Fabiola Quintero‐Rivera

4.8k total citations · 1 hit paper
54 papers, 1.4k citations indexed

About

Fabiola Quintero‐Rivera is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Fabiola Quintero‐Rivera has authored 54 papers receiving a total of 1.4k indexed citations (citations by other indexed papers that have themselves been cited), including 27 papers in Genetics, 22 papers in Molecular Biology and 8 papers in Genetics. Recurrent topics in Fabiola Quintero‐Rivera's work include Genomic variations and chromosomal abnormalities (15 papers), Congenital heart defects research (11 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Fabiola Quintero‐Rivera is often cited by papers focused on Genomic variations and chromosomal abnormalities (15 papers), Congenital heart defects research (11 papers) and Genetics and Neurodevelopmental Disorders (7 papers). Fabiola Quintero‐Rivera collaborates with scholars based in United States, Canada and United Kingdom. Fabiola Quintero‐Rivera's co-authors include Kerry K. Brown, Sarah T. South, Erik C. Thorland, Hutton M. Kearney, Julián A. Martínez-Agosto, Wayne W. Grody, Joshua L. Deignan, Hane Lee, Éric Vilain and Stanley F. Nelson and has published in prestigious journals such as Nature Communications, SHILAP Revista de lepidopterología and The American Journal of Human Genetics.

In The Last Decade

Fabiola Quintero‐Rivera

49 papers receiving 1.4k citations

Hit Papers

American College of Medical Genetics standards and guidel... 2011 2026 2016 2021 2011 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants
    2011 643 citations Hutton M. Kearney, Erik C. Thorland et al. Genetics in Medicine profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fabiola Quintero‐Rivera United States 16 907 634 357 123 99 54 1.4k
Teresa Mattina Italy 18 839 0.9× 764 1.2× 181 0.5× 65 0.5× 101 1.0× 59 1.4k
Roberto Ciccone Italy 23 956 1.1× 681 1.1× 283 0.8× 64 0.5× 102 1.0× 51 1.4k
Elizabeth Roeder United States 21 972 1.1× 1.2k 1.8× 346 1.0× 165 1.3× 216 2.2× 37 1.9k
Sibel Kantarci United States 15 1.0k 1.1× 821 1.3× 385 1.1× 142 1.2× 248 2.5× 23 1.8k
Līvija Medne United States 25 928 1.0× 1.1k 1.7× 342 1.0× 145 1.2× 102 1.0× 53 1.8k
Daniela del Gaudio United States 18 1.0k 1.1× 854 1.3× 388 1.1× 67 0.5× 254 2.6× 47 1.8k
Erica Andersen United States 16 773 0.9× 612 1.0× 340 1.0× 65 0.5× 86 0.9× 28 1.5k
Emmanuelle Lemyre Canada 22 879 1.0× 550 0.9× 276 0.8× 55 0.4× 129 1.3× 52 1.3k
Carol Saunders United States 22 635 0.7× 744 1.2× 110 0.3× 93 0.8× 72 0.7× 59 1.3k
Karine Hovanes United States 17 444 0.5× 978 1.5× 262 0.7× 75 0.6× 89 0.9× 28 1.9k

Countries citing papers authored by Fabiola Quintero‐Rivera

Since Specialization
Citations

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

Fields of papers citing papers by Fabiola Quintero‐Rivera

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fabiola Quintero‐Rivera. 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 Fabiola Quintero‐Rivera. The network helps show where Fabiola Quintero‐Rivera may publish in the future.

