| Year |
Citation |
Score |
| 2023 |
Wei WQ, Guardo C, Gandireddy S, Yan C, Ong H, Kerchberger V, Dickson A, Pfaff E, Master H, Basford M, Tran N, Mancuso S, Syed T, Zhao Z, Feng Q, et al. Genetic and Survey Data Improves Performance of Machine Learning Model for Long COVID. Research Square. PMID 38196610 DOI: 10.21203/rs.3.rs-3749510/v1 |
0.462 |
|
| 2023 |
Grabowska ME, Van Driest SL, Robinson JR, Patrick AE, Guardo C, Gangireddy S, Ong HH, Feng Q, Carroll R, Kannankeril PJ, Wei WQ. Developing and evaluating pediatric phecodes (Peds-Phecodes) for high-throughput phenotyping using electronic health records. Journal of the American Medical Informatics Association : Jamia. PMID 38041473 DOI: 10.1093/jamia/ocad233 |
0.494 |
|
| 2023 |
Gupta Y, Friedman DJ, McNulty MT, Khan A, Lane B, Wang C, Ke J, Jin G, Wooden B, Knob AL, Lim TY, Appel GB, Huggins K, Liu L, Mitrotti A, ... ... Wei WQ, et al. Strong protective effect of the APOL1 p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. Nature Communications. 14: 7836. PMID 38036523 DOI: 10.1038/s41467-023-43020-9 |
0.499 |
|
| 2023 |
Linder JE, Tao R, Chung WK, Kiryluk K, Liu C, Weng C, Connolly JJ, Hakonarson H, Harr M, Leppig KA, Jarvik GP, Veenstra DL, Aufox S, Chisholm RL, Gordon AS, ... ... Wei WQ, et al. Prospective, multi-site study of healthcare utilization after actionable monogenic findings from clinical sequencing. American Journal of Human Genetics. PMID 37883979 DOI: 10.1016/j.ajhg.2023.10.006 |
0.452 |
|
| 2023 |
Jiang L, Liu G, Oeser A, Ihegword A, Dickson AL, Daniel LL, Hung AM, Cox NJ, Chung CP, Wei WQ, Stein CM, Feng Q. Association between risk variants and the occurrence of sepsis in Black patients hospitalized with infections: a retrospective cohort study. Elife. 12. PMID 37882666 DOI: 10.7554/eLife.88538 |
0.69 |
|
| 2023 |
Grabowska ME, Huang A, Wen Z, Li B, Wei WQ. Drug repurposing for Alzheimer's disease from 2012-2022-a 10-year literature review. Frontiers in Pharmacology. 14: 1257700. PMID 37745051 DOI: 10.3389/fphar.2023.1257700 |
0.44 |
|
| 2023 |
Pividori M, Lu S, Li B, Su C, Johnson ME, Wei WQ, Feng Q, Namjou B, Kiryluk K, Kullo IJ, Luo Y, Sullivan BD, Voight BF, Skarke C, Ritchie MD, et al. Projecting genetic associations through gene expression patterns highlights disease etiology and drug mechanisms. Nature Communications. 14: 5562. PMID 37689782 DOI: 10.1038/s41467-023-41057-4 |
0.694 |
|
| 2023 |
Mosley JD, Shelley JP, Dickson AL, Zanussi J, Daniel LL, Zheng NS, Bastarache L, Wei WQ, Shi M, Jarvik GP, Rosenthal EA, Khan A, Sherafati A, Kullo IJ, Walunas TL, et al. Clinical consequences of a polygenic predisposition to benign lower white blood cell counts. Medrxiv : the Preprint Server For Health Sciences. PMID 37662324 DOI: 10.1101/2023.08.20.23294331 |
0.6 |
|
| 2023 |
Grabowska ME, Van Driest SL, Robinson JR, Patrick AE, Guardo C, Gangireddy S, Ong H, Feng Q, Carroll R, Kannankeril PJ, Wei WQ. Developing and Evaluating Pediatric Phecodes (Peds-Phecodes) for High-Throughput Phenotyping Using Electronic Health Records. Medrxiv : the Preprint Server For Health Sciences. PMID 37662278 DOI: 10.1101/2023.08.22.23294435 |
0.791 |
|
| 2023 |
Gupta Y, Friedman DJ, McNulty M, Khan A, Lane B, Wang C, Ke J, Jin G, Wooden B, Knob AL, Lim TY, Appel GB, Huggins K, Liu L, Mitrotti A, ... ... Wei WQ, et al. Strong protective effect of the p.N264K variant against G2-associated focal segmental glomerulosclerosis and kidney disease. Medrxiv : the Preprint Server For Health Sciences. PMID 37577628 DOI: 10.1101/2023.08.02.23293554 |
0.69 |
|
| 2023 |
Zanussi JT, Zhao J, Wei WQ, Karakoc G, Chung CP, Feng Q, Olsen NJ, Stein CM, Kawai VK. Clinical diagnoses associated with a positive antinuclear antibody test in patients with and without autoimmune disease. Bmc Rheumatology. 7: 24. PMID 37550754 DOI: 10.1186/s41927-023-00349-4 |
0.7 |
|
| 2023 |
Wei WQ, Yan C, Grabowska M, Dickson A, Li B, Wen Z, Roden D, Stein C, Embí P, Peterson J, Feng Q, Malin B. Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets. Research Square. PMID 37503019 DOI: 10.21203/rs.3.rs-3125859/v1 |
0.718 |
|
| 2023 |
Yan C, Grabowska ME, Dickson AL, Li B, Wen Z, Roden DM, Stein CM, Embí PJ, Peterson JF, Feng Q, Malin BA, Wei WQ. Leveraging Generative AI to Prioritize Drug Repurposing Candidates: Validating Identified Candidates for Alzheimer's Disease in Real-World Clinical Datasets. Medrxiv : the Preprint Server For Health Sciences. PMID 37461512 DOI: 10.1101/2023.07.07.23292388 |
0.718 |
|
| 2023 |
Lennon NJ, Kottyan LC, Kachulis C, Abul-Husn N, Arias J, Belbin G, Below JE, Berndt S, Chung W, Cimino JJ, Clayton EW, Connolly JJ, Crosslin D, Dikilitas O, Velez Edwards DR, ... ... Wei WQ, et al. Selection, optimization, and validation of ten chronic disease polygenic risk scores for clinical implementation in diverse populations. Medrxiv : the Preprint Server For Health Sciences. PMID 37333246 DOI: 10.1101/2023.05.25.23290535 |
0.734 |
|
| 2023 |
Robinson-Cohen C, Triozzi JL, Rowan B, He J, Chen HC, Zheng NS, Wei WQ, Wilson OD, Hellwege JN, Tsao PS, Gaziano JM, Bick A, Matheny ME, Chung CP, Lipworth L, et al. Genome-Wide Association Study of Chronic Kidney Disease Progression. Journal of the American Society of Nephrology : Jasn. PMID 37261792 DOI: 10.1681/ASN.0000000000000170 |
0.492 |
|
| 2023 |
Connolly JJ, Berner ES, Smith M, Levy S, Terek S, Harr M, Karavite D, Suckiel S, Holm IA, Dufendach K, Nelson C, Khan A, Chisholm RL, Allworth A, Wei WQ, et al. Education and Electronic Medical Records and Genomics Network, Challenges and Lessons Learned from a Large-Scale Clinical Trial Using Polygenic Risk Scores. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100906. PMID 37246632 DOI: 10.1016/j.gim.2023.100906 |
0.484 |
|
| 2023 |
Graham SE, Clarke SL, Wu KH, Kanoni S, Zajac GJM, Ramdas S, Surakka I, Ntalla I, Vedantam S, Winkler TW, Locke AE, Marouli E, Hwang MY, Han S, Narita A, ... ... Wei WB, ... ... Wei WQ, et al. Author Correction: The power of genetic diversity in genome-wide association studies of lipids. Nature. PMID 37237109 DOI: 10.1038/s41586-023-06194-2 |
0.683 |
|
| 2023 |
Pfaff ER, Girvin AT, Crosskey M, Gangireddy S, Master H, Wei WQ, Kerchberger VE, Weiner M, Harris PA, Basford M, Lunt C, Chute CG, Moffitt RA, Haendel M. De-black-boxing health AI: demonstrating reproducible machine learning computable phenotypes using the N3C-RECOVER Long COVID model in the All of Us data repository. Journal of the American Medical Informatics Association : Jamia. PMID 37218289 DOI: 10.1093/jamia/ocad077 |
0.588 |
|
| 2023 |
Spotnitz M, Acharya N, Cimino JJ, Murphy S, Namjou B, Crimmins N, Walunas T, Liu C, Crosslin D, Benoit B, Rosenthal E, Pacheco JA, Ostropolets A, Reyes Nieva H, Patterson JS, ... Wei WQ, et al. A metadata framework for computational phenotypes. Jamia Open. 6: ooad032. PMID 37181728 DOI: 10.1093/jamiaopen/ooad032 |
0.487 |
|
| 2023 |
