R. Prates

840 total citations
13 papers, 615 citations indexed

About

R. Prates is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Surgery. According to data from OpenAlex, R. Prates has authored 13 papers receiving a total of 615 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Pediatrics, Perinatology and Child Health, 10 papers in Genetics and 2 papers in Surgery. Recurrent topics in R. Prates's work include Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genetic Syndromes and Imprinting (5 papers). R. Prates is often cited by papers focused on Prenatal Screening and Diagnostics (13 papers), Genomic variations and chromosomal abnormalities (9 papers) and Genetic Syndromes and Imprinting (5 papers). R. Prates collaborates with scholars based in United States, United Kingdom and Netherlands. R. Prates's co-authors include S. Munné, Dagan Wells, P. Colls, Cristina Gutiérrez-Mateo, K. Ketterson, Jorge Sánchez-García, Tomás Escudero, N.-N. Goodall, William B. Schoolcraft and S. Alfarawati and has published in prestigious journals such as Genome Research, Human Reproduction and Fertility and Sterility.

In The Last Decade

R. Prates

13 papers receiving 567 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
R. Prates United States 7 536 321 181 148 52 13 615
N.-N. Goodall United States 7 467 0.9× 223 0.7× 227 1.3× 145 1.0× 52 1.0× 14 548
L. Spizzichino Italy 8 652 1.2× 394 1.2× 216 1.2× 166 1.1× 52 1.0× 12 759
D. Wells United Kingdom 5 466 0.9× 275 0.9× 198 1.1× 126 0.9× 54 1.0× 7 561
Eftychia Dimitriadou Belgium 15 488 0.9× 315 1.0× 175 1.0× 251 1.7× 92 1.8× 26 715
G. Gemelos United States 5 633 1.2× 300 0.9× 185 1.0× 148 1.0× 45 0.9× 10 702
Christian S. Ottolini United Kingdom 14 468 0.9× 270 0.8× 262 1.4× 247 1.7× 109 2.1× 28 683
D Babariya United Kingdom 6 449 0.8× 187 0.6× 209 1.2× 136 0.9× 22 0.4× 15 505
Vanessa Peinado Spain 16 566 1.1× 241 0.8× 326 1.8× 216 1.5× 34 0.7× 22 719
Andrea R. Victor United States 11 499 0.9× 184 0.6× 258 1.4× 152 1.0× 27 0.5× 20 585

Countries citing papers authored by R. Prates

Since Specialization
Citations

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

Fields of papers citing papers by R. Prates

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

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

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

All Works

13 of 13 papers shown
1.
Konstantinidis, M., Krithika Ravichandran, R. Prates, et al.. (2019). Aneuploidy and recombination in the human preimplantation embryo. Copy number variation analysis and genome-wide polymorphism genotyping. Reproductive BioMedicine Online. 40(4). 479–493. 9 indexed citations
2.
Konstantinidis, M., et al.. (2015). Human leukocyte antigen (HLA) matching of preimplantation embryos using a polymerase chain reaction (PCR) based methodology and karyomapping. Human Reproduction. 30. 402–402. 1 indexed citations
3.
Peters, Brock A., Bahram G. Kermani, Misha R. Agarwal, et al.. (2015). Detection and phasing of single base de novo mutations in biopsies from human in vitro fertilized embryos by advanced whole-genome sequencing. Genome Research. 25(3). 426–434. 37 indexed citations
4.
Konstantinidis, M., R. Prates, N.-N. Goodall, et al.. (2015). Live births following Karyomapping of human blastocysts: experience from clinical application of the method. Reproductive BioMedicine Online. 31(3). 394–403. 54 indexed citations
5.
Coşkun, Serdar, R. Prates, S. Munné, et al.. (2014). Genome-wide karyomapping accurately identifies the inheritance of single-gene defects in human preimplantation embryos in vitro. Genetics in Medicine. 16(11). 838–845. 136 indexed citations
6.
Prates, R., M. Konstantinidis, N.-N. Goodall, et al.. (2014). Clinical experience with karyomapping for preimplantation genetic diagnosis (PGD) of single gene disorders. Fertility and Sterility. 102(3). e25–e26. 1 indexed citations
7.
Prates, R., et al.. (2013). Multiple advantages of blastocyst versus cleavage stage biopsy for preimplantation genetic diagnosis (PGD) of single gene disorders. Fertility and Sterility. 100(3). S84–S84. 1 indexed citations
8.
Prates, R., et al.. (2013). Simultaneous analysis of single gene disorders and aneuploidy by PCR and array CGH. Fertility and Sterility. 100(3). S35–S36. 1 indexed citations
9.
Gutiérrez-Mateo, Cristina, P. Colls, Jorge Sánchez-García, et al.. (2010). Validation of microarray comparative genomic hybridization for comprehensive chromosome analysis of embryos. Fertility and Sterility. 95(3). 953–958. 244 indexed citations
10.
Escudero, T., et al.. (2010). Preimplantation genetic diagnosis (PGD) for reciprocal translocations using array comparative genome hybridization (aCGH). Fertility and Sterility. 94(4). S80–S81. 1 indexed citations
11.
12.
Fragouli, E., M. Katz-Jaffe, S. Alfarawati, et al.. (2009). Comprehensive chromosome screening of polar bodies and blastocysts from couples experiencing repeated implantation failure. Fertility and Sterility. 94(3). 875–887. 122 indexed citations
13.
Munné, S., et al.. (2009). Validation of microarray CGH for PGD by FISH reanalysis. Fertility and Sterility. 92(3). S2–S2. 2 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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