Qiao Q - Search Results

1

SOX17 loss-of-function variation underlying familial congenital heart disease.

Zhao L, Jiang WF, Yang CX, Qiao Q, Xu YJ, Shi HY, Qiu XB, Wu SH, Yang YQ. Zhao L, et al. Among authors: qiao q. Eur J Med Genet. 2021 May;64(5):104211. doi: 10.1016/j.ejmg.2021.104211. Epub 2021 Mar 29. Eur J Med Genet. 2021. PMID: 33794346

2

GATA6 loss-of-function mutation contributes to congenital bicuspid aortic valve.

Xu YJ, Di RM, Qiao Q, Li XM, Huang RT, Xue S, Liu XY, Wang J, Yang YQ. Xu YJ, et al. Among authors: qiao q. Gene. 2018 Jul 15;663:115-120. doi: 10.1016/j.gene.2018.04.018. Epub 2018 Apr 10. Gene. 2018. PMID: 29653232

3

HAND2 loss-of-function mutation causes familial dilated cardiomyopathy.

Liu H, Xu YJ, Li RG, Wang ZS, Zhang M, Qu XK, Qiao Q, Li XM, Di RM, Qiu XB, Yang YQ. Liu H, et al. Among authors: qiao q. Eur J Med Genet. 2019 Sep;62(9):103540. doi: 10.1016/j.ejmg.2018.09.007. Epub 2018 Sep 12. Eur J Med Genet. 2019. PMID: 30217752

4

ISL1 loss-of-function mutation contributes to congenital heart defects.

Ma L, Wang J, Li L, Qiao Q, Di RM, Li XM, Xu YJ, Zhang M, Li RG, Qiu XB, Li X, Yang YQ. Ma L, et al. Among authors: qiao q. Heart Vessels. 2019 Apr;34(4):658-668. doi: 10.1007/s00380-018-1289-z. Epub 2018 Nov 2. Heart Vessels. 2019. PMID: 30390123

5

A SHOX2 loss-of-function mutation underlying familial atrial fibrillation.

Li N, Wang ZS, Wang XH, Xu YJ, Qiao Q, Li XM, Di RM, Guo XJ, Li RG, Zhang M, Qiu XB, Yang YQ. Li N, et al. Among authors: qiao q. Int J Med Sci. 2018 Oct 20;15(13):1564-1572. doi: 10.7150/ijms.27424. eCollection 2018. Int J Med Sci. 2018. PMID: 30443179 Free PMC article.

6

Identification and Functional Characterization of an ISL1 Mutation Predisposing to Dilated Cardiomyopathy.

Xu YJ, Wang ZS, Yang CX, Di RM, Qiao Q, Li XM, Gu JN, Guo XJ, Yang YQ. Xu YJ, et al. Among authors: qiao q. J Cardiovasc Transl Res. 2019 Jun;12(3):257-267. doi: 10.1007/s12265-018-9851-8. Epub 2018 Dec 10. J Cardiovasc Transl Res. 2019. PMID: 30536204

7

NR2F2 loss‑of‑function mutation is responsible for congenital bicuspid aortic valve.

Wang J, Abhinav P, Xu YJ, Li RG, Zhang M, Qiu XB, Di RM, Qiao Q, Li XM, Huang RT, Xue S, Yang YQ. Wang J, et al. Among authors: qiao q. Int J Mol Med. 2019 Apr;43(4):1839-1846. doi: 10.3892/ijmm.2019.4087. Epub 2019 Jan 31. Int J Mol Med. 2019. PMID: 30720060

8

Identification and functional characterization of KLF5 as a novel disease gene responsible for familial dilated cardiomyopathy.

Di RM, Yang CX, Zhao CM, Yuan F, Qiao Q, Gu JN, Li XM, Xu YJ, Yang YQ. Di RM, et al. Among authors: qiao q. Eur J Med Genet. 2020 Apr;63(4):103827. doi: 10.1016/j.ejmg.2019.103827. Epub 2019 Dec 16. Eur J Med Genet. 2020. PMID: 31857253

9

A New TBX5 Loss-of-Function Mutation Contributes to Congenital Heart Defect and Atrioventricular Block.

Zhang Y, Sun YM, Xu YJ, Zhao CM, Yuan F, Guo XJ, Guo YH, Yang CX, Gu JN, Qiao Q, Wang J, Yang YQ. Zhang Y, et al. Among authors: qiao q. Int Heart J. 2020 Jul 30;61(4):761-768. doi: 10.1536/ihj.19-650. Epub 2020 Jul 8. Int Heart J. 2020. PMID: 32641638 Free article.

10

ISL1 loss-of-function variation causes familial atrial fibrillation.

Wu SH, Wang XH, Xu YJ, Gu JN, Yang CX, Qiao Q, Guo XJ, Guo YH, Qiu XB, Jiang WF, Yang YQ. Wu SH, et al. Among authors: qiao q. Eur J Med Genet. 2020 Nov;63(11):104029. doi: 10.1016/j.ejmg.2020.104029. Epub 2020 Aug 6. Eur J Med Genet. 2020. PMID: 32771629

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