Darwin Muir - Related publications

Affiliations: 
Queen's University, Kingston, ON, Canada 
Website:
http://psyc.queensu.ca/faculty/muir/muir.html
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 Mountjoy E, Schmidt EM, Carmona M, Schwartzentruber J, Peat G, Miranda A, Fumis L, Hayhurst J, Buniello A, Karim MA, Wright D, Hercules A, Papa E, Fauman EB, Barrett JC, et al. An open approach to systematically prioritize causal variants and genes at all published human GWAS trait-associated loci. Nature Genetics. 53: 1527-1533. PMID 34711957 DOI: 10.1038/s41588-021-00945-5   
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 Ma S, Dalgleish J, Lee J, Wang C, Liu L, Gill R, Buxbaum JD, Chung WK, Aschard H, Silverman EK, Cho MH, He Z, Ionita-Laza I. Powerful gene-based testing by integrating long-range chromatin interactions and knockoff genotypes. Proceedings of the National Academy of Sciences of the United States of America. 118. PMID 34799441 DOI: 10.1073/pnas.2105191118   
2021 Kim YC, Jeong MJ, Jeong BH. Regulatory Single Nucleotide Polymorphism of the Bovine Gene Induces Differential Transcriptional Capacities of Hanwoo and Holstein Cattle. Genes. 12. PMID 34828268 DOI: 10.3390/genes12111662   
2021 Zhang X, Zhu Y, Kremling KAG, Romay MC, Bukowski R, Sun Q, Gao S, Buckler ES, Lu F. Genome-wide analysis of deletions in maize population reveals abundant genetic diversity and functional impact. Tag. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik. PMID 34661697 DOI: 10.1007/s00122-021-03965-1   
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 Sinclair-Waters M, Piavchenko N, Ruokolainen A, Aykanat T, Erkinaro J, Primmer CR. Refining the genomic location of single nucleotide polymorphism variation affecting Atlantic salmon maturation timing at a key large-effect locus. Molecular Ecology. PMID 34716945 DOI: 10.1111/mec.16256   
2021 Ng B, Casazza W, Kim NH, Wang C, Farhadi F, Tasaki S, Bennett DA, De Jager PL, Gaiteri C, Mostafavi S. Cascading epigenomic analysis for identifying disease genes from the regulatory landscape of GWAS variants. Plos Genetics. 17: e1009918. PMID 34807913 DOI: 10.1371/journal.pgen.1009918   
2021 Li H, Hua L, Rouse MN, Li T, Pang S, Bai S, Shen T, Luo J, Li H, Zhang W, Wang X, Dubcovsky J, Chen S. Mapping and Characterization of a Wheat Stem Rust Resistance Gene in Durum Wheat "Kronos". Frontiers in Plant Science. 12: 751398. PMID 34721479 DOI: 10.3389/fpls.2021.751398   
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 Li YK, Zhang XX, Yang Y, Gao J, Shi Q, Liu SD, Fu WP, Sun C. Convergent Evidence Supports TH2LCRR as a Novel Asthma Susceptibility Gene. American Journal of Respiratory Cell and Molecular Biology. PMID 34851809 DOI: 10.1165/rcmb.2020-0481OC   
2021 Qi X, Wang XQ, Jin L, Gao LX, Guo HF. Uncovering potential single nucleotide polymorphisms, copy number variations and related signaling pathways in primary Sjogren's syndrome. Bioengineered. PMID 34723755 DOI: 10.1080/21655979.2021.2000245   
2021 Chen DP, Chang SW, Jaing TH, Wang WT, Hsu FP, Tseng CP. Single nucleotide polymorphisms within HLA region are associated with the outcomes of unrelated cord blood transplantation. Scientific Reports. 11: 21925. PMID 34753965 DOI: 10.1038/s41598-021-01155-z   
