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Page 1
Aberrant interchromosomal exchanges are the predominant cause of the 22q11.2 deletion.
Saitta SC, Harris SE, Gaeth AP, Driscoll DA, McDonald-McGinn DM, Maisenbacher MK, Yersak JM, Chakraborty PK, Hacker AM, Zackai EH, Ashley T, Emanuel BS. Saitta SC, et al. Among authors: harris se. Hum Mol Genet. 2004 Feb 15;13(4):417-28. doi: 10.1093/hmg/ddh041. Epub 2003 Dec 17. Hum Mol Genet. 2004. PMID: 14681306 Free PMC article.
Effects of COMT genotype on behavioral symptomatology in the 22q11.2 Deletion Syndrome.
Bearden CE, Jawad AF, Lynch DR, Monterossso JR, Sokol S, McDonald-McGinn DM, Saitta SC, Harris SE, Moss E, Wang PP, Zackai E, Emanuel BS, Simon TJ. Bearden CE, et al. Among authors: harris se. Child Neuropsychol. 2005 Feb;11(1):109-17. doi: 10.1080/09297040590911239. Child Neuropsychol. 2005. PMID: 15846854 Free PMC article.
Fine mapping of the Darier's disease locus on chromosome 12q.
Richard G, Wright AR, Harris S, Doyle SZ, Korge B, Mazzanti C, Tanaka T, Harth W, McBride OW, Compton JG, Bale SJ, DiGiovanna JJ. Richard G, et al. J Invest Dermatol. 1994 Nov;103(5):665-8. doi: 10.1111/1523-1747.ep12398429. J Invest Dermatol. 1994. PMID: 7963653 Free article.
Familial deletion of chromosome 18 (p11.2).
Velagaleti GV, Harris S, Carpenter NJ, Coldwell J, Say B. Velagaleti GV, et al. Ann Genet. 1996;39(4):201-4. Ann Genet. 1996. PMID: 9037347
DNA methylation-based predictors of metabolic traits in Scottish and Singaporean cohorts.
Smith HM, Ng HK, Moodie JE, Gadd DA, McCartney DL, Bernabeu E, Campbell A, Redmond P, Taylor A, Page D, Corley J, Harris SE, Tay D, Deary IJ, Evans KL, Robinson MR, Chambers JC, Loh M, Cox SR, Marioni RE, Hillary RF. Smith HM, et al. Among authors: harris se. Am J Hum Genet. 2024 Dec 13:S0002-9297(24)00421-X. doi: 10.1016/j.ajhg.2024.11.012. Online ahead of print. Am J Hum Genet. 2024. PMID: 39706196 Free article.
Effects of gene dosage on cognitive ability: A function-based association study across brain and non-brain processes.
Huguet G, Renne T, Poulain C, Dubuc A, Kumar K, Kazem S, Engchuan W, Shanta O, Douard E, Proulx C, Jean-Louis M, Saci Z, Mollon J, Schultz LM, Knowles EEM, Cox SR, Porteous D, Davies G, Redmond P, Harris SE, Schumann G, Dumas G, Labbe A, Pausova Z, Paus T, Scherer SW, Sebat J, Almasy L, Glahn DC, Jacquemont S. Huguet G, et al. Among authors: harris se. Cell Genom. 2024 Dec 11;4(12):100721. doi: 10.1016/j.xgen.2024.100721. Cell Genom. 2024. PMID: 39667348 Free article.
622 results