R. Queralt

562 total citations
11 papers, 421 citations indexed

About

R. Queralt is a scholar working on Molecular Biology, Physiology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, R. Queralt has authored 11 papers receiving a total of 421 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 3 papers in Physiology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in R. Queralt's work include Alzheimer's disease research and treatments (3 papers), RNA and protein synthesis mechanisms (3 papers) and Computational Drug Discovery Methods (2 papers). R. Queralt is often cited by papers focused on Alzheimer's disease research and treatments (3 papers), RNA and protein synthesis mechanisms (3 papers) and Computational Drug Discovery Methods (2 papers). R. Queralt collaborates with scholars based in Spain, Canada and France. R. Queralt's co-authors include Rafael Oliva, Robert J. Winkfein, Gordon H. Dixon, Jacques Retief, F Ballesta, Ester Margarit, Vanessa Bach, Paloma Jara, Miquel Bruguera and Ana Carrió and has published in prestigious journals such as Neurology, Biochemical and Biophysical Research Communications and Journal of Neurology Neurosurgery & Psychiatry.

In The Last Decade

R. Queralt

11 papers receiving 412 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
R. Queralt Spain	8	202	125	121	72	70	11	421
Inoru HASHIMOTO Japan	13	155 0.8×	12 0.1×	125 1.0×	46 0.6×	130 1.9×	25	563
Shangang Li China	11	252 1.2×	17 0.1×	80 0.7×	17 0.2×	36 0.5×	32	396
M. C. Richardson United Kingdom	15	135 0.7×	25 0.2×	84 0.7×	18 0.3×	215 3.1×	27	665
B Turner Australia	10	288 1.4×	40 0.3×	270 2.2×	214 3.0×	12 0.2×	16	700
Robert Fraser Canada	13	303 1.5×	10 0.1×	143 1.2×	17 0.2×	75 1.1×	16	603
Adriana S. Moreno Brazil	9	216 1.1×	15 0.1×	94 0.8×	26 0.4×	365 5.2×	32	625
Fatih Temiz Türkiye	9	238 1.2×	38 0.3×	137 1.1×	38 0.5×	362 5.2×	35	563
Márcia S. Wagner Brazil	8	182 0.9×	5 0.0×	119 1.0×	39 0.5×	119 1.7×	9	580
Yayoi Yoshida Japan	13	120 0.6×	199 1.6×	38 0.3×	106 1.5×	7 0.1×	28	580
Eveline P. C. T. de Rijk Netherlands	14	153 0.8×	6 0.0×	40 0.3×	38 0.5×	81 1.2×	22	571

Countries citing papers authored by R. Queralt

Since Specialization

Citations

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

Fields of papers citing papers by R. Queralt

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of R. Queralt

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

All Works

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11 of 11 papers shown

Margarit, Ester, Vanessa Bach, Miquel Bruguera, et al.. (2005). Mutation analysis of Wilson disease in the Spanish population - identification of a prevalent substitution and eight novel mutations in the ATP7B gene. Clinical Genetics. 68(1). 61–68. 71 indexed citations

Rosiñol, Laura, Joan Bladé, Jordi Esteve, et al.. (2003). Smoldering multiple myeloma: natural history and recognition of an evolving type. British Journal of Haematology. 123(4). 631–636. 95 indexed citations

Queralt, R.. (2002). A novel mutation (V89L) in the presenilin 1 gene in a family with early onset Alzheimer's disease and marked behavioural disturbances. Journal of Neurology Neurosurgery & Psychiatry. 72(2). 266–269. 43 indexed citations

Lleó, Alberto, Rafael Blesa, Magda Castellvı́, et al.. (2001). A novel presenilin 2 gene mutation (D439A) in a patient with early-onset Alzheimer’s disease. Neurology. 57(10). 1926–1928. 28 indexed citations

Soler, Anna, Ester Margarit, Ana Carrió, et al.. (1999). Trisomy/tetrasomy 21 mosaicism in CVS: interpretation of cytogenetic discrepancies between placental and fetal chromosome complements. Journal of Medical Genetics. 36(4). 333–334. 5 indexed citations

Ballesta, F, et al.. (1999). Parental origin and meiotic stage of non-disjunction in 139 cases of trisomy 21.. PubMed. 42(1). 11–5. 21 indexed citations

Ezquerra, Mario, F Ballesta, R. Queralt, et al.. (1998). Apolipoprotein E ϵ4 alleles and meiotic origin of non-disjunction in Down syndrome children and in their corresponding fathers and mothers. Neuroscience Letters. 248(1). 1–4. 6 indexed citations

Queralt, R. & Rafael Oliva. (1995). Demonstration of Trans-acting Factors Binding to the Promoter Region of the Testis-Specific Rat Protamine P1 Gene. Biochemical and Biophysical Research Communications. 208(2). 802–812. 14 indexed citations

Queralt, R., et al.. (1995). Evolution of protamine P1 genes in mammals. Journal of Molecular Evolution. 40(6). 601–607. 75 indexed citations

10.

Retief, Jacques, Robert J. Winkfein, Gordon H. Dixon, et al.. (1993). Evolution of protamine P1 genes in primates. Journal of Molecular Evolution. 37(4). 426–34. 56 indexed citations

11.

Queralt, R., Oriol de Fàbregues, M. Gené, et al.. (1993). Direct Sequencing of the Human Protamine P1 Gene and Application in Forensic Medicine. Journal of Forensic Sciences. 38(6). 1491–1501. 7 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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