Maria Soller

3.9k total citations
46 papers, 884 citations indexed

About

Maria Soller is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Maria Soller has authored 46 papers receiving a total of 884 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 21 papers in Genetics and 8 papers in Cancer Research. Recurrent topics in Maria Soller's work include Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (6 papers) and Renal and related cancers (6 papers). Maria Soller is often cited by papers focused on Prenatal Screening and Diagnostics (7 papers), Genomics and Rare Diseases (6 papers) and Renal and related cancers (6 papers). Maria Soller collaborates with scholars based in Sweden, Denmark and Australia. Maria Soller's co-authors include Inger Björck, Juscelino Tovar, Josef Davidsson, Anna Collin, Ioannis Panagopoulos, Å. Nilsson, Felix Mitelman, Leif Johansson, Michael Dictor and Mats Jerkeman and has published in prestigious journals such as PLoS ONE, Stroke and Scientific Reports.

In The Last Decade

Maria Soller

44 papers receiving 858 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Maria Soller Sweden 20 359 267 153 132 128 46 884
Koichi Yano Japan 17 276 0.8× 148 0.6× 185 1.2× 176 1.3× 191 1.5× 80 946
Yumiko Okubo Japan 10 336 0.9× 135 0.5× 78 0.5× 82 0.6× 77 0.6× 27 791
Rachel Reynaud France 24 538 1.5× 495 1.9× 84 0.5× 96 0.7× 249 1.9× 99 1.6k
Antony Lafferty Australia 16 558 1.6× 367 1.4× 166 1.1× 189 1.4× 548 4.3× 30 1.6k
Siddharth Banka United Kingdom 18 339 0.9× 480 1.8× 63 0.4× 55 0.4× 104 0.8× 55 991
Thomas Rothämel Germany 13 229 0.6× 116 0.4× 126 0.8× 101 0.8× 172 1.3× 35 798
Naotake Shimoda Japan 12 256 0.7× 99 0.4× 236 1.5× 104 0.8× 95 0.7× 41 696
Ko-En Huang Taiwan 18 423 1.2× 463 1.7× 234 1.5× 151 1.1× 103 0.8× 22 1.6k
Liguang Sun China 18 356 1.0× 87 0.3× 78 0.5× 104 0.8× 81 0.6× 54 1.1k
Ko‐En Huang Taiwan 22 442 1.2× 190 0.7× 128 0.8× 108 0.8× 73 0.6× 43 1.1k

Countries citing papers authored by Maria Soller

Since Specialization
Citations

This map shows the geographic impact of Maria Soller'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 Maria Soller with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Maria Soller more than expected).

Fields of papers citing papers by Maria Soller

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Maria Soller. 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 Maria Soller. The network helps show where Maria Soller may publish in the future.

Co-authorship network of co-authors of Maria Soller

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Soller. A scholar is included among the top collaborators of Maria Soller 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 Maria Soller. Maria Soller 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.
Friedman, Mikaela, et al.. (2025). Self-assessed knowledge of genomic medicine among non-genetics physicians – results from a nationwide Swedish survey. Journal of Community Genetics. 16(6). 669–677.
2.
Pettersson, Maria, Anna Hammarsjö, Ann Nordgren, et al.. (2023). The cost-effectiveness of whole genome sequencing in neurodevelopmental disorders. Scientific Reports. 13(1). 6904–6904. 17 indexed citations
3.
4.
Lagerstedt‐Robinson, Kristina, Izabella Baranowska Körberg, Erik Björck, et al.. (2022). A retrospective two centre study of Birt-Hogg-Dubé syndrome reveals a pathogenic founder mutation in FLCN in the Swedish population. PLoS ONE. 17(2). e0264056–e0264056. 6 indexed citations
5.
Nozohoor, Shahab, et al.. (2018). Radical pericardiectomy for chronic constrictive pericarditis. Journal of Cardiac Surgery. 33(6). 301–307. 16 indexed citations
6.
Ilinca, Andreea, et al.. (2018). A stroke gene panel for whole-exome sequencing. European Journal of Human Genetics. 27(2). 317–324. 24 indexed citations
7.
Valind, Anders, Caroline Haikal, Maria C. Johansson, et al.. (2016). The fetal thymus has a unique genomic copy number profile resulting from physiological T cell receptor gene rearrangement. Scientific Reports. 6(1). 23500–23500. 2 indexed citations
8.
Tovar, Juscelino, Maria Soller, & Inger Björck. (2015). A multifunctional diet improves cardiometabolic-related biomarkers independently of weight changes: an 8-week randomized controlled intervention in healthy overweight and obese subjects. European Journal of Nutrition. 55(7). 2295–2306. 25 indexed citations
9.
Taroni, Franco, et al.. (2014). Atypical Friedreich ataxia in patients with FXN p.R165P point mutation or comorbid hemochromatosis. Parkinsonism & Related Disorders. 20(8). 919–923. 9 indexed citations
10.
Collin, Anna, P. Sladkevicius, & Maria Soller. (2009). False‐positive prenatal diagnosis of trisomy 18 by interphase FISH: hybridization of chromosome 18 alpha‐satellite probe (D18Z1) to chromosome 2. Prenatal Diagnosis. 29(13). 1279–1281. 1 indexed citations
11.
Soller, Maria, et al.. (2009). The expression of pluripotency marker Oct 3/4 in prostate cancer and benign prostate hyperplasia. The Prostate. 69(9). 909–916. 25 indexed citations
12.
13.
Davidsson, Josef, Anna Collin, Mia Olsson, Johan Lundgren, & Maria Soller. (2008). Deletion of the SCN gene cluster on 2q24.4 is associated with severe epilepsy: An array-based genotype–phenotype correlation and a comprehensive review of previously published cases. Epilepsy Research. 81(1). 69–79. 34 indexed citations
14.
Nilbert, Mef, et al.. (2007). Discrepancies Between Estimated and Perceived Risk of Cancer among Individuals with Hereditary Nonpolyposis Colorectal Cancer. Genetic Testing. 11(2). 183–186. 9 indexed citations
15.
Soller, Maria, et al.. (2007). Cytogenetic findings in pediatric renal cell carcinoma. Cancer Genetics and Cytogenetics. 173(1). 75–80. 3 indexed citations
16.
Kremeyer, Bárbara, Maria Soller, Kristina Lagerstedt‐Robinson, et al.. (2005). The BRCA1 exon 13 duplication in the Swedish population. Familial Cancer. 4(2). 191–194. 14 indexed citations
17.
Frigyesi, Attila, David Gisselsson, Gunnar B. Hansen, et al.. (2004). A model for karyotypic evolution in testicular germ cell tumors. Genes Chromosomes and Cancer. 40(3). 172–178. 12 indexed citations
18.
Höglund, Mattias, David Gisselsson, Maria Soller, et al.. (2004). Dissecting karyotypic patterns in renal cell carcinoma: an analysis of the accumulated cytogenetic data. Cancer Genetics and Cytogenetics. 153(1). 1–9. 31 indexed citations
19.
Higashi, Koichiro, Maria Soller, Sverre Heim, et al.. (1991). Rearrangement of 9p13 as the primary chromosomal aberration in adenoid cystic carcinoma of the respiratory tract. Genes Chromosomes and Cancer. 3(1). 21–23. 42 indexed citations
20.
Örndal, Charlotte, Maria Soller, Sverre Heim, et al.. (1990). Parathyroid adenoma with t(1;5)(p22;q32) as the sole clonal chromosome abnormality. Cancer Genetics and Cytogenetics. 48(2). 225–228. 9 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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