Emily Germain-Lee
Chief, Pediatric Endocrinology · University of Connecticut School of Medicine
Credentials: · ·
History
- Present
Pediatric Endocrinology Division · University of Connecticut School of Medicine
- Present
Division of Pediatric Endocrinology · University of Connecticut School of Medicine
- Present
Center for Rare Disease · University of Connecticut School of Medicine
- 1989–1992
- 1986–1989
Pediatrics
- 1982–1986
1978–1982
Research
Review · Nature Reviews Endocrinology · 2018 · 240 citations
Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders
Nature Genetics · 1997 · 193 citations
The Journal of Clinical Endocrinology & Metabolism · 2007 · Last of 5 authors · 139 citations
13 papers
5 papers · 5 as a resident
4 papers
- BR
4 papers
4 papers
4 papers · 1 as a resident
- AS
3 papers · 1 as a fellow
3 papers
Grants
- 2022–2027
National Institute of Arthritis and Musculoskeletal and Skin Diseases · R01
PI · $3.1M · University of Connecticut Sch of Med/Dnt
- 2022–2026
Elucidating Extragonadal Functions of Follicle Stimulating Hormone Using Genetic Approaches in Mice
National Institute on Aging · R21
Contact PI · $493.5K · University of Connecticut Sch of Med/Dnt
- 2016–2020
The Role of G Protein-Coupled Signaling in Neurocognitive and Psychosocialabnormalities
National Institute of Child Health and Human Development · R21
Contact PI · $451.4K · University of Connecticut Sch of Med/Dnt
- 2010–2015
Phase 2 of Growth Hormone for Treatment of Albright Hereditary Osteodystrophy
Food and Drug Administration · R01
Contact PI · $359.4K · Hugo w. Moser Res Inst Kennedy Krieger
Clinical trials
- 2003–2030
Albright Hereditary Osteodystrophy: Natural History, Growth, and Cognitive/Behavioral Assessments
Principal investigator · Active not recruiting
Connecticut Children's Medical Center