Manu Sharma - Related publications

Affiliations: 
2005 Princeton University, Princeton, NJ 
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50 most relevant papers in past 60 days:
Year Citation  Score
2021 Jiang L, Mei JP, Zhao YW, Zhang R, Pan HX, Yang Y, Sun QY, Xu Q, Yan XX, Tan JQ, Li JC, Tang BS, Guo JF. Low-frequency and rare coding variants of NUS1 contribute to susceptibility and phenotype of Parkinson's disease. Neurobiology of Aging. PMID 34635350 DOI: 10.1016/j.neurobiolaging.2021.09.003   
2021 Chairta PP, Hadjisavvas A, Georgiou AN, Loizidou MA, Yiangou K, Demetriou CA, Christou YP, Pantziaris M, Michailidou K, Zamba-Papanicolaou E. Prediction of Parkinson's Disease Risk Based on Genetic Profile and Established Risk Factors. Genes. 12. PMID 34440451 DOI: 10.3390/genes12081278   
2021 Chu YT, Tai CH, Lin CH, Wu RM. Updates on the Genetics of Parkinson's Disease: Clinical Implications and Future Treatment. Acta Neurologica Taiwanica. 30: 83-93. PMID 34841503   
2021 Han J, Feng G, Wu J, Zhang Y, Long Z, Yao X. Association of ATG5 gene polymorphism with Parkinson's disease in a Han Chinese population. Acta Neurologica Belgica. PMID 34661876 DOI: 10.1007/s13760-021-01814-y   
2021 Wallom KL, Fernández-Suárez ME, Priestman DA, Te Vruchte D, Huebecker M, Hallett PJ, Isacson O, Platt FM. Glycosphingolipid metabolism and its role in ageing and Parkinson's disease. Glycoconjugate Journal. PMID 34757540 DOI: 10.1007/s10719-021-10023-x   
2021 Pérez-Santamarina E, García-Ruiz P, Martínez-Rubio D, Ezquerra M, Pla-Navarro I, Puente J, Martí MJ, Palau F, Hoenicka J. Regulatory rare variants of the dopaminergic gene ANKK1 as potential risk factors for Parkinson's disease. Scientific Reports. 11: 9879. PMID 33972609 DOI: 10.1038/s41598-021-89300-6   
2021 Jarazo J, Barmpa K, Modamio J, Saraiva C, Sabaté-Soler S, Rosety I, Griesbeck A, Skwirblies F, Zaffaroni G, Smits LM, Su J, Arias-Fuenzalida J, Walter J, Gomez-Giro G, Monzel AS, et al. Parkinson's Disease Phenotypes in Patient Neuronal Cultures and Brain Organoids Improved by 2-Hydroxypropyl-β-Cyclodextrin Treatment. Movement Disorders : Official Journal of the Movement Disorder Society. PMID 34637165 DOI: 10.1002/mds.28810   
2021 Nalls MA, Blauwendraat C, Sargent L, Vitale D, Leonard H, Iwaki H, Song Y, Bandres-Ciga S, Menden K, Faghri F, Heutink P, Cookson MR, Singleton AB. Evidence for connecting multiple neurodegenerative diseases. Brain Communications. 3: fcab095. PMID 34693284 DOI: 10.1093/braincomms/fcab095   
2021 Siokas V, Aloizou AM, Liampas I, Bakirtzis C, Tsouris Z, Sgantzos M, Liakos P, Bogdanos DP, Hadjigeorgiou GM, Dardiotis E. Myelin-associated oligodendrocyte basic protein rs616147 polymorphism as a risk factor for Parkinson's disease. Acta Neurologica Scandinavica. PMID 34694630 DOI: 10.1111/ane.13538   
2021 Prince C, Mitchell RE, Richardson TG. Integrative multiomics analysis highlights immune-cell regulatory mechanisms and shared genetic architecture for 14 immune-associated diseases and cancer outcomes. American Journal of Human Genetics. PMID 34741802 DOI: 10.1016/j.ajhg.2021.10.003   
