Julia Pinsonneault - Related publications

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50 most relevant papers in past 60 days:
Year Citation  Score
2021 Mulvey B, Dougherty JD. Transcriptional-regulatory convergence across functional MDD risk variants identified by massively parallel reporter assays. Translational Psychiatry. 11: 403. PMID 34294677 DOI: 10.1038/s41398-021-01493-6   
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 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 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 Li X, Pan X, Zhou H, Wang P, Gao Y, Shang S, Guo S, Sun J, Xiong Z, Ning S, Zhi H, Li X. Comprehensive characterization genetic regulation and chromatin landscape of enhancer-associated long non-coding RNAs and their implication in human cancer. Briefings in Bioinformatics. PMID 34581409 DOI: 10.1093/bib/bbab401   
2021 Pineda-Cirera L, Cabana-Domínguez J, Lee PH, Fernàndez-Castillo N, Cormand B. Identification of genetic variants influencing methylation in brain with pleiotropic effects on psychiatric disorders. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 110454. PMID 34637873 DOI: 10.1016/j.pnpbp.2021.110454   
2021 Cui Y, Peng F, Wang D, Li Y, Li JS, Li L, Li W. 3'aQTL-atlas: an atlas of 3'UTR alternative polyadenylation quantitative trait loci across human normal tissues. Nucleic Acids Research. PMID 34432052 DOI: 10.1093/nar/gkab740   
2021 Gürsoy G, Lu N, Wagner S, Gerstein M. Recovering genotypes and phenotypes using allele-specific genes. Genome Biology. 22: 263. PMID 34493313 DOI: 10.1186/s13059-021-02477-x   
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 Mei L, Gao Y, Chen M, Zhang X, Yue W, Zhang D, Yu H. Overlapping common genetic architecture between major depressive disorders and anxiety and stress-related disorders. Progress in Neuro-Psychopharmacology & Biological Psychiatry. 110450. PMID 34634379 DOI: 10.1016/j.pnpbp.2021.110450   
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 Wang S, Said MA, Groot HE, van der Most PJ, Thio CHL, van de Vegte YJ, Verweij N, Snieder H, van der Harst P. Search for a Functional Genetic Variant Mimicking the Effect of SGLT2 Inhibitor Treatment. Genes. 12. PMID 34440348 DOI: 10.3390/genes12081174   
2021 Tian P, Zhong M, Wei GH. Mechanistic insights into genetic susceptibility to prostate cancer. Cancer Letters. 522: 155-163. PMID 34560228 DOI: 10.1016/j.canlet.2021.09.025   
2021 Yang C, Li S, Ma Y, Chen B, Li M, Bosker FJ, Li J, Nolte IM. Lack of association of FKBP5 SNPs and haplotypes with susceptibility and treatment response phenotypes in Han Chinese with major depressive disorder: A pilot case-control study (STROBE). Medicine. 100: e26983. PMID 34516490 DOI: 10.1097/MD.0000000000026983   
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 Yurko R, Roeder K, Devlin B, G'Sell M. An approach to gene-based testing accounting for dependence of tests among nearby genes. Briefings in Bioinformatics. PMID 34459489 DOI: 10.1093/bib/bbab329   
2021 Gamache I, Legault MA, Grenier JC, Sanchez R, Rhéaume E, Asgari S, Barhdadi A, Zada YF, Trochet H, Luo Y, Lecca L, Murray M, Raychaudhuri S, Tardif JC, Dubé MP, et al. A sex-specific evolutionary interaction between and . Elife. 10. PMID 34609279 DOI: 10.7554/eLife.69198   
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 Zhang Q, He Y, Xu H, Li L, Guo Y, Zhang J, Cheng L, Yu H, Dai Y, Yang Q, Yang Z, Li C, Zhang S, Zhu S, Luo B, et al. Modulation of STIM1 by a risk insertion/deletion polymorphism underlying genetics susceptibility to sudden cardiac death originated from coronary artery disease. Forensic Science International. 328: 111010. PMID 34592581 DOI: 10.1016/j.forsciint.2021.111010   
