Matthew Farrer, PhD, Imperial College - Related publications

Affiliations: 
Neurogenetics and Translational Medicine University of British Columbia, Vancouver, Vancouver, BC, Canada 
Area:
Neurodegenerative diseases
Website:
http://www.cmmt.ubc.ca/research/investigators/farrer/lab
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50 most relevant papers in past 60 days:
Year Citation  Score
2021 Torrealba-Acosta G, Yu E, Lobo-Prada T, Ruíz-Martínez J, Gorostidi-Pagola A, Gan-Or Z, Carazo-Céspedes K, Trempe JF, Mata IF, Fornaguera-Trías J. Clinical and Genetic Analysis of Costa Rican Patients With Parkinson's Disease. Frontiers in Neurology. 12: 656342. PMID 34421783 DOI: 10.3389/fneur.2021.656342   
2021 Guo Y, Sun Y, Song Z, Zheng W, Xiong W, Yang Y, Yuan L, Deng H. Genetic Analysis and Literature Review of Variants in Parkinson's Disease. Frontiers in Aging Neuroscience. 13: 648151. PMID 34456707 DOI: 10.3389/fnagi.2021.648151   
2021 Cui X, Xu C, Zhang L, Wang Y. Identification of Parkinson's Disease-Causing Genes via Omics Data. Frontiers in Genetics. 12: 712164. PMID 34394198 DOI: 10.3389/fgene.2021.712164   
2021 Chandler RJ, Cogo S, Lewis PA, Kevei E. Modelling the Functional Genomics of Parkinson's in Caenorhabditis elegans: LRRK2 and Beyond. Bioscience Reports. PMID 34397087 DOI: 10.1042/BSR20203672   
2021 Usnich T, Vollstedt EJ, Schell N, Skrahina V, Bogdanovic X, Gaber H, Förster TM, Heuer A, Koleva-Alazeh N, Csoti I, Basak AN, Ertan S, Genc G, Bauer P, Lohmann K, ... , et al. LIPAD (LRRK2/Luebeck International Parkinson's Disease) Study Protocol: Deep Phenotyping of an International Genetic Cohort. Frontiers in Neurology. 12: 710572. PMID 34475849 DOI: 10.3389/fneur.2021.710572   
2021 Mehmood A, Ali W, Din ZU, Song S, Sohail M, Shah W, Guo J, Guo RY, Ilahi I, Shah S, Al-Shaebi F, Zeb L, Asiamah EA, Al-Dhamin Z, Bilal H, et al. Clustered regularly interspaced short palindromic repeats as an advanced treatment for Parkinson's disease. Brain and Behavior. PMID 34291612 DOI: 10.1002/brb3.2280   
2021 Wallen ZD, Stone WJ, Factor SA, Molho E, Zabetian CP, Standaert DG, Payami H. Exploring human-genome gut-microbiome interaction in Parkinson's disease. Npj Parkinson's Disease. 7: 74. PMID 34408160 DOI: 10.1038/s41531-021-00218-2   
2021 Li C, Ou R, Hou Y, Chen Y, Gu X, Wei Q, Cao B, Zhang L, Liu K, Chen X, Song W, Zhao B, Wu Y, Shang H. Genetic analysis of TRIM family genes for early-onset Parkinson's disease in Chinese population. Parkinsonism & Related Disorders. 90: 105-113. PMID 34419804 DOI: 10.1016/j.parkreldis.2021.08.005   
2021 Yao S, Zhang X, Zou SC, Zhu Y, Li B, Kuang WP, Guo Y, Li XS, Li L, Wang XY. A transcriptome-wide association study identifies susceptibility genes for Parkinson's disease. Npj Parkinson's Disease. 7: 79. PMID 34504106 DOI: 10.1038/s41531-021-00221-7   
