Lista de obras - Minh Bui - Dominio Público Uruguay

Aetiological overlap between obsessive-compulsive related and anxiety disorder symptoms: multivariate twin study.

artículo científico publicado en 2015

Architecture of cortical bone determines in part its remodelling and structural decay

artículo científico publicado en 2013

Are the Relationships of Lean Mass and Fat Mass With Bone Microarchitecture Causal or Due to Familial Confounders? A Novel Study of Adult Female Twin Pairs

artículo científico publicado en 2020

Autism spectrum phenotype in males and females with fragile X full mutation and premutation

artículo científico publicado en 2007

Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation females.

artículo científico publicado en 2016

Cerebellar volume mediates the relationship between FMR1 mRNA levels and voluntary step initiation in males with the premutation.

artículo científico publicado en 2016

Childhood Lung Function Predicts Adult Chronic Obstructive Pulmonary Disease and Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome

artículo científico publicado en 2017

Childhood body mass index and adult mammographic density measures that predict breast cancer risk

artículo científico publicado en 2016

Chronic effects of stroke on hip bone density and tibial morphology: a longitudinal study.

artículo científico publicado en 2015

Common Pediatric Pain Disorders and Their Clinical Associations

artículo científico publicado en 2017

DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome

artículo científico publicado en 2020

Dairy food supplementation may reduce malnutrition risk in institutionalised elderly

artículo científico publicado en 2017

Delineation of the working memory profile in female FMR1 premutation carriers: the effect of cognitive load on ocular motor responses.

artículo científico publicado en 2015

Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis

artículo científico publicado en 2015

Development of the oral resistome during the first decade of life

scientific article published in 2023

Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots

artículo científico publicado en 2014

Effect of Turner's syndrome and X-linked imprinting on cognitive status: analysis based on pedigree data.

artículo científico publicado en 2005

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis

artículo científico publicado en 2003

Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis

artículo científico publicado en 2002

Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X.

artículo científico publicado en 2003

Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation

artículo científico publicado en 2014

Executive Dysfunction in Female FMR1 Premutation Carriers.

artículo científico publicado en 2016

Explaining variance in the cumulus mammographic measures that predict breast cancer risk: a twins and sisters study.

artículo científico publicado en 2013

Fracture risk and height: an association partly accounted for by cortical porosity of relatively thinner cortices

artículo científico publicado en 2013

Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study.

artículo científico publicado en 2012

Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study

artículo científico publicado en 2012

Genetic and environmental variances of bone microarchitecture and bone remodeling markers: a twin study

artículo científico publicado en 2015

Genetics of febrile seizure subtypes and syndromes: a twin study

artículo científico publicado en 2013

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

artículo científico publicado en 2016

Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype

artículo científico publicado en 2014

Genome-wide association analysis identifies three new breast cancer susceptibility loci

artículo científico publicado en 2012

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

artículo científico publicado en 2013

Growth in stature and head circumference in high-functioning autism and Asperger disorder during the first 3 years of life

artículo científico publicado en 2006

Hallux Valgus, By Nature or Nurture? A Twin Study

artículo científico publicado en 2016

Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-X.

artículo científico publicado en 2004

Immortalized Parkinson's disease lymphocytes have enhanced mitochondrial respiratory activity

artículo científico publicado en 2016

Irreversible Deterioration of Cortical and Trabecular Microstructure Associated With Breastfeeding

artículo científico publicado en 2016

MicroRNA related polymorphisms and breast cancer risk

artículo científico publicado en 2014

New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease

artículo científico publicado en 2012

Novel Blood Biomarkers Are Associated with White Matter Lesions in Fragile X- Associated Tremor/Ataxia Syndrome.

artículo científico publicado en 2016

Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women

artículo científico publicado en 2015

Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion.

artículo científico publicado en 2014

Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspective

artículo científico publicado en 2003

Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and pubert

artículo científico publicado en 2013

Remodeling markers are associated with larger intracortical surface area but smaller trabecular surface area: a twin study

artículo científico publicado en 2011

Serum 25-Hydroxyvitamin D Insufficiency in Search of a Bone Disease

artículo científico publicado en 2017

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

artículo científico publicado en 2009

The effects of stress-tension on depression and anxiety symptoms: evidence from a novel twin modelling analysis.

artículo científico publicado en 2016

The heterogeneity in femoral neck structure and strength

artículo científico publicado en 2013

Trabecular and cortical microstructure and fragility of the distal radius in women

artículo científico publicado en 2015

Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.

artículo científico publicado en 2006

White matter changes in patients with Parkinson's disease carrying small CGG expansion FMR1 alleles: a pilot study

artículo científico publicado en 2013

β-glucuronidase mRNA levels are correlated with gait and working memory in premutation females: understanding the role of FMR1 premutation alleles

artículo científico publicado en 2016

Lista de obras de Minh Bui

Aetiological overlap between obsessive-compulsive related and anxiety disorder symptoms: multivariate twin study.

