Genetics of kidney stone disease von Howles, Sarah A., Thakker, Rajesh V.

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Pregnancy and parenthood in surgical training: a cross-sectional survey in the UK von Whitburn, Jessica, Miah, Saiful, Howles, Sarah A

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Genetic variants of calcium and vitamin D metabolism in kidney stone disease von Howles, Sarah A., Wiberg, Akira, Goldsworthy, Michelle, Bayliss, Asha L., Gluck, Anna K., Ng, Michael, Grout, Emily, Tanikawa, Chizu, Kamatani, Yoichiro, Terao, Chikashi, Takahashi, Atsushi, Kubo, Michiaki, Matsuda, Koichi, Thakker, Rajesh V., Turney, Benjamin W., Furniss, Dominic

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Mutations Affecting G-Protein Subunit α11 in Hypercalcemia and Hypocalcemia von Nesbit, M. Andrew, Hannan, Fadil M, Howles, Sarah A, Babinsky, Valerie N, Head, Rosie A, Cranston, Treena, Rust, Nigel, Hobbs, Maurine R, Heath, Hunter, Thakker, Rajesh V

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Causal inference in health and disease: a review of the principles and applications of Mendelian randomization von Lovegrove, Catherine E, Howles, Sarah A, Furniss, Dominic, Holmes, Michael V

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Mutations in AP2S1 cause familial hypocalciuric hypercalcemia type 3 von Nesbit, M Andrew, Hannan, Fadil M, Howles, Sarah A, Reed, Anita A C, Cranston, Treena, Thakker, Clare E, Gregory, Lorna, Rimmer, Andrew J, Rust, Nigel, Graham, Una, Morrison, Patrick J, Hunter, Steven J, Whyte, Michael P, McVean, Gil, Buck, David, Thakker, Rajesh V

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Utility of blood tests in screening for metabolic disorders in kidney stone disease von Eyre, Katie S., Lewis, Francesca, Cui, Helen, Grout, Emily, Mihai, Radu, Turney, Benjamin W., Howles, Sarah A.

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Matched pair analysis of wide versus narrow focus during shockwave lithotripsy for urolithiasis von Sharp, Anna J., Lovegrove, Catherine E., Sreekumar, Roshan, Spencer, Mandy, Turney, Benjamin W., Howles, Sarah A.

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Calcium sensing receptor expression is downregulated in gastroenteropancreatic neuroendocrine tumours via epigenetic mechanisms von English, Katherine A, Goldsworthy, Michelle, Willis, Brittannie, Kooblall, Kreepa G, Birla, Shweta, Selberherr, Andreas, Stevenson, Mark, Shariq, Omair A, Oberg, Ann L, Wang, Tony, Carmichael, James, Mavrommatis, Konstantinos, Escoubet, Laure, Thakker, Rajesh V, Howles, Sarah A, Lines, Kate E

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Central Adiposity Increases Risk of Kidney Stone Disease through Effects on Serum Calcium Concentrations von Lovegrove, Catherine E, Bešević, Jelena, Wiberg, Akira, Lacey, Ben, Littlejohns, Thomas J, Allen, Naomi E, Goldsworthy, Michelle, Kim, Jihye, Hannan, Fadil M, Curhan, Gary C, Turney, Ben W, McCarthy, Mark I, Mahajan, Anubha, Thakker, Rajesh V, Holmes, Michael V, Furniss, Dominic, Howles, Sarah A

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Cinacalcet Reverses Short QT Interval in Familial Hypocalciuric Hypercalcemia Type 1 von Cuny, Thomas, Romanet, Pauline, Goldsworthy, Michelle, Guérin, Carole, Wilkin, Marie, Roche, Philippe, Sebag, Frédéric, van Summeren, Lynn E, Stevenson, Mark, Howles, Sarah A, Deharo, Jean-Claude, Thakker, Rajesh V, Taïeb, David

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Urology never events in the United Kingdom: A retrospective 10‐year review von Loyala, Jerocin Vishani, Ang, Andrew, Down, Billy, Howles, Sarah A.

