PubMed (Bookshelf cited) for id: 761671

Year	Number of Results
1998	1
1999	1
2000	1
2001	1
2004	1
2006	1
2007	2
2008	5
2010	1
2011	3
2012	1
2013	6
2014	2
2015	3
2016	4
2017	2
2018	2
2019	2
2020	6
2021	5
2022	1
2024	0

1

Variation among DNA banking consent forms: points for clinicians to bank on.

Huang SJ, Amendola LM, Sternen DL. Huang SJ, et al. J Community Genet. 2022 Aug;13(4):389-397. doi: 10.1007/s12687-022-00601-3. Epub 2022 Jul 14. J Community Genet. 2022. PMID: 35834113 Free PMC article.

2

Analyses of oligodontia phenotypes and genetic etiologies.

Zhou M, Zhang H, Camhi H, Seymen F, Koruyucu M, Kasimoglu Y, Kim JW, Kim-Berman H, Yuson NMR, Benke PJ, Wu Y, Wang F, Zhu Y, Simmer JP, Hu JC. Zhou M, et al. Int J Oral Sci. 2021 Sep 30;13(1):32. doi: 10.1038/s41368-021-00135-3. Int J Oral Sci. 2021. PMID: 34593752 Free PMC article.

3

Characterization of EDARADD gene mutations responsible for hypohidrotic ectodermal dysplasia.

Asano N, Yasuno S, Hayashi R, Shimomura Y. Asano N, et al. J Dermatol. 2021 Oct;48(10):1533-1541. doi: 10.1111/1346-8138.16044. Epub 2021 Jul 4. J Dermatol. 2021. PMID: 34219261

4

WNT10A, dermatology and dentistry.

Doolan BJ, Onoufriadis A, Kantaputra P, McGrath JA. Doolan BJ, et al. Br J Dermatol. 2021 Dec;185(6):1105-1111. doi: 10.1111/bjd.20601. Epub 2021 Sep 7. Br J Dermatol. 2021. PMID: 34184264 Review.

5

Lrp6 Dynamic Expression in Tooth Development and Mutations in Oligodontia.

Yu M, Fan Z, Wong SW, Sun K, Zhang L, Liu H, Feng H, Liu Y, Han D. Yu M, et al. J Dent Res. 2021 Apr;100(4):415-422. doi: 10.1177/0022034520970459. Epub 2020 Nov 9. J Dent Res. 2021. PMID: 33164649

6

Functional Effects of WNT10A Rare Variants Associated with Tooth Agenesis.

Zeng Y, Baugh E, Akyalcin S, Letra A. Zeng Y, et al. J Dent Res. 2021 Mar;100(3):302-309. doi: 10.1177/0022034520962728. Epub 2020 Oct 9. J Dent Res. 2021. PMID: 33034246

7

The Human Gene Mutation Database (HGMD^®): optimizing its use in a clinical diagnostic or research setting.

Stenson PD, Mort M, Ball EV, Chapman M, Evans K, Azevedo L, Hayden M, Heywood S, Millar DS, Phillips AD, Cooper DN. Stenson PD, et al. Hum Genet. 2020 Oct;139(10):1197-1207. doi: 10.1007/s00439-020-02199-3. Epub 2020 Jun 28. Hum Genet. 2020. PMID: 32596782 Free PMC article. Review.

8

Safety and immunogenicity of Fc-EDA, a recombinant ectodysplasin A1 replacement protein, in human subjects.

Körber I, Klein OD, Morhart P, Faschingbauer F, Grange DK, Clarke A, Bodemer C, Maitz S, Huttner K, Kirby N, Durand C, Schneider H. Körber I, et al. Br J Clin Pharmacol. 2020 Oct;86(10):2063-2069. doi: 10.1111/bcp.14301. Epub 2020 Apr 24. Br J Clin Pharmacol. 2020. PMID: 32250462 Free PMC article.

9

LEF1 haploinsufficiency causes ectodermal dysplasia.

Lévy J, Capri Y, Rachid M, Dupont C, Vermeesch JR, Devriendt K, Verloes A, Tabet AC, Bailleul-Forestier I. Lévy J, et al. Clin Genet. 2020 Apr;97(4):595-600. doi: 10.1111/cge.13714. Epub 2020 Feb 17. Clin Genet. 2020. PMID: 32022899

10

Natural history of X-linked hypohidrotic ectodermal dysplasia: a 5-year follow-up study.

Wohlfart S, Meiller R, Hammersen J, Park J, Menzel-Severing J, Melichar VO, Huttner K, Johnson R, Porte F, Schneider H. Wohlfart S, et al. Orphanet J Rare Dis. 2020 Jan 10;15(1):7. doi: 10.1186/s13023-019-1288-x. Orphanet J Rare Dis. 2020. PMID: 31924237 Free PMC article.

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