Evrony G - Search Results

1

Pangenome graphs improve the analysis of structural variants in rare genetic diseases.

Groza C, Schwendinger-Schreck C, Cheung WA, Farrow EG, Thiffault I, Lake J, Rizzo WB, Evrony G, Curran T, Bourque G, Pastinen T. Groza C, et al. Among authors: evrony g. Nat Commun. 2024 Jan 22;15(1):657. doi: 10.1038/s41467-024-44980-2. Nat Commun. 2024. PMID: 38253606 Free PMC article.

2

METTL23, a transcriptional partner of GABPA, is essential for human cognition.

Reiff RE, Ali BR, Baron B, Yu TW, Ben-Salem S, Coulter ME, Schubert CR, Hill RS, Akawi NA, Al-Younes B, Kaya N, Evrony GD, Al-Saffar M, Felie JM, Partlow JN, Sunu CM, Schembri-Wismayer P, Alkuraya FS, Meyer BF, Walsh CA, Al-Gazali L, Mochida GH. Reiff RE, et al. Hum Mol Genet. 2014 Jul 1;23(13):3456-66. doi: 10.1093/hmg/ddu054. Epub 2014 Feb 5. Hum Mol Genet. 2014. PMID: 24501276 Free PMC article.

3

Single-neuron sequencing analysis of L1 retrotransposition and somatic mutation in the human brain.

Evrony GD, Cai X, Lee E, Hills LB, Elhosary PC, Lehmann HS, Parker JJ, Atabay KD, Gilmore EC, Poduri A, Park PJ, Walsh CA. Evrony GD, et al. Cell. 2012 Oct 26;151(3):483-96. doi: 10.1016/j.cell.2012.09.035. Cell. 2012. PMID: 23101622 Free PMC article.

4

A PIECE OF MY MIND. A Wild Rotation.

Evrony GD. Evrony GD. JAMA. 2016 Aug 16;316(7):713-4. doi: 10.1001/jama.2016.4994. JAMA. 2016. PMID: 27533153 Free PMC article. No abstract available.

5

Evolutionarily dynamic alternative splicing of GPR56 regulates regional cerebral cortical patterning.

Bae BI, Tietjen I, Atabay KD, Evrony GD, Johnson MB, Asare E, Wang PP, Murayama AY, Im K, Lisgo SN, Overman L, Šestan N, Chang BS, Barkovich AJ, Grant PE, Topçu M, Politsky J, Okano H, Piao X, Walsh CA. Bae BI, et al. Science. 2014 Feb 14;343(6172):764-8. doi: 10.1126/science.1244392. Science. 2014. PMID: 24531968 Free PMC article.

6

Somatic activation of AKT3 causes hemispheric developmental brain malformations.

Poduri A, Evrony GD, Cai X, Elhosary PC, Beroukhim R, Lehtinen MK, Hills LB, Heinzen EL, Hill A, Hill RS, Barry BJ, Bourgeois BF, Riviello JJ, Barkovich AJ, Black PM, Ligon KL, Walsh CA. Poduri A, et al. Neuron. 2012 Apr 12;74(1):41-8. doi: 10.1016/j.neuron.2012.03.010. Neuron. 2012. PMID: 22500628 Free PMC article.

7

Loss of PCLO function underlies pontocerebellar hypoplasia type III.

Ahmed MY, Chioza BA, Rajab A, Schmitz-Abe K, Al-Khayat A, Al-Turki S, Baple EL, Patton MA, Al-Memar AY, Hurles ME, Partlow JN, Hill RS, Evrony GD, Servattalab S, Markianos K, Walsh CA, Crosby AH, Mochida GH. Ahmed MY, et al. Neurology. 2015 Apr 28;84(17):1745-50. doi: 10.1212/WNL.0000000000001523. Epub 2015 Apr 1. Neurology. 2015. PMID: 25832664 Free PMC article.

8

Resolving rates of mutation in the brain using single-neuron genomics.

Evrony GD, Lee E, Park PJ, Walsh CA. Evrony GD, et al. Elife. 2016 Feb 22;5:e12966. doi: 10.7554/eLife.12966. Elife. 2016. PMID: 26901440 Free PMC article.

9

Microcephaly gene links trithorax and REST/NRSF to control neural stem cell proliferation and differentiation.

Yang YJ, Baltus AE, Mathew RS, Murphy EA, Evrony GD, Gonzalez DM, Wang EP, Marshall-Walker CA, Barry BJ, Murn J, Tatarakis A, Mahajan MA, Samuels HH, Shi Y, Golden JA, Mahajnah M, Shenhav R, Walsh CA. Yang YJ, et al. Cell. 2012 Nov 21;151(5):1097-112. doi: 10.1016/j.cell.2012.10.043. Cell. 2012. PMID: 23178126 Free PMC article.

10

Single-cell, genome-wide sequencing identifies clonal somatic copy-number variation in the human brain.

Cai X, Evrony GD, Lehmann HS, Elhosary PC, Mehta BK, Poduri A, Walsh CA. Cai X, et al. Cell Rep. 2015 Feb 3;10(4):645. doi: 10.1016/j.celrep.2015.01.028. Epub 2015 Feb 3. Cell Rep. 2015. PMID: 25832109 Free article. No abstract available.

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