Probing genetic overlap among complex human phenotypes

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Disease network delineates the disease progression profile of cardiovascular diseases

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Gene-Rich Large Deletions Are Overrepresented in POAG Patients of Indian and Caucasian Origins

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The Aberrant Connectivity Hypothesis in Schizophrenia

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Integrated molecular, clinical, and ontological analysis identifies overlooked disease relationshipsPreprint

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Overlap of genetic factors among craniosynostosis and autism spectrum disorder: the presence of autistic cases without craniosynostosis in carriers of shared variants

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A Multi‐Dimensional Approach to Map Disease Relationships Challenges Classical Disease Views

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Biomechanisms of Comorbidity: Reviewing Integrative Analyses of Multi-omics Datasets and Electronic Health Records

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Biobanking across the phenome - at the center of chronic disease research

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Network-Based Analysis of Comorbidities: Case Study of Diabetes Mellitus

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Phenotypic categorization of genetic skin diseases reveals new relations between phenotypes, genes and pathways

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Pan-disease clustering analysis of the trend of period prevalence

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The Genetic Basis of Phenotypic Diversity: Autism as an Extreme Tail of a Complex Dimensional Trait

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Decoding Neuromuscular Disorders Using Phenotypic Clusters Obtained From Co-Occurrence Networks

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Associations between Multimorbidity Patterns and Subsequent Labor Market Marginalization among Refugees and Swedish-Born Young Adults—A Nationwide Registered-Based Cohort Study

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Linking traits based on their shared molecular mechanisms

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Systems biology: An emerging strategy for discovering novel pathogenetic mechanisms that promote cardiovascular disease

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Disease universe: Visualisation of population-wide disease-wide associationsPreprint

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How Data Anonymisation Techniques influence Disease Triage in Digital Health

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Dimensional and Categorical Approaches to Mental Illness

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Multimorbidity analysis with low condition counts: a robust Bayesian approach for small but important subgroups

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Hereditary Multiple Cerebral Cavernous Malformations Associated with Wilson Disease and Multiple Lipomatosis

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Autoimmune Disorders

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The architecture of co-morbidity networks of physical and mental health conditions in military veterans

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Genetic comorbidity of hypertension and bronchial asthma

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A network approach for the comorbidities of HIV/AIDS in Taiwan

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Developmental social vulnerability as the intrinsic origin of psychopathology: A paradigm shift from disease entities to psychiatric derivatives within human diversity

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Structure and dynamics of human complication-disease network

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A Network based Approach to Identify the Genetic Influence Caused by Associated Factors and Disorders for the Parkinsons Disease ProgressionPreprint

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Network Pharmacology to Aid the Drug Discovery Process

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Interconnectivity of human cellular metabolism and disease prevalence

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‘Stoned’: Schneiderian first-rank symptoms as a manifestation of bilateral obstructive urolithiasis

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Network Analysis of Comorbidities: Case Study of HIV/AIDS in Taiwan

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Viruses and Psychiatric Disorders

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The Origin of Population Diversity: Stochastic Interactions between a Modifier Variant and the Individual Genetic Background

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Retinoic Acid Signalling in Neuropsychiatric Disease: Possible Markers and Treatment Agents

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Behavioral and cognitive core domains shared between autism spectrum disorder and schizophrenia

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Downstream targets of GWAS-detected genes for breast, lung, and prostate and colon cancer converge to G1/S transition pathway

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Quantifying the Potential for Future Gene Therapy to Lower Lifetime Risk of Polygenic Late-Onset Diseases

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Translating genome wide association study results to associations among common diseases: In silico study with an electronic medical record

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Systems Biology Approaches to Study Disease Comorbidities

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Systematic Analysis of GWAS Data Reveals Genomic Hotspots for Shared Mechanisms between Neurodegenerative Diseases

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Disease networks and their contribution to disease understanding and drug repurposing: Evolution of the concept, techniques and data sourcesPreprint

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Genetic outline of the hermeneutics of the diseases connection phenomenon in human

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MOLECULAR GENETIC STUDIES OF COMORBIDITY

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Exploring Hepatocellular Carcinoma Pathogenesis: The Influence of Genetic Polymorphisms

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Immune Activity and Psychopathology

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A Network-Based Approach on Big Data for the Comorbidities of Urticaria

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Constructing Disease Comorbidity Networks Using Statistical Methods from Electronic Health Records

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Integrated Pleiotropic Gene Set Unveils Comorbidity Insights across Digestive Cancers and Other Diseases

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Preventing Common Hereditary Disorders through Time-Separated Twinning

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Phenome-Wide Association Study

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A multi-trait evaluation of network propagation for GWAS results

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Constructing and analyzing a disease network based on proteins

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Autism and Emotion: A Narrative Review

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Retinoid Signaling in the Central Nervous System

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Phenotype-guided disease investigation using bioinformatics.

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Cancer predisposition in children: genetics, phenotypes & screening

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A New Model for Mining Data on Shared Phenotypes for Autism, Schizophrenia, and Bipolar Illness

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3D Visualisation of the Radiological Features of Type II Collagenopathies Associated with Skeletal Dysplasias

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Association Study between Gene Expression and Multiple Relevant Phenotypes with Cluster Analysis

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Genome wide search for genetic determinants of habitual alcohol, tobacco and coffee use, obesity-related traits, response to mental and physical stress and hemodynamic traits

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Artificial intelligence applied to medical genetics

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Integration of heterogeneous data sources for identification of disease genes using computational techniques

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Schizophrenia and Affective Psychotic Disorders – Inputs from a Genetic Perspective

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The Science Behind Autism and the 'Developmental Disorders': Tortuous or Tortured?

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Biologically relevant subgroups within the schizophrenia syndrome

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Network Paradigm and Medicine: Achievements and Prospects

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Integrative Network Analysis Interweaves the Missing Links in Cardiomyopathy DiseasomePreprint

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Faculty Opinions recommendation of A nondegenerate code of deleterious variants in Mendelian loci contributes to complex disease risk.

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Authors' reply

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Creation of Networks for the Analysis of Disease Similarities

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Learning healthcare delivery network with longitudinal electronic health records data

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The Autoimmune Diseases

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Étude des anomalies du développement humain# un modèle d’analyse phénotypique

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Additional file 1 of High-risk multimorbidity patterns on the road to cardiovascular mortality

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Additional file 1 of Where do obesity and male infertility collide?

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Collective behavior of blood indicators in lung cancer

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Pleiotropic genes underlying genetic correlations across human diseases

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Network analysis of cultural funding in Brazil: uncovering regional differences and signatures

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Genetic-linkage mapping of complex hereditary disorders to a whole-genome molecular-interaction networkPreprint

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Sharing of Genes and Pathways Across Complex Phenotypes: A Multilevel Genome-Wide Analysis

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Bivariate causal mixture model quantifies polygenic overlap between complex traits beyond genetic correlation

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Identifying the genetic basis and molecular mechanisms underlying phenotypic correlation between complex human traits using a gene-based approachPreprint

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Charting the Landscape of Genetic Overlap Between Mental Disorders and Related Traits Beyond Genetic Correlation

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