Emily L Germain-Lee

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2024
Publications (10 Years): 10

Top Venues

Proceedings of the National Academy of Sciences of the United States of America

PloS one

bioRxiv : the preprint server for biology

JBMR plus

University of Connecticut School of Medicine

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Connecticut School of Medicine Oct 28 2016

United States

Professor, Division Chief of Pediatric Endocrinology :: Pediatrics

Publications

Patrick McMullan, Peter Maye, Sierra H Root, Qingfen Yang, Sarah Edie, David Rowe, Ivo Kalajzic, Emily L Germain-Lee
Hair follicle-resident progenitor cells are a major cellular contributor to heterotopic subcutaneous ossifications in a mouse model of Albright hereditary osteodystrophy. bioRxiv : the preprint server for biology (2024)
Patrick McMullan, Peter Maye, Sierra H Root, Qingfen Yang, Sarah Edie, David Rowe, Ivo Kalajzic, Emily L Germain-Lee
Hair follicle-resident progenitor cells are a major cellular contributor to heterotopic subcutaneous ossifications in a mouse model of Albright hereditary osteodystrophy. bioRxiv : the preprint server for biology (2024)
Neetu Krishnan, Patrick McMullan, Qingfen Yang, Alexzandrea N Buscarello, Emily L Germain-Lee
Prevalence of Chiari malformation type 1 is increased in pseudohypoparathyroidism type 1A and associated with aberrant bone development. PloS one 18 (1) (2023)
Neetu Krishnan, Patrick McMullan, Qingfen Yang, Alexzandrea N Buscarello, Emily L Germain-Lee
Prevalence of Chiari malformation type 1 is increased in pseudohypoparathyroidism type 1A and associated with aberrant bone development. PloS one 18 (1) (2023)
Neetu Krishnan, Patrick McMullan, Qingfen Yang, Alexzandrea N Buscarello, Emily L Germain-Lee
Prevalence of Chiari malformation type 1 is increased in pseudohypoparathyroidism type 1A and associated with aberrant bone development. PloS one 18 (1) (2023)
Patrick McMullan, Emily L Germain-Lee
Aberrant Bone Regulation in Albright Hereditary Osteodystrophy dueto Gnas Inactivation: Mechanisms and Translational Implications. Current osteoporosis reports 20 (1) (2022)
Yewei Liu, Adam Lehar, Renata Rydzik, Harshpreet Chandok, Yun-Sil Lee, Daniel W Youngstrom, Joshy George, Martin M Matzuk, Emily L Germain-Lee, Se-Jin Lee
Local versus systemic control of bone and skeletal muscle mass by components of the transforming growth factor-β signaling pathway. Proceedings of the National Academy of Sciences of the United States of America 118 (33) (2021)
Patrick McMullan, Peter Maye, Qingfen Yang, David W Rowe, Emily L Germain-Lee
Parental Origin of Gsα Inactivation Differentially Affects Bone Remodeling in a Mouse Model of Albright Hereditary Osteodystrophy. JBMR plus 6 (1) (2021)
Se-Jin Lee, Adam Lehar, Yewei Liu, Chi Hai Ly, Quynh-Mai Pham, Michael Michaud, Renata Rydzik, Daniel W Youngstrom, Michael M Shen, Vesa Kaartinen, Emily L Germain-Lee, Thomas A Rando
Functional redundancy of type I and type II receptors in the regulation of skeletal muscle growth by myostatin and activin A. Proceedings of the National Academy of Sciences of the United States of America 117 (49) (2020)
Se-Jin Lee, Adam Lehar, Jessica U Meir, Christina Koch, Andrew Morgan, Lara E Warren, Renata Rydzik, Daniel W Youngstrom, Harshpreet Chandok, Joshy George, Joseph Gogain, Michael Michaud, Thomas A Stoklasek, Yewei Liu, Emily L Germain-Lee
Targeting myostatin/activin A protects against skeletal muscle and bone loss during spaceflight. Proceedings of the National Academy of Sciences of the United States of America 117 (38) (2020)

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Publication Activity (10 Years)

Top Topics

Top Venues

Emily L Germain-Lee