| Year |
Citation |
Score |
| 2020 |
Bush WS, Wheeler N, Beaulieu-Jones B, Darabos C. Packaging Biocomputing Software to Maximize Distribution and Reuse. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 25: 739-742. PMID 31797644 |
0.68 |
|
| 2020 |
Crawford DC, Lin J, Cooke Bailey JN, Kinzy T, Sedor JR, O'Toole JF, Bush WS. Frequency of ClinVar Pathogenic Variants in Chronic Kidney Disease Patients Surveyed for Return of Research Results at a Cleveland Public Hospital. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 25: 575-586. PMID 31797629 |
0.44 |
|
| 2020 |
Wheeler NR, Benchek P, Kunkle BW, Hamilton-Nelson KL, Warfe M, Fondran JR, Haines JL, Bush WS. Hadoop and PySpark for reproducibility and scalability of genomic sequencing studies. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 25: 523-534. PMID 31797624 |
0.4 |
|
| 2019 |
Bis JC, Jian X, Kunkle BW, Chen Y, Hamilton-Nelson KL, Bush WS, Salerno WJ, Lancour D, Ma Y, Renton AE, Marcora E, Farrell JJ, Zhao Y, Qu L, Ahmad S, et al. Correction: Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry. PMID 31636380 DOI: 10.1038/s41380-019-0529-7 |
0.4 |
|
| 2019 |
Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, Bush WS, Gifford KA, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Crane PK, Resnick SM, Keene CD, Montine TJ, et al. Sex differences in the genetic predictors of Alzheimer's pathology. Brain : a Journal of Neurology. 142: 2581-2589. PMID 31497858 DOI: 10.1093/brain/awz206 |
0.4 |
|
| 2019 |
Bush WS, Cooke Bailey JN, Beno MF, Crawford DC. Bridging the Gaps in Personalized Medicine Value Assessment: A Review of the Need for Outcome Metrics across Stakeholders and Scientific Disciplines. Public Health Genomics. 1-9. PMID 31454805 DOI: 10.1159/000501974 |
0.44 |
|
| 2019 |
Gardner OK, Wang L, Van Booven D, Whitehead PL, Hamilton-Nelson KL, Adams LD, Starks TD, Hofmann NK, Vance JM, Cuccaro ML, Martin ER, Byrd GS, Haines JL, Bush WS, Beecham GW, et al. RNA editing alterations in a multi-ethnic Alzheimer disease cohort converge on immune and endocytic molecular pathways. Human Molecular Genetics. PMID 31162550 DOI: 10.1093/hmg/ddz110 |
0.4 |
|
| 2018 |
Bis JC, Jian X, Kunkle BW, Chen Y, Hamilton-Nelson KL, Bush WS, Salerno WJ, Lancour D, Ma Y, Renton AE, Marcora E, Farrell JJ, Zhao Y, Qu L, Ahmad S, et al. Whole exome sequencing study identifies novel rare and common Alzheimer's-Associated variants involved in immune response and transcriptional regulation. Molecular Psychiatry. PMID 30108311 DOI: 10.1038/s41380-018-0112-7 |
0.4 |
|
| 2018 |
Igo RP, Hall NB, Malone LL, Hall JB, Truitt B, Qiu F, Tao L, Mupere E, Schnell A, Hawn TR, Bush WS, Joloba M, Boom WH, Stein CM. Fine-mapping analysis of a chromosome 2 region linked to resistance to Mycobacterium tuberculosis infection in Uganda reveals potential regulatory variants. Genes and Immunity. PMID 30100616 DOI: 10.1038/s41435-018-0040-1 |
1 |
|
| 2018 |
Deming Y, Dumitrescu L, Barnes LL, Thambisetty M, Kunkle B, Gifford KA, Bush WS, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Huentelman M, Crane PK, Resnick SM, Keene CD, et al. Sex-specific genetic predictors of Alzheimer's disease biomarkers. Acta Neuropathologica. PMID 29967939 DOI: 10.1007/s00401-018-1881-4 |
0.4 |
|
| 2018 |
Cooke Bailey JN, Crawford DC, Goldenberg A, Slaven A, Pencak J, Schachere M, Bush WS, Sedor JR, O'Toole JF. Willingness to Participate in a National Precision Medicine Cohort: Attitudes of Chronic Kidney Disease Patients at a Cleveland Public Hospital. Journal of Personalized Medicine. 8. PMID 29949895 DOI: 10.3390/jpm8030021 |
