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Ruikun Cai

Observed names: Cai Ruikun, Cai, Ruikun, Rui‐Kun Cai
ORCID: 0000-0001-9810-7559
Observed ORCID: 0000-0001-9810-7559
OpenAlex ID: A5045061359
Molecular diagnose of a large hearing loss population from China by targeted genome sequencing
2022 · Jie Wu, Zongfu Cao, et al. · Journal of Human Genetics · 49
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Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome
2021 · Minna Luo, Zaisheng Lin, et al. · Genetics in Medicine · 39
High throughput sequencing reveals the diversity of TRB-CDR3 repertoire in patients with psoriasis vulgaris
2016 · Xiaofang Cao, Qingbiao Wa, et al. · International Immunopharmacology · 22
Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy
2022 · Zhang Chuan, Cai Ruikun, et al. · Frontiers in Genetics · 18
High-Throughput Sequencing Reveals Immunological Characteristics of the TRB-/IgH-CDR3 Region of Umbilical Cord Blood
2016 · Changlong Guo, Qidi Wang, et al. · The Journal of Pediatrics · 17
Clinical heterogeneity and intrafamilial variability of Joubert syndrome in two siblings with CPLANE1 variants
2021 · Xiujuan Zhang, Yue Shen, et al. · Molecular Genetics & Genomic Medicine · 14
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Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome
2020 · Yue Shen, Hao Wang, et al. · BMC Medical Genetics · 13
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Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndrome
2019 · Minna Luo, Li Cao, et al. · Molecular Genetics & Genomic Medicine · 13
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Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome
2021 · Ruikun Cai, Yichao Dong, et al. · Frontiers in Cell and Developmental Biology · 12
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De novo genome assembly of a Han Chinese male and genome-wide detection of structural variants using Oxford Nanopore sequencing
2020 · Ruikun Cai, Yichao Dong, et al. · Molecular Genetics and Genomics · 9
GPS-MBA: Computational Analysis of MHC Class II Epitopes in Type 1 Diabetes
2012 · Ruikun Cai, Zexian Liu, et al. · PLoS ONE · 8
VarfromPDB: An Automated and Integrated Tool to Mine Disease-Gene-Variant Relations from the Public Databases and Literature
2017 · Zongfu Cao, Lei Wang, et al. · Journal of Proteomics & Bioinformatics · 5
Correction to: Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome
2021 · Minna Luo, Zaisheng Lin, et al. · Genetics in Medicine · 4
Deep targeted sequencing reveals the diversity of TRB-CDR3 repertoire in patients with preeclampsia
2019 · Changlong Guo, Ruikun Cai, et al. · Human Immunology · 4
Correction: GPS-MBA: Computational Analysis of MHC Class II Epitopes in Type 1 Diabetes
2012 · Ruikun Cai, Zexian Liu, et al. · PLoS ONE · 2
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A defined serum‐free culture system for human long‐term haematopoietic stem cells
2023 · Yichao Dong, Ruikun Cai, et al. · British Journal of Haematology · 1
Prevention and Control of Pathogens Based on Big-Data Mining and Visualization Analysis
2021 · Cui‐Xia Chen, Li‐Na Sun, et al. · Frontiers in Molecular Biosciences · 1
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Platform Construction for the Early-Warning Forecast in Prevention and Control of Influenza Based on Multi-Source Heterogeneous Big-Data Mining
2020 · Cuixia Chen, Xiaolong Wang, et al. · Zhongguo shengwu gongcheng zazhi · 1
Additional file 1 of Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome
2020 · Shen, Yue, Wang, Hao, et al. · Figshare
Automatic analysis and interpretation of genetic variations for monogenic diseases
2019 · Zongfu Cao, Yufei Yu, et al.
Sequence similarity analysis of non-self CTL epitopes and mouse proteins using sequence alignment
2011 · Ruikun Cai, Xi Cheng, et al. · Wuhan University Journal of Natural Sciences
Works count: 21
Citation count: 232
H-index: 9
I10-index: 9
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