Human Genome Epidemiology Literature Finder
Records 1 - 30 (of 156 Records) |
Query Trace: SORL1[original query] |
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Association between Alzheimer's disease genes and trajectories of cognitive function decline in Han Chinese in Taiwan. Aging 2021 Jul 13 . Hsieh Tsung-Jen, Lee Wei-Ju, Liao Yi-Chu, Hsu Chih-Cheng, Fang Yao-Hwei, Chen Tzu-Yu, Lin Yung-Shuan, Chang I-Shou, Wang Shuu-Jiun, Hsiung Chao A, Fuh Jong-Ling, |
Plasma lipidome is dysregulated in Alzheimer's disease and is associated with disease risk genes. Translational psychiatry 2021 6 11 (1): 344. Liu Yue, Thalamuthu Anbupalam, Mather Karen A, Crawford John, Ulanova Marina, Wong Matthew Wai Kin, Pickford Russell, Sachdev Perminder S, Braidy Na |
Novel Rare SORL1 Variants in Early-Onset Dementia. Journal of Alzheimer's disease : JAD 2021 6 82 (2): 761-770. Korpioja Anita, Krüger Johanna, Koivuluoma Susanna, Pylkäs Katri, Moilanen Virpi, Helisalmi Seppo, Hiltunen Mikko, Remes Anne |
Identification of two pathogenic mutations in SORL1 in early-onset Alzheimer's disease. Journal of clinical neuroscience : official journal of the Neurosurgical Society of Australasia 2021 6 89 243-248. Qiu Guozhen, Zhu Fei-Qi, Xu Chuny |
THE EXPRESSION OF THE MAIN AND ALTERNATIVE TRANSCRIPT (SORL1 Delta2) OF THE SORL1 GENE IN CHRONIC LYMPHOCYTIC LEUKEMIA PATIENTS AFFECTED BY THE CHORNOBYL ACCIDENT. Problemy radiatsiinoi medytsyny ta radiobiolohii 2021 12 26 273-283. Abramenko I V, Bilous N I, Chumak A A, Diagil I S, Martina Z |
Investigating the Endo-Lysosomal System in Major Neurocognitive Disorders Due to Alzheimer's Disease, Frontotemporal Lobar Degeneration and Lewy Body Disease: Evidence for SORL1 as a Cross-Disease Gene. International journal of molecular sciences 2021 12 22 (24): . Benussi Luisa, Longobardi Antonio, Kocoglu Cemile, Carrara Matteo, Bellini Sonia, Ferrari Clarissa, Nicsanu Roland, Saraceno Claudia, Bonvicini Cristian, Fostinelli Silvia, Zanardini Roberta, Catania Marcella, Moisse Matthieu, Van Damme Philip, Di Fede Giuseppe, Binetti Giuliano, Van Broeckhoven Christine, van der Zee Julie, Ghidoni Rober |
Analysis of cognitive performance and polymorphisms of SORL1, PVRL2, CR1, TOMM40, APOE, PICALM, GWAS_14q, CLU, and BIN1 in patients with mild cognitive impairment and cognitively healthy controls. Neurologia 0 36 (9): 681-691. Cruz-Sanabria F, Bonilla-Vargas K, Estrada K, Mancera O, Vega E, Guerrero E, Ortega-Rojas J, Mahecha María F, Romero A, Montañés P, Celeita V, Arboleda H, Pardo |
Analysis of Genotype-Phenotype Correlations in Patients With Degenerative Dementia Through the Whole Exome Sequencing. Frontiers in aging neuroscience 2021 11 13 745407. Sun Lin, Zhang Jianye, Su Ning, Zhang Shaowei, Yan Feng, Lin Xiang, Yu Jie, Li Wei, Li Xia, Xiao Shi |
Association and Gene-Gene Interactions Study of Late-Onset Alzheimer's Disease in the Russian Population. Genes 2021 Oct 12 (10): . Bocharova Anna, Vagaitseva Kseniya, Marusin Andrey, Zhukova Natalia, Zhukova Irina, Minaycheva Larisa, Makeeva Oksana, Stepanov Vad |
Endophenotypic effects of the SORL1 variant rs2298813 on regional brain volume in patients with late-onset Alzheimer's disease. Frontiers in aging neuroscience 2022 8 14 885090. Chen Chun-Yu, Lin Yung-Shuan, Lee Wei-Ju, Liao Yi-Chu, Kuo Yu-Shan, Yang Albert C, Fuh Jong-Li |
Generation of two iPSC lines (UMi038-A & UMi039-A) from siblings bearing an Alzheimer's disease-associated variant in SORL1. Stem cell research 2022 6 62 102823. DeRosa Brooke A, Simon Shaina A, Velez Christina A, Vance Jeffery M, Pericak-Vance Margaret A, Dykxhoorn Derek |
Penetrance estimation of Alzheimer disease in SORL1 loss-of-function variant carriers using a family-based strategy and stratification by APOE genotypes. Genome medicine 2022 Jun 14 (1): 69. Schramm Catherine, Charbonnier Camille, Zaréa Aline, Lacour Morgane, Wallon David, , Boland Anne, Deleuze Jean-François, Olaso Robert, , Alarcon Flora, Campion Dominique, Nuel Grégory, Nicolas Ga |