2021 Jin J, Wang Y. T2-DAG: a powerful test for differentially expressed gene pathways via graph-informed structural equation modeling. Bioinformatics (Oxford, England). PMID 34755844 DOI: 10.1093/bioinformatics/btab770   
2021 Reza MN, Ferdous N, Emon MTH, Islam MS, Mohiuddin AKM, Hossain MU. Pathogenic genetic variants from highly connected cancer susceptibility genes confer the loss of structural stability. Scientific Reports. 11: 19264. PMID 34584144 DOI: 10.1038/s41598-021-98547-y   
2021 He Y, Huang L, Tang Y, Yang Z, Han Z. Genome-wide Identification and Analysis of Splicing QTLs in Multiple Sclerosis by RNA-Seq Data. Frontiers in Genetics. 12: 769804. PMID 34868258 DOI: 10.3389/fgene.2021.769804   
2021 Wu L, Chang Y, Wang L, Wang S, Wu J. The aquaporin gene PvXIP1;2 conferring drought resistance identified by GWAS at seedling stage in common bean. Tag. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik. PMID 34698878 DOI: 10.1007/s00122-021-03978-w   
2021 Arthur VL, Li Z, Cao R, Oetting WS, Israni AK, Jacobson PA, Ritchie MD, Guan W, Chen J. A Multi-Marker Test for Analyzing Paired Genetic Data in Transplantation. Frontiers in Genetics. 12: 745773. PMID 34721531 DOI: 10.3389/fgene.2021.745773   
2021 Curtis D. Analysis of 200,000 Exome-Sequenced UK Biobank Subjects Implicates Genes Involved in Increased and Decreased Risk of Hypertension. Pulse (Basel, Switzerland). 9: 17-29. PMID 34722352 DOI: 10.1159/000517419   
2021 Teng MS, Wu S, Hsu LA, Chou HH, Ko YL. Pleiotropic Effects of Functional Variants on Cardiometabolic, Renal, and Hematological Traits in the Taiwanese Population. International Journal of Molecular Sciences. 22. PMID 34638981 DOI: 10.3390/ijms221910641   
2021 Tian Y, Soupir A, Liu Q, Wu L, Huang CC, Park JY, Wang L. Novel role of prostate cancer risk variant rs7247241 on PPP1R14A isoform transition through allelic TF binding and CpG methylation. Human Molecular Genetics. PMID 34849858 DOI: 10.1093/hmg/ddab347   
2021 Mostafa T, Abdel-Hamid I, Taymour M, Ali O. Genetic variants in varicocele-related male infertility: a systematic review and future directions. Human Fertility (Cambridge, England). 1-17. PMID 34587863 DOI: 10.1080/14647273.2021.1983214   
2021 He Z, Le Guen Y, Liu L, Lee J, Ma S, Yang AC, Liu X, Rutledge J, Losada PM, Song B, Belloy ME, Butler RR, Longo FM, Tang H, Mormino EC, et al. Genome-wide analysis of common and rare variants via multiple knockoffs at biobank scale, with an application to Alzheimer disease genetics. American Journal of Human Genetics. 108: 2336-2353. PMID 34767756 DOI: 10.1016/j.ajhg.2021.10.009   
2021 Casares-Marfil D, Kerick M, Andrés-León E, Bosch-Nicolau P, Molina I, , Martin J, Acosta-Herrera M. GWAS loci associated with Chagas cardiomyopathy influences DNA methylation levels. Plos Neglected Tropical Diseases. 15: e0009874. PMID 34714828 DOI: 10.1371/journal.pntd.0009874   
2021 Schneider N, Sundaresan Y, Gopalakrishnan P, Beryozkin A, Hanany M, Levanon EY, Banin E, Ben-Aroya S, Sharon D. Inherited retinal diseases: Linking genes, disease-causing variants, and relevant therapeutic modalities. Progress in Retinal and Eye Research. 101029. PMID 34839010 DOI: 10.1016/j.preteyeres.2021.101029   
