Anna Allavena

620 total citations
4 papers, 34 citations indexed

About

Anna Allavena is a scholar working on Molecular Biology, Pathology and Forensic Medicine and Oncology. According to data from OpenAlex, Anna Allavena has authored 4 papers receiving a total of 34 indexed citations (citations by other indexed papers that have themselves been cited), including 2 papers in Molecular Biology, 2 papers in Pathology and Forensic Medicine and 2 papers in Oncology. Recurrent topics in Anna Allavena's work include Cancer Genomics and Diagnostics (2 papers), Genetic factors in colorectal cancer (2 papers) and Dermatological and Skeletal Disorders (1 paper). Anna Allavena is often cited by papers focused on Cancer Genomics and Diagnostics (2 papers), Genetic factors in colorectal cancer (2 papers) and Dermatological and Skeletal Disorders (1 paper). Anna Allavena collaborates with scholars based in Italy. Anna Allavena's co-authors include Enrico Grosso, Nicola Migone, Caterina Carbonara, Silvia Polidoro, Lucia Longa, Alfredo Brusco, Ivana Sarotto, Luisa Delsedime, I Borelli and Barbara Pasini and has published in prestigious journals such as Human Genetics, European Journal of Human Genetics and Cerebrovascular Diseases.

In The Last Decade

Anna Allavena

4 papers receiving 32 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna Allavena Italy	3	16	14	13	11	6	4	34
Mingxia Shi China	4	18 1.1×	8 0.6×	7 0.5×	4 0.4×	16 2.7×	5	48
Jolanta Kalniņa Latvia	3	8 0.5×	3 0.2×	18 1.4×	5 0.5×	17 2.8×	10	38
Bruce M. Wollison United States	3	13 0.8×	32 2.3×	10 0.8×	6 0.5×	13 2.2×	4	44
Davide Bondavalli Italy	4	4 0.3×	7 0.5×	12 0.9×	5 0.5×	15 2.5×	7	33
Barbara Wölfel Germany	3	10 0.6×	2 0.1×	5 0.4×	9 0.8×	13 2.2×	4	45
Liane Rapatoni Brazil	3	33 2.1×	4 0.3×	6 0.5×	15 1.4×	8 1.3×	7	42
Satoshi Asai Japan	3	11 0.7×	2 0.1×	6 0.5×	6 0.5×	16 2.7×	3	32
E. Steve Roach United States	2	8 0.5×	23 1.6×	3 0.2×	2 0.2×	8 1.3×	2	37
Sarah K. Macklin‐Mantia United States	4	7 0.4×	2 0.1×	7 0.5×	6 0.5×	12 2.0×	6	22
M.‐M. Garcia‐Barceló Hong Kong	2	7 0.4×	3 0.2×	3 0.2×	6 0.5×	19 3.2×	2	30

Countries citing papers authored by Anna Allavena

Since Specialization

Citations

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

Fields of papers citing papers by Anna Allavena

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Allavena

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

All Works

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4 of 4 papers shown

1.

Borelli, I, Tiziana Venesio, Ivana Sarotto, et al.. (2014). A founder MLH1 mutation in Lynch syndrome families from Piedmont, Italy, is associated with an increased risk of pancreatic tumours and diverse immunohistochemical patterns. Familial Cancer. 13(3). 401–413. 9 indexed citations

2.

Borelli, I, Marco Barberis, Anna Allavena, et al.. (2012). A unique MSH2 exon 8 deletion accounts for a major portion of all mismatch repair gene mutations in Lynch syndrome families of Sardinian origin. European Journal of Human Genetics. 21(2). 154–161. 5 indexed citations

3.

Cerrato, Paolo, Mauro Bergui, Maria Grazia Grasso, et al.. (2005). Juvenile Vertebrobasilar Ischaemic Stroke in a Patient with Camurati-Engelmann Disease. Cerebrovascular Diseases. 20(4). 283–284. 2 indexed citations

4.

Longa, Lucia, Alfredo Brusco, Silvia Polidoro, et al.. (2001). TSC1 and TSC2 deletions differ in size, preference for recombinatorial sequences, and location within the gene. Human Genetics. 108(2). 156–166. 18 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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