Keloth VK, Banda JM, Gurley M, Heider PM, Kennedy G, Liu H, Liu F, Miller T, Natarajan K, V Patterson O, Peng Y, Raja K, Reeves RM, Rouhizadeh M, Shi J, ... Wei WQ, et al. Representing and Utilizing Clinical Textual Data for Real World Studies: An OHDSI Approach. Journal of Biomedical Informatics. 104343. PMID 36935011 DOI: 10.1016/j.jbi.2023.104343 |
0.487 |
|
| 2023 |
Xiao B, Velez Edwards DR, Lucas A, Drivas T, Gray K, Keating B, Weng C, Jarvik GP, Hakonarson H, Kottyan L, Elhadad N, Wei WQ, Luo Y, Kim D, Ritchie M, et al. Inference of Causal Relationships Between Genetic Risk Factors for Cardiometabolic Phenotypes and Female-Specific Health Conditions. Journal of the American Heart Association. e026561. PMID 36846987 DOI: 10.1161/JAHA.121.026561 |
0.532 |
|
| 2023 |
Sunthankar SD, Zhao J, Wei WQ, Hill GD, Parra DA, Kohl K, McCoy A, Jayaram NM, Godown J. Machine Learning to Predict Interstage Mortality Following Single Ventricle Palliation: A NPC-QIC Database Analysis. Pediatric Cardiology. PMID 36820914 DOI: 10.1007/s00246-023-03130-z |
0.55 |
|
| 2023 |
Zhang Y, Hu H, Fokaidis V, Colby LV, Xu J, Zang C, Xu Z, Wang F, Koropsak M, Bian J, Hall J, Rothman RL, Shenkman EA, Wei WQ, Weiner MG, et al. Identifying Environmental Risk Factors for Post-Acute Sequelae of SARS-CoV-2 Infection: An EHR-based Cohort Study from the RECOVER Program. Environmental Advances. 11: 100352. PMID 36785842 DOI: 10.1016/j.envadv.2023.100352 |
0.488 |
|
| 2023 |
Dorand RD, Zheng NS, Agarwal R, Carroll RJ, Rubinstein SM, Winkfield KM, Wei WQ, Berlin J, Shu XO. Correlates of Taxane-Induced Neuropathy, an Electronic Health Record Based Observational Study. Cancers. 15. PMID 36765713 DOI: 10.3390/cancers15030754 |
0.603 |
|
| 2023 |
Jiang L, Liu G, Oeser A, Ihegword A, Dickson AL, Daniel LL, Hung AM, Cox NJ, Chung CP, Wei WQ, Stein CM, Feng Q. Association between risk variants and progression from infection to sepsis. Medrxiv : the Preprint Server For Health Sciences. PMID 36747677 DOI: 10.1101/2023.01.27.23284540 |
0.695 |
|
| 2023 |
Pacheco JA, Rasmussen LV, Wiley K, Person TN, Cronkite DJ, Sohn S, Murphy S, Gundelach JH, Gainer V, Castro VM, Liu C, Mentch F, Lingren T, Sundaresan AS, Eickelberg G, ... Wei W, et al. Evaluation of the portability of computable phenotypes with natural language processing in the eMERGE network. Scientific Reports. 13: 1971. PMID 36737471 DOI: 10.1038/s41598-023-27481-y |
0.469 |
|
| 2023 |
Davis A, Dickson AL, Daniel LL, Nepal P, Zanussi J, Miller-Fleming TW, Straub PS, Wei WQ, Liu G, Cox NJ, Hung AM, Feng Q, Stein CM, Chung CP. Association Between Genetically Predicted Expression of TPMT and Azathioprine Adverse Events. Research Square. PMID 36711487 DOI: 10.21203/rs.3.rs-2444787/v1 |
0.711 |
|
| 2023 |
Li F, Wu P, Ong HH, Peterson JF, Wei WQ, Zhao J. Evaluating and Mitigating Bias in Machine Learning Models for Cardiovascular Disease Prediction. Journal of Biomedical Informatics. 104294. PMID 36706849 DOI: 10.1016/j.jbi.2023.104294 |
0.754 |
|
| 2023 |
Liu G, Jiang L, Kerchberger VE, Oeser A, Ihegword A, Dickson AL, Daniel LL, Shaffer C, Linton MF, Cox N, Chung CP, Wei WQ, Stein CM, Feng Q. The relationship between high density lipoprotein cholesterol and sepsis: A clinical and genetic approach. Clinical and Translational Science. PMID 36645160 DOI: 10.1111/cts.13462 |
0.68 |
|
| 2023 |
Linder JE, Allworth A, Bland ST, Caraballo PJ, Chisholm RL, Clayton EW, Crosslin DR, Dikilitas O, DiVietro A, Esplin ED, Forman S, Freimuth RR, Gordon AS, Green R, Harden MV, ... Wei WQ, et al. Returning integrated genomic risk and clinical recommendations: the eMERGE study. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 100006. PMID 36621880 DOI: 10.1016/j.gim.2023.100006 |
0.577 |
|
| 2022 |
Kanoni S, Graham SE, Wang Y, Surakka I, Ramdas S, Zhu X, Clarke SL, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, Zajac GJM, Wu KH, Ntalla I, ... ... Wei WB, ... ... Wei WQ, et al. Implicating genes, pleiotropy, and sexual dimorphism at blood lipid loci through multi-ancestry meta-analysis. Genome Biology. 23: 268. PMID 36575460 DOI: 10.1186/s13059-022-02837-1 |
0.688 |
|
| 2022 |
Hui D, Xiao B, Dikilitas O, Freimuth RR, Irvin MR, Jarvik GP, Kottyan L, Kullo I, Limdi NA, Liu C, Luo Y, Namjou B, Puckelwartz MJ, Schaid D, Tiwari H, ... Wei WQ, et al. Quantifying factors that affect polygenic risk score performance across diverse ancestries and age groups for body mass index. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 28: 437-448. PMID 36540998 |
0.503 |
|
| 2022 |
Hellwege JN, Dorn C, Irvin MR, Limdi NA, Cimino J, Beasley TM, Tsao PS, Damrauer SM, Roden DM, Velez Edwards DR, Wei WQ, Edwards TL. Predictive models for abdominal aortic aneurysms using polygenic scores and PheWAS-derived risk factors. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 28: 425-436. PMID 36540997 |
0.597 |
|
| 2022 |
Brandt PS, Kho A, Luo Y, Pacheco JA, Walunas TL, Hakonarson H, Hripcsak G, Liu C, Shang N, Weng C, Walton N, Carrell DS, Crane PK, Larson EB, Chute CG, ... ... Wei WQ, et al. Characterizing variability of electronic health record-driven phenotype definitions. Journal of the American Medical Informatics Association : Jamia. PMID 36474423 DOI: 10.1093/jamia/ocac235 |
0.779 |
|
| 2022 |
Wan NC, Yaqoob AA, Ong HH, Zhao J, Wei WQ. Evaluating resources composing the PheMAP knowledge base to enhance high-throughput phenotyping. Journal of the American Medical Informatics Association : Jamia. PMID 36451277 DOI: 10.1093/jamia/ocac234 |
0.581 |
|
| 2022 |
Song J, Forrest N, Gordon A, Kottyan L, Mittendorf KF, Wei WQ, Ramsey-Goldman R, Walunas T, Kho A. Utilization of electronic health record data to evaluate the association of urban environment on systemic lupus erythematosus symptoms. Rheumatology (Oxford, England). PMID 36383166 DOI: 10.1093/rheumatology/keac647 |
0.463 |
|
| 2022 |
Robinson JR, Carroll RJ, Bastarache L, Chen Q, Pirruccello J, Mou Z, Wei WQ, Connolly J, Mentch F, Crane PK, Hebbring SJ, Crosslin DR, Gordon AS, Rosenthal EA, Stanaway IB, ... Wei W, et al. Quantifying the phenome-wide disease burden of obesity using electronic health records and genomics. Obesity (Silver Spring, Md.). PMID 36372681 DOI: 10.1002/oby.23561 |
0.794 |
|
| 2022 |
Zhang Y, Hu H, Fokaidis V, Lewis V C, Xu J, Zang C, Xu Z, Wang F, Koropsak M, Bian J, Hall J, Rothman RL, Shenkman EA, Wei WQ, Weiner MG, et al. Identifying Contextual and Spatial Risk Factors for Post-Acute Sequelae of SARS-CoV-2 Infection: An EHR-based Cohort Study from the RECOVER Program. Medrxiv : the Preprint Server For Health Sciences. PMID 36263067 DOI: 10.1101/2022.10.13.22281010 |
0.469 |
|
| 2022 |
Jiang L, Kerchberger VE, Shaffer C, Dickson AL, Ormseth MJ, Daniel LL, Leon BGC, Cox NJ, Chung CP, Wei WQ, Stein CM, Feng Q. Genome-wide association analyses of common infections in a large practice-based biobank. Bmc Genomics. 23: 672. PMID 36167494 DOI: 10.1186/s12864-022-08888-9 |
