Marta Codina‐Solà

724 total citations
21 papers, 210 citations indexed

About

Marta Codina‐Solà is a scholar working on Molecular Biology, Genetics and Genetics. According to data from OpenAlex, Marta Codina‐Solà has authored 21 papers receiving a total of 210 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Molecular Biology, 8 papers in Genetics and 5 papers in Genetics. Recurrent topics in Marta Codina‐Solà's work include Genomics and Rare Diseases (5 papers), Neurogenetic and Muscular Disorders Research (4 papers) and RNA modifications and cancer (4 papers). Marta Codina‐Solà is often cited by papers focused on Genomics and Rare Diseases (5 papers), Neurogenetic and Muscular Disorders Research (4 papers) and RNA modifications and cancer (4 papers). Marta Codina‐Solà collaborates with scholars based in Spain, Palestinian Territory and United States. Marta Codina‐Solà's co-authors include Ivon Cuscó, Luis A. Pérez‐Jurado, Benjamín Rodríguez‐Santiago, Gemma Aznar‐Laín, Guillermo Antiñolo, Elisabeth Gabau, Maria Rigau, Blanca Gener, Miguel Del Campo and M.P. Botella and has published in prestigious journals such as SHILAP Revista de lepidopterología, Molecular Biology and Evolution and Journal of Autism and Developmental Disorders.

In The Last Decade

Marta Codina‐Solà

19 papers receiving 206 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Marta Codina‐Solà Spain 7 125 96 72 18 15 21 210
Naila Cristina Vilaça Lourenço Brazil 9 129 1.0× 125 1.3× 46 0.6× 15 0.8× 5 0.3× 16 214
Dima El‐Khechen United States 8 208 1.7× 125 1.3× 49 0.7× 6 0.3× 6 0.4× 10 294
Simona Carone Italy 6 107 0.9× 76 0.8× 88 1.2× 12 0.7× 4 0.3× 12 200
Aurora Arghir Romania 7 87 0.7× 78 0.8× 31 0.4× 7 0.4× 4 0.3× 30 187
Kirsty McWalter United States 10 118 0.9× 78 0.8× 15 0.2× 8 0.4× 19 1.3× 24 221
Alinoë Lavillaureix France 7 90 0.7× 68 0.7× 48 0.7× 4 0.2× 6 0.4× 12 169
Barbara Wiśniowiecka‐Kowalnik Poland 8 306 2.4× 214 2.2× 155 2.2× 20 1.1× 10 0.7× 11 445
Anne Chun‐Hui Tsai United States 10 117 0.9× 126 1.3× 27 0.4× 7 0.4× 14 0.9× 22 295
Louisa Kalsner United States 6 150 1.2× 126 1.3× 66 0.9× 4 0.2× 5 0.3× 14 247
Sorina Mihaela Papuc Romania 10 116 0.9× 166 1.7× 31 0.4× 7 0.4× 5 0.3× 29 327

