PubMed for id: 60529

Year	Number of Results
1993	1
1995	1
1996	1
1999	1
2000	2
2001	3
2002	1
2003	1
2004	2
2005	1
2006	3
2007	1
2009	4
2010	5
2011	1
2012	2
2013	3
2014	3
2015	2
2016	1
2017	4
2019	2
2020	6
2021	3
2023	1
2024	0

1

Dominant frontonasal dysplasia with ectodermal defects results from increased activity of ALX4.

Peled A, Sarig O, Mohamad J, Eskin-Schwartz M, Vodo D, Bochner R, Malchin N, Isakov O, Shomron N, Fainberg G, Bertolini M, Paus R, Sprecher E. Peled A, et al. Am J Med Genet A. 2023 Dec;191(12):2806-2812. doi: 10.1002/ajmg.a.63408. Epub 2023 Sep 19. Am J Med Genet A. 2023. PMID: 37724761

2

De novo ALX4 variant detected in child with non-syndromic craniosynostosis.

Fonteles CS, Finnell RH, Lei Y, Zurita-Jimenez ME, Monteiro AJ, George TM, Harshbarger RJ. Fonteles CS, et al. Braz J Med Biol Res. 2021 Sep 24;54(11):e11396. doi: 10.1590/1414-431X2021e11396. eCollection 2021. Braz J Med Biol Res. 2021. PMID: 34586326 Free article.

3

Variants in ALX4 and their association with genitourinary defects.

Chen CH, Bournat JC, Wilken N, Rosenfeld JA, Zhang J, Seth A, Jorgez CJ. Chen CH, et al. Andrology. 2020 Sep;8(5):1243-1255. doi: 10.1111/andr.12815. Epub 2020 Jul 16. Andrology. 2020. PMID: 32385972 Free PMC article.

4

ALX4, an epigenetically down regulated tumor suppressor, inhibits breast cancer progression by interfering Wnt/β-catenin pathway.

Yang J, Han F, Liu W, Chen H, Hao X, Jiang X, Yin L, Huang Y, Cao J, Zhang H, Liu J. Yang J, et al. J Exp Clin Cancer Res. 2017 Nov 28;36(1):170. doi: 10.1186/s13046-017-0643-9. J Exp Clin Cancer Res. 2017. PMID: 29183346 Free PMC article.

5

[Mother and son with enlarged parietal foramina, persistent fetal vein, and ALX4 mutation].

Morita M, Nanba E, Adachi K, Ohno K. Morita M, et al. No To Hattatsu. 2016 May;48(3):205-8. No To Hattatsu. 2016. PMID: 27349084 Japanese.

6

Mild nasal clefting may be predictive for ALX4 heterozygotes.

Altunoglu U, Satkın B, Uyguner ZO, Kayserili H. Altunoglu U, et al. Am J Med Genet A. 2014 Aug;164A(8):2054-8. doi: 10.1002/ajmg.a.36578. Epub 2014 Apr 24. Am J Med Genet A. 2014. PMID: 24764194

7

Vertical transmission of a frontonasal phenotype caused by a novel ALX4 mutation.

Bertola DR, Rodrigues MG, Quaio CR, Kim CA, Passos-Bueno MR. Bertola DR, et al. Am J Med Genet A. 2013 Mar;161A(3):600-4. doi: 10.1002/ajmg.a.35762. Epub 2013 Feb 7. Am J Med Genet A. 2013. PMID: 23401352

8

ALX4 gain-of-function mutations in nonsyndromic craniosynostosis.

Yagnik G, Ghuman A, Kim S, Stevens CG, Kimonis V, Stoler J, Sanchez-Lara PA, Bernstein JA, Naydenov C, Drissi H, Cunningham ML, Kim J, Boyadjiev SA. Yagnik G, et al. Hum Mutat. 2012 Dec;33(12):1626-9. doi: 10.1002/humu.22166. Epub 2012 Aug 13. Hum Mutat. 2012. PMID: 22829454 Free PMC article.

9

Loss of ALX4 expression in epithelial cells and adjacent stromal cells in breast cancer.

Chang H, Mohabir N, Done S, Hamel PA. Chang H, et al. J Clin Pathol. 2009 Oct;62(10):908-14. doi: 10.1136/jcp.2009.067298. J Clin Pathol. 2009. PMID: 19783719

10

Construction of a natural panel of 11p11.2 deletions and further delineation of the critical region involved in Potocki-Shaffer syndrome.

Wakui K, Gregato G, Ballif BC, Glotzbach CD, Bailey KA, Kuo PL, Sue WC, Sheffield LJ, Irons M, Gomez EG, Hecht JT, Potocki L, Shaffer LG. Wakui K, et al. Eur J Hum Genet. 2005 May;13(5):528-40. doi: 10.1038/sj.ejhg.5201366. Eur J Hum Genet. 2005. PMID: 15852040

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