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The Journal of Pediatrics|June 8, 2001
Bleeding disorders: A common cause of menorrhagia in adolescentsJ A Bevan, K W Maloney, C A Hillery, et al.
Contraception|October 27, 2019
Contraceptive counseling practices and patient experience: Results from a cluster randomized controlled trial at Planned ParenthoodHannah R Simons, Jordan Leon-Atkins, Julia E Kohn, et al.
Blood|August 30, 2003
Increased erythrocyte adhesion in mice and humans with hereditary spherocytosis and hereditary elliptocytosisNancy J Wandersee, Scott C Olson, Sandra L Holzhauer, et al.
Cell Reports|February 16, 2022
cis-Regulatory changes in locomotor genes are associated with the evolution of burrowing behaviorCaroline K Hu, Ryan A York, Hillery C Metz, et al.
JAMA Network Open|October 28, 2025
Time to Total Hip Arthroplasty Among Patients in the US Military Health SystemBrandon L Hillery, Ashton H Goldman, Alexander G Velosky, et al.
Biochimie|May 13, 2024
FicD regulates adaptation to the unfolded protein response in the murine liverAmanda K Casey, Nathan M Stewart, Naqi Zaidi, et al.
Biorxiv : the Preprint Server for Biology|April 25, 2024
FicD regulates adaptation to the unfolded protein response in the murine liverAmanda K Casey, Nathan M Stewart, Naqi Zaidi, et al.
British Journal of Haematology|August 20, 2016
Substance P is increased in patients with sickle cell disease and associated with haemolysis and hydroxycarbamide useAmanda M Brandow, Nancy J Wandersee, Mahua Dasgupta, et al.
British Journal of Haematology|May 21, 2011
Methaemalbumin formation in sickle cell disease: effect on oxidative protein modification and HO-1 inductionMadelyn S Hanson, Barbora Piknova, Agnes Keszler, et al.
American Journal of Medical Genetics. Part C, Seminars in Medical Genetics|July 28, 2023
Applications of artificial intelligence in clinical laboratory genomicsSwaroop Aradhya, Flavia M Facio, Hillery Metz, et al.
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