Lista de obras - Hilary Coon - Dominio Público Uruguay

A diversified approach for PKU treatment: routine screening yields high incidence of psychiatric distress in phenylketonuria clinics

artículo científico publicado en 2012

A genome scan for loci influencing anti-atherogenic serum bilirubin levels

artículo científico publicado en 2002

A genome-wide scan for common alleles affecting risk for autism

scientific journal article

A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study

artículo científico publicado en 2002

A new NOS2 promoter polymorphism associated with increased nitric oxide production and protection from severe malaria in Tanzanian and Kenyan children

artículo científico publicado en 2002

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

artículo científico publicado en 2011

A simple method of model fitting for adoption data.

artículo científico publicado en 1990

A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.

artículo científico publicado en 2014

A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families

artículo científico publicado en 2010

APOH interacts with FTO to predispose to healthy thinness

artículo científico publicado en 2015

Altitude is a risk factor for completed suicide in bipolar disorder.

artículo científico publicado en 2014

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

artículo científico publicado en 2018

An investigation of the effects of lipid-lowering medications: genome-wide linkage analysis of lipids in the HyperGEN study

artículo científico publicado en 2007

Analysis of chromosome 18 DNA markers in multiplex pedigrees with manic depression

article

Analysis of chromosome 22 markers in nine schizophrenia pedigrees

article

Are there altered antibody responses to measles, mumps, or rubella viruses in autism?

artículo científico publicado en 2007

Are there enhanced MBP autoantibodies in autism?

artículo científico publicado en 2007

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

artículo científico publicado en 2015

Associations between phenylthiocarbamide gene polymorphisms and cigarette smoking

artículo científico publicado en 2005

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

artículo científico publicado en 2009

Autism spectrum disorder reclassified: a second look at the 1980s Utah/UCLA Autism Epidemiologic Study

artículo científico publicado en 2013

Autism, regression, and the broader autism phenotype

artículo científico publicado en 2002

C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families

article

Common genetic variants on 5p14.1 associate with autism spectrum disorders

artículo científico publicado en 2009

Comparative analysis of suicide, accidental, and undetermined cause of death classification

artículo científico publicado en 2014

Confirmation of the association of the C4B null allelle in autism

artículo científico publicado en 2005

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

artículo científico publicado en 2014

Current perspectives on the genetic analysis of autism.

artículo científico publicado en 2006

Developmental and genetic influences on the P50 sensory gating phenotype

artículo científico publicado en 1996

Differential Vulnerability to Early-Life Parental Death: The Moderating Effects of Family Suicide History on Risks for Major Depression and Substance Abuse in Later Life

artículo científico publicado en 2016

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

artículo científico publicado en 2013

Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q.

artículo científico publicado en 2004

Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree

artículo científico publicado en 2005

Excess Mortality and Causes of Death in Autism Spectrum Disorders: A Follow up of the 1980s Utah/UCLA Autism Epidemiologic Study ⬇️

artículo científico publicado el 1 de mayo de 2013

Familial Aggregation and Genome-Wide Linkage Analysis of Carotid Artery Plaque: The NHLBI Family Heart Study

article

Functional impact of global rare copy number variation in autism spectrum disorders

artículo científico publicado en 2010

Genetic and developmental factors in spontaneous selective attention: a study of normal twins ⬇️

artículo científico publicado el 8 de agosto de 1997

Genetic epidemiological study of schizophrenia in Palau, Micronesia: Prevalence and familiality

article

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

artículo científico publicado en 2013

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

artículo científico publicado en 2003

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

artículo científico publicado en 2009

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

artículo científico publicado en 2018

Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders

artículo científico publicado en 2010

Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study.