Co-authorship network of co-authors of Fabiola Quintero‐Rivera

This figure shows the co-authorship network connecting the top 25 collaborators of Fabiola Quintero‐Rivera. A scholar is included among the top collaborators of Fabiola Quintero‐Rivera 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 Fabiola Quintero‐Rivera. Fabiola Quintero‐Rivera 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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Platt, Julia, et al.. (2024). Analysis of financial barriers experienced by prospective genetic counseling students. Genetics in Medicine. 26(11). 101175–101175. 1 indexed citations
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Wang, Jinglong, Oliver S. Eng, Sora Park Tanjasiri, et al.. (2024). Increased AID results in mutations at the CRLF2 locus implicated in Latin American ALL health disparities. Nature Communications. 15(1). 6331–6331. 1 indexed citations
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Quinn, Colin, et al.. (2023). Novel Variants in the VCP Gene Causing Multisystem Proteinopathy 1. Genes. 14(3). 676–676. 4 indexed citations
7.
Senaratne, T. Niroshini, et al.. (2023). Outcomes of two different unbalanced segregations from a maternal t(4;10)(q33;p15.1) translocation. BMC Medical Genomics. 16(1). 65–65. 1 indexed citations
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Massingham, Lauren, Jonathan A. Bernstein, David P. Gardner, et al.. (2022). 2022 Association of Professors of Human and Medical Genetics (APHMG) consensus–based update of the core competencies for undergraduate medical education in genetics and genomics. Genetics in Medicine. 24(10). 2167–2179. 7 indexed citations
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Quintero‐Rivera, Fabiola, et al.. (2014). Duodenal atresia in 17q12 microdeletion including HNF1B: A new associated malformation in this syndrome. American Journal of Medical Genetics Part A. 164(12). 3076–3082. 20 indexed citations
11.
Strom, Samuel P., Reymundo Lozano, Hane Lee, et al.. (2014). De Novo variants in the KMT2A (MLL) gene causing atypical Wiedemann-Steiner syndrome in two unrelated individuals identified by clinical exome sequencing. BMC Medical Genetics. 15(1). 49–49. 44 indexed citations
12.
Amarillo, Ina, Katrina M. Dipple, & Fabiola Quintero‐Rivera. (2013). Familial Microdeletion of 17q24.3 Upstream of SOX9 Is Associated With Isolated Pierre Robin Sequence Due to Position Effect. American Journal of Medical Genetics Part A. 161(5). 1167–1172. 29 indexed citations
13.
Quintero‐Rivera, Fabiola, et al.. (2013). Ring 2 chromosome associated with failure to thrive, microcephaly and dysmorphic facial features. Gene. 529(1). 65–68. 4 indexed citations
14.
Kearney, Hutton M., Erik C. Thorland, Kerry K. Brown, Fabiola Quintero‐Rivera, & Sarah T. South. (2011). American College of Medical Genetics standards and guidelines for interpretation and reporting of postnatal constitutional copy number variants. Genetics in Medicine. 13(7). 680–685. 643 indexed citations breakdown →
15.
Quintero‐Rivera, Fabiola, Joshua L. Deignan, Wayne W. Grody, et al.. (2010). An exon 1 deletion in OTC identified using chromosomal microarray analysis in a mother and her two affected deceased newborns: Implications for the prenatal diagnosis of ornithine transcarbamylase deficiency. Molecular Genetics and Metabolism. 101(4). 413–416. 7 indexed citations
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Quintero‐Rivera, Fabiola & Julián A. Martínez-Agosto. (2010). Bilateral exophthalmos: Report of a case and review of a fibroblast growth factor receptor 2 mutation associated with non‐penetrant Crouzon syndrome. Journal of Paediatrics and Child Health. 46(11). 693–695. 2 indexed citations
17.
Chang, Vivian Y., Fabiola Quintero‐Rivera, Erin E. Baldwin, et al.. (2010). B‐Acute lymphoblastic leukemia and cystinuria in a patient with duplication 22q11.21 detected by chromosomal microarray analysis. Pediatric Blood & Cancer. 56(3). 470–473. 7 indexed citations
18.
Llerena, Juan Clinton, et al.. (2008). Deletion (1)(p32.2–p32.3) detected by array‐CGH in a patient with developmental delay/mental retardation, dysmorphic features and low cholesterol: A new microdeletion syndrome?. American Journal of Medical Genetics Part A. 146A(17). 2284–2290. 10 indexed citations
19.
Quintero‐Rivera, Fabiola, Caroline D. Robson, Rosemary Reiss, et al.. (2006). Apert syndrome: what prenatal radiographic findings should prompt its consideration?. Prenatal Diagnosis. 26(10). 966–972. 14 indexed citations
20.
Maya, Walter D. Cardona, et al.. (2006). Inherited thrombophilia is associated with deep vein thrombosis in a Colombian population. American Journal of Hematology. 81(12). 933–937. 21 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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