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European Journal of Clinical Investigation|March 23, 2016
Lifestyle and clinical determinants of skin autofluorescence in a population-based cohort studyRobert P van Waateringe, Sandra N Slagter, Melanie M van der Klauw, et al.Arteriosclerosis, Thrombosis, and Vascular Biology|September 5, 2009
Genome-wide association identifies the ABO blood group as a major locus associated with serum levels of soluble E-selectinAndrew D Paterson, Maria F Lopes-Virella, Daryl Waggott, et al.Physical Review Letters|March 14, 2003
Measurement of the spatial coherence function of undulator radiation using a phase maskJ J A Lin, D Paterson, A G Peele, et al.Clinical Journal of the American Society of Nephrology : CJASN|February 19, 2021
Patients with Protein-Truncating PKD1 Mutations and Mild ADPKDMatthew B Lanktree, Elsa Guiard, Pedram Akbari, et al.American Journal of Human Genetics|April 5, 2008
CC2D2A, encoding a coiled-coil and C2 domain protein, causes autosomal-recessive mental retardation with retinitis pigmentosaAbdul Noor, Christian Windpassinger, Megha Patel, et al.Journal of the American Society of Nephrology : JASN|October 17, 1998
A spectrum of mutations in the polycystic kidney disease-2 (PKD2) gene from eight Canadian kindredsY Pei, N He, K Wang, et al.Cardiovascular Diabetology|April 27, 2018
Novel risk genes identified in a genome-wide association study for coronary artery disease in patients with type 1 diabetesRomain Charmet, Seamus Duffy, Sareh Keshavarzi, et al.Clinical Journal of the American Society of Nephrology : CJASN|November 1, 2016
Albuminuria Changes and Cardiovascular and Renal Outcomes in Type 1 Diabetes: The DCCT/EDIC StudyIan H de Boer, Xiaoyu Gao, Patricia A Cleary, et al.Diabetic Medicine : a Journal of the British Diabetic Association|February 4, 2010
The associations of apolipoprotein E and angiotensin-converting enzyme polymorphisms and cognitive function in Type 1 diabetes based on an 18-year follow-up of the DCCT cohortA M Jacobson, A D Paterson, C M Ryan, et al.Clinical Journal of the American Society of Nephrology : CJASN|January 17, 2019
Integration of Genetic Testing and Pathology for the Diagnosis of Adults with FSGSTony Yao, Khalil Udwan, Rohan John, et al.Pageof 44