Caitrin W. McDonough, Ph.D. - Related publications

2010 Wake Forest University, Winston-Salem, NC, United States 
Genetics, Endocrinology Biology
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50 most relevant papers in past 60 days:
Year Citation  Score
2020 Olvany JM, Sausville LN, White MJ, Tacconelli A, Tavera G, Sobota RS, Ciccacci C, Bohlbro AS, Wejse C, Williams SM, Sirugo G. CLEC4E (Mincle) genetic variation associates with pulmonary tuberculosis in Guinea-Bissau (West Africa). Infection, Genetics and Evolution : Journal of Molecular Epidemiology and Evolutionary Genetics in Infectious Diseases. 104560. PMID 32971250 DOI: 10.1016/j.meegid.2020.104560   
2020 León-Reyes G, Rivera-Paredez B, López JCF, Ramírez-Salazar EG, Aquino-Gálvez A, Gallegos-Carrillo K, Denova-Gutiérrez E, Salmerón J, Velázquez-Cruz R. The Variant rs1784042 of the Gene is Associated with Metabolic Syndrome through Low HDL-c Levels in a Mexican Population. Genes. 11. PMID 33066450 DOI: 10.3390/genes11101192   
2020 Iacoangeli A, Lin T, Al Khleifat A, Jones AR, Opie-Martin S, Coleman JRI, Shatunov A, Sproviero W, Williams KL, Garton F, Restuadi R, Henders AK, Mather KA, Needham M, Mathers S, et al. Genome-wide Meta-analysis Finds the ACSL5-ZDHHC6 Locus Is Associated with ALS and Links Weight Loss to the Disease Genetics. Cell Reports. 33: 108323. PMID 33113361 DOI: 10.1016/j.celrep.2020.108323   
2020 Nakamura R, Misawa K, Tohnai G, Nakatochi M, Furuhashi S, Atsuta N, Hayashi N, Yokoi D, Watanabe H, Watanabe H, Katsuno M, Izumi Y, Kanai K, Hattori N, Morita M, et al. A multi-ethnic meta-analysis identifies novel genes, including ACSL5, associated with amyotrophic lateral sclerosis. Communications Biology. 3: 526. PMID 32968195 DOI: 10.1038/s42003-020-01251-2   
2020 Komaravalli PL, Rani S V, Dalal A, Jahan P. Association analysis of FMR1 genetic variants and primary ovarian insufficiency in South Indian women with a novel approach of CGG repeats classification. European Journal of Medical Genetics. 63: 104081. PMID 33039683 DOI: 10.1016/j.ejmg.2020.104081   
2020 Lu G, Zhou B, He Y, Liu H, Luo S, Amos CI, Lee JE, Yang K, Qureshi A, Han J, Wei Q. Novel genetic variants of and of the endosome-related pathway predict cutaneous melanoma-specific survival. American Journal of Cancer Research. 10: 3382-3394. PMID 33163277   
2020 Vergara C, Duggal P, Thio CL, Valencia A, Brien TRO, Latanich R, Timp W, Johnson EO, Kral AH, Mangia A, Goedert JJ, Piazzola V, Mehta SH, Kirk GD, Peters MG, et al. Multi-ancestry fine mapping of interferon lambda and the outcome of acute hepatitis C virus infection. Genes and Immunity. PMID 33116245 DOI: 10.1038/s41435-020-00115-3   
2020 Ran H, Xiao H, Zhou X, Guo L, Lu S. Single-nucleotide polymorphisms and haplotypes in the interleukin-33 gene are associated with a risk of allergic rhinitis in the Chinese population. Experimental and Therapeutic Medicine. 20: 102. PMID 32973951 DOI: 10.3892/etm.2020.9232   
