Brian H. Shirts, Ph.D. - Publications

2006 University of Pittsburgh, Pittsburgh, PA, United States 
Genetics, Clinical Psychology, Immunology, Pathology

40 high-probability publications. We are testing a new system for linking publications to authors. You can help! If you notice any inaccuracies, please sign in and mark papers as correct or incorrect matches. If you identify any major omissions or other inaccuracies in the publication list, please let us know.

Year Citation  Score
2016 Garrett LT, Hickman N, Jacobson A, Bennett RL, Amendola LM, Rosenthal EA, Shirts BH. Family Studies for Classification of Variants of Uncertain Classification: Current Laboratory Clinical Practice and a New Web-Based Educational Tool. Journal of Genetic Counseling. PMID 27422780 DOI: 10.1007/S10897-016-9993-2  0.32
2016 Green RC, Goddard KA, Jarvik GP, Amendola LM, Appelbaum PS, Berg JS, Bernhardt BA, Biesecker LG, Biswas S, Blout CL, Bowling KM, Brothers KB, Burke W, Caga-Anan CF, Chinnaiyan AM, ... ... Shirts B, et al. Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine. American Journal of Human Genetics. PMID 27181682 DOI: 10.1016/J.Ajhg.2016.04.011  0.32
2016 Aziz A, Kawamoto K, Eilbeck K, Williams MS, Freimuth RR, Hoffman MA, Rasmussen LV, Overby CL, Shirts BH, Hoffman JM, Welch BM. The Genomic CDS Sandbox: An Assessment Among Domain Experts. Journal of Biomedical Informatics. PMID 26778834 DOI: 10.1016/J.Jbi.2015.12.019  0.32
2015 Nishimura AA, Shirts BH, Salama J, Smith JW, Devine B, Tarczy-Hornoch P. Physician perspectives of CYP2C19 and clopidogrel drug-gene interaction active clinical decision support alerts. International Journal of Medical Informatics. PMID 26642939 DOI: 10.1016/J.Ijmedinf.2015.11.004  0.32
2015 Gallego CJ, Perez ML, Burt A, Amendola LM, Shirts BH, Pritchard CC, Hisama FM, Bennett RL, Veenstra DL, Jarvik GP. Next Generation Sequencing in the Clinic: a Patterns of Care Study in a Retrospective Cohort of Subjects Referred to a Genetic Medicine Clinic for Suspected Lynch Syndrome. Journal of Genetic Counseling. PMID 26637299 DOI: 10.1007/S10897-015-9902-0  0.32
2015 Shirts BH, Salama JS, Aronson SJ, Chung WK, Gray SW, Hindorff LA, Jarvik GP, Plon SE, Stoffel EM, Tarczy-Hornoch PZ, Van Allen EM, Weck KE, Chute CG, Freimuth RR, Grundmeier RW, et al. CSER and eMERGE: current and potential state of the display of genetic information in the electronic health record. Journal of the American Medical Informatics Association : Jamia. PMID 26142422 DOI: 10.1093/Jamia/Ocv065  0.32
2015 Gallego CJ, Shirts BH, Bennette CS, Guzauskas G, Amendola LM, Horike-Pyne M, Hisama FM, Pritchard CC, Grady WM, Burke W, Jarvik GP, Veenstra DL. Next-Generation Sequencing Panels for the Diagnosis of Colorectal Cancer and Polyposis Syndromes: A Cost-Effectiveness Analysis. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 33: 2084-91. PMID 25940718 DOI: 10.1200/Jco.2014.59.3665  0.32
2015 Nishimura AA, Shirts BH, Dorschner MO, Amendola LM, Smith JW, Jarvik GP, Tarczy-Hornoch P. Development of clinical decision support alerts for pharmacogenomic incidental findings from exome sequencing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 25741865 DOI: 10.1038/Gim.2015.5  0.32
