Welander J - Search Results

1

A universal method for species identification of mammals utilizing next generation sequencing for the analysis of DNA mixtures.

Tillmar AO, Dell'Amico B, Welander J, Holmlund G. Tillmar AO, et al. Among authors: welander j. PLoS One. 2013 Dec 16;8(12):e83761. doi: 10.1371/journal.pone.0083761. eCollection 2013. PLoS One. 2013. PMID: 24358309 Free PMC article.

2

DNA microarray as a tool in establishing genetic relatedness--Current status and future prospects.

Kling D, Welander J, Tillmar A, Skare O, Egeland T, Holmlund G. Kling D, et al. Among authors: welander j. Forensic Sci Int Genet. 2012 May;6(3):322-9. doi: 10.1016/j.fsigen.2011.07.007. Epub 2011 Aug 2. Forensic Sci Int Genet. 2012. PMID: 21813350

3

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. 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.

4

Consensus Statement on next-generation-sequencing-based diagnostic testing of hereditary phaeochromocytomas and paragangliomas.

NGS in PPGL (NGSnPPGL) Study Group; Toledo RA, Burnichon N, Cascon A, Benn DE, Bayley JP, Welander J, Tops CM, Firth H, Dwight T, Ercolino T, Mannelli M, Opocher G, Clifton-Bligh R, Gimm O, Maher ER, Robledo M, Gimenez-Roqueplo AP, Dahia PL. NGS in PPGL (NGSnPPGL) Study Group, et al. Among authors: welander j. Nat Rev Endocrinol. 2017 Apr;13(4):233-247. doi: 10.1038/nrendo.2016.185. Epub 2016 Nov 18. Nat Rev Endocrinol. 2017. PMID: 27857127 Free article. Review.

5

Germline SDHA mutation detected by next-generation sequencing in a young index patient with large paraganglioma.

Welander J, Garvin S, Bohnmark R, Isaksson L, Wiseman RW, Söderkvist P, Gimm O. Welander J, et al. J Clin Endocrinol Metab. 2013 Aug;98(8):E1379-80. doi: 10.1210/jc.2013-1963. Epub 2013 Jun 7. J Clin Endocrinol Metab. 2013. PMID: 23750034 No abstract available.

6

Colistin- and carbapenem-resistant Klebsiella pneumoniae carrying mcr-1 and blaOXA-48 isolated at a paediatric hospital in Vietnam.

Berglund B, Hoang NTB, Tärnberg M, Le NK, Welander J, Nilsson M, Khu DTK, Nilsson LE, Olson L, Le HT, Larsson M, Hanberger H. Berglund B, et al. Among authors: welander j. J Antimicrob Chemother. 2018 Apr 1;73(4):1100-1102. doi: 10.1093/jac/dkx491. J Antimicrob Chemother. 2018. PMID: 29253209 No abstract available.

7

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. 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

8

Characterization of extended-spectrum β-lactamase-producing Escherichia coli harboring mcr-1 and toxin genes from human fecal samples from China.

Berglund B, Chen B, Tärnberg M, Sun Q, Xu L, Welander J, Li Y, Bi Z, Nilsson M, Nilsson LE. Berglund B, et al. Among authors: welander j. Future Microbiol. 2018 Nov;13:1647-1655. doi: 10.2217/fmb-2018-0242. Epub 2018 Nov 29. Future Microbiol. 2018. PMID: 30489158

9

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: welander j. World J Surg. 2014 Mar;38(3):724-32. doi: 10.1007/s00268-013-2373-2. World J Surg. 2014. PMID: 24322175

10

YAP1 is a potential biomarker for cetuximab resistance in head and neck cancer.

Jerhammar F, Johansson AC, Ceder R, Welander J, Jansson A, Grafström RC, Söderkvist P, Roberg K. Jerhammar F, et al. Among authors: welander j. Oral Oncol. 2014 Sep;50(9):832-9. doi: 10.1016/j.oraloncology.2014.06.003. Epub 2014 Jun 30. Oral Oncol. 2014. PMID: 24993889

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