Dai Pu - Search Results

Year	Number of Results
2002	2
2004	2
2005	3
2006	9
2007	18
2008	9
2009	16
2010	13
2011	14
2012	14
2013	11
2014	15
2015	12
2016	8
2017	10
2018	9
2019	14
2020	12
2021	20
2022	24
2023	15
2024	8

1

Molecular diagnose of a large hearing loss population from China by targeted genome sequencing.

Wu J, Cao Z, Su Y, Wang Y, Cai R, Chen J, Gao B, Han M, Li X, Zhang D, Gao X, Huang S, Huang Q, Yuan Y, Ma X, Dai P. Wu J, et al. Among authors: dai p. J Hum Genet. 2022 Nov;67(11):643-649. doi: 10.1038/s10038-022-01066-5. Epub 2022 Aug 19. J Hum Genet. 2022. PMID: 35982127 Free PMC article.

2

KCNJ10 may not be a contributor to nonsyndromic enlargement of vestibular aqueduct (NSEVA) in Chinese subjects.

Zhao J, Yuan Y, Huang S, Huang B, Cheng J, Kang D, Wang G, Han D, Dai P. Zhao J, et al. Among authors: dai p. PLoS One. 2014 Nov 5;9(11):e108134. doi: 10.1371/journal.pone.0108134. eCollection 2014. PLoS One. 2014. PMID: 25372295 Free PMC article.

3

Genetic architecture and phenotypic landscape of deafness and onychodystrophy syndromes.

Gao X, Dai P, Yuan YY. Gao X, et al. Among authors: dai p. Hum Genet. 2022 Apr;141(3-4):821-838. doi: 10.1007/s00439-021-02310-2. Epub 2021 Jul 7. Hum Genet. 2022. PMID: 34232384 Review.

4

Evolutionary origin of pathogenic GJB2 alleles in China.

Jiang Y, Huang S, Zhang Y, Fang N, Liu Q, Liu Y, Bai L, Han D, Dai P. Jiang Y, et al. Among authors: dai p. Clin Genet. 2022 Oct;102(4):305-313. doi: 10.1111/cge.14191. Epub 2022 Jul 24. Clin Genet. 2022. PMID: 35841299

5

[Clinical case analysis and literature review of mandibulofacial dysostosis with microcephaly syndrome].

Li X, Hong M, Dai P, Yuan Y. Li X, et al. Among authors: dai p. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2022 Jan;36(1):36-40. doi: 10.13201/j.issn.2096-7993.2022.01.008. Lin Chuang Er Bi Yan Hou Tou Jing Wai Ke Za Zhi. 2022. PMID: 34979617 Free PMC article. Review. Chinese.

6

Variant analysis of 92 Chinese Han families with hearing loss.

Jin X, Huang S, An L, Zhang C, Dai P, Gao H, Ma X. Jin X, et al. Among authors: dai p. BMC Med Genomics. 2022 Jan 21;15(1):12. doi: 10.1186/s12920-022-01158-3. BMC Med Genomics. 2022. PMID: 35062939 Free PMC article.

7

The genetic bases for non-syndromic hearing loss among Chinese.

Ouyang XM, Yan D, Yuan HJ, Pu D, Du LL, Han DY, Liu XZ. Ouyang XM, et al. Among authors: pu d. J Hum Genet. 2009 Mar;54(3):131-40. doi: 10.1038/jhg.2009.4. Epub 2009 Feb 6. J Hum Genet. 2009. PMID: 19197336 Free PMC article. Review.

8

Exploration of a Novel Noninvasive Prenatal Testing Approach for Monogenic Disorders Based on Fetal Nucleated Red Blood Cells.

Li X, Zhang D, Zhao X, Huang S, Han M, Wang G, Li Y, Kang D, Zhang X, Dai P, Yuan Y. Li X, et al. Among authors: dai p. Clin Chem. 2023 Dec 1;69(12):1396-1408. doi: 10.1093/clinchem/hvad165. Clin Chem. 2023. PMID: 37963809

9

Surgical management of endolymphatic sac tumor: classification, outcomes and strategy. A single institution's experience.

Wu N, Ma X, Shen W, Hou Z, Han W, Dai P, Zhao H, Huang D, Han D, Yang S. Wu N, et al. Among authors: dai p. Eur Arch Otorhinolaryngol. 2023 Jan;280(1):69-76. doi: 10.1007/s00405-022-07447-y. Epub 2022 Jun 23. Eur Arch Otorhinolaryngol. 2023. PMID: 35739425 Review.

10

Digital storytelling to facilitate consumer engagement in healthcare research.

Pu D, Bonnici R, Shorr R, Haines T. Pu D, et al. Health Promot J Austr. 2022 Jul;33(3):758-767. doi: 10.1002/hpja.565. Epub 2022 Jan 2. Health Promot J Austr. 2022. PMID: 34923697 Clinical Trial.

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