0.44 |
|
| 2018 |
Crawford DC, Bailey JNC, Miskimen K, Miron P, McCauley JL, Sedor JR, ƠToole JF, Bush WS. Somatic T-cell Receptor Diversity in a Chronic Kidney Disease PatientPopulation Linked to Electronic Health Records. Amia Joint Summits On Translational Science Proceedings. Amia Joint Summits On Translational Science. 2017: 63-71. PMID 29888042 |
0.44 |
|
| 2018 |
Jones CC, Mercaldo SF, Blume JD, Wenzlaff AS, Schwartz AG, Chen H, Deppen SA, Bush WS, Crawford DC, Chanock SJ, Blot WJ, Grogan EL, Aldrich MC. Racial disparities in lung cancer survival: The contribution of stage, treatment, and ancestry. Journal of Thoracic Oncology : Official Publication of the International Association For the Study of Lung Cancer. PMID 29885480 DOI: 10.1016/j.jtho.2018.05.032 |
0.44 |
|
| 2018 |
Naj AC, Lin H, Vardarajan BN, White S, Lancour D, Ma Y, Schmidt M, Sun F, Butkiewicz M, Bush WS, Kunkle BW, Malamon J, Amin N, Choi SH, Hamilton-Nelson KL, et al. Quality control and integration of genotypes from two calling pipelines for whole genome sequence data in the Alzheimer's disease sequencing project. Genomics. PMID 29857119 DOI: 10.1016/j.ygeno.2018.05.004 |
0.4 |
|
| 2018 |
Hohman TJ, Dumitrescu L, Barnes LL, Thambisetty M, Beecham G, Kunkle B, Gifford KA, Bush WS, Chibnik LB, Mukherjee S, De Jager PL, Kukull W, Crane PK, Resnick SM, Keene CD, et al. Sex-Specific Association of Apolipoprotein E With Cerebrospinal Fluid Levels of Tau. Jama Neurology. PMID 29801024 DOI: 10.1001/jamaneurol.2018.0821 |
0.4 |
|
| 2018 |
Butkiewicz M, Blue E, Leung F, Jian X, Marcora E, Renton A, Kuzma A, Wang LS, Koboldt D, Haines JL, Bush WS. Functional Annotation of genomic variants in studies of Late-Onset Alzheimer's Disease. Bioinformatics (Oxford, England). PMID 29590295 DOI: 10.1093/bioinformatics/bty177 |
0.4 |
|
| 2018 |
Blue EE, Bis JC, Dorschner MO, Tsuang DW, Barral SM, Beecham G, Below JE, Bush WS, Butkiewicz M, Cruchaga C, DeStefano A, Farrer LA, Goate A, Haines J, Jaworski J, et al. Genetic Variation in Genes Underlying Diverse Dementias May Explain a Small Proportion of Cases in the Alzheimer's Disease Sequencing Project. Dementia and Geriatric Cognitive Disorders. 45: 1-17. PMID 29486463 DOI: 10.1159/000485503 |
0.4 |
|
| 2018 |
Sivley RM, Dou X, Meiler J, Bush WS, Capra JA. Comprehensive Analysis of Constraint on the Spatial Distribution of Missense Variants in Human Protein Structures. American Journal of Human Genetics. PMID 29455857 DOI: 10.1016/j.ajhg.2018.01.017 |
0.72 |
|
| 2018 |
Sivley RM, Sheehan JH, Kropski JA, Cogan J, Blackwell TS, Phillips JA, Bush WS, Meiler J, Capra JA. Three-dimensional spatial analysis of missense variants in RTEL1 identifies pathogenic variants in patients with Familial Interstitial Pneumonia. Bmc Bioinformatics. 19: 18. PMID 29361909 DOI: 10.1186/s12859-018-2010-z |
0.72 |
|
| 2018 |
Bush WS, Crawford DC, Briggs F, Freedman D, Sloan C. INTEGRATING COMMUNITY-LEVEL DATA RESOURCES FOR PRECISION MEDICINE RESEARCH. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 23: 618-622. PMID 29218920 |
0.44 |
|
| 2018 |
Fish AE, Crawford DC, Capra JA, Bush WS. Local ancestry transitions modify snp-trait associations. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 23: 424-435. PMID 29218902 |
0.72 |
|
| 2017 |
Goodloe R, Farber-Eger E, Boston J, Crawford DC, Bush WS. Reducing Clinical Noise for Body Mass Index Measures Due to Unit and Transcription Errors in the Electronic Health Record. Amia Joint Summits On Translational Science Proceedings. Amia Joint Summits On Translational Science. 2017: 102-111. PMID 28815116 |
