Maria Anvret

7.4k total citations
125 papers, 4.7k citations indexed

About

Maria Anvret is a scholar working on Molecular Biology, Genetics and Cellular and Molecular Neuroscience. According to data from OpenAlex, Maria Anvret has authored 125 papers receiving a total of 4.7k indexed citations (citations by other indexed papers that have themselves been cited), including 63 papers in Molecular Biology, 40 papers in Genetics and 31 papers in Cellular and Molecular Neuroscience. Recurrent topics in Maria Anvret's work include Genetic Neurodegenerative Diseases (25 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Porphyrin Metabolism and Disorders (11 papers). Maria Anvret is often cited by papers focused on Genetic Neurodegenerative Diseases (25 papers), Genetics and Neurodevelopmental Disorders (16 papers) and Porphyrin Metabolism and Disorders (11 papers). Maria Anvret collaborates with scholars based in Sweden, United Kingdom and United States. Maria Anvret's co-authors include Kerstin Hall, Lars Edström, Margareta Blombäck, Silvia Buervenich, Andrea Carmine, Ulla Grandell, George Klein, Gunnar Falk, E. Almqvist and Fengqing Xiang and has published in prestigious journals such as Nature, New England Journal of Medicine and Proceedings of the National Academy of Sciences.

In The Last Decade

Maria Anvret

124 papers receiving 4.5k citations

Peers

Maria Anvret
Mireille Claustres France
Marco Seri Italy
Lionel Van Maldergem Belgium
Alan Y. Sakaguchi United States
David W. Stockton United States
Hans G. Dauwerse Netherlands
A. Westerveld Netherlands
Elias I. Traboulsi United States
Haluk Topaloğlu Türkiye
M. Leppert United States
Mireille Claustres France
Maria Anvret
Citations per year, relative to Maria Anvret Maria Anvret (= 1×) peers Mireille Claustres

Countries citing papers authored by Maria Anvret

Since Specialization
Citations

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

Fields of papers citing papers by Maria Anvret

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Maria Anvret

This figure shows the co-authorship network connecting the top 25 collaborators of Maria Anvret. A scholar is included among the top collaborators of Maria Anvret 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 Anvret. Maria Anvret 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.
Carmine, Andrea, Milan G. Chheda, Erik G. Jönsson, et al.. (2003). Two NOTCH4 polymorphisms and their relation to schizophrenia susceptibility and different personality traits. Psychiatric Genetics. 13(1). 23–28. 15 indexed citations
2.
3.
Moore, Richard C., Fengqing Xiang, Dong Han, et al.. (2001). Huntington Disease Phenocopy Is a Familial Prion Disease. The American Journal of Human Genetics. 69(6). 1385–1388. 95 indexed citations
4.
Eriksson, Maria, Tor Ansved, Maria Anvret, & Nessa Carey. (2001). A Mammalian Radial Spokehead-Like Gene, RSHL1, at the Myotonic Dystrophy-1 Locus. Biochemical and Biophysical Research Communications. 281(4). 835–841. 14 indexed citations
5.
Buervenich, Silvia, et al.. (2000). Alcohol dehydrogenase alleles in Parkinson's disease. Movement Disorders. 15(5). 813–818. 42 indexed citations
6.
7.
Xiang, Fengqing, Lars‐Gunnar Gunnarsson, Bruno Giometto, et al.. (1999). Autosomal Dominant Myopathy with Proximal Weakness and Early Respiratory Muscle Involvement Maps to Chromosome 2q. The American Journal of Human Genetics. 64(3). 788–792. 34 indexed citations
8.
Zhang, Zhiping, Maria Eriksson, Gunnar Falk, et al.. (1998). Failure to Achieve Gene Conversion with Chimeric Circular Oligonucleotides: Potentially Misleading PCR Artifacts Observed. Antisense and Nucleic Acid Drug Development. 8(6). 531–536. 34 indexed citations
9.
Åhlberg, Gabrielle, Kristian Borg, Lars Edström, & Maria Anvret. (1998). Welander hereditary distal myopathy, a molecular genetic comparison to hereditary myopathies with inclusion bodies. Neuromuscular Disorders. 8(2). 111–114. 13 indexed citations
10.
Lundin, Gunnel & Maria Anvret. (1997). Characterization and Regulation of the Nonerythroid Porphobilinogen Deaminase Promoter. Biochemical and Biophysical Research Communications. 231(2). 409–411. 4 indexed citations
11.
Nordenskjöld, Agneta, et al.. (1996). No evidence of WT1 gene mutations in children with congenital diaphragmatic hernia. Journal of Pediatric Surgery. 31(7). 925–927. 18 indexed citations
12.
Anvret, Maria, et al.. (1995). PARENTAL EXPOSURE TO HYDROCARBONS IN PRADER‐WILLI SYNDROME. Developmental Medicine & Child Neurology. 37(12). 1101–1109. 11 indexed citations
13.
Anvret, Maria, et al.. (1994). Rett Syndrome: The bcl-2 Gene - A Mediator of Neurotrophic Mechanisms?. Neuropediatrics. 25(6). 323–324. 8 indexed citations
14.
Hagberg, Bengt, Maria Anvret, & Jan Wahlström. (1993). Rett syndrome—Clinical & biological aspects.. 13 indexed citations
15.
Dahl, Niklas, Ulla Grandell, Tommy Martinsson, et al.. (1993). Frequency of four cystic fibrosis mutations in a Swedish population. Acta Paediatrica. 82(6-7). 609–609. 7 indexed citations
16.
Blombäck, Margareta, et al.. (1992). Dinucleotide repeat polymorphism in the promoter region of the human von Willebrand factor gene (vWF gene). Human Molecular Genetics. 1(9). 780–780. 12 indexed citations
17.
Dahl, Niklas, P. Goonewardena, Jayanti Chotai, Maria Anvret, & U. Pettersson. (1988). DNA linkage analysis of X-linked retinoschisis. Human Genetics. 78(3). 228–232. 24 indexed citations
18.
Johnson, Keith, Elaine R. Nimmo, P A Jones, et al.. (1988). Segregation of linked probes to myotonic dystrophy in a family demonstrating that 152 and APOC2 are on the same side of DM on 19q. Human Genetics. 80(4). 379–381. 4 indexed citations
19.
Berkel, A.I. van, Werner Henle, Gertrude Henle, et al.. (1981). Epstein-Barr-virus-carrying lymphoma in a patient with ataxia-telangiectasia.. BMJ. 282(6262). 425–427. 79 indexed citations
20.
Saemundsen, Ari K., David T. Purtilo, Kiyoshi Sakamoto, et al.. (1981). Documentation of Epstein-Barr virus infection in immunodeficient patients with life-threatening lymphoproliferative diseases by Epstein-Barr virus complementary RNA/DNA and viral DNA/DNA hybridization.. PubMed. 41(11 Pt 1). 4237–42. 111 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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