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Year Number of Results
2017 1
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2019 3
2020 2
2021 2
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2023 1
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11 results

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Page 1
Optimizing Stem Cell Therapy after Ischemic Brain Injury.
Zhang S, Lachance BB, Moiz B, Jia X. Zhang S, et al. Among authors: moiz b. J Stroke. 2020 Sep;22(3):286-305. doi: 10.5853/jos.2019.03048. Epub 2020 Sep 29. J Stroke. 2020. PMID: 33053945 Free PMC article. Review.
Myopia in Chinese families shows linkage to 10q26.13.
Musolf AM, Simpson CL, Long KA, Moiz BA, Lewis DD, Middlebrooks CD, Portas L, Murgia F, Ciner EB, Bailey-Wilson JE, Stambolian D. Musolf AM, et al. Among authors: moiz ba. Mol Vis. 2018 Jan 14;24:29-42. eCollection 2018. Mol Vis. 2018. PMID: 29383007 Free PMC article.
Genetic Variation and Recurrent Haplotypes on Chromosome 6q23-25 Risk Locus in Familial Lung Cancer.
Musolf AM, Simpson CL, Moiz BA, Pikielny CW, Middlebrooks CD, Mandal D, de Andrade M, Cole MD, Gaba C, Yang P, You M, Li Y, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, Amos CI, Bailey-Wilson JE. Musolf AM, et al. Among authors: moiz ba. Cancer Res. 2021 Jun 15;81(12):3162-3173. doi: 10.1158/0008-5472.CAN-20-3196. Epub 2021 Apr 14. Cancer Res. 2021. PMID: 33853833 Free PMC article.
Caucasian Families Exhibit Significant Linkage of Myopia to Chromosome 11p.
Musolf AM, Simpson CL, Moiz BA, Long KA, Portas L, Murgia F, Ciner EB, Stambolian D, Bailey-Wilson JE. Musolf AM, et al. Among authors: moiz ba. Invest Ophthalmol Vis Sci. 2017 Jul 1;58(9):3547-3554. doi: 10.1167/iovs.16-21271. Invest Ophthalmol Vis Sci. 2017. PMID: 28715588 Free PMC article.
Whole Exome Sequencing of Highly Aggregated Lung Cancer Families Reveals Linked Loci for Increased Cancer Risk on Chromosomes 12q, 7p, and 4q.
Musolf AM, Moiz BA, Sun H, Pikielny CW, Bossé Y, Mandal D, de Andrade M, Gaba C, Yang P, Li Y, You M, Govindan R, Wilson RK, Kupert EY, Anderson MW, Schwartz AG, Pinney SM, Amos CI, Bailey-Wilson JE. Musolf AM, et al. Among authors: moiz ba. Cancer Epidemiol Biomarkers Prev. 2020 Feb;29(2):434-442. doi: 10.1158/1055-9965.EPI-19-0887. Epub 2019 Dec 11. Cancer Epidemiol Biomarkers Prev. 2020. PMID: 31826912 Free PMC article.
Small posterior fossa in Chiari I malformation affected families is significantly linked to 1q43-44 and 12q23-24.11 using whole exome sequencing.
Musolf AM, Ho WSC, Long KA, Zhuang Z, Argersinger DP, Sun H, Moiz BA, Simpson CL, Mendelevich EG, Bogdanov EI, Bailey-Wilson JE, Heiss JD. Musolf AM, et al. Among authors: moiz ba. Eur J Hum Genet. 2019 Oct;27(10):1599-1610. doi: 10.1038/s41431-019-0457-7. Epub 2019 Jun 21. Eur J Hum Genet. 2019. PMID: 31227808 Free PMC article.
11 results