2020 Nakatsuka N, Patterson N, Patsopoulos NA, Altemose N, Tandon A, Beecham AH, McCauley JL, Isobe N, Hauser S, De Jager PL, Hafler DA, Oksenberg JR, Reich D. Two genetic variants explain the association of European ancestry with multiple sclerosis risk in African-Americans. Scientific Reports. 10: 16902. PMID 33037294 DOI: 10.1038/s41598-020-74035-7   
2020 Zhang H, Deng S, Zhang J, Zhu G, Zhou J, Ye W, Wang Q, Wang Y, Zou B, Zhang P, Zhang S, Lang J, Lu S. Single nucleotide polymorphisms within NFKBIA are associated with nasopharyngeal carcinoma susceptibility in Chinese Han population. Cytokine. 155356. PMID 33160813 DOI: 10.1016/j.cyto.2020.155356   
2020 Kumar S, Kumar S, Singh RV, Chauhan A, Kumar A, Bharati J, Singh SV. Association of genetic variability in gene with bovine paratuberculosis disease: a case-control study in the Indian cattle population. Animal Biotechnology. 1-8. PMID 32985930 DOI: 10.1080/10495398.2020.1823400   
2020 Jiang K, Du F, Lv L, Zhuo H, Xu T, Peng L, Chen Y, Li L, Zhang J. Genetic Fine Mapping and Genomic Annotation Defines Causal Mechanisms at A Novel Colorectal Cancer Susceptibility Locus in Han Chinese. Journal of Cancer. 11: 6841-6849. PMID 33123275 DOI: 10.7150/jca.47189   
2020 Feofanova EV, Chen H, Dai Y, Jia P, Grove ML, Morrison AC, Qi Q, Daviglus M, Cai J, North KE, Laurie CC, Kaplan RC, Boerwinkle E, Yu B. A Genome-wide Association Study Discovers 46 Loci of the Human Metabolome in the Hispanic Community Health Study/Study of Latinos. American Journal of Human Genetics. PMID 33031748 DOI: 10.1016/j.ajhg.2020.09.003   
2020 Shinohara T, Urayama KY, Watanabe A, Akahane K, Goi K, Huang M, Kagami K, Abe M, Sugita K, Okada Y, Goto H, Minegishi M, Iwamoto S, Inukai T. Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. Journal of Cellular and Molecular Medicine. PMID 33002292 DOI: 10.1111/jcmm.15882   
2020 Shinohara T, Urayama KY, Watanabe A, Akahane K, Goi K, Huang M, Kagami K, Abe M, Sugita K, Okada Y, Goto H, Minegishi M, Iwamoto S, Inukai T. Inherited genetic variants associated with glucocorticoid sensitivity in leukaemia cells. Journal of Cellular and Molecular Medicine. PMID 33002292 DOI: 10.1111/jcmm.15882   
2020 Zhang Q, Cai Z, Lhomme M, Sahana G, Lesnik P, Guerin M, Fredholm M, Karlskov-Mortensen P. Inclusion of endophenotypes in a standard GWAS facilitate a detailed mechanistic understanding of genetic elements that control blood lipid levels. Scientific Reports. 10: 18434. PMID 33116219 DOI: 10.1038/s41598-020-75612-6   
2020 Gialluisi A, Andlauer TFM, Mirza-Schreiber N, Moll K, Becker J, Hoffmann P, Ludwig KU, Czamara D, Pourcain BS, Honbolygó F, Tóth D, Csépe V, Huguet G, Chaix Y, Iannuzzi S, et al. Genome-wide association study reveals new insights into the heritability and genetic correlates of developmental dyslexia. Molecular Psychiatry. PMID 33057169 DOI: 10.1038/s41380-020-00898-x   
2020 Fataki Asina O, Noyes H, Bucheton B, Ilboudo H, MacLeod A, Mumba Ngoyi D, . SNPs in IL4 and IFNG show no protective associations with human African trypanosomiasis in the Democratic Republic of the Congo: a case-control study. Aas Open Research. 3: 35. PMID 32964195 DOI: 10.12688/aasopenres.12999.1   