0.682 |
|
| 2022 |
Kerchberger VE, Peterson JF, Wei WQ. Scanning the medical phenome to identify new diagnoses after recovery from COVID-19 in a US cohort. Journal of the American Medical Informatics Association : Jamia. PMID 36005898 DOI: 10.1093/jamia/ocac159 |
0.46 |
|
| 2022 |
Ramdas S, Judd J, Graham SE, Kanoni S, Wang Y, Surakka I, Wenz B, Clarke SL, Chesi A, Wells A, Bhatti KF, Vedantam S, Winkler TW, Locke AE, Marouli E, ... Wei WB, ... Wei WQ, et al. A multi-layer functional genomic analysis to understand noncoding genetic variation in lipids. American Journal of Human Genetics. 109: 1366-1387. PMID 35931049 DOI: 10.1016/j.ajhg.2022.06.012 |
0.689 |
|
| 2022 |
Ge T, Irvin MR, Patki A, Srinivasasainagendra V, Lin YF, Tiwari HK, Armstrong ND, Benoit B, Chen CY, Choi KW, Cimino JJ, Davis BH, Dikilitas O, Etheridge B, Feng YA, ... Wei WQ, et al. Development and validation of a trans-ancestry polygenic risk score for type 2 diabetes in diverse populations. Genome Medicine. 14: 70. PMID 35765100 DOI: 10.1186/s13073-022-01074-2 |
0.491 |
|
| 2022 |
Dickson AL, Daniel LL, Jackson E, Zanussi J, Yang W, Plummer WD, Dupont WD, Wei WQ, Nepal P, Hung AM, Cox NJ, Van Driest SL, Feng Q, Yang JJ, Stein CM, et al. Race, Genotype, and Azathioprine Discontinuation : A Cohort Study. Annals of Internal Medicine. PMID 35724382 DOI: 10.7326/M21-4675 |
0.682 |
|
| 2022 |
Zhang X, Lucas AM, Veturi Y, Drivas TG, Bone WP, Verma A, Chung WK, Crosslin D, Denny JC, Hebbring S, Jarvik GP, Kullo I, Larson EB, Rasmussen-Torvik LJ, Schaid DJ, ... Wei WQ, et al. Large-scale genomic analyses reveal insights into pleiotropy across circulatory system diseases and nervous system disorders. Nature Communications. 13: 3428. PMID 35701404 DOI: 10.1038/s41467-022-30678-w |
0.633 |
|
| 2022 |
Shadrina AS, Elgaeva EE, Stanaway IB, Jarvik GP, Namjou B, Wei WQ, Glessner J, Hakonarson H, Suri P, Tsepilov YA. Mendelian randomization analysis of plasma levels of CD209 and MICB proteins and the risk of varicose veins of lower extremities. Plos One. 17: e0268725. PMID 35594287 DOI: 10.1371/journal.pone.0268725 |
0.463 |
|
| 2022 |
Feng YA, Stanaway IB, Connolly JJ, Denny JC, Luo Y, Weng C, Wei WQ, Weiss ST, Karlson EW, Smoller JW. Psychiatric manifestations of rare variation in medically actionable genes: a PheWAS approach. Bmc Genomics. 23: 385. PMID 35590255 DOI: 10.1186/s12864-022-08600-x |
0.618 |
|
| 2022 |
Krantz MS, Kerchberger VE, Wei WQ. Novel Analysis Methods to Mine Immune-Mediated Phenotypes and Find Genetic Variation Within the Electronic Health Record (Roadmap for Phenotype to Genotype: Immunogenomics). The Journal of Allergy and Clinical Immunology. in Practice. PMID 35487368 DOI: 10.1016/j.jaip.2022.04.016 |
0.529 |
|
| 2022 |
Zhao J, Feng Q, Wei WQ. Integration of Omics and Phenotypic Data for Precision Medicine. Methods in Molecular Biology (Clifton, N.J.). 2486: 19-35. PMID 35437716 DOI: 10.1007/978-1-0716-2265-0_2 |
0.744 |
|
| 2022 |
Denaxas S, Liu G, Feng Q, Fatemifar G, Bastarache L, Kerchberger EV, Hingorani AD, Lumbers T, Peterson JF, Wei WQ, Hemingway H. Mapping the Read2/CTV3 controlled clinical terminologies to Phecodes in UK Biobank primary care electronic health records: implementation and evaluation. Amia ... Annual Symposium Proceedings. Amia Symposium. 2021: 362-371. PMID 35308936 |
0.658 |
|
| 2022 |
Daniel LL, Dickson AL, Zanussi JT, Miller-Fleming TW, Straub PS, Wei WQ, Plummer WD, Dupont WD, Liu G, Anandi P, Reese TS, Birdwell KA, Kawai VK, Hung AM, Cox NJ, et al. Predicted expression of genes involved in the thiopurine metabolic pathway and azathioprine discontinuation due to myelotoxicity. Clinical and Translational Science. PMID 35118815 DOI: 10.1111/cts.13243 |
0.684 |
|
| 2022 |
Yu J, Pacheco JA, Ghosh AS, Luo Y, Weng C, Shang N, Benoit B, Carrell DS, Carroll RJ, Dikilitas O, Freimuth RR, Gainer VS, Hakonarson H, Hripcsak G, Kullo IJ, ... Wei WQ, et al. Under-specification as the source of ambiguity and vagueness in narrative phenotype algorithm definitions. Bmc Medical Informatics and Decision Making. 22: 23. PMID 35090449 DOI: 10.1186/s12911-022-01759-z |
0.702 |
|
| 2022 |
Wu P, Feng Q, Kerchberger VE, Nelson SD, Chen Q, Li B, Edwards TL, Cox NJ, Phillips EJ, Stein CM, Roden DM, Denny JC, Wei WQ. Integrating gene expression and clinical data to identify drug repurposing candidates for hyperlipidemia and hypertension. Nature Communications. 13: 46. PMID 35013250 DOI: 10.1038/s41467-021-27751-1 |
0.781 |
|
| 2021 |
Glazer AM, Davogustto GE, Shaffer CM, Vanoye CG, Desai RR, Farber-Eger E, Dikilitas O, Shang N, Pacheco JA, Yang T, Muhammad A, Mosley JD, Van Driest SL, Wells QS, Shaffer LL, ... Wei WQ, et al. Arrhythmia Variant Associations and Reclassifications in the eMERGE-III Sequencing Study. Circulation. PMID 34930020 DOI: 10.1161/CIRCULATIONAHA.121.055562 |
0.799 |
|
| 2021 |
Graham SE, Clarke SL, Wu KH, Kanoni S, Zajac GJM, Ramdas S, Surakka I, Ntalla I, Vedantam S, Winkler TW, Locke AE, Marouli E, Hwang MY, Han S, Narita A, ... Wei WB, ... Wei WQ, et al. The power of genetic diversity in genome-wide association studies of lipids. Nature. PMID 34887591 DOI: 10.1038/s41586-021-04064-3 |
0.726 |
|
| 2021 |
Zanussi JT, Zhao J, Dorn CA, Liu G, Feng Q, Wei W, Mosley JD, Stein CM, Kawai VK. Identifying potential therapeutic applications and diagnostic harms of increased bilirubin concentrations - a clinical and genetic approach. Clinical Pharmacology and Therapeutics. PMID 34625956 DOI: 10.1002/cpt.2441 |
0.751 |
|
| 2021 |
Dickson AL, Daniel LL, Zanussi J, Plummer WD, Wei WQ, Liu G, Reese T, Anandi P, Birdwell KA, Kawai V, Cox NJ, Dupont WD, Hung AM, Feng Q, Stein CM, et al. TPMT and NUDT15 Variants Predict Discontinuation of Azathioprine for Myelotoxicity in Patients with Inflammatory Disease: Real-World Clinical Results. Clinical Pharmacology and Therapeutics. PMID 34582038 DOI: 10.1002/cpt.2428 |
0.7 |
|
| 2021 |
Zheng NS, Kerchberger VE, Borza VA, Eken HN, Smith JC, Wei WQ. An updated, computable MEDication-Indication resource for biomedical research. Scientific Reports. 11: 18953. PMID 34556781 DOI: 10.1038/s41598-021-98579-4 |
0.461 |
|
| 2021 |
Zheng NS, Wang F, Agarwal R, Carroll RJ, Wei WQ, Berlin J, Shu XO. Racial disparity in taxane-induced neutropenia among cancer patients. Cancer Medicine. PMID 34547180 DOI: 10.1002/cam4.4181 |
0.571 |
|
| 2021 |
Wells QS, Bagheri M, Aday AW, Gupta DK, Shaffer CM, Wei WQ, Sarna Vaitinadin N, Khan SS, Greenland P, Wang TJ, Stein CM, Roden DM, Mosley JD. Polygenic Risk Score to Identify Subclinical Coronary Heart Disease Risk in Young Adults. Circulation. Genomic and Precision Medicine. CIRCGEN121003341. PMID 34463132 DOI: 10.1161/CIRCGEN.121.003341 |
0.548 |
|
| 2021 |