artículo científico publicado en 2004

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees ⬇️

artículo científico publicado el 8 de abril de 2010

Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide

article

Genomewide Multipoint Linkage Analysis of Seven Extended Palauan Pedigrees with Schizophrenia, by a Markov-Chain Monte Carlo Method ⬇️

artículo científico publicado el 19 de octubre de 2001

Genomic scan for genes predisposing to schizophrenia

article

Head circumference and height in autism: a study by the Collaborative Program of Excellence in Autism

artículo científico publicado en 2006

Heterogeneous association between engrailed-2 and autism in the CPEA network

artículo científico publicado en 2008

How relevant are GFAP autoantibodies in autism and Tourette Syndrome?

artículo científico publicado en 2007

Human Dopamine Transporter Gene Not Linked to Schizophrenia in Multigenerational Pedigrees

article

Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q

artículo científico publicado en 1999

Identifying Children in the Colorado Adoption Project at Risk for Conduct Disorder

artículo científico publicado en 1992

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

artículo científico publicado en 2012

Individual common variants exert weak effects on the risk for autism spectrum disorders

scientific journal article

Lineage: Visualizing Multivariate Clinical Data in Genealogy Graphs

artículo científico publicado en 2018

Linkage Analysis between Schizophrenia and Index Simple-Sequence Repeat Loci for Chromosome 21

article

Linkage Analysis of Schizophrenia: The D1 Dopamine Receptor Gene and Several Flanking DNA Markers

article

Linkage analysis of Tourette syndrome in a large Utah pedigree

artículo científico publicado en 2010

Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families

artículo científico publicado en 1999

Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat.

artículo científico publicado en 2002

Male suspected suicide decedents in Utah: A comparison of Veterans and nonveterans

artículo científico publicado en 2016

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

artículo científico publicado en 2007

Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

artículo científico publicado en 2015

Model-fitting and linkage analysis of sodium–lithium countertransport

article

Mutation scan of the D1 dopamine receptor gene in 22 cases of bipolar I disorder

article

Neuropathy target esterase gene mutations cause motor neuron disease

artículo científico publicado en 2008

No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.

artículo científico publicado en 2011

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

article

Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.

artículo científico publicado en 2018

Ocular motor delayed-response task performance among patients with schizophrenia and their biological relatives

artículo científico publicado en 2001

Parent-offspring and sibling adoption analyses of parental ratings of temperament in infancy and childhood

artículo científico publicado en 1991

Performance on Cambridge Neuropsychological Test Automated Battery subtests sensitive to frontal lobe function in people with autistic disorder: evidence from the Collaborative Programs of Excellence in Autism network

artículo científico publicado en 2004

Possible association between autism and variants in the brain-expressed tryptophan hydroxylase gene (TPH2).

artículo científico publicado en 2005

Predicting Diabetic Control from Competence, Adherence, Adjustment, and Psychopathology

article

Psychiatric comorbidity and medication use in adults with autism spectrum disorder.

artículo científico publicado en 2014

Psychiatric symptoms in adults with phenylketonuria.

artículo científico

SSCP at the HTR1DA locus

article

Schizophrenia and nicotinic receptors.

artículo científico publicado en 1994

Search for a gene predisposing to manic-depression on chromosome 21

article

Search for a schizophrenia susceptibility locus on human chromosome 22

article

Segregation analysis of HDL cholesterol in the NHLBI Family Heart Study and in Utah pedigrees.

artículo científico publicado en 2002

Severity of cough in idiopathic pulmonary fibrosis is associated with MUC5 B genotype.

artículo científico publicado en 2014

Smoking influences the association between apolipoprotein E and lipids: the National Heart, Lung, and Blood Institute Family Heart Study.

artículo científico publicado en 2000

Spatial relative risk patterns of autism spectrum disorders in Utah

artículo científico publicado en 2015

Synaptic, transcriptional and chromatin genes disrupted in autism

artículo científico publicado en 2014

Temporal lobe, autism, and macrocephaly.

