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

Year Number of Results
1990 2
1992 1
1999 2
2000 1
2001 3
2002 1
2003 3
2004 6
2005 2
2006 1
2007 2
2009 3
2010 2
2012 1
2014 4
2015 2
2017 3
2018 3
2019 4
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2024 1

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47 results

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Page 1
Recent Advances in Craniosynostosis.
Yilmaz E, Mihci E, Nur B, Alper ÖM, Taçoy Ş. Yilmaz E, et al. Among authors: alper om. Pediatr Neurol. 2019 Oct;99:7-15. doi: 10.1016/j.pediatrneurol.2019.01.018. Epub 2019 Feb 2. Pediatr Neurol. 2019. PMID: 31421914 Review.
Novel insights into c-Src.
Alper O, Bowden ET. Alper O, et al. Curr Pharm Des. 2005;11(9):1119-30. doi: 10.2174/1381612053507576. Curr Pharm Des. 2005. PMID: 15853660 Review.
Genome sequencing identifies coding and non-coding variants for non-syndromic hearing loss.
Ramzan M, Duman D, Hendricks LCP, Guo S, Mutlu A, Kalcioglu MT, Seyhan S, Carranza C, Bonyadi M, Mahdieh N, Yildirim-Baylan M, Figueroa-Ildefonso E, Alper O, Atik T, Ayral A, Bozan N, Balta B, Rivas C, Manzoli GN, Huesca-Hernandez F, Kuchay RAH, Durgut M, Bademci G, Tekin M. Ramzan M, et al. Among authors: alper o. J Hum Genet. 2023 Oct;68(10):657-669. doi: 10.1038/s10038-023-01159-9. Epub 2023 May 22. J Hum Genet. 2023. PMID: 37217689
Novel Gene Variants Associated with Primary Ciliary Dyskinesia.
Demir Eksi D, Yilmaz E, Basaran AE, Erduran G, Nur B, Mihci E, Karadag B, Bingol A, Alper OM. Demir Eksi D, et al. Among authors: alper om. Indian J Pediatr. 2022 Jul;89(7):682-691. doi: 10.1007/s12098-022-04098-z. Epub 2022 Mar 3. Indian J Pediatr. 2022. PMID: 35239159
Novel anti-filamin-A antibody detects a secreted variant of filamin-A in plasma from patients with breast carcinoma and high-grade astrocytoma.
Alper O, Stetler-Stevenson WG, Harris LN, Leitner WW, Ozdemirli M, Hartmann D, Raffeld M, Abu-Asab M, Byers S, Zhuang Z, Oldfield EH, Tong Y, Bergmann-Leitner E, Criss WE, Nagasaki K, Mok SC, Cramer DW, Karaveli FS, Goldbach-Mansky R, Leo P, Stromberg K, Weil RJ. Alper O, et al. Cancer Sci. 2009 Sep;100(9):1748-56. doi: 10.1111/j.1349-7006.2009.01244.x. Epub 2009 Jun 17. Cancer Sci. 2009. PMID: 19594548 Free PMC article.
A novel AXIN2 gene mutation in sagittal synostosis.
Yilmaz E, Mihci E, Guzel Nur B, Alper OM. Yilmaz E, et al. Among authors: alper om. Am J Med Genet A. 2018 Sep;176(9):1976-1980. doi: 10.1002/ajmg.a.40373. Epub 2018 Aug 8. Am J Med Genet A. 2018. PMID: 30088857
47 results