Emily L. Germain‐Lee

Mutations in PEX1 are the most common cause of peroxisome biogenesis disorders

Bernadette E. Reuber, Emily L. Germain‐Lee, Cynthia S. Collins et al. · Nature Genetics · 1997 · 234 citations

Peroxisome Biogenesis Disorders, Mendelian Disorder, Genetic Disorder +8

Body Mass Index Differences in Pseudohypoparathyroidism Type 1a<i>Versus</i>Pseudopseudohypoparathyroidism May Implicate Paternal Imprinting of Gαs in the Development of Human Obesity

Dominique Long, Sarah McGuire, Michael A. Levine et al. · The Journal of Clinical Endocrinology & Metabolism · 2006 · 181 citations · Full text

Growth Hormone Deficiency in Pseudohypoparathyroidism Type 1a: Another Manifestation of Multihormone Resistance

Emily L. Germain‐Lee, Joshua D. Groman, Janet L. Crane et al. · The Journal of Clinical Endocrinology & Metabolism · 2003 · 157 citations

Php Type 1A, Human Growth, Genetics +18

Paternal imprinting of Gαs in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a

Emily L. Germain‐Lee, Chang-Lin Ding, Zhi‐chao Deng et al. · Biochemical and Biophysical Research Communications · 2002 · 145 citations

Human Thyroid, Tsh Resistance, Paternal Imprinting +9

A Mouse Model of Albright Hereditary Osteodystrophy Generated by Targeted Disruption of Exon 1 of the Gnas Gene

Emily L. Germain‐Lee, William F. Schwindinger, Janet L. Crane et al. · Endocrinology · 2005 · 127 citations