Nordling M - Search Results

1

Integrative genetic characterization and phenotype correlations in pheochromocytoma and paraganglioma tumours.

Crona J, Nordling M, Maharjan R, Granberg D, Stålberg P, Hellman P, Björklund P. Crona J, et al. Among authors: nordling m. PLoS One. 2014 Jan 22;9(1):e86756. doi: 10.1371/journal.pone.0086756. eCollection 2014. PLoS One. 2014. PMID: 24466223 Free PMC article.

2

Genotype-phenotype correlations, and retinal function and structure in von Hippel-Lindau disease.

Wittström E, Nordling M, Andréasson S. Wittström E, et al. Among authors: nordling m. Ophthalmic Genet. 2014 Jun;35(2):91-106. doi: 10.3109/13816810.2014.886265. Epub 2014 Feb 20. Ophthalmic Genet. 2014. PMID: 24555745

3

Delimitation of a critical tumour suppressor region at distal 1p in neuroblastoma tumours.

Martinsson T, Sjöberg RM, Hallstensson K, Nordling M, Hedborg F, Kogner P. Martinsson T, et al. Among authors: nordling m. Eur J Cancer. 1997 Oct;33(12):1997-2001. doi: 10.1016/s0959-8049(97)00278-5. Eur J Cancer. 1997. PMID: 9516841

4

A large deletion disrupts the exon 3 transcription activation domain of the BRCA2 gene in a breast/ovarian cancer family.

Nordling M, Karlsson P, Wahlström J, Engwall Y, Wallgren A, Martinsson T. Nordling M, et al. Cancer Res. 1998 Apr 1;58(7):1372-5. Cancer Res. 1998. PMID: 9537232

5

A high frequency of germline BRCA1/2 mutations in western Sweden detected with complementary screening techniques.

Bergman A, Flodin A, Engwall Y, Arkblad EL, Berg K, Einbeigi Z, Martinsson T, Wahlström J, Karlsson P, Nordling M. Bergman A, et al. Among authors: nordling m. Fam Cancer. 2005;4(2):89-96. doi: 10.1007/s10689-004-5812-2. Fam Cancer. 2005. PMID: 15951958

6

Novel findings in Swedish patients with MYH-associated polyposis: mutation detection and clinical characterization.

Kanter-Smoler G, Björk J, Fritzell K, Engwall Y, Hallberg B, Karlsson G, Grönberg H, Karlsson P, Wallgren A, Wahlström J, Hultcrantz R, Nordling M. Kanter-Smoler G, et al. Among authors: nordling m. Clin Gastroenterol Hepatol. 2006 Apr;4(4):499-506. doi: 10.1016/j.cgh.2006.01.005. Clin Gastroenterol Hepatol. 2006. PMID: 16616356

7

Occurrence of both breast and ovarian cancer in a woman is a marker for the BRCA gene mutations: a population-based study from western Sweden.

Einbeigi Z, Bergman A, Meis-Kindblom JM, Flodin A, Bjursell C, Martinsson T, Kindblom LG, Wahlström J, Wallgren A, Nordling M, Karlsson P. Einbeigi Z, et al. Among authors: nordling m. Fam Cancer. 2007;6(1):35-41. doi: 10.1007/s10689-006-9101-0. Fam Cancer. 2007. PMID: 16944270

8

Genome-wide linkage scan for breast cancer susceptibility loci in Swedish hereditary non-BRCA1/2 families: suggestive linkage to 10q23.32-q25.3.

Bergman A, Karlsson P, Berggren J, Martinsson T, Björck K, Nilsson S, Wahlström J, Wallgren A, Nordling M. Bergman A, et al. Among authors: nordling m. Genes Chromosomes Cancer. 2007 Mar;46(3):302-9. doi: 10.1002/gcc.20405. Genes Chromosomes Cancer. 2007. PMID: 17171685

9

Clinical characterization and the mutation spectrum in Swedish adenomatous polyposis families.

Kanter-Smoler G, Fritzell K, Rohlin A, Engwall Y, Hallberg B, Bergman A, Meuller J, Grönberg H, Karlsson P, Björk J, Nordling M. Kanter-Smoler G, et al. Among authors: nordling m. BMC Med. 2008 Apr 24;6:10. doi: 10.1186/1741-7015-6-10. BMC Med. 2008. PMID: 18433509 Free PMC article.

10

No germline mutations in supposed tumour suppressor genes SAFB1 and SAFB2 in familial breast cancer with linkage to 19p.

Bergman A, Abel F, Behboudi A, Yhr M, Mattsson J, Svensson JH, Karlsson P, Nordling M. Bergman A, et al. Among authors: nordling m. BMC Med Genet. 2008 Dec 13;9:108. doi: 10.1186/1471-2350-9-108. BMC Med Genet. 2008. PMID: 19077293 Free PMC article.

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