De T, Zhang H, Alarcon C, Lec B, Avitia J, Smithberger E, Chen C, Horvath M, Kwan S, Young M, Adhikari S, Kwon J, Pacheco J, Jarvik G, Wei WQ, et al. Genetic association of primary nonresponse to anti-TNFα therapy in patients with inflammatory bowel disease. Pharmacogenetics and Genomics. PMID 34380996 DOI: 10.1097/FPC.0000000000000445 |
0.493 |
|
| 2021 |
Xu D, Wang C, Khan A, Shang N, He Z, Gordon A, Kullo IJ, Murphy S, Ni Y, Wei WQ, Gharavi A, Kiryluk K, Weng C, Ionita-Laza I. Quantitative disease risk scores from EHR with applications to clinical risk stratification and genetic studies. Npj Digital Medicine. 4: 116. PMID 34302027 DOI: 10.1038/s41746-021-00488-3 |
0.563 |
|
| 2021 |
Satterfield BA, Dikilitas O, Safarova MS, Clarke SL, Tcheandjieu C, Zhu X, Bastarache L, Larson EB, Justice AE, Shang N, Rosenthal EA, Shah A, Namjou-Khales B, Urbina EM, Wei WQ, et al. Associations of Genetically Predicted Lipoprotein (a) Levels with Cardiovascular Traits in Individuals of European and African Ancestry. Circulation. Genomic and Precision Medicine. PMID 34282949 DOI: 10.1161/CIRCGEN.120.003354 |
0.696 |
|
| 2021 |
Eric V, Yi V, Murdock D, Kalla SE, Wu TJ, Sabo A, Li S, Meng Q, Tian X, Murugan M, Cohen M, Kovar C, Wei WQ, Chung WK, Weng C, et al. Neptune: an environment for the delivery of genomic medicine. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 34257418 DOI: 10.1038/s41436-021-01230-w |
0.512 |
|
| 2021 |
Wei WQ, Zhao J, Roden DM, Peterson JF. Machine Learning Challenges in Pharmacogenomic Research. Clinical Pharmacology and Therapeutics. PMID 34217153 DOI: 10.1002/cpt.2329 |
0.572 |
|
| 2021 |
Muhammad A, Aka IT, Birdwell KA, Gordon AS, Roden DM, Wei WQ, Mosley JD, Van Driest SL. Genome-wide approach to measure variant-based heritability of drug outcome phenotypes. Clinical Pharmacology and Therapeutics. PMID 34151428 DOI: 10.1002/cpt.2323 |
0.601 |
|
| 2021 |
Veturi Y, Lucas A, Bradford Y, Hui D, Dudek S, Theusch E, Verma A, Miller JE, Kullo I, Hakonarson H, Sleiman P, Schaid D, Stein CM, Edwards DRV, Feng Q, Wei WQ, et al. A unified framework identifies new links between plasma lipids and diseases from electronic medical records across large-scale cohorts. Nature Genetics. PMID 34140684 DOI: 10.1038/s41588-021-00879-y |
0.71 |
|
| 2021 |
Liu G, Shi M, Mosley JD, Weng C, Zhang Y, Lee MTM, Jarvik GP, Hakonarson H, Namjou-Khales B, Sleiman P, Luo Y, Mentch F, Denny JC, Linton MF, Wei WQ, et al. A Mendelian Randomization Approach Using 3-HMG-Coenzyme-A Reductase Gene Variation to Evaluate the Association of Statin-Induced Low-Density Lipoprotein Cholesterol Lowering With Noncardiovascular Disease Phenotypes. Jama Network Open. 4: e2112820. PMID 34097045 DOI: 10.1001/jamanetworkopen.2021.12820 |
0.74 |
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| 2021 |
Zheng NS, Stone CA, Jiang L, Shaffer CM, Kerchberger VE, Chung CP, Feng Q, Cox NJ, Stein CM, Roden DM, Denny JC, Phillips EJ, Wei WQ. High-throughput framework for genetic analyses of adverse drug reactions using electronic health records. Plos Genetics. 17: e1009593. PMID 34061827 DOI: 10.1371/journal.pgen.1009593 |
0.783 |
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| 2021 |
Kawai VK, Shi M, Liu G, Feng Q, Wei W, Chung CP, Walunas TL, Gordon AS, Linneman JG, Hebbring SJ, Harley JB, Cox NJ, Roden DM, Stein CM, Mosley JD. Pleiotropy of systemic lupus erythematosus risk alleles and cardiometabolic disorders: A phenome-wide association study and inverse-variance weighted meta-analysis. Lupus. 9612033211014952. PMID 33977795 DOI: 10.1177/09612033211014952 |
0.706 |
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| 2021 |
Murugan M, Babb LJ, Overby Taylor C, Rasmussen LV, Freimuth RR, Venner E, Yan F, Yi V, Granite SJ, Zouk H, Aronson SJ, Power K, Fedotov A, Crosslin DR, Fasel D, ... ... Wei W, et al. Genomic Considerations for FHIR®; eMERGE Implementation Lessons. Journal of Biomedical Informatics. 103795. PMID 33930535 DOI: 10.1016/j.jbi.2021.103795 |
0.515 |
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| 2021 |
DeLozier S, Bastarache L, Bland S, McPheeters M, Wells Q, Farber-Eger E, Bejan CA, Fabbri D, Rosenbloom T, Roden D, Johnson KB, Wei WQ, Peterson J. Phenotyping coronavirus disease 2019 during a global health pandemic: lessons learned from the characterization of an early cohort. Journal of Biomedical Informatics. 103777. PMID 33838341 DOI: 10.1016/j.jbi.2021.103777 |
0.615 |
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| 2021 |
Emdin CA, Haas ME, Khera AV, Aragam K, Chaffin M, Klarin D, Hindy G, Jiang L, Wei WQ, Feng Q, Karjalainen J, Havulinna A, Kiiskinen T, Bick A, Ardissino D, et al. Correction: A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease. Plos Genetics. 17: e1009503. PMID 33822779 DOI: 10.1371/journal.pgen.1009503 |
0.703 |
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| 2021 |
Zhao J, Grabowska ME, Eric Kerchberger V, Smith JC, Nur Eken H, Feng Q, Peterson JF, Trent Rosenbloom S, Johnson KB, Wei WQ. ConceptWAS: a high-throughput method for early identification of COVID-19 presenting symptoms and characteristics from clinical notes. Journal of Biomedical Informatics. 103748. PMID 33774203 DOI: 10.1016/j.jbi.2021.103748 |
0.716 |
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| 2021 |
Wu P, Nelson SD, Zhao J, Stone CA, Feng Q, Chen Q, Larson EA, Li B, Cox NJ, Stein CM, Phillips EJ, Roden DM, Denny JC, Wei WQ. DDIWAS: High-throughput electronic health record-based screening of drug-drug interactions. Journal of the American Medical Informatics Association : Jamia. PMID 33712848 DOI: 10.1093/jamia/ocab019 |
0.775 |
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| 2021 |
Thomas M, Sakoda LC, Hoffmeister M, Rosenthal EA, Lee JK, van Duijnhoven FJB, Platz EA, Wu AH, Dampier CH, de la Chapelle A, Wolk A, Joshi AD, Burnett-Hartman A, Gsur A, Lindblom A, ... Wei WQ, et al. Response to Li and Hopper. American Journal of Human Genetics. 108: 527-529. PMID 33667396 DOI: 10.1016/j.ajhg.2021.02.003 |
0.369 |
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| 2021 |
Li R, Duan R, Zhang X, Lumley T, Pendergrass S, Bauer C, Hakonarson H, Carrell DS, Smoller JW, Wei WQ, Carroll R, Velez Edwards DR, Wiesner G, Sleiman P, Denny JC, et al. Lossless integration of multiple electronic health records for identifying pleiotropy using summary statistics. Nature Communications. 12: 168. PMID 33420026 DOI: 10.1038/s41467-020-20211-2 |
0.631 |
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| 2021 |
Rosenthal EA, Crosslin DR, Gordon AS, Carrell DS, Stanaway IB, Larson EB, Grafton J, Wei WQ, Denny JC, Feng QP, Shah AS, Sturm AC, Ritchie MD, Pacheco JA, Hakonarson H, et al. Association between triglycerides, known risk SNVs and conserved rare variation in SLC25A40 in a multi-ancestry cohort. Bmc Medical Genomics. 14: 11. PMID 33407432 DOI: 10.1186/s12920-020-00854-2 |
0.735 |
|
| 2020 |
