Luo H - Search Results

1

Bi-allelic BRWD1 variants cause male infertility with asthenoteratozoospermia and likely primary ciliary dyskinesia.

Guo T, Tu CF, Yang DH, Ding SZ, Lei C, Wang RC, Liu L, Kang X, Shen XQ, Yang YF, Tan ZP, Tan YQ, Luo H. Guo T, et al. Among authors: luo h. Hum Genet. 2021 May;140(5):761-773. doi: 10.1007/s00439-020-02241-4. Epub 2021 Jan 3. Hum Genet. 2021. PMID: 33389130

2

Targeted expression of vascular endothelial growth factor 165 in the hrDNA locus mediated by hrDNA targeting vector.

Liang ZM, Luo H, Yang YF, Liu XH, Xie L, Xue ZG, Hu DX, Liang DS, Xia K, Xia JH. Liang ZM, et al. Among authors: luo h. Chin Med J (Engl). 2007 Mar 5;120(5):427-30. Chin Med J (Engl). 2007. PMID: 17376316 No abstract available.

3

[Association of intercellular adhesion molecule-1 gene K469E polymorphism with chronic obstructive pulmonary disease].

Huang H, Jiang H, Kong X, Liu T, Tan Z, Chen P, Luo H. Huang H, et al. Among authors: luo h. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2012 Jan;37(1):78-83. doi: 10.3969/j.issn.1672-7347.2012.01.014. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2012. PMID: 22349390 Chinese.

4

Duplication of 8q12 encompassing CHD7 is associated with a distinct phenotype but without duane anomaly.

Luo H, Xie L, Wang SZ, Chen JL, Huang C, Wang J, Yang JF, Zhang WZ, Yang YF, Tan ZP. Luo H, et al. Eur J Med Genet. 2012 Nov;55(11):646-9. doi: 10.1016/j.ejmg.2012.07.006. Epub 2012 Jul 31. Eur J Med Genet. 2012. PMID: 22902603

5

A clinical and molecular analysis of a patient with Emanuel syndrome.

Luo JW, Yang H, Tan ZP, Tu M, Luo H, Yang YF, Xie L. Luo JW, et al. Among authors: luo h. Mol Med Rep. 2017 Mar;15(3):1348-1352. doi: 10.3892/mmr.2017.6107. Epub 2017 Jan 5. Mol Med Rep. 2017. PMID: 28075445

6

Identification of two novel mutations in the SLCO2A1 prostaglandin transporter gene in a Chinese patient with primary hypertrophic osteoarthropathy.

Guo T, Yang K, Liu L, Tan ZP, Luo H. Guo T, et al. Among authors: luo h. Mol Med Rep. 2017 May;15(5):2977-2982. doi: 10.3892/mmr.2017.6391. Epub 2017 Mar 24. Mol Med Rep. 2017. PMID: 28339061 Free PMC article.

7

Detection of Folliculin Gene Mutations in Two Chinese Families with Birt-Hogg-Dube Syndrome.

Liu L, Yang K, Wang X, Shi Z, Yang Y, Yuan Y, Guo T, Xiao X, Luo H. Liu L, et al. Among authors: luo h. Biomed Res Int. 2017;2017:8751384. doi: 10.1155/2017/8751384. Epub 2017 Jul 12. Biomed Res Int. 2017. PMID: 28785590 Free PMC article.

8

An effective combination of whole-exome sequencing and runs of homozygosity for the diagnosis of primary ciliary dyskinesia in consanguineous families.

Guo T, Tan ZP, Chen HM, Zheng DY, Liu L, Huang XG, Chen P, Luo H, Yang YF. Guo T, et al. Among authors: luo h. Sci Rep. 2017 Aug 11;7(1):7905. doi: 10.1038/s41598-017-08510-z. Sci Rep. 2017. PMID: 28801648 Free PMC article.

9

Whole-Exome Sequencing Identified a Novel Compound Heterozygous Mutation of LRRC6 in a Chinese Primary Ciliary Dyskinesia Patient.

Liu L, Luo H. Liu L, et al. Among authors: luo h. Biomed Res Int. 2018 Jan 8;2018:1854269. doi: 10.1155/2018/1854269. eCollection 2018. Biomed Res Int. 2018. PMID: 29511670 Free PMC article.

10

Whole-exome sequencing identifies a novel CCDC151 mutation, c.325G>T (p.E109X), in a patient with primary ciliary dyskinesia and situs inversus.

Zhang W, Li D, Wei S, Guo T, Wang J, Luo H, Yang Y, Tan Z. Zhang W, et al. Among authors: luo h. J Hum Genet. 2019 Mar;64(3):249-252. doi: 10.1038/s10038-018-0540-x. Epub 2018 Nov 30. J Hum Genet. 2019. PMID: 30504913

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