Genome-wide association study of extreme high bone mass: Contribution of common genetic variation to extreme BMD phenotypes and potential novel BMD-associated genes by Gregson, Celia L., Newell, Felicity, Leo, Paul J., Clark, Graeme R., Paternoster, Lavinia, Marshall, Mhairi, Forgetta, Vincenzo, Morris, John A., Ge, Bing, Bao, Xiao, Duncan Bassett, J.H., Williams, Graham R., Youlten, Scott E., Croucher, Peter I., Davey Smith, George, Evans, David M., Kemp, John P., Brown, Matthew A., Tobias, Jon H., Duncan, Emma L.

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Mechanisms of action of thyroid hormones in the skeleton by Wojcicka, Anna, Bassett, J.H. Duncan, Williams, Graham R.

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Thyroid hormone metabolism in skeletal development and adult bone maintenance by Waung, Julian A, Bassett, J.H. Duncan, Williams, Graham R

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Critical role of the hypothalamic–pituitary–thyroid axis in bone by Bassett, J.H. Duncan, Williams, Graham R

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The molecular actions of thyroid hormone in bone by Duncan Bassett, J.H, Williams, Graham R

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Thyroid Hormone Receptor Beta in the Ventromedial Hypothalamus Is Essential for the Physiological Regulation of Food Intake and Body Weight by Hameed, Saira, Patterson, Michael, Dhillo, Waljit S., Rahman, Sofia A., Ma, Yue, Holton, Christopher, Gogakos, Apostolos, Yeo, Giles S.H., Lam, Brian Y.H., Polex-Wolf, Joseph, Fenske, Wiebke, Bell, Jimmy, Anastasovska, Jelena, Samarut, Jacques, Bloom, Stephen R., Bassett, J.H. Duncan, Williams, Graham R., Gardiner, James V.

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Kcnn4 Is a Regulator of Macrophage Multinucleation in Bone Homeostasis and Inflammatory Disease by Kang, Heeseog, Kerloc’h, Audrey, Rotival, Maxime, Xu, Xiaoqing, Zhang, Qing, D’Souza, Zelpha, Kim, Michael, Scholz, Jodi Carlson, Ko, Jeong-Hun, Srivastava, Prashant K., Genzen, Jonathan R., Cui, Weiguo, Aitman, Timothy J., Game, Laurence, Melvin, James E., Hanidu, Adedayo, Dimock, Janice, Zheng, Jie, Souza, Donald, Behera, Aruna K., Nabozny, Gerald, Cook, H. Terence, Bassett, J.H. Duncan, Williams, Graham R., Li, Jun, Vignery, Agnès, Petretto, Enrico, Behmoaras, Jacques

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Hypochondroplasia gain-of-function mutation in FGFR3 causes defective bone mineralization in mice by Loisay, Léa, Komla-Ebri, Davide, Morice, Anne, Heuzé, Yann, Viaut, Camille, de La Seiglière, Amélie, Kaci, Nabil, Chan, Danny, Lamouroux, Audrey, Baujat, Geneviève, Bassett, J H Duncan, Williams, Graham R, Legeai-Mallet, Laurence

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The secreted protein augurin is a novel modulator of canonical Wnt signalling involved in osteoblast differentiation by Ruggiero, Carmen, Durand, Nelly, Jarjat, Marielle, Barhanin, Jacques, Ghirardello, Elena J., Dack, Michael R.G., Williams, Graham R., Bassett, J.H. Duncan, Lalli, Enzo

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A Mouse Model with a Frameshift Mutation in the Nuclear Factor I/X (NFIX) Gene Has Phenotypic Features of Marshall‐Smith Syndrome by Kooblall, Kreepa G., Stevenson, Mark, Stewart, Michelle, Harris, Lachlan, Zalucki, Oressia, Dewhurst, Hannah, Butterfield, Natalie, Leng, Houfu, Hough, Tertius A., Ma, Da, Siow, Bernard, Potter, Paul, Cox, Roger D., Brown, Stephen D.M., Horwood, Nicole, Wright, Benjamin, Lockstone, Helen, Buck, David, Vincent, Tonia L., Hannan, Fadil M., Bassett, J.H. Duncan, Williams, Graham R., Lines, Kate E., Piper, Michael, Wells, Sara, Teboul, Lydia, Hennekam, Raoul C., Thakker, Rajesh V.

