Célia Kun‐Rodrigues

888 total citations
22 papers, 295 citations indexed

About

Célia Kun‐Rodrigues is a scholar working on Genetics, Physiology and Molecular Biology. According to data from OpenAlex, Célia Kun‐Rodrigues has authored 22 papers receiving a total of 295 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 7 papers in Physiology and 5 papers in Molecular Biology. Recurrent topics in Célia Kun‐Rodrigues's work include Genomics and Rare Diseases (5 papers), Alzheimer's disease research and treatments (4 papers) and Wildlife Ecology and Conservation (4 papers). Célia Kun‐Rodrigues is often cited by papers focused on Genomics and Rare Diseases (5 papers), Alzheimer's disease research and treatments (4 papers) and Wildlife Ecology and Conservation (4 papers). Célia Kun‐Rodrigues collaborates with scholars based in United States, Portugal and United Kingdom. Célia Kun‐Rodrigues's co-authors include Lounès Chikhi, José Brás, Rita Guerreiro, Rachel J. O’Neill, Jordi Salmona, Benoît Goossens, Reeta Sharma, Nathaniel K. Jue, Emmanuel Rasolondraibe and Miguel Tábuas‐Pereira and has published in prestigious journals such as PLoS ONE, Neurology and Human Molecular Genetics.

In The Last Decade

Célia Kun‐Rodrigues

22 papers receiving 292 citations

Peers

Célia Kun‐Rodrigues

GENET

ECOLO

PHYSI

Noriko Kamei United States

Cao Chen China

Moritz Hertel Germany

Hideki Ueno Japan

Kazutoyo Ogino Japan

Peter Nürnberg Germany

Feng‐Yu Wang China

Peter N�rnberg Germany

L. Shahul Hameed Sweden

Amanda M. Papakyrikos United States

Noriko Kamei United States

Célia Kun‐Rodrigues

64 ×0.7

GENET

40 ×0.5

ECOLO

118 ×1.5

31 ×0.5

9 ×0.1

PHYSI

Citations per year, relative to Célia Kun‐Rodrigues Célia Kun‐Rodrigues (= 1×) peers Noriko Kamei

Countries citing papers authored by Célia Kun‐Rodrigues

Since Specialization

Citations

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

Fields of papers citing papers by Célia Kun‐Rodrigues

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Célia Kun‐Rodrigues. 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 Célia Kun‐Rodrigues. The network helps show where Célia Kun‐Rodrigues may publish in the future.

Co-authorship network of co-authors of Célia Kun‐Rodrigues

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

All Works

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20 of 20 papers shown

Tábuas‐Pereira, Miguel, João Durães, Célia Kun‐Rodrigues, et al.. (2024). Exploring first-degree family history in a cohort of Portuguese Alzheimer’s disease patients: population evidence for X-chromosome linked and recessive inheritance of risk factors. Journal of Neurology. 271(10). 6983–6990. 1 indexed citations

Tábuas‐Pereira, Miguel, Rita Guerreiro, Célia Kun‐Rodrigues, et al.. (2022). Whole-exome sequencing reveals PSEN1 and ATP7B combined variants as a possible cause of early-onset Lewy body dementia: a case study of genotype–phenotype correlation. Neurogenetics. 23(4). 279–283. 2 indexed citations

Tábuas‐Pereira, Miguel, Isabel Santana, Maria Rosário Almeida, et al.. (2022). Rare variants in TP73 in a frontotemporal dementia cohort link this gene with primary progressive aphasia phenotypes. European Journal of Neurology. 29(5). 1524–1528. 2 indexed citations

Güven, Gamze, Célia Kun‐Rodrigues, Catarina Gouveia, et al.. (2021). A comprehensive analysis of copy number variation in a Turkish dementia cohort. Human Genomics. 15(1). 48–48. 2 indexed citations

Faller, Kiterie M. E., Alison E. Ridyard, Rodrigo Gutierrez‐Quintana, et al.. (2020). A deletion of IDUA exon 10 in a family of Golden Retriever dogs with an attenuated form of mucopolysaccharidosis type I. Journal of Veterinary Internal Medicine. 34(5). 1813–1824. 3 indexed citations