2021 Strafella C, Caputo V, Termine A, Assogna F, Pellicano C, Pontieri FE, Macchiusi L, Minozzi G, Gambardella S, Centonze D, Bossù P, Spalletta G, Caltagirone C, Giardina E, Cascella R. Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs Interactions. Frontiers in Genetics. 12: 651971. PMID 34149802 DOI: 10.3389/fgene.2021.651971   
2021 Strafella C, Caputo V, Termine A, Assogna F, Pellicano C, Pontieri FE, Macchiusi L, Minozzi G, Gambardella S, Centonze D, Bossù P, Spalletta G, Caltagirone C, Giardina E, Cascella R. Immune System and Neuroinflammation in Idiopathic Parkinson's Disease: Association Analysis of Genetic Variants and miRNAs Interactions. Frontiers in Genetics. 12: 651971. PMID 34149802 DOI: 10.3389/fgene.2021.651971   
2021 Lu X, Song N, Wang W, Liu Y, Song H, Xu L, Wang Y, Wei C, Chen J, Yang X, Han F. Generation of integration-free human iPSC line LCPHi001-A from a Parkinson's disease patient carrying the RecNciI mutation in GBA gene. Stem Cell Research. 56: 102514. PMID 34464855 DOI: 10.1016/j.scr.2021.102514   
2021 Zhao H, Zhang Q, Chen H, Rezanur Rahman M, Md Faruquee H. Integrated multi-omics approach identified molecular mechanism and pathogenetic processes of COVID-19 that affect patient with Parkinson's disorder. Saudi Journal of Biological Sciences. PMID 34366686 DOI: 10.1016/j.sjbs.2021.07.074   
2021 Olsen AL, Feany MB. Parkinson's disease risk genes act in glia to control neuronal α-synuclein toxicity. Neurobiology of Disease. 159: 105482. PMID 34390834 DOI: 10.1016/j.nbd.2021.105482   
2021 Kim S, Shin JY, Kwon NJ, Kim CU, Kim C, Lee CS, Seo JS. Evaluation of low-pass genome sequencing in polygenic risk score calculation for Parkinson's disease. Human Genomics. 15: 58. PMID 34454617 DOI: 10.1186/s40246-021-00357-w   
2021 Duan KM, Fang C, Yang SQ, Yang ST, Xiao JD, Chang H, Lin GX, Zhang LB, Peng MC, Liu ZQ, Wang SY. Genetic Polymorphism of rs13306146 Affects Expression and Associated With Postpartum Depressive Symptoms in Chinese Women Who Received Cesarean Section. Frontiers in Genetics. 12: 675386. PMID 34306020 DOI: 10.3389/fgene.2021.675386   
2021 Zheng R, Qiao S, Chen Y, Jin C, Fang Y, Lin Z, Xue N, Yan Y, Gu L, Gao T, Tian J, Yan Y, Yin X, Pu J, Zhang B. Association Analysis and Polygenic Risk Score Evaluation of 38 GWAS-identified Loci in a Chinese population with Parkinson's Disease. Neuroscience Letters. 136150. PMID 34352340 DOI: 10.1016/j.neulet.2021.136150   
2021 Yin Y, Liu Y, Xu M, Zhang X, Li C. Association of COMT rs4680 and MAO-B rs1799836 polymorphisms with levodopa-induced dyskinesia in Parkinson's disease-a meta-analysis. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 34346015 DOI: 10.1007/s10072-021-05509-3   
2021 Reiszadeh Jahromi S, Ramesh SR, Finkelstein DI, Haddadi M. -Synuclein E46K Mutation and Involvement of Oxidative Stress in a Model of Parkinson's Disease. Parkinson's Disease. 2021: 6621507. PMID 34285796 DOI: 10.1155/2021/6621507   
2021 Song F, Owczarek-Lipska M, Ahmels T, Book M, Aisenbrey S, Menghini M, Barthelmes D, Schrader S, Spital G, Neidhardt J. High-Throughput Sequencing to Identify Mutations Associated with Retinal Dystrophies. Genes. 12. PMID 34440443 DOI: 10.3390/genes12081269   
