Citation Impact
Citing Papers
2018 Guidelines for the Early Management of Patients With Acute Ischemic Stroke: A Guideline for Healthcare Professionals From the American Heart Association/American Stroke Association
2018 Standout
Guidelines for the Prevention of Stroke in Patients With Stroke and Transient Ischemic Attack
2014 Standout
Fungal microbiota dysbiosis in IBD
2016
Autoimmune Th17 Cells Induced Synovial Stromal and Innate Lymphoid Cell Secretion of the Cytokine GM-CSF to Initiate and Augment Autoimmune Arthritis
2018 StandoutNobel
P2RX7, a gene coding for a purinergic ligand-gated ion channel, is associated with major depressive disorder
2006
The Genetics of Major Depression
2014
Neutrophil-Derived Proteases Escalate Inflammation through Activation of IL-36 Family Cytokines
2016
Depression
2018 Standout
From stress to inflammation and major depressive disorder: A social signal transduction theory of depression.
2014 Standout
An Expanded View of Complex Traits: From Polygenic to Omnigenic
2017 Standout
Psoriasis
2014
Association of the paternally transmitted copy of common Valine allele of the Val66Met polymorphism of the brain-derived neurotrophic factor (BDNF) gene with susceptibility to ADHD
2005
Telomerase abrogation dramatically accelerates TRF2-induced epithelial carcinogenesis
2007
Elements of cancer immunity and the cancer–immune set point
2017 StandoutNature
Meta-analysis shows significant association between dopamine system genes and attention deficit hyperactivity disorder (ADHD)
2006
Support for association between ADHD and two candidate genes: NET1 and DRD1
2005
Genetic effects on gene expression across human tissues
2017 StandoutNature
Vascular dementia
2015 Standout
The epigenetic regulation of mammalian telomeres
2007
Psoriasis and Other Complex Trait Dermatoses: From Loci to Functional Pathways
2011
Associations of genetic polymorphisms of Siglecs with human diseases
2014
Evaluation of Asymmetric Dimethylarginine and Homocysteine in Microangiopathy-Related Cerebral Damage
2008
Host genetic variation impacts microbiome composition across human body sites
2015
Hallmarks of aging: An expanding universe
2023 Standout
Gene–environment interactions in psychiatry: joining forces with neuroscience
2006
The Human Intestinal Microbiome in Health and Disease
2016 Standout
Cellular Senescence in Cancer and Aging
2007 Standout
Epigenetic Studies of Psychosis: Current Findings, Methodological Approaches, and Implications for Postmortem Research
2010
Bayesian Test for Colocalisation between Pairs of Genetic Association Studies Using Summary Statistics
2014 Standout
The Science of Stroke: Mechanisms in Search of Treatments
2010 Standout
Estimation and testing of genotype and haplotype effects in case‐control studies: comparison of weighted regression and multiple imputation procedures
2006
Aspirin plus Clopidogrel as Secondary Prevention after Stroke or Transient Ischemic Attack: A Systematic Review and Meta-Analysis
2014 Standout
Psoriasis
2021 Standout
The role of regulatory variation in complex traits and disease
2015
A general framework for estimating the relative pathogenicity of human genetic variants
2014 Standout
Linking “big” personality traits to anxiety, depressive, and substance use disorders: A meta-analysis.