Santos, Mariana, Joana Damásio, Célia Kun‐Rodrigues, et al.. (2020). Novel MAG Variant Causes Cerebellar Ataxia with Oculomotor Apraxia: Molecular Basis and Expanded Clinical Phenotype. Journal of Clinical Medicine. 9(4). 1212–1212. 3 indexed citations

Guerreiro, Rita, Elizabeth Gibbons, Miguel Tábuas‐Pereira, et al.. (2020). Genetic architecture of common non-Alzheimer’s disease dementias. Neurobiology of Disease. 142. 104946–104946. 31 indexed citations

Kun‐Rodrigues, Célia, Susana Carmona, Johanna Schleutker, et al.. (2020). Whole-exome sequencing of Finnish patients with vascular cognitive impairment. European Journal of Human Genetics. 29(4). 663–671. 5 indexed citations

Kun‐Rodrigues, Célia, Haşmet Hanağası, Ebba Lohmann, et al.. (2020). Analysis of copy number variation in a Turkish dementia cohort. Alzheimer s & Dementia. 16(S3). 1 indexed citations

10.

Salmona, Jordi, et al.. (2018). Genetic Differentiation and Demographic History of the Northern Rufous Mouse Lemur (Microcebus tavaratra) Across a Fragmented Landscape in Northern Madagascar. International Journal of Primatology. 39(1). 65–89. 12 indexed citations

11.

Darwent, Lee, Susana Carmona, Ebba Lohmann, et al.. (2017). Mutations in TYROBP are not a common cause of dementia in a Turkish cohort. Neurobiology of Aging. 58. 240.e1–240.e3. 9 indexed citations

12.

Carmona, Susana, Célia Kun‐Rodrigues, José Brás, & Rita Guerreiro. (2017). Revisiting the genetics of APOE. UCL Discovery (University College London). 1 indexed citations

13.

Goossens, Benoît, Reeta Sharma, Célia Kun‐Rodrigues, et al.. (2016). Habitat fragmentation and genetic diversity in natural populations of the Bornean elephant: Implications for conservation. Biological Conservation. 196. 80–92. 53 indexed citations

14.

Faller, Kiterie M. E., José Brás, Glenn Anderson, et al.. (2016). The Chihuahua dog: A new animal model for neuronal ceroid lipofuscinosis CLN7 disease?. Journal of Neuroscience Research. 94(4). 339–347. 29 indexed citations

15.

Kun‐Rodrigues, Célia, Christos Ganos, Rita Guerreiro, et al.. (2015). A systematic screening to identifyde novomutations causing sporadic early-onset Parkinson's disease. Human Molecular Genetics. 24(23). 6711–6720. 35 indexed citations

16.

Salmona, Jordi, Emmanuel Rasolondraibe, Célia Kun‐Rodrigues, et al.. (2015). Genetic Diversity, Population Size, and Conservation of the Critically Endangered Perrier’s Sifaka (Propithecus perrieri). International Journal of Primatology. 36(6). 1132–1153. 12 indexed citations

17.

Kun‐Rodrigues, Célia, Jordi Salmona, Emmanuel Rasolondraibe, et al.. (2014). New density estimates of a threatened sifaka species (Propithecus coquereli) in Ankarafantsika National Park. American Journal of Primatology. 76(6). 515–528. 28 indexed citations

18.

Vanpé, Cécile, Jordi Salmona, Célia Kun‐Rodrigues, et al.. (2013). Noninvasive molecular sexing: An evaluation and validation of the SRY‐ and amelogenin‐based method in three new lemur species. American Journal of Physical Anthropology. 150(3). 492–503. 6 indexed citations

19.

Salmona, Jordi, Emmanuel Rasolondraibe, Célia Kun‐Rodrigues, et al.. (2013). Survey of the critically endangered Perrier’s sifaka (Propithecus Perrieri) across most if its distribution range.. Portuguese National Funding Agency for Science, Research and Technology (RCAAP Project by FCT). 17. 9–12. 4 indexed citations

20.

Sharma, Reeta, Benoît Goossens, Célia Kun‐Rodrigues, et al.. (2012). Two Different High Throughput Sequencing Approaches Identify Thousands of De Novo Genomic Markers for the Genetically Depleted Bornean Elephant. PLoS ONE. 7(11). e49533–e49533. 30 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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