Lista de obras - Desmond Campbell - Dominio Público Uruguay

A Single Nucleotide Variant in HNF-1β is Associated with Maturity-Onset Diabetes of the Young in a Large Chinese Family

artículo científico publicado en 2016

Amerind ancestry, socioeconomic status and the genetics of type 2 diabetes in a Colombian population

artículo científico publicado en 2012

CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.

artículo científico publicado en 2013

CYP2C19 genotype predicts steady state escitalopram concentration in GENDEP.

artículo científico publicado en 2011

Cognitive impairment among children at-risk for schizophrenia

artículo científico publicado en 2013

Computation of individual latent variable scores from data with multiple missingness patterns.

artículo científico publicado en 2006

Cost effective assay choice for rare disease study designs

artículo científico publicado en 2015

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

artículo científico publicado en 2014

DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage.

artículo científico publicado en 2008

Erratum: Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort

artículo científico publicado en 2015

Erratum: The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

article

Error in sample size formula

artículo científico publicado en 2014

Gene Variants at Loci Related to Blood Pressure Account for Variation in Response to Antihypertensive Drugs Between Black and White Individuals

artículo científico publicado en 2019

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

artículo científico publicado en 2016

Genome-wide association study of Tourette's syndrome

artículo científico publicado en 2013

Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations

artículo científico publicado en 2014

Interplay between Schizophrenia Polygenic Risk Score and Childhood Adversity in First-Presentation Psychotic Disorder: A Pilot Study.

artículo científico publicado en 2016

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings

artículo científico publicado en 2008

Local True Discovery Rate Weighted Polygenic Scores Using GWAS Summary Data.

artículo científico publicado en 2016

Multifactorial disease risk calculator: Risk prediction for multifactorial disease pedigrees

artículo científico publicado en 2017

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

artículo científico publicado en 2013

Personality traits are linked to crime among men and women: evidence from a birth cohort

artículo científico publicado en 1994

Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort

artículo científico publicado en 2014

Reconstructing Native American population history

artículo científico publicado en 2012

Sacral agenesis: a pilot whole exome sequencing and copy number study

artículo científico publicado en 2016

Salt stress in the renal tubules is linked to TAL-specific expression of uromodulin and an upregulation of heat shock genes

article

Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates

artículo científico publicado en 2010

Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes

artículo científico publicado en 2009

Suicidal ideation during treatment of depression with escitalopram and nortriptyline in genome-based therapeutic drugs for depression (GENDEP): a clinical trial

artículo científico publicado en 2009

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

artículo científico publicado en 2006

The emerging molecular architecture of schizophrenia, polygenic risk scores and the clinical implications for GxE research

artículo científico publicado en 2014

Two subtypes of intervertebral disc degeneration distinguished by large-scale population-based study.

artículo científico publicado en 2016

Lista de obras de Desmond Campbell

A Single Nucleotide Variant in HNF-1β is Associated with Maturity-Onset Diabetes of the Young in a Large Chinese Family

Amerind ancestry, socioeconomic status and the genetics of type 2 diabetes in a Colombian population

CNV analysis in Tourette syndrome implicates large genomic rearrangements in COL8A1 and NRXN1.

CYP2C19 genotype predicts steady state escitalopram concentration in GENDEP.

Cognitive impairment among children at-risk for schizophrenia

Computation of individual latent variable scores from data with multiple missingness patterns.

Cost effective assay choice for rare disease study designs

Cross-disorder genome-wide analyses suggest a complex genetic relationship between Tourette's syndrome and OCD.

DSM-IV combined type ADHD shows familial association with sibling trait scores: a sampling strategy for QTL linkage.

Erratum: Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort

Erratum: The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

Error in sample size formula

Gene Variants at Loci Related to Blood Pressure Account for Variation in Response to Antihypertensive Drugs Between Black and White Individuals

Genetic study of congenital bile-duct dilatation identifies de novo and inherited variants in functionally related genes

Genome-wide association study of Tourette's syndrome

Identifying gene-environment interactions in schizophrenia: contemporary challenges for integrated, large-scale investigations

Interplay between Schizophrenia Polygenic Risk Score and Childhood Adversity in First-Presentation Psychotic Disorder: A Pilot Study.

Linkage to chromosome 1p36 for attention-deficit/hyperactivity disorder traits in school and home settings

Local True Discovery Rate Weighted Polygenic Scores Using GWAS Summary Data.

Multifactorial disease risk calculator: Risk prediction for multifactorial disease pedigrees

Partitioning the heritability of Tourette syndrome and obsessive compulsive disorder reveals differences in genetic architecture

Personality traits are linked to crime among men and women: evidence from a birth cohort

Reciprocal causation models of cognitive vs volumetric cerebral intermediate phenotypes for schizophrenia in a pan-European twin cohort

Reconstructing Native American population history

Sacral agenesis: a pilot whole exome sequencing and copy number study

Salt stress in the renal tubules is linked to TAL-specific expression of uromodulin and an upregulation of heat shock genes

Software for generating liability distributions for pedigrees conditional on their observed disease states and covariates

Strong association of socioeconomic status with genetic ancestry in Latinos: implications for admixture studies of type 2 diabetes

Suicidal ideation during treatment of depression with escitalopram and nortriptyline in genome-based therapeutic drugs for depression (GENDEP): a clinical trial

The analysis of 51 genes in DSM-IV combined type attention deficit hyperactivity disorder: association signals in DRD4, DAT1 and 16 other genes

The emerging molecular architecture of schizophrenia, polygenic risk scores and the clinical implications for GxE research

Two subtypes of intervertebral disc degeneration distinguished by large-scale population-based study.