2021 Lim JL, Lohmann K, Tan AH, Tay YW, Ibrahim KA, Abdul Aziz Z, Mawardi AS, Puvanarajah SD, Lim TT, Looi I, Ooi JCE, Chia YK, Muthusamy KA, Bauer P, Rolfs A, et al. Glucocerebrosidase (GBA) gene variants in a multi-ethnic Asian cohort with Parkinson's disease: mutational spectrum and clinical features. Journal of Neural Transmission (Vienna, Austria : 1996). PMID 34779914 DOI: 10.1007/s00702-021-02421-0   
2021 Quan W, Li J, Jin X, Liu L, Zhang Q, Qin Y, Pei X, Chen J. Identification of Potential Core Genes in Parkinson's Disease Using Bioinformatics Analysis. Parkinson's Disease. 2021: 1690341. PMID 34580608 DOI: 10.1155/2021/1690341   
2021 Fang HS, Chao CY, Wang CC, Fan WL, Huang PJ, Fung HC, Wu YR. Association of AXIN1 With Parkinson's Disease in a Taiwanese Population. Journal of Movement Disorders. PMID 34781631 DOI: 10.14802/jmd.21073   
2021 König E, Nicoletti A, Pattaro C, Annesi G, Melotti R, Gialluisi A, Schwienbacher C, Picard A, Blankenburg H, Pichler I, Modugno N, Ciullo M, Esposito T, Domingues FS, Hicks AA, et al. Exome-wide association study of levodopa-induced dyskinesia in Parkinson's disease. Scientific Reports. 11: 19582. PMID 34599261 DOI: 10.1038/s41598-021-99393-8   
2021 Gu X, Hou Y, Chen Y, Ou R, Cao B, Wei Q, Zhang L, Song W, Zhao B, Wu Y, Shang H. Comprehensive Analysis of LIN28A in Chinese Patients With Early Onset Parkinson's Disease. Frontiers in Genetics. 12: 740096. PMID 34733315 DOI: 10.3389/fgene.2021.740096   
2021 Zazuli Z, de Jong C, Xu W, Vijverberg SJH, Masereeuw R, Patel D, Mirshams M, Khan K, Cheng D, Ordonez-Perez B, Huang S, Spreafico A, Hansen AR, Goldstein DP, de Almeida JR, et al. Association between Genetic Variants and Cisplatin-Induced Nephrotoxicity: A Genome-Wide Approach and Validation Study. Journal of Personalized Medicine. 11. PMID 34834585 DOI: 10.3390/jpm11111233   
2021 Das S, Pearson M, Taylor K, Bouchet V, Møller GL, Hall TO, Strivens M, Tzeng KTH, Gardner S. Combinatorial Analysis of Phenotypic and Clinical Risk Factors Associated With Hospitalized COVID-19 Patients. Frontiers in Digital Health. 3: 660809. PMID 34713134 DOI: 10.3389/fdgth.2021.660809   
2021 Katz DH, Tahir UA, Bick AG, Pampana A, Ngo D, Benson MD, Yu Z, Robbins JM, Chen ZZ, Cruz DE, Deng S, Farrell L, Sinha S, Schmaier AA, Shen D, ... , et al. Whole Genome Sequence Analysis of the Plasma Proteome in Black Adults Provides Novel Insights into Cardiovascular Disease. Circulation. PMID 34814699 DOI: 10.1161/CIRCULATIONAHA.121.055117   
2021 Haydock L, Garneau AP, Tremblay L, Yen HY, Gao H, Harrisson R, Isenring P. Genetic abnormalities in biopsy-proven, adult-onset hemolytic uremic syndrome and C3 glomerulopathy. Journal of Molecular Medicine (Berlin, Germany). PMID 34714369 DOI: 10.1007/s00109-021-02102-1   
