Jonasson JG - Search Results

1

Loss-of-function variants in ATM confer risk of gastric cancer.

Helgason H, Rafnar T, Olafsdottir HS, Jonasson JG, Sigurdsson A, Stacey SN, Jonasdottir A, Tryggvadottir L, Alexiusdottir K, Haraldsson A, le Roux L, Gudmundsson J, Johannsdottir H, Oddsson A, Gylfason A, Magnusson OT, Masson G, Jonsson T, Skuladottir H, Gudbjartsson DF, Thorsteinsdottir U, Sulem P, Stefansson K. Helgason H, et al. Among authors: jonasson jg. Nat Genet. 2015 Aug;47(8):906-10. doi: 10.1038/ng.3342. Epub 2015 Jun 22. Nat Genet. 2015. PMID: 26098866

2

Linkage to BRCA2 region in hereditary male breast cancer.

Thorlacius S, Tryggvadottir L, Olafsdottir GH, Jonasson JG, Ogmundsdottir HM, Tulinius H, Eyfjord JE. Thorlacius S, et al. Among authors: jonasson jg. Lancet. 1995 Aug 26;346(8974):544-5. doi: 10.1016/s0140-6736(95)91383-1. Lancet. 1995. PMID: 7658781

3

Loss of heterozygosity on chromosome 9 in human breast cancer: association with clinical variables and genetic changes at other chromosome regions.

Eiriksdottir G, Sigurdsson A, Jonasson JG, Agnarsson BA, Sigurdsson H, Gudmundsson J, Bergthorsson JT, Barkardottir RB, Egilsson V, Ingvarsson S. Eiriksdottir G, et al. Among authors: jonasson jg. Int J Cancer. 1995 Dec 20;64(6):378-82. doi: 10.1002/ijc.2910640605. Int J Cancer. 1995. PMID: 8550238

4

A single BRCA2 mutation in male and female breast cancer families from Iceland with varied cancer phenotypes.

Thorlacius S, Olafsdottir G, Tryggvadottir L, Neuhausen S, Jonasson JG, Tavtigian SV, Tulinius H, Ogmundsdottir HM, Eyfjörd JE. Thorlacius S, et al. Among authors: jonasson jg. Nat Genet. 1996 May;13(1):117-9. doi: 10.1038/ng0596-117. Nat Genet. 1996. PMID: 8673089

5

TP53 mutation analyses on breast carcinomas: a study of paraffin-embedded archival material.

Gretarsdottir S, Tryggvadottir L, Jonasson JG, Sigurdsson H, Olafsdottir K, Agnarsson BA, Ogmundsdottir H, Eyfjörd JE. Gretarsdottir S, et al. Among authors: jonasson jg. Br J Cancer. 1996 Aug;74(4):555-61. doi: 10.1038/bjc.1996.400. Br J Cancer. 1996. PMID: 8761369 Free PMC article.

6

Loss of heterozygosity at chromosome 7q in human breast cancer: association with clinical variables.

Kristjansson AK, Eiriksdottir G, Ragnarsson G, Sigurdsson A, Gudmundsson J, Barkardottir RB, Jonasson JG, Egilsson V, Ingvarsson S. Kristjansson AK, et al. Among authors: jonasson jg. Anticancer Res. 1997 Jan-Feb;17(1A):93-8. Anticancer Res. 1997. PMID: 9066635

7

Genomic instability and poor prognosis associated with abnormal TP53 in breast carcinomas. Molecular and immunohistochemical analysis.

Valgardsdottir R, Tryggvadottir L, Steinarsdottir M, Olafsdottir K, Jonasdottir S, Jonasson JG, Ogmundsdottir HM, Eyfjörd JE. Valgardsdottir R, et al. Among authors: jonasson jg. APMIS. 1997 Feb;105(2):121-30. doi: 10.1111/j.1699-0463.1997.tb00550.x. APMIS. 1997. PMID: 9113074

8

Study of a single BRCA2 mutation with high carrier frequency in a small population.

Thorlacius S, Sigurdsson S, Bjarnadottir H, Olafsdottir G, Jonasson JG, Tryggvadottir L, Tulinius H, Eyfjörd JE. Thorlacius S, et al. Among authors: jonasson jg. Am J Hum Genet. 1997 May;60(5):1079-84. Am J Hum Genet. 1997. PMID: 9150155 Free PMC article.

9

High incidence of loss of heterozygosity in breast tumors from carriers of the BRCA2 999del5 mutation.

Ingvarsson S, Geirsdottir EK, Johannesdottir G, Sigbjörnsdóttir BI, Eiriksdottir G, Ragnarsson G, Agnarsson BA, Gudmundsson J, Jonasson JG, Sigurdsson A, Egilsson V, Barkardottir RB. Ingvarsson S, et al. Among authors: jonasson jg. Cancer Res. 1998 Oct 1;58(19):4421-5. Cancer Res. 1998. PMID: 9766673

10

Mapping loss of heterozygosity at chromosome 13q: loss at 13q12-q13 is associated with breast tumour progression and poor prognosis.

Eiriksdottir G, Johannesdottir G, Ingvarsson S, Björnsdottir IB, Jonasson JG, Agnarsson BA, Hallgrimsson J, Gudmundsson J, Egilsson V, Sigurdsson H, Barkardottir RB. Eiriksdottir G, et al. Among authors: jonasson jg. Eur J Cancer. 1998 Dec;34(13):2076-81. doi: 10.1016/s0959-8049(98)00241-x. Eur J Cancer. 1998. PMID: 10070314

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