Publications by authors named "Cai Ruikun"

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A defined serum-free culture system for human long-term haematopoietic stem cells.
Yichao Dong, Ruikun Cai, Mingxia Fang, Yuqi Chen, Peng Li

Br J Haematol· January 2024

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Molecular diagnose of a large hearing loss population from China by targeted genome sequencing.
Jie Wu, Zongfu Cao, Yu Su, Yang Wang, Ruikun Cai

J Hum Genet· November 2022

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Genetic and Phenotype Analysis of a Chinese Cohort of Infants and Children With Epilepsy.
Zhang Chuan, Cai Ruikun, Li Qian, Mei Shiyue, Hao Shengju

Front Genet· April 2022

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Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.
Minna Luo, Zaisheng Lin, Tian Zhu, Minjun Jin, Dan Meng, Ruikun Cai

Genet Med· June 2021

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Clinical heterogeneity and intrafamilial variability of Joubert syndrome in two siblings with CPLANE1 variants.
Xiujuan Zhang, Yue Shen, Ping Li, Ruikun Cai, Chao Lu

Mol Genet Genomic Med· June 2021

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Correction to: Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.
Minna Luo, Zaisheng Lin, Tian Zhu, Minjun Jin, Dan Meng, Ruikun Cai

Genet Med· June 2021

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Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome.
Ruikun Cai, Yichao Dong, Mingxia Fang, Yuxuan Fan, Zian Cheng

Front Cell Dev Biol· March 2021

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Prevention and Control of Pathogens Based on Big-Data Mining and Visualization Analysis.
Cui-Xia Chen, Li-Na Sun, Xue-Xin Hou, Peng-Cheng Du, Xiao-Long Wang

Front Mol Biosci· February 2021

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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.
Yue Shen, Hao Wang, Zhimin Liu, Minna Luo, Siyu Ma, Ruikun Cai

BMC Med Genet· October 2020

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De novo genome assembly of a Han Chinese male and genome-wide detection of structural variants using Oxford Nanopore sequencing.
Ruikun Cai, Yichao Dong, Mingxia Fang, Changlong Guo, Xu Ma

Mol Genet Genomics· July 2020

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Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndrome.
Minna Luo, Li Cao, Zongfu Cao, Siyu Ma, Yue Shen, Ruikun Cai

Mol Genet Genomic Med· December 2019

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Deep targeted sequencing reveals the diversity of TRB-CDR3 repertoire in patients with preeclampsia.
Changlong Guo, Ruikun Cai, Xiaofang Cao, Ying Yang, Qidi Wang

Hum Immunol· October 2019

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High throughput sequencing reveals the diversity of TRB-CDR3 repertoire in patients with psoriasis vulgaris.
Xiaofang Cao, Qingbiao Wa, Qidi Wang, Lin Li, Xin Liu, Ruikun Cai

Int Immunopharmacol· November 2016

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High-Throughput Sequencing Reveals Immunological Characteristics of the TRB-/IgH-CDR3 Region of Umbilical Cord Blood.
Changlong Guo, Qidi Wang, Xiaofang Cao, Ying Yang, Xin Liu, Ruikun Cai

J Pediatr· September 2016

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GPS-MBA: computational analysis of MHC class II epitopes in type 1 diabetes.
Ruikun Cai, Zexian Liu, Jian Ren, Chuang Ma, Tianshun Gao

PLoS One· November 2012

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