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European Heart Journal Open|April 6, 2026
Circulating biomarkers and mortality in atrial fibrillation: the REasons for Geographic And Racial Differences in Stroke studyErin M Hald, Katherine Wilkinson, Samuel A P Short, et al.Clinical and Experimental Allergy : Journal of the British Society for Allergy and Clinical Immunology|March 11, 2010
Disconnect between standardized field-based testing and mannitol challenge in Scottish elite swimmersK L Clearie, P A Williamson, S Vaidyanathan, et al.American Journal of Medical Genetics. Part A|January 25, 2014
Germline CBL mutation associated with a noonan-like syndrome with primary lymphedema and teratoma associated with acquired uniparental isodisomy of chromosome 11q23Helen L Hanson, Meredith J Wilson, John P Short, et al.Kidney International Reports|April 11, 2020
Bleeding Complications After Percutaneous Native Kidney Biopsy: Results From the Boston Kidney Biopsy CohortRagnar Palsson, Samuel A P Short, Zoe A Kibbelaar, et al.American Journal of Human Genetics|August 1, 1996
Allelic loss is frequent in tuberous sclerosis kidney lesions but rare in brain lesionsE P Henske, B W Scheithauer, M P Short, et al.American Journal of Human Genetics|October 1, 1991
Localization of one gene for tuberous sclerosis within 9q32-9q34, and further evidence for heterogeneityJ L Haines, M P Short, D J Kwiatkowski, et al.Plos One|May 26, 2011
Adenoma formation following limited ablation of p120-catenin in the mouse intestineWhitney G Smalley-Freed, Andrey Efimov, Sarah P Short, et al.Nephrology, Dialysis, Transplantation : Official Publication of the European Dialysis and Transplant Association - European Renal Association|November 18, 2021
A randomized controlled trial of two dialysate sodium concentrations in hospitalized hemodialysis patientsFinnian R Mc Causland, Katherine Scovner Ravi, Katherine A Curtis, et al.Nature Genetics|September 1, 1992
Linkage of an important gene locus for tuberous sclerosis to a chromosome 16 marker for polycystic kidney diseaseR S Kandt, J L Haines, M Smith, et al.American Journal of Human Genetics|August 1, 1994
Mutational analysis of patients with neurofibromatosis 2M MacCollin, V Ramesh, L B Jacoby, et al.Pageof 17