Elizabeth Chao - Publications

Affiliations: 
2014-2015 California Institute for Biomedical Research 

8/69 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
2018 Muppidi A, Lee SJ, Hsu CH, Zou H, Lee C, Pflimlin E, Mahankali M, Yang P, Chao E, Ahmad I, Crameri A, Wang D, Woods A, Shen W. Design and Synthesis of Potent, Long-Acting Lipidated Relaxin-2 Analogs. Bioconjugate Chemistry. PMID 30543420 DOI: 10.1021/acs.bioconjchem.8b00764  0.52
2018 Yang P, Zou H, Lee C, Muppidi A, Chao E, Fu Q, Luo X, Wang D, Schultz PG, Shen W. A Stapled, Long-Acting Glucagon-like Peptide 2 Analog with Efficacy in Dextran Sodium Sulfate-Induced Mouse Colitis Models. Journal of Medicinal Chemistry. PMID 29528634 DOI: 10.1021/acs.jmedchem.7b00768  0.52
2017 Lee SJ, Mahankali M, Bitar A, Zou H, Chao E, Nguyen H, Gonzalez J, Caballero D, Hull M, Wang D, Schultz PG, Shen W. A Novel Role for RARα Agonists as Apolipoprotein CIII Inhibitors Identified from High Throughput Screening. Scientific Reports. 7: 5824. PMID 28724938 DOI: 10.1038/s41598-017-05163-w  0.52
2016 Liu Y, Wang Y, Zhang Y, Liu T, Jia H, Zou H, Fu Q, Zhang Y, Lu L, Chao E, Parker H, Nguyen-Tran V, Shen W, Wang D, Schultz PG, et al. Rational Design of Dual Agonist-Antibody Fusions as Long-acting Therapeutic Hormones. Acs Chemical Biology. PMID 27704775 DOI: 10.1021/acschembio.6b00630  0.52
2016 Wang Y, Du J, Zou H, Liu Y, Zhang Y, Gonzalez J, Chao E, Lu L, Yang P, Parker H, Nguyen-Tran V, Shen W, Wang D, Schultz PG, Wang F. Multifunctional Antibody Agonists Targeting Glucagon-like Peptide-1, Glucagon, and Glucose-Dependent Insulinotropic Polypeptide Receptors. Angewandte Chemie (International Ed. in English). PMID 27595986 DOI: 10.1002/anie.201606321  0.52
2016 Yang PY, Zou H, Chao E, Sherwood L, Nunez V, Keeney M, Ghartey-Tagoe E, Ding Z, Quirino H, Luo X, Welzel G, Chen G, Singh P, Woods AK, Schultz PG, et al. Engineering a long-acting, potent GLP-1 analog for microstructure-based transdermal delivery. Proceedings of the National Academy of Sciences of the United States of America. 113: 4140-5. PMID 27035989 DOI: 10.1073/pnas.1601653113  0.52
2016 Muppidi A, Zou H, Yang PY, Chao E, Sherwood L, Nunez V, Woods AK, Schultz PG, Lin Q, Shen W. Design of Potent and Proteolytically Stable Oxyntomodulin Analogs. Acs Chemical Biology. 11: 324-8. PMID 26727558 DOI: 10.1021/acschembio.5b00787  0.52
2015 Zhang Y, Zou H, Wang Y, Caballero D, Gonzalez J, Chao E, Welzel G, Shen W, Wang D, Schultz PG, Wang F. Rational design of a humanized glucagon-like peptide-1 receptor agonist antibody. Angewandte Chemie (International Ed. in English). 54: 2126-30. PMID 25556336 DOI: 10.1002/anie.201410049  0.52
Low-probability matches
2017 LaDuca H, Farwell KD, Vuong H, Lu HM, Mu W, Shahmirzadi L, Tang S, Chen J, Bhide S, Chao EC. Exome sequencing covers >98% of mutations identified on targeted next generation sequencing panels. Plos One. 12: e0170843. PMID 28152038 DOI: 10.1371/journal.pone.0170843  0.2
2019 Tian Y, Pesaran T, Chamberlin A, Fenwick RB, Li S, Gau CL, Chao EC, Lu HM, Black MH, Qian D. REVEL and BayesDel outperform other in silico meta-predictors for clinical variant classification. Scientific Reports. 9: 12752. PMID 31484976 DOI: 10.1038/s41598-019-49224-8  0.08
