Andrea Carmine Belin - Related publications

Affiliations: 
Karolinska Institute, Stockholm, Sweden 
Area:
Parkinson genetics
NOTE: We are testing a new system for identifying relevant work based on semantic analysis that identifies similarities between recently published papers and the current author's publications. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches.
50 most relevant papers in past 60 days:
Year Citation  Score
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 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 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 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 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 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 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 Pan HX, Wang YG, Zhao YW, Zeng Q, Wang Z, Fang ZH, Zhang Y, Zhou X, He RC, Xu Q, Sun QY, Tan JQ, Yan XX, Li JC, Tang BS, et al. Evaluating the role of ARSA in Chinese patients with Parkinson's disease. Neurobiology of Aging. PMID 34531044 DOI: 10.1016/j.neurobiolaging.2021.08.008   
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 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 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 Yang Z, Li Z, Teasdale RD. Retromer dependent changes in cellular homeostasis and Parkinson's disease. Essays in Biochemistry. PMID 34528672 DOI: 10.1042/EBC20210023   
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 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 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 Gu X, Hou Y, Chen Y, Ou R, Cao B, Wei Q, Zhang L, Song W, Zhao B, Wu Y, Li C, Shang H. Enrichment of rare variants in E3 ubiquitin ligase genes in Early onset Parkinson's disease. Neurobiology of Aging. PMID 34544586 DOI: 10.1016/j.neurobiolaging.2021.08.013   
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 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 Patel S, Howard D, French L. A pH-eQTL Interaction at the - Parkinson's Disease Risk Locus in the Substantia Nigra. Frontiers in Aging Neuroscience. 13: 690632. PMID 34305570 DOI: 10.3389/fnagi.2021.690632   
2021 Arendt M, Ambrosen A, Fall T, Kierczak M, Tengvall K, Meadows JRS, Karlsson Å, Lagerstedt AS, Bergström T, Andersson G, Lindblad-Toh K, Hagman R. The ABCC4 gene is associated with pyometra in golden retriever dogs. Scientific Reports. 11: 16647. PMID 34404837 DOI: 10.1038/s41598-021-95936-1   
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 Claussnitzer M, Susztak K. Gaining insight into metabolic diseases from human genetic discoveries. Trends in Genetics : Tig. PMID 34315631 DOI: 10.1016/j.tig.2021.07.005   
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 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 Chen Y, Yu X, Kong J. Identification of Neuropeptides as Potential Crosstalks Linking Down Syndrome and Periodontitis Revealed by Transcriptomic Analyses. Disease Markers. 2021: 7331821. PMID 34545294 DOI: 10.1155/2021/7331821   
2021 Dagli-Hernandez C, Zhou Y, Lauschke VM, Genvigir FDV, Hirata TDC, Hirata MH, Hirata RDC. Pharmacogenomics of statins: lipid response and other outcomes in Brazilian cohorts. Pharmacological Reports : Pr. PMID 34403130 DOI: 10.1007/s43440-021-00319-y   
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 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 Gui Y, Grzyb K, Thomas MH, Ohnmacht J, Garcia P, Buttini M, Skupin A, Sauter T, Sinkkonen L. Single-nuclei chromatin profiling of ventral midbrain reveals cell identity transcription factors and cell-type-specific gene regulatory variation. Epigenetics & Chromatin. 14: 43. PMID 34503558 DOI: 10.1186/s13072-021-00418-3   
