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

Year Number of Results
2002 1
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2008 3
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2011 1
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2013 2
2014 5
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Page 1
Clinical Phenotypes of CDHR1-Associated Retinal Dystrophies.
Malechka VV, Cukras CA, Chew EY, Sergeev YV, Blain D, Jeffrey BG, Ullah E, Hufnagel RB, Brooks BP, Huryn LA, Zein WM. Malechka VV, et al. Among authors: sergeev yv. Genes (Basel). 2022 May 22;13(5):925. doi: 10.3390/genes13050925. Genes (Basel). 2022. PMID: 35627310 Free PMC article.
Haplotype-based analysis resolves missing heritability in oculocutaneous albinism type 1B.
Loftus SK, Gillis MF, Lundh L, Baxter LL, Wedel JC, Watkins-Chow DE, Donovan FX; NISC Comparative Sequencing Program; Sergeev YV, Oetting WS, Pavan WJ, Adams DR. Loftus SK, et al. Among authors: sergeev yv. Am J Hum Genet. 2023 Jul 6;110(7):1123-1137. doi: 10.1016/j.ajhg.2023.05.012. Epub 2023 Jun 15. Am J Hum Genet. 2023. PMID: 37327787 Free PMC article.
59 results