Alice Dica

434 total citations
7 papers, 70 citations indexed

About

Alice Dica is a scholar working on Genetics, Public Health, Environmental and Occupational Health and Molecular Biology. According to data from OpenAlex, Alice Dica has authored 7 papers receiving a total of 70 indexed citations (citations by other indexed papers that have themselves been cited), including 4 papers in Genetics, 3 papers in Public Health, Environmental and Occupational Health and 2 papers in Molecular Biology. Recurrent topics in Alice Dica's work include Down syndrome and intellectual disability research (2 papers), Glycogen Storage Diseases and Myoclonus (1 paper) and RNA modifications and cancer (1 paper). Alice Dica is often cited by papers focused on Down syndrome and intellectual disability research (2 papers), Glycogen Storage Diseases and Myoclonus (1 paper) and RNA modifications and cancer (1 paper). Alice Dica collaborates with scholars based in Romania, Netherlands and Belgium. Alice Dica's co-authors include Dana Craiu, Catrinel Iliescu, Diana Bârcă, Magdalena Budișteanu, Arndt Rolfs, Mihaela Gherghiceanu, Nahid Nahavandi, Dorota Hoffman‐Zacharska, Alexandra Bastian and Monika Goś and has published in prestigious journals such as Clinical Genetics, European Journal of Paediatric Neurology and European Journal of Medical Genetics.

In The Last Decade

Alice Dica

6 papers receiving 70 citations

Peers

Countries citing papers authored by Alice Dica

Since Specialization

Citations

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

Fields of papers citing papers by Alice Dica

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Alice Dica

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

All Works

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7 of 7 papers shown

#	Work	Indexed citations
1	Age-Onset-Related Particularities of Pediatric MS—Understanding the Spectrum: A Tertiary Center Experience 2025 ·Diseases ·Alice Dica, Dana Craiu, (unknown), Magdalena Budișteanu, Catrinel Iliescu, (unknown), (unknown), Diana Bârcă, (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), (unknown), Daniela Adriana Ion	0
2	Endocrine Disorders in a Newborn with Heterozygous Galactosemia, Down Syndrome and Complex Cardiac Malformation: Case Report 2023 ·Medicina ·(unknown), (unknown), (unknown), (unknown), (unknown), Alice Dica, Elvira Brătilă, (unknown), (unknown)	5
3	Clinical and genomic findings in brain heterotopia: Report of a pediatric patient cohort from Romania 2021 ·Experimental and Therapeutic Medicine ·Magdalena Budișteanu, Sorina Mihaela Papuc, (unknown), Catrinel Iliescu, Maria Dobre, Diana Bârcă, (unknown), (unknown), Alice Dica, (unknown), (unknown), Dana Craiu, Aurora Arghir	3
4	Biallelic mutations in RTTN are associated with microcephaly, short stature and a wide range of brain malformations 2018 ·European Journal of Medical Genetics ·Katrien Stouffs, Stéphanie Moortgat, Tim Vanderhasselt, (unknown), Alice Dica, (unknown), Kathelijn Keymolen, Sara Seneca, Alexander Gheldof, Linda De Meırleır, Anna Jansen	8
5	Expanding the clinical spectrum of biallelic ZNF335 variants 2018 ·Clinical Genetics ·Katrien Stouffs, Andrew B. Stergachis, Tim Vanderhasselt, Alice Dica, Sandra Janssens, (unknown), Alexander Gheldof, Olaf A. Bodamer, Kathelijn Keymolen, Sara Seneca, I. Liebærs, Durai Jayaraman, (unknown), Jennifer N. Partlow, Christopher A. Walsh, Anna Jansen	12
6	Rett-like onset in late-infantile neuronal ceroid lipofuscinosis (CLN7) caused by compound heterozygous mutation in the MFSD8 gene and review of the literature data on clinical onset signs 2014 ·European Journal of Paediatric Neurology ·Dana Craiu, (unknown), Alice Dica, Dorota Hoffman‐Zacharska, Monika Goś, Alexandra Bastian, Mihaela Gherghiceanu, Arndt Rolfs, Nahid Nahavandi, (unknown), Catrinel Iliescu	23
7	Intellectual disability and epilepsy in down syndrome. 2014 ·PubMed ·Diana Bârcă, (unknown), Alice Dica, Catrinel Iliescu, Magdalena Budișteanu, (unknown), (unknown), Dana Craiu	19

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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