Iria Roca

478 total citations
13 papers, 295 citations indexed

About

Iria Roca is a scholar working on Clinical Biochemistry, Molecular Biology and Genetics. According to data from OpenAlex, Iria Roca has authored 13 papers receiving a total of 295 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Clinical Biochemistry, 6 papers in Molecular Biology and 4 papers in Genetics. Recurrent topics in Iria Roca's work include Metabolism and Genetic Disorders (8 papers), Genomics and Rare Diseases (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Iria Roca is often cited by papers focused on Metabolism and Genetic Disorders (8 papers), Genomics and Rare Diseases (3 papers) and Genomic variations and chromosomal abnormalities (3 papers). Iria Roca collaborates with scholars based in Spain, Palestinian Territory and China. Iria Roca's co-authors include María L. Couce, Ana Fernández‐Marmiesse, Rosaura Leis, Luis Aldámiz‐Echevarría, Isidro Vitoria, Paula Sánchez‐Pintos, Á. Hermida Ameijeiras, Fernando Andrade, Jaime Dalmau and Segundo Rite Gracia and has published in prestigious journals such as Scientific Reports, International Journal of Molecular Sciences and Movement Disorders.

In The Last Decade

Iria Roca

13 papers receiving 292 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Iria Roca Spain	11	165	147	109	71	44	13	295
Anke Schumann Germany	11	149 0.9×	179 1.2×	75 0.7×	64 0.9×	37 0.8×	32	379
Magalie Barth France	12	171 1.0×	274 1.9×	92 0.8×	35 0.5×	27 0.6×	32	378
Emma Glamuzina New Zealand	11	149 0.9×	148 1.0×	68 0.6×	62 0.9×	61 1.4×	30	323
Haq Nawaz Khan Pakistan	9	80 0.5×	88 0.6×	63 0.6×	72 1.0×	51 1.2×	25	325
Sabine Grønborg Denmark	11	74 0.4×	207 1.4×	64 0.6×	69 1.0×	42 1.0×	25	330
Mary Anne D. Chiong Philippines	10	142 0.9×	168 1.1×	54 0.5×	36 0.5×	41 0.9×	31	295
Tessa van Dijk Netherlands	10	114 0.7×	170 1.2×	60 0.6×	49 0.7×	111 2.5×	18	320
Christine Makowski Germany	10	143 0.9×	229 1.6×	51 0.5×	51 0.7×	94 2.1×	18	480
Darius J. Adams United States	10	328 2.0×	328 2.2×	102 0.9×	71 1.0×	76 1.7×	17	464
Rebecca Mardach United States	11	164 1.0×	193 1.3×	100 0.9×	40 0.6×	28 0.6×	17	351

Countries citing papers authored by Iria Roca

Since Specialization

Citations

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

Fields of papers citing papers by Iria Roca

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Iria Roca

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

All Works

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13 of 13 papers shown

Roca, Iria, et al.. (2019). PattRec: An easy-to-use CNV detection tool optimized for targeted NGS assays with diagnostic purposes. Genomics. 112(2). 1245–1256. 7 indexed citations

Roca, Iria, et al.. (2019). Free-access copy-number variant detection tools for targeted next-generation sequencing data. Mutation Research/Reviews in Mutation Research. 779. 114–125. 43 indexed citations

Couce, María L., Paula Sánchez‐Pintos, Luis Aldámiz‐Echevarría, et al.. (2019). Evolution of tyrosinemia type 1 disease in patients treated with nitisinone in Spain. Medicine. 98(39). e17303–e17303. 18 indexed citations

Gil, Marta, et al.. (2018). Retrospective study to identify risk factors for chronic kidney disease in children with congenital solitary functioning kidney detected by neonatal renal ultrasound screening. Medicine. 97(32). e11819–e11819. 11 indexed citations

Couce, María L., Paula Sánchez‐Pintos, Isidro Vitoria, et al.. (2018). Carbohydrate status in patients with phenylketonuria. Orphanet Journal of Rare Diseases. 13(1). 103–103. 41 indexed citations

Roca, Iria, et al.. (2018). Prioritization of Variants Detected by Next Generation Sequencing According to the Mutation Tolerance and Mutational Architecture of the Corresponding Genes. International Journal of Molecular Sciences. 19(6). 1584–1584. 13 indexed citations

Fernández‐Marmiesse, Ana, Hirofumi Kusumoto, Iria Roca, et al.. (2018). A novel missense mutation in GRIN2A causes a nonepileptic neurodevelopmental disorder. Movement Disorders. 33(6). 992–999. 22 indexed citations

Ameijeiras, Á. Hermida, et al.. (2017). Arterial stiffness assessment in patients with phenylketonuria. Medicine. 96(51). e9322–e9322. 22 indexed citations

Sánchez‐Pintos, Paula, et al.. (2017). Similarities between acylcarnitine profiles in large for gestational age newborns and obesity. Scientific Reports. 7(1). 16267–16267. 21 indexed citations

10.

Emperador, Sonia, M. Pilar Bayona‐Bafaluy, Ana Fernández‐Marmiesse, et al.. (2016). Molecular-genetic characterization and rescue of a TSFM mutation causing childhood-onset ataxia and nonobstructive cardiomyopathy. European Journal of Human Genetics. 25(1). 153–156. 16 indexed citations

11.

Couce, María L., Isidro Vitoria, Luis Aldámiz‐Echevarría, et al.. (2016). Lipid profile status and other related factors in patients with Hyperphenylalaninaemia. Orphanet Journal of Rare Diseases. 11(1). 123–123. 31 indexed citations

12.

Aldámiz‐Echevarría, Luis, Isidro Vitoria, Fernando Andrade, et al.. (2015). Micronutrient in hyperphenylalaninemia. Data in Brief. 4. 614–621. 5 indexed citations

13.

Aldámiz‐Echevarría, Luis, Jaime Dalmau, Isidro Vitoria, et al.. (2015). Vitamin and mineral status in patients with hyperphenylalaninemia. Molecular Genetics and Metabolism. 115(4). 145–150. 45 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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