0.44 |
|
| 2017 |
Farber-Eger E, Goodloe R, Boston J, Bush WS, Crawford DC. Extracting Country-of-Origin from Electronic Health Records for Gene- Environment Studies as Part of the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) Study. Amia Joint Summits On Translational Science Proceedings. Amia Joint Summits On Translational Science. 2017: 50-57. PMID 28815105 |
0.44 |
|
| 2017 |
Jones CC, Bush WS, Crawford DC, Wenzlaff AS, Schwartz AG, Wiencke JK, Wrensch MR, Blot WJ, Chanock SJ, Grogan EL, Aldrich MC. Germline genetic variants and lung cancer survival in African Americans. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. PMID 28619829 DOI: 10.1158/1055-9965.EPI-16-0998 |
0.44 |
|
| 2017 |
Fernández-Rhodes L, Gong J, Haessler J, Franceschini N, Graff M, Nishimura KK, Wang Y, Highland HM, Yoneyama S, Bush WS, Goodloe R, Ritchie MD, Crawford D, Gross M, Fornage M, et al. Trans-ethnic fine-mapping of genetic loci for body mass index in the diverse ancestral populations of the Population Architecture using Genomics and Epidemiology (PAGE) Study reveals evidence for multiple signals at established loci. Human Genetics. PMID 28391526 DOI: 10.1007/s00439-017-1787-6 |
0.68 |
|
| 2017 |
Butkiewicz M, Haines JL, Bush WS. Introducing COCOS: codon consequence scanner for annotating reading frame changes induced by stop-lost and frame shift variants. Bioinformatics (Oxford, England). PMID 28122779 DOI: 10.1093/bioinformatics/btw820 |
0.4 |
|
| 2016 |
Zubair N, Graff M, Luis Ambite J, Bush WS, Kichaev G, Lu Y, Manichaikul A, Sheu WH, Absher D, Assimes TL, Bielinski SJ, Bottinger EP, Buzkova P, Chuang LM, Chung RH, et al. Fine-mapping of lipid regions in global populations discovers ethnic-specific signals and refines previously identified lipid loci. Human Molecular Genetics. 25: 5500-5512. PMID 28426890 DOI: 10.1093/hmg/ddw358 |
0.44 |
|
| 2016 |
Bush WS, Crawford DC. Predicting Incident Coronary Heart Disease Many Markers at a Time. Circulation. Cardiovascular Genetics. 9: 472-473. PMID 27998944 DOI: 10.1161/CIRCGENETICS.116.001645 |
0.44 |
|
| 2016 |
Hall JB, Bush WS. Analysis of Heritability Using Genome-Wide Data. Current Protocols in Human Genetics. 91: 1.30.1-1.30.10. PMID 27727439 DOI: 10.1002/cphg.25 |
1 |
|
| 2016 |
Fish AE, Capra JA, Bush WS. Are Interactions between cis-Regulatory Variants Evidence for Biological Epistasis or Statistical Artifacts? American Journal of Human Genetics. PMID 27640306 DOI: 10.1016/j.ajhg.2016.07.022 |
0.72 |
|
| 2016 |
Verma A, Verma SS, Pendergrass SA, Crawford DC, Crosslin DR, Kuivaniemi H, Bush WS, Bradford Y, Kullo I, Bielinski SJ, Li R, Denny JC, Peissig P, Hebbring S, De Andrade M, et al. eMERGE Phenome-Wide Association Study (PheWAS) identifies clinical associations and pleiotropy for stop-gain variants. Bmc Medical Genomics. 9: 32. PMID 27535653 DOI: 10.1186/s12920-016-0191-8 |
0.76 |
|
| 2016 |
Oetjens MT, Bush WS, Denny JC, Birdwell K, Kodaman N, Verma A, Dilks HH, Pendergrass SA, Ritchie MD, Crawford DC. Evidence for extensive pleiotropy among pharmacogenes. Pharmacogenomics. 0. PMID 27249515 DOI: 10.2217/pgs-2015-0007 |
0.76 |
|
| 2016 |
Bartlett J, Predazzi IM, Williams SM, Bush WS, Kim Y, Havas S, Toth PP, Fazio S, Miller M. Is Isolated Low High-Density Lipoprotein Cholesterol a Cardiovascular Disease Risk Factor? New Insights From the Framingham Offspring Study. Circulation. Cardiovascular Quality and Outcomes. PMID 27166203 DOI: 10.1161/CIRCOUTCOMES.115.002436 |
0.76 |
|
| 2016 |
