Anna Di Rienzo, PhD - Related publications

Affiliations: 
Human Genetics University of Chicago, Chicago, IL 
Area:
Genetics, Evolution, Developmental Biology
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50 most relevant papers in past 60 days:
Year Citation  Score
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 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 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 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 Garcia JA, Lohmueller KE. Negative linkage disequilibrium between amino acid changing variants reveals interference among deleterious mutations in the human genome. Plos Genetics. 17: e1009676. PMID 34319975 DOI: 10.1371/journal.pgen.1009676   
2021 Wang Y. Association of pigmentation related-genes polymorphisms and geographic environmental variables in the Chinese population. Hereditas. 158: 24. PMID 34238381 DOI: 10.1186/s41065-021-00189-7   
2021 Wang Y. Association of pigmentation related-genes polymorphisms and geographic environmental variables in the Chinese population. Hereditas. 158: 24. PMID 34238381 DOI: 10.1186/s41065-021-00189-7   
2021 Yan Q, Forno E, Celedón JC, Chen W, Weeks DE. CHIT: an allele-specific method for testing the association between molecular quantitative traits and phenotype-genotype interaction. Bioinformatics (Oxford, England). PMID 34323937 DOI: 10.1093/bioinformatics/btab554   
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 Nabi RBS, Cho KS, Tayade R, Oh KW, Lee MH, Kim JI, Kim S, Pae SB, Oh E. Genetic diversity analysis of Korean peanut germplasm using 48 K SNPs 'Axiom_Arachis' Array and its application for cultivar differentiation. Scientific Reports. 11: 16630. PMID 34404839 DOI: 10.1038/s41598-021-96074-4   
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 Li P, Zhou J, Wang D, Li L, Xiao L, Quan M, Lu W, Yao L, Fang Y, Lv C, Song F, Du Q, Zhang D. Genetic Architecture and Genome-Wide Adaptive Signatures Underlying Stem Lenticel Traits in . International Journal of Molecular Sciences. 22. PMID 34502156 DOI: 10.3390/ijms22179249   
2021 Sofer T, Lee J, Kurniansyah N, Jain D, Laurie CA, Gogarten SM, Conomos MP, Heavner B, Hu Y, Kooperberg C, Haessler J, Vasan RS, Cupples LA, Coombes BJ, Seyerle A, ... , et al. BinomiRare: A robust test for association of a rare genetic variant with a binary outcome for mixed models and any case-control proportion. Hgg Advances. 2. PMID 34337551 DOI: 10.1016/j.xhgg.2021.100040   
2021 Ahmed S, Gul S, Akhlaq M, Hussain A, Tariq Khan S, Rehman H, Hanif Bangash M, Al Mughairbi F, Hamid Hamdard M. Estimation of polymorphisms in the drug-metabolizing enzyme, cytochrome gene in six major ethnicities of Pakistan. Bioengineered. 12: 4442-4451. PMID 34308762 DOI: 10.1080/21655979.2021.1955809   
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 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 Al Alawi I, Al Riyami M, Barroso-Gil M, Powell L, Olinger E, Al Salmi I, Sayer JA. The diagnostic yield of whole exome sequencing as a first approach in consanguineous Omani renal ciliopathy syndrome patients. F1000research. 10: 207. PMID 34354814 DOI: 10.12688/f1000research.40338.2   
2021 Kehdy FSG, Pita-Oliveira M, Scudeler MM, Torres-Loureiro S, Zolini C, Moreira R, Michelin LA, Alvim I, Silva-Carvalho C, Furlan VC, Aquino MM, Santolalla ML, Borda V, Soares-Souza GB, Jaramillo-Valverde L, et al. Human-SARS-CoV-2 interactome and human genetic diversity: TMPRSS2-rs2070788, associated with severe influenza, and its population genetics caveats in Native Americans. Genetics and Molecular Biology. 44: e20200484. PMID 34436507 DOI: 10.1590/1678-4685-GMB-2020-0484   
