Chanjuan Hao[Author] - Search Results

Year	Number of Results
2005	2
2007	1
2008	3
2011	1
2012	4
2013	3
2014	1
2016	1
2018	1
2019	6
2020	10
2021	10
2022	8
2023	10
2024	2

1

Clinical and Genetic Spectrum of Children With Primary Ciliary Dyskinesia in China.

Guan Y, Yang H, Yao X, Xu H, Liu H, Tang X, Hao C, Zhang X, Zhao S, Ge W, Ni X. Guan Y, et al. Among authors: hao c. Chest. 2021 May;159(5):1768-1781. doi: 10.1016/j.chest.2021.02.006. Epub 2021 Feb 10. Chest. 2021. PMID: 33577779 Free PMC article.

2

New insights into the pathogenesis of Hermansky-Pudlak syndrome.

Li W, Hao CJ, Hao ZH, Ma J, Wang QC, Yuan YF, Gong JJ, Chen YY, Yu JY, Wei AH. Li W, et al. Pigment Cell Melanoma Res. 2022 May;35(3):290-302. doi: 10.1111/pcmr.13030. Epub 2022 Feb 13. Pigment Cell Melanoma Res. 2022. PMID: 35129281 Review.

3

[Clinical practice guidelines for albinism].

Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, Li W, Wei A, Bai D, Qi Z, Hao C. Writing Group For Practice Guidelines For Diagnosis And Treatment Of Genetic Diseases Medical Genetics Branch Of Chinese Medical Association, et al. Among authors: hao c. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020 Mar 10;37(3):252-257. doi: 10.3760/cma.j.issn.1003-9406.2020.03.005. Zhonghua Yi Xue Yi Chuan Xue Za Zhi. 2020. PMID: 32128740 Chinese.

4

A gain-of-function TPC2 variant R210C increases affinity to PI(3,5)P₂ and causes lysosome acidification and hypopigmentation.

Wang Q, Wang Z, Wang Y, Qi Z, Bai D, Wang C, Chen Y, Xu W, Zhu X, Jeon J, Xiong J, Hao C, Zhu MX, Wei A, Li W. Wang Q, et al. Among authors: hao c. Nat Commun. 2023 Jan 14;14(1):226. doi: 10.1038/s41467-023-35786-9. Nat Commun. 2023. PMID: 36641477 Free PMC article.

5

Biological implications of genetic variations in autism spectrum disorders from genomics studies.

Zhang Y, Liu X, Guo R, Xu W, Guo Q, Hao C, Ni X, Li W. Zhang Y, et al. Among authors: hao c. Biosci Rep. 2021 Jul 30;41(7):BSR20210593. doi: 10.1042/BSR20210593. Biosci Rep. 2021. PMID: 34240107 Free PMC article. Review.

6

Phenylalanyl-tRNA synthetase deficiency caused by biallelic variants in FARSA gene and literature review.

Guo R, Chen Y, Hu X, Qi Z, Guo J, Li Y, Hao C. Guo R, et al. Among authors: hao c. BMC Med Genomics. 2023 Oct 13;16(1):245. doi: 10.1186/s12920-023-01662-0. BMC Med Genomics. 2023. PMID: 37833669 Free PMC article. Review.

7

The BLOC interactomes form a network in endosomal transport.

Li W, Feng Y, Hao C, Guo X, Cui Y, He M, He X. Li W, et al. Among authors: hao c. J Genet Genomics. 2007 Aug;34(8):669-82. doi: 10.1016/S1673-8527(07)60076-9. J Genet Genomics. 2007. PMID: 17707211 Review.

8

Behavioural deficits of autism spectrum disorder and associations with different gene clusters: a study with the whole-genome transmission disequilibrium test.

Guo Q, Xia L, Guo R, Xu W, Zhang Y, Zhao C, Zhang P, Bai T, Ni X, Hao C, Xia K, Li W. Guo Q, et al. Among authors: hao c. BMJ Paediatr Open. 2023 Jul;7(1):e001930. doi: 10.1136/bmjpo-2023-001930. BMJ Paediatr Open. 2023. PMID: 37407249 Free PMC article.

9

Whole exome sequencing for non-selective pediatric patients with hyperlipidemia.

Hu X, Chen L, Gong C, Guo J, Chen Y, Wang Q, Guo R, Li W, Hao C. Hu X, et al. Among authors: hao c. Gene. 2021 Feb 5;768:145310. doi: 10.1016/j.gene.2020.145310. Epub 2020 Nov 18. Gene. 2021. PMID: 33217533

10

BLOS1 mediates kinesin switch during endosomal recycling of LDL receptor.

Zhang C, Hao C, Shui G, Li W. Zhang C, et al. Among authors: hao c. Elife. 2020 Nov 12;9:e58069. doi: 10.7554/eLife.58069. Elife. 2020. PMID: 33179593 Free PMC article.

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