Emdin CA, Haas M, Ajmera V, Simon TG, Homburger J, Neben C, Jiang L, Wei WQ, Feng Q, Zhou A, Denny J, Corey K, Loomba R, Kathiresan S, Khera AV. Association of genetic variation with cirrhosis: a multi-trait genome-wide association and gene-environment interaction study. Gastroenterology. PMID 33310085 DOI: 10.1053/j.gastro.2020.12.011 |
0.755 |
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| 2020 |
Zheng NS, Warner JL, Osterman TJ, Wells QS, Shu XO, Deppen SA, Karp SJ, Dwyer S, Feng Q, Cox NJ, Peterson JF, Michael Stein C, Roden DM, Johnson KB, Wei WQ. A retrospective approach to evaluating potential adverse outcomes associated with delay of procedures for cardiovascular and cancer-related diagnoses in the context of COVID-19. Journal of Biomedical Informatics. 103657. PMID 33309899 DOI: 10.1016/j.jbi.2020.103657 |
0.783 |
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| 2020 |
Bonkowsky JL, Wilkes J, Ying J, Wei WQ. Novel and known morbidities of leukodystrophies identified using a phenome-wide association study. Neurology. Clinical Practice. 10: 406-414. PMID 33299668 DOI: 10.1212/CPJ.0000000000000783 |
0.489 |
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| 2020 |
Zhao J, Grabowska ME, Kerchberger VE, Smith JC, Eken HN, Feng Q, Peterson JF, Rosenbloom ST, Johnson KB, Wei WQ. ConceptWAS: a high-throughput method for early identification of COVID-19 presenting symptoms. Medrxiv : the Preprint Server For Health Sciences. PMID 33200151 DOI: 10.1101/2020.11.06.20227165 |
0.71 |
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| 2020 |
Zheng NS, Feng Q, Kerchberger VE, Zhao J, Edwards TL, Cox NJ, Stein CM, Roden DM, Denny JC, Wei WQ. PheMap: a multi-resource knowledge base for high-throughput phenotyping within electronic health records. Journal of the American Medical Informatics Association : Jamia. PMID 32974638 DOI: 10.1093/jamia/ocaa104 |
0.781 |
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| 2020 |
Johnson KB, Wei WQ, Weeraratne D, Frisse ME, Misulis K, Rhee K, Zhao J, Snowdon JL. Precision medicine, AI, and the future of personalized health care. Clinical and Translational Science. PMID 32961010 DOI: 10.1111/cts.12884 |
0.569 |
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| 2020 |
Krebs K, Bovijn J, Zheng N, Lepamets M, Censin JC, Jürgenson T, Särg D, Abner E, Laisk T, Luo Y, Skotte L, Geller F, Feenstra B, Wang W, Auton A, ... Wei WQ, et al. Genome-wide Study Identifies Association between HLA-B55:01 and Self-Reported Penicillin Allergy. American Journal of Human Genetics. PMID 32888428 DOI: 10.1016/J.Ajhg.2020.08.008 |
0.643 |
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| 2020 |
Thomas M, Sakoda LC, Hoffmeister M, Rosenthal EA, Lee JK, van Duijnhoven FJB, Platz EA, Wu AH, Dampier CH, de la Chapelle A, Wolk A, Joshi AD, Burnett-Hartman A, Gsur A, Lindblom A, ... Wei WQ, et al. Genome-wide Modeling of Polygenic Risk Score in Colorectal Cancer Risk. American Journal of Human Genetics. PMID 32758450 DOI: 10.1016/J.Ajhg.2020.07.006 |
0.556 |
|
| 2020 |
Coleman DT, Stone CA, Wei WQ, Phillips EJ. Penicillin allergy labels drive perioperative prophylactic antibiotic selection in orthopedic procedures. The Journal of Allergy and Clinical Immunology. in Practice. PMID 32693215 DOI: 10.1016/J.Jaip.2020.07.007 |
0.44 |
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| 2020 |
Mitchell SL, Leon DAC, Chaugai S, Kawai VK, Levinson RT, Wei WQ, Stein CM. Pharmacogenetics of hypoglycemia associated with sulfonylurea therapy in usual clinical care. The Pharmacogenomics Journal. PMID 32504053 DOI: 10.1038/S41397-020-0171-4 |
0.587 |
|
| 2020 |
Dikilitas O, Schaid DJ, Kosel ML, Carroll RJ, Chute CG, Denny JA, Fedotov A, Feng Q, Hakonarson H, Jarvik GP, Lee MTM, Pacheco JA, Rowley R, Sleiman PM, Stein CM, ... Wei WQ, et al. Predictive Utility of Polygenic Risk Scores for Coronary Heart Disease in Three Major Racial and Ethnic Groups. American Journal of Human Genetics. 106: 707-716. PMID 32386537 DOI: 10.1016/J.Ajhg.2020.04.002 |
0.78 |
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| 2020 |
Coleman DT, Stone CA, Wei WQ, Phillips EJ. Readiness for PENicillin allergy testing: Perception of Allergy Label (PEN-PAL) Survey. The Journal of Allergy and Clinical Immunology. in Practice. PMID 32304843 DOI: 10.1016/J.Jaip.2020.03.049 |
0.477 |
|
| 2020 |
Emdin CA, Haas ME, Khera AV, Aragam K, Chaffin M, Klarin D, Hindy G, Jiang L, Wei WQ, Feng Q, Karjalainen J, Havulinna A, Kiiskinen T, Bick A, Ardissino D, et al. A missense variant in Mitochondrial Amidoxime Reducing Component 1 gene and protection against liver disease. Plos Genetics. 16: e1008629. PMID 32282858 DOI: 10.1371/Journal.Pgen.1008629 |
0.735 |
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| 2020 |
Bajaj A, Ihegword A, Qiu C, Small AM, Wei WQ, Bastarache L, Feng Q, Kember RL, Risman M, Bloom RD, Birtwell DL, Williams H, Shaffer CM, Chen J, Center RG, et al. Phenome-wide association analysis suggests the APOL1 linked disease spectrum primarily drives kidney-specific pathways. Kidney International. PMID 32247630 DOI: 10.1016/J.Kint.2020.01.027 |
0.765 |
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| 2020 |
Hu Y, Graff M, Haessler J, Buyske S, Bien SA, Tao R, Highland HM, Nishimura KK, Zubair N, Lu Y, Verbanck M, Hilliard AT, Klarin D, Damrauer SM, Ho YL, ... Wei WQ, et al. Minority-centric meta-analyses of blood lipid levels identify novel loci in the Population Architecture using Genomics and Epidemiology (PAGE) study. Plos Genetics. 16: e1008684. PMID 32226016 DOI: 10.1371/journal.pgen.1008684 |
0.71 |
|
| 2020 |
Anandi P, Dickson AL, Feng Q, Wei WQ, Dupont WD, Plummer D, Liu G, Octaria R, Barker KA, Kawai VK, Birdwell K, Cox NJ, Hung A, Stein CM, Chung CP. Combining clinical and candidate gene data into a risk score for azathioprine-associated leukopenia in routine clinical practice. The Pharmacogenomics Journal. PMID 32054992 DOI: 10.1038/S41397-020-0163-4 |
0.719 |
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| 2020 |
Emdin CA, Haas ME, Khera AV, Aragam K, Chaffin M, Klarin D, Hindy G, Jiang L, Wei W, Feng Q, Karjalainen J, Havulinna A, Kiiskinen T, Bick A, Ardissino D, et al. Association of MARC1 A165T with metabolic traits. Plos Genetics. DOI: 10.1371/Journal.Pgen.1008629.S005 |
0.677 |
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| 2020 |
Emdin CA, Haas ME, Khera AV, Aragam K, Chaffin M, Klarin D, Hindy G, Jiang L, Wei W, Feng Q, Karjalainen J, Havulinna A, Kiiskinen T, Bick A, Ardissino D, et al. Distribution of ancestry in each cohort. Plos Genetics. DOI: 10.1371/Journal.Pgen.1008629.S003 |
0.643 |
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| 2019 |
Li X, Meng X, He Y, Spiliopoulou A, Timofeeva M, Wei WQ, Gifford A, Yang T, Varley T, Tzoulaki I, Joshi P, Denny JC, Mckeigue P, Campbell H, Theodoratou E. Genetically determined serum urate levels and cardiovascular and other diseases in UK Biobank cohort: A phenome-wide mendelian randomization study. Plos Medicine. 16: e1002937. PMID 31626644 DOI: 10.1371/Journal.Pmed.1002937 |
