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Page 1
Human prefrontal cortex gene regulatory dynamics from gestation to adulthood at single-cell resolution.
Herring CA, Simmons RK, Freytag S, Poppe D, Moffet JJD, Pflueger J, Buckberry S, Vargas-Landin DB, Clément O, Echeverría EG, Sutton GJ, Alvarez-Franco A, Hou R, Pflueger C, McDonald K, Polo JM, Forrest ARR, Nowak AK, Voineagu I, Martelotto L, Lister R. Herring CA, et al. Among authors: voineagu i. Cell. 2022 Nov 10;185(23):4428-4447.e28. doi: 10.1016/j.cell.2022.09.039. Epub 2022 Oct 31. Cell. 2022. PMID: 36318921 Free article.
Alu-minating the Mechanisms Underlying Primate Cortex Evolution.
Wang J, Weatheritt R, Voineagu I. Wang J, et al. Among authors: voineagu i. Biol Psychiatry. 2022 Nov 15;92(10):760-771. doi: 10.1016/j.biopsych.2022.04.021. Epub 2022 May 19. Biol Psychiatry. 2022. PMID: 35981906 Review.
Circular RNAs: The Brain Transcriptome Comes Full Circle.
Gokool A, Loy CT, Halliday GM, Voineagu I. Gokool A, et al. Among authors: voineagu i. Trends Neurosci. 2020 Oct;43(10):752-766. doi: 10.1016/j.tins.2020.07.007. Epub 2020 Aug 20. Trends Neurosci. 2020. PMID: 32829926 Review.
De novo variants predicting haploinsufficiency for DIP2C are associated with expressive speech delay.
Ha T, Morgan A, Bartos MN, Beatty K, Cogné B, Braun D, Gerber CB, Gaspar H, Kopps AM, Rieubland C, Hurst ACE, Amor DJ, Nizon M, Pasquier L, Pfundt R, Reis A, Siu VM, Tessarech M, Thompson ML, Vincent M, de Vries BBA, Walsh MB, Wechsler SB, Zweier C, Schnur RE, Guillen Sacoto MJ, Margot H, Masotto B, Palafoll MIV, Nawaz U, Voineagu I, Slavotinek A. Ha T, et al. Among authors: voineagu i. Am J Med Genet A. 2024 Jul;194(7):e63559. doi: 10.1002/ajmg.a.63559. Epub 2024 Feb 29. Am J Med Genet A. 2024. PMID: 38421105 Free article.
Autism: from genetics to biomarkers.
Voineagu I. Voineagu I. Dis Markers. 2012;33(5):223-4. doi: 10.3233/DMA-2012-0931. Dis Markers. 2012. PMID: 22960343 Free PMC article. No abstract available.
Evolutionary dynamics of circular RNAs in primates.
Santos-Rodriguez G, Voineagu I, Weatheritt RJ. Santos-Rodriguez G, et al. Among authors: voineagu i. Elife. 2021 Sep 20;10:e69148. doi: 10.7554/eLife.69148. Elife. 2021. PMID: 34542404 Free PMC article.
De Novo ZMYND8 variants result in an autosomal dominant neurodevelopmental disorder with cardiac malformations.
Dias KR, Carlston CM, Blok LER, De Hayr L, Nawaz U, Evans CA, Bayrak-Toydemir P, Htun S, Zhu Y, Ma A, Lynch SA, Moorwood C, Stals K, Ellard S, Bainbridge MN, Friedman J, Pappas JG, Rabin R, Nowak CB, Douglas J, Wilson TE, Guillen Sacoto MJ, Mullegama SV, Palculict TB, Kirk EP, Pinner JR, Edwards M, Montanari F, Graziano C, Pippucci T, Dingmann B, Glass I, Mefford HC, Shimoji T, Suzuki T, Yamakawa K, Streff H, Schaaf CP, Slavotinek AM, Voineagu I, Carey JC, Buckley MF, Schenck A, Harvey RJ, Roscioli T. Dias KR, et al. Among authors: voineagu i. Genet Med. 2022 Sep;24(9):1952-1966. doi: 10.1016/j.gim.2022.06.001. Epub 2022 Aug 1. Genet Med. 2022. PMID: 35916866 Free article.
40 results