Fadil M Hannan
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Explore the profile of Fadil M Hannan including associated specialties, affiliations and a list of published articles.
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66
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1743
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Recent Articles
1.
Hannan F, Kooblall K, Stevenson M, Elajnaf T, Liu F, Lines K, et al.
J Biol Chem
. 2025 Mar;
:108404.
PMID: 40086735
Germline gain-of-function mutations of the calcium-sensing receptor (CaSR) result in autosomal dominant hypocalcemia type 1 (ADH1), which may cause symptomatic hypocalcemia with low parathyroid hormone (PTH) concentrations. Negative allosteric CaSR...
2.
Hannan F, Leow M, Lee J, Kovats S, Elajnaf T, Kennedy S, et al.
Nat Rev Endocrinol
. 2024 Jul;
20(11):673-684.
PMID: 39080505
Climate change is increasing both seasonal temperatures and the frequency and severity of heat extremes. As the endocrine system facilitates physiological adaptations to temperature changes, diseases with an endocrinological basis...
3.
Knopfel N, Zecchin D, Richardson H, Polubothu S, Barberan-Martin S, Cullup T, et al.
J Invest Dermatol
. 2023 Oct;
144(4):820-832.e9.
PMID: 37802294
Mosaic mutations in genes GNAQ or GNA11 lead to a spectrum of diseases including Sturge-Weber syndrome and phakomatosis pigmentovascularis with dermal melanocytosis. The pathognomonic finding of localized "tramlining" on plain...
4.
Zecchin D, Knopfel N, Gluck A, Stevenson M, Sauvadet A, Polubothu S, et al.
J Invest Dermatol
. 2023 Oct;
144(4):811-819.e4.
PMID: 37802293
Mosaic variants in genes GNAQ or GNA11 lead to a spectrum of vascular and pigmentary diseases including Sturge-Weber syndrome, in which progressive postnatal neurological deterioration led us to seek biologically...
5.
Lovegrove C, Besevic J, Wiberg A, Lacey B, Littlejohns T, Allen N, et al.
J Am Soc Nephrol
. 2023 Oct;
34(12):1991-2011.
PMID: 37787550
Significance Statement: Kidney stone disease is a common disorder with poorly understood pathophysiology. Observational and genetic studies indicate that adiposity is associated with an increased risk of kidney stone disease....
6.
Kooblall K, Stevenson M, Stewart M, Harris L, Zalucki O, Dewhurst H, et al.
JBMR Plus
. 2023 Jun;
7(6):e10739.
PMID: 37283649
The nuclear factor I/X () gene encodes a ubiquitously expressed transcription factor whose mutations lead to two allelic disorders characterized by developmental, skeletal, and neural abnormalities, namely, Malan syndrome (MAL)...
7.
Howles S, Gorvin C, Cranston T, Rogers A, Gluck A, Boon H, et al.
J Bone Miner Res
. 2023 Mar;
38(6):907-917.
PMID: 36970776
Familial hypocalciuric hypercalcemia type 2 (FHH2) and autosomal dominant hypocalcemia type 2 (ADH2) are due to loss- and gain-of-function mutations, respectively, of the GNA11 gene that encodes the G protein...
8.
Chinoy A, Nicholson J, Skae M, Hannan F, Thakker R, Mughal M, et al.
J Pediatr
. 2023 Mar;
257:113367.
PMID: 36868303
Objectives: To evaluate the prevalence and degree of any neurodevelopmental abnormalities in children with familial hypocalciuric hypercalcemia type 3 (FHH3). Study Design: A formal neurodevelopmental assessment was performed in children...
9.
Minisola S, Arnold A, Belaya Z, Brandi M, Clarke B, Hannan F, et al.
J Bone Miner Res
. 2022 Oct;
37(11):2315-2329.
PMID: 36245271
In this narrative review, we present data gathered over four decades (1980-2020) on the epidemiology, pathophysiology and genetics of primary hyperparathyroidism (PHPT). PHPT is typically a disease of postmenopausal women,...
10.
Hannan F, Elajnaf T, Vandenberg L, Kennedy S, Thakker R
Nat Rev Endocrinol
. 2022 Oct;
19(1):46-61.
PMID: 36192506
Lactation is critical to infant short-term and long-term health and protects mothers from breast cancer, ovarian cancer and type 2 diabetes mellitus. The mammary gland is a dynamic organ, regulated...