Maria Soller

4.0k citations
48 papers · 961 · h-index 21

Impact in

  • Genetics top 10%
    • Genomic variations and chromosomal abnormalities
    • Genomics and Rare Diseases
    • BRCA gene mutations in cancer
    • Cancer Genomics and Diagnostics

Papers in

    • Renal and related cancers 5
    • BRCA gene mutations in cancer 5
    • Genomics and Rare Diseases 4
    • Genomic variations and chromosomal abnormalities 3

Maria Soller

44 papers receiving 921 citations

Peers

Maria Soller
Comparison fields: 5 of 87
  • Genetics 248
  • Cancer Research 86
  • Genetics 49
  • Molecular Biology 333
  • Pulmonary and Respiratory Medicine 139
Replace Rachel Reynaud with:
Rachel Reynaud France
Amy P. Webster United Kingdom
Michael H. Guo United States
Anatoly Tiulpakov Russia
Philip Murray United Kingdom
Young Bae Sohn South Korea
Marie‐Laure Raffin‐Sanson France
Charles Sultan France
Antony Lafferty Australia
Wendy K. Chung United States
Maria Soller relative to Rachel Reynaud France Rachel Reynaud's profile →
Citations per field
00.5×1.5×1.8×
Rachel Reynaud · 1×
Citations per year

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-authors

The 25 scholars most cited alongside Maria Soller, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Maria Soller Line = papers co-authored together Maria Soller links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 48 papers — load more, or switch the sort, to bring in the rest.

#Work
1 200668
2 201254
3 201350
4 201149
5 200848
6 199145
7 200839
8 200837
9 200436
10 201331
11 200928
12 199528
13 202026
14 201226
15 201526
16 201826
17 200925
18 200325
19 201921
20 199421

About Maria Soller

Maria Soller is a scholar working on Molecular Biology, Genetics, Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Pulmonary and Respiratory Medicine, having authored 48 papers that have together received 961 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (6 papers), Renal and related cancers (5 papers), BRCA gene mutations in cancer (5 papers), Renal cell carcinoma treatment (4 papers), Cancer Genomics and Diagnostics (4 papers), Tumors and Oncological Cases (4 papers), Genomics and Rare Diseases (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Genetics (248 citations), Cancer Research (86 citations), Genetics (49 citations), Molecular Biology (333 citations) and Pulmonary and Respiratory Medicine (139 citations). Maria Soller has collaborated with scholars based in Sweden, Denmark and United Kingdom. Frequent co-authors include Inger Björck, Juscelino Tovar, Anna Collin, Josef Davidsson, Felix Mitelman, Å. Nilsson, Ioannis Panagopoulos, Leif Johansson, Michael Dictor and Göran Hambraeus. Their work appears in journals such as Prenatal Diagnosis, Parkinsonism & Related Disorders, Genes Chromosomes and Cancer, Scientific Reports and BMC Cancer.

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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