Chen Q - Search Results

1

Whole exome sequencing identified a rare WT1 loss-of-function variant in a non-syndromic POI patient.

Wang Y, Chen Q, Zhang F, Yang X, Shang L, Ren S, Pan Y, Zhou Z, Li G, Fang Y, Jin L, Wu Y, Zhang X. Wang Y, et al. Among authors: chen q. Mol Genet Genomic Med. 2022 Jan;10(1):e1820. doi: 10.1002/mgg3.1820. Epub 2021 Nov 29. Mol Genet Genomic Med. 2022. PMID: 34845858 Free PMC article.

2

Whole-exome sequencing reveals SALL4 variants in premature ovarian insufficiency: an update on genotype-phenotype correlations.

Wang Q, Li D, Cai B, Chen Q, Li C, Wu Y, Jin L, Wang X, Zhang X, Zhang F. Wang Q, et al. Among authors: chen q. Hum Genet. 2019 Jan;138(1):83-92. doi: 10.1007/s00439-018-1962-4. Epub 2019 Jan 2. Hum Genet. 2019. PMID: 30603774

3

Rare variants in FANCA induce premature ovarian insufficiency.

Yang X, Zhang X, Jiao J, Zhang F, Pan Y, Wang Q, Chen Q, Cai B, Tang S, Zhou Z, Chen S, Yin H, Fu W, Luo Y, Li D, Li G, Shang L, Yang J, Jin L, Shi Q, Wu Y. Yang X, et al. Among authors: chen q, chen s. Hum Genet. 2019 Dec;138(11-12):1227-1236. doi: 10.1007/s00439-019-02059-9. Epub 2019 Sep 18. Hum Genet. 2019. PMID: 31535215 Free PMC article.

4

Rare deleterious BUB1B variants induce premature ovarian insufficiency and early menopause.

Chen Q, Ke H, Luo X, Wang L, Wu Y, Tang S, Li J, Jin L, Zhang F, Qin Y, Chen X. Chen Q, et al. Among authors: chen x. Hum Mol Genet. 2020 Sep 29;29(16):2698-2707. doi: 10.1093/hmg/ddaa153. Hum Mol Genet. 2020. PMID: 32716490

5

Haploinsufficiency in non-homologous end joining factor 1 induces ovarian dysfunction in humans and mice.

Li G, Yang X, Wang L, Pan Y, Chen S, Shang L, Zhang Y, Wu Y, Zhou Z, Chen Q, Zhang X, Zhang L, Wang Y, Li J, Jin L, Wu Y, Zhang X, Zhang F. Li G, et al. Among authors: chen q, chen s. J Med Genet. 2022 Jun;59(6):579-588. doi: 10.1136/jmedgenet-2020-107398. Epub 2021 Apr 22. J Med Genet. 2022. PMID: 33888552

6

HSD17B12 dosage insufficiency induced premature ovarian insufficiency in humans and mice.

Wang Q, Chen Q, Zhang Y, Zhang X, Liu C, Wang D, Wu Y, Sun Y, Zhang L, Song C, Wang Y, An Y, Tang H, Xu C, Wu Y, Jin L, Huang H, Zhang F. Wang Q, et al. Among authors: chen q. Clin Transl Med. 2022 Feb;12(2):e737. doi: 10.1002/ctm2.737. Clin Transl Med. 2022. PMID: 35187845 Free PMC article. No abstract available.

7

Rare variants in FANCJ induce premature ovarian insufficiency in humans and mice.

Yang X, Ren S, Yang J, Pan Y, Zhou Z, Chen Q, Fang Y, Shang L, Zhang F, Zhang X, Wu Y. Yang X, et al. Among authors: chen q. J Genet Genomics. 2024 Feb;51(2):252-255. doi: 10.1016/j.jgg.2023.03.013. Epub 2023 Apr 14. J Genet Genomics. 2024. PMID: 37062450 No abstract available.

8

Recombinant human GLP-1 beinaglutide regulates lipid metabolism of adipose tissues in diet-induced obese mice.

Zhang F, Chen Z, Wu D, Tian L, Chen Q, Ye Y, Chen W, Wu X, Wu P, Yuan W, Qiu Y, Zhou Z, Du Z, Hu F. Zhang F, et al. Among authors: chen z, chen q, chen w. iScience. 2021 Oct 30;24(12):103382. doi: 10.1016/j.isci.2021.103382. eCollection 2021 Dec 17. iScience. 2021. PMID: 34841227 Free PMC article.

9

Effect of a Personalized Enteral Nutrition Protocol on the Postoperative Nutritional Status in Patients Who Underwent Oral Cancer Surgery.

Ding C, Chen Q, Zhang F, Xu B, Zhang H. Ding C, et al. Among authors: chen q. Nutr Cancer. 2023;75(3):815-824. doi: 10.1080/01635581.2022.2157449. Epub 2022 Dec 19. Nutr Cancer. 2023. PMID: 36533888

10

Functional analysis of a de novo mutation c.1692 del A of the PHEX gene in a Chinese family with X-linked hypophosphataemic rickets.

Huang J, Bao X, Xia W, Zhu L, Zhang J, Ma J, Jiang N, Yang J, Chen Q, Jing T, Liu J, Ma D, Xu G. Huang J, et al. Among authors: chen q. Bone Joint Res. 2019 Sep 3;8(8):405-413. doi: 10.1302/2046-3758.88.BJR-2018-0276.R1. eCollection 2019 Aug. Bone Joint Res. 2019. PMID: 31537998 Free PMC article.

Zhu, J. Zhang, J. Ma, N. Jiang, J. Yang, Q. Chen, T. Jing, J. Liu, D. Ma, G. Xu. Functional analysis of a de novo mutation c.1692 del A of the PHEX gene in a Chinese family with X-linked hypophosphataemic rickets. ...

Zhu, J. Zhang, J. Ma, N. Jiang, J. Yang, Q. Chen, T. Jing, J. Liu, D. Ma, G. Xu. Functional analysis of a de novo mutation c.1 …

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