Margrét Steinarsdóttir

927 total citations
28 papers, 611 citations indexed

About

Margrét Steinarsdóttir is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Margrét Steinarsdóttir has authored 28 papers receiving a total of 611 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Molecular Biology, 13 papers in Genetics and 11 papers in Oncology. Recurrent topics in Margrét Steinarsdóttir's work include Genomic variations and chromosomal abnormalities (8 papers), Cancer-related Molecular Pathways (7 papers) and Cancer Genomics and Diagnostics (6 papers). Margrét Steinarsdóttir is often cited by papers focused on Genomic variations and chromosomal abnormalities (8 papers), Cancer-related Molecular Pathways (7 papers) and Cancer Genomics and Diagnostics (6 papers). Margrét Steinarsdóttir collaborates with scholars based in Iceland, Switzerland and Denmark. Margrét Steinarsdóttir's co-authors include Jórunn E. Eyfjörd, Jón G. Jónasson, Helga M. Ögmundsdóttir, Kesara Anamthawat‐Jónsson, Rut Valgardsdottir, Steinunn Thorlacius, Kristrún Ólafsdóttir, Óskar Þór Jóhannsson, Sigríður Klara Böðvarsdóttir and Ólafur Andri Stefánsson and has published in prestigious journals such as Nucleic Acids Research, Cancer Letters and Journal of Medical Genetics.

In The Last Decade

Margrét Steinarsdóttir

28 papers receiving 593 citations

Peers

Margrét Steinarsdóttir
Massimo Bogliolo Spain
Deborah Yebon Kang South Korea
J.M. Trent United States
Ashleen Shadeo Canada
Emmanuelle Despras France
Åke Borg Sweden
Małgorzata Krajewska Netherlands
Dragana Kopanja United States
Oksana I. Dukhanina United States
Emmanuel Tubacher France
Massimo Bogliolo Spain
Margrét Steinarsdóttir
Citations per year, relative to Margrét Steinarsdóttir Margrét Steinarsdóttir (= 1×) peers Massimo Bogliolo

Countries citing papers authored by Margrét Steinarsdóttir

Since Specialization
Citations

This map shows the geographic impact of Margrét Steinarsdóttir's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Margrét Steinarsdóttir with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Margrét Steinarsdóttir more than expected).

Fields of papers citing papers by Margrét Steinarsdóttir

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Margrét Steinarsdóttir. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Margrét Steinarsdóttir. The network helps show where Margrét Steinarsdóttir may publish in the future.

