Estudos de associação genética em epilepsia de lobo temporal mesial e acidente vascular cerebral

• Grant number: 13/19524-0
• Support Opportunities: Scholarships in Brazil - Post-Doctoral
• Start date: March 01, 2014
• End date: November 30, 2018
• Field of knowledge: Health Sciences - Medicine - Medical Clinics
• Principal Investigator: Fernando Cendes
• Grantee: Rodrigo Secolin
• Host Institution: Faculdade de Ciências Médicas (FCM). Universidade Estadual de Campinas (UNICAMP). Campinas , SP, Brazil
• Associated research grant: 13/07559-3 - BRAINN - The Brazilian Institute of Neuroscience and Neurotechnology., AP.CEPID
• Associated scholarship(s): 16/14423-9 - Studying the genetic structure of a population from a specific geographic region: a comparative study using common, rare and structural variants., BE.EP.PD

Abstract

Epilepsia and stroke are the most cause of death linked to neurological field in Brazil and worldwide. This project is inserted in Brazilian Institute of Neurosciences and Neurotechnology and its objective is to use several strategies to identify susceptibility genes for these two conditions.

Scientific publications

(The scientific publications listed on this page originate from the Web of Science or SciELO databases. Their authors have cited FAPESP grant or fellowship project numbers awarded to Principal Investigators or Fellowship Recipients, whether or not they are among the authors. This information is collected automatically and retrieved directly from those bibliometric databases.)

MAGALHAES, PEDRO H. M.; MORAES, HELENA T.; ATHIE, MARIA C. P.; SECOLIN, RODRIGO; LOPES-CENDES, ISCIA. New avenues in molecular genetics for the diagnosis and application of therapeutics to the epilepsies. Epilepsy & Behavior, v. 121, n. B, AUG 2021. (13/07559-3, 17/00648-1, 13/19524-0)

ROCHA, CRISTIANE S.; SECOLIN, RODRIGO; RODRIGUES, MAIRA R.; CARVALHO, BENILTON S.; LOPES-CENDES, ISCIA. The Brazilian Initiative on Precision Medicine (BIPMed): fostering genomic data-sharing of underrepresented populations. NPJ GENOMIC MEDICINE, v. 5, n. 1, p. 7-pg., 2020-10-02. (16/26173-7, 13/07559-3, 13/19524-0)