2019 LaDuca H, Polley EC, Yussuf A, Hoang L, Gutierrez S, Hart SN, Yadav S, Hu C, Na J, Goldgar DE, Fulk K, Smith LP, Horton C, Profato J, Pesaran T, ... ... Chao EC, et al. A clinical guide to hereditary cancer panel testing: evaluation of gene-specific cancer associations and sensitivity of genetic testing criteria in a cohort of 165,000 high-risk patients. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31406321 DOI: 10.1038/s41436-019-0633-8  0.08
2020 Deignan JL, Chao E, Gannon JL, Greely HT, Hagman KDF, Mao R, Topper S. Points to consider when assessing relationships (or suspecting misattributed relationships) during family-based clinical genomic testing: a statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32404921 DOI: 10.1038/s41436-020-0821-6  0.04
2020 Li MM, Chao E, Esplin ED, Miller DT, Nathanson KL, Plon SE, Scheuner MT, Stewart DR. Points to consider for reporting of germline variation in patients undergoing tumor testing: a statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 32321997 DOI: 10.1038/s41436-020-0783-8  0.04
2019 Li H, LaDuca H, Pesaran T, Chao EC, Dolinsky JS, Parsons M, Spurdle AB, Polley EC, Shimelis H, Hart SN, Hu C, Couch FJ, Goldgar DE. Classification of variants of uncertain significance in BRCA1 and BRCA2 using personal and family history of cancer from individuals in a large hereditary cancer multigene panel testing cohort. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31853058 DOI: 10.1038/s41436-019-0729-1  0.04
2019 Li S, Qian D, Thompson BA, Gutierrez S, Wu S, Pesaran T, LaDuca H, Lu HM, Chao EC, Black M. Tumour characteristics provide evidence for germline mismatch repair missense variant pathogenicity. Journal of Medical Genetics. PMID 31391288 DOI: 10.1136/jmedgenet-2019-106096  0.04
2019 Fulk K, Milam MR, Li S, Yussuf A, Black MH, Chao EC, LaDuca H, Stany MP. Women with breast and uterine cancer are more likely to harbor germline mutations than women with breast or uterine cancer alone: A case for expanded gene testing. Gynecologic Oncology. PMID 30612783 DOI: 10.1016/j.ygyno.2018.12.021  0.04
2018 Eno C, Bayrak-Toydemir P, Bean L, Braxton A, Chao EC, El-Khechen D, Esplin ED, Friedman B, Hagman KDF, Hambuch T, Hernandez A, Juusola J, Londre G, Machado J, Mao R, et al. Misattributed parentage as an unanticipated finding during exome/genome sequencing: current clinical laboratory practices and an opportunity for standardization. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 30214068 DOI: 10.1038/s41436-018-0265-4  0.04
2018 Powis Z, Espenschied CR, LaDuca H, Hagman KD, Paudyal T, Li S, Inaba H, Mauer A, Nathanson KL, Knost J, Chao EC, Tang S. Clinical germline diagnostic exome sequencing for hereditary cancer: Findings within novel candidate genes are prevalent. Cancer Genetics. 224: 12-20. PMID 29778231 DOI: 10.1016/j.cancergen.2018.04.002  0.04
