Imma Hernán

918 total citations
31 papers, 712 citations indexed

About

Imma Hernán is a scholar working on Molecular Biology, Ophthalmology and Genetics. According to data from OpenAlex, Imma Hernán has authored 31 papers receiving a total of 712 indexed citations (citations by other indexed papers that have themselves been cited), including 19 papers in Molecular Biology, 5 papers in Ophthalmology and 5 papers in Genetics. Recurrent topics in Imma Hernán's work include Retinal Development and Disorders (12 papers), Advanced biosensing and bioanalysis techniques (5 papers) and CRISPR and Genetic Engineering (4 papers). Imma Hernán is often cited by papers focused on Retinal Development and Disorders (12 papers), Advanced biosensing and bioanalysis techniques (5 papers) and CRISPR and Genetic Engineering (4 papers). Imma Hernán collaborates with scholars based in Spain, Poland and United States. Imma Hernán's co-authors include Miguel Carballo, María José Gamundi, Emma Borràs, Miguel Dias, Carmen Ayuso, Montserrat Baiget, Elena Millá, José A. G. Agúndez, Miguel Blanca and Ignasi Roig and has published in prestigious journals such as PLoS ONE, Journal of Allergy and Clinical Immunology and Journal of Experimental Botany.

In The Last Decade

Imma Hernán

31 papers receiving 703 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Imma Hernán Spain 16 386 134 95 78 64 31 712
Denis A. Akkad Germany 16 396 1.0× 36 0.3× 135 1.4× 12 0.2× 132 2.1× 26 702
Roberta La Piana Canada 19 475 1.2× 57 0.4× 93 1.0× 56 0.7× 76 1.2× 62 1.1k
Lamei Yuan China 19 551 1.4× 80 0.6× 268 2.8× 56 0.7× 34 0.5× 83 1.0k
Séverine Drunat France 21 581 1.5× 19 0.1× 443 4.7× 30 0.4× 22 0.3× 57 1.1k
Mark B. Skeen United States 8 207 0.5× 47 0.4× 198 2.1× 35 0.4× 193 3.0× 21 1.1k
Toru Kurokawa Japan 20 589 1.5× 241 1.8× 97 1.0× 76 1.0× 47 0.7× 62 1.4k
Karin Weigelt Germany 15 409 1.1× 92 0.7× 80 0.8× 15 0.2× 19 0.3× 18 834
Maria Grigoriadou Greece 18 329 0.9× 108 0.8× 191 2.0× 30 0.4× 24 0.4× 48 723
Oliver Puk Germany 17 404 1.0× 186 1.4× 158 1.7× 19 0.2× 33 0.5× 30 681
Javier Ruiz‐Ederra Spain 17 784 2.0× 442 3.3× 52 0.5× 99 1.3× 33 0.5× 42 1.1k

