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Page 1
Linkage of familial essential tremor to chromosome 5q35.
Hicks JE, Konidari I, Scott BL, Stajich JM, Ashley-Koch AE, Gilbert JR, Scott WK. Hicks JE, et al. Among authors: konidari i. Mov Disord. 2016 Jul;31(7):1059-62. doi: 10.1002/mds.26582. Epub 2016 Feb 26. Mov Disord. 2016. PMID: 26918299
Variants in several genomic regions associated with asperger disorder.
Salyakina D, Ma DQ, Jaworski JM, Konidari I, Whitehead PL, Henson R, Martinez D, Robinson JL, Sacharow S, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Salyakina D, et al. Among authors: konidari i. Autism Res. 2010 Dec;3(6):303-10. doi: 10.1002/aur.158. Autism Res. 2010. PMID: 21182207 Free PMC article.
Association and gene-gene interaction of SLC6A4 and ITGB3 in autism.
Ma DQ, Rabionet R, Konidari I, Jaworski J, Cukier HN, Wright HH, Abramson RK, Gilbert JR, Cuccaro ML, Pericak-Vance MA, Martin ER. Ma DQ, et al. Among authors: konidari i. Am J Med Genet B Neuropsychiatr Genet. 2010 Mar 5;153B(2):477-483. doi: 10.1002/ajmg.b.31003. Am J Med Genet B Neuropsychiatr Genet. 2010. PMID: 19588468 Free PMC article.
A genome-wide association study of autism reveals a common novel risk locus at 5p14.1.
Ma D, Salyakina D, Jaworski JM, Konidari I, Whitehead PL, Andersen AN, Hoffman JD, Slifer SH, Hedges DJ, Cukier HN, Griswold AJ, McCauley JL, Beecham GW, Wright HH, Abramson RK, Martin ER, Hussman JP, Gilbert JR, Cuccaro ML, Haines JL, Pericak-Vance MA. Ma D, et al. Among authors: konidari i. Ann Hum Genet. 2009 May;73(Pt 3):263-73. doi: 10.1111/j.1469-1809.2009.00523.x. Ann Hum Genet. 2009. PMID: 19456320 Free PMC article.
Novel variants identified in methyl-CpG-binding domain genes in autistic individuals.
Cukier HN, Rabionet R, Konidari I, Rayner-Evans MY, Baltos ML, Wright HH, Abramson RK, Martin ER, Cuccaro ML, Pericak-Vance MA, Gilbert JR. Cukier HN, et al. Among authors: konidari i. Neurogenetics. 2010 Jul;11(3):291-303. doi: 10.1007/s10048-009-0228-7. Epub 2009 Nov 18. Neurogenetics. 2010. PMID: 19921286 Free PMC article.
Copy number variants in extended autism spectrum disorder families reveal candidates potentially involved in autism risk.
Salyakina D, Cukier HN, Lee JM, Sacharow S, Nations LD, Ma D, Jaworski JM, Konidari I, Whitehead PL, Wright HH, Abramson RK, Williams SM, Menon R, Haines JL, Gilbert JR, Cuccaro ML, Pericak-Vance MA. Salyakina D, et al. Among authors: konidari i. PLoS One. 2011;6(10):e26049. doi: 10.1371/journal.pone.0026049. Epub 2011 Oct 7. PLoS One. 2011. PMID: 22016809 Free PMC article.
32 results