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Table representation of search results timeline featuring number of search results per year.
Year | Number of Results |
---|---|
2023 | 2 |
2024 | 5 |
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7 results
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Page 1
The contributions of rare inherited and polygenic risk to ASD in multiplex families.
Proc Natl Acad Sci U S A. 2023 Aug;120(31):e2215632120. doi: 10.1073/pnas.2215632120. Epub 2023 Jul 28.
Proc Natl Acad Sci U S A. 2023.
PMID: 37506195
Free PMC article.
Whole-Genome Sequencing Analysis Reveals New Susceptibility Loci and Structural Variants Associated with Progressive Supranuclear Palsy.
Wang H, Chang TS, Dombroski BA, Cheng PL, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Rajput A, De Deyn PP, Bastard NL, Gearing M, Kaat LD, Swieten JCV, Dopper E, Ghetti BF, Newell KL, Troakes C, de Yébenes JG, Rábano-Gutierrez A, Meller T, Oertel WH, Respondek G, Stamelou M, Arzberger T, Roeber S, Müller U, Hopfner F, Pastor P, Brice A, Durr A, Ber IL, Beach TG, Serrano GE, Hazrati LN, Litvan I, Rademakers R, Ross OA, Galasko D, Boxer AL, Miller BL, Seeley WW, Deerlin VMV, Lee EB, White CL 3rd, Morris H, de Silva R, Crary JF, Goate AM, Friedman JS, Leung YY, Coppola G, Naj AC, Wang LS; PSP genetics study group; Dickson DW, Höglinger GU, Schellenberg GD, Geschwind DH, Lee WP.
Wang H, et al.
medRxiv [Preprint]. 2024 Jan 30:2023.12.28.23300612. doi: 10.1101/2023.12.28.23300612.
medRxiv. 2024.
PMID: 38234807
Free PMC article.
Preprint.
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Defining the distance between diseases using SNOMED CT embeddings.
Fu M, Yan Y, Olde Loohuis LM, Chang TS.
Fu M, et al.
J Biomed Inform. 2023 Mar;139:104307. doi: 10.1016/j.jbi.2023.104307. Epub 2023 Feb 3.
J Biomed Inform. 2023.
PMID: 36738869
Free article.
Item in Clipboard
Multi-class Modeling Identifies Shared Genetic Risk for Late-onset Epilepsy and Alzheimer's Disease.
Fu M, Tran T, Eskin E, Lajonchere C, Pasaniuc B, Geschwind DH, Vossel K, Chang TS.
Fu M, et al.
medRxiv [Preprint]. 2024 Feb 6:2024.02.05.24302353. doi: 10.1101/2024.02.05.24302353.
medRxiv. 2024.
PMID: 38370677
Free PMC article.
Preprint.
Item in Clipboard
Association of Structural Forms of 17q21.31 with the Risk of Progressive Supranuclear Palsy and MAPT Sub-haplotypes.
Wang H, Chang TS, Dombroski BA, Cheng PL, Si YQ, Tucci A, Patil V, Valiente-Banuet L, Farrell K, Mclean C, Molina-Porcel L, Alex R, Paul De Deyn P, Le Bastard N, Gearing M, Donker Kaat L, Van Swieten JC, Dopper E, Ghetti BF, Newell KL, Troakes C, G de Yébenes J, Rábano-Gutierrez A, Meller T, Oertel WH, Respondek G, Stamelou M, Arzberger T, Roeber S, Müller U, Hopfner F, Pastor P, Brice A, Durr A, Ber IL, Beach TG, Serrano GE, Hazrati LN, Litvan I, Rademakers R, Ross OA, Galasko D, Boxer AL, Miller BL, Seeley WW, Van Deerlin VM, Lee EB, White CL 3rd, Morris HR, de Silva R, Crary JF, Goate AM, Friedman JS, Leung YY, Coppola G, Naj AC, Wang LS; PSP genetics study group; Dickson DW, Höglinger GU, Tzeng JY, Geschwind DH, Schellenberg GD, Lee WP.
Wang H, et al.
medRxiv [Preprint]. 2024 Feb 28:2024.02.26.24303379. doi: 10.1101/2024.02.26.24303379.
medRxiv. 2024.
PMID: 38464214
Free PMC article.
Preprint.
Item in Clipboard
Improving genetic risk modeling of dementia from real-world data in underrepresented populations.
Fu M, Valiente-Banuet L, Wadhwa SS; UCLA Precision Health Data Discovery Repository Working Group; UCLA Precision Health ATLAS Working Group; Pasaniuc B, Vossel K, Chang TS.
Fu M, et al.
medRxiv [Preprint]. 2024 Feb 6:2024.02.05.24302355. doi: 10.1101/2024.02.05.24302355.
medRxiv. 2024.
PMID: 38370649
Free PMC article.
Preprint.
Item in Clipboard
Improving genetic risk modeling of dementia from real-world data in underrepresented populations.
Chang T, Fu M, Valiente-Banuet L, Wadhwa S, Pasaniuc B, Vossel K.
Chang T, et al.
Res Sq [Preprint]. 2024 Feb 15:rs.3.rs-3911508. doi: 10.21203/rs.3.rs-3911508/v1.
Res Sq. 2024.
PMID: 38410460
Free PMC article.
Preprint.
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