2020 Pan X, Li M, Huang L, Mo D, Liang Y, Huang Z, Zhu B, Fang M. , , and Gene Polymorphisms on Hepatocellular Carcinoma Susceptibility in the Chinese Population. Biomed Research International. 2020: 2918517. PMID 33062675 DOI: 10.1155/2020/2918517   
2020 Gorski M, Jung B, Li Y, Matias-Garcia PR, Wuttke M, Coassin S, Thio CHL, Kleber ME, Winkler TW, Wanner V, Chai JF, Chu AY, Cocca M, Feitosa MF, Ghasemi S, ... , ... , et al. Meta-analysis uncovers genome-wide significant variants for rapid kidney function decline. Kidney International. PMID 33137338 DOI: 10.1016/j.kint.2020.09.030   
2020 Feng W, Wang Z, Feng D, Zhu Y, Zhang K, Huang W. The effects of common variants in MDM2 and GNRH2 genes on the risk and survival of osteosarcoma in Han populations from Northwest China. Scientific Reports. 10: 15939. PMID 32994424 DOI: 10.1038/s41598-020-72995-4   
2020 Xu W, Tan CC, Cao XP, Tan L, . Association of Alzheimer's disease risk variants on the gene with PICALM expression, core biomarkers, and feature neurodegeneration. Aging. 12. PMID 33170153 DOI: 10.18632/aging.103814   
2020 Pei YF, Liu YZ, Yang XL, Zhang H, Feng GJ, Wei XT, Zhang L. The genetic architecture of appendicular lean mass characterized by association analysis in the UK Biobank study. Communications Biology. 3: 608. PMID 33097823 DOI: 10.1038/s42003-020-01334-0   
2020 Sun R, Lin X. Genetic Variant Set-Based Tests Using the Generalized Berk-Jones Statistic with Application to a Genome-Wide Association Study of Breast Cancer. Journal of the American Statistical Association. 115: 1079-1091. PMID 33041403 DOI: 10.1080/01621459.2019.1660170   
2020 Jha CK, Mir R, Elfaki I, Javid J, Babakr AT, Banu S, Chahal SMS. Reply to Comment: Evaluation of the Association of Omentin 1 rs2274907 A > T and rs2274908 G > A Gene Polymorphisms with Coronary Artery Disease in Indian Population: A Case-Control Study. Journal of Personalized Medicine. 10. PMID 33114503 DOI: 10.3390/jpm10040194   
2020 Cismaru AL, Rudin D, Ibañez L, Liakoni E, Bonadies N, Kreutz R, Carvajal A, Lucena MI, Martin J, Sancho Ponce E, Molokhia M, Eriksson N, EuDAC Collaborators, Krähenbühl S, Largiadèr CR, et al. Genome-Wide Association Study of Metamizole-Induced Agranulocytosis in European Populations. Genes. 11. PMID 33138277 DOI: 10.3390/genes11111275   
2020 Du B, Jia X, Tian W, Yan X, Wang N, Cai D, Li X, Zhang H, Jin M, Wu N, Qiu C, Zhang Q. Associations of SUCNR1, GRK4, CAMK1D gene polymorphisms and the susceptibility of type 2 diabetes mellitus and essential hypertension in a northern Chinese Han population. Journal of Diabetes and Its Complications. 107752. PMID 33127268 DOI: 10.1016/j.jdiacomp.2020.107752   
2020 Magotra A, Gupta ID, Ahmad T, Alex R. Polymorphism in DNA repair gene BRCA1 associated with clinical mastitis and production traits in indigenous dairy cattle. Research in Veterinary Science. 133: 194-201. PMID 33011602 DOI: 10.1016/j.rvsc.2020.09.013   
2020 Pu W, Wu W, Liu Q, Ma Y, Tu W, Zuo X, Guo G, Jiang S, Zhao Y, Zuo X, Wang Q, Yang L, Xiao R, Chu H, Wang L, et al. Exome-wide association analysis suggests LRP2BP as a susceptibility gene for endothelial injury in systemic sclerosis in Han Chinese population. The Journal of Investigative Dermatology. PMID 33069728 DOI: 10.1016/j.jid.2020.07.039   