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Fgfr3 gain-of-function mutation impacts bone homeostasis in hypochondroplasia mouse model by Loisay, Léa, Ebri, Davide Komla, Kaci, Nabil, Bassett, J.H. Duncan, Williams, Graham R., Mallet, Laurence Legeai

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Frequent falls and confusion: recurrent hypoglycemia in a patient with tuberous sclerosis complex by Comninos, Alexander N., Yang, Lisa, Abbara, Ali, Dhillo, Waljit S., Bassett, J.H. Duncan, Todd, Jeannie F.

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Functional validation of the osteoporosis GWAS candidate FUBP3 in knockout mice by Watts, Laura, Freudenthal, Bernard, Butterfield, Natalie C., Pollard, Andrea, Komla-Ebri, Davide, Leitch, Victoria, Logan, John, Mannan, Naila, Bassett, J.H. Duncan, Williams, Graham R.

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Slc38a10 is a novel regulator of osteoblastic bone formation by Pollard, Andrea S., Ebri, Davide Komla, Sparkes, Penny, Gogakos, Apostolos, Logan, John G., Butterfield, Natalie C., Leitch, Victoria, Bassett, J.H. Duncan, Williams, Graham R.

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Mitoguardin-2 deficiency results in severe osteoporosis by Komla-Ebri, Davide, Pollard, Andrea S., Sparkes, Penny C., Ghirardello, Elena J., Gogakos, Apostolos, Logan, John G., Williams, Graham R., Bassett, J.H. Duncan

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Classification and Proposed Nomenclature for Inherited Defects of Thyroid Hormone Action, Cell Transport, and Metabolism by Refetoff, Samuel, Bassett, J.H. Duncan, Beck-Peccoz, Paolo, Bernal, Juan, Brent, Gregory, Chatterjee, Krishna, De Groot, Leslie J., Dumitrescu, Alexandra M., Jameson, J. Larry, Kopp, Peter A., Murata, Yoshiharu, Persani, Luca, Samarut, Jacques, Weiss, Roy E., Williams, Graham R., Yen, Paul M.

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Type 2 deiodinase polymorphism causes ER stress and hypothyroidism in the brain by Jo, Sungro, Fonseca, Tatiana L, Bocco, Barbara M L C, Fernandes, Gustavo W, McAninch, Elizabeth A, Bolin, Anaysa P, Da Conceição, Rodrigo R, Werneck-de-Castro, Joao Pedro, Ignacio, Daniele L, Egri, Péter, Németh, Dorottya, Fekete, Csaba, Bernardi, Maria Martha, Leitch, Victoria D, Mannan, Naila S, Curry, Katharine F, Butterfield, Natalie C, Bassett, J H Duncan, Williams, Graham R, Gereben, Balázs, Ribeiro, Miriam O, Bianco, Antonio C

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Thyroid and bone by Gogakos, Apostolos I., Duncan Bassett, J.H., Williams, Graham R.

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The Thyroid Hormone Transporter MCT10 Is a Novel Regulator of Trabecular Bone Mass and Bone Turnover in Male Mice by Lademann, Franziska, Mayerl, Steffen, Tsourdi, Elena, Verrey, Francois, Leitch, Victoria D, Williams, Graham R, Bassett, J H Duncan, Hofbauer, Lorenz C, Heuer, Heike, Rauner, Martina

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PYY is a negative regulator of bone mass and strength by Leitch, Victoria D., Brassill, Mary Jane, Rahman, Sofia, Butterfield, Natalie C., Ma, Pattara, Logan, John G., Boyde, Alan, Evans, Holly, Croucher, Peter I., Batterham, Rachel L., Williams, Graham R., Bassett, J.H. Duncan

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