| Alterações genéticas na doença de Alzheimer C Fridman, SP Gregório, E Dias Neto, ÉPB Ojopi Archives of Clinical Psychiatry (São Paulo) 31, 19-25, 2004 | 147 | 2004 |
| Epilepsy in patients with Angelman syndrome caused by deletion of the chromosome 15q11-13 KD Valente, CP Koiffmann, C Fridman, M Varella, F Kok, JQ Andrade, ... Archives of neurology 63 (1), 122-128, 2006 | 121 | 2006 |
| Assessment of the relationship between self-declared ethnicity, mitochondrial haplogroups and genomic ancestry in Brazilian individuals MMSG Cardena, A Ribeiro-dos-Santos, S Santos, AJ Mansur, AC Pereira, ... PloS one 8 (4), e62005, 2013 | 108 | 2013 |
| Angelman syndrome: difficulties in EEG pattern recognition and possible misinterpretations KD Valente, JQ Andrade, RM Grossmann, F Kok, C Fridman, ... Epilepsia 44 (8), 1051-1063, 2003 | 79 | 2003 |
| The GHEP–EMPOP collaboration on mtDNA population data—A new resource for forensic casework L Prieto, B Zimmermann, A Goios, A Rodriguez-Monge, GG Paneto, ... Forensic Science International: Genetics 5 (2), 146-151, 2011 | 63 | 2011 |
| DNA phenotyping: current application in forensic science LA Marano, C Fridman Research and Reports in Forensic Medical Science, 1-8, 2019 | 57 | 2019 |
| Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the P gene C Fridman, N Hosomi, MC Varela, AH Souza, K Fukai, CP Koiffmann American Journal of Medical Genetics Part A 119 (2), 180-183, 2003 | 52 | 2003 |
| Paternal UPD15: further genetic and clinical studies in four Angelman syndrome patients C Fridman, MC Varela, F Kok, A Diament, CP Koiffmann American journal of medical genetics 92 (5), 322-327, 2000 | 50 | 2000 |
| Molecular and cytogenetic analyses on Brazilian youths with pervasive developmental disorders MR Higino Estécio, AC Fett-Conte, M Varella-Garcia, C Fridman, AE Silva Journal of Autism and Developmental Disorders 32, 35-41, 2002 | 49 | 2002 |
| Rett syndrome in a boy with a 47, XXY karyotype JS Schwartzman, M Zatz, L dos Reis Vasquez, RR Gomes, CP Koiffmann, ... The American Journal of Human Genetics 64 (6), 1781-1784, 1999 | 49 | 1999 |
| Origin of uniparental disomy 15 in patients with Prader‐Willi or Angelman syndrome C Fridman, CP Koiffmann American journal of medical genetics 94 (3), 249-253, 2000 | 42 | 2000 |
| MYH9 and APOL1 gene polymorphisms and the risk of CKD in patients with lupus nephritis from an admixture population VS Colares, SMO Titan, AC Pereira, P Malafronte, MM Cardena, S Santos, ... PLoS One 9 (3), e87716, 2014 | 39 | 2014 |
| The E180splice mutation in the GHR gene causing Laron syndrome: Witness of a Sephardic Jewish exodus from the Iberian Peninsula to the New World? FT Gonçalves, C Fridman, EM Pinto, J Guevara‐Aguirre, O Shevah, ... American Journal of Medical Genetics Part A 164 (5), 1204-1208, 2014 | 37 | 2014 |
| Prader-Willi syndrome: genetic tests and clinical findings C Fridman, MC Varela, F Kok, N Setian, CP Koiffmann Genetic Testing 4 (4), 387-392, 2000 | 37 | 2000 |
| Association of a new polymorphism in ALOX12 gene with bipolar disorder C Fridman, ÉPB Ojopi, SP Gregório, EH Ikenaga, DH Moreno, ... European archives of psychiatry and clinical neuroscience 253, 40-43, 2003 | 33 | 2003 |
| Unusual clinical features in an Angelman syndrome patient with uniparental disomy due to a translocation 15q15q C Fridman, MC Varela, RD Nicholls, CP Koiffmann Clinical genetics 54 (4), 303-308, 1998 | 32 | 1998 |
| Brazilian population profile of 15 STR markers C Fridman, PCC dos Santos, P Kohler, CF Garcia, LF Lopez, E Massad, ... Forensic Science International: Genetics 2 (2), e1-e4, 2008 | 27 | 2008 |
| Haplotype diversity in mitochondrial DNA hypervariable region in a population of southeastern Brazil C Fridman, RS Gonzalez, AC Pereira, M Cardena International journal of legal medicine 128, 589-593, 2014 | 24 | 2014 |
| O genoma humano e as perspectivas para o estudo da esquizofrenia EPB Ojopi, SP Gregorio, PEM Guimarães, C Fridman, E Dias Neto Archives of Clinical Psychiatry (São Paulo) 31, 9-18, 2004 | 23 | 2004 |
| Male lineages in Brazilian populations and performance of haplogroup prediction tools J Jannuzzi, J Ribeiro, C Alho, GOL e Arão, R Cicarelli, HSD Corrêa, ... Forensic Science International: Genetics 44, 102163, 2020 | 22 | 2020 |