2021 van Eyk CL, Webber DL, Minoche AE, Pérez-Jurado LA, Corbett MA, Gardner AE, Berry JG, Harper K, MacLennan AH, Gecz J. Yield of clinically reportable genetic variants in unselected cerebral palsy by whole genome sequencing. Npj Genomic Medicine. 6: 74. PMID 34531397 DOI: 10.1038/s41525-021-00238-0   
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 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 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 Weisschuh N, Schimpf-Linzenbold S, Mazzola P, Kieninger S, Xiao T, Kellner U, Neuhann T, Kelbsch C, Tonagel F, Wilhelm H, Kohl S, Wissinger B. Mutation spectrum of the OPA1 gene in a large cohort of patients with suspected dominant optic atrophy: Identification and classification of 48 novel variants. Plos One. 16: e0253987. PMID 34242285 DOI: 10.1371/journal.pone.0253987   
2021 Lalami I, Abo C, Borghese B, Chapron C, Vaiman D. Genomics of Endometriosis: From Genome Wide Association Studies to Exome Sequencing. International Journal of Molecular Sciences. 22. PMID 34298916 DOI: 10.3390/ijms22147297   
2021 Nair V, Sankaranarayanan R, Vasavada AR. Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract. Indian Journal of Ophthalmology. 69: 2064-2070. PMID 34304179 DOI: 10.4103/ijo.IJO_3062_20   
2021 Nair V, Sankaranarayanan R, Vasavada AR. Deciphering the association of intronic single nucleotide polymorphisms of crystallin gene family with congenital cataract. Indian Journal of Ophthalmology. 69: 2064-2070. PMID 34304179 DOI: 10.4103/ijo.IJO_3062_20   
2021 Wu Z, Liang Y, Zuo Y, Xu Y, Mai H, Pi L, Che D, Gu X. The Rs6983267 G Variant Contributes to Increased Sepsis Susceptibility in a Southern Chinese Population. Infection and Drug Resistance. 14: 2969-2976. PMID 34377001 DOI: 10.2147/IDR.S311717   
2021 Wang Q, Dhindsa RS, Carss K, Harper AR, Nag A, Tachmazidou I, Vitsios D, Deevi SVV, Mackay A, Muthas D, Hühn M, Monkley S, Olsson H, , Wasilewski S, et al. Rare variant contribution to human disease in 281,104 UK Biobank exomes. Nature. PMID 34375979 DOI: 10.1038/s41586-021-03855-y   
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 Sin S, Choi HM, Lim J, Kim J, Bak SH, Choi SS, Park J, Lee JH, Oh YM, Lee MK, Hobbs BD, Cho MH, Silverman EK, Kim WJ. A genome-wide association study of quantitative computed tomographic emphysema in Korean populations. Scientific Reports. 11: 16692. PMID 34404834 DOI: 10.1038/s41598-021-95887-7   
2021 Inoue M, Arichi S, Hachiya T, Ohtera A, Kim SW, Yu E, Nishimura M, Shiosakai K, Ohira T. An exploratory assessment of the applicability of direct-to-consumer genetic testing to translational research in Japan. Bmc Research Notes. 14: 282. PMID 34301328 DOI: 10.1186/s13104-021-05696-4   
2021 Inoue M, Arichi S, Hachiya T, Ohtera A, Kim SW, Yu E, Nishimura M, Shiosakai K, Ohira T. An exploratory assessment of the applicability of direct-to-consumer genetic testing to translational research in Japan. Bmc Research Notes. 14: 282. PMID 34301328 DOI: 10.1186/s13104-021-05696-4   
2021 Jan A, Saeed M, Afridi MH, Khuda F, Shabbir M, Khan H, Ali S, Hassan M, Samiullah, Akbar R, Zakiullah. Association of HLA-B Gene Polymorphisms with Type 2 Diabetes in Pashtun Ethnic Population of Khyber Pakhtunkhwa, Pakistan. Journal of Diabetes Research. 2021: 6669731. PMID 34258292 DOI: 10.1155/2021/6669731   
2021 Nowomiejska K, Nasser F, Stingl K, Schimpf-Linzenbold S, Biskup S, Brzozowska A, Rejdak R, Kohl S, Zrenner E. Disease expression caused by different variants in the BEST1 gene: genotype and phenotype findings in bestrophinopathies. Acta Ophthalmologica. PMID 34327816 DOI: 10.1111/aos.14958