2010 Standout
Multiple sclerosis
2008 Standout
Metagenomic biomarker discovery and explanation
2011 Standout
The immunogenetics of Psoriasis: A comprehensive review
2015
Reactive oxygen species (ROS) as pleiotropic physiological signalling agents
2020 Standout
Psoriasis
2015 Standout
Activating CARD14 Mutations Are Associated with Generalized Pustular Psoriasis but Rarely Account for Familial Recurrence in Psoriasis Vulgaris
2015
Multimodal biomedical AI
2022 Standout
Crohn's disease
2016 Standout
Neutrophil extracellular traps in immunity and disease
2017 Standout
The gut microbiota and inflammatory bowel diseases
2016
A new multipoint method for genome-wide association studies by imputation of genotypes
2007 Standout
Deficient mismatch repair improves organismal fitness and survival of mice with dysfunctional telomeres
2007
Genes, endothelial function and cerebral small vessel disease in man
2007
Non-B DNA conformations, mutagenesis and disease
2007
Inclusion of a priori information in genome‐wide association analysis
2009
IL-1 and IL-36 are dominant cytokines in generalized pustular psoriasis
2017
Family‐based association study of serotonin transporter gene polymorphisms in attention deficit hyperactivity disorder: No evidence for association in UK and Taiwanese samples
2005
The genetic background of generalized pustular psoriasis: IL36RN mutations and CARD14 gain-of-function variants
2014
Mitochondria in the signaling pathways that control longevity and health span
2019
Physiology and Pathophysiology of Purinergic Neurotransmission
2007 Standout
Beyond diathesis stress: Differential susceptibility to environmental influences.
2009 Standout
Nod2: The intestinal gate keeper
2017
Integrative omics for health and disease
2018
Current understanding of the human microbiome
2018 Standout
PSORS2 Is Due to Mutations in CARD14
2012
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
2018 Standout
Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder
2011 Standout
Family-based association study of serotonergic candidate genes and attention-deficit/hyperactivity disorder in a German sample
2006
Psoriasis: a mixed autoimmune and autoinflammatory disease
2017
Maternal programming of defensive responses through sustained effects on gene expression
2006
Gut microbiota, metabolites and host immunity
2016 Standout
Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets
2016 Standout
Relations between multi-informant assessments of ADHD symptoms, DAT1, and DRD4.
2008
Characterizing the ADHD phenotype for genetic studies
2005
Proteobacteria: microbial signature of dysbiosis in gut microbiota
2015 Standout
Prenatal Smoking Exposure and Dopaminergic Genotypes Interact to Cause a Severe ADHD Subtype
2006
The Hallmarks of Aging
2013 Standout
Chromatin remodeller SMARCA4 recruits topoisomerase 1 and suppresses transcription-associated genomic instability
2016 StandoutNobel
Epigenetic Profiling in Schizophrenia and Major Mental Disorders
2009
Interleukin 7 receptor α chain ( IL7R ) shows allelic and functional association with multiple sclerosis
2007
The Pathobiology of Vascular Dementia
2013 Standout
The SNAP25 gene as a susceptibility gene contributing to attention-deficit hyperactivity disorder
2005
Dopamine and serotonin transporter genotypes moderate sensitivity to maternal expressed emotion: the case of conduct and emotional problems in attention deficit/hyperactivity disorder
2009
Human DNA methylomes at base resolution show widespread epigenomic differences
2009 StandoutNature
DNA methyltransferases control telomere length and telomere recombination in mammalian cells
2006
Joint Analysis of Functional Genomic Data and Genome-wide Association Studies of 18 Human Traits
2014
Single-cell transcriptomic analysis of Alzheimer’s disease
2019 StandoutNature
Low blood pressure during the acute period of ischemic stroke is associated with decreased survival
2014
Circulating Markers of Endothelial Dysfunction and Platelet Activation in Patients with Severe Symptomatic Cerebral Small Vessel Disease
2013
Endothelial Dysfunction in Lacunar Stroke: A Systematic Review
2009
Small RNAs are modified with N-glycans and displayed on the surface of living cells
2021 StandoutNobel
The IL-23/T17 pathogenic axis in psoriasis is amplified by keratinocyte responses
2013
