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A searchable database of genetic evidence for psychiatric disorders.
Konneker T, Barnes T, Furberg H, Losh M, Bulik CM, Sullivan PF. Konneker T, et al. Among authors: losh m. Am J Med Genet B Neuropsychiatr Genet. 2008 Sep 5;147B(6):671-5. doi: 10.1002/ajmg.b.30802. Am J Med Genet B Neuropsychiatr Genet. 2008. PMID: 18548508 Free PMC article.
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: losh m. 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: losh m. Mol Psychiatry. 2020 Dec;25(12):3450. doi: 10.1038/s41380-019-0526-x. Mol Psychiatry. 2020. PMID: 31548576
72 results