L. Mellor-Crummey

Disrupted nitric oxide signaling due to GUCY1A3 mutations increases risk for moyamoya disease, achalasia and hypertension

D. Nickerson, M. Bamshad, D. Saunders, 2016, Clinical genetics.

Loss-of-Function Mutations in YY1AP1 Lead to Grange Syndrome and a Fibromuscular Dysplasia-Like Vascular Disease.

R. Pfundt, B. D. de Vries, D. Nickerson, 2017, American journal of human genetics.

Clinical History and Management Recommendations of the Smooth Muscle Dysfunction Syndrome Due to ACTA2 Arginine 179 Alterations

M. Tekin, B. Lorenz, D. Milewicz, 2018, Genetics in Medicine.

A Comparison of the Liver Fat Score and CT Liver-to-Spleen Ratio as Predictors of Fatty Liver Disease by HIV Serostatus.

M. Budoff, L. Kingsley, W. Post, 2018, Journal of clinical gastroenterology and hepatology.

Genotype in BRCA‐associated Breast Cancers

Funda Meric-Bernstam, G. Hortobagyi, F. Meric-Bernstam, 2013, The breast journal.