J. R. Oliveira

发表

In Silico Identification of New Genetic Variations as Potential Risk Factors for Alzheimer’s Disease in a Microarray-oriented Simulation

R. Lemos, CH Castelletti, J. L. Lima Filho, 2009, Journal of Molecular Neuroscience.

Exploring the Implications of INDELs in Neuropsychiatric Genetics: Challenges and Perspectives

R. Lemos, J. R. Oliveira, M. B. R. Souza, 2012, Journal of Molecular Neuroscience.

Immunodominant B cell epitope in SARS-CoV-2 RBD comprises a B.1.351 and P.1 mutation hotspot: implications for viral spread and antibody escape

H. Nakaya, G. Schmitz, D. Schechtman, 2021, medRxiv.

Vitamin-D receptor agonist calcitriol reduces calcification in vitro through selective upregulation of SLC20A2 but not SLC20A1 or XPR1

R. Lemos, J. R. Oliveira, T. Hagg, 2016, Scientific Reports.

Analysis of Candidate Genes at the IBGC1 Locus Associated with Idiopathic Basal Ganglia Calcification (“Fahr” Disease’)

D. Geschwind, E. Spiteri, G. Meroni, 2007, Journal of Molecular Neuroscience.

Analysis of candidate genes at the IBGC1 locus associated with idiopathic basal ganglia calcification ("Fahr's disease").

D. Geschwind, E. Spiteri, G. Meroni, 2007, Journal of molecular neuroscience : MN.

Primary brain calcification: an international study reporting novel variants and associated phenotypes

D. Geschwind, M. Vidailhet, D. Galasko, 2018, European Journal of Human Genetics.

First Report of a De Novo Mutation at SLC20A2 in a Patient with Brain Calcification

J. R. Oliveira, J. Ferreira, M. Keasey, 2014, Journal of Molecular Neuroscience.

Update and Mutational Analysis of SLC20A2: A Major Cause of Primary Familial Brain Calcification

Y. Crow, G. Coppola, D. Campion, 2015, Human mutation.

Genetic heterogeneity in familial idiopathic basal ganglia calcification (Fahr disease)

D H Geschwind, D B Calne, D. Geschwind, 2004, Neurology.

Analysis of the disease risk locus DXS1047 polymorphism in Brazilian Alzheimer patients

M. Zatz, J. R. Oliveira, V. Bahia, 2000, Molecular Psychiatry.

The use of apolipoprotein E genotype for preclinical detection of risk's group for Alzheimer's disease.

M. Passos-Bueno, M. Zatz, J. L. Lima Filho, 1997, American journal of medical genetics.

News about disturbances of neuronal migration bring views to bipolar disorder

J. R. Oliveira, 2000, Molecular Psychiatry.

Exploring the Implications of INDELs in Neuropsychiatric Genetics: Challenges and Perspectives

R. Lemos, J. R. Oliveira, M. B. R. Souza, 2012, Journal of Molecular Neuroscience.

Genetic heterogeneity for Duchenne-like muscular dystrophy (DLMD) based on linkage and 50 DAG analysis.

K. Campbell, M. Passos-Bueno, M. Zatz, 1993, Human molecular genetics.

Main clinical features of the three mapped autosomal recessive limb-girdle muscular dystrophies and estimated proportion of each form in 13 Brazilian families.

K. Bushby, T. Strachan, M. Passos-Bueno, 1996, Journal of medical genetics.

Revising the M235T Polymorphism Position for the AGT Gene and Reporting a Modifying Variant in the Brazilian Population with Potential Cardiac and Neural Impact

R. Lemos, J. R. Oliveira, C. Ayres, 2012, Journal of Molecular Neuroscience.

The short variant of the polymorphism within the promoter region of the serotonin transporter gene is a risk factor for late onset Alzheimer's disease

M. Passos-Bueno, M. Zatz, P. Otto, 1998, Molecular Psychiatry.

Obstructive Sleep Apnea Severity Correlates with Cellular and Plasma Oxidative Stress Parameters and Affective Symptoms

J. R. Oliveira, O. Lins, A. M. J. Lima, 2012, Journal of Molecular Neuroscience.

Combined Genome-Wide CSF Aβ-42’s Associations and Simple Network Properties Highlight New Risk Factors for Alzheimer’s Disease

Ivan G. Costa, G. Araújo, J. R. Oliveira, 2015, Journal of Molecular Neuroscience.

