1. Absence of KMT2D/MLL2 mutations in abdominal paraganglioma. (22nd September 2015) Authors: Stenman, Adam; Juhlin, Carl C.; Haglund, Felix; Brown, Taylor C.; Clark, Victoria E.; Svahn, Fredrika; Bilguvar, Kaya; Goh, Gerald; Korah, Reju; Lifton, Richard P.; Carling, Tobias Journal: Clinical endocrinology Issue: Volume 84:Number 4(2016) Page Start: 632 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
2. Characterization of the mutational landscape of anaplastic thyroid cancer via whole-exome sequencing. (9th January 2015) Authors: Kunstman, John W.; Juhlin, C. Christofer; Goh, Gerald; Brown, Taylor C.; Stenman, Adam; Healy, James M.; Rubinstein, Jill C.; Choi, Murim; Kiss, Nimrod; Nelson-Williams, Carol; Mane, Shrikant; Rimm, David L.; Prasad, Manju L.; Höög, Anders; Zedenius, Jan; Larsson, Catharina; Korah, Reju; Lifton, ... Journal: Human molecular genetics Issue: Volume 24:Number 8(2015:Apr. 15) Page Start: 2318 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
3. Novel somatic mutations in primary hyperaldosteronism are related to the clinical, radiological and pathological phenotype. (23rd September 2015) Authors: Scholl, Ute I.; Healy, James M.; Thiel, Anne; Fonseca, Annabelle L.; Brown, Taylor C.; Kunstman, John W.; Horne, Matthew J.; Dietrich, Dimo; Riemer, Jasmin; Kücükköylü, Seher; Reimer, Esther N.; Reis, Anna‐Carinna; Goh, Gerald; Kristiansen, Glen; Mahajan, Amit; Korah, Reju; Lifton, Richard P.; Pr... Journal: Clinical endocrinology Issue: Volume 83:Number 6(2015:Dec.) Page Start: 779 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
4. PIK3CA Mutational Analysis of Parathyroid Adenomas. (13th April 2020) Authors: Riccardi, Aaliyah; Lemos, Carolina; Ramos, Ryan; Bellizzi, Justin; Parham, Kourosh; Brown, Taylor C.; Korah, Reju; Carling, Tobias; Costa‐Guda, Jessica; Arnold, Andrew Journal: JBMR plus Issue: Volume 4:Number 6(2020) Page Start: n/a Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗
5. Whole‐exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene. Issue 9 (29th May 2015) Authors: Juhlin, C. Christofer; Stenman, Adam; Haglund, Felix; Clark, Victoria E.; Brown, Taylor C.; Baranoski, Jacob; Bilguvar, Kaya; Goh, Gerald; Welander, Jenny; Svahn, Fredrika; Rubinstein, Jill C.; Caramuta, Stefano; Yasuno, Katsuhito; Günel, Murat; Bäckdahl, Martin; Gimm, Oliver; Söderkvist, Peter; ... Journal: Genes, chromosomes & cancer Issue: Volume 54:Issue 9(2015:Sep.) Page Start: 542 Record Type: Journal Article View Content: Available online (eLD content is only available in our Reading Rooms) ↗