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GNA11 Variants Identified in Patients with Hypercalcemia or Hypocalcemia von Howles, Sarah A., Gorvin, Caroline M., Cranston, Treena, Rogers, Angela, Gluck, Anna K., Boon, Hannah, Gibson, Kate, Rahman, Mushtaqur, Root, Allen, Nesbit, M. Andrew, Hannan, Fadil M., Thakker, Rajesh V.

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Author Correction: Genetic variants of calcium and vitamin D metabolism in kidney stone disease von Howles, Sarah A., Wiberg, Akira, Goldsworthy, Michelle, Bayliss, Asha L., Gluck, Anna K., Ng, Michael, Grout, Emily, Tanikawa, Chizu, Kamatani, Yoichiro, Terao, Chikashi, Takahashi, Atsushi, Kubo, Michiaki, Matsuda, Koichi, Thakker, Rajesh V., Turney, Benjamin W., Furniss, Dominic

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Cinacalcet for Symptomatic Hypercalcemia Caused by AP2S1 Mutations von Howles, Sarah A, Hannan, Fadil M, Babinsky, Valerie N, Rogers, Angela, Gorvin, Caroline M, Rust, Nigel, Richardson, Tristan, McKenna, Malachi J, Nesbit, M. Andrew, Thakker, Rajesh V

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Identification of a G‐Protein Subunit‐α11 Gain‐of‐Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2) von Piret, Sian E, Gorvin, Caroline M, Pagnamenta, Alistair T, Howles, Sarah A, Cranston, Treena, Rust, Nigel, Nesbit, M Andrew, Glaser, Ben, Taylor, Jenny C, Buchs, Andreas E, Hannan, Fadil M, Thakker, Rajesh V

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Adaptor protein-2 sigma subunit mutations causing familial hypocalciuric hypercalcaemia type 3 (FHH3) demonstrate genotype-phenotype correlations, codon bias and dominant-negative... von Hannan, Fadil M, Howles, Sarah A, Rogers, Angela, Cranston, Treena, Gorvin, Caroline M, Babinsky, Valerie N, Reed, Anita A, Thakker, Clare E, Bockenhauer, Detlef, Brown, Rosalind S, Connell, John M, Cook, Jacqueline, Darzy, Ken, Ehtisham, Sarah, Graham, Una, Hulse, Tony, Hunter, Steven J, Izatt, Louise, Kumar, Dhavendra, McKenna, Malachi J, McKnight, John A, Morrison, Patrick J, Mughal, M Zulf, O'Halloran, Domhnall, Pearce, Simon H, Porteous, Mary E, Rahman, Mushtaqur, Richardson, Tristan, Robinson, Robert, Scheers, Isabelle, Siddique, Haroon, Van't Hoff, William G, Wang, Timothy, Whyte, Michael P, Nesbit, M Andrew, Thakker, Rajesh V

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Allosteric Modulation of the Calcium-sensing Receptor Rectifies Signaling Abnormalities Associated with G-protein α-11 Mutations Causing Hypercalcemic and Hypocalcemic Disorders von Babinsky, Valerie N., Hannan, Fadil M., Gorvin, Caroline M., Howles, Sarah A., Nesbit, M. Andrew, Rust, Nigel, Hanyaloglu, Aylin C., Hu, Jianxin, Spiegel, Allen M., Thakker, Rajesh V.

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Mucinous Adenocarcinoma of the Prostate With Normal Prostate-Specific Antigen Levels, Pulmonary Metastasis, and the Absence of Nodal Disease: A Case Report von Khokhar, Arham A, Howles, Sarah A, Leiblich, Aaron W, Samdani, Khubaib, Ahmed, Mubariz

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Identification of a G-Protein Subunit-[alpha]11 Gain-of-Function Mutation, Val340Met, in a Family With Autosomal Dominant Hypocalcemia Type 2 (ADH2) von Piret, Sian E, Gorvin, Caroline M, Pagnamenta, Alistair T, Howles, Sarah A, Cranston, Treena, Rust, Nigel, Nesbit, M Andrew, Glaser, Ben, Taylor, Jenny C, Buchs, Andreas E, Hannan, Fadil M, Thakker, Rajesh V

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