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Variation in FGF1, FOXE1, and TIMP2 genes is associated with nonsyndromic cleft lip with or without cleft palate.
Nikopensius T, Kempa I, Ambrozaitytė L, Jagomägi T, Saag M, Matulevičienė A, Utkus A, Krjutškov K, Tammekivi V, Piekuse L, Akota I, Barkane B, Krumina A, Klovins J, Lace B, Kučinskas V, Metspalu A. Nikopensius T, et al. Among authors: krumina a. Birth Defects Res A Clin Mol Teratol. 2011 Apr;91(4):218-25. doi: 10.1002/bdra.20791. Epub 2011 Apr 1. Birth Defects Res A Clin Mol Teratol. 2011. PMID: 21462296
Genetic variants in COL2A1, COL11A2, and IRF6 contribute risk to nonsyndromic cleft palate.
Nikopensius T, Jagomägi T, Krjutskov K, Tammekivi V, Saag M, Prane I, Piekuse L, Akota I, Barkane B, Krumina A, Ambrozaityte L, Matuleviciene A, Kucinskiene ZA, Lace B, Kucinskas V, Metspalu A. Nikopensius T, et al. Among authors: krumina a. Birth Defects Res A Clin Mol Teratol. 2010 Sep;88(9):748-56. doi: 10.1002/bdra.20700. Birth Defects Res A Clin Mol Teratol. 2010. PMID: 20672350
BCL3 gene role in facial morphology.
Lace B, Kempa I, Klovins J, Stavusis J, Krumina A, Akota I, Barkane B, Vieira AR, Nagle E, Grinfelde I, Maulina I. Lace B, et al. Among authors: krumina a. Birth Defects Res A Clin Mol Teratol. 2012 Nov;94(11):918-24. doi: 10.1002/bdra.23085. Epub 2012 Nov 1. Birth Defects Res A Clin Mol Teratol. 2012. PMID: 23115114
Mitochondrial DNA origins of the Latvian clefting population.
Vieira AR, Pliss L, Pelnena I, Krumina A, Baumanis V, Lace B. Vieira AR, et al. Among authors: krumina a. Mitochondrion. 2011 Mar;11(2):357-9. doi: 10.1016/j.mito.2010.10.001. Epub 2010 Oct 12. Mitochondrion. 2011. PMID: 20946971
Robust genotyping tool for autosomal recessive type of limb-girdle muscular dystrophies.
Inashkina I, Jankevics E, Stavusis J, Vasiljeva I, Viksne K, Micule I, Strautmanis J, Naudina MS, Cimbalistiene L, Kucinskas V, Krumina A, Utkus A, Burnyte B, Matuleviciene A, Lace B. Inashkina I, et al. Among authors: krumina a. BMC Musculoskelet Disord. 2016 May 4;17:200. doi: 10.1186/s12891-016-1058-z. BMC Musculoskelet Disord. 2016. PMID: 27142102 Free PMC article.
A New Baltic Population-Specific Human Genetic Marker in the PMCA4 Gene.
Stavusis J, Inashkina I, Lace B, Pelnena D, Limborska S, Khrunin A, Kucinskas V, Krumina A, Piekuse L, Zorn B, Fodina V, Punab M, Erenpreiss J. Stavusis J, et al. Among authors: krumina a. Hum Hered. 2016;82(3-4):140-146. doi: 10.1159/000481434. Epub 2017 Nov 2. Hum Hered. 2016. PMID: 29131013
78 results