Sandra Leistner-Segal

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Roberto GiuglianiHead of Rare Diseases DASA, Founder CASA DOS RAROS, Med Genet Serv HCPA, Dep Genetics & PPGBM UFRGSEmail confirmado em hcpa.edu.br
Gisele Gus ManfroUniversidade Federal do Rio Grande do Sul/Hospital de Clínicas de Porto AlegreEmail confirmado em hcpa.edu.br
Ida SchwartzProfessor, Federal University of Rio Grande do SulEmail confirmado em hcpa.edu.br
Carolina Blaya DreherHCPA - Ufrgs - UfcspaEmail confirmado em hcpa.edu.br
Giovanni Abrahão SalumChild Mind InstituteEmail confirmado em childmind.org
Marino Bianchin, Marino Muxfeldt Bian...Universidade Federal do Rio Grande do SulEmail confirmado em hcpa.edu.br
Angelina AcostaProfessora da Faculdade de Medicina da Bahia da Universidade Federal da BahiaEmail confirmado em ufba.br
Ursula MatteHospital de Clinicas de Porto AlegreEmail confirmado em hcpa.edu.br
MARIA TERESA V SANSEVERINOProfessora adjunta de Genética Medica da Escola de Medicina da Pontificia Universidade Catolica doEmail confirmado em pucrs.br
Chong Ae KimProfessora Associada do Departamento de Pediatria FMUSPEmail confirmado em hc.fm.usp.br
José Augusto BragattiHospital de Clínicas de Porto AlegreEmail confirmado em hcpa.edu.br
Laura Bannach JardimProfessora da Faculdade de Medicina, Universidade Federal do Rio Grande do Sul, e Serviço deEmail confirmado em hcpa.edu.br
Jose Antonio de Azevedo MagalhaesProfessor de Medicina do Hospital de Clinicas de Porto Alegre/ Universidade Federal do Rio Grande do SulEmail confirmado em hcpa.ufrgs.br
Filippo Pinto e VairoMayo ClinicEmail confirmado em mayo.edu
Temis Maria FelixHospital de Clínicas de Porto AlegreEmail confirmado em hcpa.edu.br
Jordan SmollerMassachusetts General HospitalEmail confirmado em broadinstitute.org
Diogo André PilgerUniversidade Federal do Rio Grande do SulEmail confirmado em ufrgs.br
shunji tomatsuAIDHCEmail confirmado em nemours.org
Fernanda Sales Luiz ViannaUniversidade Federal do Rio Grande do SulEmail confirmado em hcpa.edu.br
Gabriela PasqualimUniversidade Federal do Rio GrandeEmail confirmado em furg.br

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Sandra Leistner-Segal

Hospital de Clínicas de Porto Alegre/Medical Genetics Service/Molecular Genetics Laboratory

