Geoffrey N. Hendy - Concepedia

Author

Geoffrey N. Hendy

McGill University ORCID

Also Known As

B. Levy, David Goltzman, G HENDY, G Hendy, G N Hendy, G. Hendy, G. N. HENDY, G. N. Hendy, G.N Hendy, G.N. Hendy

1.2K

Publications

15.6K

Citations

H-Index

156

Concepts

All Affiliations

McGill University Royal Victoria Hospital University of Toronto Royal Victoria Regional Health Centre McGill University Health Centre

About

Geoffrey N. Hendy is an author at McGill University specializing in medicine, endocrinology, and cell biology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	45	84	6K
2	Natural Sciences	14	14	1.2K
3	Health Sciences	12	12	1.1K
4	Education	2	2	44
5	Engineering	2	2	83

Geoffrey N. Hendy

182

Publications

13.1K

Citations

H-Index

Page 1

	Year	Citations
Targeted ablation of the 25-hydroxyvitamin D 1α-hydroxylase enzyme: Evidence for skeletal, reproductive, and immune dysfunction Dibyendu K. Panda, Dengshun Miao, Michel L. Tremblay, Proceedings of the National Academy of Sciences Pseudovitamin D-deficiency RicketsImmunologyPathologyOsteoporosisOxidative Stress	2001	635
Human Calcium-sensing Receptor Gene Lucie Canaff, Geoffrey N. Hendy Journal of Biological Chemistry	2002	393
Inactivation of the 25-Hydroxyvitamin D 1α-Hydroxylase and Vitamin D Receptor Demonstrates Independent and Interdependent Effects of Calcium and Vitamin D on Skeletal and Mineral Homeostasis Dibyendu K. Panda, Dengshun Miao, Isabel Bolivar, Journal of Biological Chemistry	2004	390
Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus Walter Rosenthal, Anita Seibold, Anaid Antaramián, Nature Genetic DeterminantDevelopmental BiologyGenetic DisorderGeneticsDiabetes	1992	331
Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type β signaling Hiroshi Kaji, Lucie Canaff, Jean‐Jacques Lebrun, Proceedings of the National Academy of Sciences	2001	293
Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype. Martin R. Pollak, Yah-Huei Chou, Stephen J. Marx, Journal of Clinical Investigation GeneticsGenetic EpidemiologyParathyroid DiseaseParathyroid GlandEpigenetics	1994	281
Autosomal dominant pseudohypoparathyroidism type Ib is associated with a heterozygous microdeletion that likely disrupts a putative imprinting control element of GNAS Murat Bastepe, Leopold F. Fröhlich, Geoffrey N. Hendy, Journal of Clinical Investigation	2003	256
Influence of Calcium and 1,25-Dihydroxycholecalciferol on Proliferation and Proto-Oncogene Expression in Primary Cultures of Bovine Parathyroid Cells* Richard Kremer, Isabel Bolivar, David Goltzman, Endocrinology	1989	231
The gene responsible for pseudohypoparathyroidism type Ib is paternally imprinted and maps in four unrelated kindreds to chromosome 20q13.3 Harald Jüppner, Ernestina Schipani, Murat Bastepe, Proceedings of the National Academy of Sciences CytogeneticsGeneticsParathyroid DiseaseMolecular BiologyMolecular Genetics	1998	194
Characterization of the human parathyroid hormone-like peptide gene Toshiyuki Yasuda, Debra L. Banville, Geoffrey N. Hendy, Journal of Biological Chemistry GeneticsExon ViiParathyroid DiseaseMolecular BiologyGenomic Mechanism	1989	180

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