| TIM-4 is the ligand for TIM-1, and the TIM-1–TIM-4 interaction regulates T cell proliferation JH Meyers, S Chakravarti, D Schlesinger, Z Illes, H Waldner, SE Umetsu, ... Nature immunology 6 (5), 455-464, 2005 | 445 | 2005 |
| Mutations in the KIAA0196 Gene at the SPG8 Locus Cause Hereditary Spastic Paraplegia PN Valdmanis, IA Meijer, A Reynolds, A Lei, P MacLeod, D Schlesinger, ... The American Journal of Human Genetics 80 (1), 152-161, 2007 | 227 | 2007 |
| A defect in the RNA-processing protein HNRPDL causes limb-girdle muscular dystrophy 1G (LGMD1G) NM Vieira, MS Naslavsky, L Licinio, F Kok, D Schlesinger, M Vainzof, ... Human molecular genetics 23 (15), 4103-4110, 2014 | 128 | 2014 |
| Screening of ARHSP‐TCC patients expands the spectrum of SPG11 mutations and includes a large scale gene deletion PS Denora, D Schlesinger, C Casali, F Kok, A Tessa, A Boukhris, ... Human mutation 30 (3), E500-E519, 2009 | 74 | 2009 |
| Ocular Toxoplasmosis: More Than Just What Meets the Eye* AL Vallochi, MV Nakamura, D Schlesinger, MC Martins, C Silveira, ... Scandinavian journal of immunology 55 (4), 324-328, 2002 | 66 | 2002 |
| African ancestry protects against Alzheimer's disease-related neuropathology D Schlesinger, LT Grinberg, JG Alba, MS Naslavsky, L Licinio, JM Farfel, ... Molecular psychiatry 18 (1), 79-85, 2013 | 62 | 2013 |
| Autosomal recessive ataxias: 20 types, and counting EK Embiruçu, ML Martyn, D Schlesinger, F Kok Arquivos de neuro-psiquiatria 67, 1143-1156, 2009 | 58 | 2009 |
| Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil LA Brito, LMR Paranaiba, CFS Bassi, C Masotti, C Malcher, D Schlesinger, ... Birth Defects Research Part A: Clinical and Molecular Teratology 94 (6), 464-468, 2012 | 53 | 2012 |
| IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population LA Brito, CFS Bassi, C Masotti, C Malcher, KM Rocha, D Schlesinger, ... American Journal of Medical Genetics Part A 158 (9), 2170-2175, 2012 | 49 | 2012 |
| Experimental autoimmune encephalomyelitis can be prevented and cured by infection with Trypanosoma cruzi CE Tadokoro, AL Vallochi, LS Rios, GA Martins, D Schlesinger, T Mosca, ... Journal of autoimmunity 23 (2), 103-115, 2004 | 43 | 2004 |
| Association between the p27 rs2066827 variant and tumor multiplicity in patients harboring MEN1 germline mutations VC Longuini, DM Lourenco Jr, T Sekiya, O Meirelles, TD Goncalves, ... European journal of endocrinology 171 (3), 335-342, 2014 | 33 | 2014 |
| Detection of germline variants in Brazilian breast cancer patients using multigene panel testing RSC Guindalini, DV Viana, JPFW Kitajima, VM Rocha, RVM López, ... Scientific reports 12 (1), 4190, 2022 | 30 | 2022 |
| Genomic monitoring unveil the early detection of the SARS‐CoV‐2 B. 1.351 (beta) variant (20H/501Y. V2) in Brazil SN Slavov, JSL Patané, RS Bezerra, M Giovanetti, V Fonseca, AJ Martins, ... Journal of medical virology 93 (12), 6782-6787, 2021 | 27 | 2021 |
| p27 variant and corticotropinoma susceptibility: a genetic and in vitro study T Sekiya, MD Bronstein, K Benfini, VC Longuini, RS Jallad, MC Machado, ... Endocrine-related cancer 21 (3), 395-404, 2014 | 22 | 2014 |
| A family with McLeod syndrome and calpainopathy with clinically overlapping diseases A Starling, D Schlesinger, F Kok, MR Passos-Bueno, M Vainzof, M Zatz Neurology 65 (11), 1832-1833, 2005 | 19 | 2005 |
| Extensive CFTR sequencing through NGS in Brazilian individuals with cystic fibrosis: unravelling regional discrepancies in the country LVRF da Silva, PJC Maróstica, RA Athanazio, FJC Reis, N Damaceno, ... Journal of Cystic Fibrosis 20 (3), 473-484, 2021 | 15 | 2021 |
| Germline DNA copy number variation in individuals with Argyrophilic grain disease reveals CTNS as a plausible candidate gene D Villela, L Kimura, D Schlesinger, A Gonçalves, PL Pearson, ... Genetics and molecular biology 36, 498-501, 2013 | 13 | 2013 |
| Lack of evidence for superantigen activity of Toxoplasma gondii towards human T cells AL Vallochi, JH Yamamoto, D Schlesinger, MAC Machado, C Silveira, ... Brazilian Journal of Medical and Biological Research 34, 1023-1031, 2001 | 11 | 2001 |
| Chromosomal microarray analyses from 5778 patients with neurodevelopmental disorders and congenital anomalies in Brazil ACV Krepischi, D Villela, SS da Costa, PC Mazzonetto, J Schauren, ... Scientific Reports 12 (1), 15184, 2022 | 10 | 2022 |
| Mutation analysis in the FKRP gene provides an explanation for a rare cause of intrafamilial clinical variability in LGMD2I NM Vieira, D Schlesinger, F de Paula, M Vainzof, M Zatz Neuromuscular Disorders 16 (12), 870-873, 2006 | 9 | 2006 |
Fernando KokProfessor Associado, Departamento de Neurologia da FMUSPVerified email at mendelics.com.br