Genetic landscape of early-onset dementia in Hungary. Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology 2022 Jun . Csaban Dora, Illes Anett, Renata Toth-Bencsik, Balicza Peter, Pentelenyi Klara, Molnar Viktor, Gezsi Andras, Grosz Zoltan, Gal Aniko, Kovacs Tibor, Klivenyi Peter, Molnar Maria Jud |
Mapping the genetic landscape of early-onset Alzheimer's disease in a cohort of 36 families. Alzheimer's research & therapy 2022 Jun 14 (1): 77. Mol Merel O, van der Lee Sven J, Hulsman Marc, Pijnenburg Yolande A L, Scheltens Phillip, , Seelaar Harro, van Swieten John C, Kaat Laura Donker, Holstege Henne, van Rooij Jeroen G |
GWAS of Hematuria. Clinical journal of the American Society of Nephrology : CJASN 2022 4 17 (5): 672-683. Gagliano Taliun Sarah A, Sulem Patrick, Sveinbjornsson Gardar, Gudbjartsson Daniel F, Stefansson Kari, Paterson Andrew D, Barua Moumi |
SORL1 Polymorphisms in Mexican Patients with Alzheimer's Disease. Genes 2022 4 13 (4): . Toral-Rios Danira, Ruiz-Sánchez Elizabeth, Rodríguez Nancy Lucero Martínez, Maury-Rosillo Marlene, Rosas-Carrasco Óscar, Becerril-Pérez Fernando, Mena-Barranco Francisco, Carvajal-García Rosa, Silva-Adaya Daniela, Delgado-Namorado Yair, Ramos-Palacios Gerardo, Sánchez-Torres Carmen, Campos-Peña Victor |
Evaluation of the relationship between SORL1 gene polymorphism and Parkinson's disease in the Chinese population. Neuroscience letters 2022 4 778 136602. Wang Ying, Luan Mengting, Xue Li, Jin Jianing, Xie An |
An association test of the spatial distribution of rare missense variants within protein structures identifies Alzheimer's disease-related patterns. Genome research 2022 2 32 (4): 778-790. Jin Bowen, Capra John A, Benchek Penelope, Wheeler Nicholas, Naj Adam C, Hamilton-Nelson Kara L, Farrell John J, Leung Yuk Yee, Kunkle Brian, Vadarajan Badri, Schellenberg Gerard D, Mayeux Richard, Wang Li-San, Farrer Lindsay A, Pericak-Vance Margaret A, Martin Eden R, Haines Jonathan L, Crawford Dana C, Bush William |
Exome sequencing identifies rare damaging variants in ATP8B4 and ABCA1 as risk factors for Alzheimer's disease. Nature genetics 2022 11 54 (12): 1786-1794. Holstege Henne, Hulsman Marc, Charbonnier Camille, Grenier-Boley Benjamin, Quenez Olivier, Grozeva Detelina, van Rooij Jeroen G J, Sims Rebecca, Ahmad Shahzad, Amin Najaf, Norsworthy Penny J, Dols-Icardo Oriol, Hummerich Holger, Kawalia Amit, Amouyel Philippe, Beecham Gary W, Berr Claudine, Bis Joshua C, Boland Anne, Bossù Paola, Bouwman Femke, Bras Jose, Campion Dominique, Cochran J Nicholas, Daniele Antonio, Dartigues Jean-François, Debette Stéphanie, Deleuze Jean-François, Denning Nicola, DeStefano Anita L, Farrer Lindsay A, Fernández Maria Victoria, Fox Nick C, Galimberti Daniela, Genin Emmanuelle, Gille Johan J P, Le Guen Yann, Guerreiro Rita, Haines Jonathan L, Holmes Clive, Ikram M Arfan, Ikram M Kamran, Jansen Iris E, Kraaij Robert, Lathrop Marc, Lemstra Afina W, Lleó Alberto, Luckcuck Lauren, Mannens Marcel M A M, Marshall Rachel, Martin Eden R, Masullo Carlo, Mayeux Richard, Mecocci Patrizia, Meggy Alun, Mol Merel O, Morgan Kevin, Myers Richard M, Nacmias Benedetta, Naj Adam C, Napolioni Valerio, Pasquier Florence, Pastor Pau, Pericak-Vance Margaret A, Raybould Rachel, Redon Richard, Reinders Marcel J T, Richard Anne-Claire, Riedel-Heller Steffi G, Rivadeneira Fernando, Rousseau Stéphane, Ryan Natalie S, Saad Salha, Sanchez-Juan Pascual, Schellenberg Gerard D, Scheltens Philip, Schott Jonathan M, Seripa Davide, Seshadri Sudha, Sie Daoud, Sistermans Erik A, Sorbi Sandro, van Spaendonk Resie, Spalletta Gianfranco, Tesi Niccolo', Tijms Betty, Uitterlinden André G, van der Lee Sven J, Visser Pieter Jelle, Wagner Michael, Wallon David, Wang Li-San, Zarea Aline, Clarimon Jordi, van Swieten John C, Greicius Michael D, Yokoyama Jennifer S, Cruchaga Carlos, Hardy John, Ramirez Alfredo, Mead Simon, van der Flier Wiesje M, van Duijn Cornelia M, Williams Julie, Nicolas Gaël, Bellenguez Céline, Lambert Jean-Charl |
