World's Best Scientists 2026 revealed!

D-Index & Metrics

Biology and Biochemistry

D-Index
83
Citations
19789
World Ranking
3582
National Ranking
112

Medicine

D-Index
83
Citations
20225
World Ranking
15805
National Ranking
662

Overview

Geoffrey N. Hendy was affiliated with the McGill University Health Centre in Canada. Their research contributions spanned the fields of Biochemistry, Genetics and Molecular Biology, and Medicine, with a total of six publications in each area. Within these broader disciplines, Hendy focused on subfields including Molecular Biology, Genetics, Oncology, Immunology, and Neurology.

The scientific work of Hendy covered several key topics, notably:

  • Bone health and treatments
  • Barrier Structure and Function Studies
  • Gut microbiota and health
  • Inflammatory Bowel Disease
  • TGF-β signaling in diseases
  • Connective tissue disorders research
  • Pancreatitis Pathology and Treatment

Throughout their career, Hendy collaborated frequently with several researchers, including:

  • David Goltzman (3 joint publications)
  • Nour Eissa (2 joint publications)
  • Hayam Hussein (2 joint publications)
  • Çharles N. Bernstein (2 joint publications)
  • Jean-Eric Ghia (2 joint publications)

The publication venues where Hendy's research appeared most often include:

  • Plastic & Reconstructive Surgery Global Open (2 papers)
  • International Journal of Molecular Sciences (1 paper)
  • Biomimetics (1 paper)
  • Biomedicines (1 paper)
  • Journal of Bone and Mineral Research (1 paper)

Notable papers authored or coauthored by Hendy include:

  • Interdependence between Chromogranin-A, Alternatively Activated Macrophages, Tight Junction Proteins and the Epithelial Functions. A Human and In-Vivo/In-Vitro Descriptive Study, 2020, International Journal of Molecular Sciences
  • Effect of Menin Deletion in Early Osteoblast Lineage on the Mineralization of an In Vitro 3D Osteoid-like Dense Collagen Gel Matrix, 2022, Biomimetics
  • Pancreastatin Reduces Alternatively Activated Macrophages, Disrupts the Epithelial Homeostasis and Aggravates Colonic Inflammation. A Descriptive Analysis, 2021, Biomedicines
  • Exogenous PTH-Related Protein and PTH Improve Mineral and Skeletal Status in 25-Hydroxyvitamin D-1α-Hydroxylase and PTH Double Knockout Mice, 2020, Journal of Bone and Mineral Research
  • Abstract 29: An Experimental And Computational Analysis Of Mouse Femur Biomechanics Following The Deletion Of Menin In The Osteoblast Lineage, 2020, Plastic & Reconstructive Surgery Global Open

Best Publications

  • The relationship between specific RET proto-oncogene mutations and disease phenotype in multiple endocrine neoplasia type 2. International RET mutation consortium analysis.

    Charis Eng;Charis Eng;David Clayton;Isabelle Schuffenecker;Gilbert Lenoir

  • 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;Jacinthe Sirois

  • Human Calcium-sensing Receptor Gene: VITAMIN D RESPONSE ELEMENTS IN PROMOTERS P1 AND P2 CONFER TRANSCRIPTIONAL RESPONSIVENESS TO 1,25-DIHYDROXYVITAMIN D

    Lucie Canaff;Geoffrey N. Hendy

  • 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;Jiarong Li

  • Molecular identification of the gene responsible for congenital nephrogenic diabetes insipidus

    Walter Rosenthal;Anita Seibold;Anaid Antaramian;Michèle Lonergan

  • Inactivation of menin, a Smad3-interacting protein, blocks transforming growth factor type β signaling

    Hiroshi Kaji;Lucie Canaff;Jean-Jacques Lebrun;David Goltzman

  • Familial isolated hyperparathyroidism: clinical and genetic characteristics of 36 kindreds.

    William F. Simonds;Laura A. James-Newton;Sunita K. Agarwal;Bing Yang

  • Mutations of the calcium-sensing receptor (CASR) in familial hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.

    Geoffrey N. Hendy;Lilia D'Souza-Li;Bing Yang;Lucie Canaff

  • Familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism. Effects of mutant gene dosage on phenotype.

    M R Pollak;Y H Chou;S J Marx;B Steinmann

  • 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;Olafur S. Indridason

  • Characterization of the human parathyroid hormone-like peptide gene. Functional and evolutionary aspects.

    T Yasuda;D Banville;G N Hendy;D Goltzman

  • Nucleotide sequence of cloned cDNAs encoding human preproparathyroid hormone.

    Geoffrey N. Hendy;Henry M. Kronenberg;John T. Potts;Alexander Rich

  • 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;Geoffrey N. Hendy

  • Nucleotide sequence of the human parathyroid hormone gene.

    Thomas J. Vasicek;Barbara E. McDevitt;Mason W. Freeman;Barbara J. Fennick

  • Familial isolated hyperparathyroidism is rarely caused by germline mutation in HRPT2, the gene for the hyperparathyroidism-jaw tumor syndrome.

    William F. Simonds;Christiane M. Robbins;Sunita K. Agarwal;Geoffrey N. Hendy

  • Insertion of an Alu sequence in the Ca(2+)-sensing receptor gene in familial hypocalciuric hypercalcemia and neonatal severe hyperparathyroidism.

    N. Janicic;Z. Pausova;D. E. C. Cole;G. N. Hendy

  • CASRdb: calcium-sensing receptor locus-specific database for mutations causing familial (benign) hypocalciuric hypercalcemia, neonatal severe hyperparathyroidism, and autosomal dominant hypocalcemia.

    Svetlana Pidasheva;Lilia D'Souza-Li;Lucie Canaff;David E.C. Cole

  • A Syndrome of Hypocalciuric Hypercalcemia Caused by Autoantibodies Directed at the Calcium-Sensing Receptor

    Olga Kifor;Francis D. Moore;Miriam Delaney;Jeffrey Garber;Jeffrey Garber

  • X-linked nephrogenic diabetes insipidus mutations in North America and the Hopewell hypothesis.

    D G Bichet;M F Arthus;M Lonergan;G N Hendy

  • Calcium sensing receptor in human colon carcinoma: Interaction with Ca2+ and 1,25-dihydroxyvitamin D3

    Subhas Chakrabarty;Hongmei Wang;Lucie Canaff;Geoffrey N. Hendy

Frequent Co-Authors

David Goltzman
David Goltzman McGill University
David E. C. Cole
David E. C. Cole University of Toronto
John H. White
John H. White McGill University
Toshitsugu Sugimoto
Toshitsugu Sugimoto Shimane University
Edward M. Brown
Edward M. Brown University of Rochester Medical Center
John T. Potts
John T. Potts Harvard University
Charles N. Bernstein
Charles N. Bernstein University of Manitoba
Socrates E. Papapoulos
Socrates E. Papapoulos Leiden University Medical Center
Anna Spada
Anna Spada University of Milan
Henry T. Keutmann
Henry T. Keutmann Harvard University

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