2015 Amendola LM, Dorschner MO, Robertson PD, Salama JS, Hart R, Shirts BH, Murray ML, Tokita MJ, Gallego CJ, Kim DS, Bennett JT, Crosslin DR, Ranchalis J, Jones KL, Rosenthal EA, et al. Actionable exomic incidental findings in 6503 participants: challenges of variant classification. Genome Research. 25: 305-15. PMID 25637381 DOI: 10.1101/Gr.183483.114  0.32
2014 Overby CL, Rasmussen LV, Hartzler A, Connolly JJ, Peterson JF, Hedberg RE, Freimuth RR, Shirts BH, Denny JC, Larson EB, Chute CG, Jarvik GP, Ralston JD, Shuldiner AR, Starren J, et al. A Template for Authoring and Adapting Genomic Medicine Content in the eMERGE Infobutton Project. Amia ... Annual Symposium Proceedings / Amia Symposium. Amia Symposium. 2014: 944-53. PMID 25954402  0.32
2014 Hauser RG, Shirts BH. Do we now know what inappropriate laboratory utilization is? An expanded systematic review of laboratory clinical audits. American Journal of Clinical Pathology. 141: 774-83. PMID 24838320 DOI: 10.1309/Ajcpx1Hiem4Klgnu  0.32
2014 Dorschner MO, Amendola LM, Shirts BH, Kiedrowski L, Salama J, Gordon AS, Fullerton SM, Tarczy-Hornoch P, Byers PH, Jarvik GP. Refining the structure and content of clinical genomic reports. American Journal of Medical Genetics. Part C, Seminars in Medical Genetics. 166: 85-92. PMID 24616401 DOI: 10.1002/Ajmg.C.31395  0.32
2014 Shirts BH, Jacobson A, Jarvik GP, Browning BL. Large numbers of individuals are required to classify and define risk for rare variants in known cancer risk genes. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 529-34. PMID 24357849 DOI: 10.1038/Gim.2013.187  0.32
2013 Dorschner MO, Amendola LM, Turner EH, Robertson PD, Shirts BH, Gallego CJ, Bennett RL, Jones KL, Tokita MJ, Bennett JT, Kim JH, Rosenthal EA, Kim DS, Tabor HK, et al. Actionable, pathogenic incidental findings in 1,000 participants' exomes. American Journal of Human Genetics. 93: 631-40. PMID 24055113 DOI: 10.1016/J.Ajhg.2013.08.006  0.32
2013 Shirts BH, Bennett ST, Jackson BR. Using patients like my patient for clinical decision support: institution-specific probability of celiac disease diagnosis using simplified near-neighbor classification. Journal of General Internal Medicine. 28: 1565-72. PMID 23645451 DOI: 10.1007/S11606-013-2443-Z  0.32
2013 Shirts BH, Welch RJ, Couturier MR. Seropositivity rates for measles, mumps, and rubella IgG and costs associated with testing and revaccination. Clinical and Vaccine Immunology : Cvi. 20: 443-5. PMID 23345583 DOI: 10.1128/Cvi.00503-12  0.32
2012 Shirts BH, Rodgers GM, Smock KJ. Prothrombin time, activated partial thromboplastin time and dilute Russell's Viper Venom times are not shorter in patients with the prothrombin G20210A mutation, and dilute Russell's Viper Venom time may be longer. Thrombosis Research. 130: e134-8. PMID 22542363 DOI: 10.1016/J.Thromres.2012.04.002  0.32
2012 Shirts BH, Howard MT, Hasstedt SJ, Nanjee MN, Knight S, Carlquist JF, Anderson JL, Hopkins PN, Hunt SC. Vitamin D dependent effects of APOA5 polymorphisms on HDL cholesterol. Atherosclerosis. 222: 167-74. PMID 22425169 DOI: 10.1016/J.Atherosclerosis.2012.02.030  0.32
