Lista de obras - Rodrigo Secolin - Dominio Público Uruguay

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

artículo científico publicado en 2017

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

artículo científico publicado en 2015

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

artículo científico publicado en 2008

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

artículo científico publicado en 2017

Analysis of energetically biased transcripts of viruses and transposable elements

artículo científico publicado en 2012

Association between IL8 haplotypes and pathogen levels in chronic periodontitis

artículo científico publicado en 2013

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

artículo científico publicado en 2017

Association of matrix metalloproteinase gene polymorphism with temporomandibular joint degeneration

artículo científico publicado en 2011

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

artículo científico publicado en 2013

Demographic history differences between Hispanics and Brazilians imprint haplotype features

artículo científico publicado en 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.

artículo científico publicado en 2018

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

artículo científico publicado en 2014

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

artículo científico publicado en 2011

Family-Based Genetic Association for Molar-Incisor Hypomineralization

scientific article published on 14 May 2016

Family-based association study for bipolar affective disorder.

artículo científico publicado en 2010

Genetic association study between Interleukin 10 gene and dental implant loss

artículo científico publicado en 2012

Genetic interaction of GSH metabolic pathway genes in cystic fibrosis

artículo científico publicado en 2013

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

artículo científico publicado en 2017

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

artículo científico publicado en 2012

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

artículo científico publicado en 2017

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

artículo científico publicado en 2017

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

artículo científico publicado en 2008

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

artículo científico publicado en 2015

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

artículo científico publicado en 2007

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

artículo científico publicado en 2003

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

artículo científico publicado en 2017

Neurocysticercotic Calcifications and Hippocampal Sclerosis: A Case-Control Study

artículo científico publicado en 2015

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

artículo científico publicado en 2012

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

artículo científico publicado en 2014

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

artículo científico publicado en 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

artículo científico publicado en 2012

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

artículo científico publicado en 2012

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

artículo científico publicado en 2014

Segregation analysis in mesial temporal lobe epilepsy with hippocampal atrophy

artículo científico publicado en 2010

Study of candidate genes for dyslexia in Brazilian individuals.

artículo científico publicado en 2013

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

artículo científico publicado en 2006

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

artículo científico publicado en 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

artículo científico publicado en 2020

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

artículo científico publicado en 2012

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

artículo científico publicado en 2015

Lista de obras de 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.