Felix Beuschlein
Felix Beuschlein
University Clinic Zurich
Verified email at usz.ch
TitleCited byYear
Adrenal insufficiency
W Arlt, B Allolio
The Lancet 361 (9372), 1881-1893, 2003
9582003
Evidence for two types of brown adipose tissue in humans
ME Lidell, MJ Betz, OD Leinhard, M Heglind, L Elander, M Slawik, ...
Nature medicine 19 (5), 631, 2013
4942013
Combination chemotherapy in advanced adrenocortical carcinoma
M Fassnacht, M Terzolo, B Allolio, E Baudin, H Haak, A Berruti, S Welin, ...
New England Journal of Medicine 366 (23), 2189-2197, 2012
4922012
Limited prognostic value of the 2004 International Union Against Cancer staging classification for adrenocortical carcinoma: proposal for a Revised TNM Classification
M Fassnacht, S Johanssen, M Quinkler, P Bucsky, HS Willenberg, ...
Cancer 115 (2), 243-250, 2009
4262009
Somatic mutations in ATP1A1 and ATP2B3 lead to aldosterone-producing adenomas and secondary hypertension
F Beuschlein, S Boulkroun, A Osswald, T Wieland, HN Nielsen, ...
Nature genetics 45 (4), 440, 2013
3622013
Integrated genomic characterization of adrenocortical carcinoma
G Assié, E Letouzé, M Fassnacht, A Jouinot, W Luscap, O Barreau, ...
Nature genetics 46 (6), 607, 2014
3332014
The immune landscape of cancer
V Thorsson, DL Gibbs, SD Brown, D Wolf, DS Bortone, THO Yang, ...
Immunity 48 (4), 812-830. e14, 2018
3142018
Comprehensive characterization of cancer driver genes and mutations
MH Bailey, C Tokheim, E Porta-Pardo, S Sengupta, D Bertrand, ...
Cell 173 (2), 371-385. e18, 2018
2852018
Constitutive activation of PKA catalytic subunit in adrenal Cushing's syndrome
F Beuschlein, M Fassnacht, G Assié, D Calebiro, CA Stratakis, A Osswald, ...
New England Journal of Medicine 370 (11), 1019-1028, 2014
2472014
MAX mutations cause hereditary and sporadic pheochromocytoma and paraganglioma
N Burnichon, A Cascón, F Schiavi, NP Morales, I Comino-Méndez, ...
Clinical Cancer Research 18 (10), 2828-2837, 2012
2332012
Prevalence, Clinical, and Molecular Correlates of KCNJ5 Mutations in Primary Aldosteronism
S Boulkroun, F Beuschlein, GP Rossi, JF Golib-Dzib, E Fischer, L Amar, ...
Hypertension 59 (3), 592-598, 2012
2312012
Comprehensive pan-genomic characterization of adrenocortical carcinoma
S Zheng, AD Cherniack, N Dewal, RA Moffitt, L Danilova, BA Murray, ...
Cancer cell 29 (5), 723-736, 2016
2262016
Cardiovascular and cerebrovascular comorbidities of hypokalemic and normokalemic primary aldosteronism: results of the German Conn’s Registry
E Born-Frontsberg, M Reincke, LC Rump, S Hahner, S Diederich, ...
The Journal of Clinical Endocrinology & Metabolism 94 (4), 1125-1130, 2009
2222009
Oncogenic signaling pathways in the cancer genome atlas
F Sanchez-Vega, M Mina, J Armenia, WK Chatila, A Luna, KC La, ...
Cell 173 (2), 321-337. e10, 2018
2212018
Mutations in the deubiquitinase gene USP8 cause Cushing's disease
M Reincke, S Sbiera, A Hayakawa, M Theodoropoulou, A Osswald, ...
Nature genetics 47 (1), 31, 2015
2212015
Cell-of-origin patterns dominate the molecular classification of 10,000 tumors from 33 types of cancer
KA Hoadley, C Yau, T Hinoue, DM Wolf, AJ Lazar, E Drill, R Shen, ...
Cell 173 (2), 291-304. e6, 2018
2092018
High diagnostic and prognostic value of steroidogenic factor-1 expression in adrenal tumors
S Sbiera, S Schmull, G Assie, HU Voelker, L Kraus, M Beyer, B Ragazzon, ...
The Journal of Clinical Endocrinology & Metabolism 95 (10), E161-E171, 2010
1822010
Genetic spectrum and clinical correlates of somatic mutations in aldosterone-producing adenoma
FL Fernandes-Rosa, TA Williams, A Riester, O Steichen, F Beuschlein, ...
Hypertension 64 (2), 354-361, 2014
1782014
Comprehensive molecular characterization of pheochromocytoma and paraganglioma
L Fishbein, I Leshchiner, V Walter, L Danilova, AG Robertson, ...
Cancer cell 31 (2), 181-193, 2017
1732017
High incidence of adrenal crisis in educated patients with chronic adrenal insufficiency: a prospective study
S Hahner, C Spinnler, M Fassnacht, S Burger-Stritt, K Lang, ...
The Journal of Clinical Endocrinology & Metabolism 100 (2), 407-416, 2015
1682015
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