Co-authorship network of co-authors of Margrét Steinarsdóttir

This figure shows the co-authorship network connecting the top 25 collaborators of Margrét Steinarsdóttir. A scholar is included among the top collaborators of Margrét Steinarsdóttir based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Margrét Steinarsdóttir. Margrét Steinarsdóttir is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Steinarsdóttir, Margrét, et al.. (2021). BRCA2 Haploinsufficiency in Telomere Maintenance. Genes. 13(1). 83–83. 1 indexed citations
2.
Lúðvígsson, Pétur, et al.. (2012). A de novo 1.13 Mb microdeletion in 12q13.13 associated with congenital distal arthrogryposis, intellectual disability and mild dysmorphism. European Journal of Medical Genetics. 55(6-7). 437–440. 9 indexed citations
3.
Böðvarsdóttir, Sigríður Klara, et al.. (2011). Dysfunctional telomeres in human BRCA2 mutated breast tumors and cell lines. Mutation research. Fundamental and molecular mechanisms of mutagenesis. 729(1-2). 90–99. 19 indexed citations
4.
Steinarsdóttir, Margrét, et al.. (2011). Cytogenetic polyclonality of breast carcinomas: Association with Clinico‐Pathological Characteristics and Outcome. Genes Chromosomes and Cancer. 50(11). 930–939. 4 indexed citations
5.
Ingþórsson, Sævar, Þórhallur I. Halldórsson, Valgarður Sigurðsson, et al.. (2010). Selection for EGFR gene amplification in a breast epithelial cell line with basal-like phenotype and hereditary background. In Vitro Cellular & Developmental Biology - Animal. 47(2). 139–148. 1 indexed citations
6.
Stefánsson, Ólafur Andri, Jón G. Jónasson, Óskar Þór Jóhannsson, et al.. (2009). Genomic profiling of breast tumours in relation to BRCAabnormalities and phenotypes. Breast Cancer Research. 11(4). R47–R47. 108 indexed citations
7.
Halldórsson, Skarphéðinn, et al.. (2007). Differentiation potential of a basal epithelial cell line established from human bronchial explant. In Vitro Cellular & Developmental Biology - Animal. 43(8-9). 283–289. 41 indexed citations
8.
Böðvarsdóttir, Sigríður Klara, Margrét Steinarsdóttir, Hólmfríður Hilmarsdóttir, Jón G. Jónasson, & Jórunn E. Eyfjörd. (2007). MYC amplification and TERT expression in breast tumor progression. Cancer Genetics and Cytogenetics. 176(2). 93–99. 13 indexed citations
9.
Viđarsson, Hilmar, et al.. (2006). Effect of hypoxia and TP53 mutation status and cytogenetics of normal and malignant mammary epithelium. Cancer Genetics and Cytogenetics. 165(2). 144–150. 1 indexed citations
10.
Böðvarsdóttir, Sigríður Klara, et al.. (2006). Aurora-A amplification associated with BRCA2 mutation in breast tumours. Cancer Letters. 248(1). 96–102. 24 indexed citations
11.
Sigurðsson, Valgarður, Agla J. Fridriksdottir, Jens Kjartansson, et al.. (2006). HUMAN BREAST MICROVASCULAR ENDOTHELIAL CELLS RETAIN PHENOTYPIC TRAITS IN LONG-TERM FINITE LIFE SPAN CULTURE. In Vitro Cellular & Developmental Biology - Animal. 42(10). 332–40. 18 indexed citations
12.
Fridriksdottir, Agla J., Þórarinn Guðjónsson, Þórhallur I. Halldórsson, et al.. (2005). Establishment of three human breast epithelial cell lines derived from carriers of the 999del5 BRCA2 icelandic founder mutation. In Vitro Cellular & Developmental Biology - Animal. 41(10). 337–342. 7 indexed citations
13.
Steinarsdóttir, Margrét, et al.. (2004). Cytogenetic changes in nonmalignant breast tissue. Genes Chromosomes and Cancer. 41(1). 47–55. 12 indexed citations
14.
Sigurðsson, Stefán, Sigríður Klara Böðvarsdóttir, Kesara Anamthawat‐Jónsson, et al.. (2000). p53 Abnormality and Chromosomal Instability in the Same Breast Tumor Cells. Cancer Genetics and Cytogenetics. 121(2). 150–155. 17 indexed citations
15.
Valgardsdottir, Rut, Laufey Tryggvadóttír, Margrét Steinarsdóttir, et al.. (1997). Genomic instability and poor prognosis associated with abnormal TP53 in breast carcinomas. Molecular and immunohistochemical analysis. Apmis. 105(1-6). 121–130. 23 indexed citations
16.
Eyfjörd, Jórunn E., et al.. (1996). Instability of chromosomes 1, 3, 16, and 17 in primary breast carcinomas inferred by fluorescence in situ hybridization. Cancer Genetics and Cytogenetics. 88(1). 1–7. 16 indexed citations
17.
Steinarsdóttir, Margrét, et al.. (1995). Cytogenetic studies of breast carcinomas: Different karyotypic profiles detected by direct harvesting and short‐term culture. Genes Chromosomes and Cancer. 13(4). 239–248. 48 indexed citations
18.
Eyfjörd, Jórunn E., Steinunn Thorlacius, Rut Valgardsdottir, et al.. (1995). TP53 Abnormalities and Genetic Instability in Breast Cancer. Acta Oncologica. 34(5). 663–667. 18 indexed citations
19.
Thorlacius, Steinunn, et al.. (1995). p53 abnormalities and genomic instability in primary human breast carcinomas.. PubMed. 55(3). 646–51. 94 indexed citations
20.
Steinarsdóttir, Margrét, et al.. (1994). Cytogenetic studies of breast carcinomas. Cancer Genetics and Cytogenetics. 77(2). 185–185. 3 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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