Analysis of Gene Expression Pattern and Neuroanatomical Correlates for SLC20A2 (PiT-2) Shows a Molecular Network with Potential Impact in Idiopathic Basal Ganglia Calcification (“Fahr’s Disease”)

J. R. Oliveira, R. J. G. D. Silva, I. Pereira, 2013, Journal of Molecular Neuroscience.

Analysis of the serotonin transporter polymorphism (5-HTTLPR) in Brazilian patients affected by dysthymia, major depression and bipolar disorder

M. Passos-Bueno, M. Zatz, H. Vallada, 2000, Molecular Psychiatry.

A novel locus for late onset amyotrophic lateral sclerosis/motor neurone disease variant at 20q13

M. Zatz, A. Nishimura, M. Vainzof, 2004, Journal of Medical Genetics.

Combined Genome-Wide CSF Aβ-42’s Associations and Simple Network Properties Highlight New Risk Factors for Alzheimer’s Disease

Ivan G. Costa, for the Alzheimer’s Disease Neuroimaging Initiative, G. Araújo, 2015, Journal of Molecular Neuroscience.

The study of genetic polymorphisms related to serotonin in Alzheimer's disease: a new perspective in a heterogenic disorder.

M. Zatz, J. R. Oliveira, 1999, Brazilian journal of medical and biological research = Revista brasileira de pesquisas medicas e biologicas.

Primary brain calcification in patients undergoing treatment with the biphosphanate alendronate

J. R. Oliveira, M. F. Oliveira, 2016, Scientific Reports.

Identical twins with Idiopathic Basal Ganglia Calcification ("Fahr's Disease") presenting with a remarkably similar pattern of neuroimaging findings.

M. Zatz, J. L. Lima Filho, J. R. Oliveira, 2009, Parkinsonism & related disorders.

XPR1: a Gene Linked to Primary Familial Brain Calcification Might Help Explain a Spectrum of Neuropsychiatric Disorders

J. R. Oliveira, D. Moura, 2015, Journal of Molecular Neuroscience.

MiR-9-5p Down-Regulates PiT2, but not PiT1 in Human Embryonic Kidney 293 Cells

J. R. Oliveira, M. Keasey, D. P. Paiva, 2017, Journal of Molecular Neuroscience.

The Genetics of Alzheimer’s Disease in Brazil: 10 Years of Analysis in a Unique Population

R. Lemos, J. R. Oliveira, Mayana Zatz, 2008, Journal of Molecular Neuroscience.

A comorbid case of familial Idiopathic Basal Ganglia Calcification ("Fahr´s Disease") associated with post-polio syndrome.

J. R. Oliveira, M. Oliveira, 2012, The Journal of neuropsychiatry and clinical neurosciences.

Phosphate Transporters Expression in Patients with Primary Familial Brain Calcifications

J. R. Oliveira, L. Pimentel, R. Lemos, 2017, Journal of Molecular Neuroscience.

The association of the short variant of the 5-HTTPLR polymorphism and the apoE4 allele does not increase the risk for late onset Alzheimer's disease

M. Passos-Bueno, M. Zatz, P. Otto, 1999, Molecular Psychiatry.

Improving Significance in Association Studies: a New Perspective for Association Studies Submitted to the Journal of Molecular Neuroscience

J. R. Oliveira, C. Charbonnier, G. Nicolas, 2015, Journal of Molecular Neuroscience.