0.666 |
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| 2019 |
Robinson JR, Carroll RJ, Bastarache L, Chen Q, Mou Z, Wei WQ, Connolly JJ, Mentch F, Sleiman P, Crane PK, Hebbring SJ, Stanaway IB, Crosslin DR, Gordon AS, Rosenthal EA, ... ... Wei W, et al. Association of Genetic Risk of Obesity with Postoperative Complications Using Mendelian Randomization. World Journal of Surgery. PMID 31605180 DOI: 10.1007/S00268-019-05202-9 |
0.776 |
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| 2019 |
Wu P, Gifford A, Meng X, Li X, Campbell H, Varley T, Zhao J, Carroll R, Bastarache L, Denny JC, Theodoratou E, Wei WQ. Developing and Evaluating Mappings of ICD-10 and ICD-10-CM Codes to PheCodes. Jmir Medical Informatics. PMID 31553307 DOI: 10.2196/14325 |
0.793 |
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| 2019 |
Shang N, Liu C, Rasmussen LV, Ta CN, Caroll RJ, Benoit B, Lingren T, Dikilitas O, Mentch FD, Carrell DS, Wei WQ, Luo Y, Gainer VS, Kullo IJ, Pacheco JA, et al. Making work visible for electronic phenotype implementation: lessons learned from the eMERGE network. Journal of Biomedical Informatics. 103293. PMID 31542521 DOI: 10.1016/J.Jbi.2019.103293 |
0.57 |
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| 2019 |
Meng X, Li X, Timofeeva MN, He Y, Spiliopoulou A, Wei WQ, Gifford A, Wu H, Varley T, Joshi P, Denny JC, Farrington SM, Zgaga L, Dunlop MG, McKeigue P, et al. Phenome-wide Mendelian-randomization study of genetically determined vitamin D on multiple health outcomes using the UK Biobank study. International Journal of Epidemiology. PMID 31518429 DOI: 10.1093/Ije/Dyz182 |
0.588 |
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| 2019 |
Feng Q, Wei WQ, Chaugai S, Carranza Leon BG, Kawai V, Carranza Leon DA, Jiang L, Zhong X, Liu G, Ihegword A, Shaffer CM, Linton MF, Chung CP, Stein CM. A Genetic Approach to the Association Between PCSK9 and Sepsis. Jama Network Open. 2: e1911130. PMID 31509211 DOI: 10.1001/jamanetworkopen.2019.11130 |
0.685 |
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| 2019 |
Zhao J, Zhang Y, Schlueter DJ, Wu P, Eric Kerchberger V, Trent Rosenbloom S, Wells QS, Feng Q, Denny JC, Wei WQ. Detecting Time-Evolving Phenotypic Topics via Tensor Factorization on Electronic Health Records: Cardiovascular Disease Case Study. Journal of Biomedical Informatics. 103270. PMID 31445983 DOI: 10.1016/J.Jbi.2019.103270 |
0.803 |
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| 2019 |
Hripcsak G, Shang N, Peissig PL, Rasmussen LV, Liu C, Benoit B, Carroll RJ, Carrell DS, Denny JC, Dikilitas O, Gainer VS, Marie Howell K, Klann JG, Kullo IJ, Lingren T, ... Wei WQ, et al. Facilitating phenotype transfer using a common data model. Journal of Biomedical Informatics. 103253. PMID 31325501 DOI: 10.1016/J.Jbi.2019.103253 |
0.665 |
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| 2019 |
Namjou B, Lingren T, Huang Y, Parameswaran S, Cobb BL, Stanaway IB, Connolly JJ, Mentch FD, Benoit B, Niu X, Wei WQ, Carroll RJ, Pacheco JA, Harley ITW, Divanovic S, et al. GWAS and enrichment analyses of non-alcoholic fatty liver disease identify new trait-associated genes and pathways across eMERGE Network. Bmc Medicine. 17: 135. PMID 31311600 DOI: 10.1186/S12916-019-1364-Z |
0.662 |
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| 2019 |
Gill D, Georgakis MK, Koskeridis F, Jiang L, Feng Q, Wei WQ, Theodoratou E, Elliott P, Denny JC, Malik R, Evangelou E, Dehghan A, Dichgans M, Tzoulaki I. Use of Genetic Variants Related to Antihypertensive Drugs to Inform on Efficacy and Side Effects. Circulation. PMID 31234639 DOI: 10.1161/Circulationaha.118.038814 |
0.742 |
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| 2019 |
Brackman DJ, Yee SW, Enogieru OJ, Shaffer C, Ranatunga D, Denny JC, Wei WQ, Kamatani Y, Kubo M, Roden DM, Jorgenson E, Giacomini KM. Genome-wide Association and Functional Studies Reveal Novel Pharmacological Mechanisms for Allopurinol. Clinical Pharmacology and Therapeutics. PMID 30924126 DOI: 10.1002/Cpt.1439 |
0.674 |
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| 2019 |
Zhang X, Veturi Y, Verma S, Bone W, Verma A, Lucas A, Hebbring S, Denny JC, Stanaway IB, Jarvik GP, Crosslin D, Larson EB, Rasmussen-Torvik L, Pendergrass SA, Smoller JW, ... Wei WQ, et al. Detecting potential pleiotropy across cardiovascular and neurological diseases using univariate, bivariate, and multivariate methods on 43,870 individuals from the eMERGE network. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 24: 272-283. PMID 30864329 |
0.668 |
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| 2019 |
Safarova MS, Satterfield BA, Fan X, Austin EE, Ye Z, Bastarache L, Zheng N, Ritchie MD, Borthwick KM, Williams MS, Larson EB, Scrol A, Jarvik GP, Crosslin DR, Leppig K, ... Wei WQ, et al. A phenome-wide association study to discover pleiotropic effects of , , and . Npj Genomic Medicine. 4: 3. PMID 30774981 DOI: 10.1038/S41525-019-0078-7 |
0.816 |
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| 2019 |
Zhao J, Feng Q, Wu P, Warner JL, Denny JC, Wei WQ. Using topic modeling via non-negative matrix factorization to identify relationships between genetic variants and disease phenotypes: A case study of Lipoprotein(a) (LPA). Plos One. 14: e0212112. PMID 30759150 DOI: 10.1371/Journal.Pone.0212112 |
0.824 |
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| 2019 |
Zhao J, Feng Q, Wu P, Lupu RA, Wilke RA, Wells QS, Denny JC, Wei WQ. Learning from Longitudinal Data in Electronic Health Record and Genetic Data to Improve Cardiovascular Event Prediction. Scientific Reports. 9: 717. PMID 30679510 DOI: 10.1038/S41598-018-36745-X |
0.8 |
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| 2019 |
Feng Q, Wei WQ, Chaugai S, Leon BGC, Mosley JD, Leon DAC, Jiang L, Ihegword A, Shaffer CM, Linton MF, Chung CP, Stein CM. Association Between Low-Density Lipoprotein Cholesterol Levels and Risk for Sepsis Among Patients Admitted to the Hospital With Infection. Jama Network Open. 2: e187223. PMID 30657536 DOI: 10.1001/jamanetworkopen.2018.7223 |
0.663 |
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| 2019 |
Giri A, Hellwege JN, Keaton JM, Park J, Qiu C, Warren HR, Torstenson ES, Kovesdy CP, Sun YV, Wilson OD, Robinson-Cohen C, Roumie CL, Chung CP, Birdwell KA, Damrauer SM, ... Wei WQ, et al. Trans-ethnic association study of blood pressure determinants in over 750,000 individuals. Nature Genetics. 51: 51-62. PMID 30578418 DOI: 10.1038/S41588-018-0303-9 |
0.578 |
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| 2019 |
Stone CA, Wei W, Phillips EJ. Characteristics of Persistent Penicillin Allergy Labels in a Large Electronic Health Record Database Journal of Allergy and Clinical Immunology. 143: AB24. DOI: 10.1016/J.Jaci.2018.12.077 |
0.307 |
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| 2018 |
