Cai R - Search Results

1

Genome-Wide Association Identifies Risk Pathways for SAPHO Syndrome.

Cai R, Dong Y, Fang M, Fan Y, Cheng Z, Zhou Y, Gao J, Han F, Guo C, Ma X. Cai R, et al. Front Cell Dev Biol. 2021 Mar 18;9:643644. doi: 10.3389/fcell.2021.643644. eCollection 2021. Front Cell Dev Biol. 2021. PMID: 33816493 Free PMC article.

2

High-Throughput Sequencing Reveals Immunological Characteristics of the TRB-/IgH-CDR3 Region of Umbilical Cord Blood.

Guo C, Wang Q, Cao X, Yang Y, Liu X, An L, Cai R, Du M, Wang G, Qiu Y, Peng Z, Han J, Ni S, Tan X, Jin L, Yu S, Wang H, Wang C, Wang X, Ma X. Guo C, et al. Among authors: cai r. J Pediatr. 2016 Sep;176:69-78.e1. doi: 10.1016/j.jpeds.2016.05.078. Epub 2016 Jun 30. J Pediatr. 2016. PMID: 27373756

3

High throughput sequencing reveals the diversity of TRB-CDR3 repertoire in patients with psoriasis vulgaris.

Cao X, Wa Q, Wang Q, Li L, Liu X, An L, Cai R, Du M, Qiu Y, Han J, Wang C, Wang X, Guo C, Lu Y, Ma X. Cao X, et al. Among authors: cai r. Int Immunopharmacol. 2016 Nov;40:487-491. doi: 10.1016/j.intimp.2016.10.004. Epub 2016 Oct 13. Int Immunopharmacol. 2016. PMID: 27743555

4

Deep targeted sequencing reveals the diversity of TRB-CDR3 repertoire in patients with preeclampsia.

Guo C, Cai R, Cao X, Yang Y, Wang Q, He R, An L, Peng Z, Chen Y, Ni S, Tan X, Han J, Liu X, Lin L, Yu S, Wang X, Wang C, Ma X. Guo C, et al. Among authors: cai r. Hum Immunol. 2019 Oct;80(10):848-854. doi: 10.1016/j.humimm.2019.04.003. Epub 2019 Apr 6. Hum Immunol. 2019. PMID: 30965079

5

Whole exome sequencing reveals novel CEP104 mutations in a Chinese patient with Joubert syndrome.

Luo M, Cao L, Cao Z, Ma S, Shen Y, Yang D, Lu C, Lin Z, Liu Z, Yu Y, Cai R, Chen C, Gao H, Wang X, Cao M, Ma X. Luo M, et al. Among authors: cai r. Mol Genet Genomic Med. 2019 Dec;7(12):e1004. doi: 10.1002/mgg3.1004. Epub 2019 Oct 18. Mol Genet Genomic Med. 2019. PMID: 31625690 Free PMC article.

6

De novo genome assembly of a Han Chinese male and genome-wide detection of structural variants using Oxford Nanopore sequencing.

Cai R, Dong Y, Fang M, Guo C, Ma X. Cai R, et al. Mol Genet Genomics. 2020 Jul;295(4):871-876. doi: 10.1007/s00438-020-01672-y. Epub 2020 Apr 9. Mol Genet Genomics. 2020. PMID: 32274588

7

Identification of two novel pathogenic variants of PIBF1 by whole exome sequencing in a 2-year-old boy with Joubert syndrome.

Shen Y, Wang H, Liu Z, Luo M, Ma S, Lu C, Cao Z, Yu Y, Cai R, Chen C, Li Q, Gao H, Peng Y, Xu B, Ma X. Shen Y, et al. Among authors: cai r. BMC Med Genet. 2020 Oct 1;21(1):192. doi: 10.1186/s12881-020-01130-x. BMC Med Genet. 2020. PMID: 33004012 Free PMC article.

8

Disrupted intraflagellar transport due to IFT74 variants causes Joubert syndrome.

Luo M, Lin Z, Zhu T, Jin M, Meng D, He R, Cao Z, Shen Y, Lu C, Cai R, Zhao Y, Wang X, Li H, Wu S, Zou X, Luo G, Cao L, Huang M, Jiao H, Gao H, Sui R, Zhao C, Ma X, Cao M. Luo M, et al. Among authors: cai r. Genet Med. 2021 Jun;23(6):1041-1049. doi: 10.1038/s41436-021-01106-z. Epub 2021 Feb 2. Genet Med. 2021. PMID: 33531668 Free article.

9

Prevention and Control of Pathogens Based on Big-Data Mining and Visualization Analysis.

Chen CX, Sun LN, Hou XX, Du PC, Wang XL, Du XC, Yu YF, Cai RK, Yu L, Li TJ, Luo MN, Shen Y, Lu C, Li Q, Zhang C, Gao HF, Ma X, Lin H, Cao ZF. Chen CX, et al. Front Mol Biosci. 2021 Feb 25;7:626595. doi: 10.3389/fmolb.2020.626595. eCollection 2020. Front Mol Biosci. 2021. PMID: 33718431 Free PMC article.

10

Clinical heterogeneity and intrafamilial variability of Joubert syndrome in two siblings with CPLANE1 variants.

Zhang X, Shen Y, Li P, Cai R, Lu C, Li Q, Chen C, Yu Y, Cheng T, Wang X, Luo M, Cao M, Cao Z, Ma X. Zhang X, et al. Among authors: cai r. Mol Genet Genomic Med. 2021 Jun;9(6):e1682. doi: 10.1002/mgg3.1682. Epub 2021 Apr 6. Mol Genet Genomic Med. 2021. PMID: 33822487 Free PMC article.

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