Imma Hernán

928 citations
32 papers · 740 · h-index 17

Impact in

Papers in

    • Retinal Development and Disorders 13
    • Retinoids in leukemia and cellular processes 2
    • BRCA gene mutations in cancer 2

Imma Hernán

31 papers receiving 729 citations

Peers

Imma Hernán
Comparison fields: 5 of 75
  • Ophthalmology 84
  • Gastroenterology 52
  • Molecular Biology 359
  • Cellular and Molecular Neuroscience 56
  • Pathology and Forensic Medicine 49
Replace Muhammad Mahajnah with:
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J CLARK United States
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Citations per year

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-authors

The 25 scholars most cited alongside Imma Hernán, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Imma Hernán Line = papers co-authored together Imma Hernán links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 32 papers — load more, or switch the sort, to bring in the rest.

#Work
1 200384
2 201169
3 201268
4 200557
5 200750
6 201242
7 200835
8 201431
9
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.
201331
10 200830
11
High prevalence of mutations in peripherin/RDS in autosomal dominant macular dystrophies in a Spanish population.
200728
12 200427
13
Detection of novel mutations that cause autosomal dominant retinitis pigmentosa in candidate genes by long-range PCR amplification and next-generation sequencing.
201321
14 201120
15 200618
16 200518
17 202117
18 201114
19
Sequence variations in the retinal fascin FSCN2 gene in a Spanish population with autosomal dominant retinitis pigmentosa or macular degeneration.
200513
20
Novel LMX1B mutation in familial nail-patella syndrome with variable expression of open angle glaucoma.
200712

About Imma Hernán

Imma Hernán is a scholar working on Molecular Biology, Genetics, Clinical Psychology, Ophthalmology and Pharmacology, having authored 32 papers that have together received 740 indexed citations. Recurring topics across this work include Retinal Development and Disorders (13 papers), BRCA gene mutations in cancer (2 papers), Retinoids in leukemia and cellular processes (2 papers), Glaucoma and retinal disorders (2 papers), Eating Disorders and Behaviors (2 papers), Colorectal Cancer Treatments and Studies (2 papers), Autism Spectrum Disorder Research (2 papers) and Retinal Diseases and Treatments (2 papers). The work is most often cited by research in Ophthalmology (84 citations), Gastroenterology (52 citations), Molecular Biology (359 citations), Cellular and Molecular Neuroscience (56 citations) and Pathology and Forensic Medicine (49 citations). Imma Hernán has collaborated with scholars based in Spain, Poland and United States. Frequent co-authors include Miguel Carballo, María José Gamundi, Emma Borràs, Carmen Ayuso, Miguel Dias, Montserrat Baiget, Elena Millá, Ignasi Roig, José A. G. Agúndez and Miguel Blanca. Their work appears in journals such as Clinical Genetics, PLoS ONE, Investigative Ophthalmology & Visual Science, Frontiers in Genetics and Clinical and Experimental Optometry.

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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