Works matching AU Challis, Benjamin G.

Results: 20

Peptidomic analysis of endogenous plasma peptides from patients with pancreatic neuroendocrine tumours.

Published in:

Rapid Communications in Mass Spectrometry: RCM, 2018, v. 32, n. 16, p. 1414, doi. 10.1002/rcm.8183

By:

Kay, Richard G.;
Challis, Benjamin G.;
Casey, Ruth T.;
Roberts, Geoffrey P.;
Meek, Claire L.;
Reimann, Frank;
Gribble, Fiona M.

Publication type:

Article

Precision Medicine in Phaeochromocytoma and Paraganglioma.

Published in:

Journal of Personalized Medicine, 2021, v. 11, n. 11, p. 1239, doi. 10.3390/jpm11111239

By:

Winzeler, Bettina;
Challis, Benjamin G.;
Casey, Ruth T.

Publication type:

Article

A review of the tumour spectrum of germline succinate dehydrogenase gene mutations: Beyond phaeochromocytoma and paraganglioma.

Published in:

Clinical Endocrinology, 2020, v. 93, n. 5, p. 528, doi. 10.1111/cen.14289

By:

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.

Publication type:

Article

What is the appropriate management of nonfunctioning pancreatic neuroendocrine tumours disclosed on screening in adult patients with multiple endocrine neoplasia type 1?

Published in:

Clinical Endocrinology, 2019, v. 91, n. 6, p. 708, doi. 10.1111/cen.14094

By:

Challis, Benjamin G.;
Casey, Ruth T.;
Grossman, Ashley;
Newell‐Price, John;
Newey, Paul;
Thakker, Rajesh V.

Publication type:

Article

Clinical Practice Guidance: Surveillance for phaeochromocytoma and paraganglioma in paediatric succinate dehydrogenase gene mutation carriers.

Published in:

Clinical Endocrinology, 2019, v. 90, n. 4, p. 499, doi. 10.1111/cen.13926

By:

Wong, Mei Yin;
Andrews, Katrina A.;
Challis, Benjamin G.;
Park, Soo‐Mi;
Acerini, Carlo L.;
Maher, Eamonn R.;
Casey, Ruth T.

Publication type:

Article

Nephrogenic syndrome of inappropriate antidiuresis secondary to an activating mutation in the arginine vasopressin receptor AVPR2.

Published in:

Clinical Endocrinology, 2016, v. 85, n. 2, p. 306, doi. 10.1111/cen.13011

By:

Powlson, Andrew S.;
Challis, Benjamin G.;
Halsall, David J.;
Schoenmakers, Erik;
Gurnell, Mark

Publication type:

Article

Familial adult onset hyperinsulinism due to an activating glucokinase mutation: implications for pharmacological glucokinase activation.

Published in:

Clinical Endocrinology, 2014, v. 81, n. 6, p. 855, doi. 10.1111/cen.12517

By:

Challis, Benjamin G.;
Harris, Julie;
Sleigh, Alison;
Isaac, Iona;
Orme, Steve M.;
Seevaratnam, Nandini;
Dhatariya, Ketan;
Simpson, Helen L.;
Semple, Robert K.

Publication type:

Article

Mutations in the human melanocortin-4 receptor gene associated with severe familial obesity disrupts receptor function through multiple molecular mechanisms.

Published in:

Human Molecular Genetics, 2003, v. 12, n. 5, p. 561, doi. 10.1093/hmg/ddg057

By:

Yeo, Giles S.H.;
Lank, Emma J.;
Farooqi, I. Sadaf;
Keogh, Julia;
Challis, Benjamin G.;
O'Rahilly, Stephen

Publication type:

Article

A missense mutation disrupting a dibasic prohormone processing site in pro-opiomelanocortin (POMC) increases susceptibility to early-onset obesity through a novel molecular mechanism.

Published in:

Human Molecular Genetics, 2002, v. 11, n. 17, p. 1997, doi. 10.1093/hmg/11.17.1997

By:

Challis, Benjamin G.;
Pritchard, Lynn E.;
Creemers, John W.M.;
Delplanque, Jerome;
Keogh, Julia M.;
Luan, Jian'an;
Wareham, Nicholas J.;
Yeo, Giles S.H.;
Bhattacharyya, Sumit;
Froguel, Phillipe;
White, Anne;
Farooqi, I. Sadaf;
O'Rahilly, Stephen

Publication type:

Article

Proopiomelanocortin and energy balance: insights from human and murine genetics.

