Eva Richard

1.5k total citations
61 papers, 1.2k citations indexed

About

Eva Richard is a scholar working on Molecular Biology, Clinical Biochemistry and Rheumatology. According to data from OpenAlex, Eva Richard has authored 61 papers receiving a total of 1.2k indexed citations (citations by other indexed papers that have themselves been cited), including 50 papers in Molecular Biology, 39 papers in Clinical Biochemistry and 10 papers in Rheumatology. Recurrent topics in Eva Richard's work include Metabolism and Genetic Disorders (39 papers), Mitochondrial Function and Pathology (22 papers) and Biochemical and Molecular Research (12 papers). Eva Richard is often cited by papers focused on Metabolism and Genetic Disorders (39 papers), Mitochondrial Function and Pathology (22 papers) and Biochemical and Molecular Research (12 papers). Eva Richard collaborates with scholars based in Spain, United States and United Kingdom. Eva Richard's co-authors include Lourdes R. Desviat, Magdalena Ugarte, Belén Pérez, Celia Pérez‐Cerdá, Belén Pérez, Pilar Rodríguez‐Pombo, Francisco X. Arredondo-Vega, Michael S. Hershfield, B. Merinero and Silvia Muro and has published in prestigious journals such as Journal of Biological Chemistry, The Journal of Experimental Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Eva Richard

57 papers receiving 1.1k citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Eva Richard Spain	23	820	609	218	121	104	61	1.2k
Zuhair N. Al‐Hassnan Saudi Arabia	18	549 0.7×	291 0.5×	114 0.5×	105 0.9×	248 2.4×	78	1.0k
Yolanda Cámara Spain	19	1.5k 1.8×	448 0.7×	84 0.4×	75 0.6×	137 1.3×	35	1.7k
Nancy G. Kennaway United States	22	1.5k 1.9×	906 1.5×	75 0.3×	90 0.7×	120 1.2×	37	2.0k
Elena J. Tucker Australia	19	1.3k 1.6×	580 1.0×	58 0.3×	46 0.4×	348 3.3×	41	1.7k
Stephanie Grünewald United Kingdom	28	1.4k 1.7×	558 0.9×	251 1.2×	217 1.8×	354 3.4×	85	2.1k
Emmanuelle Sarzi France	17	1.6k 1.9×	865 1.4×	35 0.2×	50 0.4×	109 1.0×	25	1.7k
Hezhi Fang China	22	996 1.2×	260 0.4×	73 0.3×	74 0.6×	76 0.7×	64	1.3k
Yves Labelle Canada	18	489 0.6×	146 0.2×	170 0.8×	39 0.3×	150 1.4×	31	1.0k
Florin Sasarman Canada	26	2.3k 2.8×	831 1.4×	31 0.1×	100 0.8×	109 1.0×	33	2.5k
Shlomo Almashanu Israel	16	390 0.5×	271 0.4×	67 0.3×	63 0.5×	136 1.3×	45	838

Countries citing papers authored by Eva Richard

Since Specialization

Citations

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

Fields of papers citing papers by Eva Richard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Eva Richard

This figure shows the co-authorship network connecting the top 25 collaborators of Eva Richard. A scholar is included among the top collaborators of Eva Richard 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 Eva Richard. Eva Richard 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

Schauer, Tamás, Jianfeng Sun, Jonas J. Funke, et al.. (2025). H4K16 acylations destabilize chromatin architecture and facilitate transcriptional response during metabolic perturbations. Molecular Cell. 86(1). 24–40.e10.

Richard, Eva, Lourdes R. Desviat, Sarah P. Young, et al.. (2024). The attenuated hepatic clearance of propionate increases cardiac oxidative stress in propionic acidemia. Basic Research in Cardiology. 119(6). 1045–1062. 3 indexed citations

Picó, Sara, Arístides López‐Márquez, Mar Álvarez, et al.. (2024). PAH deficient pathology in humanized c.1066-11G>A phenylketonuria mice. Human Molecular Genetics. 33(12). 1074–1089. 1 indexed citations

Álvarez, Mar, Maja Dembić, Margarita Castro, et al.. (2024). Splice-Switching Antisense Oligonucleotides Correct Phenylalanine Hydroxylase Exon 11 Skipping Defects and Rescue Enzyme Activity in Phenylketonuria. Nucleic Acid Therapeutics. 34(3). 134–142. 2 indexed citations

