Mark Stevenson

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2020-2023
Publications (10 Years): 4

Top Topics

Induced Pluripotent Stem Cells

Dna Methylation

Total Knee Arthroplasty

Angiotensin Converting Enzyme

Top Venues

American journal of medical genetics. Part A

The Journal of clinical endocrinology and metabolism

Nature communications

Journal of the Endocrine Society

This page only lists publications with an associated author ORCID identifier.

Publications

Thomas Cuny, Pauline Romanet, Michelle Goldsworthy, Carole Guérin, Marie Wilkin, Philippe Roche, Frédéric A Sebag, Lynn E van Summeren, Mark Stevenson, Sarah A Howles, Jean Claude Deharo, Rajesh V Thakker, David Taïeb
Cinacalcet reverses short QT interval in Familial Hypocalciuric Hypercalcemia type 1. The Journal of clinical endocrinology and metabolism (2023)
Mark Stevenson, Alistair T Pagnamenta, Heather G Mack, Judith Savige, Edoardo Giacopuzzi, Kate E Lines, Jenny C Taylor, Rajesh V Thakker
The Bartter-Gitelman Spectrum: 50-Year Follow-up With Revision of Diagnosis After Whole-Genome Sequencing. Journal of the Endocrine Society 6 (7) (2022)
Mark Stevenson, Alistair T Pagnamenta, Silvia Reichart, Charlotte Philpott, Kate E Lines, null null, Caroline M Gorvin, Karl Lhotta, Jenny C Taylor, Rajesh V Thakker
Whole genome sequence analysis identifies a PAX2 mutation to establish a correct diagnosis for a syndromic form of hyperuricemia. American journal of medical genetics. Part A 182 (11) (2020)
Esra Karakose, Huan Wang, William Inabnet, Rajesh V Thakker, Steven Libutti, Gustavo Fernandez-Ranvier, Hyunsuk Suh, Mark Stevenson, Yayoi Kinoshita, Michael Donovan, Yevgeniy Antipin, Yan Li, Xiaoxiao Liu, Fulai Jin, Peng Wang, Andrew V Uzilov, Carmen A Argmann, Eric E Schadt, Andrew F Stewart, Donald K Scott, Luca Lambertini
Aberrant methylation underlies insulin gene expression in human insulinoma. Nature communications 11 (1) (2020)