Filtros de búsqueda

Lista de obras de Andrew J Schork

1q21.1 distal copy number variants are associated with cerebral and cognitive alterations in humans

artículo científico publicado en 2021

A genome-wide association study of shared risk across psychiatric disorders implicates gene regulation during fetal neurodevelopment

artículo científico publicado en 2019

A large population-based investigation into the genetics of susceptibility to gastrointestinal infections and the link between gastrointestinal infections and mental illness

artículo científico publicado en 2020

A large-scale genomic investigation of susceptibility to infection and its association with mental disorders in the Danish population

scientific article published on 11 November 2019

A molecule-based genetic association approach implicates a range of voltage-gated calcium channels associated with schizophrenia

A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function

article

Abundant genetic overlap between blood lipids and immune-mediated diseases indicates shared molecular genetic mechanisms

artículo científico publicado en 2015

All SNPs are not created equal: genome-wide association studies reveal a consistent pattern of enrichment among functionally annotated SNPs

artículo científico publicado en 2013

An Empirical Bayes Mixture Model for Effect Size Distributions in Genome-Wide Association Studies

artículo científico publicado en 2015

Analysis of potential protein-modifying variants in 9000 endometriosis patients and 150000 controls of European ancestry

artículo científico publicado en 2017

Association Between Genetic Traits for Immune-Mediated Diseases and Alzheimer Disease

artículo científico publicado en 2016

Association between Mental Disorders and Subsequent Medical Conditions

artículo científico publicado en 2020

Association of Copy Number Variation of the 15q11.2 BP1-BP2 Region With Cortical and Subcortical Morphology and Cognition

artículo científico publicado en 2019

Author Correction: A new common functional coding variant at the DDC gene change renal enzyme activity and modify renal dopamine function

artículo científico publicado en 2020

Autonomic and hemodynamic origins of pre-hypertension: central role of heredity

artículo científico publicado en 2012

Beyond heritability: Improving discoverability in imaging genetics

artículo científico publicado en 2018

Common genetic variants influence human subcortical brain structures

artículo científico publicado en 2015

Conservation of Distinct Genetically-Mediated Human Cortical Pattern

artículo científico publicado en 2016

Correction: Abundant Genetic Overlap between Blood Lipids and Immune-Mediated Diseases Indicates Shared Molecular Genetic Mechanisms

artículo científico publicado en 2015

Correction: Dose response of the 16p11.2 distal copy number variant on intracranial volume and basal ganglia

artículo científico publicado en 2020

Correction: Improved Detection of Common Variants Associated with Schizophrenia and Bipolar Disorder Using Pleiotropy-Informed Conditional False Discovery Rate

artículo científico publicado en 2015

Covariate-modulated local false discovery rate for genome-wide association studies

artículo científico publicado en 2014

Dense genotyping of immune-related disease regions identifies nine new risk loci for primary sclerosing cholangitis.

artículo científico publicado en 2013

Dynamic changes in the copy number of pluripotency and cell proliferation genes in human ESCs and iPSCs during reprogramming and time in culture

artículo científico publicado en 2011

Enrichment of genetic markers of recent human evolution in educational and cognitive traits

artículo científico publicado en 2018

Estimating Effect Sizes and Expected Replication Probabilities from GWAS Summary Statistics

artículo científico publicado en 2016

Exploring Comorbidity Within Mental Disorders Among a Danish National Population

artículo científico publicado en 2019

Genes and environment: novel, functional polymorphism in the human cathepsin L (CTSL1) promoter disrupts a xenobiotic response element (XRE) to alter transcription and blood pressure

artículo científico publicado en 2012

Genetic Architecture of Subcortical Brain Structures in Over 40,000 Individuals Worldwide

scholarly article published 28 August 2017

Genetic Markers of Human Evolution Are Enriched in Schizophrenia

artículo científico publicado en 2015

Genetic Sharing with Cardiovascular Disease Risk Factors and Diabetes Reveals Novel Bone Mineral Density Loci

artículo científico publicado en 2015

Genetic analyses of gynecological disease identify genetic relationships between uterine fibroids and endometrial cancer, and a novel endometrial cancer genetic risk region at the WNT4 1p36.12 locus

artículo científico publicado en 2021

Genetic architecture of sporadic frontotemporal dementia and overlap with Alzheimer's and Parkinson's diseases

artículo científico publicado en 2016

Genetic architecture of subcortical brain structures in 38,851 individuals

scientific article published on 21 October 2019

Genetic assessment of age-associated Alzheimer disease risk: Development and validation of a polygenic hazard score

artículo científico publicado en 2017

Genetic correlations of polygenic disease traits: from theory to practice

artículo científico publicado en 2019

Genetic factors underlying the bidirectional relationship between autoimmune and mental disorders - findings from a Danish population-based study

artículo científico publicado en 2020

Genetic implication of a novel thiamine transporter in human hypertension

artículo científico publicado en 2014

Genetic overlap between multiple sclerosis and several cardiovascular disease risk factors

artículo científico publicado en 2016

Genetic predictors of educational attainment and intelligence test performance predict voter turnout

scientific article published on 09 November 2020

Genetic risks and clinical rewards

scientific article published on 01 September 2018

Genetic variation at the delta-sarcoglycan (SGCD) locus elevates heritable sympathetic nerve activity in human twin pairs

artículo científico publicado en 2013

Genetics of suicide attempts in individuals with and without mental disorders: a population-based genome-wide association study

