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 · 235 citations

Life Sciences, Genetics, Molecular Genetics +13

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 · 183 citations · Full text

Medicine, Endocrinology, Genetics +17

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 · 159 citations

Medicine, Endocrinology, Genetics +16

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

Medicine, Endocrinology, Genetics +15

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 · 128 citations

Medicine, Genetics, Molecular Genetics +17