Countries citing papers authored by Imma Hernán

Since Specialization
Citations

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

Fields of papers citing papers by Imma Hernán

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Imma Hernán

This figure shows the co-authorship network connecting the top 25 collaborators of Imma Hernán. A scholar is included among the top collaborators of Imma Hernán 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 Imma Hernán. Imma Hernán 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.
Millá, Elena, María José Gamundi, Emma Borràs, et al.. (2024). Next-generation sequencing-based gene panel tests for the detection of rare variants and hypomorphic alleles associated with primary open-angle glaucoma. PLoS ONE. 19(1). e0282133–e0282133. 1 indexed citations
2.
Beyer, Frauke, A. Veronica Witte, Imma Hernán, et al.. (2023). From the reward network to whole-brain metrics: structural connectivity in adolescents and young adults according to body mass index and genetic risk of obesity. International Journal of Obesity. 48(4). 567–574. 1 indexed citations
3.
Arzalluz-Luque, Ángeles, José Luis Cabrera, Heli Skottman, et al.. (2021). Mutant PRPF8 Causes Widespread Splicing Changes in Spliceosome Components in Retinitis Pigmentosa Patient iPSC-Derived RPE Cells. Frontiers in Neuroscience. 15. 636969–636969. 14 indexed citations
4.
Lukovic, Dunja, et al.. (2017). Generation of a human iPSC line from a patient with retinitis pigmentosa caused by mutation in PRPF8 gene. Stem Cell Research. 21. 23–25. 3 indexed citations
5.
Hernán, Imma, Emma Borràs, Miguel Dias, et al.. (2015). Two novel frameshift mutations in BRCA2 gene detected by next generation sequencing in a survey of Spanish patients of breast cancer. Clinical & Translational Oncology. 17(7). 576–580. 3 indexed citations
6.
Marqués‐Iturria, Idoia, Maite Garolera, Roser Pueyo, et al.. (2014). The interaction effect between BDNF val66met polymorphism and obesity on executive functions and frontal structure. American Journal of Medical Genetics Part B Neuropsychiatric Genetics. 165(3). 245–253. 30 indexed citations
7.
Millá, Elena, Susana Duch, Imma Hernán, et al.. (2013). Survey of familial glaucoma shows a high incidence of cytochrome P450, family 1, subfamily B, polypeptide 1 (CYP1B1) mutations in non-consanguineous congenital forms in a Spanish population.. PubMed. 19. 1707–22. 29 indexed citations
8.
Borràs, Emma, E. Dotor, Àngels Arcusa, et al.. (2013). High-resolution melting analysis of the common c.1905+1G>A mutation causing dihydropyrimidine dehydrogenase deficiency and lethal 5-fluorouracil toxicity. Frontiers in Genetics. 3. 312–312. 10 indexed citations
9.
Borràs, Emma, et al.. (2013). Detection of novel genetic variation in autosomal dominant retinitis pigmentosa. Clinical Genetics. 84(5). 441–452. 8 indexed citations
10.
Hernán, Imma, Emma Borràs, Miguel Dias, et al.. (2012). Detection of Genomic Variations in BRCA1 and BRCA2 Genes by Long-Range PCR and Next-Generation Sequencing. Journal of Molecular Diagnostics. 14(3). 286–293. 40 indexed citations
11.
Hernán, Imma, Emma Borràs, Blanca Garcı́a-Sandoval, et al.. (2011). Novel p.M96T variant of NRL and shRNA‐based suppression and replacement of NRL mutants associated with autosomal dominant retinitis pigmentosa. Clinical Genetics. 82(5). 446–452. 14 indexed citations
12.
Borràs, Emma, Imma Hernán, María José Gamundi, et al.. (2011). Clinical pharmacogenomic testing of KRAS, BRAF and EGFRmutations by high resolution melting analysis and ultra-deep pyrosequencing. BMC Cancer. 11(1). 406–406. 68 indexed citations
13.
Jaijo, Teresa, Elena Aller, Gema García‐García, et al.. (2010). Functional analysis of splicing mutations in MYO7A and USH2A genes. Clinical Genetics. 79(3). 282–288. 11 indexed citations
14.
Gamundi, María José, Imma Hernán, Pedro López‐Romero, et al.. (2008). Transcriptional expression ofcis-acting andtrans-acting splicing mutations cause autosomal dominant retinitis pigmentosa. Human Mutation. 29(6). 869–878. 30 indexed citations
15.
Bernal, Sara, Imma Hernán, Miguel Carballo, et al.. (2008). Analysis of the involvement of the NR2E3 gene in autosomal recessive retinal dystrophies. Clinical Genetics. 73(4). 360–366. 33 indexed citations
16.
Cornejo‐García, J.A., Tahía D. Fernández, Cristobalina Mayorga, et al.. (2007). Cytokine and Transcription Factors Expression in Patients with Delayed Allergic Reactions to Drugs. Journal of Allergy and Clinical Immunology. 119(1). S272–S272. 1 indexed citations
17.
Gamundi, María José, Imma Hernán, M.J. Trujillo, et al.. (2007). High prevalence of mutations in peripherin/RDS in autosomal dominant macular dystrophies in a Spanish population.. PubMed. 13. 1031–7. 26 indexed citations
18.
Gamundi, María José, Imma Hernán, Blanca Garcı́a-Sandoval, et al.. (2006). Three novel and the common Arg677Ter RP1 protein truncating mutations causing autosomal dominant retinitis pigmentosa in a Spanish population. BMC Medical Genetics. 7(1). 35–35. 18 indexed citations
19.
Espunya, M. Carme, et al.. (2005). Differential expression of genes encoding protein kinase CK2 subunits in the plant cell cycle. Journal of Experimental Botany. 56(422). 3183–3192. 18 indexed citations
20.
Hernán, Imma, et al.. (2004). De novo germline mutation in the serine–threonine kinase STK11/LKB1 gene associated with Peutz–Jeghers syndrome. Clinical Genetics. 66(1). 58–62. 23 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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