Alan S. Weiner - Related publications

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18 most relevant papers in past 60 days:
Year Citation  Score
2022 Dennis J, Tyrer JP, Walker LC, Michailidou K, Dorling L, Bolla MK, Wang Q, Ahearn TU, Andrulis IL, Anton-Culver H, Antonenkova NN, Arndt V, Aronson KJ, Freeman LEB, Beckmann MW, ... , ... , ... , ... , et al. Rare germline copy number variants (CNVs) and breast cancer risk. Communications Biology. 5: 65. PMID 35042965 DOI: 10.1038/s42003-021-02990-6   
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 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 Jiao B, Xiao X, Yuan Z, Guo L, Liao X, Zhou Y, Zhou L, Wang X, Liu X, Liu H, Jiang Y, Lin Z, Zhu Y, Yang Q, Zhang W, et al. Associations of risk genes with onset age and plasma biomarkers of Alzheimer's disease: a large case-control study in mainland China. Neuropsychopharmacology : Official Publication of the American College of Neuropsychopharmacology. PMID 35001095 DOI: 10.1038/s41386-021-01258-1   
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 Wan L, Zhang L, Sun P, Han L, Zhang H, Zhu B, Wang B. Association between UBAC2 gene polymorphism and the risk of noise-induced hearing loss: a cross-sectional study. Environmental Science and Pollution Research International. PMID 35020141 DOI: 10.1007/s11356-021-18360-y   
2022 Meng P, Ye J, Chu X, Cheng B, Cheng S, Liu L, Yang X, Liang C, Zhang F. Associations between genetic loci, environment factors and mental disorders: a genome-wide survival analysis using the UK Biobank data. Translational Psychiatry. 12: 17. PMID 35017462 DOI: 10.1038/s41398-022-01782-8   
2022 Null M, Yilmaz F, Astling D, Yu HC, Cole JB, Hallgrímsson B, Santorico SA, Spritz RA, Shaikh TH, Hendricks AE. Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans. Hgg Advances. 3: 100082. PMID 35047866 DOI: 10.1016/j.xhgg.2021.100082   
2022 Nam Y, Jung SH, Verma A, Sriram V, Won HH, Yun JS, , Kim D. netCRS: Network-based comorbidity risk score for prediction of myocardial infarction using biobank-scaled PheWAS data. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 27: 325-336. PMID 34890160   
2022 Chen Y, Yang Y, Zhong Y, Li J, Kong T, Zhang S, Yang S, Wu C, Cui B, Fu L, Hui R, Zhang W. Genetic risk of hyperuricemia in hypertensive patients associated with antihypertensive drug therapy: a longitudinal study. Clinical Genetics. PMID 35023146 DOI: 10.1111/cge.14110   
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 Nagy D, Verheyen S, Wigby KM, Borovikov A, Sharkov A, Slegesky V, Larson A, Fagerberg C, Brasch-Andersen C, Kibæk M, Bader I, Hernan R, High FA, Chung WK, Schieving JH, et al. Genotype-Phenotype Comparison in POGZ-Related Neurodevelopmental Disorders by Using Clinical Scoring. Genes. 13. PMID 35052493 DOI: 10.3390/genes13010154   
2022 Chen X, Huang X, Zheng C, Wang X, Zhang W. Using the optimal method-explained variance weighted genetic risk score to predict the efficacy of folic acid therapy to hyperhomocysteinemia. European Journal of Clinical Nutrition. PMID 35001080 DOI: 10.1038/s41430-021-01055-5   
2022 Polikowsky HG, Shaw DM, Petty LE, Chen HH, Pruett DG, Linklater JP, Viljoen KZ, Beilby JM, Highland HM, Levitt B, Avery CL, Mullan Harris K, Jones RM, Below JE, Kraft SJ. Population-based genetic effects for developmental stuttering. Hgg Advances. 3: 100073. PMID 35047858 DOI: 10.1016/j.xhgg.2021.100073   
2022 Jamali L, Sadeghi H, Ghasemi MR, Mohseni R, Nazemalhosseini-Mojarad E, Yassaee VR, Larki P, Zali MR, Mirfakhraie R. Autophagy ATG16L1 rs2241880 impacts the colorectal cancer risk: A case-control study. Journal of Clinical Laboratory Analysis. 36: e24169. PMID 34894411 DOI: 10.1002/jcla.24169   
2022 Tarapara B, Shah F. An analysis to identify structural, functional and regulatory role of SNPs in . Journal of Biomolecular Structure & Dynamics. 1-15. PMID 35048780 DOI: 10.1080/07391102.2022.2028678   
2022 Kaibori M, Sakai K, Matsushima H, Kosaka H, Matsui K, De Velasco MA, Sekimoto M, Nishio K. Patients with polyclonal hepatocellular carcinoma are at a high risk of early recurrence and have a poor recurrence-free survival period. Hepatology International. PMID 34973129 DOI: 10.1007/s12072-021-10278-4   
2022 Lam SY, Mommersteeg MC, Yu B, Broer L, Spaander MCW, Frost F, Weiss S, Völzke H, Lerch MM, Schöttker B, Zhang Y, Stocker H, Brenner H, Levy D, Hwang SJ, et al. Toll-like receptor 1 locus re-examined in a genome-wide association study update on anti-Helicobacter pylori IgG titers. Gastroenterology. PMID 35031300 DOI: 10.1053/j.gastro.2022.01.011