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American Journal of Medical Genetics. Part A|March 22, 2017
Multigenerational pedigree with STAR syndrome: A novel FAM58A variant and expansion of the phenotypeNicole J Boczek, Teresa Kruisselbrink, Margot A Cousin, et al.
Biorxiv : the Preprint Server for Biology|February 9, 2026
PRDM16 Coordinates Genetic and Epigenetic Programs Governing Chondrogenesis and Chondrocyte Phenotype Specification in the Knee JointEloise Fadial, Victoria Hansen, Gulzada Kulzhanova, et al.
Plos One|February 10, 2017
Molecular modeling and molecular dynamic simulation of the effects of variants in the TGFBR2 kinase domain as a paradigm for interpretation of variants obtained by next generation sequencingMichael T Zimmermann, Raul Urrutia, Gavin R Oliver, et al.
American Journal of Physiology. Heart and Circulatory Physiology|August 31, 2019
Reconstitution of autophagy ameliorates vascular function and arterial stiffening in spontaneously hypertensive ratsCameron G McCarthy, Camilla F Wenceslau, Fabiano B Calmasini, et al.
Plant Physiology|October 13, 2009
Plant MetGenMAP: an integrative analysis system for plant systems biologyJe-Gun Joung, Anthony M Corbett, Shanna Moore Fellman, et al.
The Veterinary Record|April 18, 2006
Investigations of the potential risk factors associated with cases of bovine spongiform encephalopathy in Bavaria, GermanyM Clauss, C Sauter-Louis, E Chaher, et al.
Medicine|December 17, 2017
Deceleration capacity as a risk predictor in patients presenting to the emergency department with syncope: A prospective exploratory pilot studyMartin Duckheim, Katharina Klee, Nina Götz, et al.
American Journal of Epidemiology|December 16, 2024
A hypothetical intervention on the use of hearing aids for the risk of dementia in people with hearing loss in UK BiobankJ Mur, M Klee, H R Wright, et al.
Applied Optics|September 22, 2025
Intensity control of few-cycle laser pulsesJoseph J Broughton, Hortense Allegre, Tim Klee, et al.
Molecular Genetics and Metabolism|November 14, 2020
Fetal glycosylation defect due to ALG3 and COG5 variants detected via amniocentesis: Complex glycosylation defect with embryonic lethal phenotypeAlejandro Ferrer, Rodrigo Tzovenos Starosta, Wasantha Ranatunga, et al.
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