2018 Farwell Hagman KD, Shinde DN, Mroske C, Smith E, Radtke K, Shahmirzadi L, El-Khechen D, Powis Z, Chao EC, Alcaraz WA, Helbig KL, Sajan SA, Rossi M, Lu HM, Huether R, et al. Erratum: Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29388939 DOI: 10.1038/gim.2017.263  0.04
2017 Chao E, Meenan CK, Ferris LK. Smartphone-Based Applications for Skin Monitoring and Melanoma Detection. Dermatologic Clinics. 35: 551-557. PMID 28886812 DOI: 10.1016/j.det.2017.06.014  0.04
2016 Leedom TP, LaDuca H, McFarland R, Li S, Dolinsky JS, Chao EC. Breast cancer risk is similar for CHEK2 founder and non-founder mutation carriers. Cancer Genetics. 209: 403-407. PMID 27751358 DOI: 10.1016/j.cancergen.2016.08.005  0.04
2016 Farwell Hagman KD, Shinde DN, Mroske C, Smith E, Radtke K, Shahmirzadi L, El-Khechen D, Powis Z, Chao EC, Alcaraz WA, Helbig KL, Sajan SA, Rossi M, Lu HM, Huether R, et al. Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27513193 DOI: 10.1038/gim.2016.95  0.04
2015 Cohen JS, Srivastava S, Farwell KD, Lu HM, Zeng W, Lu H, Chao EC, Fatemi A. ELP2 is a novel gene implicated in neurodevelopmental disabilities. American Journal of Medical Genetics. Part A. 167: 1391-5. PMID 25847581 DOI: 10.1002/ajmg.a.36935  0.04
2015 Chao E, Dolinsky J, Pal T. Response to Cragun et al. Clinical Genetics. 88: 201. PMID 25381838 DOI: 10.1111/cge.12512  0.04
2015 Farwell KD, Shahmirzadi L, El-Khechen D, Powis Z, Chao EC, Tippin Davis B, Baxter RM, Zeng W, Mroske C, Parra MC, Gandomi SK, Lu I, Li X, Lu H, Lu HM, et al. Enhanced utility of family-centered diagnostic exome sequencing with inheritance model-based analysis: results from 500 unselected families with undiagnosed genetic conditions. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 17: 578-86. PMID 25356970 DOI: 10.1038/gim.2014.154  0.04
2014 Chong HK, Wang T, Lu HM, Seidler S, Lu H, Keiles S, Chao EC, Stuenkel AJ, Li X, Elliott AM. The validation and clinical implementation of BRCAplus: a comprehensive high-risk breast cancer diagnostic assay. Plos One. 9: e97408. PMID 24830819 DOI: 10.1371/journal.pone.0097408  0.04
2014 LaDuca H, Stuenkel AJ, Dolinsky JS, Keiles S, Tandy S, Pesaran T, Chen E, Gau CL, Palmaer E, Shoaepour K, Shah D, Speare V, Gandomi S, Chao E. Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 830-7. PMID 24763289 DOI: 10.1038/gim.2014.40  0.04
2014 Butterfield RJ, Stevenson TJ, Xing L, Newcomb TM, Nelson B, Zeng W, Li X, Lu HM, Lu H, Farwell Gonzalez KD, Wei JP, Chao EC, Prior TW, Snyder PJ, Bonkowsky JL, et al. Congenital lethal motor neuron disease with a novel defect in ribosome biogenesis. Neurology. 82: 1322-30. PMID 24647030 DOI: 10.1212/WNL.0000000000000305  0.04
2014 Bakry D, Aronson M, Durno C, Rimawi H, Farah R, Alharbi QK, Alharbi M, Shamvil A, Ben-Shachar S, Mistry M, Constantini S, Dvir R, Qaddoumi I, Gallinger S, Lerner-Ellis J, ... ... Chao E, et al. Genetic and clinical determinants of constitutional mismatch repair deficiency syndrome: report from the constitutional mismatch repair deficiency consortium. European Journal of Cancer (Oxford, England : 1990). 50: 987-96. PMID 24440087 DOI: 10.1016/j.ejca.2013.12.005  0.04