Published in:

2004

By:

Coll, Anthony P;
Farooqi, I Sadaf;
Challis, Benjamin G;
Yeo, Giles S H;
O'Rahilly, Stephen

Publication type:

journal article

Characterisation of proguanylin expressing cells in the intestine – evidence for constitutive luminal secretion.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-52049-0

By:

Dye, Florent Serge;
Larraufie, Pierre;
Kay, Richard;
Darwish, Tamana;
Rievaj, Juraj;
Goldspink, Deborah A.;
Meek, Claire L.;
Middleton, Stephen J.;
Hardwick, Richard H.;
Roberts, Geoffrey P.;
Percival-Alwyn, Jennifer L.;
Vaughan, Tris;
Ferraro, Franco;
Challis, Benjamin G.;
O'Rahilly, Stephen;
Groves, Maria;
Gribble, Fiona M.;
Reimann, Frank

Publication type:

Article

SDHC epi-mutation testing in gastrointestinal stromal tumours and related tumours in clinical practice.

Published in:

Scientific Reports, 2019, v. 9, n. 1, p. N.PAG, doi. 10.1038/s41598-019-46124-9

By:

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.

Publication type:

Article

Clinical and Molecular Features of Renal and Pheochromocytoma/Paraganglioma Tumor Association Syndrome (RAPTAS): Case Series and Literature Review.

Published in:

2017

By:

Casey, Ruth T;
Warren, Anne Y;
Rodrigues, 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

Publication type:

journal article

Familial Adrenocortical Carcinoma in Association With Lynch Syndrome.

Published in:

2016

By:

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

Publication type:

journal article

Past, present and future strategies to study the genetics of body weight regulation.

Published in:

Briefings in Functional Genomics & Proteomics, 2002, v. 1, n. 3, p. 290, doi. 10.1093/bfgp/1.3.290

By:

Challis, Benjamin G.;
Yeo, Giles S. H.

Publication type:

Article

Heterozygosity for a POMC-Null Mutation and Increased Obesity Risk in Humans.

Published in:

Diabetes, 2006, v. 55, n. 9, p. 2549, doi. 10.2337/db06-0214

By:

Farooqi, I. Sadaf;
Drop, Stenvert;
Clements, Agnes;
Keogh, Julia M.;
Biernacka, Joanna;
Lowenbein, Sarah;
Challis, Benjamin G.;
O'Rahilly, Stephen

Publication type:

Article

Proopiomelanocortin-Deficient Mice Are Hypersensitive to the Adverse Metabolic Effects of Glucocorticoids.

Published in:

Diabetes, 2005, v. 54, n. 8, p. 2269, doi. 10.2337/diabetes.54.8.2269

By:

Coll, Anthony P.;
Challis, Benjamin G.;
López, Miguel;
Piper, Sarah;
Yeo, Giles S. H.;
O'Rahilly, Stephen

Publication type:

Article

The CART Gene and Human Obesity.

Published in:

Diabetes, 2000, v. 49, n. 5, p. 872, doi. 10.2337/diabetes.49.5.872

By:

Challis, Benjamin G.;
Yeo, Giles S.H.;
Farooqi, I. Sadaf;
Luan, Jian'an;
Aminian, Shiva;
Halsall, David J.;
Keogh, Julia M.;
Wareham, Nicholas J.;
O'Rahilly, Stephen

Publication type:

Article

Do glucagonomas always produce glucagon?

Published in:

Bosnian Journal of Basic Medical Sciences, 2016, v. 16, n. 1, p. 1, doi. 10.17305/bjbms.2015.794

By:

Albrechtsen, Nicolai Jacob Wewer;
Challis, Benjamin G.;
Damjanov, Ivan;
Holst, Jens Juul

Publication type:

Article

An Approach to a Patient With Primary Hyperparathyroidism and a Suspected Ectopic Parathyroid Adenoma.

Published in:

Journal of Clinical Endocrinology & Metabolism, 2022, v. 107, n. 6, p. 1706, doi. 10.1210/clinem/dgac024

By:

Glasgow, Clark;
Lau, Eunice Y. C.;
Aloj, Luigi;
Harper, Ines;
Heok Cheow;
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

Publication type:

Article