2021 Chen YP, Yu SH, Wei QQ, Cao B, Gu XJ, Chen XP, Song W, Zhao B, Wu Y, Sun MM, Liu FF, Hou YB, Ou RW, Zhang LY, Liu KC, et al. Role of genetics in amyotrophic lateral sclerosis: a large cohort study in Chinese mainland population. Journal of Medical Genetics. PMID 34544842 DOI: 10.1136/jmedgenet-2021-107965   
2021 Majeed MM, Ahmed I, Roome T, Fatima T, Amin R. Association between Interleukin-1β Gene Polymorphism and Chronic Periodontitis. European Journal of Dentistry. PMID 34303316 DOI: 10.1055/s-0041-1730041   
2021 Weisschuh N, Schimpf-Linzenbold S, Mazzola P, Kieninger S, Xiao T, Kellner U, Neuhann T, Kelbsch C, Tonagel F, Wilhelm H, Kohl S, Wissinger B. Mutation spectrum of the OPA1 gene in a large cohort of patients with suspected dominant optic atrophy: Identification and classification of 48 novel variants. Plos One. 16: e0253987. PMID 34242285 DOI: 10.1371/journal.pone.0253987   
2021 Ziadi W, Boussetta S, Elkamel S, Pakstis AJ, Kidd KK, Medimegh I, Ben Ammar Elgaaied A, Cherni L. STAT3 polymorphisms in North Africa and its implication in breast cancer. Molecular Genetics & Genomic Medicine. e1744. PMID 34251094 DOI: 10.1002/mgg3.1744   
2021 Yuan Y, Zhang H, Yi G, You Z, Zhao C, Yuan H, Wang K, Li J, Yang N, Lian L. Genetic Diversity of MHC B-F/B-L Region in 21 Chicken Populations. Frontiers in Genetics. 12: 710770. PMID 34484301 DOI: 10.3389/fgene.2021.710770   
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 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 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 Abrahams-October Z, Xhakaza L, Pearce B, Mandisa Masilela C, Benjeddou M, Vincent Adeniyi O, Johnson R, Jebio Ongole J. Genetic Association of Solute Carrier Transporter Gene Variants with Metformin Response. Balkan Journal of Medical Genetics : Bjmg. 24: 47-56. PMID 34447659 DOI: 10.2478/bjmg-2021-0004   
2021 Westerman KE, Lin J, Sevilla-Gonzalez M, Tadess B, Marchek C, Manning AK. Gene-environment interaction analysis incorporating sex, cardiometabolic diseases, and multiple deprivation index reveals novel genetic associations with COVID-19 severity. Medrxiv : the Preprint Server For Health Sciences. PMID 34462758 DOI: 10.1101/2021.08.13.21261910   
2021 Inoue Y, Hasebe Y, Igarashi T, Kawagishi-Hotta M, Okuno R, Yamada T, Hasegawa S. Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Experimental Dermatology. PMID 34265127 DOI: 10.1111/exd.14430   
2021 Inoue Y, Hasebe Y, Igarashi T, Kawagishi-Hotta M, Okuno R, Yamada T, Hasegawa S. Search for genetic loci involved in the constitution and skin type of a Japanese women using a genome-wide association study. Experimental Dermatology. PMID 34265127 DOI: 10.1111/exd.14430   
2021 Alharazy S, Naseer MI, Alissa E, Robertson MD, Lanham-New S, Alqahtani MH, Chaudhary AG. Association of SNPs in GC and CYP2R1 with total and directly measured free 25-hydroxyvitamin D in multi-ethnic postmenopausal women in Saudi Arabia. Saudi Journal of Biological Sciences. 28: 4626-4632. PMID 34354449 DOI: 10.1016/j.sjbs.2021.04.071   
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 Zhang Y, Lu Q, Ye Y, Huang K, Liu W, Wu Y, Zhong X, Li B, Yu Z, Travers BG, Werling DM, Li JJ, Zhao H. SUPERGNOVA: local genetic correlation analysis reveals heterogeneous etiologic sharing of complex traits. Genome Biology. 22: 262. PMID 34493297 DOI: 10.1186/s13059-021-02478-w   
2021 Fisher V, Sebastiani P, Cupples LA, Liu CT. ANNORE: Genetic fine mapping with functional annotation. Human Molecular Genetics. PMID 34302344 DOI: 10.1093/hmg/ddab210   
2021 Fisher V, Sebastiani P, Cupples LA, Liu CT. ANNORE: Genetic fine mapping with functional annotation. Human Molecular Genetics. PMID 34302344 DOI: 10.1093/hmg/ddab210   
2021 Othman H, da Rocha JEB, Hazelhurst S. Single Nucleotide Polymorphism Induces Divergent Dynamic Patterns in CYP3A5: A Microsecond Scale Biomolecular Simulation of Variants Identified in Sub-Saharan African Populations. International Journal of Molecular Sciences. 22. PMID 34360551 DOI: 10.3390/ijms22157786   