2020 Trajanoska K, Seppala LJ, Medina-Gomez C, Hsu YH, Zhou S, van Schoor NM, de Groot LCPGM, Karasik D, Richards JB, Kiel DP, Uitterlinden AG, Perry JRB, van der Velde N, Day FR, Rivadeneira F. Genetic basis of falling risk susceptibility in the UK Biobank Study. Communications Biology. 3: 543. PMID 32999390 DOI: 10.1038/s42003-020-01256-x   
2020 Brandão A, Paulo P, Maia S, Pinheiro M, Peixoto A, Cardoso M, Silva MP, Santos C, Eeles RA, Kote-Jarai Z, Muir K, Ukgpcs Collaborators, Schleutker J, Wang Y, Pashayan N, et al. The Variant C.349A>G Is Associated with Prostate Cancer Risk and Carriers Share a Common Ancestor. Cancers. 12. PMID 33158149 DOI: 10.3390/cancers12113254   
2020 Koyama S, Ito K, Terao C, Akiyama M, Horikoshi M, Momozawa Y, Matsunaga H, Ieki H, Ozaki K, Onouchi Y, Takahashi A, Nomura S, Morita H, Akazawa H, Kim C, et al. Population-specific and trans-ancestry genome-wide analyses identify distinct and shared genetic risk loci for coronary artery disease. Nature Genetics. PMID 33020668 DOI: 10.1038/s41588-020-0705-3   
2020 Yadav BK, Yadav R, Kang HG, Kim KW, Lee CH, Shin BS. Association of Genetic Variation in a Wnt Signaling Pathway Gene () with Susceptibility to Leukoaraiosis. Genetic Testing and Molecular Biomarkers. PMID 33026847 DOI: 10.1089/gtmb.2020.0111   
2020 Hou B, Jia X, Deng Z, Liu X, Liu H, Yu H, Liu S. Exploration of CYP21A2 and CYP17A1 polymorphisms and preeclampsia risk among Chinese Han population: a large-scale case-control study based on 5021 subjects. Human Genomics. 14: 33. PMID 32977860 DOI: 10.1186/s40246-020-00286-0   
2020 Han YG, Zeng Y, Huang YF, Huang DL, Peng P, Na RS. A nonsynonymous SNP within the gene is associated with litter size in Dazu black goats. Animal Biotechnology. 1-5. PMID 33151107 DOI: 10.1080/10495398.2020.1842750   
2020 Owen KA, Price A, Ainsworth H, Aidukaitis BN, Bachali P, Catalina MD, Dittman JM, Howard TD, Kingsmore KM, Labonte AC, Marion MC, Robl RD, Zimmerman KD, Langefeld CD, Grammer AC, et al. Analysis of Trans-Ancestral SLE Risk Loci Identifies Unique Biologic Networks and Drug Targets in African and European Ancestries. American Journal of Human Genetics. PMID 33031749 DOI: 10.1016/j.ajhg.2020.09.007   
2020 Ma C, Li X, Chen J, Li Z, Guan J, Li Y, Yin S, Shi Y. Association Analysis Between Common Variants of the Gene and Three Mental Disorders in the Han Chinese Population. Genetic Testing and Molecular Biomarkers. PMID 33001715 DOI: 10.1089/gtmb.2019.0096   
2020 Chen J, Guan L, Liu H, Liu Q, Fan P, Bai H. GALNT2 Gene Variant rs4846914 Is Associated with Insulin and Insulin Resistance Depending on BMI in PCOS Patients: a Case-Control Study. Reproductive Sciences (Thousand Oaks, Calif.). PMID 33171515 DOI: 10.1007/s43032-020-00380-7   
2020 Li J, Abedi V, , Zand R, Griessenauer CJ. Replication of Top Loci From COL4A1/2 Associated With White Matter Hyperintensity Burden in Patients With Ischemic Stroke. Stroke. STROKEAHA120030260. PMID 33148145 DOI: 10.1161/STROKEAHA.120.030260   
