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Results by year

Table representation of search results timeline featuring number of search results per year.

Year Number of Results
1999 1
2000 6
2001 3
2003 1
2004 1
2005 1
2006 1
2007 2
2008 3
2009 2
2010 1
2011 3
2012 2
2013 1
2014 1
2015 3
2017 2
2018 1
2019 1
2020 1
2021 1
2023 2
2024 0

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Cited In for PMID: 10231032

37 results

Results by year

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Page 1
CEP162 deficiency causes human retinal degeneration and reveals a dual role in ciliogenesis and neurogenesis.
Nuzhat N, Van Schil K, Liakopoulos S, Bauwens M, Rey AD, Käseberg S, Jäger M, Willer JR, Winter J, Truong HM, Gruartmoner N, Van Heetvelde M, Wolf J, Merget R, Grasshoff-Derr S, Van Dorpe J, Hoorens A, Stöhr H, Mansard L, Roux AF, Langmann T, Dannhausen K, Rosenkranz D, Wissing KM, Van Lint M, Rossmann H, Häuser F, Nürnberg P, Thiele H, Zechner U, Pearring JN, De Baere E, Bolz HJ. Nuzhat N, et al. J Clin Invest. 2023 Apr 17;133(8):e161156. doi: 10.1172/JCI161156. J Clin Invest. 2023. PMID: 36862503 Free PMC article.
BAHD1 haploinsufficiency results in anxiety-like phenotypes in male mice.
Pourpre R, Naudon L, Meziane H, Lakisic G, Jouneau L, Varet H, Legendre R, Wendling O, Selloum M, Proux C, Coppée JY, Herault Y, Bierne H. Pourpre R, et al. PLoS One. 2020 May 14;15(5):e0232789. doi: 10.1371/journal.pone.0232789. eCollection 2020. PLoS One. 2020. PMID: 32407325 Free PMC article.
Review of the phenotypic spectrum associated with haploinsufficiency of MYRF.
Rossetti LZ, Glinton K, Yuan B, Liu P, Pillai N, Mizerik E, Magoulas P, Rosenfeld JA, Karaviti L, Sutton VR, Lalani SR, Scott DA. Rossetti LZ, et al. Am J Med Genet A. 2019 Jul;179(7):1376-1382. doi: 10.1002/ajmg.a.61182. Epub 2019 May 8. Am J Med Genet A. 2019. PMID: 31069960 Free PMC article. Review.
37 results