Countries citing papers authored by Marta Codina‐Solà

Since Specialization
Citations

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

Fields of papers citing papers by Marta Codina‐Solà

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Marta Codina‐Solà

This figure shows the co-authorship network connecting the top 25 collaborators of Marta Codina‐Solà. A scholar is included among the top collaborators of Marta Codina‐Solà 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 Codina‐Solà. Marta Codina‐Solà 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.
Valenzuela, Irene, Marta Codina‐Solà, Anna M. Cueto‐González, et al.. (2025). Deep phenotyping of 11 individuals with pathogenic variants in RNU4-2 reveals a clinically recognizable syndrome. Genetics in Medicine. 28(1). 101633–101633.
2.
Campeau, Philippe M., et al.. (2024). Functional studies in yeast confirm the pathogenicity of a new GINS3 Meier–Gorlin syndrome variant. Clinical Genetics. 106(3). 342–346.
3.
Codina‐Solà, Marta, Mar Xunclà, Elena García‐Arumí, et al.. (2024). A novel FAM83G variant from palmoplantar keratoderma patient disrupts WNT signalling via loss of FAM83G-CK1α interaction. Open Biology. 14(7). 240075–240075. 2 indexed citations
4.
Blasco, Laura Campello, Marta Codina‐Solà, Pascale Saugier-Véber, et al.. (2024). Complex SMN Hybrids Detected in a Cohort of 31 Patients With Spinal Muscular Atrophy. Neurology Genetics. 10(4). e200175–e200175. 4 indexed citations
5.
Valenzuela, Irene, Marta Codina‐Solà, Anna M. Cueto‐González, et al.. (2024). Deep phenotyping of 11 individuals with pathogenic variants in RNU4-2 reveals a clinically recognizable syndrome. Genetics in Medicine. 26(12). 101288–101288. 5 indexed citations
6.
Abulí, Anna, et al.. (2023). The diagnosis communication process in spinal muscular atrophy: A cross-cutting view of the new challenges facing the therapeutic era. SHILAP Revista de lepidopterología. 1(1). 100825–100825. 1 indexed citations
7.
Restrepo‐Vera, Juan Luis, Jordi Pérez‐Rodon, Marta Codina‐Solà, et al.. (2023). Limb-girdle myopathy and mild intellectual disability: The expanding spectrum of TANGO2-related disease. Neuromuscular Disorders. 33(6). 463–467. 1 indexed citations
8.
Díaz, Francisca, Manuel Parrón, Silvia Modamio‐Høybjør, et al.. (2023). Evolution of clinical and radiological presentations of spondyloepimetaphyseal dysplasia, RPL13‐related: Description of 11 further cases. Clinical Genetics. 104(1). 100–106. 2 indexed citations
9.
Restrepo‐Vera, Juan Luis, Marta Codina‐Solà, Arnau Llauradó, et al.. (2023). Identification of two novel RRM2B variants associated with autosomal recessive progressive external ophthalmoplegia in a family with pseudodominant inheritance pattern. Journal of Human Genetics. 68(8). 527–532. 1 indexed citations
10.
Restrepo‐Vera, Juan Luis, Marta Codina‐Solà, Arnau Llauradó, et al.. (2022). An Atypical Presentation of Upper Motor Neuron Predominant Juvenile Amyotrophic Lateral Sclerosis Associated with TARDBP Gene: A Case Report and Review of the Literature. Genes. 13(8). 1483–1483. 1 indexed citations
11.
Abulí, Anna, Marta Codina‐Solà, Irene Valenzuela, et al.. (2022). Experience using singleton exome sequencing of probands as an approach to preconception carrier screening in consanguineous couples. Journal of Medical Genetics. 60(6). 540–546. 1 indexed citations
12.
Milligan, John N., et al.. (2022). Recommendations for Interpreting and Reporting Silent Carrier and Disease-Modifying Variants in SMA Testing Workflows. Genes. 13(9). 1657–1657. 9 indexed citations
13.
Gran, Ferrán, Marta Garrido, Alexandra Navarro, et al.. (2021). Differences between genetic dilated cardiomyopathy and myocarditis in children presenting with severe cardiac dysfunction. European Journal of Pediatrics. 181(1). 287–294. 4 indexed citations
14.
Fernández‐Álvarez, Paula, Marta Codina‐Solà, Irene Valenzuela, et al.. (2021). A systematic study and literature review of parental somatic mosaicism of FBN1 pathogenic variants in Marfan syndrome. Journal of Medical Genetics. 59(6). 605–612. 7 indexed citations
15.
Abulí, Anna, Marta Codina‐Solà, Irene Valenzuela, et al.. (2020). Beyond the disease itself: A cross‐cutting educational initiative for patients and families with rare diseases. Journal of Genetic Counseling. 30(3). 693–700. 2 indexed citations
16.
Codina‐Solà, Marta, et al.. (2019). Genetic factors contributing to autism spectrum disorder in Williams-Beuren syndrome. Journal of Medical Genetics. 56(12). 801–808. 11 indexed citations
17.
Codina‐Solà, Marta, Luis A. Pérez‐Jurado, Ivon Cuscó, & Clara Serra‐Juhé. (2017). Provision of Genetic Services for Autism and its Impact on Spanish Families. Journal of Autism and Developmental Disorders. 47(10). 2947–2956. 15 indexed citations
18.
Codina‐Solà, Marta, Benjamín Rodríguez‐Santiago, Cristina M. Villanueva, et al.. (2016). Genetic and epigenetic methylation defects and implication of the ERMN gene in autism spectrum disorders. Translational Psychiatry. 6(7). e855–e855. 31 indexed citations
19.
Engelken, Johannes, Guadalupe Espadas, Francesco M. Mancuso, et al.. (2015). Signatures of Evolutionary Adaptation in Quantitative Trait Loci Influencing Trace Element Homeostasis in Liver. Molecular Biology and Evolution. 33(3). 738–754. 18 indexed citations
20.
Codina‐Solà, Marta, Benjamín Rodríguez‐Santiago, Javier Santoyo‐López, et al.. (2015). Integrated analysis of whole-exome sequencing and transcriptome profiling in males with autism spectrum disorders. Molecular Autism. 6(1). 21–21. 89 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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