List of works - Rodrigo Secolin

A Prediction Algorithm for Drug Response in Patients with Mesial Temporal Lobe Epilepsy Based on Clinical and Genetic Information

scientific article

A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population.

scientific article published on 13 August 2015

A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27

scientific article published on 01 May 2008

Acute liver failure is associated with altered cerebral expression profiles of long non-coding RNAs.

scientific article published on 22 June 2017

Analysis of energetically biased transcripts of viruses and transposable elements

scientific article published on 13 November 2012

Association between IL8 haplotypes and pathogen levels in chronic periodontitis

scientific article published on 10 May 2013

Association between interleukin-8 levels and chronic periodontal disease: A PRISMA-compliant systematic review and meta-analysis

scientific article published on June 2017

Association of matrix metalloproteinase gene polymorphism with temporomandibular joint degeneration

scientific article published on 01 February 2011

Clinical outcomes of periodontal therapy are not influenced by the ATC/TTC haplotype in the IL8 gene.

scientific article published on 29 August 2013

Demographic history differences between Hispanics and Brazilians imprint haplotype features

scientific article published in 2022

Distribution of local ancestry and evidence of adaptation in admixed populations

scientific article published on 25 September 2019

Dysregulation of NEUROG2 plays a key role in focal cortical dysplasia.

scientific article published on 20 February 2018

Elevated micronucleus frequency in patients with type 2 diabetes, dyslipidemia and periodontitis.

scientific article published on 18 September 2014

Evidence that polymorphisms in detoxification genes modulate the susceptibility for sporadic medullary thyroid carcinoma.

scientific article published on 2 November 2011

Family-Based Genetic Association for Molar-Incisor Hypomineralization

scientific article published on 14 May 2016

Family-based association study for bipolar affective disorder.

scientific article published in June 2010

Genetic association study between Interleukin 10 gene and dental implant loss

scientific article published on 16 March 2012

Genetic interaction of GSH metabolic pathway genes in cystic fibrosis

scientific article

Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients

scientific article

Haplotypes of susceptibility to chronic periodontitis in the Interleukin 8 gene do not influence protein level in the gingival crevicular fluid

scientific article published on 09 August 2012

Inducible Nitric Oxide Synthase Polymorphisms and Nitric Oxide Levels in Individuals with Chronic Periodontitis.

scientific article

Is cerebral microbleed prevalence relevant as a biomarker in amnestic mild cognitive impairment and mild Alzheimer's disease?

scientific article published in January 2017

LINKGEN: a new algorithm to process data in genetic linkage studies.

scientific article

Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy

scientific article published on April 2015

Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy.

scientific article

Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras

scientific article published in November 2003

MicroRNA hsa-miR-134 is a circulating biomarker for mesial temporal lobe epilepsy.

scientific article

Neurocysticercotic Calcifications and Hippocampal Sclerosis: A Case-Control Study

scientific article published on July 2015

Normal ATXN3 Allele but Not CHIP Polymorphisms Modulates Age at Onset in Machado-Joseph Disease.

scientific article published on 19 November 2012

PER2 rs2304672, CLOCK rs1801260, and PER3 rs57875989 polymorphisms are not associated with juvenile myoclonic epilepsy

scientific article

Polymorphisms of cell cycle control genes influence the development of sporadic medullary thyroid carcinoma.

scientific article published in December 2014

Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function

article

Preliminary Analysis of the Nonsynonymous Polymorphism rs17563 in BMP4 Gene in Brazilian Population Suggests Protection for Nonsyndromic Cleft Lip and Palate

scientific article

Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorder

scientific article published on 31 December 2012

SLC23A2-05 (rs4987219) and KRAS-LCS6 (rs61764370) polymorphisms in patients with squamous cell carcinoma of the head and neck

scientific article

Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy

scientific article published in February 2010

Study of candidate genes for dyslexia in Brazilian individuals.

scientific article published on 7 November 2013

THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy

scientific article published on 17 August 2006

TSHR intronic polymorphisms (rs179247 and rs12885526) and their role in the susceptibility of the Brazilian population to Graves' disease and Graves' ophthalmopathy.

scientific article published on 28 December 2014

The Brazilian Initiative on Precision Medicine (BIPMed): fostering genomic data-sharing of underrepresented populations

scientific article published on 02 October 2020

The genetic architecture of the human cerebral cortex

scientific article

The periodized resistance training promotes similar changes in lipid profile in middle-aged men and women

scientific article published on 01 June 2012

p.Q192R SNP of PON1 seems not to be Associated with Carotid Atherosclerosis Risk Factors in an Asymptomatic and Normolipidemic Brazilian Population Sample.

scientific article published on 29 May 2015

List of works by Rodrigo Secolin

A Prediction Algorithm for Drug Response in Patients with Mesial Temporal Lobe Epilepsy Based on Clinical and Genetic Information

A multicentric association study between 39 genes and nonsyndromic cleft lip and palate in a Brazilian population.