Architecture of cortical bone determines in part its remodelling and structural decay

Are the Relationships of Lean Mass and Fat Mass With Bone Microarchitecture Causal or Due to Familial Confounders? A Novel Study of Adult Female Twin Pairs

Autism spectrum phenotype in males and females with fragile X full mutation and premutation

Brain structure and intragenic DNA methylation are correlated, and predict executive dysfunction in fragile X premutation females.

Cerebellar volume mediates the relationship between FMR1 mRNA levels and voluntary step initiation in males with the premutation.

Childhood Lung Function Predicts Adult Chronic Obstructive Pulmonary Disease and Asthma-Chronic Obstructive Pulmonary Disease Overlap Syndrome

Childhood body mass index and adult mammographic density measures that predict breast cancer risk

Chronic effects of stroke on hip bone density and tibial morphology: a longitudinal study.

Common Pediatric Pain Disorders and Their Clinical Associations

DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome

Dairy food supplementation may reduce malnutrition risk in institutionalised elderly

Delineation of the working memory profile in female FMR1 premutation carriers: the effect of cognitive load on ocular motor responses.

Detection of skewed X-chromosome inactivation in Fragile X syndrome and X chromosome aneuploidy using quantitative melt analysis

Development of the oral resistome during the first decade of life

Early detection of fragile X syndrome: applications of a novel approach for improved quantitative methylation analysis in venous blood and newborn blood spots

Effect of Turner's syndrome and X-linked imprinting on cognitive status: analysis based on pedigree data.

Effect of fragile X status categories and FMRP deficits on cognitive profiles estimated by robust pedigree analysis

Effect of the deficits of fragile X mental retardation protein on cognitive status of fragile x males and females assessed by robust pedigree analysis

Effect of the fragile X status categories and the fragile X mental retardation protein levels on executive functioning in males and females with fragile X.

Evidence linking FMR1 mRNA and attentional demands of stepping and postural control in women with the premutation

Executive Dysfunction in Female FMR1 Premutation Carriers.

Explaining variance in the cumulus mammographic measures that predict breast cancer risk: a twins and sisters study.

Fracture risk and height: an association partly accounted for by cortical porosity of relatively thinner cortices

Fragile X mental retardation 1 (FMR1) intron 1 methylation in blood predicts verbal cognitive impairment in female carriers of expanded FMR1 alleles: evidence from a pilot study.

Fragile X-related element 2 methylation analysis may provide a suitable option for inclusion of fragile X syndrome and/or sex chromosome aneuploidy into newborn screening: a technical validation study

Genetic and environmental variances of bone microarchitecture and bone remodeling markers: a twin study

Genetics of febrile seizure subtypes and syndromes: a twin study

Genome-wide analysis identifies 12 loci influencing human reproductive behavior

Genome-wide association analysis identifies 11 risk variants associated with the asthma with hay fever phenotype

Genome-wide association analysis identifies three new breast cancer susceptibility loci

Genome-wide association studies identify four ER negative-specific breast cancer risk loci

Growth in stature and head circumference in high-functioning autism and Asperger disorder during the first 3 years of life

Hallux Valgus, By Nature or Nurture? A Twin Study

Hierarchical Bayes model for random haplotype and family effects in the transmission of fragile-X.

Immortalized Parkinson's disease lymphocytes have enhanced mitochondrial respiratory activity

Irreversible Deterioration of Cortical and Trabecular Microstructure Associated With Breastfeeding

MicroRNA related polymorphisms and breast cancer risk

New evidence for, and challenges in, linking small CGG repeat expansion FMR1 alleles with Parkinson's disease

Novel Blood Biomarkers Are Associated with White Matter Lesions in Fragile X- Associated Tremor/Ataxia Syndrome.

Novel methylation markers of the dysexecutive-psychiatric phenotype in FMR1 premutation women

Psychological status in female carriers of premutation FMR1 allele showing a complex relationship with the size of CGG expansion.

Relationship of deficits of FMR1 gene specific protein with physical phenotype of fragile X males and females in pedigrees: a new perspective

Relationships between age and epi-genotype of the FMR1 exon 1/intron 1 boundary are consistent with non-random X-chromosome inactivation in FM individuals, with the selection for the unmethylated state being most significant between birth and pubert

Remodeling markers are associated with larger intracortical surface area but smaller trabecular surface area: a twin study

Serum 25-Hydroxyvitamin D Insufficiency in Search of a Bone Disease

Small CGG repeat expansion alleles of FMR1 gene are associated with parkinsonism

The effects of stress-tension on depression and anxiety symptoms: evidence from a novel twin modelling analysis.

The heterogeneity in femoral neck structure and strength

Trabecular and cortical microstructure and fragility of the distal radius in women

Transcript levels of the intermediate size or grey zone fragile X mental retardation 1 alleles are raised, and correlate with the number of CGG repeats.

White matter changes in patients with Parkinson's disease carrying small CGG expansion FMR1 alleles: a pilot study

β-glucuronidase mRNA levels are correlated with gait and working memory in premutation females: understanding the role of FMR1 premutation alleles