Similar articles for PMID: 35058298

Year	Number of Results
1997	3
1998	5
1999	5
2000	4
2001	4
2002	2
2003	2
2004	6
2005	3
2006	9
2007	6
2008	4
2009	6
2010	4
2011	5
2012	1
2013	5
2014	6
2015	2
2016	1
2017	2
2018	4
2019	4
2020	4
2021	9
2022	6

1

Re-Examining the Cochlea in Branchio-Oto-Renal Syndrome: Genotype-Phenotype Correlation.

Pao J, D'Arco F, Clement E, Picariello S, Moonis G, Robson CD, Juliano AF. Pao J, et al. AJNR Am J Neuroradiol. 2022 Feb;43(2):309-314. doi: 10.3174/ajnr.A7396. Epub 2022 Jan 20. AJNR Am J Neuroradiol. 2022. PMID: 35058298

2

Genetic research progress in branchio-oto syndrome/ branchio-oto-renal syndrome.

Chen A, Ling J, Feng Y. Chen A, et al. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2022 Jan 28;47(1):129-138. doi: 10.11817/j.issn.1672-7347.2022.210251. Zhong Nan Da Xue Xue Bao Yi Xue Ban. 2022. PMID: 35545373 Free article. Chinese, English.

3

The Unwound Cochlea: A Specific Imaging Marker of Branchio-Oto-Renal Syndrome.

Hsu A, Desai N, Paldino MJ. Hsu A, et al. AJNR Am J Neuroradiol. 2018 Dec;39(12):2345-2349. doi: 10.3174/ajnr.A5856. Epub 2018 Nov 1. AJNR Am J Neuroradiol. 2018. PMID: 30385470 Free PMC article.

4

Mutation screening of the EYA1, SIX1, and SIX5 genes in an East Asian cohort with branchio-oto-renal syndrome.

Wang SH, Wu CC, Lu YC, Lin YH, Su YN, Hwu WL, Yu IS, Hsu CJ. Wang SH, et al. Laryngoscope. 2012 May;122(5):1130-6. doi: 10.1002/lary.23217. Epub 2012 Mar 23. Laryngoscope. 2012. PMID: 22447252

5

Mutational analysis of EYA1, SIX1 and SIX5 genes and strategies for management of hearing loss in patients with BOR/BO syndrome.

Song MH, Kwon TJ, Kim HR, Jeon JH, Baek JI, Lee WS, Kim UK, Choi JY. Song MH, et al. PLoS One. 2013 Jun 28;8(6):e67236. doi: 10.1371/journal.pone.0067236. Print 2013. PLoS One. 2013. PMID: 23840632 Free PMC article.

6

Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutations.

Krug P, Morinière V, Marlin S, Koubi V, Gabriel HD, Colin E, Bonneau D, Salomon R, Antignac C, Heidet L. Krug P, et al. Hum Mutat. 2011 Feb;32(2):183-90. doi: 10.1002/humu.21402. Hum Mutat. 2011. PMID: 21280147 Free article.

7

Branchio-oto-renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses.

Sanggaard KM, Rendtorff ND, Kjaer KW, Eiberg H, Johnsen T, Gimsing S, Dyrmose J, Nielsen KO, Lage K, Tranebjaerg L. Sanggaard KM, et al. Eur J Hum Genet. 2007 Nov;15(11):1121-31. doi: 10.1038/sj.ejhg.5201900. Epub 2007 Jul 18. Eur J Hum Genet. 2007. PMID: 17637804

8

Branchio-oto-renal syndrome: comprehensive review based on nationwide surveillance in Japan.

Morisada N, Nozu K, Iijima K. Morisada N, et al. Pediatr Int. 2014 Jun;56(3):309-14. doi: 10.1111/ped.12357. Pediatr Int. 2014. PMID: 24730701 Review.

9

SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.

Kochhar A, Orten DJ, Sorensen JL, Fischer SM, Cremers CW, Kimberling WJ, Smith RJ. Kochhar A, et al. Hum Mutat. 2008 Apr;29(4):565. doi: 10.1002/humu.20714. Hum Mutat. 2008. PMID: 18330911

10

Identification of a Novel CNV at 8q13 in a Family With Branchio-Oto-Renal Syndrome and Epilepsy.

Men M, Li W, Chen H, Wu J, Feng Y, Guo H, Li JD. Men M, et al. Laryngoscope. 2020 Feb;130(2):526-532. doi: 10.1002/lary.27941. Epub 2019 Mar 25. Laryngoscope. 2020. PMID: 30908667

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