Simonti CN, Vernot B, Bastarache L, Bottinger E, Carrell DS, Chisholm RL, Crosslin DR, Hebbring SJ, Jarvik GP, Kullo IJ, Li R, Pathak J, Ritchie MD, Roden DM, Verma SS, ... ... Bush WS, et al. The phenotypic legacy of admixture between modern humans and Neandertals. Science (New York, N.Y.). 351: 737-41. PMID 26912863 DOI: 10.1126/science.aad2149 |
0.76 |
|
| 2016 |
Bush WS, Oetjens MT, Crawford DC. Unravelling the human genome-phenome relationship using phenome-wide association studies. Nature Reviews. Genetics. 17: 129-45. PMID 26875678 DOI: 10.1038/nrg.2015.36 |
0.76 |
|
| 2016 |
Hohman TJ, Bush WS, Jiang L, Brown-Gentry KD, Torstenson ES, Dudek SM, Mukherjee S, Naj A, Kunkle BW, Ritchie MD, Martin ER, Schellenberg GD, Mayeux R, Farrer LA, Pericak-Vance MA, et al. Discovery of gene-gene interactions across multiple independent data sets of late onset Alzheimer disease from the Alzheimer Disease Genetics Consortium. Neurobiology of Aging. 38: 141-50. PMID 26827652 DOI: 10.1016/j.neurobiolaging.2015.10.031 |
0.76 |
|
| 2016 |
Van Driest SL, Wells QS, Stallings S, Bush WS, Gordon A, Nickerson DA, Kim JH, Crosslin DR, Jarvik GP, Carrell DS, Ralston JD, Larson EB, Bielinski SJ, Olson JE, Ye Z, et al. Association of Arrhythmia-Related Genetic Variants With Phenotypes Documented in Electronic Medical Records. Jama. 315: 47-57. PMID 26746457 DOI: 10.1001/jama.2015.17701 |
0.76 |
|
| 2016 |
Butkiewicz M, Bush WS. In Silico Functional Annotation of Genomic Variation. Current Protocols in Human Genetics / Editorial Board, Jonathan L. Haines ... [Et Al.]. 88: 6.15.1-6.15.17. PMID 26724722 DOI: 10.1002/0471142905.hg0615s88 |
0.4 |
|
| 2015 |
Dumitrescu L, Restrepo NA, Goodloe R, Boston J, Farber-Eger E, Pendergrass SA, Bush WS, Crawford DC. Towards a phenome-wide catalog of human clinical traits impacted by genetic ancestry. Biodata Mining. 8: 35. PMID 26566401 DOI: 10.1186/s13040-015-0068-y |
0.44 |
|
| 2015 |
Hall JB, Cooke Bailey JN, Hoffman JD, Pericak-Vance MA, Scott WK, Kovach JL, Schwartz SG, Agarwal A, Brantley MA, Haines JL, Bush WS. Estimating cumulative pathway effects on risk for age-related macular degeneration using mixed linear models. Bmc Bioinformatics. 16: 329. PMID 26467978 DOI: 10.1186/s12859-015-0760-4 |
1 |
|
| 2015 |
Wiley LK, Moretz JD, Denny JC, Peterson JF, Bush WS. Phenotyping Adverse Drug Reactions: Statin-Related Myotoxicity. Amia Joint Summits On Translational Science Proceedings Amia Summit On Translational Science. 2015: 466-70. PMID 26306287 |
0.44 |
|
| 2015 |
Crawford DC, Goodloe R, Farber-Eger E, Boston J, Pendergrass SA, Haines JL, Ritchie MD, Bush WS. Leveraging Epidemiologic and Clinical Collections for Genomic Studies of Complex Traits. Human Heredity. 79: 137-46. PMID 26201699 DOI: 10.1159/000381805 |
0.68 |
|
| 2015 |
Hohman TJ, Chibnik L, Bush WS, Jefferson AL, De Jaeger PL, Thornton-Wells TA, Bennett DA, Schneider JA. GSK3β Interactions with Amyloid Genes: An Autopsy Verification and Extension. Neurotoxicity Research. 28: 232-8. PMID 26194614 DOI: 10.1007/s12640-015-9541-0 |
0.32 |
|
| 2015 |
Predazzi IM, Sobota RS, Sanna S, Bush WS, Bartlett J, Lilley JS, Linton MF, Schlessinger D, Cucca F, Fazio S, Williams SM. Sex-Specific Parental Effects on Offspring Lipid Levels. Journal of the American Heart Association. 4. PMID 26126546 DOI: 10.1161/JAHA.115.001951 |
0.68 |
|
| 2015 |
Chapman KA, Bush WS, Zhang Z. Gene expression in cell lines from propionic acidemia patients, carrier parents, and controls. Molecular Genetics and Metabolism. PMID 25963861 DOI: 10.1016/j.ymgme.2015.05.004 |
0.76 |
|
| 2015 |