2021 Ritchie SC, Lambert SA, Arnold M, Teo SM, Lim S, Scepanovic P, Marten J, Zahid S, Chaffin M, Liu Y, Abraham G, Ouwehand WH, Roberts DJ, Watkins NA, Drew BG, et al. Integrative analysis of the plasma proteome and polygenic risk of cardiometabolic diseases. Nature Metabolism. PMID 34750571 DOI: 10.1038/s42255-021-00478-5   
2021 Verma A, Tsao NL, Thomann L, Ho YL, Iyengar SK, Luoh SW, Carr R, Crawford D, Efird JT, Huffman J, Hung A, Ivey KL, Levin M, Lynch J, Natarajan P, ... , et al. A Phenome-Wide Association Study of genes associated with COVID-19 severity reveals shared genetics with complex diseases in the Million Veteran Program. Medrxiv : the Preprint Server For Health Sciences. PMID 34642702 DOI: 10.1101/2021.05.18.21257396   
2021 Kurul SH, Oktay Y, Töpf A, Szabó NZ, Güngör S, Yaramis A, Sonmezler E, Matalonga L, Yis U, Schon K, Paramonov I, Kalafatcilar İP, Gao F, Rieger A, Arslan N, ... , et al. High diagnostic rate of trio exome sequencing in consanguineous families with neurogenetic diseases. Brain : a Journal of Neurology. PMID 34791078 DOI: 10.1093/brain/awab395   
2021 Sadhukhan S, Maity S, Chakraborty S, Paul S, Munian D, Pattanayak AK, Jana B, Das M. Molecular Insight into the Effect of a Single-Nucleotide Polymorphic Variation on the Structure and Dynamics of Methionine Synthase Reductase and Its Association with Neural Tube Defects. Acs Omega. 6: 26372-26380. PMID 34667917 DOI: 10.1021/acsomega.1c03563   
2021 Reith MEA, Kortagere S, Wiers CE, Sun H, Kurian MA, Galli A, Volkow ND, Lin Z. The dopamine transporter gene SLC6A3: multidisease risks. Molecular Psychiatry. PMID 34650206 DOI: 10.1038/s41380-021-01341-5   
2021 Yang Y, Li D, He C, Peng L, Xing S, Bai M, Rong H, Yuan D, He Y, He X, Wang L, Jin T. Fc receptor-like 1, 3, and 6 variants are associated with rheumatoid arthritis risk in the Chinese Han population. Genes and Environment : the Official Journal of the Japanese Environmental Mutagen Society. 43: 42. PMID 34620245 DOI: 10.1186/s41021-021-00213-2   
2021 Backman JD, Li AH, Marcketta A, Sun D, Mbatchou J, Kessler MD, Benner C, Liu D, Locke AE, Balasubramanian S, Yadav A, Banerjee N, Gillies C, Damask A, Liu S, ... , ... , et al. Exome sequencing and analysis of 454,787 UK Biobank participants. Nature. PMID 34662886 DOI: 10.1038/s41586-021-04103-z   
2021 Márquez A, Martín J. Genetic overlap between type 1 diabetes and other autoimmune diseases. Seminars in Immunopathology. PMID 34595540 DOI: 10.1007/s00281-021-00885-6   
2021 Belbin GM, Rutledge S, Dodatko T, Cullina S, Turchin MC, Kohli S, Torre D, Yee MC, Gignoux CR, Abul-Husn NS, Houten SM, Kenny EE. Leveraging health systems data to characterize a large effect variant conferring risk for liver disease in Puerto Ricans. American Journal of Human Genetics. PMID 34678161 DOI: 10.1016/j.ajhg.2021.09.016   
2021 Sidhu I, Barwe SP, Pillai RK, Gopalakrishnapillai A. Harnessing the Power of Induced Pluripotent Stem Cells and Gene Editing Technology: Therapeutic Implications in Hematological Malignancies. Cells. 10. PMID 34685678 DOI: 10.3390/cells10102698   