Robinson JR, Wei WQ, Roden DM, Denny JC. Defining Phenotypes from Clinical Data to Drive Genomic Research. Annual Review of Biomedical Data Science. 1: 69-92. PMID 34109303 DOI: 10.1146/annurev-biodatasci-080917-013335 |
0.79 |
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| 2018 |
Chaugai S, Dickson AL, Shuey MM, Feng Q, Barker KA, Wei WQ, Luther JM, Stein CM, Chung CP. Co-prescription of Strong CYP1A2 Inhibitors and the Risk of Tizanidine-Associated Hypotension: A Retrospective Cohort Study. Clinical Pharmacology and Therapeutics. PMID 30223305 DOI: 10.1002/Cpt.1233 |
0.698 |
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| 2018 |
Mosley JD, Feng Q, Wells QS, Van Driest SL, Shaffer CM, Edwards TL, Bastarache L, Wei WQ, Davis LK, McCarty CA, Thompson W, Chute CG, Jarvik GP, Gordon AS, Palmer MR, et al. A study paradigm integrating prospective epidemiologic cohorts and electronic health records to identify disease biomarkers. Nature Communications. 9: 3522. PMID 30166544 DOI: 10.1038/S41467-018-05624-4 |
0.784 |
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| 2018 |
Feng Q, Wei WQ, Chung CP, Levinson RT, Sundermann AC, Mosley JD, Bastarache L, Ferguson JF, Cox NJ, Roden DM, Denny JC, Linton MF, Edwards DRV, Stein CM. Relationship between very low low-density lipoprotein cholesterol concentrations not due to statin therapy and risk of type 2 diabetes: A US-based cross-sectional observational study using electronic health records. Plos Medicine. 15: e1002642. PMID 30153257 DOI: 10.1371/Journal.Pmed.1002642 |
0.767 |
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| 2018 |
Zhou W, Nielsen JB, Fritsche LG, Dey R, Gabrielsen ME, Wolford BN, LeFaive J, VandeHaar P, Gagliano SA, Gifford A, Bastarache LA, Wei WQ, Denny JC, Lin M, Hveem K, et al. Efficiently controlling for case-control imbalance and sample relatedness in large-scale genetic association studies. Nature Genetics. PMID 30104761 DOI: 10.1038/S41588-018-0184-Y |
0.602 |
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| 2018 |
Ji X, Bossé Y, Landi MT, Gui J, Xiao X, Qian D, Joubert P, Lamontagne M, Li Y, Gorlov I, de Biasi M, Han Y, Gorlova O, Hung RJ, Wu X, ... Wei WQ, et al. Identification of susceptibility pathways for the role of chromosome 15q25.1 in modifying lung cancer risk. Nature Communications. 9: 3221. PMID 30104567 DOI: 10.1038/S41467-018-05074-Y |
0.44 |
|
| 2018 |
Wei WQ, Li X, Feng Q, Kubo M, Kullo IJ, Peissig PL, Karlson EW, Jarvik GP, Lee MTM, Shang N, Larson EA, Edwards T, Shaffer C, Mosley JD, Maeda S, et al. Variants are Associated with Residual Cardiovascular Risk in Patients Receiving Statins. Circulation. PMID 29703846 DOI: 10.1161/Circulationaha.117.031356 |
0.773 |
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| 2018 |
Bastarache L, Hughey JJ, Hebbring S, Marlo J, Zhao W, Ho WT, Van Driest SL, McGregor TL, Mosley JD, Wells QS, Temple M, Ramirez AH, Carroll R, Osterman T, Edwards T, ... Wei WQ, et al. Phenotype risk scores identify patients with unrecognized Mendelian disease patterns. Science (New York, N.Y.). 359: 1233-1239. PMID 29590070 DOI: 10.1126/Science.Aal4043 |
0.809 |
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| 2018 |
Li X, Meng X, Spiliopoulou A, Timofeeva M, Wei WQ, Gifford A, Shen X, He Y, Varley T, McKeigue P, Tzoulaki I, Wright AF, Joshi P, Denny JC, Campbell H, et al. MR-PheWAS: exploring the causal effect of SUA level on multiple disease outcomes by using genetic instruments in UK Biobank. Annals of the Rheumatic Diseases. PMID 29437585 DOI: 10.1136/Annrheumdis-2017-212534 |
0.598 |
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| 2018 |
Robinson JR, Wei W, Roden DM, Denny JC. Defining Phenotypes from Clinical Data to Drive Genomic Research Annual Review of Biomedical Data Science. 1: 69-92. DOI: 10.1146/ANNUREV-BIODATASCI-080917-013335 |
0.462 |
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| 2018 |
Phillips EJ, Wei W, Shaffer CM, Feng Q, Stone CA, Stein CM, Roden DM, Denny JC. A High-Throughput Genetic Analysis of Common Drug Allergy Labels Using Data from a Large Biobank Journal of Allergy and Clinical Immunology. 141: AB399. DOI: 10.1016/J.Jaci.2017.12.937 |
0.733 |
|
| 2017 |
Denny JC, Van Driest SL, Wei WQ, Roden DM. The influence of big (clinical) data and genomics on precision medicine and drug development. Clinical Pharmacology and Therapeutics. PMID 29171014 DOI: 10.1002/Cpt.951 |
0.712 |
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| 2017 |
Wei WQ, Bastarache LA, Carroll RJ, Marlo JE, Osterman TJ, Gamazon ER, Cox NJ, Roden DM, Denny JC. Evaluating phecodes, clinical classification software, and ICD-9-CM codes for phenome-wide association studies in the electronic health record. Plos One. 12: e0175508. PMID 28686612 DOI: 10.1371/Journal.Pone.0175508 |
0.796 |
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| 2017 |
Feng Q, Wei WQ, Levinson RT, Mosley JD, Stein CM. Replication and fine-mapping of genetic predictors of lipid traits in African-Americans. Journal of Human Genetics. PMID 28539666 DOI: 10.1038/Jhg.2017.55 |
0.719 |
|
| 2016 |
Postmus I, Warren HR, Trompet S, Arsenault BJ, Avery CL, Bis JC, Chasman DI, de Keyser CE, Deshmukh HA, Evans DS, Feng Q, Li X, Smit RA, Smith AV, Sun F, ... Wei WQ, et al. Meta-analysis of genome-wide association studies of HDL cholesterol response to statins. Journal of Medical Genetics. PMID 27587472 DOI: 10.1136/Jmedgenet-2016-103966 |
0.733 |
|
| 2016 |
Teixeira PL, Wei WQ, Cronin RM, Mo H, VanHouten JP, Carroll RJ, LaRose E, Bastarache LA, Rosenbloom ST, Edwards TL, Roden DM, Lasko TA, Dart RA, Nikolai AM, Peissig PL, et al. Evaluating electronic health record data sources and algorithmic approaches to identify hypertensive individuals. Journal of the American Medical Informatics Association : Jamia. PMID 27497800 DOI: 10.1093/Jamia/Ocw071 |
0.79 |
|
| 2016 |
Adefurin A, Darghosian L, Okafor C, Kawai V, Li C, Shah A, Wei WQ, Kurnik D, Stein CM. Alpha2A adrenergic receptor genetic variation contributes to hyperglycemia after myocardial infarction. International Journal of Cardiology. 215: 482-486. PMID 27131769 DOI: 10.1016/J.Ijcard.2016.04.079 |
0.474 |
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| 2016 |
Osterman TJ, Bastarache L, Wei W, Mosley JD, Denny JC. Using a gene-environment interaction study to evaluate risk for lung cancer. Journal of Clinical Oncology. 34: 1524-1524. DOI: 10.1200/Jco.2016.34.15_Suppl.1524 |
0.712 |
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| 2015 |
Wei WQ, Teixeira PL, Mo H, Cronin RM, Warner JL, Denny JC. Combining billing codes, clinical notes, and medications from electronic health records provides superior phenotyping performance. Journal of the American Medical Informatics Association : Jamia. PMID 26338219 DOI: 10.1093/Jamia/Ocv130 |
0.78 |
|
| 2015 |