artículo científico publicado en 2003

The Autism Simplex Collection: an international, expertly phenotyped autism sample for genetic and phenotypic analyses

artículo científico publicado en 2014

The PHQ-9 as a brief assessment of lifetime major depression

article

The sensitivity of the Spontaneous Selective Attention Test (SSAT): a study of schizophrenic inpatients and outpatients versus normal controls

artículo científico publicado en 1998

Twenty-year outcome for individuals with autism and average or near-average cognitive abilities

artículo científico publicado en 2009

Upstream stimulatory factor 1 associated with familial combined hyperlipidemia, LDL cholesterol, and triglycerides

artículo científico publicado en 2005

Use of a genealogical database demonstrates heritability of pulmonary fibrosis

artículo científico publicado en 2013

Use of a neurophysiological trait in linkage analysis of schizophrenia

article

Whole exome sequencing in extended families with autism spectrum disorder implicates four candidate genes

artículo científico publicado en 2015

Lista de obras de Hilary Coon

A diversified approach for PKU treatment: routine screening yields high incidence of psychiatric distress in phenylketonuria clinics

A genome scan for loci influencing anti-atherogenic serum bilirubin levels

A genome-wide scan for common alleles affecting risk for autism

A genome-wide screen reveals evidence for a locus on chromosome 11 influencing variation in LDL cholesterol in the NHLBI Family Heart Study

A new NOS2 promoter polymorphism associated with increased nitric oxide production and protection from severe malaria in Tanzanian and Kenyan children

A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

A simple method of model fitting for adoption data.

A unified test of linkage analysis and rare-variant association for analysis of pedigree sequence data.

A unified theory of autism revisited: linkage evidence points to chromosome X using a high-risk subset of AGRE families

APOH interacts with FTO to predispose to healthy thinness

Altitude is a risk factor for completed suicide in bipolar disorder.

An analytical framework for whole-genome sequence association studies and its implications for autism spectrum disorder

An investigation of the effects of lipid-lowering medications: genome-wide linkage analysis of lipids in the HyperGEN study

Analysis of chromosome 18 DNA markers in multiplex pedigrees with manic depression

Analysis of chromosome 22 markers in nine schizophrenia pedigrees

Are there altered antibody responses to measles, mumps, or rubella viruses in autism?

Are there enhanced MBP autoantibodies in autism?

Association of the OPRM1 Variant rs1799971 (A118G) with Non-Specific Liability to Substance Dependence in a Collaborative de novo Meta-Analysis of European-Ancestry Cohorts

Associations between phenylthiocarbamide gene polymorphisms and cigarette smoking

Autism genome-wide copy number variation reveals ubiquitin and neuronal genes

Autism spectrum disorder reclassified: a second look at the 1980s Utah/UCLA Autism Epidemiologic Study

Autism, regression, and the broader autism phenotype

C to T nucleotide substitution in codon 713 of amyloid precursor protein gene not found in 86 unrelated schizophrenics from multiplex families

Common genetic variants on 5p14.1 associate with autism spectrum disorders

Comparative analysis of suicide, accidental, and undetermined cause of death classification

Confirmation of the association of the C4B null allelle in autism

Convergence of genes and cellular pathways dysregulated in autism spectrum disorders

Current perspectives on the genetic analysis of autism.

Developmental and genetic influences on the P50 sensory gating phenotype

Differential Vulnerability to Early-Life Parental Death: The Moderating Effects of Family Suicide History on Risks for Major Depression and Substance Abuse in Later Life

Distinct loci in the CHRNA5/CHRNA3/CHRNB4 gene cluster are associated with onset of regular smoking

Evidence for a gene influencing fasting LDL cholesterol and triglyceride levels on chromosome 21q.