Email confirmado em hcpa.edu.br

Human Molecular Genetics/ Molecular Diagnosis of Familial Disorders


Título Ordenar por citações Ordenar por ano Ordenar por título	Citado por Citado por	Ano
A clinical study of 77 patients with mucopolysaccharidosis type II IVD Schwartz, MG Ribeiro, JG Mota, MBP Toralles, P Correia, D Horovitz, ... Acta Paediatrica 96, 63-70, 2007	176	2007
Hematopoietic stem cell transplantation for patients with mucopolysaccharidosis II F Kubaski, H Yabe, Y Suzuki, T Seto, T Hamazaki, RW Mason, L Xie, ... Biology of Blood and Marrow Transplantation 23 (10), 1795-1803, 2017	103	2017
Lack of association between the Serotonin Transporter Promoter Polymorphism (5-HTTLPR) and Panic Disorder: a systematic review and meta-analysis C Blaya, GA Salum, MS Lima, S Leistner-Segal, GG Manfro Behavioral and brain functions 3, 1-10, 2007	94	2007
Detection of human bocavirus and human metapneumovirus by real-time PCR from patients with respiratory symptoms in Southern Brazil DA Pilger, VV Cantarelli, SL Amantea, S Leistner-Segal Memorias do Instituto Oswaldo Cruz 106, 56-60, 2011	87	2011
Diagnosis of mucopolysaccharidoses F Kubaski, F de Oliveira Poswar, K Michelin-Tirelli, MG Burin, ... Diagnostics 10 (3), 172, 2020	82	2020
Diagnostic and treatment strategies in mucopolysaccharidosis VI F Vairo, A Federhen, G Baldo, M Riegel, M Burin, S Leistner-Segal, ... The application of clinical genetics, 245-255, 2015	82	2015
The multidimensional evaluation and treatment of anxiety in children and adolescents: rationale, design, methods and preliminary findings GA Salum, LR Isolan, VL Bosa, AG Tocchetto, SP Teche, I Schuch, ... Brazilian Journal of Psychiatry 33, 181-195, 2011	74	2011
The BDNF Val66Met polymorphism is an independent risk factor for high lethality in suicide attempts of depressed patients LC Schenkel, J Segal, JA Becker, GG Manfro, MM Bianchin, ... Progress in Neuro-Psychopharmacology and Biological Psychiatry 34 (6), 940-944, 2010	73	2010
Intellectual disability in a birth cohort: prevalence, etiology, and determinants at the age of 4 years SM Karam, AJD Barros, A Matijasevich, IS Dos Santos, L Anselmi, ... Public Health Genomics 19 (5), 290-297, 2016	61	2016
Molecular testing of 163 patients with Morquio A (Mucopolysaccharidosis IVA) identifies 39 novel GALNS mutations A Morrone, KL Tylee, M Al-Sayed, AC Brusius-Facchin, A Caciotti, ... Molecular Genetics and Metabolism 112 (2), 160-170, 2014	61	2014
Mucopolysaccharidosis type II: identification of 30 novel mutations among Latin American patients AC Brusius-Facchin, IVD Schwartz, C Zimmer, MG Ribeiro, AX Acosta, ... Molecular genetics and metabolism 111 (2), 133-138, 2014	56	2014
Panic disorder and serotonergic genes (SLC6A4, HTR1A and HTR2A): association and interaction with childhood trauma and parenting C Blaya, GA Salum, P Moorjani, AC Seganfredo, E Heldt, ... Neuroscience letters 485 (1), 11-15, 2010	55	2010
Genetic studies in a cluster of mucopolysaccharidosis type VI patients in Northeast Brazil FM Costa-Motta, AX Acosta, K Abé-Sandes, F Bender, IVD Schwartz, ... Molecular Genetics and Metabolism 104 (4), 603-607, 2011	53	2011
A community-based study of mucopolysaccharidosis type VI in Brazil: the influence of founder effect, endogamy and consanguinity FM Costa-Motta, F Bender, A Acosta, K Abé-Sandes, T Machado, ... Human heredity 77 (1-4), 189-196, 2014	50	2014
Mucopolysaccharidosis type VI: Identification of novel mutations on the arylsulphatase B gene in South American patients MFG Petry, K Nonemacher, JC Sebben, IVD Schwartz, ACM Azevedo, ... Journal of inherited metabolic disease 28, 1027-1034, 2005	45	2005
Prevalence of 185delAG and 5382insC mutations in BRCA1, and 6174delT in BRCA2 in women of Ashkenazi Jewish origin in southern Brazil CV Dillenburg, IC Bandeira, TV Tubino, LG Rossato, ES Dias, ... Genetics and molecular biology 35, 599-602, 2012	43	2012
Analysis of KIR gene frequencies and HLA class I genotypes in breast cancer and control group MR Jobim, M Jobim, PH Salim, P Portela, LF Jobim, S Leistner-Segal, ... Human Immunology 74 (9), 1130-1133, 2013	42	2013
Val66Met polymorphism association with serum BDNF and inflammatory biomarkers in major depression MA Caldieraro, M McKee, S Leistner-Segal, EA Vares, F Kubaski, ... The World Journal of Biological Psychiatry 19 (5), 402-409, 2018	41	2018
Serotonin transporter gene (5HTT) polymorphisms and temporal lobe epilepsy LC Schenkel, JA Bragatti, CM Torres, KC Martin, G Gus-Manfro, ... Epilepsy Research 95 (1-2), 152-157, 2011	40	2011
Evidence of association between Val66Met polymorphism at BDNF gene and anxiety disorders in a community sample of children and adolescents A Tocchetto, GA Salum, C Blaya, S Teche, L Isolan, A Bortoluzzi, ... Neuroscience letters 502 (3), 197-200, 2011	39	2011

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