2020 Al-Thuwaini TM, Al-Shuhaib MBS, Lepretre F, Mahdi ZA. Co-inherited novel SNPs of the LIPE gene associated with increased carcass dressing and decreased fat-tail weight in Awassi breed. Tropical Animal Health and Production. PMID 32939705 DOI: 10.1007/s11250-020-02400-9   
2020 Hatmal MM, Abderrahman SM, Nimer W, Al-Eisawi Z, Al-Ameer HJ, Al-Hatamleh MAI, Mohamud R, Alshaer W. Artificial Neural Networks Model for Predicting Type 2 Diabetes Mellitus Based on Gene Polymorphism, Lipid Profile and Demographic Data. Biology. 9. PMID 32823649 DOI: 10.3390/biology9080222   
2020 Teissier M, Larroque H, Brito LF, Rupp R, Schenkel FS, Robert-Granié C. Genomic predictions based on haplotypes fitted as pseudo-SNP for milk production and udder type traits and SCS in French dairy goats. Journal of Dairy Science. PMID 33041034 DOI: 10.3168/jds.2020-18662   
2020 Malik A, Saha S, Morya RK, Bhadada SK, Singh PK, Rana SV. Angiotensin-Converting Enzyme Gene Polymorphism Influences Gastrointestinal Motility in Type 2 Diabetes Mellitus. Biochemical Genetics. PMID 33136283 DOI: 10.1007/s10528-020-10011-0   
2020 Lai E, Danner AL, Famula TR, Oberbauer AM. Genome-Wide Association Studies Reveal Susceptibility Loci for Digital Dermatitis in Holstein Cattle. Animals : An Open Access Journal From Mdpi. 10. PMID 33142934 DOI: 10.3390/ani10112009   
2020 Yuan L, Liu Z, Wei G, Yang P, Hu XE, Qu F, Lu J, He X, Bao G. Genetic polymorphisms in folate-metabolizing genes associated with gastric cancer prognosis in northwest China subjects. Journal of Cancer. 11: 6413-6420. PMID 33033524 DOI: 10.7150/jca.46978   
2020 Herrera-Luis E, Lorenzo-Diaz F, Samedy-Bates LA, Eng C, Villar J, Rodriguez-Santana JR, Burchard EG, Pino-Yanes M. A Deoxyribonuclease 1 Like 3 genetic variant associates with asthma exacerbations. The Journal of Allergy and Clinical Immunology. PMID 33035569 DOI: 10.1016/j.jaci.2020.09.027   
2020 Akhatar J, Singh MP, Sharma A, Kaur H, Kaur N, Sharma S, Bharti B, Sardana VK, Banga SS. Association Mapping of Seed Quality Traits Under Varying Conditions of Nitrogen Application in L. Czern & Coss. Frontiers in Genetics. 11: 744. PMID 33088279 DOI: 10.3389/fgene.2020.00744   
2020 Ovejero-Benito MC, Muñoz-Aceituno E, Sabador D, Almoguera B, Prieto-Pérez R, Hakonarson H, Coto-Segura P, Carretero G, Reolid A, Llamas-Velasco M, Abad-Santos F, Daudén E. Genome-wide association analysis of psoriasis patients treated with anti-TNF drugs. Experimental Dermatology. PMID 33058233 DOI: 10.1111/exd.14215   
2020 Ali MW, Patro CPK, Zhu JJ, Dampier CH, Plummer SJ, Kuscu C, Adli M, Lau C, Lai RK, Casey G. A Functional Variant on 20q13.33 Related to Glioma Risk Alters Enhancer Activity and Modulates Expression of Multiple Genes. Human Mutation. PMID 33169458 DOI: 10.1002/humu.24134   
2020 Liu J, Chen Q, Alkam E, Zheng X, Li Y, Wang L, Fang J. Association between gene polymorphisms of TGF-β and Smad3 and susceptibility to arthritis: a meta-analysis. Expert Review of Clinical Immunology. 1-12. PMID 33012198 DOI: 10.1080/1744666X.2020.1816826