2014 Shahmirzadi L, Chao EC, Palmaer E, Parra MC, Tang S, Gonzalez KD. Patient decisions for disclosure of secondary findings among the first 200 individuals undergoing clinical diagnostic exome sequencing. Genetics in Medicine : Official Journal of the American College of Medical Genetics. 16: 395-9. PMID 24113345 DOI: 10.1038/gim.2013.153  0.04
2010 Lipkin SM, Chao EC, Moreno V, Rozek LS, Rennert H, Pinchev M, Dizon D, Rennert G, Kopelovich L, Gruber SB. Genetic variation in 3-hydroxy-3-methylglutaryl CoA reductase modifies the chemopreventive activity of statins for colorectal cancer. Cancer Prevention Research (Philadelphia, Pa.). 3: 597-603. PMID 20403997 DOI: 10.1158/1940-6207.CAPR-10-0007  0.04
2008 Chao EC, Velasquez JL, Witherspoon MS, Rozek LS, Peel D, Ng P, Gruber SB, Watson P, Rennert G, Anton-Culver H, Lynch H, Lipkin SM. Accurate classification of MLH1/MSH2 missense variants with multivariate analysis of protein polymorphisms-mismatch repair (MAPP-MMR). Human Mutation. 29: 852-60. PMID 18383312 DOI: 10.1002/humu.20735  0.04
2006 Chao EC, Lipkin SM. Molecular models for the tissue specificity of DNA mismatch repair-deficient carcinogenesis. Nucleic Acids Research. 34: 840-52. PMID 16464822 DOI: 10.1093/nar/gkj489  0.04
2003 Hu Z, Pfeifer BA, Chao E, Murli S, Kealey J, Carney JR, Ashley G, Khosla C, Hutchinson CR. A specific role of the Saccharopolyspora erythraea thioesterase II gene in the function of modular polyketide synthases. Microbiology (Reading, England). 149: 2213-25. PMID 12904561  0.04
2020 Kim DJ, Makdisi J, Regan C, Chen PC, Chao E, Rotunda AM. Reconstruction of Distal Nasal Defects Using Free Cartilage Batten Grafting With Secondary Intention Healing: A Retrospective Case Series of 129 Patients. Dermatologic Surgery : Official Publication For American Society For Dermatologic Surgery [Et Al.]. PMID 33165075 DOI: 10.1097/DSS.0000000000002714  0.01
2020 Yadav S, LaDuca H, Polley EC, Hu C, Niguidula N, Shimelis H, Lilyquist J, Na J, Lee KY, Gutierrez S, Yussuf A, Hart SN, Davis BT, Chao EC, Pesaran T, et al. Racial and ethnic differences in multigene hereditary cancer panel test results for women with breast cancer. Journal of the National Cancer Institute. PMID 33146377 DOI: 10.1093/jnci/djaa167  0.01
2020 Kimonis V, Al Dubaisi R, Maclean AE, Hall K, Weiss L, Stover AE, Schwartz PH, Berg B, Cheng C, Parikh S, Conner BR, Wu S, Hasso AN, Scott DA, Koenig MK, ... Chao E, et al. mitochondrial disease: new patients and review of the genetic and clinical spectrum. Journal of Medical Genetics. PMID 32518176 DOI: 10.1136/jmedgenet-2020-106846  0.01
2020 Landrith T, Li B, Cass AA, Conner BR, LaDuca H, McKenna DB, Maxwell KN, Domchek S, Morman NA, Heinlen C, Wham D, Koptiuch C, Vagher J, Rivera R, Bunnell A, ... ... Chao E, et al. Splicing profile by capture RNA-seq identifies pathogenic germline variants in tumor suppressor genes. Npj Precision Oncology. 4: 4. PMID 32133419 DOI: 10.1038/s41698-020-0109-y  0.01
2019 Karam R, Conner B, LaDuca H, McGoldrick K, Krempely K, Richardson ME, Zimmermann H, Gutierrez S, Reineke P, Hoang L, Allen K, Yussuf A, Farber-Katz S, Rana HQ, Culver S, ... ... Chao E, et al. Assessment of Diagnostic Outcomes of RNA Genetic Testing for Hereditary Cancer. Jama Network Open. 2: e1913900. PMID 31642931 DOI: 10.1001/jamanetworkopen.2019.13900  0.01