2021 Kozin MS, Kiselev IS, Baulina NM, Pavlova GV, Boyko AN, Kulakova OG, Favorova OO. [Risk of Multiple Sclerosis: Analysis of Interactions Between Variants of Nuclear and Mitochondrial Genomes]. Molekuliarnaia Biologiia. 55: 956-964. PMID 34837699 DOI: 10.31857/S0026898421060070   
2021 Joo JY, Lim KH, Yang S, Kim SH, Cocco L, Suh PG. Prediction of genetic alteration of phospholipase C isozymes in brain disorders: Studies with deep learning. Advances in Biological Regulation. 82: 100833. PMID 34773889 DOI: 10.1016/j.jbior.2021.100833   
2021 Chen T, Lin YX, Zha Y, Sun Y, Tian J, Yang Z, Lin SW, Yu F, Chen ZS, Kuang BH, Lei JJ, Nie YJ, Xu Y, Tian DB, Li YZ, et al. A Low-Producing Haplotype of Interleukin-6 Disrupting CTCF Binding Is Protective against Severe COVID-19. Mbio. e0137221. PMID 34634929 DOI: 10.1128/mBio.01372-21   
2021 Ahmed H, Alarabi L, El-Sappagh S, Soliman H, Elmogy M. Genetic variations analysis for complex brain disease diagnosis using machine learning techniques: opportunities and hurdles. Peerj. Computer Science. 7: e697. PMID 34616886 DOI: 10.7717/peerj-cs.697   
2021 Velasco-Ruiz A, Nuñez-Torres R, Pita G, Wildiers H, Lambrechts D, Hatse S, Delombaerde D, Van Brussel T, Alonso MR, Alvarez N, Herraez B, Vulsteke C, Zamora P, Lopez-Fernandez T, Gonzalez-Neira A. as a Novel Susceptibility Gene for Cardiotoxicity in Epirubicin Treatment of Breast Cancer Patients. Pharmaceutics. 13. PMID 34834357 DOI: 10.3390/pharmaceutics13111942   
2021 de Jorge Martínez C, Rukh G, Williams MJ, Gaudio S, Brooks S, Schiöth HB. Genetics of anorexia nervosa: an overview of genome-wide association studies and emerging biological links. Journal of Genetics and Genomics = Yi Chuan Xue Bao. PMID 34634498 DOI: 10.1016/j.jgg.2021.09.005   
2021 Sakaue S, Kanai M, Tanigawa Y, Karjalainen J, Kurki M, Koshiba S, Narita A, Konuma T, Yamamoto K, Akiyama M, Ishigaki K, Suzuki A, Suzuki K, Obara W, Yamaji K, ... , et al. A cross-population atlas of genetic associations for 220 human phenotypes. Nature Genetics. 53: 1415-1424. PMID 34594039 DOI: 10.1038/s41588-021-00931-x   
2021 Barros JBS, Santos KF, Azevedo RM, de Oliveira RPD, Leobas ACD, Bento DDCP, Santos RDS, Reis AADS. No association of GSTP1 rs1695 polymorphism with amyotrophic lateral sclerosis: A case-control study in the Brazilian population. Plos One. 16: e0247024. PMID 33606765 DOI: 10.1371/journal.pone.0247024   
2021 Roy J, Shaikh TM, Del Río Mendoza L, Hosain S, Chapara V, Rahman M. Genome-wide association mapping and genomic prediction for adult stage sclerotinia stem rot resistance in Brassica napus (L) under field environments. Scientific Reports. 11: 21773. PMID 34741104 DOI: 10.1038/s41598-021-01272-9   
2021 Li Y, Lu X, Zhang J, Liu Q, Zhou D, Deng X, Qiu Y, Chen Q, Li M, Yang G, Zheng H, Dai J. Significance of Parkinson Family Genes in the Prognosis and Treatment Outcome Prediction for Lung Adenocarcinoma. Frontiers in Molecular Biosciences. 8: 735263. PMID 34616772 DOI: 10.3389/fmolb.2021.735263   