artículo científico

Genome-wide Pleiotropy Between Parkinson Disease and Autoimmune Diseases

artículo científico publicado en 2017

Genome-wide analyses for personality traits identify six genomic loci and show correlations with psychiatric disorders

artículo científico publicado en 2016

Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals

artículo científico publicado en 2020

Heritability of Biomarkers of Oxidized Lipoproteins: Twin Pair Study

artículo científico publicado en 2015

Human Disease Variation in the Light of Population Genomics

artículo científico publicado en 2019

Human heart rate: heritability of resting and stress values in twin pairs, and influence of genetic variation in the adrenergic pathway at a microribonucleic acid (microrna) motif in the 3'-UTR of cytochrome b561 [corrected]

artículo científico publicado en 2013

Identification of Gene Loci That Overlap Between Schizophrenia and Educational Attainment

artículo científico publicado en 2016

Identification of novel loci affecting circulating chromogranins and related peptides.

artículo científico publicado en 2016

Identification of shared genetic variants between schizophrenia and lung cancer.

artículo científico publicado en 2018

Identifying Novel Gene Variants in Coronary Artery Disease and Shared Genes With Several Cardiovascular Risk Factors

artículo científico publicado en 2015

Identifying common genetic variants in blood pressure due to polygenic pleiotropy with associated phenotypes

artículo científico publicado en 2014

Improved detection of common variants associated with schizophrenia and bipolar disorder using pleiotropy-informed conditional false discovery rate

artículo científico publicado en 2013

Improved detection of common variants associated with schizophrenia by leveraging pleiotropy with cardiovascular-disease risk factors

artículo científico publicado en 2013

Integrated computational and experimental analysis of the neuroendocrine transcriptome in genetic hypertension identifies novel control points for the cardiometabolic syndrome

artículo científico publicado en 2012

Large-scale genome-wide association meta-analysis of endometriosis reveals 13 novel loci and genetically-associated comorbidity with other pain conditions

Large-scale genomics unveil polygenic architecture of human cortical surface area

artículo científico publicado en 2015

Leveraging Genomic Annotations and Pleiotropic Enrichment for Improved Replication Rates in Schizophrenia GWAS.

artículo científico publicado en 2016

Leveraging genome characteristics to improve gene discovery for putamen subcortical brain structure

artículo científico publicado en 2017

Meta-analysis identifies five novel loci associated with endometriosis highlighting key genes involved in hormone metabolism

artículo científico publicado en 2017

MicroRNAs enrichment in GWAS of complex human phenotypes

artículo científico publicado en 2015

Modeling prior information of common genetic variants improves gene discovery for neuroticism

artículo científico publicado en 2017

Modeling the 3D geometry of the cortical surface with genetic ancestry

artículo científico publicado en 2015

Neuropeptide Y (NPY): genetic variation in the human promoter alters glucocorticoid signaling, yielding increased NPY secretion and stress responses

artículo científico publicado en 2012

New statistical approaches exploit the polygenic architecture of schizophrenia--implications for the underlying neurobiology

artículo científico publicado en 2015

Novel Loci Associated With Attention-Deficit/Hyperactivity Disorder Are Revealed by Leveraging Polygenic Overlap With Educational Attainment

artículo científico publicado en 2017

Novel genetic loci associated with hippocampal volume

scientific article published on 18 January 2017

Novel genetic loci underlying human intracranial volume identified through genome-wide association

artículo científico publicado en 2016

O4.6. GENOME-WIDE ASSOCIATION STUDY, HERITABILITY ESTIMATION AND POLYGENIC RISK ANALYSIS OF SUSCEPTIBILITY TO INFECTIONS IN 65,534 INDIVIDUALS WITH SEVERE MENTAL DISORDERS AND POPULATION CONTROLS.

artículo científico publicado en 2018

Pleiotropic Analysis of Lung Cancer and Blood Triglycerides

artículo científico publicado en 2016

Polygenic Overlap Between C-Reactive Protein, Plasma Lipids, and Alzheimer Disease

artículo científico publicado en 2015

Probing the Association between Early Evolutionary Markers and Schizophrenia

artículo científico publicado en 2017

Restricted ethnic diversity in human embryonic stem cell lines

artículo científico publicado en 2010

Shared Molecular Neuropathology Across Major Psychiatric Disorders Parallels Polygenic Overlap

artículo científico publicado en 2019

Shared common variants in prostate cancer and blood lipids

artículo científico publicado en 2014

Shared molecular neuropathology across major psychiatric disorders parallels polygenic overlap.

artículo científico publicado en 2018

Spatial fine-mapping for gene-by-environment effects identifies risk hot spots for schizophrenia

scientific article published in Nature Communications

Subcortical brain volume differences in participants with attention deficit hyperactivity disorder in children and adults: a cross-sectional mega-analysis.

artículo científico publicado en 2017

The ENIGMA Consortium: large-scale collaborative analyses of neuroimaging and genetic data

artículo científico publicado en 2014

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 are associated with gestational duration

article

Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration

artículo científico publicado en 2019

Williams Syndrome neuroanatomical score associates with GTF2IRD1 in large-scale magnetic resonance imaging cohorts: a proof of concept for multivariate endophenotypes.

artículo científico publicado en 2018

Williams syndrome-specific neuroanatomical profile and its associations with behavioral features

artículo científico publicado en 2017

Dominio Público Uruguay está sostenido por:

Acerca de Dominio Público Uruguay

Ayuda