Disorders of the calcium-sensing receptor and partner proteins: insights into the molecular basis of calcium homeostasis. by Hannan, F, Babinsky, V, Thakker, R

Genetic approaches to metabolic bone diseases by Hannan, F, Newey, P, Whyte, M, Thakker, R

Association of calcium-sensing receptor polymorphisms with indices of vascular calcification in renal transplant recipients by Babinsky, V, Hannan, F, Youhanna, S, Devuyst, O, Thakker, R

The calcium-sensing receptor in physiology and in calcitropic and noncalcitropic diseases by Hannan, F, Kallay, E, Chang, W, Brandi, M, Thakker, R

Familial Hypocalciuric Hypercalcaemia Type 3 (FHH3) Identified in a Family in Northern Ireland Leading to Identification of a Causative Mutation in the Adaptor Protein 2 Sigma 1 (A... by Graham, U, Nesbit, M, Hannan, F, Howles, SA, Thakker, R, Hunter, S

Oncogenic hypophosphataemic osteomalacia: biomarker roles of fibroblast growth factor 23, 1,25-dihydroxyvitamin D3 and lymphatic vessel endothelial hyaluronan receptor 1. by Hannan, F, Athanasou, N, Teh, J, Gibbons, C, Shine, B, Thakker, R

Identification of a second kindred with familial hypocalciuric hypercalcemia type 3 (FHH3) narrows localization to a <3.5 megabase pair region on chromosome 19q13.3. by Nesbit, M, Hannan, F, Graham, U, Whyte, M, Morrison, P, Hunter, S, Thakker, R

A G-protein subunit-α11 loss-of-function mutation, Thr54Met, causes familial hypocalciuric hypercalcemia type 2 (FHH2) by Gorvin, C, Cranston, T, Hannan, F, Rust, N, Qureshi, A, Nesbit, M, Thakker, R

Familial isolated primary hyperparathyroidism caused by mutations of the MEN1 gene. by Hannan, F, Nesbit, M, Christie, P, Fratter, C, Dudley, N, Sadler, G, Thakker, R

Cinacalcet rectifies hypercalcemia in a patient with familial hypocalciuric hypercalcemia type 2 (FHH2) caused by a germline loss‐of‐function Gα11 mutation by Gorvin, C, Hannan, F, Cranston, T, Valta, H, Makitie, O, Schalin-Jantti, C, Thakker, R

Calcium-sensing receptor residues with loss- and gain-of-function mutations are located in regions of conformational change and cause signalling bias by Gorvin, C, Frost, M, Malinauskas, T, Cranston, T, Boon, H, Siebold, C, Jones, E, Hannan, F, Thakker, R

A homozygous inactivating calcium-sensing receptor mutation, Pro339Thr, is associated with isolated primary hyperparathyroidism: correlation between location of mutations and sever... by Hannan, F, Nesbit, M, Christie, P, Lissens, W, Van der Schueren, B, Bex, M, Bouillon, R, Thakker, R

Comparison of human chromosome 19q13 and syntenic region on mouse chromosome 7 reveals absence, in man, of 11.6 Mb containing four mouse calcium-sensing receptor-related sequences:... by Hannan, F, Nesbit, M, Turner, J, Stacey, J, Cianferotti, L, Christie, P, Conigrave, A, Whyte, M, Thakker, R

Mutations affecting G-protein subunit α11 in hypercalcemia and hypocalcemia. by Nesbit, M, Hannan, F, Howles, SA, Babinsky, V, Head, R, Cranston, T, Rust, N, Hobbs, MR, Heath, H, Thakker, R

N-ethyl-N-Nitrosourea (ENU) induced mutations within the klotho gene lead to ectopic calcification and reduced lifespan in mouse models by Esapa, C, Hannan, F, Babinsky, V, Potter, P, Thomas, G, Croucher, P, Brown, M, Brown, S, Cox, R, Thakker, R

A calcium-sensing receptor mutation causing hypocalcemia disrupts a transmembrane salt bridge to activate β-arrestin-biased signaling by Gorvin, C, Babinsky, V, Malinauskas, T, Nissen, P, Schou, A, Hanyaloglu, A, Siebold, C, Jones, E, Hannan, F, Thakker, R

Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations by Howles, S, Hannan, F, Babinsky, V, Rogers, A, Gorvin, C, Rust, N, Richardson, T, McKenna, M, Nesbit, M, Thakker, R

Cinacalcet corrects hypercalcemia in mice with an inactivating Gα11 mutation by Howles, S, Hannan, F, Gorvin, C, Piret, S, Paudyal, A, Stewart, M, Hough, T, Nesbit, M, Wells, S, Brown, S, Cox, R, Thakker, R

Activating mutations of the G-protein subunit α11 interdomain interface cause autosomal dominant hypocalcemia type 2 by Gorvin, C, Stokes, V, Boon, H, Cranston, T, Gluck, A, Bahl, S, Homfray, T, Aung, T, Shine, B, Lines, K, Hannan, F, Thakker, R

GNA11 variants identified in patients with hypercalcemia or hypocalcemia by Howles, S, Gorvin, C, Cranston, T, Rogers, A, Gluck, A, Boon, H, Gibson, K, Rahman, M, Root, A, Nesbit, M, Hannan, F, Thakker, R