Cecilia Esteves

2.6k total citations
6 papers, 98 citations indexed

About

Cecilia Esteves is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Cecilia Esteves has authored 6 papers receiving a total of 98 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 2 papers in Molecular Biology and 2 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Cecilia Esteves's work include Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Prenatal Screening and Diagnostics (2 papers). Cecilia Esteves is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Prenatal Screening and Diagnostics (2 papers). Cecilia Esteves collaborates with scholars based in United States. Cecilia Esteves's co-authors include Vaidehi Jobanputra, Dorothy Warburton, Jennie Kline, Stephen Brown, Vanessa Felice, Vamsee Pillalamarri, Ronald J. Wapner, Kelly Brennan, Avinash Abhyankar and Zehra Ordulu and has published in prestigious journals such as Journal of the American Medical Informatics Association, BMC Health Services Research and Prenatal Diagnosis.

In The Last Decade

Cecilia Esteves

6 papers receiving 97 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Cecilia Esteves United States	6	64	35	26	17	13	6	98
Ling Cheng China	4	29 0.5×	16 0.5×	33 1.3×	26 1.5×	18 1.4×	8	75
Stephanie Harris United States	9	48 0.8×	15 0.4×	45 1.7×	5 0.3×	13 1.0×	11	169
Catherine L. Mercer United Kingdom	5	49 0.8×	13 0.4×	41 1.6×	7 0.4×	15 1.2×	6	72
Israel Maldonado Rosas United States	7	20 0.3×	34 1.0×	46 1.8×	123 7.2×	5 0.4×	27	183
Daniel Moreno‐Mendoza Italy	5	69 1.1×	13 0.4×	77 3.0×	42 2.5×	12 0.9×	9	125
Sylke Singer Germany	7	113 1.8×	75 2.1×	50 1.9×	7 0.4×	41 3.2×	13	128
S Reitano Italy	4	35 0.5×	8 0.2×	26 1.0×	11 0.6×	4 0.3×	5	64
Matthieu Bouaziz France	6	70 1.1×	4 0.1×	30 1.2×	7 0.4×	7 0.5×	9	121
Christina Anagnostopoulou Switzerland	4	5 0.1×	18 0.5×	32 1.2×	49 2.9×	3 0.2×	9	135
J. P. Milazzo France	6	127 2.0×	85 2.4×	72 2.8×	144 8.5×	37 2.8×	8	273

Countries citing papers authored by Cecilia Esteves

Since Specialization

Citations

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

Fields of papers citing papers by Cecilia Esteves

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cecilia Esteves

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

All Works

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6 of 6 papers shown

1.

Tinker, Rory J., Lisa Bastarache, Cecilia Esteves, et al.. (2023). The contribution of mosaicism to genetic diseases and de novo pathogenic variants. American Journal of Medical Genetics Part A. 191(10). 2482–2492. 8 indexed citations

2.

Gutiérrez‐Sacristán, Alba, Vianney Jouhet, Kimberly LeBlanc, et al.. (2021). Finding commonalities in rare diseases through the undiagnosed diseases network. Journal of the American Medical Informatics Association. 28(8). 1694–1702. 5 indexed citations

3.

Nicole, Sophie, Loren Peña, Stephen R. Hooper, et al.. (2018). Characteristics of undiagnosed diseases network applicants: implications for referring providers. BMC Health Services Research. 18(1). 652–652. 23 indexed citations

4.

Abhyankar, Avinash, Michelle F. Lamendola-Essel, Kelly Brennan, et al.. (2017). Clinical whole exome sequencing from dried blood spot identifies novel genetic defect underlying asparagine synthetase deficiency. Clinical Case Reports. 6(1). 200–205. 13 indexed citations

5.

Macera, Michael J., Brynn Levy, Vaidehi Jobanputra, et al.. (2014). Prenatal diagnosis of chromothripsis, with nine breaks characterized by karyotyping, FISH, microarray and whole‐genome sequencing. Prenatal Diagnosis. 35(3). 299–301. 27 indexed citations

6.

Jobanputra, Vaidehi, et al.. (2011). Using FISH to increase the yield and accuracy of karyotypes from spontaneous abortion specimens. Prenatal Diagnosis. 31(8). 755–759. 22 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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