Genetic insights into common pathways and complex relationships among immune-mediated diseases
2013
Guidelines for the Early Management of Patients With Acute Ischemic Stroke
2013 Standout
Update on Genetics of Stroke and Cerebrovascular Disease 2005
2006
Living Beyond Our Physiological Means
2009
A longitudinal study of epigenetic variation in twins
2010
Psoriasis Pathogenesis and Treatment
2019 Standout
Decrease in topoisomerase I is responsible for activation-induced cytidine deaminase (AID)-dependent somatic hypermutation
2011 StandoutNobel
Immunology of Psoriasis
2014 Standout
Interventions for deliberately altering blood pressure in acute stroke
2014
AID-induced decrease in topoisomerase 1 induces DNA structural alteration and DNA cleavage for class switch recombination
2009 StandoutNobel
Short-Term Blood Pressure Variability in Acute Stroke
2015
A polymorphism in the norepinephrine transporter gene alters promoter activity and is associated with attention-deficit hyperactivity disorder
2006
Religious Orders Study and Rush Memory and Aging Project
2018 Standout
Effect of Blood Pressure Lowering in Early Ischemic Stroke
2015
Interpreting non-coding variation in complex disease genetics
2012
European consensus statement on phenotypes of pustular psoriasis
2017
Changes of brachial flow-mediated vasodilation in different ischemic stroke subtypes
2006
Histone3 lysine4 trimethylation regulated by the facilitates chromatin transcription complex is critical for DNA cleavage in class switch recombination
2010 StandoutNobel
Modest Blood Pressure Reduction with Valsartan in Acute Ischemic Stroke: A Prospective, Randomized, Open-Label, Blinded-End-Point Trial
2015
Nod2 Deficiency Augments Th17 Responses and Exacerbates Autoimmune Arthritis
2018 StandoutNobel
Molecular Genetics of Attention-Deficit/Hyperactivity Disorder
2005 Standout
Works of Jo Knight being referenced
DNA pooling identifies association of the noradrenergic transporter gene (NET1) with attention deficit hyperactivity disorder (ADHD).
2003
Complex host genetics influence the microbiome in inflammatory bowel disease
2014
Effects of antihypertensive treatment after acute stroke in the Continue Or Stop post-Stroke Antihypertensives Collaborative Study (COSSACS): a prospective, randomised, open, blinded-endpoint trial
2010
Haplotype analysis of SNAP-25 suggests a role in the aetiology of ADHD
2004
Quantitative trait locus analysis of candidate gene alleles associated with attention deficit hyperactivity disorder (ADHD) in five genes: DRD4, DAT1, DRD5, SNAP‐25, and 5HT1B
2004
Whole genome linkage scan of recurrent depressive disorder from the depression network study
2005
Examining the role of common and rare mitochondrial variants in schizophrenia
2018
Mutations in IL36RN/IL1F5 Are Associated with the Severe Episodic Inflammatory Skin Disease Known as Generalized Pustular Psoriasis
2011
TTF-1 and RET promoter SNPs: regulation of RET transcription in Hirschsprung's disease
2004
Haplotype Association Analysis of Discrete and Continuous Traits Using Mixture of Regression Models
2004
Differential methylation of the X‐chromosome is a possible source of discordance for bipolar disorder female monozygotic twins
2007
A Common Haplotype of the Dopamine Transporter Gene Associated With Attention-Deficit/Hyperactivity Disorder and Interacting With Maternal Use of Alcohol During Pregnancy
2006
A pragmatic suggestion for dealing with results for candidate genes obtained from genome wide association studies
2007
Using Functional Annotation for the Empirical Determination of Bayes Factors for Genome-Wide Association Study Analysis
2011
DNA pooling analysis of ADHD and genes regulating vesicle release of neurotransmitters
2005
DNA pooling analysis of 21 norepinephrine transporter gene SNPs with attention deficit hyperactivity disorder: No evidence for association
2005
A Bayesian Method to Incorporate Hundreds of Functional Characteristics with Association Evidence to Improve Variant Prioritization
2014
Conditional analysis identifies three novel major histocompatibility complex loci associated with psoriasis
2012
Genetic epistasis regulates amyloid deposition in resilient aging
2017
Endothelial Nitric Oxide Gene Haplotypes and Risk of Cerebral Small-Vessel Disease
2004
Introduction to Genetic Association Studies
2012