Franke, K. R., Isett, R., Robbins, A., Paquette-Straub, C., Shapiro, C. A., Lee, M. M., & Crowgey, E. L. (2022). Genomic surveillance of SARS-CoV-2 in the state of Delaware reveals tremendous genomic diversity. PLoS ONE, 17(1 January). doi:10.1371/journal.pone.0262573 View Full Publication
Huang, B. J., Smith, J. L., Wang, Y.-C., Taghizadeh, K., Leonti, A. R., Ries, R. E., & Meshinchi, S. (2021). CBFB-MYH11 fusion transcripts distinguish acute myeloid leukemias with distinct molecular landscapes and outcomes. Blood Advances, 5(23), 4963-4968. doi:10.1182/bloodadvances.2021004965 View Full Publication
Robinson, K. G., Crowgey, E. L., Lee, S. K., & Akins, R. E. (2021). Transcriptional analysis of muscle tissue and isolated satellite cells in spastic cerebral palsy. Developmental Medicine and Child Neurology, 63(10), 1213-1220. doi:10.1111/dmcn.14915 View Full Publication
Mansoor, S., Maheshwari, A., Guglielmo, Furuya, K., Wang, M., Crowgey, E., & He, Z. (2021). The PNPLA3 rs738409 Variant but not MBOAT7 rs641738 is a Risk Factor for Nonalcoholic Fatty Liver Disease in Obese U.S. Children of Hispanic Ethnicity. Pediatric Gastroenterology, Hepatology and Nutrition, 24(5), 455-469. doi:10.5223/pghn.2021.24.5.455
Crowgey, E. L., Soini, T., Shah, N., Pauniaho, S.-L., Lahdenne, P., Wilson, D. B., & Druley, T. E. (2020). Germline sequencing identifies rare variants in finnish subjects with familial germ cell tumors. Application of Clinical Genetics, 13, 127-137. doi:10.2147/TACG.S245093
Miller, R., Coyne, E., Crowgey, E. L., Eckrich, D., Myers, J. C., Villanueva, R., & Kolb, E. A. (2020). Implementation of a learning healthcare system for sickle cell disease. JAMIA Open, 3(3), 349-359. doi:10.1093/JAMIAOPEN/OOAA024
Barwe, S. P., Gopalakrisnapillai, A., Mahajan, N., Druley, T. E., Kolb, E. A., & Crowgey, E. L. (2020). Strong concordance between RNA structural and single nucleotide variants identified via next generation sequencing techniques in primary pediatric leukemia and patient-derived xenograft samples. Genomics and Informatics, 18(1). doi:10.5808/GI.2020.18.1.e6
Franke, K. R., & Crowgey, E. L. (2020). Accelerating next generation sequencing data analysis: An evaluation of optimized best practices for genome analysis toolkit algorithms. Genomics and Informatics, 18(1). doi:10.5808/GI.2020.18.1.e10
Crowgey, E. L., Mahajan, N., Wong, W. H., Gopalakrishnapillai, A., Barwe, S. P., Kolb, E. A., & Druley, T. E. (2020). Error-corrected sequencing strategies enable comprehensive detection of leukemic mutations relevant for diagnosis and minimal residual disease monitoring. BMC Medical Genomics, 13(1). doi:10.1186/s12920-020-0671-8 View Full Publication
Crowgey, E. L., Lee, M. M., Sansbury, B., & Kmiec, E. B. (2020). Perspectives on molecular diagnostic testing for the covid-19 pandemic in delaware. Delaware Journal of Public Health, 6(2). Opgehaal van https://www.scopus.com/inward/record.uri?eid=2-s2.0-85107004383&partnerID=40&md5=73e914383aa42777d87ca40b241799b1
Fert-Bober, J., Venkatraman, V., Hunter, C. L., Liu, R., Crowgey, E. L., Pandey, R., & Van Eyk, J. E. (2019). Mapping Citrullinated Sites in Multiple Organs of Mice Using Hypercitrullinated Library. Journal of Proteome Research, 18(5), 2270-2278. doi:10.1021/acs.jproteome.9b00118 View Full Publication
Guglielmo, D., Franke, K., Cox, C., & Crowgey, E. L. (2019). Whole genome metagenomic analysis of the gut microbiome of differently fed infants identifies differences in microbial composition and functional genes, including an absent CRISPR/Cas9 gene in the formula-fed cohort. Human Microbiome Journal, 12. doi:10.1016/j.humic.2019.100057
