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.
24 most relevant papers in past 60 days:
Year Citation  Score
2022 Cabana-Domínguez J, Torrico B, Reif A, Fernàndez-Castillo N, Cormand B. Comprehensive exploration of the genetic contribution of the dopaminergic and serotonergic pathways to psychiatric disorders. Translational Psychiatry. 12: 11. PMID 35013130 DOI: 10.1038/s41398-021-01771-3   
2022 Ng JW, Chong ETJ, Lee PC. An Updated Review on the Role of Single Nucleotide Polymorphisms in COVID-19 Disease Severity: A Global Aspect. Current Pharmaceutical Biotechnology. PMID 35034591 DOI: 10.2174/1389201023666220114162347   
2022 Sun Q, Crowley CA, Huang L, Wen J, Chen J, Bao EL, Auer PL, Lettre G, Reiner AP, Sankaran VG, Raffield LM, Li Y. From GWAS variant to function: A study of ∼148,000 variants for blood cell traits. Hgg Advances. 3: 100063. PMID 35047852 DOI: 10.1016/j.xhgg.2021.100063   
2022 Lin CX, Li HD, Deng C, Erhardt S, Wang J, Peng X, Wang J. AlzCode: a Platform for Multiview Analysis of Genes Related to Alzheimer's Disease. Bioinformatics (Oxford, England). PMID 35040932 DOI: 10.1093/bioinformatics/btac033   
2022 Liang J, Liu X, Yang P, Yao Z, Qu K, Wang H, Zhang Z, Liang H, Cheng B, Li Z, Ru B, Zhang J, Qi Z, Wang E, Lei C, et al. Copy number variation of gene is associated with growth traits of Chinese cattle. Animal Biotechnology. 1-7. PMID 35001788 DOI: 10.1080/10495398.2021.1996385   
2022 Downing J, D'Orsogna L. High-resolution human KIR genotyping. Immunogenetics. PMID 35050404 DOI: 10.1007/s00251-021-01247-0   
2022 Zhao Y, Pu Y, Liang B, Bai T, Liu Y, Jiang L, Ma Y. A study using single-locus and multi-locus genome-wide association study to identify genes associated with teat number in Hu sheep. Animal Genetics. PMID 35040155 DOI: 10.1111/age.13169   
2022 Chen R, Cheng RA, Wiedmann M, Orsi RH. Development of a Genomics-Based Approach To Identify Putative Hypervirulent Nontyphoidal Salmonella Isolates: Salmonella enterica Serovar Saintpaul as a Model. Msphere. e0073021. PMID 34986312 DOI: 10.1128/msphere.00730-21   
2022 T Suresh N, E R V, Krishnakumar U. Topology Driven Analysis of Protein - Protein Interactome for Prioritizing Key Comorbid Genes via Sub Graph based Average Path Length Centrality. Ieee/Acm Transactions On Computational Biology and Bioinformatics. PMID 34986099 DOI: 10.1109/TCBB.2022.3140388   
2022 Qi G, Dutta D, Leroux A, Ray D, Muschelli J, Crainiceanu C, Chatterjee N. Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Genetic Epidemiology. PMID 35043453 DOI: 10.1002/gepi.22441   
2022 Restuadi R, Steyn FJ, Kabashi E, Ngo ST, Cheng FF, Nabais MF, Thompson MJ, Qi T, Wu Y, Henders AK, Wallace L, Bye CR, Turner BJ, Ziser L, Mathers S, et al. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1. Genome Medicine. 14: 7. PMID 35042540 DOI: 10.1186/s13073-021-01006-6   
2022 Jeon S, Han J, Kim CW, Kim JG, Moon JH, Kim S. Identification of a candidate gene responsible for the G locus determining chartreuse bulb color in onion (Allium cepa L.) using bulked segregant RNA-Seq. Tag. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik. PMID 35034161 DOI: 10.1007/s00122-021-04016-5   
2022 Sahajpal NS, Jill Lai CY, Hastie A, Mondal AK, Dehkordi SR, van der Made CI, Fedrigo O, Al-Ajli F, Jalnapurkar S, Byrska-Bishop M, Kanagal-Shamanna R, Levy B, Schieck M, Illig T, Bacanu SA, ... , et al. Optical genome mapping identifies rare structural variations as predisposition factors associated with severe COVID-19. Iscience. 103760. PMID 35036860 DOI: 10.1016/j.isci.2022.103760   