Álvarez, Mar, Pedro Ruiz‐Sala, Belén Pérez, Lourdes R. Desviat, & Eva Richard. (2023). Dysregulated Cell Homeostasis and miRNAs in Human iPSC-Derived Cardiomyocytes from a Propionic Acidemia Patient with Cardiomyopathy. International Journal of Molecular Sciences. 24(3). 2182–2182. 6 indexed citations

Park, Kyung Chan, S. Krywawych, Eva Richard, Lourdes R. Desviat, & Pawel Swietach. (2020). Cardiac Complications of Propionic and Other Inherited Organic Acidemias. Frontiers in Cardiovascular Medicine. 7. 617451–617451. 25 indexed citations

Richard, Eva, et al.. (2020). プログラム化DNA除去中の包括的染色体末端リモデリング【JST・京大機械翻訳】. Current Biology. 30(17). 3397–3413. 6 indexed citations

Navarro‐García, José Alberto, Almudena Val‐Blasco, Gema Ruiz‐Hurtado, et al.. (2019). Intracellular calcium mishandling leads to cardiac dysfunction and ventricular arrhythmias in a mouse model of propionic acidemia. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1866(1). 165586–165586. 26 indexed citations

López‐Márquez, Arístides, Rosa Navarrete, Celia Pérez‐Cerdá, et al.. (2019). Generation and characterization of a human iPSC line (UAMi004-A) from a patient with propionic acidemia due to defects in the PCCB gene. Stem Cell Research. 38. 101469–101469. 5 indexed citations

10.

Navarrete, Rosa, Eva Richard, Magdalena Ugarte, et al.. (2018). Identification of 34 novel mutations in propionic acidemia: Functional characterization of missense variants and phenotype associations. Molecular Genetics and Metabolism. 125(3). 266–275. 16 indexed citations

11.

Richard, Eva, Sandra Brasil, M. Esther Gallardo, et al.. (2018). Generation and characterization of two human iPSC lines from patients with methylmalonic acidemia cblB type. Stem Cell Research. 29. 143–147. 3 indexed citations

12.

Richard, Eva, et al.. (2018). Altered Redox Homeostasis in Branched‐Chain Amino Acid Disorders, Organic Acidurias, and Homocystinuria. Oxidative Medicine and Cellular Longevity. 2018(1). 1246069–1246069. 31 indexed citations

13.

Pérez‐Cerdá, Celia, Ricardo Ramos, Michael A. Barry, et al.. (2017). Dysregulated miRNAs and their pathogenic implications for the neurometabolic disease propionic acidemia. Scientific Reports. 7(1). 5727–5727. 19 indexed citations

14.

Guenzel, Adam J., Belén Pérez, Michael A. Barry, et al.. (2016). In vivo evidence of mitochondrial dysfunction and altered redox homeostasis in a genetic mouse model of propionic acidemia: Implications for the pathophysiology of this disorder. Free Radical Biology and Medicine. 96. 1–12. 43 indexed citations

15.

Mikula, Ivan, et al.. (2015). Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients. Folia Biologica. 61(6). 219–226. 3 indexed citations

16.

Jorge‐Finnigan, Ana, Alejandra Gámez, Belén Pérez, Magdalena Ugarte, & Eva Richard. (2010). Different altered pattern expression of genes related to apoptosis in isolated methylmalonic aciduria cblB type and combined with homocystinuria cblC type. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1802(11). 959–967. 13 indexed citations

17.

Richard, Eva, et al.. (2002). Clustered Charged Amino Acids of Human Adenosine Deaminase Comprise a Functional Epitope for Binding the Adenosine Deaminase Complexing Protein CD26/Dipeptidyl Peptidase IV. Journal of Biological Chemistry. 277(22). 19720–19726. 35 indexed citations

18.

Ugarte, Magdalena, Pilar Rodríguez‐Pombo, Lourdes R. Desviat, et al.. (1999). Overview of mutations in thePCCA andPCCB genes causing propionic acidemia. Human Mutation. 14(4). 275–282. 66 indexed citations

19.

Richard, Eva, Lourdes R. Desviat, Belén Pérez, Celia Pérez‐Cerdá, & Magdalena Ugarte. (1999). Genetic heterogeneity in propionic acidemia patients with α-subunit defects. Identification of five novel mutations, one of them causing instability of the protein. Biochimica et Biophysica Acta (BBA) - Molecular Basis of Disease. 1453(3). 351–358. 21 indexed citations

20.

Hoenicka, Janet, Pilar Rodríguez‐Pombo, Celia Pérez‐Cerdá, et al.. (1998). New frequent mutation in the PCCB gene in Spanish propionic acidemia patients. Human Mutation. 11(S1). S234–S236. 11 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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