Citation Impact
Citing Papers
RepeatModeler2 for automated genomic discovery of transposable element families
2020 Standout
Intracellular Nucleic Acid Sensors and Autoimmunity
2011 StandoutNobel
Autoimmune Th17 Cells Induced Synovial Stromal and Innate Lymphoid Cell Secretion of the Cytokine GM-CSF to Initiate and Augment Autoimmune Arthritis
2018 StandoutNobel
Schizophrenia risk from complex variation of complement component 4
2016 StandoutNature
iSVP: an integrated structural variant calling pipeline from high-throughput sequencing data
2013
An Expanded View of Complex Traits: From Polygenic to Omnigenic
2017 Standout
Elements of cancer immunity and the cancer–immune set point
2017 StandoutNature
Rheumatoid arthritis
2018 Standout
Mendelian Inheritance in Man and Its Online Version, OMIM
2007
Neonatal screening for congenital adrenal hyperplasia
2009
Taking qPCR to a higher level: Analysis of CNV reveals the power of high throughput qPCR to enhance quantitative resolution
2010
The evolving landscape of biomarkers for checkpoint inhibitor immunotherapy
2019 Standout
Complement: a key system for immune surveillance and homeostasis
2010 Standout
Classification and characterization of human endogenous retroviruses; mosaic forms are common
2016
Complement associated microvascular injury and thrombosis in the pathogenesis of severe COVID-19 infection: A report of five cases
2020 Standout
Complement deficiencies in humans and animals: Links to autoimmunity
2006
Super-Enhancers in the Control of Cell Identity and Disease
2013 Standout
Sensors of the innate immune system: their link to rheumatic diseases
2010 StandoutNobel
Use of C4d as a Diagnostic Adjunct in Lung Allograft Biopsies
2003
Re-evaluation of low-resolution crystal structuresviainteractive molecular-dynamics flexible fitting (iMDFF): a case study in complement C4
2016
Genetic susceptibility to systemic lupus erythematosus in the genomic era
2010
The JAK/STAT signaling pathway: from bench to clinic
2021 Standout
Systemic Lupus Erythematosus
2011 Standout
Detection of widespread horizontal pleiotropy in causal relationships inferred from Mendelian randomization between complex traits and diseases
2018 Standout
Recent segmental and gene duplications in the mouse genome
2003
Coming of age: ten years of next-generation sequencing technologies
2016 Standout
Prescribing Personalized Nutrition for Cardiovascular Health: Are We Ready?
2014 Standout
Implant infections: adhesion, biofilm formation and immune evasion
2018 Standout
10 Years of GWAS Discovery: Biology, Function, and Translation
2017 Standout
Molecular Genetics of 21- Hydroxylase Deficiency
2010
Structural variants: changing the landscape of chromosomes and design of disease studies
2006
Reactive Astrocytes: Production, Function, and Therapeutic Potential
2017 Standout
Clinical Significance of Complement Deficiencies
2009
The Diagnosis of Polycystic Ovary Syndrome during Adolescence
2015 Standout
Pre-rheumatoid arthritis: predisposition and transition to clinical synovitis
2012
Genetic insights into common pathways and complex relationships among immune-mediated diseases
2013
Identification of copy number variants in whole-genome data using Reference Coverage Profiles
2015 StandoutNobel
Dangerous liaisons: complement, coagulation, and kallikrein/kinin cross‐talk act as a linchpin in the events leading to thromboinflammation
2016
Comprehensive Genetic Analysis of 182 Unrelated Families with Congenital Adrenal Hyperplasia due to 21-Hydroxylase Deficiency
2010
Strain-Specific Manifestation of Lupus-like Systemic Autoimmunity Caused by Zap70 Mutation
2019 StandoutNobel
UCSF ChimeraX: Meeting modern challenges in visualization and analysis
2017 Standout
The Molecular Biology, Biochemistry, and Physiology of Human Steroidogenesis and Its Disorders
2011 Standout
Sampling and energy evaluation challenges in ligand binding protein design
2017 StandoutNobel
COMPARATIVE PRIMATE GENOMICS
2004 StandoutNobel
Impaired T cell receptor signaling and development of T cell–mediated autoimmune arthritis
2020 StandoutNobel
Works of Bi Zhou being referenced
Sensitive and Specific Real-Time Polymerase Chain Reaction Assays to Accurately Determine Copy Number Variations (CNVs) of Human Complement C4A , C4B , C4-Long , C4-Short , and RCCX Modules: Elucidation of C4 CNVs in 50 Consanguineous Subjects with Defined HLA Genotypes
2007
Assessment of complement C4 gene copy number using the paralog ratio test
2010
The Intricate Role of Complement Component C4 in Human Systemic Lupus Erythematosus
2003
Great genotypic and phenotypic diversities associated with copy-number variations of complement C4 and RP-C4-CYP21-TNX (RCCX) modules: A comparison of Asian-Indian and European American populations
2009
Increased frequency of complement C4B deficiency in rheumatoid arthritis
2011
Phenotypes, genotypes and disease susceptibility associated with gene copy number variations: complement <i>C4</i> CNVs in European American healthy subjects and those with systemic lupus erythematosus
2008
Genetic, structural and functional diversities of human complement components C4A and C4B and their mouse homologues, Slp and C4
2001
Genetic Sophistication of Human Complement Components C4A and C4B and RP-C4-CYP21-TNX (RCCX) Modules in the Major Histocompatibility Complex
2002
Deficiencies of Human Complement Component C4a and C4b and Heterozygosity in Length Variants ofRP-C4-CYP21-TNX(Rccx) Modules in Caucasians
2000
Human Complement Components C4A and C4B Genetic Diversities: Complex Genotypes and Phenotypes
2005
Diversity in Intrinsic Strengths of the Human Complement System: Serum C4 Protein Concentrations Correlate withC4Gene Size and Polygenic Variations, Hemolytic Activities, and Body Mass Index
2003