Maher A. Noureddine, Ph.D. - Related publications

University of North Carolina, Chapel Hill, Chapel Hill, NC 
Cell cycle
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50 most relevant papers in past 60 days:
Year Citation  Score
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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 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 Joslin AC, Sobreira DR, Hansen GT, Sakabe NJ, Aneas I, Montefiori LE, Farris KM, Gu J, Lehman DM, Ober C, He X, Nóbrega MA. A functional genomics pipeline identifies pleiotropy and cross-tissue effects within obesity-associated GWAS loci. Nature Communications. 12: 5253. PMID 34489471 DOI: 10.1038/s41467-021-25614-3   
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 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 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 Zhang Y, Wang Y, Zhou W, Zheng S, Ye R. Detection of candidate gene networks involved in resistance to Sclerotinia sclerotiorum in soybean. Journal of Applied Genetics. PMID 34510383 DOI: 10.1007/s13353-021-00654-z   
2021 Hariharan P, Dupuis J. Mapping gene and gene pathways associated with coronary artery disease: a CARDIoGRAM exome and multi-ancestry UK biobank analysis. Scientific Reports. 11: 16461. PMID 34385509 DOI: 10.1038/s41598-021-95637-9   
2021 Arango D, Bittar A, Esmeral NP, Ocasión C, Muñoz-Camargo C, Cruz JC, Reyes LH, Bloch NI. Understanding the Potential of Genome Editing in Parkinson's Disease. International Journal of Molecular Sciences. 22. PMID 34502143 DOI: 10.3390/ijms22179241   
2021 Cleary S, Seoighe C. Perspectives on Allele-Specific Expression. Annual Review of Biomedical Data Science. 4: 101-122. PMID 34465174 DOI: 10.1146/annurev-biodatasci-021621-122219   
2021 Guan Y, Liang X, Ma Z, Hu H, Liu H, Miao Z, Linkermann A, Hellwege JN, Voight BF, Susztak K. A single genetic locus controls both expression of DPEP1/CHMP1A and kidney disease development via ferroptosis. Nature Communications. 12: 5078. PMID 34426578 DOI: 10.1038/s41467-021-25377-x   
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 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 Oluwafemi OO, Musfee FI, Mitchell LE, Goldmuntz E, Xie HM, Hakonarson H, Morrow BE, Guo T, Taylor DM, McDonald-McGinn DM, Emanuel BS, Agopian AJ. Genome-Wide Association Studies of Conotruncal Heart Defects with Normally Related Great Vessels in the United States. Genes. 12. PMID 34356046 DOI: 10.3390/genes12071030   
2021 Mo A, Nagpal S, Gettler K, Haritunians T, Giri M, Haberman Y, Karns R, Prince J, Arafat D, Hsu NY, Chuang LS, Argmann C, Kasarskis A, Suarez-Farinas M, Gotman N, et al. Stratification of risk of progression to colectomy in ulcerative colitis via measured and predicted gene expression. American Journal of Human Genetics. PMID 34450030 DOI: 10.1016/j.ajhg.2021.07.013   
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 Yaoxing H, Danchun Y, Xiaojuan S, Shuman J, Qingqing Y, Lin J. Identification of Novel Susceptible Genes of Gastric Cancer Based on Integrated Omics Data. Frontiers in Cell and Developmental Biology. 9: 712020. PMID 34354996 DOI: 10.3389/fcell.2021.712020   
2021 Zhan L, Li J, Jew B, Sul JH. Rare variants in the endocytic pathway are associated with Alzheimer's disease, its related phenotypes, and functional consequences. Plos Genetics. 17: e1009772. PMID 34516545 DOI: 10.1371/journal.pgen.1009772   
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 Kolosov N, Daly MJ, Artomov M. Prioritization of disease genes from GWAS using ensemble-based positive-unlabeled learning. European Journal of Human Genetics : Ejhg. PMID 34276057 DOI: 10.1038/s41431-021-00930-w   
2021 Reuter MS, Chaturvedi RR, Jobling RK, Pellecchia G, Hamdan O, Sung WWL, Nalpathamkalam T, Attaluri P, Silversides CK, Wald RM, Marshall CR, Williams S, Keavney BD, Thiruvahindrapuram B, Scherer SW, et al. Clinical Genetic Risk Variants Inform a Functional Protein Interaction Network for Tetralogy of Fallot. Circulation. Genomic and Precision Medicine. PMID 34328347 DOI: 10.1161/CIRCGEN.121.003410   
2021 Soler-Garzón A, McClean PE, Miklas PN. Genome-Wide Association Mapping of and Reveals Candidate Genes and New Adjustments to the Host-Pathogen Interaction for Resistance to in Common Bean. Frontiers in Plant Science. 12: 699569. PMID 34267774 DOI: 10.3389/fpls.2021.699569   
2021 Ruan X, Wang Z, Su Y, Wang T. Population Genomics Reveals Gene Flow and Adaptive Signature in Invasive Weed . Genes. 12. PMID 34440453 DOI: 10.3390/genes12081279   
2021 Shen F, Cai W, Gan X, Feng J, Chen Z, Guo M, Wei F, Cao J, Xu B. Prediction of Genetic Factors of Hyperthyroidism Based on Gene Interaction Network. Frontiers in Cell and Developmental Biology. 9: 700355. PMID 34409035 DOI: 10.3389/fcell.2021.700355   
2021 Jiang X, Pan W, Chen M, Wang W, Song W, Lin GN. Integrative enrichment analysis of gene expression based on an artificial neuron. Bmc Medical Genomics. 14: 173. PMID 34433483 DOI: 10.1186/s12920-021-00988-x   
2021 Zhu D, Yao S, Wu H, Ke X, Zhou X, Geng S, Dong S, Chen H, Yang T, Cheng Y, Guo Y. A transcriptome-wide association study identifies novel susceptibility genes for psoriasis. Human Molecular Genetics. PMID 34409462 DOI: 10.1093/hmg/ddab237   
2021 Chen J, Ali MW, Yan L, Dighe SG, Dai JY, Vaughan TL, Casey G, Buas MF. Prioritization and functional analysis of GWAS risk loci for Barrett's esophagus and esophageal adenocarcinoma. Human Molecular Genetics. PMID 34505128 DOI: 10.1093/hmg/ddab259   
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 Kim SS, Hudgins AD, Yang J, Zhu Y, Tu Z, Rosenfeld MG, DiLorenzo TP, Suh Y. A comprehensive integrated post-GWAS analysis of Type 1 diabetes reveals enhancer-based immune dysregulation. Plos One. 16: e0257265. PMID 34529725 DOI: 10.1371/journal.pone.0257265   
2021 Xu J, Liu X, Cai C, Su W, Xie J, Zhang Z, Yang P, Lyu S, Li Z, Lei C, Chen H, Wang E, Ru B, Huang Y. Two cSNPs sites in the fatty acid-binding protein 4 () gene and their association analysis with body measurement data in five Chinese cattle breeds. Animal Biotechnology. 1-8. PMID 34392778 DOI: 10.1080/10495398.2021.1916511   
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 Audain E, Wilsdon A, Breckpot J, Izarzugaza JM, Fitzgerald TW, Kahlert AK, Sifrim A, Wünnemann F, Perez-Riverol Y, Abdul-Khaliq H, Bak M, Bassett AS, Benson WD, Berger F, Daehnert I, et al. Integrative analysis of genomic variants reveals new associations of candidate haploinsufficient genes with congenital heart disease. Plos Genetics. 17: e1009679. PMID 34324492 DOI: 10.1371/journal.pgen.1009679