Citation Impact
Citing Papers
Human Inborn Errors of Immunity: 2019 Update on the Classification from the International Union of Immunological Societies Expert Committee
2020 Standout
FoxP3+ T regulatory cells in cancer: Prognostic biomarkers and therapeutic targets
2020
Transcriptional and epigenetic basis of Treg cell development and function: its genetic anomalies or variations in autoimmune diseases
2020 StandoutNobel
Regulatory T cells in tumor microenvironment: new mechanisms, potential therapeutic strategies and future prospects
2020
DisGeNET: a comprehensive platform integrating information on human disease-associated genes and variants
2016 Standout
Toward an Optimized Process for Clinical Manufacturing of CAR-Treg Cell Therapy
2020
30 Years of NF-κB: A Blossoming of Relevance to Human Pathobiology
2017 Nobel
Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome/Velocardiofacial Syndrome)
2010
The STRING database in 2017: quality-controlled protein–protein association networks, made broadly accessible
2016 Standout
Selective loss of function variants in IL6ST cause Hyper-IgE syndrome with distinct impairments of T-cell phenotype and function
2018
Big data and machine learning algorithms for health-care delivery
2019 Standout
The Human Phenotype Ontology: Semantic Unification of Common and Rare Disease
2015
NRF2 and NF-қB interplay in cerebrovascular and neurodegenerative disorders: Molecular mechanisms and possible therapeutic approaches
2018 Standout
The non-canonical NF-κB pathway in immunity and inflammation
2017
OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
2014 Standout
Inflammation and tumor progression: signaling pathways and targeted intervention
2021 Standout
The JAK/STAT signaling pathway: from bench to clinic
2021 Standout
Settling the score: variant prioritization and Mendelian disease
2017
Primary immunodeficiencies
2009
Functional mapping and annotation of genetic associations with FUMA
2017 Standout
The Transcription Factor Foxp3 Shapes Regulatory T Cell Identity by Tuning the Activity of trans-Acting Intermediaries
2020
The Diverse Clinical Features of Chromosome 22q11.2 Deletion Syndrome (DiGeorge Syndrome)
2013
Deletion of PD-1 destabilizes the lineage identity and metabolic fitness of tumor-infiltrating regulatory T cells
2022
Metabolic Control of Treg Cell Stability, Plasticity, and Tissue-Specific Heterogeneity
2019
Lessons learned from the study of human inborn errors of innate immunity
2018
Targeting ferroptosis as a vulnerability in cancer
2022 Standout
Transcription factor Ikzf1 associates with Foxp3 to repress gene expression in Treg cells and limit autoimmunity and anti-tumor immunity
2024 StandoutNobel
New Treg cell-based therapies of autoimmune diseases: towards antigen-specific immune suppression
2020 StandoutNobel
ClinVar: public archive of interpretations of clinically relevant variants
2015 Standout
22q11.2 deletion syndrome
2015 Standout
NF-κB, inflammation, immunity and cancer: coming of age
2018 Standout
Tumor-infiltrating regulatory T cells as targets of cancer immunotherapy
2023 StandoutNobel
The IUPHAR/BPS Guide to PHARMACOLOGY in 2018: updates and expansion to encompass the new guide to IMMUNOPHARMACOLOGY
2017 Standout
Ontology learning algorithm for similarity measuring and ontology mapping using linear programming
2017 Standout
Classification, Ontology, and Precision Medicine
2018
STRING v11: protein–protein association networks with increased coverage, supporting functional discovery in genome-wide experimental datasets
2018 Standout
The DisGeNET knowledge platform for disease genomics: 2019 update
2019 Standout
2013 IDSA Clinical Practice Guideline for Vaccination of the Immunocompromised Host
2013 Standout
WebGestalt 2019: gene set analysis toolkit with revamped UIs and APIs
2019 Standout
Works of Karin Chen being referenced
Phevor Combines Multiple Biomedical Ontologies for Accurate Identification of Disease-Causing Alleles in Single Individuals and Small Nuclear Families
2014
Germline Mutations in NFKB2 Implicate the Noncanonical NF-κB Pathway in the Pathogenesis of Common Variable Immunodeficiency
2013
Long-term results of bone marrow transplantation in complete DiGeorge syndrome
2007
Autosomal Dominant Hyper-IgE Syndrome in the USIDNET Registry
2017
Functional reprogramming of regulatory T cells in the absence of Foxp3
2019