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

Year Number of Results
1996 1
1997 1
1998 4
1999 4
2000 2
2001 2
2002 5
2003 3
2004 7
2005 7
2006 5
2007 3
2008 8
2009 7
2010 7
2011 7
2012 8
2013 19
2014 16
2015 14
2016 12
2017 16
2018 10
2019 12
2020 8
2021 1
2022 13
2023 12
2024 15
2025 1

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208 results

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Page 1
Expanding the genetics and phenotypes of ocular congenital cranial dysinnervation disorders.
Jurgens JA, Barry BJ, Chan WM, MacKinnon S, Whitman MC, Matos Ruiz PM, Pratt BM, England EM, Pais L, Lemire G, Groopman E, Glaze C, Russell KA, Singer-Berk M, Di Gioia SA, Lee AS, Andrews C, Shaaban S, Wirth MM, Bekele S, Toffoloni M, Bradford VR, Foster EE, Berube L, Rivera-Quiles C, Mensching FM, Sanchis-Juan A, Fu JM, Wong I, Zhao X, Wilson MW, Weisburd B, Lek M; Ocular CCDD Phenotyping Consortium; Brand H, Talkowski ME, MacArthur DG, O'Donnell-Luria A, Robson CD, Hunter DG, Engle EC. Jurgens JA, et al. Genet Med. 2024 Jul 17:101216. doi: 10.1016/j.gim.2024.101216. Online ahead of print. Genet Med. 2024. PMID: 39033378 Free article.
Genetic Aspects of Glaucoma: An Updated Review.
Chacon-Camacho OF, Arce-Gonzalez R, Sanchez-de la Rosa F, Urióstegui-Rojas A, Hofmann-Blancas ME, Mata-Flores F, Zenteno JC. Chacon-Camacho OF, et al. Among authors: zenteno jc. Curr Mol Med. 2024;24(10):1231-1249. doi: 10.2174/1566524023666230602143617. Curr Mol Med. 2024. PMID: 37272463 Review.
Familial Hypercholesterolemia: Update and Review.
Chacón-Camacho OF, Pozo-Molina G, Méndez-Catalá CF, Reyes-Reali J, Méndez-Cruz R, Zenteno JC. Chacón-Camacho OF, et al. Among authors: zenteno jc. Endocr Metab Immune Disord Drug Targets. 2022;22(2):198-211. doi: 10.2174/1871530321666210208212148. Endocr Metab Immune Disord Drug Targets. 2022. PMID: 33563162
Genes relacionados con microftalmia y anoftalmia hereditarias.
Matías-Pérez D, García-Montalvo IA, Zenteno JC. Matías-Pérez D, et al. Among authors: zenteno jc. Gac Med Mex. 2017;153(7):824-829. doi: 10.24875/GMM.17002604. Gac Med Mex. 2017. PMID: 29414965 Free article. Review.
MTSS2-related neurodevelopmental disorder: Further delineation of the phenotype.
Corona-Rivera JR, Zenteno JC, Ordoñez-Labastida V, Cruz-Cruz JP, Cortés-Pastrana RC, Peña-Padilla C, Bobadilla-Morales L, Corona-Rivera A, Martínez-Herrera A. Corona-Rivera JR, et al. Among authors: zenteno jc. Eur J Med Genet. 2023 Oct;66(10):104826. doi: 10.1016/j.ejmg.2023.104826. Epub 2023 Aug 30. Eur J Med Genet. 2023. PMID: 37657631
208 results