2019 Deignan JL, Chung WK, Kearney HM, Monaghan KG, Rehder CW, Chao EC. Points to consider in the reevaluation and reanalysis of genomic test results: a statement of the American College of Medical Genetics and Genomics (ACMG). Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 31015575 DOI: 10.1038/s41436-019-0478-1  0.01
2019 Hjelm BE, Rollins B, Morgan L, Sequeira A, Mamdani F, Pereira F, Damas J, Webb MG, Weber MD, Schatzberg AF, Barchas JD, Lee FS, Akil H, Watson SJ, Myers RM, Chao EC, et al. Splice-Break: exploiting an RNA-seq splice junction algorithm to discover mitochondrial DNA deletion breakpoints and analyses of psychiatric disorders. Nucleic Acids Research. PMID 30869147 DOI: 10.1093/nar/gkz164  0.01
2019 Salvador MU, Truelson MRF, Mason C, Souders B, LaDuca H, Dougall B, Black MH, Fulk K, Profato J, Gutierrez S, Jasperson K, Tippin-Davis B, Lu HM, Gray P, Shah S, Chao EC, et al. Comprehensive Paired Tumor/Germline Testing for Lynch Syndrome: Bringing Resolution to the Diagnostic Process. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. JCO1800696. PMID 30702970 DOI: 10.1200/JCO.18.00696  0.01
2018 Lee K, Krempely K, Roberts ME, Anderson MJ, Carneiro F, Chao E, Dixon K, Figueiredo J, Ghosh R, Huntsman D, Kaurah P, Kesserwan C, Landrith T, Li S, Mensenkamp AR, et al. Specifications of the ACMG/AMP variant curation guidelines for the analysis of germline CDH1 sequence variants. Human Mutation. 39: 1553-1568. PMID 30311375 DOI: 10.1002/humu.23650  0.01
2018 Walsh MF, Ritter DI, Kesserwan C, Sonkin D, Chakravarty D, Chao E, Ghosh R, Kemel Y, Wu G, Lee K, Kulkarni S, Hedges D, Mandelker D, Ceyhan-Birsoy O, Luo M, et al. Integrating somatic variant data and biomarkers for germline variant classification in cancer predisposition genes. Human Mutation. 39: 1542-1552. PMID 30311369 DOI: 10.1002/humu.23640  0.01
2018 Rana HQ, Gelman R, LaDuca H, McFarland R, Dalton E, Thompson J, Speare V, Dolinsky JS, Chao EC, Garber JE. Differences in TP53 Mutation Carrier Phenotypes Emerge From Panel-Based Testing. Journal of the National Cancer Institute. PMID 29529297 DOI: 10.1093/jnci/djy001  0.01
2017 Weitzel JN, Chao EC, Nehoray B, Van Tongeren LR, LaDuca H, Blazer KR, Slavin T, Facmg DABMD, Pesaran T, Rybak C, Solomon I, Niell-Swiller M, Dolinsky JS, Castillo D, Elliott A, et al. Somatic TP53 variants frequently confound germ-line testing results. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 29189820 DOI: 10.1038/gim.2017.196  0.01
2017 Couch FJ, Shimelis H, Hu C, Hart SN, Polley EC, Na J, Hallberg E, Moore R, Thomas A, Lilyquist J, Feng B, McFarland R, Pesaran T, Huether R, LaDuca H, ... Chao EC, et al. Associations Between Cancer Predisposition Testing Panel Genes and Breast Cancer. Jama Oncology. PMID 28418444 DOI: 10.1001/jamaoncol.2017.0424  0.01
