Gunnarsson C - Search Results

1

A new polymorphism in the coding region of exon four in HSD17B2 in relation to risk of sporadic and hereditary breast cancer.

Jansson A, Carlsson J, Olsson A, Storm P, Margolin S, Gunnarsson C, Stenmark-Askmalm M, Lindblom A, Persson B, Stål O. Jansson A, et al. Among authors: gunnarsson c. Breast Cancer Res Treat. 2007 Nov;106(1):57-64. doi: 10.1007/s10549-006-9477-4. Epub 2007 Jan 27. Breast Cancer Res Treat. 2007. PMID: 17260097

2

Case report: KPTN gene-related syndrome associated with a spectrum of neurodevelopmental anomalies including severe epilepsy.

Horn S, Danyel M, Erdmann N, Boschann F, Gunnarsson C, Biskup S, Juengling J, Potratz C, Prager C, Kaindl AM. Horn S, et al. Among authors: gunnarsson c. Front Neurol. 2023 Jan 10;13:1113811. doi: 10.3389/fneur.2022.1113811. eCollection 2022. Front Neurol. 2023. PMID: 36703628 Free PMC article.

3

Two epilepsy-associated variants in KCNA2 (K_V 1.2) at position H310 oppositely affect channel functional expression.

Mínguez-Viñas T, Prakash V, Wang K, Lindström SH, Pozzi S, Scott SA, Spiteri E, Stevenson DA, Ashley EA, Gunnarsson C, Pantazis A. Mínguez-Viñas T, et al. Among authors: gunnarsson c. J Physiol. 2023 Dec;601(23):5367-5389. doi: 10.1113/JP285052. Epub 2023 Oct 26. J Physiol. 2023. PMID: 37883018 Free article.

4

Rapid Implementation of Telegenetic Counseling in the COVID-19 and Swedish Healthcare Context: A Feasibility Study.

Pestoff R, Johansson P, Danielsson H, Neher M, Gunnarsson C. Pestoff R, et al. Among authors: gunnarsson c. Front Health Serv. 2022 Jun 23;2:848512. doi: 10.3389/frhs.2022.848512. eCollection 2022. Front Health Serv. 2022. PMID: 36925809 Free PMC article.

5

Definition and clinical variability of SHANK3-related Phelan-McDermid syndrome.

Schön M, Lapunzina P, Nevado J, Mattina T, Gunnarsson C, Hadzsiev K, Verpelli C, Bourgeron T, Jesse S, van Ravenswaaij-Arts CMA; European Phelan-McDermid syndrome consortium; Hennekam RC. Schön M, et al. Among authors: gunnarsson c. Eur J Med Genet. 2023 Jul;66(7):104754. doi: 10.1016/j.ejmg.2023.104754. Epub 2023 Mar 31. Eur J Med Genet. 2023. PMID: 37003575 Free article.

6

Translation, cross-cultural adaptation, and preliminary validation of a patient-reported outcome measure for genetic counseling outcomes in Sweden.

Pestoff R, Danielsson H, McAllister M, Johansson P, Gunnarsson C. Pestoff R, et al. Among authors: gunnarsson c. J Genet Couns. 2024 Apr 26. doi: 10.1002/jgc4.1896. Online ahead of print. J Genet Couns. 2024. PMID: 38665117

7

Abnormal expression of 17beta-hydroxysteroid dehydrogenases in breast cancer predicts late recurrence.

Gunnarsson C, Olsson BM, Stål O; Southeast Sweden Breast Cancer Group. Gunnarsson C, et al. Cancer Res. 2001 Dec 1;61(23):8448-51. Cancer Res. 2001. PMID: 11731426

8

Amplification of HSD17B1 and ERBB2 in primary breast cancer.

Gunnarsson C, Ahnström M, Kirschner K, Olsson B, Nordenskjöld B, Rutqvist LE, Skoog L, Stål O. Gunnarsson C, et al. Oncogene. 2003 Jan 9;22(1):34-40. doi: 10.1038/sj.onc.1206078. Oncogene. 2003. PMID: 12527905

9

17beta-Hydroxysteroid dehydrogenases involved in local oestrogen synthesis have prognostic significance in breast cancer.

Gunnarsson C, Hellqvist E, Stål O. Gunnarsson C, et al. Br J Cancer. 2005 Feb 14;92(3):547-52. doi: 10.1038/sj.bjc.6602375. Br J Cancer. 2005. PMID: 15685233 Free PMC article.

10

Expression of COX-2 and steroid converting enzymes in breast cancer.

Gunnarsson C, Jansson A, Holmlund B, Ferraud L, Nordenskjöld B, Rutqvist LE, Skoog L, Stål O. Gunnarsson C, et al. Oncol Rep. 2006 Aug;16(2):219-24. Oncol Rep. 2006. PMID: 16820896

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