Mafalda Barbosa

5.5k total citations
8 papers, 330 citations indexed

About

Mafalda Barbosa is a scholar working on Genetics, Molecular Biology and Cell Biology. According to data from OpenAlex, Mafalda Barbosa has authored 8 papers receiving a total of 330 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 4 papers in Molecular Biology and 2 papers in Cell Biology. Recurrent topics in Mafalda Barbosa's work include Genetics and Neurodevelopmental Disorders (4 papers), Dermatological and Skeletal Disorders (2 papers) and Skin and Cellular Biology Research (2 papers). Mafalda Barbosa is often cited by papers focused on Genetics and Neurodevelopmental Disorders (4 papers), Dermatological and Skeletal Disorders (2 papers) and Skin and Cellular Biology Research (2 papers). Mafalda Barbosa collaborates with scholars based in Portugal, United States and Sweden. Mafalda Barbosa's co-authors include Patrı́cia Maciel, Fátima Lopes, José Pedro Vieira, Teresa Temudo, Jorge Pinto‐Basto, Gabriela Soares, Joaquim Sá, Ann‐Christine Syvänen, Sascha Sauer and Inger Jonasson and has published in prestigious journals such as Journal of Bone and Mineral Research, Journal of Medical Genetics and JAMA Neurology.

In The Last Decade

Mafalda Barbosa

7 papers receiving 302 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Mafalda Barbosa Portugal	7	221	166	68	46	33	8	330
Shino Shimada Japan	15	318 1.4×	315 1.9×	68 1.0×	35 0.8×	62 1.9×	36	545
Takuya Hiraide Japan	12	185 0.8×	271 1.6×	82 1.2×	17 0.4×	26 0.8×	34	441
Saghar Ghasemi Firouzabadi Iran	13	121 0.5×	205 1.2×	48 0.7×	16 0.3×	22 0.7×	22	328
Eleonora Di Gregorio Italy	17	170 0.8×	389 2.3×	134 2.0×	25 0.5×	28 0.8×	32	569
Sébastien Moutton France	12	211 1.0×	212 1.3×	64 0.9×	26 0.6×	33 1.0×	17	367
Ábel Vértesy Austria	9	80 0.4×	310 1.9×	43 0.6×	49 1.1×	11 0.3×	12	437
Sara Bizzotto United States	8	216 1.0×	303 1.8×	46 0.7×	12 0.3×	54 1.6×	11	468
Magdi M. Sobeih United States	5	107 0.5×	211 1.3×	97 1.4×	27 0.6×	37 1.1×	6	370
Kirsten Cremer Germany	10	144 0.7×	326 2.0×	26 0.4×	17 0.4×	23 0.7×	14	436
Barbara Utermann Austria	13	177 0.8×	128 0.8×	46 0.7×	17 0.4×	100 3.0×	18	336

Countries citing papers authored by Mafalda Barbosa

Since Specialization

Citations

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

Fields of papers citing papers by Mafalda Barbosa

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mafalda Barbosa

This figure shows the co-authorship network connecting the top 25 collaborators of Mafalda Barbosa. A scholar is included among the top collaborators of Mafalda Barbosa 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 Mafalda Barbosa. Mafalda Barbosa 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:

8 of 8 papers shown

1.

Lopes, Fátima, Mafalda Barbosa, Adam Ameur, et al.. (2016). Identification of novel genetic causes of Rett syndrome-like phenotypes. Journal of Medical Genetics. 53(3). 190–199. 126 indexed citations

2.

Lopes, Fátima, Mafalda Barbosa, Teresa Temudo, et al.. (2015). ISDN2014_0322: REMOVED: Identification of novel genetic causes of Rett syndrome‐like phenotypes by whole exome sequencing. International Journal of Developmental Neuroscience. 47(Part_A). 99–99.

3.

Vieira, José Pedro, Fátima Lopes, Anabela Silva‐Fernandes, et al.. (2015). Variant Rett syndrome in a girl with a pericentric X‐chromosome inversion leading to epigenetic changes and overexpression of the MECP2 gene. International Journal of Developmental Neuroscience. 46(1). 82–87. 24 indexed citations

4.

Barbosa, Mafalda, et al.. (2015). Recurrent copy number variations as risk factors for neurodevelopmental disorders: critical overview and analysis of clinical implications. Journal of Medical Genetics. 53(2). 73–90. 80 indexed citations

5.

Loureiro, José Leal, Luís Ruano, Ana M. Lopes, et al.. (2013). Autosomal Dominant Spastic Paraplegias. JAMA Neurology. 70(4). 481–481. 37 indexed citations

6.

Barbosa, Mafalda, et al.. (2011). [Osteopathia striata with cranial sclerosis].. PubMed. 23(6). 1147–50. 7 indexed citations

7.

Perdu, Bram, Fenna de Freitas, Suzanna G.M. Frints, et al.. (2009). Osteopathia striata with cranial sclerosis owing to WTX gene defect. Journal of Bone and Mineral Research. 25(1). 82–90. 50 indexed citations

8.

Barbosa, Mafalda, et al.. (2008). Muenke syndrome with osteochondroma. American Journal of Medical Genetics Part A. 149A(2). 260–261. 6 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.

Explore authors with similar magnitude of impact