2021 Castelo Rueda MP, Raftopoulou A, Gögele M, Borsche M, Emmert D, Fuchsberger C, Hantikainen EM, Vukovic V, Klein C, Pramstaller PP, Pichler I, Hicks AA. Frequency of Heterozygous Parkin () Variants and Penetrance of Parkinson's Disease Risk Markers in the Population-Based CHRIS Cohort. Frontiers in Neurology. 12: 706145. PMID 34434164 DOI: 10.3389/fneur.2021.706145   
2021 Brendza R, Lin H, Stark K, Foreman O, Tao J, Pierce A, Ngu H, Shen K, Easton AE, Bhangale T, Chang D, Bingol B, Friedman BA. Genetic ablation of Gpnmb does not alter synuclein-related pathology. Neurobiology of Disease. 105494. PMID 34464706 DOI: 10.1016/j.nbd.2021.105494   
2021 Kinoshita S, Ando M, Ando J, Ishii M, Furukawa Y, Tomita O, Azusawa Y, Shirane S, Kishita Y, Yatsuka Y, Eguchi H, Okazaki Y, Komatsu N. Trigenic // mutations in myelodysplasia with Usher syndrome. Heliyon. 7: e07804. PMID 34458631 DOI: 10.1016/j.heliyon.2021.e07804   
2021 Ferese R, Campopiano R, Scala S, D'Alessio C, Storto M, Buttari F, Centonze D, Logroscino G, Zecca C, Zampatti S, Fornai F, Cianci V, Manfroi E, Giardina E, Magnani M, et al. Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants. Frontiers in Genetics. 12: 682050. PMID 34354735 DOI: 10.3389/fgene.2021.682050   
2021 Yeh TH, Liu HF, Chiu CC, Cheng ML, Huang GJ, Huang YC, Liu YC, Huang YZ, Lu CS, Chen YC, Chen HY, Cheng YC. PLA2G6 mutations cause motor dysfunction phenotypes of young-onset dystonia-parkinsonism type 14 and can be relieved by DHA treatment in animal models. Experimental Neurology. 113863. PMID 34520727 DOI: 10.1016/j.expneurol.2021.113863   
2021 Wang X, Xiao H, Yao Y, Xu K, Liu X, Su B, Zhang H, Guan N, Zhong X, Zhang Y, Ding J, Wang F. Spectrum of Mutations in Pediatric Non-glomerular Chronic Kidney Disease Stages 2-5. Frontiers in Genetics. 12: 697085. PMID 34295353 DOI: 10.3389/fgene.2021.697085   
2021 Jiang X, Chen M, Song W, Lin GN. Label propagation-based semi-supervised feature selection on decoding clinical phenotypes with RNA-seq data. Bmc Medical Genomics. 14: 141. PMID 34465339 DOI: 10.1186/s12920-021-00985-0   
2021 Feliciano CM, Wu K, Watry HL, Marley CBE, Ramadoss GN, Ghanim HY, Liu AZ, Zholudeva LV, McDevitt TC, Saporta MA, Conklin BR, Judge LM. Allele-Specific Gene Editing Rescues Pathology in a Human Model of Charcot-Marie-Tooth Disease Type 2E. Frontiers in Cell and Developmental Biology. 9: 723023. PMID 34485306 DOI: 10.3389/fcell.2021.723023   
2021 Chen ZR, Bao MH, Wang XY, Yang YM, Huang B, Han ZL, Cai J, Fan XH. Genetic variants in Chinese patients with sporadic Stanford type A aortic dissection. Journal of Thoracic Disease. 13: 4008-4022. PMID 34422331 DOI: 10.21037/jtd-20-2758   
2021 Stoker TB, Mason SL, Greenland JC, Holden ST, Santini H, Barker RA. Huntington's disease: diagnosis and management. Practical Neurology. PMID 34413240 DOI: 10.1136/practneurol-2021-003074   
