Wang L - Search Results

1

Novel RSPH4A Variants Associated With Primary Ciliary Dyskinesia-Related Infertility in Three Chinese Families.

Wang L, Wang R, Yang D, Lu C, Xu Y, Liu Y, Guo T, Lei C, Luo H. Wang L, et al. Among authors: wang r. Front Genet. 2022 Jun 22;13:922287. doi: 10.3389/fgene.2022.922287. eCollection 2022. Front Genet. 2022. PMID: 35812741 Free PMC article.

2

DRC1 deficiency caused primary ciliary dyskinesia and MMAF in a Chinese patient.

Lei C, Yang D, Wang R, Ding S, Wang L, Guo T, Luo H. Lei C, et al. Among authors: wang l, wang r. J Hum Genet. 2022 Apr;67(4):197-201. doi: 10.1038/s10038-021-00985-z. Epub 2021 Nov 24. J Hum Genet. 2022. PMID: 34815526

3

Novel Compound Heterozygous Variants in CCDC40 Associated with Primary Ciliary Dyskinesia and Multiple Morphological Abnormalities of the Sperm Flagella.

Xu Y, Yang B, Lei C, Yang D, Ding S, Lu C, Wang L, Guo T, Wang R, Luo H. Xu Y, et al. Among authors: wang l, wang r. Pharmgenomics Pers Med. 2022 Apr 15;15:341-350. doi: 10.2147/PGPM.S359821. eCollection 2022. Pharmgenomics Pers Med. 2022. PMID: 35449766 Free PMC article.

4

Case Report: Pirfenidone in the Treatment of Post-COVID-19 Pulmonary Fibrosis.

Zhou X, Yang D, Kong X, Wei C, LvQiu S, Wang L, Lin Y, Yin Z, Zhou Z, Luo H. Zhou X, et al. Among authors: wang l. Front Med (Lausanne). 2022 Jun 6;9:925703. doi: 10.3389/fmed.2022.925703. eCollection 2022. Front Med (Lausanne). 2022. PMID: 35733875 Free PMC article.

5

Identification of a Novel OFD1 Variant in a Patient with Primary Ciliary Dyskinesia.

Yang B, Lei C, Yang D, Lu C, Xu Y, Wang L, Guo T, Wang R, Luo H. Yang B, et al. Among authors: wang l, wang r. Pharmgenomics Pers Med. 2022 Jul 11;15:697-704. doi: 10.2147/PGPM.S365740. eCollection 2022. Pharmgenomics Pers Med. 2022. PMID: 35847568 Free PMC article.

6

Case Report: Whole-Exome Sequencing-Based Copy Number Variation Analysis Identified a Novel DRC1 Homozygous Exon Deletion in a Patient With Primary Ciliary Dyskinesia.

Liu Y, Lei C, Wang R, Yang D, Yang B, Xu Y, Lu C, Wang L, Ding S, Guo T, Liu S, Luo H. Liu Y, et al. Among authors: wang l, wang r. Front Genet. 2022 Jul 6;13:940292. doi: 10.3389/fgene.2022.940292. eCollection 2022. Front Genet. 2022. PMID: 35873463 Free PMC article.

7

A novel COL3A1 variant associated with vascular Ehlers-Danlos syndrome in a patient presents as recurrent pneumothorax with cavities.

Guo T, Liu Y, Lvqiu S, Lei C, He WL, Jiang Y, Yang D, Wang R, Yang B, Lu C, Xu Y, Ding S, Wang L, Luo H, Peng H. Guo T, et al. Among authors: wang l, wang r. QJM. 2023 Sep 12;116(8):691-693. doi: 10.1093/qjmed/hcad059. QJM. 2023. PMID: 37074961 No abstract available.

8

Dynein axonemal heavy chain 10 deficiency causes primary ciliary dyskinesia in humans and mice.

Wang R, Yang D, Tu C, Lei C, Ding S, Guo T, Wang L, Liu Y, Lu C, Yang B, Ouyang S, Gong K, Tan Z, Deng Y, Tan Y, Qing J, Luo H. Wang R, et al. Among authors: wang l. Front Med. 2023 Oct;17(5):957-971. doi: 10.1007/s11684-023-0988-8. Epub 2023 Jun 13. Front Med. 2023. PMID: 37314648

9

The effect of gut microbiome and plasma metabolome on systemic sclerosis: a bidirectional two-sample Mendelian randomization study.

Xie S, Meng Q, Wang L. Xie S, et al. Among authors: wang l. Front Microbiol. 2024 Jul 17;15:1427195. doi: 10.3389/fmicb.2024.1427195. eCollection 2024. Front Microbiol. 2024. PMID: 39086645 Free PMC article.

10

Identification of gross deletions in FBN1 gene by MLPA.

Yang H, Ma Y, Luo M, Zhao K, Zhang Y, Zhu G, Sun X, Luo F, Wang L, Shu C, Zhou Z. Yang H, et al. Among authors: wang l. Hum Genomics. 2018 Oct 4;12(1):46. doi: 10.1186/s40246-018-0178-y. Hum Genomics. 2018. PMID: 30286810 Free PMC article.

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