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Page 1
Common-variant associations with fragile X syndrome.
Crowley JJ, Szatkiewicz J, Kähler AK, Giusti-Rodriguez P, Ancalade N, Booker JK, Carr JL, Crawford GE, Losh M, Stockmeier CA, Taylor AK, Piven J, Sullivan PF. Crowley JJ, et al. Among authors: booker jk. Mol Psychiatry. 2019 Mar;24(3):338-344. doi: 10.1038/s41380-018-0290-3. Epub 2018 Dec 7. Mol Psychiatry. 2019. PMID: 30531935 Free PMC article.
Correction: Common-variant associations with fragile X syndrome.
Crowley JJ, Szatkiewicz J, Kähler AK, Giusti-Rodriguez P, Ancalade N, Booker JK, Carr JL, Giamberardino SN, Crawford GE, Losh M, Stockmeier CA, Taylor AK, Piven J, Sullivan PF. Crowley JJ, et al. Among authors: booker jk. Mol Psychiatry. 2020 Dec;25(12):3450. doi: 10.1038/s41380-019-0526-x. Mol Psychiatry. 2020. PMID: 31548576
Mosaicism for an FMR1 gene deletion in a fragile X female.
Fan H, Booker JK, McCandless SE, Shashi V, Fleming A, Farber RA. Fan H, et al. Among authors: booker jk. Am J Med Genet A. 2005 Jul 15;136(2):214-7. doi: 10.1002/ajmg.a.30807. Am J Med Genet A. 2005. PMID: 15940701
Detection of common disease-causing mutations in mitochondrial DNA (mitochondrial encephalomyopathy, lactic acidosis with stroke-like episodes MTTL1 3243 A>G and myoclonic epilepsy associated with ragged-red fibers MTTK 8344A>G) by real-time polymerase chain reaction.
Fan H, Civalier C, Booker JK, Gulley ML, Prior TW, Farber RA. Fan H, et al. Among authors: booker jk. J Mol Diagn. 2006 May;8(2):277-81. doi: 10.2353/jmoldx.2006.050066. J Mol Diagn. 2006. PMID: 16645216 Free PMC article.
Genomic Sequencing for Newborn Screening: Results of the NC NEXUS Project.
Roman TS, Crowley SB, Roche MI, Foreman AKM, O'Daniel JM, Seifert BA, Lee K, Brandt A, Gustafson C, DeCristo DM, Strande NT, Ramkissoon L, Milko LV, Owen P, Roy S, Xiong M, Paquin RS, Butterfield RM, Lewis MA, Souris KJ, Bailey DB Jr, Rini C, Booker JK, Powell BC, Weck KE, Powell CM, Berg JS. Roman TS, et al. Among authors: booker jk. Am J Hum Genet. 2020 Oct 1;107(4):596-611. doi: 10.1016/j.ajhg.2020.08.001. Epub 2020 Aug 26. Am J Hum Genet. 2020. PMID: 32853555 Free PMC article.
CSF1R mosaicism in a family with hereditary diffuse leukoencephalopathy with spheroids.
Eichler FS, Li J, Guo Y, Caruso PA, Bjonnes AC, Pan J, Booker JK, Lane JM, Tare A, Vlasac I, Hakonarson H, Gusella JF, Zhang J, Keating BJ, Saxena R. Eichler FS, et al. Among authors: booker jk. Brain. 2016 Jun;139(Pt 6):1666-72. doi: 10.1093/brain/aww066. Epub 2016 May 5. Brain. 2016. PMID: 27190017 Free PMC article.
22 results