| PTCH gene mutations in odontogenic keratocysts DC Barreto, RS Gomez, AE Bale, WL Boson, L De Marco Journal of dental research 79 (6), 1418-1422, 2000 | 309 | 2000 |
| Report of 33 novel AVPR2 mutations and analysis of 117 families with X-linked nephrogenic diabetes insipidus MJ CRUMLEY, AK NAUMOVA, D MORIN, LA DE MARCO, BS KAPLAN, ... Journal of the American Society of Nephrology 11 (6), 1044-1054, 2000 | 228 | 2000 |
| HRPT2 gene alterations in ossifying fibroma of the jaws FJ Pimenta, LFG Silveira, GC Tavares, AC Silva, PF Perdigão, WH Castro, ... Oral oncology 42 (7), 735-739, 2006 | 145 | 2006 |
| Allelic loss from chromosome 11 in parathyroid tumors E Friedman, L De Marco, PV Gejman, JA Norton, AE Bale, GD Aurbach, ... Cancer Research 52 (24), 6804-6809, 1992 | 120 | 1992 |
| Normal structural dopamine type 2 receptor gene in prolactin-secreting and other pituitary tumors E Friedman, EF Adams, A Höög, PV Gejman, E Carson, C Larsson, ... The Journal of Clinical Endocrinology & Metabolism 78 (3), 568-574, 1994 | 113 | 1994 |
| The effect of a muscle weight-bearing and aerobic exercise program on the body composition, muscular strength, biochemical markers, and bone mass of obese patients who have … L Campanha-Versiani, DAG Pereira, GA Ribeiro-Samora, AV Ramos, ... Obesity surgery 27 (8), 2129-2137, 2017 | 107 | 2017 |
| β-catenin mutations in craniopharyngiomas and pituitary adenomas E Oikonomou, DC Barreto, B Soares, LD Marco, M Buchfelder, EF Adams Journal of neuro-oncology 73 (3), 205-209, 2005 | 106 | 2005 |
| Carcinoid tumors frequently display genetic abnormalities involving chromosome 11 O Jakobovitz, D Nass, L DeMarco, AJ Barbosa, FB Simoni, G Rechavi, ... The Journal of Clinical Endocrinology & Metabolism 81 (9), 3164-3167, 1996 | 103 | 1996 |
| Sequence-specific" gene signatures" can be obtained by PCR with single specific primers at low stringency. SD Pena, G Barreto, AR Vago, L De Marco, FC Reinach, E Dias Neto, ... Proceedings of the National Academy of Sciences 91 (5), 1946-1949, 1994 | 97 | 1994 |
| A novel mutation of the cathepsin C gene in Papillon‐Lefevre syndrome VF Cury, JE Costa, RS Gomez, WL Boson, CG Loures, L De Marco Journal of periodontology 73 (3), 307-312, 2002 | 93 | 2002 |
| Decision-making impairment is related to serotonin transporter promoter polymorphism in a sample of patients with obsessive–compulsive disorder FF da Rocha, L Malloy-Diniz, NV Lage, MA Romano-Silva, LA de Marco, ... Behavioural brain research 195 (1), 159-163, 2008 | 84 | 2008 |
| Immunolocalization of PTCH protein in odontogenic cysts and tumors DC Barreto, AE Bale, L De Marco, RS Gomez Journal of dental research 81 (11), 757-760, 2002 | 83 | 2002 |
| Molecular and immunohistochemical investigation of protein kinase a regulatory subunit type 1A (PRKAR1A) in odontogenic myxomas PF Perdigão, SG Stergiopoulos, L De Marco, L Matyakhina, SA Boikos, ... Genes, Chromosomes and Cancer 44 (2), 204-211, 2005 | 82 | 2005 |
| Is the 5‐HTTLPR polymorphism associated with bipolar disorder or with suicidal behavior of bipolar disorder patients? FS Neves, G Silveira, MA Romano‐Silva, L Malloy‐Diniz, AA Ferreira, ... American Journal of Medical Genetics Part B: Neuropsychiatric Genetics 147 …, 2008 | 75 | 2008 |
| The 5-HTTLPR polymorphism, impulsivity and suicide behavior in euthymic bipolar patients LF Malloy-Diniz, FS Neves, PHP de Moraes, LA De Marco, ... Journal of affective disorders 133 (1-2), 221-226, 2011 | 73 | 2011 |
| Familial hyperparathyroidism: surgical outcome after 30 years of follow-up in three families with germline HRPT2 mutations MS Sarquis, LG Silveira, FJ Pimenta, EP Dias, BT Teh, E Friedman, ... Surgery 143 (5), 630-640, 2008 | 70 | 2008 |
| Thiopurine methyltransferase polymorphisms in a Brazilian population WL Boson, MA Romano-Silva, H Correa, RP Falcão, PV Teixeira-Vidigal, ... The pharmacogenomics journal 3 (3), 178-182, 2003 | 70 | 2003 |
| An association study between the Val66Met polymorphism of the BDNF gene and postpartum depression P Figueira, L Malloy-Diniz, SB Campos, DM Miranda, MA Romano-Silva, ... Archives of women's mental health 13 (3), 285-289, 2010 | 68 | 2010 |
| Novel mutations of the BSCL2 and AGPAT2 genes in 10 families with Berardinelli–Seip congenital generalized lipodystrophy syndrome DM Miranda, BL Wajchenberg, MR Calsolari, MJ Aguiar, JMCL Silva, ... Clinical Endocrinology 71 (4), 512-517, 2009 | 62 | 2009 |
| Novel mutations in the SH3BP2 gene associated with sporadic central giant cell lesions and cherubism VM Carvalho, PF Perdigão, FR Amaral, PEA De Souza, L De Marco, ... Oral diseases 15 (1), 106-110, 2009 | 61 | 2009 |
