| Body Mass Index Differences in Pseudohypoparathyroidism Type 1a Versus Pseudopseudohypoparathyroidism May Implicate Paternal Imprinting of Gαs in the … DN Long, S McGuire, MA Levine, LS Weinstein, EL Germain-Lee The Journal of Clinical Endocrinology & Metabolism 92 (3), 1073-1079, 2007 | 207 | 2007 |
| Growth hormone deficiency in pseudohypoparathyroidism type 1a: another manifestation of multihormone resistance EL Germain-Lee, J Groman, JL Crane, SM Jan de Beur, MA Levine The Journal of Clinical Endocrinology & Metabolism 88 (9), 4059-4069, 2003 | 177 | 2003 |
| Paternal imprinting of Gαs in the human thyroid as the basis of TSH resistance in pseudohypoparathyroidism type 1a EL Germain-Lee, CL Ding, Z Deng, JL Crane, M Saji, MD Ringel, ... Biochemical and biophysical research communications 296 (1), 67-72, 2002 | 161 | 2002 |
| A mouse model of Albright hereditary osteodystrophy generated by targeted disruption of exon 1 of the Gnas gene EL Germain-Lee, W Schwindinger, JL Crane, R Zewdu, LS Zweifel, ... Endocrinology 146 (11), 4697-4709, 2005 | 136 | 2005 |
| Physiological functions of the imprinted Gnas locus and its protein variants Galpha (s) and XLalpha (s) in human and mouse A Plagge, G Kelsey, EL Germain-Lee The Journal of endocrinology 196 (2), 193-214, 2008 | 134 | 2008 |
| Expression of a type I insulin-like growth factor receptor with low affinity for insulin-like growth factor II EL Germain-Lee, M Janicot, R Lammers, A Ullrich, SJ Casella Biochemical Journal 281 (2), 413-417, 1992 | 105 | 1992 |
| Age‐related anti‐thyroid antibodies and thyroid abnormalities in Turner syndrome EL GERMAIN, LP PLOTNICK Acta Paediatrica 75 (5), 750-755, 1986 | 84 | 1986 |
| Short stature, obesity, and growth hormone deficiency in pseudohypoparathyroidism type 1a. EL Germain-Lee Pediatric endocrinology reviews: PER 3, 318-327, 2006 | 66 | 2006 |
| Growth hormone deficiency in Sturge–Weber syndrome RS Miller, KL Ball, AM Comi, EL Germain-Lee Archives of disease in childhood 91 (4), 340-341, 2006 | 65 | 2006 |
| Central hypothyroidism and Sturge-Weber syndrome AM Comi, S Bellamkonda, LM Ferenc, BA Cohen, EL Germain-Lee Pediatric neurology 39 (1), 58-62, 2008 | 62 | 2008 |
| Bone mineral density in pseudohypoparathyroidism type 1a DN Long, MA Levine, EL Germain-Lee The Journal of Clinical Endocrinology & Metabolism 95 (9), 4465-4475, 2010 | 53 | 2010 |
| Osteogenesis imperfecta: effecting the transition from adolescent to adult medical care J Shapiro, E Germain-Lee | 43 | 2012 |
| NVL: a new member of the AAA family of ATPases localized to the nucleus EL Germain-Lee, C Obie, D Valle Genomics 44 (1), 22-34, 1997 | 36 | 1997 |
| Increased prevalence of carpal tunnel syndrome in Albright hereditary osteodystrophy AW Joseph, AH Shoemaker, EL Germain-Lee The Journal of Clinical Endocrinology & Metabolism 96 (7), 2065-2073, 2011 | 22 | 2011 |
| Twenty‐nail dystrophy associated with hematologic abnormalities EL GERMAIN‐LEE, WH ZINKHAM Acta Pædiatrica 80 (10), 977-980, 1991 | 18 | 1991 |
| Imprinting Status of GαS, NESP55, and XLαs in Cell Cultures Derived from Human Embryonic Germ Cells: GNAS Imprinting in Human Embryonic Germ Cells JL Crane, MJ Shamblott, J Axelman, S Hsu, MA Levine, EL Germain‐Lee Clinical and translational science 2 (5), 355-360, 2009 | 14 | 2009 |
| Selective deficiency of antibody responses to polysaccharide antigens in a child mosaic for partial trisomy 1 (46, XX, dir dup (1)(q12→ q23)/46, XX) EL Germain-Lee, G Schiffman, EH Mules, HM Lederman The Journal of pediatrics 117 (1), 96-99, 1990 | 13 | 1990 |
| Heterotopic subcutaneous ossifications in a mouse model of Albright hereditary osteodystrophy DL Huso, S McGuire, EL Germain-Lee 89th Annual Meeting of The Endocrine Society, 2007 | 9 | 2007 |
| Endoderm-secreted factor stimulates growth of embyronal carcinoma stem cells E Germain, J Littlefield In Vitro Cellular and Developmental Biology, 1986 | 8 | 1986 |
| A new culprit in osteogenesis imperfecta EL Germain‐Lee Journal of Bone and Mineral Research 26 (12), 2795-2797, 2011 | 7 | 2011 |
