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

Year Number of Results
1994 3
1996 1
1997 1
1998 1
1999 1
2000 3
2002 2
2003 3
2004 1
2005 5
2006 4
2007 4
2008 1
2009 3
2010 4
2011 6
2012 6
2013 4
2014 7
2015 1
2016 1
2017 3
2018 1
2019 2
2020 4
2021 2
2022 3
2023 1
2024 1

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74 results

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Page 1
Pegunigalsidase alfa, a novel PEGylated enzyme replacement therapy for Fabry disease, provides sustained plasma concentrations and favorable pharmacodynamics: A 1-year Phase 1/2 clinical trial.
Schiffmann R, Goker-Alpan O, Holida M, Giraldo P, Barisoni L, Colvin RB, Jennette CJ, Maegawa G, Boyadjiev SA, Gonzalez D, Nicholls K, Tuffaha A, Atta MG, Rup B, Charney MR, Paz A, Szlaifer M, Alon S, Brill-Almon E, Chertkoff R, Hughes D. Schiffmann R, et al. Among authors: boyadjiev sa. J Inherit Metab Dis. 2019 May;42(3):534-544. doi: 10.1002/jimd.12080. Epub 2019 Apr 8. J Inherit Metab Dis. 2019. PMID: 30834538 Clinical Trial.
Genetic advances in craniosynostosis.
Lattanzi W, Barba M, Di Pietro L, Boyadjiev SA. Lattanzi W, et al. Among authors: boyadjiev sa. Am J Med Genet A. 2017 May;173(5):1406-1429. doi: 10.1002/ajmg.a.38159. Epub 2017 Feb 4. Am J Med Genet A. 2017. PMID: 28160402 Free PMC article. Review.
The genetic overlap between osteoporosis and craniosynostosis.
Kague E, Medina-Gomez C, Boyadjiev SA, Rivadeneira F. Kague E, et al. Among authors: boyadjiev sa. Front Endocrinol (Lausanne). 2022 Sep 26;13:1020821. doi: 10.3389/fendo.2022.1020821. eCollection 2022. Front Endocrinol (Lausanne). 2022. PMID: 36225206 Free PMC article. Review.
Genetics of craniosynostosis.
Kimonis V, Gold JA, Hoffman TL, Panchal J, Boyadjiev SA. Kimonis V, et al. Among authors: boyadjiev sa. Semin Pediatr Neurol. 2007 Sep;14(3):150-61. doi: 10.1016/j.spen.2007.08.008. Semin Pediatr Neurol. 2007. PMID: 17980312 Review.
Joint multi-ancestry and admixed GWAS reveals the complex genetics behind human cranial vault shape.
Goovaerts S, Hoskens H, Eller RJ, Herrick N, Musolf AM, Justice CM, Yuan M, Naqvi S, Lee MK, Vandermeulen D, Szabo-Rogers HL, Romitti PA, Boyadjiev SA, Marazita ML, Shaffer JR, Shriver MD, Wysocka J, Walsh S, Weinberg SM, Claes P. Goovaerts S, et al. Among authors: boyadjiev sa. Nat Commun. 2023 Nov 16;14(1):7436. doi: 10.1038/s41467-023-43237-8. Nat Commun. 2023. PMID: 37973980 Free PMC article. Review.
Bladder exstrophy-epispadias complex.
Ludwig M, Ching B, Reutter H, Boyadjiev SA. Ludwig M, et al. Among authors: boyadjiev sa. Birth Defects Res A Clin Mol Teratol. 2009 Jun;85(6):509-22. doi: 10.1002/bdra.20557. Birth Defects Res A Clin Mol Teratol. 2009. PMID: 19161161 Review.
Genetic analysis of non-syndromic craniosynostosis.
Boyadjiev SA; International Craniosynostosis Consortium. Boyadjiev SA, et al. Orthod Craniofac Res. 2007 Aug;10(3):129-37. doi: 10.1111/j.1601-6343.2007.00393.x. Orthod Craniofac Res. 2007. PMID: 17651129 Review.
SMAD6 variants in craniosynostosis: genotype and phenotype evaluation.
Calpena E, Cuellar A, Bala K, Swagemakers SMA, Koelling N, McGowan SJ, Phipps JM, Balasubramanian M, Cunningham ML, Douzgou S, Lattanzi W, Morton JEV, Shears D, Weber A, Wilson LC, Lord H, Lester T, Johnson D, Wall SA, Twigg SRF, Mathijssen IMJ, Boardman-Pretty F; Genomics England Research Consortium; Boyadjiev SA, Wilkie AOM. Calpena E, et al. Among authors: boyadjiev sa. Genet Med. 2020 Sep;22(9):1498-1506. doi: 10.1038/s41436-020-0817-2. Epub 2020 Jun 5. Genet Med. 2020. PMID: 32499606 Free PMC article.
74 results