Söderkvist P - Search Results

1

A somatic mutation in CLCN2 identified in a sporadic aldosterone-producing adenoma.

Dutta RK, Arnesen T, Heie A, Walz M, Alesina P, Söderkvist P, Gimm O. Dutta RK, et al. Among authors: soderkvist p. Eur J Endocrinol. 2019 Nov;181(5):K37-K41. doi: 10.1530/EJE-19-0377. Eur J Endocrinol. 2019. PMID: 31491746

2

Complementary somatic mutations of KCNJ5, ATP1A1, and ATP2B3 in sporadic aldosterone producing adrenal adenomas.

Dutta RK, Welander J, Brauckhoff M, Walz M, Alesina P, Arnesen T, Söderkvist P, Gimm O. Dutta RK, et al. Among authors: soderkvist p. Endocr Relat Cancer. 2014 Jan 8;21(1):L1-4. doi: 10.1530/ERC-13-0466. Print 2014 Feb. Endocr Relat Cancer. 2014. PMID: 24179102 Free article. No abstract available.

3

Genetics of primary hyperaldosteronism.

Dutta RK, Söderkvist P, Gimm O. Dutta RK, et al. Among authors: soderkvist p. Endocr Relat Cancer. 2016 Oct;23(10):R437-54. doi: 10.1530/ERC-16-0055. Epub 2016 Aug 2. Endocr Relat Cancer. 2016. PMID: 27485459 Review.

4

X-chromosome variants are associated with aldosterone producing adenomas.

Dutta RK, Larsson M, Arnesen T, Heie A, Walz M, Alesina P, Gimm O, Söderkvist P. Dutta RK, et al. Among authors: soderkvist p. Sci Rep. 2021 May 18;11(1):10562. doi: 10.1038/s41598-021-89986-8. Sci Rep. 2021. PMID: 34006971 Free PMC article.

5

The NF1 gene: a frequent mutational target in sporadic pheochromocytomas and beyond.

Welander J, Söderkvist P, Gimm O. Welander J, et al. Among authors: soderkvist p. Endocr Relat Cancer. 2013 Jul 4;20(4):C13-7. doi: 10.1530/ERC-13-0046. Print 2013 Aug. Endocr Relat Cancer. 2013. PMID: 23756430

6

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: soderkvist p. 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.

7

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: soderkvist p. 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.

8

Activating FGFR1 Mutations in Sporadic Pheochromocytomas.

Welander J, Łysiak M, Brauckhoff M, Brunaud L, Söderkvist P, Gimm O. Welander J, et al. Among authors: soderkvist p. World J Surg. 2018 Feb;42(2):482-489. doi: 10.1007/s00268-017-4320-0. World J Surg. 2018. PMID: 29159601 Free PMC article.

9

Genetics and clinical characteristics of hereditary pheochromocytomas and paragangliomas.

Welander J, Söderkvist P, Gimm O. Welander J, et al. Among authors: soderkvist p. Endocr Relat Cancer. 2011 Dec 1;18(6):R253-76. doi: 10.1530/ERC-11-0170. Print 2011 Dec. Endocr Relat Cancer. 2011. PMID: 22041710 Review.

10

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: soderkvist p. 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

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