McCallion AS - Search Results

1

Functional Characterization of Schizophrenia-Associated Variation in CACNA1C.

Eckart N, Song Q, Yang R, Wang R, Zhu H, McCallion AS, Avramopoulos D. Eckart N, et al. Among authors: mccallion as. PLoS One. 2016 Jun 8;11(6):e0157086. doi: 10.1371/journal.pone.0157086. eCollection 2016. PLoS One. 2016. PMID: 27276213 Free PMC article.

2

Functional variants in DPYSL2 sequence increase risk of schizophrenia and suggest a link to mTOR signaling.

Liu Y, Pham X, Zhang L, Chen PL, Burzynski G, McGaughey DM, He S, McGrath JA, Wolyniec P, Fallin MD, Pierce MS, McCallion AS, Pulver AE, Avramopoulos D, Valle D. Liu Y, et al. Among authors: mccallion as. G3 (Bethesda). 2014 Nov 20;5(1):61-72. doi: 10.1534/g3.114.015636. G3 (Bethesda). 2014. PMID: 25416705 Free PMC article.

3

Parkinson-Associated SNCA Enhancer Variants Revealed by Open Chromatin in Mouse Dopamine Neurons.

McClymont SA, Hook PW, Soto AI, Reed X, Law WD, Kerans SJ, Waite EL, Briceno NJ, Thole JF, Heckman MG, Diehl NN, Wszolek ZK, Moore CD, Zhu H, Akiyama JA, Dickel DE, Visel A, Pennacchio LA, Ross OA, Beer MA, McCallion AS. McClymont SA, et al. Among authors: mccallion as. Am J Hum Genet. 2018 Dec 6;103(6):874-892. doi: 10.1016/j.ajhg.2018.10.018. Epub 2018 Nov 29. Am J Hum Genet. 2018. PMID: 30503521 Free PMC article.

4

Leveraging mouse chromatin data for heritability enrichment informs common disease architecture and reveals cortical layer contributions to schizophrenia.

Hook PW, McCallion AS. Hook PW, et al. Among authors: mccallion as. Genome Res. 2020 Apr;30(4):528-539. doi: 10.1101/gr.256578.119. Epub 2020 Apr 17. Genome Res. 2020. PMID: 32303558 Free PMC article.

5

A Functional Schizophrenia-associated genetic variant near the TSNARE1 and ADGRB1 genes.

Wahbeh MH, Boyd RJ, Yovo C, Rike B, McCallion AS, Avramopoulos D. Wahbeh MH, et al. Among authors: mccallion as. bioRxiv [Preprint]. 2023 Dec 18:2023.12.18.570831. doi: 10.1101/2023.12.18.570831. bioRxiv. 2023. PMID: 38187620 Free PMC article. Updated. Preprint.

6

Genome-wide association study and mouse model identify interaction between RET and EDNRB pathways in Hirschsprung disease.

Carrasquillo MM, McCallion AS, Puffenberger EG, Kashuk CS, Nouri N, Chakravarti A. Carrasquillo MM, et al. Among authors: mccallion as. Nat Genet. 2002 Oct;32(2):237-44. doi: 10.1038/ng998. Epub 2002 Sep 23. Nat Genet. 2002. PMID: 12355085

7

A common sex-dependent mutation in a RET enhancer underlies Hirschsprung disease risk.

Emison ES, McCallion AS, Kashuk CS, Bush RT, Grice E, Lin S, Portnoy ME, Cutler DJ, Green ED, Chakravarti A. Emison ES, et al. Among authors: mccallion as. Nature. 2005 Apr 14;434(7035):857-63. doi: 10.1038/nature03467. Nature. 2005. PMID: 15829955

8

Efficient array-based identification of novel cardiac genes through differentiation of mouse ESCs.

Miller RA, Christoforou N, Pevsner J, McCallion AS, Gearhart JD. Miller RA, et al. Among authors: mccallion as. PLoS One. 2008 May 14;3(5):e2176. doi: 10.1371/journal.pone.0002176. PLoS One. 2008. PMID: 18478100 Free PMC article.

9

A rare myelin protein zero (MPZ) variant alters enhancer activity in vitro and in vivo.

Antonellis A, Dennis MY, Burzynski G, Huynh J, Maduro V, Hodonsky CJ, Khajavi M, Szigeti K, Mukkamala S, Bessling SL, Pavan WJ, McCallion AS, Lupski JR, Green ED; NISC Comparative Sequencing Program. Antonellis A, et al. Among authors: mccallion as. PLoS One. 2010 Dec 16;5(12):e14346. doi: 10.1371/journal.pone.0014346. PLoS One. 2010. PMID: 21179557 Free PMC article.

10

SOX10 directly modulates ERBB3 transcription via an intronic neural crest enhancer.

Prasad MK, Reed X, Gorkin DU, Cronin JC, McAdow AR, Chain K, Hodonsky CJ, Jones EA, Svaren J, Antonellis A, Johnson SL, Loftus SK, Pavan WJ, McCallion AS. Prasad MK, et al. Among authors: mccallion as. BMC Dev Biol. 2011 Jun 14;11:40. doi: 10.1186/1471-213X-11-40. BMC Dev Biol. 2011. PMID: 21672228 Free PMC article.

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