Maria Aminoff

2.9k total citations
10 papers, 915 citations indexed

About

Maria Aminoff is a scholar working on Molecular Biology, Rheumatology and Physiology. According to data from OpenAlex, Maria Aminoff has authored 10 papers receiving a total of 915 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 8 papers in Rheumatology and 3 papers in Physiology. Recurrent topics in Maria Aminoff's work include Folate and B Vitamins Research (7 papers), Porphyrin Metabolism and Disorders (6 papers) and Metabolism and Genetic Disorders (2 papers). Maria Aminoff is often cited by papers focused on Folate and B Vitamins Research (7 papers), Porphyrin Metabolism and Disorders (6 papers) and Metabolism and Genetic Disorders (2 papers). Maria Aminoff collaborates with scholars based in Finland, France and United States. Maria Aminoff's co-authors include Søren K. Moestrup, P Verroust, Albert de la Chapelle, Christian Jacobsen, Ralf Krahe, Erik Christensen, Renata Kozyraki, John C. Fyfe, Harald Broch and Ralph Gräsbeck and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Medicine and Nature Genetics.

In The Last Decade

Maria Aminoff

9 papers receiving 897 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Maria Aminoff Finland	9	397	271	209	184	154	10	915
Yo‐ichi Takei Japan	20	739 1.9×	123 0.5×	216 1.0×	45 0.2×	92 0.6×	70	1.3k
George B.M. Lindop United Kingdom	21	474 1.2×	110 0.4×	202 1.0×	59 0.3×	173 1.1×	77	1.3k
Bernadette Chadefaux-Vekemans France	16	207 0.5×	371 1.4×	159 0.8×	180 1.0×	50 0.3×	31	919
Eric T. Rush United States	13	386 1.0×	181 0.7×	126 0.6×	61 0.3×	41 0.3×	51	815
Manish P. Ponda United States	14	309 0.8×	47 0.2×	130 0.6×	290 1.6×	250 1.6×	24	1.0k
Yuansheng Xie China	13	322 0.8×	173 0.6×	87 0.4×	63 0.3×	228 1.5×	29	767
Susan K. Durham United States	24	732 1.8×	59 0.2×	179 0.9×	79 0.4×	55 0.4×	33	1.5k
Masataka Adachi Japan	20	694 1.7×	33 0.1×	204 1.0×	101 0.5×	327 2.1×	51	1.3k
Tina Storm Denmark	11	280 0.7×	69 0.3×	56 0.3×	93 0.5×	151 1.0×	17	603
Taichi Kitaoka Japan	16	273 0.7×	201 0.7×	93 0.4×	88 0.5×	113 0.7×	49	798

Countries citing papers authored by Maria Aminoff

Since Specialization

Citations

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

Fields of papers citing papers by Maria Aminoff

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Aminoff

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Aminoff. A scholar is included among the top collaborators of Maria Aminoff 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 Aminoff. Maria Aminoff is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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10 of 10 papers shown

1.

Pettersson, Tom, et al.. (2003). Proteinuria in cubilin-deficient patients with selective vitamin B12 malabsorption. Pediatric Nephrology. 18(5). 417–421. 61 indexed citations

2.

Tanner, Stephan M., Maria Aminoff, Fred A. Wright, et al.. (2003). Amnionless, essential for mouse gastrulation, is mutated in recessive hereditary megaloblastic anemia. Nature Genetics. 33(3). 426–429. 99 indexed citations

3.

Nykjær, Anders, John C. Fyfe, Renata Kozyraki, et al.. (2001). Cubilin dysfunction causes abnormal metabolism of the steroid hormone 25(OH) vitamin D ₃. Proceedings of the National Academy of Sciences. 98(24). 13895–13900. 246 indexed citations

4.

Kristiansen, Mette, Maria Aminoff, Christian Jacobsen, et al.. (2000). Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor–vitamin B12 by cubilin. Blood. 96(2). 405–409. 46 indexed citations

5.

Kristiansen, Mette, Maria Aminoff, Christian Jacobsen, et al.. (2000). Cubilin P1297L mutation associated with hereditary megaloblastic anemia 1 causes impaired recognition of intrinsic factor–vitamin B12 by cubilin. Blood. 96(2). 405–409. 17 indexed citations

6.

Aminoff, Maria, Robert B. Chadwick, Cheryl K.H. Johnson, et al.. (1999). Mutations in CUBN, encoding the intrinsic factor-vitamin B12 receptor, cubilin, cause hereditary megaloblastic anaemia 1. Nature Genetics. 21(3). 309–313. 191 indexed citations

7.

Kozyraki, Renata, John C. Fyfe, Mette Kristiansen, et al.. (1999). The intrinsic factor–vitamin B12 receptor, cubilin, is a high-affinity apolipoprotein A-I receptor facilitating endocytosis of high-density lipoprotein. Nature Medicine. 5(6). 656–661. 220 indexed citations

8.

Dugué, Benoît, et al.. (1998). A Urinary Radioisotope‐Binding Assay to Diagnose Gräsbeck‐Imerslund Disease. Journal of Pediatric Gastroenterology and Nutrition. 26(1). 21–25.

9.

Dugué, Benoît, et al.. (1998). A Urinary Radioisotope-Binding Assay to Diagnose Gräsbeck-Imerslund Disease. Journal of Pediatric Gastroenterology and Nutrition. 26(1). 21–25. 8 indexed citations

10.

Aminoff, Maria, Esa Tahvanainen, R. Gräsbeck, et al.. (1995). Selective intestinal malabsorption of vitamin B12 displays recessive mendelian inheritance: assignment of a locus to chromosome 10 by linkage.. PubMed. 57(4). 824–31. 27 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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