Mosley JD, Shaffer CM, Van Driest SL, Weeke PE, Wells QS, Karnes JH, Velez Edwards DR, Wei WQ, Teixeira PL, Bastarache L, Crawford DC, Li R, Manolio TA, Bottinger EP, McCarty CA, et al. A genome-wide association study identifies variants in KCNIP4 associated with ACE inhibitor-induced cough. The Pharmacogenomics Journal. PMID 26169577 DOI: 10.1038/Tpj.2015.51 |
0.762 |
|
| 2015 |
Owens AP, Edwards TL, Antoniak S, Geddings JE, Jahangir E, Wei WQ, Denny JC, Boulaftali Y, Bergmeier W, Daugherty A, Sampson UK, Mackman N. Platelet Inhibitors Reduce Rupture in a Mouse Model of Established Abdominal Aortic Aneurysm. Arteriosclerosis, Thrombosis, and Vascular Biology. 35: 2032-41. PMID 26139462 DOI: 10.1161/Atvbaha.115.305537 |
0.537 |
|
| 2015 |
Wei WQ, Denny JC. Extracting research-quality phenotypes from electronic health records to support precision medicine. Genome Medicine. 7: 41. PMID 25937834 DOI: 10.1186/S13073-015-0166-Y |
0.665 |
|
| 2015 |
Bejan CA, Wei WQ, Denny JC. Assessing the role of a medication-indication resource in the treatment relation extraction from clinical text. Journal of the American Medical Informatics Association : Jamia. 22: e162-76. PMID 25336593 DOI: 10.1136/Amiajnl-2014-002954 |
0.612 |
|
| 2014 |
Wei WQ, Feng Q, Weeke P, Bush W, Waitara MS, Iwuchukwu OF, Roden DM, Wilke RA, Stein CM, Denny JC. Creation and Validation of an EMR-based Algorithm for Identifying Major Adverse Cardiac Events while on Statins. Amia Joint Summits On Translational Science Proceedings Amia Summit On Translational Science. 2014: 112-9. PMID 25717410 |
0.768 |
|
| 2014 |
Iwuchukwu OF, Feng Q, Wei WQ, Jiang L, Jiang M, Xu H, Denny JC, Wilke RA, Krauss RM, Roden DM, Stein CM. Genetic variation in the UGT1A locus is associated with simvastatin efficacy in a clinical practice setting. Pharmacogenomics. 15: 1739-1747. PMID 25493567 DOI: 10.2217/Pgs.14.128 |
0.766 |
|
| 2014 |
Postmus I, Trompet S, Deshmukh HA, Barnes MR, Li X, Warren HR, Chasman DI, Zhou K, Arsenault BJ, Donnelly LA, Wiggins KL, Avery CL, Griffin P, Feng Q, Taylor KD, ... Wei WQ, et al. Pharmacogenetic meta-analysis of genome-wide association studies of LDL cholesterol response to statins. Nature Communications. 5: 5068. PMID 25350695 DOI: 10.1038/ncomms6068 |
0.745 |
|
| 2014 |
Wei WQ, Feng Q, Jiang L, Waitara MS, Iwuchukwu OF, Roden DM, Jiang M, Xu H, Krauss RM, Rotter JI, Nickerson DA, Davis RL, Berg RL, Peissig PL, McCarty CA, et al. Characterization of statin dose response in electronic medical records. Clinical Pharmacology and Therapeutics. 95: 331-8. PMID 24096969 DOI: 10.1038/Clpt.2013.202 |
0.742 |
|
| 2013 |
Wei WQ, Mosley JD, Bastarache L, Denny JC. Validation and enhancement of a computable medication indication resource (MEDI) using a large practice-based dataset Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 2013: 1448-1456. PMID 24551419 |
0.579 |
|
| 2013 |
Wei WQ, Cronin RM, Xu H, Lasko TA, Bastarache L, Denny JC. Development of an ensemble resource linking MEDications to their Indications (MEDI). Amia Joint Summits On Translational Science Proceedings Amia Summit On Translational Science. 2013: 172. PMID 24303333 |
0.725 |
|
| 2013 |
Wu Y, Lei J, Wei WQ, Tang B, Denny JC, Rosenbloom ST, Miller RA, Giuse DA, Zheng K, Xu H. Analyzing differences between chinese and english clinical text: a cross-institution comparison of discharge summaries in two languages. Studies in Health Technology and Informatics. 192: 662-6. PMID 23920639 DOI: 10.3233/978-1-61499-289-9-662 |
0.714 |
|
| 2013 |
DeGorter MK, Tirona RG, Schwarz UI, Choi YH, Dresser GK, Suskin N, Myers K, Zou G, Iwuchukwu O, Wei WQ, Wilke RA, Hegele RA, Kim RB. Clinical and pharmacogenetic predictors of circulating atorvastatin and rosuvastatin concentrations in routine clinical care. Circulation. Cardiovascular Genetics. 6: 400-8. PMID 23876492 DOI: 10.1161/Circgenetics.113.000099 |
0.465 |
|
| 2013 |
Wei WQ, Cronin RM, Xu H, Lasko TA, Bastarache L, Denny JC. Development and evaluation of an ensemble resource linking medications to their indications. Journal of the American Medical Informatics Association : Jamia. 20: 954-61. PMID 23576672 DOI: 10.1136/Amiajnl-2012-001431 |
0.72 |
|
| 2013 |
Tao C, Pathak J, Solbrig HR, Wei WQ, Chute CG. Terminology representation guidelines for biomedical ontologies in the semantic web notations. Journal of Biomedical Informatics. 46: 128-38. PMID 23026232 DOI: 10.1016/J.Jbi.2012.09.003 |
0.559 |
|
| 2013 |
Wei WQ, Leibson CL, Ransom JE, Kho AN, Chute CG. The absence of longitudinal data limits the accuracy of high-throughput clinical phenotyping for identifying type 2 diabetes mellitus subjects. International Journal of Medical Informatics. 82: 239-47. PMID 22762862 DOI: 10.1016/J.Ijmedinf.2012.05.015 |
0.569 |
|
| 2012 |
Wei WQ, Leibson CL, Ransom JE, Kho AN, Caraballo PJ, Chai HS, Yawn BP, Pacheco JA, Chute CG. Impact of data fragmentation across healthcare centers on the accuracy of a high-throughput clinical phenotyping algorithm for specifying subjects with type 2 diabetes mellitus. Journal of the American Medical Informatics Association : Jamia. 19: 219-24. PMID 22249968 DOI: 10.1136/Amiajnl-2011-000597 |
0.567 |
|
| 2012 |
Kho AN, Hayes MG, Rasmussen-Torvik L, Pacheco JA, Thompson WK, Armstrong LL, Denny JC, Peissig PL, Miller AW, Wei WQ, Bielinski SJ, Chute CG, Leibson CL, Jarvik GP, Crosslin DR, et al. Use of diverse electronic medical record systems to identify genetic risk for type 2 diabetes within a genome-wide association study. Journal of the American Medical Informatics Association : Jamia. 19: 212-8. PMID 22101970 DOI: 10.1136/Amiajnl-2011-000439 |
0.708 |
|
| 2010 |
Wei WQ, Tao C, Jiang G, Chute CG. A high throughput semantic concept frequency based approach for patient identification: a case study using type 2 diabetes mellitus clinical notes. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 2010: 857-61. PMID 21347100 |
0.577 |
|
| 2010 |
Tao C, Wei WQ, Solbrig HR, Savova G, Chute CG. CNTRO: A Semantic Web Ontology for Temporal Relation Inferencing in Clinical Narratives. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 2010: 787-91. PMID 21347086 |
0.559 |
|
| 2010 |
Tao C, Solbrig HR, Sharma DK, Wei WQ, Savova GK, Chute CG. Time-oriented question answering from clinical narratives using semantic-web techniques Lecture Notes in Computer Science (Including Subseries Lecture Notes in Artificial Intelligence and Lecture Notes in Bioinformatics). 6497: 241-256. DOI: 10.1007/978-3-642-17749-1_16 |
0.371 |
|
| 2009 |
Tao C, Pathak J, Solbrig HR, Wei WQ, Chute CG. LexRDF Model: An RDF-based Unified Model for Heterogeneous Biomedical Ontologies. Ceur Workshop Proceedings. 521: 3. PMID 21804785 |
0.557 |
|
| 2004 |
Wei WQ, Zhu GJ, Xu CL, Han SM, Qi BS, Chen L, Zu SY, Zhou XM, Hu WF, Zhang ZG. The physiology constant database of teen-agers in Beijing. Thescientificworldjournal. 4: 442-8. PMID 15258669 DOI: 10.1100/tsw.2004.98 |
0.424 |
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