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Genome-wide association study of pediatric obsessive-compulsive traits: shared genetic risk between traits and disorder.
Burton CL, Lemire M, Xiao B, Corfield EC, Erdman L, Bralten J, Poelmans G, Yu D, Shaheen SM, Goodale T, Sinopoli VM; OCD Working Group of the Psychiatric Genomics Consortium; Soreni N, Hanna GL, Fitzgerald KD, Rosenberg D, Nestadt G, Paterson AD, Strug LJ, Schachar RJ, Crosbie J, Arnold PD. Burton CL, et al. Among authors: strug lj. Transl Psychiatry. 2021 Feb 2;11(1):91. doi: 10.1038/s41398-020-01121-9. Transl Psychiatry. 2021. PMID: 33531474 Free PMC article.
A microRNA-328 binding site in PAX6 is associated with centrotemporal spikes of rolandic epilepsy.
Panjwani N, Wilson MD, Addis L, Crosbie J, Wirrell E, Auvin S, Caraballo RH, Kinali M, McCormick D, Oren C, Taylor J, Trounce J, Clarke T, Akman CI, Kugler SL, Mandelbaum DE, McGoldrick P, Wolf SM, Arnold P, Schachar R, Pal DK, Strug LJ. Panjwani N, et al. Among authors: strug lj. Ann Clin Transl Neurol. 2016 Jun 2;3(7):512-22. doi: 10.1002/acn3.320. eCollection 2016 Jul. Ann Clin Transl Neurol. 2016. PMID: 27386500 Free PMC article.
Statistical power in COVID-19 case-control host genomic study design.
Lin YC, Brooks JD, Bull SB, Gagnon F, Greenwood CMT, Hung RJ, Lawless J, Paterson AD, Sun L, Strug LJ; Genetic Epidemiology Committee of the Canadian COVID Genomics Network (CanCOGeN) HostSeq Project. Lin YC, et al. Among authors: strug lj. Genome Med. 2020 Dec 28;12(1):115. doi: 10.1186/s13073-020-00818-2. Genome Med. 2020. PMID: 33371892 Free PMC article.
Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities.
Price KM, Wigg KG, Eising E, Feng Y, Blokland K, Wilkinson M, Kerr EN, Guger SL; Quantitative Trait Working Group of the GenLang Consortium; Fisher SE, Lovett MW, Strug LJ, Barr CL. Price KM, et al. Among authors: strug lj. Transl Psychiatry. 2022 Nov 29;12(1):495. doi: 10.1038/s41398-022-02250-z. Transl Psychiatry. 2022. PMID: 36446759 Free PMC article.
123 results