Kocarnik JM, Park SL, Han J, Dumitrescu L, Cheng I, Wilkens LR, Schumacher FR, Kolonel L, Carlson CS, Crawford DC, Goodloe RJ, Dilks HH, Baker P, Richardson D, Matise TC, ... ... Bush WS, et al. Pleiotropic and sex-specific effects of cancer GWAS SNPs on melanoma risk in the population architecture using genomics and epidemiology (PAGE) study. Plos One. 10: e0120491. PMID 25789475 DOI: 10.1371/journal.pone.0120491 |
0.76 |
|
| 2015 |
Kayton NS, Poffenberger G, Henske J, Dai C, Thompson C, Aramandla R, Shostak A, Nicholson W, Brissova M, Bush WS, Powers AC. Human islet preparations distributed for research exhibit a variety of insulin-secretory profiles. American Journal of Physiology. Endocrinology and Metabolism. 308: E592-602. PMID 25648831 DOI: 10.1152/ajpendo.00437.2014 |
0.76 |
|
| 2015 |
Kolek MJ, Muehlschlegel JD, Bush WS, Parvez B, Murray KT, Stein CM, Shoemaker MB, Blair MA, Kor KC, Roden DM, Donahue BS, Fox AA, Shernan SK, Collard CD, Body SC, et al. Genetic and clinical risk prediction model for postoperative atrial fibrillation. Circulation. Arrhythmia and Electrophysiology. 8: 25-31. PMID 25567478 DOI: 10.1161/CIRCEP.114.002300 |
0.76 |
|
| 2014 |
Bush WS, Haines JL. Genotype Correlation Analysis Reveals Pathway-Based Functional Disequilibrium and Potential Epistasis in the Human Interactome. Applications of Evolutionary Computation : 17th European Conference, Evoapplications 2014, Granada, Spain, April 23-25, 2014 : Revised Selected Papers. Evoapplications (Conference) (17th : 2014 : Granada, Spain). 8602: 890-901. PMID 28393142 DOI: 10.1007/978-3-662-45523-4_72 |
0.4 |
|
| 2014 |
Xie W, Kantarcioglu M, Bush WS, Crawford D, Denny JC, Heatherly R, Malin BA. SecureMA: protecting participant privacy in genetic association meta-analysis. Bioinformatics (Oxford, England). 30: 3334-41. PMID 25147357 DOI: 10.1093/bioinformatics/btu561 |
0.76 |
|
| 2014 |
Park SL, Caberto CP, Lin Y, Goodloe RJ, Dumitrescu L, Love SA, Matise TC, Hindorff LA, Fowke JH, Schumacher FR, Beebe-Dimmer J, Chen C, Hou L, Thomas F, Deelman E, ... ... Bush WS, et al. Association of cancer susceptibility variants with risk of multiple primary cancers: The population architecture using genomics and epidemiology study. Cancer Epidemiology, Biomarkers & Prevention : a Publication of the American Association For Cancer Research, Cosponsored by the American Society of Preventive Oncology. 23: 2568-78. PMID 25139936 DOI: 10.1158/1055-9965.EPI-14-0129 |
0.76 |
|
| 2014 |
Crawford DC, Crosslin DR, Tromp G, Kullo IJ, Kuivaniemi H, Hayes MG, Denny JC, Bush WS, Haines JL, Roden DM, McCarty CA, Jarvik GP, Ritchie MD. eMERGEing progress in genomics-the first seven years. Frontiers in Genetics. 5: 184. PMID 24987407 DOI: 10.3389/fgene.2014.00184 |
0.76 |
|
| 2014 |
Hall JB, Dumitrescu L, Dilks HH, Crawford DC, Bush WS. Accuracy of administratively-assigned ancestry for diverse populations in an electronic medical record-linked biobank. Plos One. 9: e99161. PMID 24896101 DOI: 10.1371/journal.pone.0099161 |
1 |
|
| 2014 |
De R, Bush WS, Moore JH. Bioinformatics challenges in genome-wide association studies (GWAS). Methods in Molecular Biology (Clifton, N.J.). 1168: 63-81. PMID 24870131 DOI: 10.1007/978-1-4939-0847-9_5 |
0.44 |
|
| 2014 |
Anderson LL, Thompson CH, Hawkins NA, Nath RD, Petersohn AA, Rajamani S, Bush WS, Frankel WN, Vanoye CG, Kearney JA, George AL. Antiepileptic activity of preferential inhibitors of persistent sodium current. Epilepsia. 55: 1274-83. PMID 24862204 DOI: 10.1111/epi.12657 |
0.76 |
|
| 2014 |
