Marta Amorim

573 total citations
7 papers, 46 citations indexed

About

Marta Amorim is a scholar working on Molecular Biology, Surgery and Genetics. According to data from OpenAlex, Marta Amorim has authored 7 papers receiving a total of 46 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 2 papers in Surgery and 2 papers in Genetics. Recurrent topics in Marta Amorim's work include Genomics and Chromatin Dynamics (2 papers), Tuberous Sclerosis Complex Research (1 paper) and Hypothalamic control of reproductive hormones (1 paper). Marta Amorim is often cited by papers focused on Genomics and Chromatin Dynamics (2 papers), Tuberous Sclerosis Complex Research (1 paper) and Hypothalamic control of reproductive hormones (1 paper). Marta Amorim collaborates with scholars based in Portugal, United Kingdom and France. Marta Amorim's co-authors include Luís Pereira‐da‐Silva, Jayne Houghton, Ana María Simón Pita, José Brás, Nicolas Lévy, Jorge Saraiva, Lina Ramos, Sofia Duarte, Rita Guerreiro and Susana Carmona and has published in prestigious journals such as SHILAP Revista de lepidopterología, American Journal of Medical Genetics Part A and European Journal of Medical Genetics.

In The Last Decade

Marta Amorim

6 papers receiving 45 citations

Peers

Marta Amorim

SURGE

MB

GENET

PPCH

Julie McCarrier United States

M Abbott United States

Hadeel Alsharif Saudi Arabia

Alice Gardham United Kingdom

Matthew Regan Australia

Véronique Manel France

Meredith Schultz United States

Wang Xiao China

Aidan Thomas Canada

Lina Ramos Portugal

Julie McCarrier United States

Marta Amorim

11 ×0.5

SURGE

22 ×1.2

MB

37 ×2.1

GENET

5 ×0.6

GENET

10 ×1.4

PPCH

Citations per year, relative to Marta Amorim Marta Amorim (= 1×) peers Julie McCarrier

Countries citing papers authored by Marta Amorim

Since Specialization

Citations

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

Fields of papers citing papers by Marta Amorim

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Amorim

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

All Works

Sort: Min cites: Since: Top N: Style:

7 of 7 papers shown

1.

Amorim, Marta, et al.. (2023). Multidisciplinary Outpatient Clinic of Neurocutaneous Diseases: Five-year Experience of a Pediatric Tertiary Hospital in Portugal. Acta Médica Portuguesa. 37(3). 187–197. 3 indexed citations

2.

Amorim, Marta, et al.. (2022). A novel variant of DeSanto-Shinawi Syndrome with joint manifestations. European Journal of Medical Genetics. 65(7). 104534–104534.

3.

Amorim, Marta, et al.. (2020). Hypogonadotropic hypogonadism due to compound heterozygous mutations TACR3 in siblings. SHILAP Revista de lepidopterología. 8(12). 3125–3128. 2 indexed citations

4.

Carmona, Susana, et al.. (2018). AP4S1 splice-site mutation in a case of spastic paraplegia type 52 with polymicrogyria. Neurology Genetics. 4(5). e273–e273. 5 indexed citations

5.

Marques, Bárbara, Cristina Ferreira, Sónia N. Pedro, et al.. (2016). Molecular characterization of a rare analphoid supernumerary marker chromosome derived from 7q35 → qter: a case report. Molecular Cytogenetics. 9(1). 87–87. 1 indexed citations

6.

Amorim, Marta, et al.. (2015). Mitchell-Riley Syndrome: A Novel Mutation in RFX6 Gene. SHILAP Revista de lepidopterología. 2015. 1–3. 18 indexed citations

7.

Sousa, Sérgio B., Lina Ramos, Wiktor Borozdin, et al.. (2008). Tetra‐amelia and lung hypo/aplasia syndrome: New case report and review. American Journal of Medical Genetics Part A. 146A(21). 2799–2803. 17 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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