2011 Furtado LV, Thaker HM, Erickson LK, Shirts BH, Opitz JM. Cervical ribs are more prevalent in stillborn fetuses than in live-born infants and are strongly associated with fetal aneuploidy. Pediatric and Developmental Pathology : the Official Journal of the Society For Pediatric Pathology and the Paediatric Pathology Society. 14: 431-7. PMID 21711209 DOI: 10.2350/11-01-0974-Oa.1  0.32
2011 Shirts BH, Hasstedt SJ, Hopkins PN, Hunt SC. Evaluation of the gene-age interactions in HDL cholesterol, LDL cholesterol, and triglyceride levels: the impact of the SORT1 polymorphism on LDL cholesterol levels is age dependent. Atherosclerosis. 217: 139-41. PMID 21466885 DOI: 10.1016/J.Atherosclerosis.2011.03.008  0.32
2011 Shirts BH, Wilson AR, Jackson BR. Partitioning reference intervals by use of genetic information. Clinical Chemistry. 57: 475-81. PMID 21164036 DOI: 10.1373/Clinchem.2010.154005  0.32
2010 Shirts BH, Burt RW, Mulvihill SJ, Cannon-Albright LA. A population-based description of familial clustering of pancreatic cancer. Clinical Gastroenterology and Hepatology : the Official Clinical Practice Journal of the American Gastroenterological Association. 8: 812-6. PMID 20570637 DOI: 10.1016/J.Cgh.2010.05.012  0.32
2010 Prasad KM, Bamne MN, Shirts BH, Goradia D, Mannali V, Pancholi KM, Xue B, McClain L, Yolken RH, Keshavan MS, Nimgaonkar VL. Grey matter changes associated with host genetic variation and exposure to Herpes Simplex Virus 1 (HSV1) in first episode schizophrenia. Schizophrenia Research. 118: 232-9. PMID 20138739 DOI: 10.1016/J.Schres.2010.01.007  0.32
2009 Shirts BH, Gundlapalli AV, Jackson B. Pilot study of linking Web-based supplemental interpretive information to laboratory test reports. American Journal of Clinical Pathology. 132: 818-23. PMID 19926571 DOI: 10.1309/Ajcpt7Chn8Dlfvgu  0.32
2009 Shirts BH, Perera S, Hanlon JT, Roumani YF, Studenski SA, Nace DA, Becich MJ, Handler SM. Provider management of and satisfaction with laboratory testing in the nursing home setting: results of a national internet-based survey. Journal of the American Medical Directors Association. 10: 161-166.e3. PMID 19233055 DOI: 10.1016/J.Jamda.2008.08.018  0.32
2008 Shirts BH, Parker LS. Changing interpretations, stable genes: responsibilities of patients, professionals, and policy makers in the clinical interpretation of complex genetic information. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 10: 778-83. PMID 18941419 DOI: 10.1097/Gim.0B013E31818Bb38F  0.32
2008 Shirts BH, Prasad KM, Pogue-Geile MF, Dickerson F, Yolken RH, Nimgaonkar VL. Antibodies to cytomegalovirus and Herpes Simplex Virus 1 associated with cognitive function in schizophrenia. Schizophrenia Research. 106: 268-74. PMID 18801645 DOI: 10.1016/J.Schres.2008.07.017  0.32
2008 Handler SM, Shirts BH, Perera S, Becich MJ, Castle NG, Hanlon JT. Frequency of laboratory monitoring of chronic medications administered to nursing facility residents: results of a national Internet-based study. The Consultant Pharmacist : the Journal of the American Society of Consultant Pharmacists. 23: 387-95. PMID 18540792 DOI: 10.4140/Tcp.N.2008.387  0.32
2008 Shirts BH, Wood J, Yolken RH, Nimgaonkar VL. Comprehensive evaluation of positional candidates in the IL-18 pathway reveals suggestive associations with schizophrenia and herpes virus seropositivity. American Journal of Medical Genetics. Part B, Neuropsychiatric Genetics : the Official Publication of the International Society of Psychiatric Genetics. 147: 343-50. PMID 18092318 DOI: 10.1002/Ajmg.B.30603  0.32