2021 Ding J, Frantzeskos A, Orozco G. Functional interrogation of autoimmune disease genetics using CRISPR/Cas9 technologies and massively parallel reporter assays. Seminars in Immunopathology. PMID 34508276 DOI: 10.1007/s00281-021-00887-4   
2021 Shalash AS, Rösler TW, Abdelrahman IY, Abulmakarem HS, Müller SH, Hopfner F, Kuhlenbäumer G, Höglinger GU, Salama M. Atypical pantothenate kinase-associated neurodegeneration with variable phenotypes in an Egyptian family. Heliyon. 7: e07469. PMID 34286134 DOI: 10.1016/j.heliyon.2021.e07469   
2021 Cao L, Yan Y, Zhao G. NOTCH2NLC-related repeat expansion disorders: an expanding group of neurodegenerative disorders. Neurological Sciences : Official Journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology. PMID 34333668 DOI: 10.1007/s10072-021-05498-3   
2021 Sortwell CE, Hacker ML, Fischer DL, Konrad PE, Davis TL, Neimat JS, Wang L, Song Y, Mattingly ZR, Cole-Strauss A, Lipton JW, Charles PD. BDNF rs6265 Genotype Influences Outcomes of Pharmacotherapy and Subthalamic Nucleus Deep Brain Stimulation in Early-Stage Parkinson's Disease. Neuromodulation : Journal of the International Neuromodulation Society. PMID 34288271 DOI: 10.1111/ner.13504   
2021 Jiao B, Liu H, Guo L, Xiao X, Liao X, Zhou Y, Weng L, Zhou L, Wang X, Jiang Y, Yang Q, Zhu Y, Zhou L, Zhang W, Wang J, et al. The role of genetics in neurodegenerative dementia: a large cohort study in South China. Npj Genomic Medicine. 6: 69. PMID 34389718 DOI: 10.1038/s41525-021-00235-3   
2021 Kang JH, Park JH, Park JS, Lee SK, Lee S, Baik HW. Molecular diagnosis of McArdle disease using whole-exome sequencing. Experimental and Therapeutic Medicine. 22: 1029. PMID 34373715 DOI: 10.3892/etm.2021.10461   
2021 Liu YH, Zhang HF, Jin JY, Wei YQ, Wang CY, Fan LL, Liu L. Case Report: A Homozygous Mutation (p.Y62X) of May Lead to a New Leukoencephalopathy Syndrome. Frontiers in Aging Neuroscience. 13: 671296. PMID 34267643 DOI: 10.3389/fnagi.2021.671296   
2021 Müller U. Spinocerebellar ataxias (SCAs) caused by common mutations. Neurogenetics. PMID 34401960 DOI: 10.1007/s10048-021-00662-5   
2021 Sánchez-Rodríguez A, Martínez-Rodríguez I, Sánchez-Juan P, Sierra M, González-Aramburu I, Rivera-Sánchez M, Andrés-Pacheco J, Gutierrez-González Á, García-Hernández A, Madera J, Delgado-Alvarado M, Infante J. Serial DaT-SPECT imaging in asymptomatic carriers of LRRK2 G2019S mutation: 8-years follow-up. European Journal of Neurology. PMID 34407293 DOI: 10.1111/ene.15070   
2021 Cooper-Knock J, Harvey C, Zhang S, Moll T, Timpanaro IS, Kenna KP, Iacoangeli A, Veldink JH. Advances in the genetic classification of amyotrophic lateral sclerosis. Current Opinion in Neurology. PMID 34343141 DOI: 10.1097/WCO.0000000000000986   
2021 He D, Shang L, Liu Q, Shen D, Sun X, Cai Z, Zhao X, Liu L, Yang X, Liu M, Zhang X, Cui L. Association of apolipoprotein E ε4 allele and amyotrophic lateral sclerosis in Chinese population. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-8. PMID 34279165 DOI: 10.1080/21678421.2021.1953077   
