Feng H - Search Results

1

EDA Variants Are Responsible for Approximately 90% of Deciduous Tooth Agenesis.

Su L, Lin B, Yu M, Liu Y, Sun S, Feng H, Liu H, Han D. Su L, et al. Among authors: feng h. Int J Mol Sci. 2024 Sep 27;25(19):10451. doi: 10.3390/ijms251910451. Int J Mol Sci. 2024. PMID: 39408781 Free PMC article.

2

A case-control study of the association between tooth-development gene polymorphisms and non-syndromic hypodontia in the Chinese Han population.

Liu H, Zhang J, Song S, Zhao H, Han D, Feng H. Liu H, et al. Among authors: feng h. Eur J Oral Sci. 2012 Oct;120(5):378-85. doi: 10.1111/j.1600-0722.2012.00986.x. Epub 2012 Aug 18. Eur J Oral Sci. 2012. PMID: 22984994

3

Functional Study of Ectodysplasin-A Mutations Causing Non-Syndromic Tooth Agenesis.

Shen W, Wang Y, Liu Y, Liu H, Zhao H, Zhang G, Snead ML, Han D, Feng H. Shen W, et al. Among authors: feng h. PLoS One. 2016 May 4;11(5):e0154884. doi: 10.1371/journal.pone.0154884. eCollection 2016. PLoS One. 2016. PMID: 27144394 Free PMC article.

4

BMP4 mutations in tooth agenesis and low bone mass.

Yu M, Wang H, Fan Z, Xie C, Liu H, Liu Y, Han D, Wong SW, Feng H. Yu M, et al. Among authors: feng h. Arch Oral Biol. 2019 Jul;103:40-46. doi: 10.1016/j.archoralbio.2019.05.012. Epub 2019 May 15. Arch Oral Biol. 2019. PMID: 31128441 Free PMC article.

5

Novel PITX2 mutations identified in Axenfeld-Rieger syndrome and the pattern of PITX2-related tooth agenesis.

Fan Z, Sun S, Liu H, Yu M, Liu Z, Wong SW, Liu Y, Han D, Feng H. Fan Z, et al. Among authors: feng h. Oral Dis. 2019 Nov;25(8):2010-2019. doi: 10.1111/odi.13196. Epub 2019 Oct 8. Oral Dis. 2019. PMID: 31529555

6

Comparative analysis of rare EDAR mutations and tooth agenesis pattern in EDAR- and EDA-associated nonsyndromic oligodontia.

Zhang L, Yu M, Wong SW, Qu H, Cai T, Liu Y, Liu H, Fan Z, Zheng J, Zhou Y, Feng H, Han D. Zhang L, et al. Among authors: feng h. Hum Mutat. 2020 Nov;41(11):1957-1966. doi: 10.1002/humu.24104. Epub 2020 Sep 16. Hum Mutat. 2020. PMID: 32906216

7

Functional study of novel PAX9 variants: The paired domain and non-syndromic oligodontia.

Sun K, Yu M, Yeh I, Zhang L, Liu H, Cai T, Feng H, Liu Y, Han D. Sun K, et al. Among authors: feng h. Oral Dis. 2021 Sep;27(6):1468-1477. doi: 10.1111/odi.13684. Epub 2020 Nov 3. Oral Dis. 2021. PMID: 33078491

8

Novel MSX1 variants identified in families with nonsyndromic oligodontia.

Zheng J, Yu M, Liu H, Cai T, Feng H, Liu Y, Han D. Zheng J, et al. Among authors: feng h. Int J Oral Sci. 2021 Jan 8;13(1):2. doi: 10.1038/s41368-020-00106-0. Int J Oral Sci. 2021. PMID: 33419968 Free PMC article.

9

Four Novel PAX9 Variants and the PAX9-Related Non-Syndromic Tooth Agenesis Patterns.

Liu H, Liu H, Su L, Zheng J, Feng H, Liu Y, Yu M, Han D. Liu H, et al. Among authors: feng h. Int J Mol Sci. 2022 Jul 24;23(15):8142. doi: 10.3390/ijms23158142. Int J Mol Sci. 2022. PMID: 35897718 Free PMC article.

10

KDF1 Novel Variant Causes Unique Dental and Oral Epithelial Defects.

Yu M, Liu H, Liu Y, Zheng J, Wu J, Sun K, Feng H, Liu H, Han D. Yu M, et al. Among authors: feng h. Int J Mol Sci. 2022 Oct 18;23(20):12465. doi: 10.3390/ijms232012465. Int J Mol Sci. 2022. PMID: 36293320 Free PMC article.

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