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The Journal of Clinical Endocrinology and Metabolism|September 10, 2010
Total testosterone assays in women with polycystic ovary syndrome: precision and correlation with hirsutismRichard S Legro, William D Schlaff, Michael P Diamond, et al.
Ophthalmology Science|October 17, 2022
Genetic Risk of Cardiovascular Disease Is Associated with Macular Ganglion Cell-Inner Plexiform Layer Thinning in an Early Glaucoma CohortHenry Marshall, Sean Mullany, Xikun Han, et al.
The Journal of Clinical Endocrinology and Metabolism|May 13, 2016
Benefit of Delayed Fertility Therapy With Preconception Weight Loss Over Immediate Therapy in Obese Women With PCOSRichard S Legro, William C Dodson, Allen R Kunselman, et al.
American Journal of Ophthalmology|August 15, 2022
Association Between Body Mass Index and Primary Open Angle Glaucoma in Three CohortsHenry Marshall, Ella C Berry, Santiago Diaz Torres, et al.
Ophthalmology|April 12, 2023
High Polygenic Risk Is Associated with Earlier Initiation and Escalation of Treatment in Early Primary Open-Angle GlaucomaHenry N Marshall, Sean Mullany, Xikun Han, et al.
Carcinogenesis|October 5, 2014
Integrative post-genome-wide association analysis of CDKN2A and TP53 SNPs and risk of esophageal adenocarcinomaMatthew F Buas, David M Levine, Karen W Makar, et al.
Pediatric Critical Care Medicine : a Journal of the Society of Critical Care Medicine and the World Federation of Pediatric Intensive and Critical Care Societies|February 20, 2025
Sepsis in Critically Ill Children in Bolivia: Multicenter Retrospective Evaluation of the Phoenix Criteria for Sepsis in a 2023 CohortRaul Copana-Olmos, Nils Casson-Rodriguez, Willmer Diaz-Villalobos, et al.
Communications Biology|November 28, 2020
A pleurocidin analogue with greater conformational flexibility, enhanced antimicrobial potency and in vivo therapeutic efficacyGiorgia Manzo, Charlotte K Hind, Philip M Ferguson, et al.
Investigative Ophthalmology & Visual Science|March 3, 2023
Physical Activity Is Associated With Macular Thickness: A Multi-Cohort Observational StudyElla C Berry, Henry N Marshall, Sean Mullany, et al.
American Journal of Human Genetics|September 13, 2011
Homozygous mutations in PXDN cause congenital cataract, corneal opacity, and developmental glaucomaKamron Khan, Adam Rudkin, David A Parry, et al.
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