Rare variant contribution to human disease in 281,104 UK Biobank exomes von Wang, Quanli, Dhindsa, Ryan S., Carss, Keren, Harper, Andrew R., Nag, Abhishek, Tachmazidou, Ioanna, Vitsios, Dimitrios, Deevi, Sri V. V., Mackay, Alex, Muthas, Daniel, Hühn, Michael, Monkley, Susan, Olsson, Henric, Wasilewski, Sebastian, Smith, Katherine R., March, Ruth, Platt, Adam, Haefliger, Carolina, Petrovski, Slavé

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CT Characteristics of Pheochromocytoma: Relevance for the Evaluation of Adrenal Incidentaloma von Canu, Letizia, Van Hemert, Janna A W, Kerstens, Michiel N, Hartman, Robert P, Khanna, Aakanksha, Kraljevic, Ivana, Kastelan, Darko, Badiu, Corin, Ambroziak, Urszula, Tabarin, Antoine, Haissaguerre, Magalie, Buitenwerf, Edward, Visser, Anneke, Mannelli, Massimo, Arlt, Wiebke, Chortis, Vasileios, Bourdeau, Isabelle, Gagnon, Nadia, Buchy, Marie, Borson-Chazot, Francoise, Deutschbein, Timo, Fassnacht, Martin, Hubalewska-Dydejczyk, Alicja, Motyka, Marcin, Rzepka, Ewelina, Casey, Ruth T, Challis, Benjamin G, Quinkler, Marcus, Vroonen, Laurent, Spyroglou, Ariadni, Beuschlein, Felix, Lamas, Cristina, Young, William F, Bancos, Irina, Timmers, Henri J L M

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A review of the tumour spectrum of germline succinate dehydrogenase gene mutations: Beyond phaeochromocytoma and paraganglioma von MacFarlane, James, Seong, Keat Cheah, Bisambar, Chad, Madhu, Basetti, Allinson, Kieren, Marker, Alison, Warren, Anne, Park, Soo‐Mi, Giger, Olivier, Challis, Benjamin G., Maher, Eamonn R., Casey, Ruth T.

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Peptidomic analysis of endogenous plasma peptides from patients with pancreatic neuroendocrine tumours von Kay, Richard G., Challis, Benjamin G., Casey, Ruth T., Roberts, Geoffrey P., Meek, Claire L., Reimann, Frank, Gribble, Fiona M.

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Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review von Casey, Ruth T, Warren, Anne Y, Martin, Jose Ezequiel, Challis, Benjamin G, Rattenberry, Eleanor, Whitworth, James, Andrews, Katrina A, Roberts, Thomas, Clark, Graeme R, West, Hannah, Smith, Philip S, Docquier, France M, Rodger, Fay, Murray, Vicki, Simpson, Helen L, Wallis, Yvonne, Giger, Olivier, Tran, Maxine, Tomkins, Susan, Stewart, Grant D, Park, Soo-Mi, Woodward, Emma R, Maher, Eamonn R

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Nephrogenic syndrome of inappropriate antidiuresis secondary to an activating mutation in the arginine vasopressin receptor AVPR2 von Powlson, Andrew S., Challis, Benjamin G., Halsall, David J., Schoenmakers, Erik, Gurnell, Mark

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An Approach to a Patient With Primary Hyperparathyroidism and a Suspected Ectopic Parathyroid Adenoma von Glasgow, Clark, Lau, Eunice Y C, Aloj, Luigi, Harper, Ines, Cheow, Heok, Das, Tilak, Berman, Laurence, Powlson, Andrew S, Bashari, Waiel A, Challis, Benjamin G, Marker, Alison, Moyle, Penelope, Mohamed, Isra Ahmed, Schoenmakers, Nadia, Broomfield, Jonathan, Oddy, Sue, Moran, Carla, Gurnell, Mark, Jani, Piyush, Masterson, Liam, Fish, Brian, Casey, Ruth T

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Heterozygosity for a POMC-Null Mutation and Increased Obesity Risk in Humans von SADAF FAROOQI, I, DROP, Stenvert, CLEMENTS, Agnes, KEOGH, Julia M, BIERNACKA, Joanna, LOWENBEIN, Sarah, CHALLIS, Benjamin G, O'RAHILLY, Stephen

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Precision Medicine in Phaeochromocytoma and Paraganglioma von Winzeler, Bettina, Challis, Benjamin G., Casey, Ruth T.

