Sun Y - Search Results

1

Panoramic variation analysis of a family with neurodevelopmental disorders caused by biallelic loss-of-function variants in TMEM141, DDHD2, and LHFPL5.

Sun L, Yang X, Khan A, Yu X, Zhang H, Han S, Habulieti X, Sun Y, Wang R, Zhang X. Sun L, et al. Among authors: sun y. Front Med. 2024 Feb;18(1):81-97. doi: 10.1007/s11684-023-1006-x. Epub 2023 Oct 14. Front Med. 2024. PMID: 37837560

2

A novel DLL4 missense mutation in a Chinese patient with Adams-Oliver syndrome.

Yu X, Wang RR, Han SR, Bai X, Habulieti X, Sun Y, Sun LW, Zhang H, Khan A, Zhang X. Yu X, et al. Among authors: sun y, sun lw. Chin Med J (Engl). 2019 Jul 20;132(14):1755-1757. doi: 10.1097/CM9.0000000000000316. Chin Med J (Engl). 2019. PMID: 31261205 Free PMC article. No abstract available.

3

Clinical and genetic features of Chinese adult patients with tumour necrosis factor receptor-associated periodic fever syndrome.

Zhao M, Luo Y, Wu D, Yang Y, Sun Y, Wang R, Shen M. Zhao M, et al. Among authors: sun y. Rheumatology (Oxford). 2020 Aug 1;59(8):1969-1974. doi: 10.1093/rheumatology/kez569. Rheumatology (Oxford). 2020. PMID: 31774538

4

Neurological manifestations of autoinflammatory diseases in Chinese adult patients.

Qin W, Wu D, Luo Y, Zhao M, Wang Y, Shi X, Zhou L, Yu W, Sun Y, Wang R, Zhang W, Liu M, Shen M. Qin W, et al. Among authors: sun y. Semin Arthritis Rheum. 2020 Dec;50(6):1500-1506. doi: 10.1016/j.semarthrit.2019.12.003. Epub 2020 Feb 3. Semin Arthritis Rheum. 2020. PMID: 32115236

5

Autoantibodies in NLRP3-associated autoinflammatory disease: a case report.

Zhang L, Sun Y, Yu W, Wu D, Shen M, Wang R. Zhang L, et al. Among authors: sun y. Clin Exp Rheumatol. 2020 Sep-Oct;38 Suppl 127(5):122-123. Epub 2020 Nov 13. Clin Exp Rheumatol. 2020. PMID: 33200730 Free article. No abstract available.

6

GATA2 mutation with recurrent haemophagocytic lymphohistiocytosis and panniculitis: a case report.

Sun L, Xu N, Shen M, Wang R, Sun Y, Zhuang J, Zhao Y, Zeng X, Zhang X. Sun L, et al. Among authors: sun y. Rheumatology (Oxford). 2021 Jul 1;60(7):e229-e231. doi: 10.1093/rheumatology/keaa913. Rheumatology (Oxford). 2021. PMID: 33410496 No abstract available.

7

Adult-onset deficiency of adenosine deaminase 2-a case report and literature review.

Zhang B, Sun Y, Xu N, Wang W, Huang X, Chen J, Shen M, Wang R, Zeng X, Zhang X. Zhang B, et al. Among authors: sun y. Clin Rheumatol. 2021 Oct;40(10):4325-4339. doi: 10.1007/s10067-021-05587-w. Epub 2021 Feb 26. Clin Rheumatol. 2021. PMID: 33638065 Review.

8

Identification and Splicing Characterization of Novel TMC6 and TMC8 Variants Associated With Epidermodysplasia Verruciformis in Three Chinese Families.

Wang R, Liu J, Yang X, Habulieti X, Yu X, Sun L, Zhang H, Sun Y, Ma D, Zhang X. Wang R, et al. Among authors: sun l, sun y. Front Genet. 2021 Jul 27;12:712275. doi: 10.3389/fgene.2021.712275. eCollection 2021. Front Genet. 2021. PMID: 34386043 Free PMC article.

9

Deep learning models of ultrasonography significantly improved the differential diagnosis performance for superficial soft-tissue masses: a retrospective multicenter study.

Long B, Zhang H, Zhang H, Chen W, Sun Y, Tang R, Lin Y, Fu Q, Yang X, Cui L, Wang K. Long B, et al. Among authors: sun y. BMC Med. 2023 Oct 26;21(1):405. doi: 10.1186/s12916-023-03099-9. BMC Med. 2023. PMID: 37880716 Free PMC article.

10

Different phenotypes caused by a STAT3 variant in a Chinese pedigree.

Sun Y, Wang X, Zhang H, Wang R, Shen M, Zhang X. Sun Y, et al. Clin Exp Rheumatol. 2024 May;42(5):1137-1138. doi: 10.55563/clinexprheumatol/qnur5o. Epub 2023 Nov 15. Clin Exp Rheumatol. 2024. PMID: 37976116 Free article. No abstract available.

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