P. Colls

4.3k total citations
51 papers, 3.0k citations indexed

About

P. Colls is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Public Health, Environmental and Occupational Health. According to data from OpenAlex, P. Colls has authored 51 papers receiving a total of 3.0k indexed citations (citations by other indexed papers that have themselves been cited), including 45 papers in Pediatrics, Perinatology and Child Health, 34 papers in Genetics and 12 papers in Public Health, Environmental and Occupational Health. Recurrent topics in P. Colls's work include Prenatal Screening and Diagnostics (45 papers), Genomic variations and chromosomal abnormalities (25 papers) and Genetic Syndromes and Imprinting (14 papers). P. Colls is often cited by papers focused on Prenatal Screening and Diagnostics (45 papers), Genomic variations and chromosomal abnormalities (25 papers) and Genetic Syndromes and Imprinting (14 papers). P. Colls collaborates with scholars based in United States, United Kingdom and Spain. P. Colls's co-authors include S. Munné, Dagan Wells, Tomás Escudero, E. Fragouli, S. Alfarawati, Cristina Gutiérrez-Mateo, J. Fischer, John Stevens, Jacques Cohen and William B. Schoolcraft and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and PLoS Genetics.

In The Last Decade

P. Colls

49 papers receiving 2.8k citations

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
P. Colls 2.4k 1.3k 1.1k 640 467 51 3.0k
Edith Coonen 2.8k 1.1× 1.3k 1.0× 1.2k 1.1× 825 1.3× 777 1.7× 69 3.5k
Francesca Vidal 1.9k 0.8× 1.7k 1.3× 2.0k 1.8× 1.1k 1.7× 1.6k 3.4× 136 4.0k
Lorena Rodrigo 1.7k 0.7× 1.2k 0.9× 598 0.6× 380 0.6× 643 1.4× 52 2.2k
M.C. Magli 2.0k 0.8× 1.4k 1.1× 739 0.7× 536 0.8× 700 1.5× 50 2.5k
Mina Alikani 2.4k 1.0× 2.9k 2.2× 659 0.6× 956 1.5× 2.0k 4.4× 78 4.1k
Tomás Escudero 1.9k 0.8× 744 0.6× 1.1k 1.0× 336 0.5× 316 0.7× 40 2.3k
Francesco Fiorentino 2.5k 1.0× 1.0k 0.8× 1.1k 1.0× 548 0.9× 462 1.0× 58 2.9k
John McBain 1.3k 0.5× 1.6k 1.3× 362 0.3× 384 0.6× 1.6k 3.4× 89 2.7k
Eric J. Forman 2.9k 1.2× 2.2k 1.7× 669 0.6× 709 1.1× 1.5k 3.3× 108 4.1k
Pedro N. Barri 1.9k 0.8× 2.5k 1.9× 326 0.3× 469 0.7× 2.8k 5.9× 135 3.8k

Countries citing papers authored by P. Colls

Since Specialization
Citations

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

Fields of papers citing papers by P. Colls

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of P. Colls

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

All Works

20 of 20 papers shown
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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
3.
Maxwell, Susan, P. Colls, B. Hodes-Wertz, et al.. (2016). Why do euploid embryos miscarry? A case-control study comparing the rate of aneuploidy within presumed euploid embryos that resulted in miscarriage or live birth using next-generation sequencing. Fertility and Sterility. 106(6). 1414–1419.e5. 131 indexed citations
4.
Colls, P., et al.. (2013). Preimplantation genetic diagnosis at blastocyst stage by array comparative genomic hybridization. Error rate determination. Fertility and Sterility. 100(3). S196–S196. 1 indexed citations
5.
McCaffrey, Caroline, et al.. (2012). Developmental morphology and continuous time-lapse microscopy (TLM) of human embryos: can we predict euploidy?. Fertility and Sterility. 98(3). S136–S136. 3 indexed citations
6.
Colls, P., Tomás Escudero, J. Fischer, et al.. (2012). Validation of array comparative genome hybridization for diagnosis of translocations in preimplantation human embryos. Reproductive BioMedicine Online. 24(6). 621–629. 65 indexed citations
7.
Alfarawati, S., E. Fragouli, P. Colls, & Dagan Wells. (2012). Embryos of Robertsonian Translocation Carriers Exhibit a Mitotic Interchromosomal Effect That Enhances Genetic Instability during Early Development. PLoS Genetics. 8(10). e1003025–e1003025. 73 indexed citations
8.
Chavez, Shawn L., Kevin Loewke, Jinnuo Han, et al.. (2012). Dynamic blastomere behaviour reflects human embryo ploidy by the four-cell stage. Nature Communications. 3(1). 1251–1251. 218 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.
Alfarawati, S., E. Fragouli, P. Colls, et al.. (2010). The relationship between blastocyst morphology, chromosomal abnormality, and embryo gender. Fertility and Sterility. 95(2). 520–524. 314 indexed citations
11.
Fischer, J., P. Colls, Tomás Escudero, & S. Munné. (2009). Preimplantation genetic diagnosis (PGD) improves pregnancy outcome for translocation carriers with a history of recurrent losses. Fertility and Sterility. 94(1). 283–289. 105 indexed citations
12.
Colls, P., N.-N. Goodall, X. Zheng, & S. Munné. (2009). Increased efficiency of preimplantation genetic diagnosis for aneuploidy by testing 12 chromosomes. Reproductive BioMedicine Online. 19(4). 532–538. 32 indexed citations
13.
Colls, P., Lee M. Silver, Jingly F. Weier, et al.. (2009). Preimplantation genetic diagnosis for gender selection in the USA. Reproductive BioMedicine Online. 19. 16–22. 17 indexed citations
14.
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
15.
Colls, P., Tomás Escudero, N. Cekleniak, et al.. (2007). Increased efficiency of preimplantation genetic diagnosis for infertility using “no result rescue”. Fertility and Sterility. 88(1). 53–61. 91 indexed citations
16.
Munné, S., P. Colls, John Garrisi, et al.. (2007). Maternal age, morphology, development and chromosome abnormalities in over 6000 cleavage-stage embryos. Reproductive BioMedicine Online. 14(5). 628–634. 199 indexed citations
17.
Vemuri, Mohan C., Tim Schimmel, P. Colls, S. Munné, & Jacques Cohen. (2007). Derivation of Human Embryonic Stem Cells in Xeno-Free Conditions. Methods in molecular biology. 407. 1–10. 15 indexed citations
18.
Munné, S., E. Velilla, P. Colls, et al.. (2005). Self-correction of chromosomally abnormal embryos in culture and implications for stem cell production. Fertility and Sterility. 84(5). 1328–1334. 115 indexed citations
19.
Colls, P.. (1998). Cytogenetic analysis of spermatozoa in the father of a child with a de- novo reciprocal translocation t(7;9) (q22;p23). Molecular Human Reproduction. 4(12). 1145–1149. 2 indexed citations
20.

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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