2021 Perez Garrido N, Pujana M, Berger M, Ramírez P, Guercio G, Belgorosky A, Marino R. Growth hormone receptor gene polymorphism. Spontaneous catch up growth in small for gestational age patients. Medicina. 81: 574-580. PMID 34453799   
2021 Sun H, Lan X, Ma L, Zhou J. Revealing modifier variations characterizations for elucidating the genetic basis of human phenotypic variations. Human Genetics. PMID 34498116 DOI: 10.1007/s00439-021-02362-4   
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 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 Melak S, Wang Q, Tian Y, Wei W, Zhang L, Elbeltagy A, Chen J. Identification and Validation of Marketing Weight-Related SNP Markers Using SLAF Sequencing in Male Yangzhou Geese. Genes. 12. PMID 34440377 DOI: 10.3390/genes12081203   
2021 Porcu E, Sadler MC, Lepik K, Auwerx C, Wood AR, Weihs A, Sleiman MSB, Ribeiro DM, Bandinelli S, Tanaka T, Nauck M, Völker U, Delaneau O, Metspalu A, Teumer A, et al. Differentially expressed genes reflect disease-induced rather than disease-causing changes in the transcriptome. Nature Communications. 12: 5647. PMID 34561431 DOI: 10.1038/s41467-021-25805-y   
2021 Dingemans AJM, Truijen KMG, Kim JH, Alaçam Z, Faivre L, Collins KM, Gerkes EH, van Haelst M, van de Laar IMBH, Lindstrom K, Nizon M, Pauling J, Heropolitańska-Pliszka E, Plomp AS, Racine C, et al. Establishing the phenotypic spectrum of ZTTK syndrome by analysis of 52 individuals with variants in SON. European Journal of Human Genetics : Ejhg. PMID 34521999 DOI: 10.1038/s41431-021-00960-4   
2021 Findley AS, Zhang X, Boye C, Lin YL, Kalita CA, Barreiro L, Lohmueller KE, Pique-Regi R, Luca F. A signature of Neanderthal introgression on molecular mechanisms of environmental responses. Plos Genetics. 17: e1009493. PMID 34570765 DOI: 10.1371/journal.pgen.1009493   
2021 Aygün N, Elwell AL, Liang D, Lafferty MJ, Cheek KE, Courtney KP, Mory J, Hadden-Ford E, Krupa O, de la Torre-Ubieta L, Geschwind DH, Love MI, Stein JL. Brain-trait-associated variants impact cell-type-specific gene regulation during neurogenesis. American Journal of Human Genetics. PMID 34416157 DOI: 10.1016/j.ajhg.2021.07.011   
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 Dlamini SN, Choudhury A, Ramsay M, Micklesfield LK, Norris SA, Crowther NJ, Crawford AA, Walker BR, Lombard Z, Goedecke JH. Associations Between and Polymorphisms, and Cardiometabolic Risk Factors in Black South Africans. Frontiers in Genetics. 12: 687335. PMID 34484290 DOI: 10.3389/fgene.2021.687335   
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 Graça R, Fernandes R, Alves AC, Menezes J, Romão L, Bourbon M. Characterization of Two Variants at Met 1 of the Human Gene Encoding the Same Amino Acid but Causing Different Functional Phenotypes. Biomedicines. 9. PMID 34572405 DOI: 10.3390/biomedicines9091219   
2021 Xue Y, Wang J, Mao X, Li C, Li L, Yang X, Hao C, Chang X, Li R, Jing R. Association Analysis Revealed That Genes Are Linked to Plant Growth Related Traits in Multiple Environment. Frontiers in Plant Science. 12: 641087. PMID 34456932 DOI: 10.3389/fpls.2021.641087   
2021 Hu Y, Qiu S, Cheng L. Integration of Multiple-Omics Data to Analyze the Population-Specific Differences for Coronary Artery Disease. Computational and Mathematical Methods in Medicine. 2021: 7036592. PMID 34447459 DOI: 10.1155/2021/7036592   
2021 Võsa U, Claringbould A, Westra HJ, Bonder MJ, Deelen P, Zeng B, Kirsten H, Saha A, Kreuzhuber R, Yazar S, Brugge H, Oelen R, de Vries DH, van der Wijst MGP, Kasela S, ... , ... , et al. Large-scale cis- and trans-eQTL analyses identify thousands of genetic loci and polygenic scores that regulate blood gene expression. Nature Genetics. PMID 34475573 DOI: 10.1038/s41588-021-00913-z   