2017 Harrison SM, Dolinsky JS, Knight Johnson AE, Pesaran T, Azzariti DR, Bale S, Chao EC, Das S, Vincent L, Rehm HL. Clinical laboratories collaborate to resolve differences in variant interpretations submitted to ClinVar. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 28301460 DOI: 10.1038/gim.2017.14  0.01
2017 Lucanic M, Plummer WT, Chen E, Harke J, Foulger AC, Onken B, Coleman-Hulbert AL, Dumas KJ, Guo S, Johnson E, Bhaumik D, Xue J, Crist AB, Presley MP, Harinath G, ... ... Chao EA, et al. Impact of genetic background and experimental reproducibility on identifying chemical compounds with robust longevity effects. Nature Communications. 8: 14256. PMID 28220799 DOI: 10.1038/ncomms14256  0.01
2016 Pritzlaff M, Summerour P, McFarland R, Li S, Reineke P, Dolinsky JS, Goldgar DE, Shimelis H, Couch FJ, Chao EC, LaDuca H. Male breast cancer in a multi-gene panel testing cohort: insights and unexpected results. Breast Cancer Research and Treatment. PMID 28008555 DOI: 10.1007/s10549-016-4085-4  0.01
2016 O'Daniel JM, McLaughlin HM, Amendola LM, Bale SJ, Berg JS, Bick D, Bowling KM, Chao EC, Chung WK, Conlin LK, Cooper GM, Das S, Deignan JL, Dorschner MO, Evans JP, et al. A survey of current practices for genomic sequencing test interpretation and reporting processes in US laboratories. Genetics in Medicine : Official Journal of the American College of Medical Genetics. PMID 27811861 DOI: 10.1038/gim.2016.152  0.01
2016 Milutinovic S, Heynen-Genel S, Chao E, Dewing A, Solano R, Milan L, Barron N, He M, Diaz PW, Matsuzawa SI, Reed JC, Hassig CA. Cardiac Glycosides Activate the Tumor Suppressor and Viral Restriction Factor Promyelocytic Leukemia Protein (PML). Plos One. 11: e0152692. PMID 27031987 DOI: 10.1371/journal.pone.0152692  0.01
2016 de la Hoya M, Soukarieh O, López-Perolio I, Vega A, Walker LC, van Ierland Y, Baralle D, Santamariña M, Lattimore V, Wijnen J, Whiley P, Blanco A, Raponi M, Hauke J, Wappenschmidt B, ... Chao E, et al. Combined genetic and splicing analysis of BRCA1 c.[594-2A>C; 641A>G] highlights the relevance of naturally occurring in-frame transcripts for developing disease gene variant classification algorithms. Human Molecular Genetics. PMID 27008870 DOI: 10.1093/hmg/ddw094  0.01
2015 Hernandez F, Huether R, Carter L, Johnston T, Thompson J, Gossage JR, Chao E, Elliott AM. Mutations in RASA1 and GDF2 identified in patients with clinical features of hereditary hemorrhagic telangiectasia. Human Genome Variation. 2: 15040. PMID 27081547 DOI: 10.1038/hgv.2015.40  0.01
2015 Karam R, Pesaran T, Chao E. ClinGen and Genetic Testing. The New England Journal of Medicine. 373: 1376-7. PMID 26422737 DOI: 10.1056/NEJMc1508700#SA1  0.01
2015 Alamillo CL, Powis Z, Farwell K, Shahmirzadi L, Weltmer EC, Turocy J, Lowe T, Kobelka C, Chen E, Basel D, Ashkinadze E, D'Augelli L, Chao E, Tang S. Exome sequencing positively identified relevant alterations in more than half of cases with an indication of prenatal ultrasound anomalies. Prenatal Diagnosis. 35: 1073-8. PMID 26147564 DOI: 10.1002/pd.4648  0.01
2015 Varga E, Chao EC, Yeager ND. The importance of proper bioinformatics analysis and clinical interpretation of tumor genomic profiling: a case study of undifferentiated sarcoma and a constitutional pathogenic BRCA2 mutation and an MLH1 variant of uncertain significance. Familial Cancer. PMID 25712765 DOI: 10.1007/s10689-015-9790-3  0.01