2021 Dhande IS, Braun MC, Doris PA. Emerging Insights Into Chronic Renal Disease Pathogenesis in Hypertension From Human and Animal Genomic Studies. Hypertension (Dallas, Tex. : 1979). 78: 1689-1700. PMID 34757770 DOI: 10.1161/HYPERTENSIONAHA.121.18112   
2021 Xie Y, Li M, Dong W, Jiang W, Zhao H. M-DATA: A statistical approach to jointly analyzing de novo mutations for multiple traits. Plos Genetics. 17: e1009849. PMID 34735430 DOI: 10.1371/journal.pgen.1009849   
2021 Shen X, Wen Y, Cui Y, Lu Q. A conditional autoregressive model for genetic association analysis accounting for genetic heterogeneity. Statistics in Medicine. PMID 34811777 DOI: 10.1002/sim.9257   
2021 Cao Z, Huang Y, Duan R, Jin P, Qin ZS, Zhang S. Disease category-specific annotation of variants using an ensemble learning framework. Briefings in Bioinformatics. PMID 34643213 DOI: 10.1093/bib/bbab438   
2021 Srivastava K, Ochuba O, Sandhu JK, Alkayyali T, Ruo SW, Waqar A, Jain A, Joseph C, Poudel S. Effect of Catechol-O-Methyltransferase Genotype Polymorphism on Neurological and Psychiatric Disorders: Progressing Towards Personalized Medicine. Cureus. 13: e18311. PMID 34725583 DOI: 10.7759/cureus.18311   
2021 Srivastava K, Ochuba O, Sandhu JK, Alkayyali T, Ruo SW, Waqar A, Jain A, Joseph C, Poudel S. Effect of Catechol-O-Methyltransferase Genotype Polymorphism on Neurological and Psychiatric Disorders: Progressing Towards Personalized Medicine. Cureus. 13: e18311. PMID 34725583 DOI: 10.7759/cureus.18311   
2021 Freitas AT, Calhau C, Antunes G, Araújo B, Bandeira M, Barreira S, Bazenga F, Braz S, Caldeira D, Santos SCR, Faria A, Faria D, Fraga M, Nogueira-Garcia B, Gonçalves L, et al. Vitamin D-related polymorphisms and vitamin D levels as risk biomarkers of COVID-19 disease severity. Scientific Reports. 11: 20837. PMID 34675344 DOI: 10.1038/s41598-021-99952-z   
2021 Mkaouar R, Riahi Z, Charfeddine C, Chelly I, Boudabbous H, Dallali H, Bonnet C, Hechmi M, Bekri S, Zitouna N, Zekri L, Tounsi A, Kefi R, Marrakchi J, Messaoud O, et al. Alpha-mannosidosis in Tunisian consanguineous families: Potential involvement of variants in GHR and SLC19A3 genes in the variable expressivity of cognitive impairment. Plos One. 16: e0258202. PMID 34614013 DOI: 10.1371/journal.pone.0258202   
2021 Zhu Y, Rao J, Wei J, Liu L, Huang S, Lan J, Xue C, Li W. Gene polymorphisms in and are associated with the risk of microscopic polyangiitis in the Guangxi Zhuang Autonomous Region in China. Peerj. 9: e12377. PMID 34820172 DOI: 10.7717/peerj.12377   
2021 Rosier F, Brisebarre A, Dupuis C, Baaklini S, Puthier D, Brun C, Pradel LC, Rihet P, Payen D. Genetic Predisposition to the Mortality in Septic Shock Patients: From GWAS to the Identification of a Regulatory Variant Modulating the Activity of a Enhancer. International Journal of Molecular Sciences. 22. PMID 34072601 DOI: 10.3390/ijms22115852   
2021 Lali R, Chong M, Omidi A, Mohammadi-Shemirani P, Le A, Cui E, Paré G. Calibrated rare variant genetic risk scores for complex disease prediction using large exome sequence repositories. Nature Communications. 12: 5852. PMID 34615865 DOI: 10.1038/s41467-021-26114-0