| alpha-Synuclein locus triplication causes Parkinson's disease alpha-Synuclein locus triplication causes Parkinson's disease Science 302 (5646), 841, 2003 | 5193* | 2003 |
| The Syk tyrosine kinase suppresses malignant growth of human breast cancer cells PJP Coopman, MTH Do, M Barth, ET Bowden, AJ Hayes, E Basyuk, ... Nature 406 (6797), 742-747, 2000 | 485 | 2000 |
| Correlation of amplification and overexpression of the c-myc oncogene in high-grade breast cancer: FISH, in situ hybridisation and immunohistochemical analyses J Blancato, B Singh, A Liu, DJ Liao, RB Dickson British journal of cancer 90 (8), 1612-1619, 2004 | 200 | 2004 |
| MicroRNAs in glioblastoma multiforme pathogenesis and therapeutics A Shea, V Harish, Z Afzal, J Chijioke, H Kedir, S Dusmatova, A Roy, ... Cancer medicine 5 (8), 1917-1946, 2016 | 191 | 2016 |
| Human T-lymphotropic virus type 1 oncoprotein tax promotes unscheduled degradation of Pds1p/securin and Clb2p/cyclin B1 and causes chromosomal instability B Liu, MH Liang, Y Kuo, W Liao, I Boros, T Kleinberger, J Blancato, ... Molecular and cellular biology 23 (15), 5269-5281, 2003 | 93 | 2003 |
| Highly skewed X-chromosome inactivation is associated with idiopathic recurrent spontaneous abortion MC Lanasa, WA Hogge, C Kubik, J Blancato, EP Hoffman The American Journal of Human Genetics 65 (1), 252-254, 1999 | 86 | 1999 |
| Principles of clinical cytogenetics N RL Thompson and Thompson Genetics in Medicine 140, 2001 | 83* | 2001 |
| Anisomastia associated with interstitial duplication of chromosome 16, mental retardation, obesity, dysmorphic facies, and digital anomalies: molecular mapping of a new … CA Stratakis, A Lafferty, SE Taymans, RI Gafni, JM Meck, J Blancato The Journal of Clinical Endocrinology & Metabolism 85 (9), 3396-3401, 2000 | 71 | 2000 |
| Clinical and molecular delineation of the Greig cephalopolysyndactyly contiguous gene deletion syndrome and its distinction from acrocallosal syndrome JJ Johnston, I Olivos‐Glander, J Turner, K Aleck, LM Bird, L Mehta, ... American Journal of Medical Genetics Part A 123 (3), 236-242, 2003 | 68 | 2003 |
| Conditional reprogramming for patient-derived cancer models and next-generation living biobanks N Palechor-Ceron, E Krawczyk, A Dakic, V Simic, H Yuan, J Blancato, ... Cells 8 (11), 1327, 2019 | 67 | 2019 |
| Respiratory insufficiency in desminopathy patients caused by introduction of proline residues in desmin C‐terminal á‐helical segment A Dagvadorj, B Goudeau, D Hilton‐Jones, JK Blancato, A Shatunov, ... Muscle & Nerve: Official Journal of the American Association of …, 2003 | 67 | 2003 |
| Hypercholesterolemia in children with Smith-Magenis syndrome: del (17)(p11. 2p11. 2) A Smith, AL Gropman, JE Bailey-Wilson, O Goker-Alpan, SH Elsea, ... Genetics in Medicine 4 (3), 118-125, 2002 | 67 | 2002 |
| Absence of donor-derived keratinocyte stem cells in skin tissues cultured from patients after mobilized peripheral blood hematopoietic stem cell transplantation P Hematti, EM Sloand, CA Carvallo, MR Albert, CL Yee, MM Fuehrer, ... Experimental hematology 30 (8), 943-949, 2002 | 58 | 2002 |
| Human APC2 localization and allelic imbalance CR Jarrett, J Blancato, T Cao, DS Bressette, M Cepeda, PE Young, ... Cancer research 61 (21), 7978-7984, 2001 | 56 | 2001 |
| Molecular analysis of the Retinoic Acid Induced 1 gene (RAI1) in patients with suspected Smith-Magenis syndrome without the 17p11. 2 deletion T Vilboux, C Ciccone, JK Blancato, GF Cox, C Deshpande, WJ Introne, ... PLoS One 6 (8), e22861, 2011 | 54 | 2011 |
| Review of disrupted sleep patterns in Smith–Magenis syndrome and normal melatonin secretion in a patient with an atypical interstitial 17p11. 2 deletion EA Boudreau, KP Johnson, AR Jackman, J Blancato, M Huizing, ... American Journal of Medical Genetics Part A 149 (7), 1382-1391, 2009 | 54 | 2009 |
| Diagnostic FISH probes for del(17)(p11.2p11.2) associated with Smith–Magenis syndrome should contain the RAI1 gene CN Vlangos, M Wilson, J Blancato, ACM Smith, SH Elsea American Journal of Medical Genetics Part A 132 (3), 278-282, 2005 | 53 | 2005 |
| Detection of chromosomal aberrations by a whole-genome microsatellite screen MJ Rosenberg, D Vaske, CE Killoran, Y Ning, D Wargowski, L Hudgins, ... The American Journal of Human Genetics 66 (2), 419-427, 2000 | 52 | 2000 |
| Molecular characterization of a large cohort of patients with chronic granulomatous disease and identification of novel CYBB mutations: an Italian multicenter study G Di Matteo, L Giordani, A Finocchi, A Ventura, M Chiriaco, J Blancato, ... Molecular immunology 46 (10), 1935-1941, 2009 | 50 | 2009 |
| Exome sequencing of oral squamous cell carcinoma in users of A rabian snuff reveals novel candidates for driver genes NN Al‐hebshi, S Li, AT Nasher, M El‐Setouhy, R Alsanosi, J Blancato, ... International journal of cancer 139 (2), 363-372, 2016 | 46 | 2016 |