2015 Minion LE, Dolinsky JS, Chase DM, Dunlop CL, Chao EC, Monk BJ. Hereditary predisposition to ovarian cancer, looking beyond BRCA1/BRCA2. Gynecologic Oncology. 137: 86-92. PMID 25622547 DOI: 10.1016/j.ygyno.2015.01.537  0.01
2015 Farwell Gonzalez KD, Li X, Lu HM, Lu H, Pellegrino JE, Miller RT, Zeng W, Chao EC. Diagnostic Exome Sequencing and Tailored Bioinformatics of the Parents of a Deceased Child with Cobalamin Deficiency Suggests Digenic Inheritance of the MTR and LMBRD1 Genes. Jimd Reports. 15: 29-37. PMID 24664876 DOI: 10.1007/8904_2014_294  0.01
2015 Milam MR, Stany M, Li S, Fulk K, Chao E, Laduca H. Women with breast and uterine cancer in relation to genetic mutation risk: A case-control analysis. Journal of Clinical Oncology. 33: 1549-1549. DOI: 10.1200/jco.2015.33.15_suppl.1549  0.01
2015 Nussbaum RL, Rehm HL. Drs. Nussbaum and Rehm reply New England Journal of Medicine. 373: 1379. DOI: 10.1056/NEJMc1508700  0.01
2013 Tsongalis GJ, Chao E, Hagenkord JM, Hambuch T, Moore JH. Bioinformatics: what the clinical laboratorian needs to know and prepare for. Clinical Chemistry. 59: 1301-5. PMID 23723312 DOI: 10.1373/clinchem.2012.198226  0.01
2013 Xu S, Vu NHT, Chao E, Simon M, Zoleikhaeian M, Kimonis V, Huang T, Mozaffar T, Wallace DC. Summary of the mitochondrial findings in a series of 300 cases Mitochondrion. 13: 936-937. DOI: 10.1016/j.mito.2013.07.098  0.01
2012 Stuenkel A, Chao E. Early clinical adoption of next-generation sequencing panels for diagnosis of hereditary cancer susceptibility: A single commercial laboratory experience. Journal of Clinical Oncology : Official Journal of the American Society of Clinical Oncology. 30: 37. PMID 28147024 DOI: 10.1200/jco.2012.30.34_suppl.37  0.01
2011 Sepehr A, Chao E, Trefrey B, Blackford A, Duncan LM, Flotte TJ, Sober A, Mihm MC, Tsao H. Long-term outcome of Spitz-type melanocytic tumors. Archives of Dermatology. 147: 1173-9. PMID 21680758 DOI: 10.1001/archdermatol.2011.170  0.01
2010 Richards-Yutz J, Grant K, Chao EC, Walther SE, Ganguly A. Update on molecular diagnosis of hereditary hemorrhagic telangiectasia. Human Genetics. 128: 61-77. PMID 20414677 DOI: 10.1007/s00439-010-0825-4  0.01
2009 Nichols KE, Walther S, Chao E, Shields C, Ganguly A. Recent advances in retinoblastoma genetic research. Current Opinion in Ophthalmology. 20: 351-5. PMID 19587599 DOI: 10.1097/ICU.0b013e32832f7f25  0.01
2002 Clemons PA, Gladstone BG, Seth A, Chao ED, Foley MA, Schreiber SL. Synthesis of calcineurin-resistant derivatives of FK506 and selection of compensatory receptors. Chemistry & Biology. 9: 49-61. PMID 11841938 DOI: 10.1016/S1074-5521(02)00085-6  0.01
2002 Tawab A, Fields J, Chao E, Kurlander RJ. Recombinant lemA without adjuvant induces extensive expansion of H2-M3-restricted CD8 effectors, which can suppress primary listeriosis in mice. International Immunology. 14: 225-32. PMID 11809741  0.01
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