2021 Cao G, Xuan X, Zhang R, Hu J, Dong H. Gene Therapy for Cardiovascular Disease: Basic Research and Clinical Prospects. Frontiers in Cardiovascular Medicine. 8: 760140. PMID 34805315 DOI: 10.3389/fcvm.2021.760140   
2021 Hu Z, Shi X, Chen X, Zheng J, Zhang A, Wang H, Fu Q. Fine-mapping and identification of a candidate gene controlling seed coat color in melon (Cucumis melo L. var. chinensis Pangalo). Tag. Theoretical and Applied Genetics. Theoretische Und Angewandte Genetik. PMID 34825925 DOI: 10.1007/s00122-021-03999-5   
2021 Han YL, Sun ZH, Chang S, Wen B, Song J, Zuo RT, Chang YQ. Application of SNP in Genetic Sex Identification and Effect of Estradiol on Gene Expression of Sex-Related Genes in . Frontiers in Endocrinology. 12: 756530. PMID 34858332 DOI: 10.3389/fendo.2021.756530   
2021 Wang CM, Jan Wu YJ, Lin JC, Huang LY, Wu J, Chen JY. Genetic effects of B3GNT2 on ankylosing spondylitis susceptibility and clinical manifestations in Taiwanese. Journal of the Formosan Medical Association = Taiwan Yi Zhi. PMID 34645591 DOI: 10.1016/j.jfma.2021.09.010   
2021 Zhang T, Liu M, Yang Y, Wang K, Zhao H, Pan C. An upstream deletion polymorphism within the goat () gene was associated with growth traits. Animal Biotechnology. 1-6. PMID 34812688 DOI: 10.1080/10495398.2021.1998091   
2021 He P, Wei P, Ma Y, Hu S, Yao J, Jiang X, Xu Y, Zhu P, Wei M, Jiang W, Peng J. Candidate sex-associated gene identification in Trachinotus ovatus (Carangidae) using an integrated SLAF-seq and bulked segregant analysis approach. Gene. 146026. PMID 34687789 DOI: 10.1016/j.gene.2021.146026   
2021 Willsey HR, Guille M, Grainger RM. Modeling Human Genetic Disorders with CRISPR Technologies in . Cold Spring Harbor Protocols. PMID 34531330 DOI: 10.1101/pdb.prot106997   
2021 Kelchtermans J, Chang X, March ME, Mentch F, Sleiman PMA, Hakonarson H. HIF-1α Pulmonary Phenotype Wide Association Study Unveils a Link to Inflammatory Airway Conditions. Frontiers in Genetics. 12: 756645. PMID 34621299 DOI: 10.3389/fgene.2021.756645   
2021 Koko M, Krause R, Sander T, Bobbili DR, Nothnagel M, May P, Lerche H, . Distinct gene-set burden patterns underlie common generalized and focal epilepsies. Ebiomedicine. 72: 103588. PMID 34571366 DOI: 10.1016/j.ebiom.2021.103588   
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 Ni G, Tan J, Wang M, Ping N, Liu M, He Y. Polymorphisms of the AS3MT gene are associated with arsenic methylation capacity and damage to the P21 gene in arsenic trioxide plant workers. Toxicology and Industrial Health. 7482337211013321. PMID 34730462 DOI: 10.1177/07482337211013321   
2021 Baba SM, Pandith AA, Shah ZA, Geelani SA, Bhat JR, Gul A, Guru SA, El-Serehy HA, Koul AM, Mansoor S. and rs156697 Polymorphism in Influence the Risk and Therapeutic Outcome of B-Acute Lymphoblastic Leukemia Patients. Frontiers in Oncology. 11: 714421. PMID 34722260 DOI: 10.3389/fonc.2021.714421   
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 Zimoń M, Huang Y, Trasta A, Halavatyi A, Liu JZ, Chen CY, Blattmann P, Klaus B, Whelan CD, Sexton D, John S, Huber W, Tsai EA, Pepperkok R, Runz H. Pairwise effects between lipid GWAS genes modulate lipid plasma levels and cellular uptake. Nature Communications. 12: 6411. PMID 34741066 DOI: 10.1038/s41467-021-26761-3   
