AR Krainer Nature genetics 30 (4), 377-384, 2002 | 960 | 2002 |
| A mechanism for exon skipping caused by nonsense or missense mutations in BRCA1 and other genes HX Liu, L Cartegni, MQ Zhang, AR Krainer Nature genetics 27 (1), 55-58, 2001 | 602 | 2001 |
| Determinants of exon 7 splicing in the spinal muscular atrophy genes, SMN1 and SMN2 L Cartegni, ML Hastings, JA Calarco, E De Stanchina, AR Krainer The American Journal of Human Genetics 78 (1), 63-77, 2006 | 384 | 2006 |
| Correction of disease-associated exon skipping by synthetic exon-specific activators L Cartegni, AR Krainer Nature structural biology 10 (2), 120-125, 2003 | 382 | 2003 |
| Exonic splicing enhancer motif recognized by human SC35 under splicing conditions HX Liu, SL Chew, L Cartegni, MQ Zhang, AR Krainer Molecular and cellular biology 20 (3), 1063-1071, 2000 | 295 | 2000 |
| hnRNP A1 selectively interacts through its Gly-rich domain with different RNA-binding proteins L Cartegni, M Maconi, E Morandi, F Cobianchi, S Riva, G Biamonti Journal of molecular biology 259 (3), 337-348, 1996 | 247 | 1996 |
| Splicing factor hnRNPH drives an oncogenic splicing switch in gliomas CV LeFave, M Squatrito, S Vorlova, GL Rocco, CW Brennan, EC Holland, ... The EMBO journal 30 (19), 4084-4097, 2011 | 193 | 2011 |
| Antitumorigenic potential of STAT3 alternative splicing modulation F Zammarchi, E De Stanchina, E Bournazou, T Supakorndej, K Martires, ... Proceedings of the National Academy of Sciences 108 (43), 17779-17784, 2011 | 183 | 2011 |
| Heart-specific localization of emerin: new insights into Emery-Dreifuss muscular dystrophy L Cartegni, MR Di Barletta, R Barresi, S Squarzoni, P Sabatelli, N Maraldi, ... Human molecular genetics 6 (13), 2257-2264, 1997 | 169 | 1997 |
| Induction of antagonistic soluble decoy receptor tyrosine kinases by intronic polyA activation S Vorlová, G Rocco, CV LeFave, FM Jodelka, K Hess, ML Hastings, ... Molecular cell 43 (6), 927-939, 2011 | 157 | 2011 |
| Seemingly neutral polymorphic variants may confer immunity to splicing-inactivating mutations: a synonymous SNP in exon 5 of MCAD protects from deleterious mutations in a … KB Nielsen, S Sørensen, L Cartegni, TJ Corydon, TK Doktor, ... The American Journal of Human Genetics 80 (3), 416-432, 2007 | 154 | 2007 |
| A novel hnRNP protein (HAP/SAF-B) enters a subset of hnRNP complexes and relocates in nuclear granules in response to heat shock F Weighardt, F Cobianchi, L Cartegni, I Chiodi, A Villa, S Riva, G Biamonti Journal of cell science 112 (10), 1465-1476, 2000 | 154 | 2000 |
| Peptide-conjugated antisense oligonucleotides for targeted inhibition of a transcriptional regulator in vivo E Henke, J Perk, J Vider, P De Candia, Y Chin, DB Solit, V Ponomarev, ... Nature biotechnology 26 (1), 91-100, 2008 | 138 | 2008 |
| BRCA2 T2722R is a deleterious allele that causes exon skipping JD Fackenthal, L Cartegni, AR Krainer, OI Olopade The American Journal of Human Genetics 71 (3), 625-631, 2002 | 117 | 2002 |
| Therapeutic hemoglobin levels after gene transfer in β-thalassemia mice and in hematopoietic cells of β-thalassemia and sickle cells disease patients L Breda, C Casu, S Gardenghi, N Bianchi, L Cartegni, M Narla, ... PloS one 7 (3), e32345, 2012 | 110 | 2012 |
| p53Ψ is a transcriptionally inactive p53 isoform able to reprogram cells toward a metastatic-like state S Senturk, Z Yao, M Camiolo, B Stiles, T Rathod, AM Walsh, ... Proceedings of the National Academy of Sciences 111 (32), E3287-E3296, 2014 | 98 | 2014 |
| KLF4 is a novel candidate tumor suppressor gene in pancreatic ductal carcinoma F Zammarchi, M Morelli, M Menicagli, C Di Cristofano, K Zavaglia, ... The American journal of pathology 178 (1), 361-372, 2011 | 97 | 2011 |
| X‐linked emery‐dreifuss muscular dystrophy can be diagnosed from skin biopsy or blood sample M Mora, L Cartegni, C Di Blasi, R Barresi, S Bione, MR Di Barletta, ... Annals of Neurology: Official Journal of the American Neurological …, 1997 | 72 | 1997 |