Setiawan VW, Schumacher F, Prescott J, Haessler J, Malinowski J, Wentzensen N, Yang H, Chanock S, Brinton L, Hartge P, Lissowska J, Park SL, Cheng I, Bush WS, Crawford DC, et al. Cross-cancer pleiotropic analysis of endometrial cancer: PAGE and E2C2 consortia. Carcinogenesis. 35: 2068-73. PMID 24832084 DOI: 10.1093/carcin/bgu107 |
0.76 |
|
| 2014 |
Mitchell SL, Hall JB, Goodloe RJ, Boston J, Farber-Eger E, Pendergrass SA, Bush WS, Crawford DC. Investigating the relationship between mitochondrial genetic variation and cardiovascular-related traits to develop a framework for mitochondrial phenome-wide association studies. Biodata Mining. 7: 6. PMID 24731735 DOI: 10.1186/1756-0381-7-6 |
1 |
|
| 2014 |
Park SL, Fesinmeyer MD, Timofeeva M, Caberto CP, Kocarnik JM, Han Y, Love SA, Young A, Dumitrescu L, Lin Y, Goodloe R, Wilkens LR, Hindorff L, Fowke JH, Carty C, ... ... Bush WS, et al. Pleiotropic associations of risk variants identified for other cancers with lung cancer risk: the PAGE and TRICL consortia. Journal of the National Cancer Institute. 106: dju061. PMID 24681604 DOI: 10.1093/jnci/dju061 |
0.76 |
|
| 2014 |
Lim U, Kocarnik JM, Bush WS, Matise TC, Caberto C, Park SL, Carlson CS, Deelman E, Duggan D, Fesinmeyer M, Haiman CA, Henderson BE, Hindorff LA, Kolonel LN, Peters U, et al. Pleiotropy of cancer susceptibility variants on the risk of non-Hodgkin lymphoma: the PAGE consortium. Plos One. 9: e89791. PMID 24598796 DOI: 10.1371/journal.pone.0089791 |
0.76 |
|
| 2014 |
Kocarnik JM, Park SL, Han J, Dumitrescu L, Cheng I, Wilkens LR, Schumacher FR, Kolonel L, Carlson CS, Crawford DC, Goodloe RJ, Dilks H, Baker P, Richardson D, Ambite JL, ... ... Bush WS, et al. Replication of associations between GWAS SNPs and melanoma risk in the Population Architecture Using Genomics and Epidemiology (PAGE) Study. The Journal of Investigative Dermatology. 134: 2049-52. PMID 24480881 DOI: 10.1038/jid.2014.53 |
0.76 |
|
| 2014 |
Oetjens M, Bush WS, Birdwell KA, Dilks HH, Bowton EA, Denny JC, Wilke RA, Roden DM, Crawford DC. Utilization of an EMR-biorepository to identify the genetic predictors of calcineurin-inhibitor toxicity in heart transplant recipients. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 253-264. PMID 24297552 |
0.76 |
|
| 2014 |
Cheng I, Kocarnik JM, Dumitrescu L, Lindor NM, Chang-Claude J, Avery CL, Caberto CP, Love SA, Slattery ML, Chan AT, Baron JA, Hindorff LA, Park SL, Schumacher FR, Hoffmeister M, ... ... Bush WS, et al. Pleiotropic effects of genetic risk variants for other cancers on colorectal cancer risk: PAGE, GECCO and CCFR consortia. Gut. 63: 800-7. PMID 23935004 DOI: 10.1136/gutjnl-2013-305189 |
0.76 |
|
| 2013 |
Sivley RM, Fish AE, Bush WS. Knowledge-constrained K-medoids Clustering of Regulatory Rare Alleles for Burden Tests. Evolutionary Computation, Machine Learning and Data Mining in Bioinformatics. Evobio (Conference), Author. 7833: 35-42. PMID 25541630 DOI: 10.1007/978-3-642-37189-9_4 |
0.76 |
|
| 2013 |
Davis MF, Sriram S, Bush WS, Denny JC, Haines JL. Automated extraction of clinical traits of multiple sclerosis in electronic medical records. Journal of the American Medical Informatics Association : Jamia. 20: e334-40. PMID 24148554 DOI: 10.1136/amiajnl-2013-001999 |
0.76 |
|
| 2013 |
Bruehl S, Denton JS, Lonergan D, Koran ME, Chont M, Sobey C, Fernando S, Bush WS, Mishra P, Thornton-Wells TA. Associations between KCNJ6 (GIRK2) gene polymorphisms and pain-related phenotypes. Pain. 154: 2853-9. PMID 23994450 DOI: 10.1016/j.pain.2013.08.026 |
0.76 |
|
| 2013 |
