Stephanie Gandomi

884 total citations
5 papers, 301 citations indexed

About

Stephanie Gandomi is a scholar working on Genetics, Molecular Biology and Pathology and Forensic Medicine. According to data from OpenAlex, Stephanie Gandomi has authored 5 papers receiving a total of 301 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 Pathology and Forensic Medicine. Recurrent topics in Stephanie Gandomi's work include BRCA gene mutations in cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Stephanie Gandomi is often cited by papers focused on BRCA gene mutations in cancer (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Genetics and Neurodevelopmental Disorders (2 papers). Stephanie Gandomi collaborates with scholars based in United States and Saudi Arabia. Stephanie Gandomi's co-authors include Chia‐Ling Gau, Aaron J. Stuenkel, Jill S. Dolinsky, Steven Keiles, Erika Palmaer, Tina Pesaran, Holly LaDuca, Virginia Speare, Elaine Chen and Divya Shah and has published in prestigious journals such as SHILAP Revista de lepidopterología, Genetics in Medicine and Molecular Genetics and Metabolism.

In The Last Decade

Stephanie Gandomi

4 papers receiving 293 citations

Peers

Stephanie Gandomi
Erika Palmaer United States
Bryce A. Seifert United States
Makia J. Marafie Kuwait
Helen Gregory United Kingdom
Alexandre Xavier Australia
A. Barroso Spain
Matthew Lubin United States
Jacopo Azzollini Italy
Simone McInerny Australia
Colyn B. Cargile United States
Erika Palmaer United States
Stephanie Gandomi
Citations per year, relative to Stephanie Gandomi Stephanie Gandomi (= 1×) peers Erika Palmaer

Countries citing papers authored by Stephanie Gandomi

Since Specialization
Citations

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

Fields of papers citing papers by Stephanie Gandomi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Stephanie Gandomi

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

All Works

5 of 5 papers shown
1.
Pilarski, Robert, Stephanie Noble, Lily Hoang, et al.. (2021). Divergent payor medical policy leads to gross disparities in access to hereditary breast and ovarian cancer genetic testing. Molecular Genetics and Metabolism. 132. S54–S54.
2.
LaDuca, Holly, Aaron J. Stuenkel, Jill S. Dolinsky, et al.. (2014). Utilization of multigene panels in hereditary cancer predisposition testing: analysis of more than 2,000 patients. Genetics in Medicine. 16(11). 830–837. 237 indexed citations
3.
Roberts, Jennifer, Stephanie Gandomi, Ira Lu, et al.. (2014). Clinical Report of a 17q12 Microdeletion with Additionally Unreported Clinical Features. SHILAP Revista de lepidopterología. 2014. 1–6. 13 indexed citations
4.
Gandomi, Stephanie, et al.. (2013). Array‐CGH is an effective first‐tier diagnostic test for EFTUD2‐associated congenital mandibulofacial dysostosis with microcephaly. Clinical Genetics. 87(1). 80–84. 16 indexed citations
5.
Gandomi, Stephanie, Kelly Gonzalez, Layla Shahmirzadi, et al.. (2013). Diagnostic Exome Sequencing Identifies Two Novel IQSEC2 Mutations Associated with X‐Linked Intellectual Disability with Seizures: Implications for Genetic Counseling and Clinical Diagnosis. Journal of Genetic Counseling. 23(3). 289–298. 35 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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2026