2021 Ferese R, Campopiano R, Scala S, D'Alessio C, Storto M, Buttari F, Centonze D, Logroscino G, Zecca C, Zampatti S, Fornai F, Cianci V, Manfroi E, Giardina E, Magnani M, et al. Cohort Analysis of 67 Charcot-Marie-Tooth Italian Patients: Identification of New Mutations and Broadening of Phenotype Expression Produced by Rare Variants. Frontiers in Genetics. 12: 682050. PMID 34354735 DOI: 10.3389/fgene.2021.682050   
2021 Hong Y, Ye J, Dong L, Li Y, Yan L, Cai G, Liu D, Tan C, Wu Z. Genome-Wide Association Study for Body Length, Body Height, and Total Teat Number in Large White Pigs. Frontiers in Genetics. 12: 650370. PMID 34408768 DOI: 10.3389/fgene.2021.650370   
2021 Combrink HM, Oosthuizen J, Visser B, Chabilal N, Buccimazza I, Foulkes WD, van der Merwe NC. Mutations in BRCA-related breast and ovarian cancer in the South African Indian population: A descriptive study. Cancer Genetics. 258: 1-6. PMID 34218100 DOI: 10.1016/j.cancergen.2021.06.002   
2021 Yang D, Jin Y, He X, Dong A, Wang J, Wu R. Inferring multilayer interactome networks shaping phenotypic plasticity and evolution. Nature Communications. 12: 5304. PMID 34489412 DOI: 10.1038/s41467-021-25086-5   
2021 Rivas L, Paine S, Dupont PY, Tiong A, Horn B, Moura A, Gilpin BJ. Genome typing and epidemiology of human listeriosis in New Zealand 1999-2018. Journal of Clinical Microbiology. JCM0084921. PMID 34406797 DOI: 10.1128/JCM.00849-21   
2021 Chamarthi SK, Kaler AS, Abdel-Haleem H, Fritschi FB, Gillman JD, Ray JD, Smith JR, Dhanapal AP, King CA, Purcell LC. Identification and Confirmation of Loci Associated With Canopy Wilting in Soybean Using Genome-Wide Association Mapping. Frontiers in Plant Science. 12: 698116. PMID 34335664 DOI: 10.3389/fpls.2021.698116   
2021 Yang C, Yan J, Jiang S, Li X, Min H, Wang X, Hao D. Resequencing 250 Soybean Accessions: New Insights into Genes Associated with Agronomic Traits and Genetic Networks. Genomics, Proteomics & Bioinformatics. PMID 34314874 DOI: 10.1016/j.gpb.2021.02.009   
2021 Yang C, Yan J, Jiang S, Li X, Min H, Wang X, Hao D. Resequencing 250 Soybean Accessions: New Insights into Genes Associated with Agronomic Traits and Genetic Networks. Genomics, Proteomics & Bioinformatics. PMID 34314874 DOI: 10.1016/j.gpb.2021.02.009   
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 Song F, Owczarek-Lipska M, Ahmels T, Book M, Aisenbrey S, Menghini M, Barthelmes D, Schrader S, Spital G, Neidhardt J. High-Throughput Sequencing to Identify Mutations Associated with Retinal Dystrophies. Genes. 12. PMID 34440443 DOI: 10.3390/genes12081269   
2021 Fu YB, Cober ER, Morrison MJ, Marsolais F, Peterson GW, Horbach C. Patterns of Genetic Variation in a Soybean Germplasm Collection as Characterized with Genotyping-by-Sequencing. Plants (Basel, Switzerland). 10. PMID 34451656 DOI: 10.3390/plants10081611   
2021 Sun Q, Graff M, Rowland B, Wen J, Huang L, Miller-Fleming TW, Haessler J, Preuss MH, Chai JF, Lee MP, Avery CL, Cheng CY, Franceschini N, Sim X, Cox NJ, et al. Analyses of biomarker traits in diverse UK biobank participants identify associations missed by European-centric analysis strategies. Journal of Human Genetics. PMID 34376796 DOI: 10.1038/s10038-021-00968-0   
2021 Zeng Z, Sun QQ, Zhang W, Wen QW, Wang TH, Qin W, Xiao DM, Zhang Z, Huang H, Mo YJ, Wu XD, Cen H. Assessment of genetic polymorphisms within nuclear factor-κB signaling pathway genes in rheumatoid arthritis: Evidence for replication and genetic interaction. International Immunopharmacology. 100: 108089. PMID 34464884 DOI: 10.1016/j.intimp.2021.108089   
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