Wiley LK, Sivley RM, Bush WS. Rapid storage and retrieval of genomic intervals from a relational database system using nested containment lists. Database : the Journal of Biological Databases and Curation. 2013: bat056. PMID 23894185 DOI: 10.1093/database/bat056 |
0.72 |
|
| 2013 |
Cummings AC, Torstenson E, Davis MF, D'Aoust LN, Scott WK, Pericak-Vance MA, Bush WS, Haines JL. Evaluating power and type 1 error in large pedigree analyses of binary traits. Plos One. 8: e62615. PMID 23658753 DOI: 10.1371/journal.pone.0062615 |
0.76 |
|
| 2013 |
Predazzi IM, Rokas A, Deinard A, Schnetz-Boutaud N, Williams ND, Bush WS, Tacconelli A, Friedrich K, Fazio S, Novelli G, Haines JL, Sirugo G, Williams SM. Putting pleiotropy and selection into context defines a new paradigm for interpreting genetic data. Circulation. Cardiovascular Genetics. 6: 299-307. PMID 23616601 DOI: 10.1161/CIRCGENETICS.113.000126 |
0.76 |
|
| 2013 |
Bush WS, Boston J, Pendergrass SA, Dumitrescu L, Goodloe R, Brown-Gentry K, Wilson S, McClellan B, Torstenson E, Basford MA, Spencer KL, Ritchie MD, Crawford DC. Enabling high-throughput genotype-phenotype associations in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project as part of the Population Architecture using Genomics and Epidemiology (PAGE) study. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 373-84. PMID 23424142 |
0.76 |
|
| 2013 |
Crawford DC, Goodloe R, Brown-Gentry K, Wilson S, Roberson J, Gillani NB, Ritchie MD, Dilks HH, Bush WS. Characterization of the Metabochip in diverse populations from the International HapMap Project in the Epidemiologic Architecture for Genes Linked to Environment (EAGLE) project. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 188-99. PMID 23424124 |
0.68 |
|
| 2013 |
Wiley LK, Shah A, Xu H, Bush WS. ICD-9 tobacco use codes are effective identifiers of smoking status. Journal of the American Medical Informatics Association : Jamia. 20: 652-8. PMID 23396545 DOI: 10.1136/amiajnl-2012-001557 |
0.76 |
|
| 2013 |
Kodaman N, Aldrich MC, Smith JR, Signorello LB, Bradley K, Breyer J, Cohen SS, Long J, Cai Q, Giles J, Bush WS, Blot WJ, Matthews CE, Williams SM. A small number of candidate gene SNPs reveal continental ancestry in African Americans. Annals of Human Genetics. 77: 56-66. PMID 23278390 DOI: 10.1111/j.1469-1809.2012.00738.x |
0.76 |
|
| 2012 |
Bush WS, Moore JH. Chapter 11: Genome-wide association studies. Plos Computational Biology. 8: e1002822. PMID 23300413 DOI: 10.1371/journal.pcbi.1002822 |
0.44 |
|
| 2012 |
Buchanan CC, Torstenson ES, Bush WS, Ritchie MD. A comparison of cataloged variation between International HapMap Consortium and 1000 Genomes Project data. Journal of the American Medical Informatics Association : Jamia. 19: 289-94. PMID 22319179 DOI: 10.1136/amiajnl-2011-000652 |
0.68 |
|
| 2011 |
Zuvich RL, Bush WS, McCauley JL, Beecham AH, De Jager PL, Ivinson AJ, Compston A, Hafler DA, Hauser SL, Sawcer SJ, Pericak-Vance MA, Barcellos LF, Mortlock DP, Haines JL. Interrogating the complex role of chromosome 16p13.13 in multiple sclerosis susceptibility: independent genetic signals in the CIITA-CLEC16A-SOCS1 gene complex. Human Molecular Genetics. 20: 3517-24. PMID 21653641 DOI: 10.1093/hmg/ddr250 |
0.76 |
|
| 2011 |
Yaspan BL, Bush WS, Torstenson ES, Ma D, Pericak-Vance MA, Ritchie MD, Sutcliffe JS, Haines JL. Genetic analysis of biological pathway data through genomic randomization. Human Genetics. 129: 563-71. PMID 21279722 DOI: 10.1007/s00439-011-0956-2 |
0.76 |
|
| 2011 |
Turner SD, Bush WS. Multivariate analysis of regulatory SNPs: empowering personal genomics by considering cis-epistasis and heterogeneity. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 276-87. PMID 21121055 |
