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Year Number of Results
2012 1
2013 1
2014 2
2015 3
2017 4
2018 6
2019 2
2020 3
2021 3
2022 3
2023 0

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24 results

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Page 1
Making every birth count: Outcomes of a perinatal mortality audit program.
Flenady V, Kettle I, Laporte J, Birthisel D, Hardiman L, Matsika A, Whelan N, Lehner C, Payton D, Utz M, Wojcieszek AM, Lawford H, Walsh T, Ellwood D. Flenady V, et al. Among authors: matsika a. Aust N Z J Obstet Gynaecol. 2021 Aug;61(4):540-547. doi: 10.1111/ajo.13325. Epub 2021 Apr 1. Aust N Z J Obstet Gynaecol. 2021. PMID: 33792893
Variable expressivity in a four-generation ACDMPV family with a non-coding hypermorphic SNV in trans to the frameshifting FOXF1 variant.
Yıldız Bölükbaşı E, Karolak JA, Szafranski P, Gambin T, Matsika A, McManus S, Scott HS, Arts P, Ha T, Barnett CP, Rodgers J, Stankiewicz P. Yıldız Bölükbaşı E, et al. Among authors: matsika a. Eur J Hum Genet. 2022 Oct;30(10):1182-1186. doi: 10.1038/s41431-022-01159-x. Epub 2022 Jul 28. Eur J Hum Genet. 2022. PMID: 35902696
Management of Xen gel stent mega-bleb due to Tenon's cyst.
Lyons D, Lee GA, Matsika A, Wong D, Shah P. Lyons D, et al. Among authors: matsika a. Clin Exp Ophthalmol. 2020 May;48(4):528-531. doi: 10.1111/ceo.13717. Epub 2020 Feb 3. Clin Exp Ophthalmol. 2020. PMID: 31975515 No abstract available.
Expanding the clinicopathological spectrum of succinate dehydrogenase-deficient renal cell carcinoma with a focus on variant morphologies: a study of 62 new tumors in 59 patients.
Fuchs TL, Maclean F, Turchini J, Vargas AC, Bhattarai S, Agaimy A, Hartmann A, Kao CS, Ellis C, Bonert M, Leroy X, Kunju LP, Schwartz L, Matsika A, Williamson SR, Rao P, Divatia M, Guarch R, Algaba F, Balancin ML, Zhou M, Samaratunga H, da Cunha IW, Brimo F, Ryan A, Clouston D, Aron M, O'Donnell M, Chan E, Hirsch MS, Moch H, Pang CY, Wah C, Yin W, Perry-Keene J, Yilmaz A, Chou A, Clarkson A, van der Westhuizen G, Morrison E, Zwi J, Hes O, Trpkov K, Gill AJ. Fuchs TL, et al. Among authors: matsika a. Mod Pathol. 2022 Jun;35(6):836-849. doi: 10.1038/s41379-021-00998-1. Epub 2021 Dec 23. Mod Pathol. 2022. PMID: 34949766
Application of Whole Genome Sequencing Technology in the Investigation of Genetic Causes of Fetal, Perinatal, and Early Infant Death.
Armes JE, Williams M, Price G, Wallis T, Gallagher R, Matsika A, Joy C, Galea M, Gardener G, Leach R, Swagemakers SM, Tearle R, Stubbs A, Harraway J, van der Spek PJ, Venter DJ. Armes JE, et al. Among authors: matsika a. Pediatr Dev Pathol. 2018 Jan-Feb;21(1):54-67. doi: 10.1177/1093526617715528. Epub 2017 Jun 22. Pediatr Dev Pathol. 2018. PMID: 28641477
Medical Education Partnership Initiative (MEPI) in Zimbabwe: Outcomes and Challenges.
Hakim JG, Chidzonga MM, Borok MZ, Nathoo KJ, Matenga J, Havranek E, Cowan F, Abas M, Aagaard E, Connors S, Nkomani S, Ndhlovu CE, Matsika A, Barry M, Campbell TB. Hakim JG, et al. Among authors: matsika a. Glob Health Sci Pract. 2018 Mar 30;6(1):82-92. doi: 10.9745/GHSP-D-17-00052. Print 2018 Mar 21. Glob Health Sci Pract. 2018. PMID: 29602867 Free PMC article.
CDCP1 enhances Wnt signaling in colorectal cancer promoting nuclear localization of β-catenin and E-cadherin.
He Y, Davies CM, Harrington BS, Hellmers L, Sheng Y, Broomfield A, McGann T, Bastick K, Zhong L, Wu A, Maresh G, McChesney S, Yau Wong K, Adams MN, Sullivan RC, Palmer JS, Burke LJ, Ewing AD, Zhang X, Margolin D, Li L, Lourie R, Matsika A, Srinivasan B, McGuckin MA, Lumley JW, Hooper JD. He Y, et al. Among authors: matsika a. Oncogene. 2020 Jan;39(1):219-233. doi: 10.1038/s41388-019-0983-3. Epub 2019 Aug 30. Oncogene. 2020. PMID: 31471585
24 results