2021 He D, Shang L, Liu Q, Shen D, Sun X, Cai Z, Zhao X, Liu L, Yang X, Liu M, Zhang X, Cui L. Association of apolipoprotein E ε4 allele and amyotrophic lateral sclerosis in Chinese population. Amyotrophic Lateral Sclerosis & Frontotemporal Degeneration. 1-8. PMID 34279165 DOI: 10.1080/21678421.2021.1953077   
2021 Kozek K, Wada Y, Sala L, Denjoy I, Egly C, O'Neill MJ, Aiba T, Shimizu W, Makita N, Ishikawa T, Crotti L, Spazzolini C, Kotta MC, Dagradi F, Castelletti S, et al. Estimating the Post-Test Probability of Long QT Syndrome Diagnosis for Rare Variants. Circulation. Genomic and Precision Medicine. PMID 34309407 DOI: 10.1161/CIRCGEN.120.003289   
2021 Kozek K, Wada Y, Sala L, Denjoy I, Egly C, O'Neill MJ, Aiba T, Shimizu W, Makita N, Ishikawa T, Crotti L, Spazzolini C, Kotta MC, Dagradi F, Castelletti S, et al. Estimating the Post-Test Probability of Long QT Syndrome Diagnosis for Rare Variants. Circulation. Genomic and Precision Medicine. PMID 34309407 DOI: 10.1161/CIRCGEN.120.003289   
2021 Wang HL, Yeh TH, Huang YZ, Weng YH, Chen RS, Lu CS, Wei KC, Liu YC, Chen YL, Chen CL, Chen YJ, Lin YW, Hsu CC, Chiu CH, Chiu CC. Functional variant rs17525453 within RAB35 gene promoter is possibly associated with increased risk of Parkinson's disease in Taiwanese population. Neurobiology of Aging. PMID 34275689 DOI: 10.1016/j.neurobiolaging.2021.06.011   
2021 Wang HL, Yeh TH, Huang YZ, Weng YH, Chen RS, Lu CS, Wei KC, Liu YC, Chen YL, Chen CL, Chen YJ, Lin YW, Hsu CC, Chiu CH, Chiu CC. Functional variant rs17525453 within RAB35 gene promoter is possibly associated with increased risk of Parkinson's disease in Taiwanese population. Neurobiology of Aging. PMID 34275689 DOI: 10.1016/j.neurobiolaging.2021.06.011   
2021 Heeney MM, Berhe S, Campagna DR, Oved JH, Kurre P, Shaw PJ, Teo J, Shanap MA, Hassab HM, Glader BE, Shah S, Yoshimi A, Ameri A, Antin JH, Boudreaux J, et al. SLC25A38 Congenital Sideroblastic Anemia: Phenotypes and genotypes of 31 individuals from 24 families, including 11 novel mutations, and a review of the literature. Human Mutation. PMID 34298585 DOI: 10.1002/humu.24267   
2021 Axente M, Shelby ES, Mirea A, Sporea C, Badina M, Padure L, Ion DA. Clinical features and genetics in non-5q spinal muscular atrophy caused by acid ceramidase deficiency. Journal of Medicine and Life. 14: 424-428. PMID 34377212 DOI: 10.25122/jml-2021-0147   
2021 Escott-Price V, Schmidt KM. Probability of Alzheimer's disease based on common and rare genetic variants. Alzheimer's Research & Therapy. 13: 140. PMID 34404470 DOI: 10.1186/s13195-021-00884-7   
2021 Xu D, Wang C, Khan A, Shang N, He Z, Gordon A, Kullo IJ, Murphy S, Ni Y, Wei WQ, Gharavi A, Kiryluk K, Weng C, Ionita-Laza I. Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies. Npj Digital Medicine. 4: 116. PMID 34302027 DOI: 10.1038/s41746-021-00488-3