Evidence for linkage on chromosome 3q25-27 in a large autism extended pedigree

Excess Mortality and Causes of Death in Autism Spectrum Disorders: A Follow up of the 1980s Utah/UCLA Autism Epidemiologic Study ⬇️

Familial Aggregation and Genome-Wide Linkage Analysis of Carotid Artery Plaque: The NHLBI Family Heart Study

Functional impact of global rare copy number variation in autism spectrum disorders

Genetic and developmental factors in spontaneous selective attention: a study of normal twins ⬇️

Genetic epidemiological study of schizophrenia in Palau, Micronesia: Prevalence and familiality

Genetic relationship between five psychiatric disorders estimated from genome-wide SNPs

Genome scan meta-analysis of schizophrenia and bipolar disorder, part III: Bipolar disorder

Genome-wide analyses of exonic copy number variants in a family-based study point to novel autism susceptibility genes

Genome-wide de novo risk score implicates promoter variation in autism spectrum disorder

Genome-wide linkage analyses of two repetitive behavior phenotypes in Utah pedigrees with autism spectrum disorders

Genome-wide linkage analysis replicates susceptibility locus for fasting plasma triglycerides: NHLBI Family Heart Study.

Genome-wide linkage using the Social Responsiveness Scale in Utah autism pedigrees ⬇️

Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide

Genomewide Multipoint Linkage Analysis of Seven Extended Palauan Pedigrees with Schizophrenia, by a Markov-Chain Monte Carlo Method ⬇️

Genomic scan for genes predisposing to schizophrenia

Head circumference and height in autism: a study by the Collaborative Program of Excellence in Autism

Heterogeneous association between engrailed-2 and autism in the CPEA network

How relevant are GFAP autoantibodies in autism and Tourette Syndrome?

Human Dopamine Transporter Gene Not Linked to Schizophrenia in Multigenerational Pedigrees

Hyperparathyroidism-jaw tumor syndrome: the HRPT2 locus is within a 0.7-cM region on chromosome 1q

Identifying Children in the Colorado Adoption Project at Risk for Conduct Disorder

Increased genetic vulnerability to smoking at CHRNA5 in early-onset smokers

Individual common variants exert weak effects on the risk for autism spectrum disorders

Lineage: Visualizing Multivariate Clinical Data in Genealogy Graphs

Linkage Analysis between Schizophrenia and Index Simple-Sequence Repeat Loci for Chromosome 21

Linkage Analysis of Schizophrenia: The D1 Dopamine Receptor Gene and Several Flanking DNA Markers

Linkage analysis of Tourette syndrome in a large Utah pedigree

Linkage of a composite inhibitory phenotype to a chromosome 22q locus in eight Utah families

Linkage of creatinine clearance to chromosome 10 in Utah pedigrees replicates a locus for end-stage renal disease in humans and renal failure in the fawn-hooded rat.

Male suspected suicide decedents in Utah: A comparison of Veterans and nonveterans

Mapping autism risk loci using genetic linkage and chromosomal rearrangements

Microdeletions of ELP4 Are Associated with Language Impairment, Autism Spectrum Disorder, and Mental Retardation

Model-fitting and linkage analysis of sodium–lithium countertransport

Mutation scan of the D1 dopamine receptor gene in 22 cases of bipolar I disorder

Neuropathy target esterase gene mutations cause motor neuron disease

No evidence for IL1RAPL1 involvement in selected high-risk autism pedigrees from the AGRE data set.

Novel genes for autism implicate both excitatory and inhibitory cell lineages in risk

Novel pedigree analysis implicates DNA repair and chromatin remodeling in multiple myeloma risk.

Ocular motor delayed-response task performance among patients with schizophrenia and their biological relatives

Parent-offspring and sibling adoption analyses of parental ratings of temperament in infancy and childhood

Performance on Cambridge Neuropsychological Test Automated Battery subtests sensitive to frontal lobe function in people with autistic disorder: evidence from the Collaborative Programs of Excellence in Autism network

Possible association between autism and variants in the brain-expressed tryptophan hydroxylase gene (TPH2).

Predicting Diabetic Control from Competence, Adherence, Adjustment, and Psychopathology

Psychiatric comorbidity and medication use in adults with autism spectrum disorder.

Psychiatric symptoms in adults with phenylketonuria.

SSCP at the HTR1DA locus