2021 Umair M, Ahmad F, Ahmad S, Alam Q, Rehan M, Alqosaibi AI, Alnamshan MM, Rafeeq MM, Haque S, Sain ZM, Ismail M, Alfadhel M. A Novel Homozygous Missense Mutation in the Zinc Finger DNA Binding Domain of GLI1 Causes Recessive Post-Axial Polydactyly. Frontiers in Genetics. 12: 746949. PMID 34721536 DOI: 10.3389/fgene.2021.746949   
2021 Dhar S, Mridha S, Bhattacharjee P. Mutational Landscape Screening Through Comprehensive In Silico Analysis for Polycystic Ovarian Syndrome-Related Genes. Reproductive Sciences (Thousand Oaks, Calif.). PMID 34697776 DOI: 10.1007/s43032-021-00752-7   
2021 Perrot N, Pelletier W, Bourgault J, Couture C, Li Z, Mitchell PL, Ghodsian N, Bossé Y, Thériault S, Mathieu P, Arsenault BJ. A trans-omic Mendelian randomization study of parental lifespan uncovers novel aging biology and therapeutic candidates for chronic diseases. Aging Cell. e13497. PMID 34704651 DOI: 10.1111/acel.13497   
2021 Perrin HJ, Currin KW, Vadlamudi S, Pandey GK, Ng KK, Wabitsch M, Laakso M, Love MI, Mohlke KL. Chromatin accessibility and gene expression during adipocyte differentiation identify context-dependent effects at cardiometabolic GWAS loci. Plos Genetics. 17: e1009865. PMID 34699533 DOI: 10.1371/journal.pgen.1009865   
2021 Huang S, Zhao G, Wu J, Li K, Wang Q, Fu Y, Zhang H, Bi Q, Li X, Wang W, Guo C, Zhang D, Wu L, Li X, Xu H, et al. Gene4HL: An Integrated Genetic Database for Hearing Loss. Frontiers in Genetics. 12: 773009. PMID 34733322 DOI: 10.3389/fgene.2021.773009   
2021 Herman I, Jolly A, Du H, Dawood M, Abdel-Salam GMH, Marafi D, Mitani T, Calame DG, Coban-Akdemir Z, Fatih JM, Hegazy I, Jhangiani SN, Gibbs RA, Pehlivan D, Posey JE, et al. Quantitative dissection of multilocus pathogenic variation in an Egyptian infant with severe neurodevelopmental disorder resulting from multiple molecular diagnoses. American Journal of Medical Genetics. Part A. PMID 34816580 DOI: 10.1002/ajmg.a.62565   
2021 Mendoza-Fandiño G, Lyra PCM, Nepomuceno TC, Harro CM, Woods NT, Li X, Rangel LB, Carvalho MA, Couch FJ, Monteiro ANA. Two distinct mechanisms underlie estrogen-receptor-negative breast cancer susceptibility at the 2p23.2 locus. European Journal of Human Genetics : Ejhg. PMID 34803163 DOI: 10.1038/s41431-021-01005-6   
2021 Mahadevan J, Pathak AK, Vemula A, Nadella RK, Viswanath B, Jain S, , Purushottam M, Mondal M. Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genes. Scientific Reports. 11: 21088. PMID 34702870 DOI: 10.1038/s41598-021-00123-x   
2021 Mahadevan J, Pathak AK, Vemula A, Nadella RK, Viswanath B, Jain S, , Purushottam M, Mondal M. Analysis of whole exome sequencing in severe mental illness hints at selection of brain development and immune related genes. Scientific Reports. 11: 21088. PMID 34702870 DOI: 10.1038/s41598-021-00123-x   
2021 Giambartolomei C, Seo JH, Schwarz T, Freund MK, Johnson RD, Spisak S, Baca SC, Gusev A, Mancuso N, Pasaniuc B, Freedman ML. H3K27ac HiChIP in prostate cell lines identifies risk genes for prostate cancer susceptibility. American Journal of Human Genetics. PMID 34822763 DOI: 10.1016/j.ajhg.2021.11.007   
2021 Wei BL, Yin RX, Liu CX, Deng GX, Guan YZ, Zheng PF. SNPs and Gene-Gene and Gene-Environment Interactions on Essential Hypertension. Frontiers in Cardiovascular Medicine. 8: 720884. PMID 34722659 DOI: 10.3389/fcvm.2021.720884