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What is the appropriate management of nonfunctioning pancreatic neuroendocrine tumours disclosed on screening in adult patients with multiple endocrine neoplasia type 1? von Challis, Benjamin G., Casey, Ruth T., Grossman, Ashley, Newell‐Price, John, Newey, Paul, Thakker, Rajesh V.

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A View on Drug Development for Cancer Prevention von Reynolds, Andrew R, Moschetta, Michele, Yohannes, Alula R, Walcott, Farzana, Ashford, Marianne, Szucs, Zoltan, Sarbajna, Tina, Hadfield, James, Harrison, Eden, Challis, Benjamin G, Hernandez, Amaya Gasco, Schiavon, Gaia, Germa, Caroline, Zorenyi, Gyorgy, Crean, Barry, Galbraith, Susan

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Clinical Practice Guidance: Surveillance for phaeochromocytoma and paraganglioma in paediatric succinate dehydrogenase gene mutation carriers von Wong, Mei Yin, Andrews, Katrina A., Challis, Benjamin G., Park, Soo‐Mi, Acerini, Carlo L., Maher, Eamonn R., Casey, Ruth T.

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Fumarate Metabolic Signature for the Detection of Reed Syndrome in Humans von Casey, Ruth T., McLean, Mary A., Challis, Benjamin G., McVeigh, Terri P., Warren, Anne Y., Mendil, Lee, Houghton, Richard, De Sanctis, Stefano, Kosmoliaptsis, Vasilis, Sandford, Richard N., Gallagher, Ferdia A., Maher, Eamonn R.

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Familial Adrenocortical Carcinoma in Association With Lynch Syndrome von Challis, Benjamin G, Kandasamy, Narayanan, Powlson, Andrew S, Koulouri, Olympia, Annamalai, Anand Kumar, Happerfield, Lisa, Marker, Alison J, Arends, Mark J, Nik-Zainal, Serena, Gurnell, Mark

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SDHC epi-mutation testing in gastrointestinal stromal tumours and related tumours in clinical practice von Casey, Ruth T., ten Hoopen, Rogier, Ochoa, Eguzkine, Challis, Benjamin G., Whitworth, James, Smith, Philip S., Martin, Jose Ezequiel, Clark, Graeme R., Rodger, Fay, Maranian, Mel, Allinson, Kieren, Madhu, Basetti, Roberts, Thomas, Campos, Luis, Anstee, Joanne, Park, Soo-Mi, Marker, Alison, Watts, Colin, Bulusu, Venkata R., Giger, Olivier T., Maher, Eamonn R.

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Multiple endocrine neoplasia type 1 in children and adolescents: Clinical features and treatment outcomes von Shariq, Omair A., Lines, Kate E., English, Katherine A., Jafar-Mohammadi, Bahram, Prentice, Philippa, Casey, Ruth, Challis, Benjamin G., Selberherr, Andreas, Boon, Hannah, Cranston, Treena, Ryan, Fiona J., Mihai, Radu, Healy, Ultan, Kurzawinski, Tom, Dattani, Mehul T., Bancos, Irina, Dy, Benzon M., Lyden, Melanie L., Young, William F., McKenzie, Travis J., Richards, Duncan, Thakker, Rajesh V.

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Proopiomelanocortin and Energy Balance: Insights from Human and Murine Genetics von Coll, Anthony P., Farooqi, I. Sadaf, Challis, Benjamin G., Yeo, Giles S. H., O’Rahilly, Stephen

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Minireview: Human Obesity—Lessons from Monogenic Disorders von O’Rahilly, Stephen, Farooqi, I. Sadaf, Yeo, Giles S. H, Challis, Benjamin G

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Metabolic dysfunction-related liver disease as a risk factor for cancer von Taylor, Alasdair, Siddiqui, Moneeza K, Ambery, Philip, Armisen, Javier, Challis, Benjamin G, Haefliger, Carolina, Pearson, Ewan R, Doney, Alex S F, Dillon, John F, Palmer, Colin N A

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Corrigendum to ‘Multiple endocrine neoplasia type 1 in children and adolescents: Clinical features and treatment outcomes’ [Surgery 171 (2021) 77–87] von Shariq, Omair A., Lines, Kate E., English, Katherine A., Jafar-Mohammadi, Bahram, Prentice, Philippa, Casey, Ruth, Challis, Benjamin G., Selberherr, Andreas, Boon, Hannah, Cranston, Treena, Ryan, Fiona J., Mihai, Radu, Healy, Ultan, Kurzawinski, Tom, Dattani, Mehul T., Bancos, Irina, Dy, Benzon M., Lyden, Melanie L., Young, William F., McKenzie, Travis J., Richards, Duncan, Thakker, Rajesh V.

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