Multiple gene variants linked to Alzheimer's-type clinical dementia via GWAS are also associated with non-Alzheimer's neuropathologic entities. Neurobiology of disease 2022 10 174 105880. Katsumata Yuriko, Shade Lincoln M, Hohman Timothy J, Schneider Julie A, Bennett David A, Farfel Jose M, , Kukull Walter A, Fardo David W, Nelson Peter |
Identification and Mechanism of the PD-1/PD-L1 Genomic Signature SORL1 as Protective Factor in Bladder Cancer. Frontiers in genetics 2022 1 12 736158. Xu Yajing, Chen Didi, Shen Lanxiao, Huang Xiaowei, Chen Yi, Su Huafa |
Associations of Germline Genetic Variants with Depression and Fatigue among Hematologic Cancer Patients Treated with Allogeneic Hematopoietic Cell Transplantation. Psychosomatic medicine 2023 9 . Aasha I Hoogland, Brian D Gonzalez, Jong Y Park, Brent J Small, Steven K Sutton, Joseph A Pidala, Kristen S Smith, Julienne E Bower, Paul B Jacobsen, Heather S L J |
Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects. medRxiv : the preprint server for health sciences 2023 9 . Hui Wang, Beth A Dombroski, Po-Liang Cheng, Albert Tucci, Ya-Qin Si, John J Farrell, Jung-Ying Tzeng, Yuk Yee Leung, John S Malamon, , Li-San Wang, Badri N Vardarajan, Lindsay A Farrer, Gerard D Schellenberg, Wan-Ping L |
Cell-type-specific regulation of APOE and CLU levels in human neurons by the Alzheimer's disease risk gene SORL1. Cell reports 2023 8 112994. Hyo Lee, Aimee J Aylward, Richard V Pearse, Alexandra M Lish, Yi-Chen Hsieh, Zachary M Augur, Courtney R Benoit, Vicky Chou, Allison Knupp, Cheryl Pan, Srilakshmi Goberdhan, Duc M Duong, Nicholas T Seyfried, David A Bennett, Mariko F Taga, Kevin Huynh, Matthias Arnold, Peter J Meikle, Philip L De Jager, Vilas Menon, Jessica E Young, Tracy L Young-Pear |
SORL1 rs1699102 Moderates the Effect of Sex on Language Network. Journal of Alzheimer's disease : JAD 2023 5 . Jialing Fan, Zhibao Zhu, Yaojing Chen, Caishui Yang, Xin Li, Kewei Chen, Xiaochun Chen, Zhanjun Zha |
Role of Single Nucleotide Polymorphism-Related Genes in Tumour Immune Cell Infiltration and Prognosis of Cutaneous Melanoma. BioMed research international 2023 5 2023 3754094. Baihe Wang, Fanxiao Liu, Yuanyuan Li, Nan Ch |
Rare variant aggregation in 148,508 exomes identifies genes associated with proxy dementia. Scientific reports 2023 2 13 (1): 2179. Wightman Douglas P, Savage Jeanne E, de Leeuw Christiaan A, Jansen Iris E, Posthuma Daniel |
Structural Variation Detection and Association Analysis of Whole-Genome-Sequence Data from 16,905 Alzheimer's Diseases Sequencing Project Subjects. Research square 2023 10 . Wan-Ping Lee, Hui Wang, Beth Dombroski, Po-Liang Cheng, Albert Tucci, Ya-Qin Si, John Farrell, Jung-Ying Tzeng, Yuk Yee Leung, John Malamon, Li-San Wang, Badri Vardarajan, Lindsay Farrer, Gerard Schellenberg, The Alzheimer's Disease Sequencing Project The Alzheimer's D Proje |
Genetic overlap between ALS and other neurodegenerative or neuromuscular disorders. Amyotrophic lateral sclerosis & frontotemporal degeneration 2023 10 1-11. Cathrine Goberg Olsen, Øyvind Løvold Busk, Øystein Lunde Holla, Kristian Tveten, Trygve Holmøy, Ole-Bjørn Tysnes, Helle Høy |
Cell type-specific histone acetylation profiling of Alzheimer's disease subjects and integration with genetics. Frontiers in molecular neuroscience 2023 1 15 948456. Ramamurthy Easwaran, Welch Gwyneth, Cheng Jemmie, Yuan Yixin, Gunsalus Laura, Bennett David A, Tsai Li-Huei, Pfenning Andreas |
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- Page last updated:Apr 22, 2024
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