2008 Talkowski ME, Kirov G, Bamne M, Georgieva L, Torres G, Mansour H, Chowdari KV, Milanova V, Wood J, McClain L, Prasad K, Shirts B, Zhang J, O'Donovan MC, Owen MJ, et al. A network of dopaminergic gene variations implicated as risk factors for schizophrenia. Human Molecular Genetics. 17: 747-58. PMID 18045777 DOI: 10.1093/Hmg/Ddm347  0.32
2007 Shirts BH, Kim JJ, Reich S, Dickerson FB, Yolken RH, Devlin B, Nimgaonkar VL. Polymorphisms in MICB are associated with human herpes virus seropositivity and schizophrenia risk. Schizophrenia Research. 94: 342-53. PMID 17561376 DOI: 10.1016/J.Schres.2007.04.021  0.32
2007 Kim JJ, Shirts BH, Dayal M, Bacanu SA, Wood J, Xie W, Zhang X, Chowdari KV, Yolken R, Devlin B, Nimgaonkar VL. Are exposure to cytomegalovirus and genetic variation on chromosome 6p joint risk factors for schizophrenia? Annals of Medicine. 39: 145-53. PMID 17453677 DOI: 10.1080/07853890601083808  0.32
2007 Prasad KM, Shirts BH, Yolken RH, Keshavan MS, Nimgaonkar VL. Brain morphological changes associated with exposure to HSV1 in first-episode schizophrenia. Molecular Psychiatry. 12: 105-13, 1. PMID 17033628 DOI: 10.1038/Sj.Mp.4001915  0.32
2007 Prasad KMR, Shirts BH, Yolken RH, Keshavan MS, Nimgaonkar VL. HSV1 exposure affects prefrontal cortical structure in schizophrenia patients Molecular Psychiatry. 12: 1. DOI: 10.1038/Sj.Mp.4001942  0.32
2006 Shirts BH, Wood J, Yolken RH, Nimgaonkar VL. Association study of IL10, IL1beta, and IL1RN and schizophrenia using tag SNPs from a comprehensive database: suggestive association with rs16944 at IL1beta. Schizophrenia Research. 88: 235-44. PMID 16905295 DOI: 10.1016/J.Schres.2006.06.037  0.32
2006 Shirts BH, Bamne M, Kim JJ, Talkowski M, Wood J, Yolken R, Nimgaonkar VL. A comprehensive genetic association and functional study of TNF in schizophrenia risk. Schizophrenia Research. 83: 7-13. PMID 16503400 DOI: 10.1016/J.Schres.2005.12.853  0.32
2004 Shirts BH, Nimgaonkar V. The genes for schizophrenia: finally a breakthrough? Current Psychiatry Reports. 6: 303-12. PMID 15260947 DOI: 10.1007/S11920-004-0081-1  0.32
2002 Hart TC, Gorry MC, Hart PS, Woodard AS, Shihabi Z, Sandhu J, Shirts B, Xu L, Zhu H, Barmada MM, Bleyer AJ. Mutations of the UMOD gene are responsible for medullary cystic kidney disease 2 and familial juvenile hyperuricaemic nephropathy. Journal of Medical Genetics. 39: 882-92. PMID 12471200 DOI: 10.1136/Jmg.39.12.882  0.32
2001 Howard MT, Shirts BH, Zhou J, Carlson CL, Matsufuji S, Gesteland RF, Weeks RS, Atkins JF. Cell culture analysis of the regulatory frameshift event required for the expression of mammalian antizymes. Genes to Cells : Devoted to Molecular & Cellular Mechanisms. 6: 931-41. PMID 11733031 DOI: 10.1046/J.1365-2443.2001.00477.X  0.32
2000 Howard MT, Shirts BH, Petros LM, Flanigan KM, Gesteland RF, Atkins JF. Sequence specificity of aminoglycoside-induced stop condon readthrough: potential implications for treatment of Duchenne muscular dystrophy. Annals of Neurology. 48: 164-9. PMID 10939566 DOI: 10.1002/1531-8249(200008)48:2<164::Aid-Ana5>3.0.Co;2-B  0.32
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