Crowgey, E. L., Washburn, M. C., Kolb, E. A., & Puffenberger, E. G. (2019). Development of a Novel Next-Generation Sequencing Assay for Carrier Screening in Old Order Amish and Mennonite Populations of Pennsylvania. Journal of Molecular Diagnostics, 21(4), 687-694. doi:10.1016/j.jmoldx.2019.03.004 View Full Publication
Crowgey, E. L., & Mahajan, N. (2018). Advancements in next-generation sequencing for detecting minimal residual disease. In Minimal Residual Disease Testing: Current Innovations and Future Directions (bll 159-192). doi:10.1007/978-3-319-94827-0_6
Crowgey, E. L., Marsh, A. G., Robinson, K. G., Yeager, S. K., & Akins, R. E. (2018). Epigenetic machine learning: Utilizing DNA methylation patterns to predict spastic cerebral palsy. BMC Bioinformatics, 19(1). doi:10.1186/s12859-018-2224-0 View Full Publication
Crowgey, E. L., Wyffels, J. T., Osborn, P. M., Wood, T. T., & Edsberg, L. E. (2018). A Systems Biology Approach for Studying Heterotopic Ossification: Proteomic Analysis of Clinical Serum and Tissue Samples. Genomics, Proteomics and Bioinformatics, 16(3), 212-220. doi:10.1016/j.gpb.2018.04.006 View Full Publication
Wang, S.-B., Venkatraman, V., Crowgey, E. L., Liu, T., Fu, Z., Holewinski, R., & Van Eyk, J. E. (2018). Protein S-Nitrosylation Controls Glycogen Synthase Kinase 3B Function Independent of Its Phosphorylation State. Circulation Research, 122(11), 1517-1531. doi:10.1161/CIRCRESAHA.118.312789 View Full Publication
Wang, Y., Gray, D. R., Robbins, A. K., Crowgey, E. L., Chanock, S. J., Greene, M. H., & Barthold, J. S. (2018). Subphenotype meta-analysis of testicular cancer genome-wide association study data suggests a role for RBFOX family genes in cryptorchidism susceptibility. Human Reproduction, 33(5), 967-977. doi:10.1093/humrep/dey066 View Full Publication
Lilley, J., Crowgey, E., & Timothy Bunnell, H. (2018). The use of machine learning and phonetic endophenotypes to discover genetic variants associated with speech sound disorder (Vol 2018-September). doi:10.21437/Interspeech.2018-2398
Fert-Bober, J., Crowgey, E. L., Sokolove, J., Giles, J. T., Bathon, J. M., & Van Eyk, J. E. (2017). The significance of myofilament protein citrullination in heart failure: Citrullination in cardiovascular diseases. In Protein Deimination in Human Health and Disease: Second Edition (bll 205-225). doi:10.1007/978-3-319-58244-3_12
Crowgey, E. L., Matlock, A., Venkatraman, V., Fert-Bober, J., & van Eyk, J. E. (2017). Mapping biological networks from quantitative data-independent acquisition mass spectrometry: Data to knowledge pipelines. In Methods in Molecular Biology (Vol 1558, bll 395-413). doi:10.1007/978-1-4939-6783-4_19 View Full Publication
Edsberg, L. E., Crowgey, E. L., Osborn, P. M., & Wyffels, J. T. (2017). A survey of proteomic biomarkers for heterotopic ossification in blood serum. Journal of Orthopaedic Surgery and Research, 12(1). doi:10.1186/s13018-017-0567-2 View Full Publication
Crowgey, E. L., . Stabley, D. L., Chen, C., Huang, H., Robbins, K. M., Polson, S. W., & Wu, C. H. (2015). An integrated approach for analyzing clinical genomic variant data from next-generation sequencing. Journal of Biomolecular Techniques, 26(1), 19-28. doi:10.7171/jbt.15-2601-002 View Full Publication
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