Ware, Stephanie M.
University Hospitals Bristol and Weston NHS Foundation Trust · Indiana University School of Medicine
3 papers on CoChatORCID 0000-0003-4714-0142
Most cited papers
- Verified
Genetic basis for congenital heart disease: Revisited: A scientific statement from the American Heart Association
Pierpont, M. E., Brueckner, M., Chung, W. K., Garg, V., Lacro, R. V., McGuire, A. L., Mital, S., Priest, J. R., Pu, W. T., Roberts, A., et al. (2018) · Circulation
Congenital heart defects researchCongenital Heart Disease Studies
Cited by 654
- Verified
High prevalence of eosinophilic esophagitis in patients with inherited connective tissue disorders
Abonia, J. P., Wen, T., Stucke, E. M., Grotjan, T., Griffith, M. S., Kemme, K. A., Collins, M. H., Putnam, P. E., Franciosi, J. P., von Tiehl, K. F., et al. (2013) · Journal of Allergy and Clinical Immunology
Eosinophilic EsophagitisFood Allergy and Anaphylaxis Research
Cited by 195
- Verified
Missense variants in ANKRD11 cause KBG syndrome by impairment of stability or transcriptional activity of the encoded protein
de Boer, E., Ockeloen, C. W., Kampen, R. A., Hampstead, J. E., Dingemans, A. J. M., Rots, D., Lütje, L., Ashraf, T., Baker, R., Barat-Houari, M., et al. (2022) · Genetics in Medicine
Genomics and Rare DiseasesGenetics and Neurodevelopmental Disorders
Cited by 28
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