2022 Wang Z, Zhou L, Lan Y, Li X, Wang J, Dong J, Guo W, Jing D, Liu Q, Zhang S, Liu Z, Shi W, Yang W, Yang T, Sun F, et al. An aspartic protease 47 causes quantitative recessive resistance to rice black-streaked dwarf virus disease and southern rice black-streaked dwarf virus disease. The New Phytologist. PMID 35015901 DOI: 10.1111/nph.17961   
2022 Zhang S, Cooper-Knock J, Weimer AK, Shi M, Moll T, Marshall JNG, Harvey C, Nezhad HG, Franklin J, Souza CDS, Ning K, Wang C, Li J, Dilliott AA, Farhan S, ... , et al. Genome-wide identification of the genetic basis of amyotrophic lateral sclerosis. Neuron. PMID 35045337 DOI: 10.1016/j.neuron.2021.12.019   
2022 Ware SM, Bhatnagar S, Dexheimer PJ, Wilkinson JD, Sridhar A, Fan X, Shen Y, Tariq M, Schubert JA, Colan SD, Shi L, Canter CE, Hsu DT, Bansal N, Webber SA, ... , et al. The genetic architecture of pediatric cardiomyopathy. American Journal of Human Genetics. PMID 35026164 DOI: 10.1016/j.ajhg.2021.12.006   
2022 Rochdi K, Cerino M, Da Silva N, Delague V, Bouzidi A, Nahili H, Zouiri G, Kriouile Y, Gorokhova S, Bartoli M, Saïle R, Barakat A, Krahn M. Identification of novel mutations by targeted NGS in Moroccan families clinically diagnosed with a neuromuscular disorder. Clinica Chimica Acta; International Journal of Clinical Chemistry. 524: 51-58. PMID 34852264 DOI: 10.1016/j.cca.2021.11.020   
2022 Annu, Rehman S, Nabi B, Sartaj A, Baboota S, Md S, Sahoo PK, Ali J. Nanoparticle mediated gene therapy: a trailblazer armament to fight CNS disorders. Current Medicinal Chemistry. PMID 34986767 DOI: 10.2174/0929867329666220105122318   
2022 Abdelrahman HA, Akawi N, Al-Shamsi AM, Ali A, Al-Jasmi F, John A, Hertecant J, Al-Gazali L, Ali BR. Bi-allelic null variant in matrix metalloproteinase-15, causes congenital cardiac defect, cholestasis jaundice, and failure to thrive. Clinical Genetics. PMID 34988996 DOI: 10.1111/cge.14107   
2022 Burton AR, Gravem SA, Barreto FS. Little evidence for genetic variation associated with susceptibility to sea star wasting syndrome in the keystone species Pisaster ochraceus. Molecular Ecology. 31: 197-205. PMID 34626020 DOI: 10.1111/mec.16212   
2022 Xia G, Li Y, Pan W, Qian C, Ma L, Zhou J, Xu H, Cheng C. SLAMF6 is associated with the susceptibility and severity of rheumatoid arthritis in the Chinese population. Journal of Orthopaedic Surgery and Research. 17: 13. PMID 35016729 DOI: 10.1186/s13018-021-02901-9   
2022 Liao Y, Liao Y, Wen F. Association of Human Hedgehog Interacting Protein Gene Polymorphisms with the Risk of Chronic Obstructive Pulmonary Disease: a Meta-Analysis. Expert Review of Respiratory Medicine. PMID 35037818 DOI: 10.1080/17476348.2022.2030226   
2022 Breeze CE, Haugen E, Reynolds A, Teschendorff A, van Dongen J, Lan Q, Rothman N, Bourque G, Dunham I, Beck S, Stamatoyannopoulos J, Franceschini N, Berndt SI. Integrative analysis of 3604 GWAS reveals multiple novel cell type-specific regulatory associations. Genome Biology. 23: 13. PMID 34996498 DOI: 10.1186/s13059-021-02560-3   
2022 Lopes KP, Snijders GJL, Humphrey J, Allan A, Sneeboer MAM, Navarro E, Schilder BM, Vialle RA, Parks M, Missall R, van Zuiden W, Gigase FAJ, Kübler R, van Berlekom AB, Hicks EM, et al. Genetic analysis of the human microglial transcriptome across brain regions, aging and disease pathologies. Nature Genetics. 54: 4-17. PMID 34992268 DOI: 10.1038/s41588-021-00976-y