Gimm O - Search Results

1

Detailed assessment of chromosome 22 aberrations in sporadic pheochromocytoma using array-CGH.

Jarbo C, Buckley PG, Piotrowski A, Mantripragada KK, Benetkiewicz M, Diaz de Ståhl T, Langford CF, Gregory SG, Dralle H, Gimm O, Bäckdahl M, Geli J, Larsson C, Westin G, Akerström G, Dumanski JP. Jarbo C, et al. Among authors: gimm o. Int J Cancer. 2006 Mar 1;118(5):1159-64. doi: 10.1002/ijc.21385. Int J Cancer. 2006. PMID: 16161042

2

Frequent EPAS1/HIF2α exons 9 and 12 mutations in non-familial pheochromocytoma.

Welander J, Andreasson A, Brauckhoff M, Bäckdahl M, Larsson C, Gimm O, Söderkvist P. Welander J, et al. Among authors: gimm o. Endocr Relat Cancer. 2014 Jun;21(3):495-504. doi: 10.1530/ERC-13-0384. Epub 2014 Apr 16. Endocr Relat Cancer. 2014. PMID: 24741025

3

HRAS mutation prevalence and associated expression patterns in pheochromocytoma.

Stenman A, Welander J, Gustavsson I, Brunaud L, Bäckdahl M, Söderkvist P, Gimm O, Juhlin CC, Larsson C. Stenman A, et al. Among authors: gimm o. Genes Chromosomes Cancer. 2016 May;55(5):452-9. doi: 10.1002/gcc.22347. Epub 2016 Feb 23. Genes Chromosomes Cancer. 2016. PMID: 26773571 Free PMC article.

4

Rare germline mutations identified by targeted next-generation sequencing of susceptibility genes in pheochromocytoma and paraganglioma.

Welander J, Andreasson A, Juhlin CC, Wiseman RW, Bäckdahl M, Höög A, Larsson C, Gimm O, Söderkvist P. Welander J, et al. Among authors: gimm o. J Clin Endocrinol Metab. 2014 Jul;99(7):E1352-60. doi: 10.1210/jc.2013-4375. Epub 2014 Apr 2. J Clin Endocrinol Metab. 2014. PMID: 24694336 Free PMC article.

5

Integrative genomics reveals frequent somatic NF1 mutations in sporadic pheochromocytomas.

Welander J, Larsson C, Bäckdahl M, Hareni N, Sivlér T, Brauckhoff M, Söderkvist P, Gimm O. Welander J, et al. Among authors: gimm o. Hum Mol Genet. 2012 Dec 15;21(26):5406-16. doi: 10.1093/hmg/dds402. Epub 2012 Sep 24. Hum Mol Genet. 2012. PMID: 23010473

6

Preoperative and surgical therapy in sporadic and familial pheochromocytoma.

Brauckhoff M, Gimm O, Dralle H. Brauckhoff M, et al. Among authors: gimm o. Front Horm Res. 2004;31:121-44. doi: 10.1159/000074661. Front Horm Res. 2004. PMID: 14674308 Review. No abstract available.

7

Mutation analysis of NTRK2 and NTRK3, encoding 2 tyrosine kinase receptors, in sporadic human medullary thyroid carcinoma reveals novel sequence variants.

Gimm O, Dziema H, Brown J, de la Puente A, Hoang-Vu C, Dralle H, Plass C, Eng C. Gimm O, et al. Int J Cancer. 2001 Apr 1;92(1):70-4. Int J Cancer. 2001. PMID: 11279608

8

Role of SDHAF2 and SDHD in von Hippel-Lindau associated pheochromocytomas.

Kugelberg J, Welander J, Schiavi F, Fassina A, Bäckdahl M, Larsson C, Opocher G, Söderkvist P, Dahia PL, Neumann HP, Gimm O. Kugelberg J, et al. Among authors: gimm o. World J Surg. 2014 Mar;38(3):724-32. doi: 10.1007/s00268-013-2373-2. World J Surg. 2014. PMID: 24322175

9

Whole-exome sequencing defines the mutational landscape of pheochromocytoma and identifies KMT2D as a recurrently mutated gene.

Juhlin CC, Stenman A, Haglund F, Clark VE, Brown TC, Baranoski J, Bilguvar K, Goh G, Welander J, Svahn F, Rubinstein JC, Caramuta S, Yasuno K, Günel M, Bäckdahl M, Gimm O, Söderkvist P, Prasad ML, Korah R, Lifton RP, Carling T. Juhlin CC, et al. Among authors: gimm o. Genes Chromosomes Cancer. 2015 Sep;54(9):542-54. doi: 10.1002/gcc.22267. Epub 2015 May 29. Genes Chromosomes Cancer. 2015. PMID: 26032282 Free PMC article.

10

Risk-oriented approach to hereditary adrenal pheochromocytoma.

Machens A, Brauckhoff M, Gimm O, Dralle H. Machens A, et al. Among authors: gimm o. Ann N Y Acad Sci. 2006 Aug;1073:417-28. doi: 10.1196/annals.1353.045. Ann N Y Acad Sci. 2006. PMID: 17102110

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