Dvora Shmulewitz, Ph.D. - Related publications

Affiliations: 
Rockefeller University, New York, NY, United States 
Area:
molecular mechanisms that regulate food intake and body weight
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.
14 most relevant papers in past 60 days:
Year Citation  Score
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 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 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 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 Kabasawa K, Hosojima M, Ito Y, Matsushima K, Tanaka J, Hara M, Nakamura K, Narita I, Saito A. Association of metabolic syndrome traits with urinary biomarkers in Japanese adults. Diabetology & Metabolic Syndrome. 14: 9. PMID 35033174 DOI: 10.1186/s13098-021-00779-5   
2022 Restuadi R, Steyn FJ, Kabashi E, Ngo ST, Cheng FF, Nabais MF, Thompson MJ, Qi T, Wu Y, Henders AK, Wallace L, Bye CR, Turner BJ, Ziser L, Mathers S, et al. Functional characterisation of the amyotrophic lateral sclerosis risk locus GPX3/TNIP1. Genome Medicine. 14: 7. PMID 35042540 DOI: 10.1186/s13073-021-01006-6   
2022 Leavitt SV, Horsburgh CR, Lee RS, Tibbs AM, White LF, Jenkins HE. What Can Genetic Relatedness Tell Us About Risk Factors for Tuberculosis Transmission? Epidemiology (Cambridge, Mass.). 33: 55-64. PMID 34847084 DOI: 10.1097/EDE.0000000000001414   
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 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 Kim C, Kim YJ, Choi W, Jang HM, Hwang MY, Jung S, Lim H, Hong SB, Yoon K, Kim BJ, Park HY, Han B. Phenome-wide association study of the major histocompatibility complex region in the Korean population identifies novel association signals. Human Molecular Genetics. PMID 35043955 DOI: 10.1093/hmg/ddac016   
2022 Zhu X, Zhu L, Wang H, Cooper RS, Chakravarti A. Genome-wide pleiotropy analysis identifies novel blood pressure variants and improves its polygenic risk scores. Genetic Epidemiology. PMID 34989438 DOI: 10.1002/gepi.22440   
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 Dharmadasa T, Scaber J, Edmond E, Marsden R, Thompson A, Talbot K, Turner MR. Genetic testing in motor neurone disease. Practical Neurology. PMID 35027459 DOI: 10.1136/practneurol-2021-002989   
2022 Qi G, Dutta D, Leroux A, Ray D, Muschelli J, Crainiceanu C, Chatterjee N. Genome-wide association studies of 27 accelerometry-derived physical activity measurements identified novel loci and genetic mechanisms. Genetic Epidemiology. PMID 35043453 DOI: 10.1002/gepi.22441