2021 Griesemer D, Xue JR, Reilly SK, Ulirsch JC, Kukreja K, Davis JR, Kanai M, Yang DK, Butts JC, Guney MH, Luban J, Montgomery SB, Finucane HK, Novina CD, Tewhey R, et al. Genome-wide functional screen of 3'UTR variants uncovers causal variants for human disease and evolution. Cell. PMID 34534445 DOI: 10.1016/j.cell.2021.08.025   
2021 Zhang Z, Huang Y, Chen H, Wu P, Deng Z, Deng G, Zheng Y, Li G, Yuan L, Xu Y. The correlation between polymorphisms in the gene and glioma susceptibility in a Chinese pediatric population. Translational Pediatrics. 10: 1896-1904. PMID 34430438 DOI: 10.21037/tp-21-301   
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 Mandozai A, Moussa AA, Zhang Q, Qu J, Du Y, Anwari G, Al Amin N, Wang P. Genome-Wide Association Study of Root and Shoot Related Traits in Spring Soybean ( L.) at Seedling Stages Using SLAF-Seq. Frontiers in Plant Science. 12: 568995. PMID 34394134 DOI: 10.3389/fpls.2021.568995   
2021 Wang YJ, Mugiyanto E, Peng YT, Huang WC, Chou WH, Lee CC, Wang YS, Irham LM, Perwitasari DA, Hsu MI, Chang WC. Genetic Association of the Functional Gene in Male Fertility. Journal of Personalized Medicine. 11. PMID 34442404 DOI: 10.3390/jpm11080760   
2021 Barowsky S, Jung JY, Nesbit N, Silberstein M, Fava M, Loggia ML, Smoller JW, Lee PH. Cross-Disorder Genomics Data Analysis Elucidates a Shared Genetic Basis Between Major Depression and Osteoarthritis Pain. Frontiers in Genetics. 12: 687687. PMID 34603368 DOI: 10.3389/fgene.2021.687687   
2021 Højland AT, Tavernier LJM, Schrauwen I, Sommen M, Topsakal V, Schatteman I, Dhooge I, Huber A, Zanetti D, Kunst HPM, Hoischen A, Petersen MB, Van Camp G, Fransen E. A wide range of protective and predisposing variants in aggrecan influence the susceptibility for otosclerosis. Human Genetics. PMID 34410490 DOI: 10.1007/s00439-021-02334-8   
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 Al-Khuzaei S, Broadgate S, Foster CR, Shah M, Yu J, Downes SM, Halford S. An Overview of the Genetics of Retinopathies, an Evolving Story. Genes. 12. PMID 34440414 DOI: 10.3390/genes12081241   
2021 Peng Y, Yang S, Huang X, Pang J, Liu J, Hu J, Shen X, Tang C, Wang H. Whole Exome Sequencing Analysis in Fetal Skeletal Dysplasia Detected by Ultrasonography: An Analysis of 38 Cases. Frontiers in Genetics. 12: 728544. PMID 34567078 DOI: 10.3389/fgene.2021.728544   
2021 Hasan MA, Hakim FT, Islam Shovon MT, Islam MM, Islam MS, Islam MA. The investigation of nonsynonymous SNPs of human gene associated with depression: An approach. Heliyon. 7: e07815. PMID 34466701 DOI: 10.1016/j.heliyon.2021.e07815   
2021 Zhang X, Yuan R, Bai Y, Yang Y, Song X, Lan X, Pan C. A deletion mutation within the goat gene is significantly associated with litter size. Animal Biotechnology. 1-7. PMID 34431749 DOI: 10.1080/10495398.2021.1968418   
2021 Mohamed SH, Hassaan MMM, Ibrahim BA, Sabbah NA. E670G (rs505151) Variant and Coronary Artery Disease Risk Among Diabetics. Genetic Testing and Molecular Biomarkers. 25: 615-623. PMID 34550777 DOI: 10.1089/gtmb.2021.0010   
2021 Kapoor M, Chao MJ, Johnson EC, Novikova G, Lai D, Meyers JL, Schulman J, Nurnberger JI, Porjesz B, Liu Y, , Foroud T, Edenberg HJ, Marcora E, Agrawal A, et al. Multi-omics integration analysis identifies novel genes for alcoholism with potential overlap with neurodegenerative diseases. Nature Communications. 12: 5071. PMID 34417470 DOI: 10.1038/s41467-021-25392-y   
2021 Akhatayeva Z, Bi Y, He Y, Khan R, Li J, Li H, Pan C, Lan X. Survey of the relationship between polymorphisms within the gene and sheep reproductive traits. Animal Biotechnology. 1-10. PMID 34586970 DOI: 10.1080/10495398.2021.1979023