Gallione CJ[au] - Search Results

Year	Number of Results
1981	2
1983	1
1984	1
1985	1
1994	1
1995	4
1996	1
1997	1
1998	3
1999	1
2000	2
2004	4
2005	1
2006	1
2011	1
2013	2
2014	2
2015	1
2019	1
2020	1
2022	2
2023	2
2024	0

1

Single-nucleus DNA sequencing reveals hidden somatic loss-of-heterozygosity in Cerebral Cavernous Malformations.

Ressler AK, Snellings DA, Girard R, Gallione CJ, Lightle R, Allen AS, Awad IA, Marchuk DA. Ressler AK, et al. Among authors: gallione cj. Nat Commun. 2023 Nov 2;14(1):7009. doi: 10.1038/s41467-023-42908-w. Nat Commun. 2023. PMID: 37919320 Free PMC article.

2

Developmental expression of the Sturge-Weber syndrome-associated genetic mutation in Gnaq: a formal test of Happle's paradominant inheritance hypothesis.

Wetzel-Strong SE, Galeffi F, Benavides C, Patrucco M, Bullock JL, Gallione CJ, Lee HK, Marchuk DA. Wetzel-Strong SE, et al. Among authors: gallione cj. Genetics. 2023 Aug 9;224(4):iyad077. doi: 10.1093/genetics/iyad077. Genetics. 2023. PMID: 37098137 Free PMC article.

3

Novel Murine Models of Cerebral Cavernous Malformations.

Detter MR, Shenkar R, Benavides CR, Neilson CA, Moore T, Lightle R, Hobson N, Shen L, Cao Y, Girard R, Zhang D, Griffin E, Gallione CJ, Awad IA, Marchuk DA. Detter MR, et al. Among authors: gallione cj. Angiogenesis. 2020 Nov;23(4):651-666. doi: 10.1007/s10456-020-09736-8. Epub 2020 Jul 24. Angiogenesis. 2020. PMID: 32710309 Free PMC article.

4

A novel somatic mutation in GNAQ in a capillary malformation provides insight into molecular pathogenesis.

Galeffi F, Snellings DA, Wetzel-Strong SE, Kastelic N, Bullock J, Gallione CJ, North PE, Marchuk DA. Galeffi F, et al. Among authors: gallione cj. Angiogenesis. 2022 Nov;25(4):493-502. doi: 10.1007/s10456-022-09841-w. Epub 2022 May 30. Angiogenesis. 2022. PMID: 35635655 Free PMC article.

5

Genetic genealogy uncovers a founder deletion mutation in the cerebral cavernous malformations 2 gene.

Gallione CJ, Detter MR, Sheline A, Christmas HM, Lee C, Marchuk DA. Gallione CJ, et al. Hum Genet. 2022 Nov;141(11):1761-1769. doi: 10.1007/s00439-022-02458-5. Epub 2022 Apr 30. Hum Genet. 2022. PMID: 35488064 Free PMC article.

6

Somatic Mutations in Vascular Malformations of Hereditary Hemorrhagic Telangiectasia Result in Bi-allelic Loss of ENG or ACVRL1.

Snellings DA, Gallione CJ, Clark DS, Vozoris NT, Faughnan ME, Marchuk DA. Snellings DA, et al. Among authors: gallione cj. Am J Hum Genet. 2019 Nov 7;105(5):894-906. doi: 10.1016/j.ajhg.2019.09.010. Epub 2019 Oct 17. Am J Hum Genet. 2019. PMID: 31630786 Free PMC article.

7

SMAD4 mutations found in unselected HHT patients.

Gallione CJ, Richards JA, Letteboer TG, Rushlow D, Prigoda NL, Leedom TP, Ganguly A, Castells A, Ploos van Amstel JK, Westermann CJ, Pyeritz RE, Marchuk DA. Gallione CJ, et al. J Med Genet. 2006 Oct;43(10):793-7. doi: 10.1136/jmg.2006.041517. Epub 2006 Apr 13. J Med Genet. 2006. PMID: 16613914 Free PMC article.

8

Exceptional aggressiveness of cerebral cavernous malformation disease associated with PDCD10 mutations.

Shenkar R, Shi C, Rebeiz T, Stockton RA, McDonald DA, Mikati AG, Zhang L, Austin C, Akers AL, Gallione CJ, Rorrer A, Gunel M, Min W, De Souza JM, Lee C, Marchuk DA, Awad IA. Shenkar R, et al. Among authors: gallione cj. Genet Med. 2015 Mar;17(3):188-196. doi: 10.1038/gim.2014.97. Epub 2014 Aug 14. Genet Med. 2015. PMID: 25122144 Free PMC article.

9

Sturge-Weber syndrome and port-wine stains caused by somatic mutation in GNAQ.

Shirley MD, Tang H, Gallione CJ, Baugher JD, Frelin LP, Cohen B, North PE, Marchuk DA, Comi AM, Pevsner J. Shirley MD, et al. Among authors: gallione cj. N Engl J Med. 2013 May 23;368(21):1971-9. doi: 10.1056/NEJMoa1213507. Epub 2013 May 8. N Engl J Med. 2013. PMID: 23656586 Free PMC article.

10

Natural genetic variation of integrin alpha L (Itgal) modulates ischemic brain injury in stroke.

Keum S, Lee HK, Chu PL, Kan MJ, Huang MN, Gallione CJ, Gunn MD, Lo DC, Marchuk DA. Keum S, et al. Among authors: gallione cj. PLoS Genet. 2013;9(10):e1003807. doi: 10.1371/journal.pgen.1003807. Epub 2013 Oct 10. PLoS Genet. 2013. PMID: 24130503 Free PMC article.

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