0.76 |
|
| 2010 |
Ritchie MD, Bush WS. Genome simulation approaches for synthesizing in silico datasets for human genomics. Advances in Genetics. 72: 1-24. PMID 21029846 DOI: 10.1016/B978-0-12-380862-2.00001-1 |
0.68 |
|
| 2010 |
Bush WS, Sawcer SJ, de Jager PL, Oksenberg JR, McCauley JL, Pericak-Vance MA, Haines JL. Evidence for polygenic susceptibility to multiple sclerosis--the shape of things to come. American Journal of Human Genetics. 86: 621-5. PMID 20362272 DOI: 10.1016/j.ajhg.2010.02.027 |
0.4 |
|
| 2010 |
Bush WS, Dudek SM, Ritchie MD. Visualizing SNP statistics in the context of linkage disequilibrium using LD-Plus. Bioinformatics (Oxford, England). 26: 578-9. PMID 20130027 DOI: 10.1093/bioinformatics/btp678 |
0.76 |
|
| 2009 |
Bush WS, Chen G, Torstenson ES, Ritchie MD. LD-spline: mapping SNPs on genotyping platforms to genomic regions using patterns of linkage disequilibrium. Biodata Mining. 2: 7. PMID 19954552 DOI: 10.1186/1756-0381-2-7 |
0.68 |
|
| 2009 |
Bush WS, Crawford DC, Alexander C, George AL, Roden DM, Ritchie MD. Genetic variation in the rhythmonome: ethnic variation and haplotype structure in candidate genes for arrhythmias. Pharmacogenomics. 10: 1043-53. PMID 19530973 DOI: 10.2217/pgs.09.67 |
0.76 |
|
| 2009 |
Bush WS, Dudek SM, Ritchie MD. Biofilter: a knowledge-integration system for the multi-locus analysis of genome-wide association studies. Pacific Symposium On Biocomputing. Pacific Symposium On Biocomputing. 368-79. PMID 19209715 |
0.76 |
|
| 2008 |
Bush WS, Edwards TL, Dudek SM, McKinney BA, Ritchie MD. Alternative contingency table measures improve the power and detection of multifactor dimensionality reduction. Bmc Bioinformatics. 9: 238. PMID 18485205 DOI: 10.1186/1471-2105-9-238 |
0.76 |
|
| 2007 |
Bush WS, Thornton-Wells TA, Ritchie MD. Association Rule Discovery Has the Ability to Model Complex Genetic Effects. Ieee Symposium On Computational Intelligence and Data Mining Ieee Symposium On Computational Intelligence and Data Mining. 2007: 624-629. PMID 20953276 DOI: 10.1109/CIDM.2007.368934 |
0.76 |
|
| 2007 |
Ritchie MD, Motsinger AA, Bush WS, Coffey CS, Moore JH. Genetic Programming Neural Networks: A Powerful Bioinformatics Tool for Human Genetics. Applied Soft Computing. 7: 471-479. PMID 20948988 DOI: 10.1016/j.asoc.2006.01.013 |
0.68 |
|
| 2007 |
Ritchie MD, Bartlett J, Bush WS, Edwards TL, Motsinger AA, Torstenson ES. Exploring epistasis in candidate genes for rheumatoid arthritis. Bmc Proceedings. 1: S70. PMID 18466572 |
0.68 |
|
| 2007 |
Bartlett CW, Vieland VJ, Bartlett J, Bell JT, Bhattacharjee S, Clerget-Darpoux F, Bush WS, Edwards TL, Gao G, Halder I, Huang Y, Kotti S, Larkin EK, Li H, Motsinger AA, et al. Discussing gene-gene interaction: warning--translating equations to English may result in jabberwocky. Genetic Epidemiology. 31: S61-7. PMID 18046759 DOI: 10.1002/gepi.20281 |
0.68 |
|
| 2007 |
Velez DR, White BC, Motsinger AA, Bush WS, Ritchie MD, Williams SM, Moore JH. A balanced accuracy function for epistasis modeling in imbalanced datasets using multifactor dimensionality reduction. Genetic Epidemiology. 31: 306-15. PMID 17323372 DOI: 10.1002/gepi.20211 |
0.76 |
|
| 2006 |
Bush WS, Dudek SM, Ritchie MD. Parallel multifactor dimensionality reduction: a tool for the large-scale analysis of gene-gene interactions. Bioinformatics (Oxford, England). 22: 2173-4. PMID 16809395 DOI: 10.1093/bioinformatics/btl347 |
0.76 |
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