Larsson C - Search Results

1

Linkage analysis with markers on 17q in 29 Swedish breast cancer families.

Lindblom A, Rotstein S, Nordenskjöld M, Larsson C. Lindblom A, et al. Among authors: larsson c. Am J Hum Genet. 1993 Apr;52(4):749-53. Am J Hum Genet. 1993. PMID: 8460641 Free PMC article.

2

Functional characterization of novel germline TP53 variants in Swedish families.

Kharaziha P, Ceder S, Axell O, Krall M, Fotouhi O, Böhm S, Lain S, Borg Å, Larsson C, Wiman KG, Tham E, Bajalica-Lagercrantz S. Kharaziha P, et al. Among authors: larsson c. Clin Genet. 2019 Sep;96(3):216-225. doi: 10.1111/cge.13564. Epub 2019 Jul 2. Clin Genet. 2019. PMID: 31081129

3

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: larsson c. 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

4

Involvement of the MEN1 gene locus in familial isolated hyperparathyroidism.

Villablanca A, Wassif WS, Smith T, Höög A, Vierimaa O, Kassem M, Dwight T, Forsberg L, Du Q, Learoyd D, Jones K, Stranks S, Juhlin C, Teh BT, Carling T, Robinson B, Larsson C. Villablanca A, et al. Among authors: larsson c. Eur J Endocrinol. 2002 Sep;147(3):313-22. doi: 10.1530/eje.0.1470313. Eur J Endocrinol. 2002. PMID: 12213668

5

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: larsson c. Int J Cancer. 2006 Mar 1;118(5):1159-64. doi: 10.1002/ijc.21385. Int J Cancer. 2006. PMID: 16161042

6

Novel and de novo mutations of the IRF6 gene detected in patients with Van der Woude or popliteal pterygium syndrome.

Peyrard-Janvid M, Pegelow M, Koillinen H, Larsson C, Fransson I, Rautio J, Hukki J, Larson O, Karsten AL, Kere J. Peyrard-Janvid M, et al. Among authors: larsson c. Eur J Hum Genet. 2005 Dec;13(12):1261-7. doi: 10.1038/sj.ejhg.5201493. Eur J Hum Genet. 2005. PMID: 16160700

7

A novel locus (RP33) for autosomal dominant retinitis pigmentosa mapping to chromosomal region 2cen-q12.1.

Zhao C, Lu S, Zhou X, Zhang X, Zhao K, Larsson C. Zhao C, et al. Among authors: larsson c. Hum Genet. 2006 Jul;119(6):617-23. doi: 10.1007/s00439-006-0168-3. Epub 2006 Apr 13. Hum Genet. 2006. PMID: 16612614

8

Characterization of 6q deletions in mature B cell lymphomas and childhood acute lymphoblastic leukemia.

Thelander EF, Ichimura K, Corcoran M, Barbany G, Nordgren A, Heyman M, Berglund M, Mungall A, Rosenquist R, Collins VP, Grandér D, Larsson C, Lagercrantz S. Thelander EF, et al. Among authors: larsson c. Leuk Lymphoma. 2008 Mar;49(3):477-87. doi: 10.1080/10428190701817282. Leuk Lymphoma. 2008. PMID: 18297524

9

Loss of chromosome 13q is a frequently acquired event in genetic progression of soft tissue sarcomas in the abdominal cavity.

Weng WH, Lerner M, Grandér D, Ahlén J, Villablanca A, Pang ST, Wejde J, Lui WO, Larsson C. Weng WH, et al. Among authors: larsson c. Int J Oncol. 2005 Jan;26(1):5-16. Int J Oncol. 2005. PMID: 15586219

10

Loss of 14q31-q32.2 in renal cell carcinoma is associated with high malignancy grade and poor survival.

Alimov A, Sundelin B, Wang N, Larsson C, Bergerheim U. Alimov A, et al. Among authors: larsson c. Int J Oncol. 2004 Jul;25(1):179-85. Int J Oncol. 2004. PMID: 15202004

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