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Investigating the contributions of circadian pathway and insomnia risk genes to autism and sleep disturbances.
Transl Psychiatry. 2022 Oct 3;12(1):424. doi: 10.1038/s41398-022-02188-2.
Transl Psychiatry. 2022.
PMID: 36192372
Free PMC article.
Assessing the NOTCH2NLC GGC expansion in European patients with essential tremor.
Liao C, Akçimen F, Diez-Fairen M, Houle G, Ross JP, Schmilovich Z, Spiegelman D, Vuokila V, Catoire H, Meijer IA, Pastor P, Rajput A, Dion PA, Rouleau GA.
Liao C, et al. Among authors: schmilovich z.
Brain. 2020 Dec 5;143(11):e89. doi: 10.1093/brain/awaa291.
Brain. 2020.
PMID: 33146671
No abstract available.
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First Ready, First to Go: Ethical Priority-Setting of Allogeneic Stem Cell Transplant at a Major Cancer Centre.
Bell JAH, Schmilovich Z, Buchman DZ, Escaf M, Costello J, Messner HA.
Bell JAH, et al. Among authors: schmilovich z.
Healthc Policy. 2020 Feb;15(3):102-115. doi: 10.12927/hcpol.2020.26127.
Healthc Policy. 2020.
PMID: 32176614
Free PMC article.
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Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
Schmilovich Z, Bourque VR, Douard E, Huguet G, Poulain C, Ross JP, Alipour P, Castonguay CÉ, Younis N, Jean-Louis M, Saci Z, Pausova Z, Paus T, Schuman G, Porteous D, Davies G, Redmond P, Harris SE, Deary IJ, Whalley H, Hayward C, Dion PA, Jacquemont S, Rouleau GA.
Schmilovich Z, et al.
Front Psychiatry. 2024 May 1;15:1369767. doi: 10.3389/fpsyt.2024.1369767. eCollection 2024.
Front Psychiatry. 2024.
PMID: 38751416
Free PMC article.
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Copy-number variants and polygenic risk for intelligence confer risk for autism spectrum disorder irrespective of their effects on cognitive ability.
Schmilovich Z, Bourque VR, Douard E, Huguet G, Poulain C, Ross JP, Alipour P, Castonguay CÉ, Younis N, Jean-Louis M, Saci Z, Pausova Z, Paus T, Schuman G, Porteous D, Davies G, Redmond P, Harris SE, Deary IJ, Whalley H, Hayward C, Dion PA, Jacquemont S, Rouleau GA.
Schmilovich Z, et al.
medRxiv [Preprint]. 2023 Nov 29:2023.11.29.23299190. doi: 10.1101/2023.11.29.23299190.
medRxiv. 2023.
PMID: 38076919
Free PMC article.
Preprint.
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Rare-variant and polygenic analyses of amyotrophic lateral sclerosis in the French-Canadian genome.
Ross JP, Akçimen F, Liao C, Kwan K, Phillips DE, Schmilovich Z, Spiegelman D, Genge A, Dupré N, Dion PA, Farhan SMK, Rouleau GA.
Ross JP, et al. Among authors: schmilovich z.
Genet Med. 2024 Jan;26(1):100967. doi: 10.1016/j.gim.2023.100967. Epub 2023 Aug 25.
Genet Med. 2024.
PMID: 37638500
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