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Common genetic variants contribute to risk of rare severe neurodevelopmental disorders.
Niemi MEK, Martin HC, Rice DL, Gallone G, Gordon S, Kelemen M, McAloney K, McRae J, Radford EJ, Yu S, Gecz J, Martin NG, Wright CF, Fitzpatrick DR, Firth HV, Hurles ME, Barrett JC. Niemi MEK, et al. Among authors: kelemen m. Nature. 2018 Oct;562(7726):268-271. doi: 10.1038/s41586-018-0566-4. Epub 2018 Sep 26. Nature. 2018. PMID: 30258228 Free PMC article.
Polygenic Prediction of Recurrent Events After Early-Onset Myocardial Infarction.
Ardissino M, Paraboschi EM, Lambert SA, Kim LG, Kelemen M, Maglietta G, Crocamo A, Magnani G, Bricoli S, Vignali L, Niccoli G, Tubaro M, Pastika L, Sau A, Ng FS, de Marvao A, Honigberg MC, Natarajan P, Nelson AJ, Inouye M, Di Angelantonio E, Asselta R, Ardissino D, Butterworth AS. Ardissino M, et al. Among authors: kelemen m. Circ Genom Precis Med. 2024 Dec;17(6):e004687. doi: 10.1161/CIRCGEN.124.004687. Epub 2024 Nov 29. Circ Genom Precis Med. 2024. PMID: 39611259 Free PMC article.
117 results