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Page 1
A novel method for analyzing genetic association with longitudinal phenotypes.
Londono D, Chen KM, Musolf A, Wang R, Shen T, Brandon J, Herring JA, Wise CA, Zou H, Jin M, Yu L, Finch SJ, Matise TC, Gordon D. Londono D, et al. Among authors: musolf a. Stat Appl Genet Mol Biol. 2013 Mar 13;12(2):241-61. doi: 10.1515/sagmb-2012-0070. Stat Appl Genet Mol Biol. 2013. PMID: 23502345
Chromatin profiling reveals regulatory network shifts and a protective role for hepatocyte nuclear factor 4α during colitis.
Chahar S, Gandhi V, Yu S, Desai K, Cowper-Sal-lari R, Kim Y, Perekatt AO, Kumar N, Thackray JK, Musolf A, Kumar N, Hoffman A, Londono D, Vazquez BN, Serrano L, Shin H, Lupien M, Gao N, Verzi MP. Chahar S, et al. Among authors: musolf a. Mol Cell Biol. 2014 Sep;34(17):3291-304. doi: 10.1128/MCB.00349-14. Epub 2014 Jun 30. Mol Cell Biol. 2014. PMID: 24980432 Free PMC article.
Genome-wide association meta-analysis of corneal curvature identifies novel loci and shared genetic influences across axial length and refractive error.
Fan Q, Pozarickij A, Tan NYQ, Guo X, Verhoeven VJM, Vitart V, Guggenheim JA, Miyake M, Tideman JWL, Khawaja AP, Zhang L, MacGregor S, Höhn R, Chen P, Biino G, Wedenoja J, Saffari SE, Tedja MS, Xie J, Lanca C, Wang YX, Sahebjada S, Mazur J, Mirshahi A, Martin NG, Yazar S, Pennell CE, Yap M, Haarman AEG, Enthoven CA, Polling J; Consortium for Refractive Error and Myopia (CREAM); UK Biobank Eye and Vision Consortium; Hewitt AW, Jaddoe VWV, van Duijn CM, Hayward C, Polasek O, Tai ES, Yoshikatsu H, Hysi PG, Young TL, Tsujikawa A, Wang JJ, Mitchell P, Pfeiffer N, Pärssinen O, Foster PJ, Fossarello M, Yip SP, Williams C, Hammond CJ, Jonas JB, He M, Mackey DA, Wong TY, Klaver CCW, Saw SM, Baird PN, Cheng CY. Fan Q, et al. Commun Biol. 2020 Mar 19;3(1):133. doi: 10.1038/s42003-020-0802-y. Commun Biol. 2020. PMID: 32193507 Free PMC article.
Linear mixed models for association analysis of quantitative traits with next-generation sequencing data.
Chiu CY, Yuan F, Zhang BS, Yuan A, Li X, Fang HB, Lange K, Weeks DE, Wilson AF, Bailey-Wilson JE, Musolf AM, Stambolian D, Lakhal-Chaieb ML, Cook RJ, McMahon FJ, Amos CI, Xiong M, Fan R. Chiu CY, et al. Among authors: musolf am. Genet Epidemiol. 2019 Mar;43(2):189-206. doi: 10.1002/gepi.22177. Epub 2018 Dec 9. Genet Epidemiol. 2019. PMID: 30537345 Free PMC article.
Whole exome sequence analysis in 51 624 participants identifies novel genes and variants associated with refractive error and myopia.
Guggenheim JA, Clark R, Cui J, Terry L, Patasova K, Haarman AEG, Musolf AM, Verhoeven VJM, Klaver CCW, Bailey-Wilson JE, Hysi PG, Williams C; CREAM Consortium; UK Biobank Eye Vision Consortium. Guggenheim JA, et al. Among authors: musolf am. Hum Mol Genet. 2022 Jun 4;31(11):1909-1919. doi: 10.1093/hmg/ddac004. Hum Mol Genet. 2022. PMID: 35022715 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. 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.
32 results