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Page 1
Rare protein-coding variants implicate genes involved in risk of suicide death.
DiBlasi E, Shabalin AA, Monson ET, Keeshin BR, Bakian AV, Kirby AV, Ferris E, Chen D, William N, Gaj E, Klein M, Jerominski L, Callor WB, Christensen E, Smith KR, Fraser A, Yu Z, Gray D; PsychChip Investigators of the Psychiatric Genomics Consortium; Camp NJ, Stahl EA, Li QS, Docherty AR, Coon H. DiBlasi E, et al. Among authors: william n. Am J Med Genet B Neuropsychiatr Genet. 2021 Dec;186(8):508-520. doi: 10.1002/ajmg.b.32861. Epub 2021 May 27. Am J Med Genet B Neuropsychiatr Genet. 2021. PMID: 34042246 Free PMC article.
Genome-wide significant regions in 43 Utah high-risk families implicate multiple genes involved in risk for completed suicide.
Coon H, Darlington TM, DiBlasi E, Callor WB, Ferris E, Fraser A, Yu Z, William N, Das SC, Crowell SE, Chen D, Anderson JS, Klein M, Jerominski L, Cannon D, Shabalin A, Docherty A, Williams M, Smith KR, Keeshin B, Bakian AV, Christensen E, Li QS, Camp NJ, Gray D. Coon H, et al. Among authors: william n. Mol Psychiatry. 2020 Nov;25(11):3077-3090. doi: 10.1038/s41380-018-0282-3. Epub 2018 Oct 23. Mol Psychiatry. 2020. PMID: 30353169 Free PMC article.
Neurexin 1 variants as risk factors for suicide death.
William N, Reissner C, Sargent R, Darlington TM, DiBlasi E, Li QS, Keeshin B, Callor WB, Ferris E, Jerominski L, Smith KR, Christensen ED, Gray DM, Camp NJ, Missler M, Williams ME, Coon H. William N, et al. Mol Psychiatry. 2021 Dec;26(12):7436-7445. doi: 10.1038/s41380-021-01190-2. Epub 2021 Jun 25. Mol Psychiatry. 2021. PMID: 34168285 Free PMC article.
RBC subpopulations in RCCs affected by donor factors.
Yazdanbakhsh M, Phan C, William N, Acker JP. Yazdanbakhsh M, et al. Among authors: william n. Transfus Apher Sci. 2024 Dec;63(6):104010. doi: 10.1016/j.transci.2024.104010. Epub 2024 Oct 15. Transfus Apher Sci. 2024. PMID: 39426025 Free article. Review.
Extended supercooled storage of red blood cells.
Isiksacan Z, William N, Senturk R, Boudreau L, Wooning C, Castellanos E, Isiksacan S, Yarmush ML, Acker JP, Usta OB. Isiksacan Z, et al. Among authors: william n. Commun Biol. 2024 Jun 24;7(1):765. doi: 10.1038/s42003-024-06463-4. Commun Biol. 2024. PMID: 38914723 Free PMC article.
The expanding clinical and genetic spectrum of DYNC1H1-related disorders.
Möller B, Becker LL, Saffari A, Afenjar A, Coci EG, Williamson R, Ward-Melver C, Gibaud M, Sedláčková L, Laššuthová P, Libá Z, Vlčková M, William N, Klee EW, Gavrilova RH, Lévy J, Capri Y, Scavina M, Körner RW, Valuvullah Z, Weiß C, Möller GM, Thiel M, Sinnema M, Kamsteeg EJ, Donkervoort S, Duboc V, Zaafrane-Khachnaoui K, Elkhateeb N, Selim L, Margot H, Marin V, Beneteau C, Isidor B, Cogne B, Keren B, Küsters B, Beggs AH, Genetti CA, Nicolai J, Dötsch J, Koy A, Bönnemann CG, von der Hagen M, von Kleist-Retzow JC, Voermans N, Jungbluth H, Dafsari HS. Möller B, et al. Among authors: william n. Brain. 2024 Jun 8:awae183. doi: 10.1093/brain/awae183. Online ahead of print. Brain. 2024. PMID: 38848546
54 results