A new candidate locus for bilateral perisylvian polymicrogyria mapped on chromosome Xq27

Acute liver failure is associated with altered cerebral expression profiles of long non-coding RNAs.

Analysis of energetically biased transcripts of viruses and transposable elements

Association between IL8 haplotypes and pathogen levels in chronic periodontitis

Association between interleukin-8 levels and chronic periodontal disease: A PRISMA-compliant systematic review and meta-analysis

Association of matrix metalloproteinase gene polymorphism with temporomandibular joint degeneration

Clinical outcomes of periodontal therapy are not influenced by the ATC/TTC haplotype in the IL8 gene.

Demographic history differences between Hispanics and Brazilians imprint haplotype features

Distribution of local ancestry and evidence of adaptation in admixed populations

Dysregulation of NEUROG2 plays a key role in focal cortical dysplasia.

Elevated micronucleus frequency in patients with type 2 diabetes, dyslipidemia and periodontitis.

Evidence that polymorphisms in detoxification genes modulate the susceptibility for sporadic medullary thyroid carcinoma.

Family-Based Genetic Association for Molar-Incisor Hypomineralization

Family-based association study for bipolar affective disorder.

Genetic association study between Interleukin 10 gene and dental implant loss

Genetic interaction of GSH metabolic pathway genes in cystic fibrosis

Genetic variation in CFH predicts phenytoin-induced maculopapular exanthema in European-descent patients

Haplotypes of susceptibility to chronic periodontitis in the Interleukin 8 gene do not influence protein level in the gingival crevicular fluid

Inducible Nitric Oxide Synthase Polymorphisms and Nitric Oxide Levels in Individuals with Chronic Periodontitis.

Is cerebral microbleed prevalence relevant as a biomarker in amnestic mild cognitive impairment and mild Alzheimer's disease?

LINKGEN: a new algorithm to process data in genetic linkage studies.

Lack of association between the prothrombin rs1799963 polymorphism and juvenile myoclonic epilepsy

Linkage study of voltage-gated potassium channels in familial mesial temporal lobe epilepsy.

Magnetic resonance imaging abnormalities in familial temporal lobe epilepsy with auditory auras

MicroRNA hsa-miR-134 is a circulating biomarker for mesial temporal lobe epilepsy.

Neurocysticercotic Calcifications and Hippocampal Sclerosis: A Case-Control Study

Normal ATXN3 Allele but Not CHIP Polymorphisms Modulates Age at Onset in Machado-Joseph Disease.

PER2 rs2304672, CLOCK rs1801260, and PER3 rs57875989 polymorphisms are not associated with juvenile myoclonic epilepsy

Polymorphisms of cell cycle control genes influence the development of sporadic medullary thyroid carcinoma.

Population analysis of the alpha hemoglobin stabilizing protein (AHSP) gene identifies sequence variants that alter expression and function

Preliminary Analysis of the Nonsynonymous Polymorphism rs17563 in BMP4 Gene in Brazilian Population Suggests Protection for Nonsyndromic Cleft Lip and Palate

Refinement of chromosome 3p22.3 region and identification of a susceptibility gene for bipolar affective disorder

SLC23A2-05 (rs4987219) and KRAS-LCS6 (rs61764370) polymorphisms in patients with squamous cell carcinoma of the head and neck

Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy

Study of candidate genes for dyslexia in Brazilian individuals.

THE SCN2A gene is not a likely candidate for familial mesial temporal lobe epilepsy

TSHR intronic polymorphisms (rs179247 and rs12885526) and their role in the susceptibility of the Brazilian population to Graves' disease and Graves' ophthalmopathy.

The Brazilian Initiative on Precision Medicine (BIPMed): fostering genomic data-sharing of underrepresented populations

The genetic architecture of the human cerebral cortex

The genetic architecture of the human cerebral cortex

The periodized resistance training promotes similar changes in lipid profile in middle-aged men and women

p.Q192R SNP of PON1 seems not to be Associated with Carotid Atherosclerosis Risk Factors in an Asymptomatic and Normolipidemic Brazilian Population Sample.