Gayle Patel

1.2k total citations
9 papers, 569 citations indexed

About

Gayle Patel is a scholar working on Genetics, Molecular Biology and Surgery. According to data from OpenAlex, Gayle Patel has authored 9 papers receiving a total of 569 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 7 papers in Molecular Biology and 1 paper in Surgery. Recurrent topics in Gayle Patel's work include Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Gayle Patel is often cited by papers focused on Genomic variations and chromosomal abnormalities (6 papers), Congenital heart defects research (5 papers) and Genetics and Neurodevelopmental Disorders (4 papers). Gayle Patel collaborates with scholars based in United States, Germany and Canada. Gayle Patel's co-authors include Amanda Gammon, Jennifer Saam, John F. Sandbach, John Kidd, Johnathan M. Lancaster, Krystal Brown, Mary B. Daly, Saundra S. Buys, LaDonna Immken and Sau Wai Cheung and has published in prestigious journals such as Nature Genetics, Journal of Clinical Oncology and Cancer.

In The Last Decade

Gayle Patel

8 papers receiving 548 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Gayle Patel United States 7 420 285 104 92 70 9 569
Qixi Wu China 14 328 0.8× 290 1.0× 92 0.9× 38 0.4× 39 0.6× 28 568
Moran Gal Israel 7 251 0.6× 188 0.7× 73 0.7× 61 0.7× 42 0.6× 9 439
Yael Laitman Israel 12 241 0.6× 181 0.6× 69 0.7× 75 0.8× 58 0.8× 39 489
Shehla Mohammed United Kingdom 12 248 0.6× 497 1.7× 92 0.9× 76 0.8× 26 0.4× 25 680
Diane Allingham‐Hawkins Canada 10 371 0.9× 283 1.0× 122 1.2× 64 0.7× 92 1.3× 21 607
Renske Olmer Netherlands 7 530 1.3× 396 1.4× 138 1.3× 44 0.5× 140 2.0× 8 855
Michèle Mathieu France 9 310 0.7× 341 1.2× 37 0.4× 36 0.4× 37 0.5× 18 622
María‐Isabel Tejada Spain 16 581 1.4× 389 1.4× 69 0.7× 49 0.5× 74 1.1× 46 758
Sung-Hae L. Kang United States 8 312 0.7× 474 1.7× 41 0.4× 52 0.6× 28 0.4× 8 756
R. Catrinel Marinescu United States 9 167 0.4× 251 0.9× 43 0.4× 29 0.3× 100 1.4× 11 389

Countries citing papers authored by Gayle Patel

Since Specialization
Citations

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

Fields of papers citing papers by Gayle Patel

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Gayle Patel

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

All Works

9 of 9 papers shown
1.
Patel, Gayle, et al.. (2021). Germline testing in community oncology patients with somatic BRCA1/2 mutations.. Journal of Clinical Oncology. 39(15_suppl). 1523–1523.
2.
Patel, Gayle, et al.. (2019). Expanding access to genetic evaluations in a large community oncology practice through a collaborative service delivery model.. Journal of Clinical Oncology. 37(27_suppl). 123–123. 1 indexed citations
3.
Buys, Saundra S., John F. Sandbach, Amanda Gammon, et al.. (2017). A study of over 35,000 women with breast cancer tested with a 25‐gene panel of hereditary cancer genes. Cancer. 123(10). 1721–1730. 267 indexed citations
4.
Carvalho, Claudia M.B., Shivakumar Vasanth, Marwan Shinawi, et al.. (2014). Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes. The American Journal of Human Genetics. 95(5). 565–578. 39 indexed citations
5.
Witsch, Jens, Przemysław Szafrański, Chun‐An Chen, et al.. (2013). Intragenic deletions of the IGF1 receptor gene in five individuals with psychiatric phenotypes and developmental delay. European Journal of Human Genetics. 21(11). 1304–1307. 10 indexed citations
6.
Celestino-Soper, Patrícia B. S., Cindy Skinner, Richard J. Schroer, et al.. (2012). Deletions in chromosome 6p22.3-p24.3, including ATXN1, are associated with developmental delay and autism spectrum disorders. Molecular Cytogenetics. 5(1). 17–17. 41 indexed citations
7.
Pearson, David, Gayle Patel, Barbara R. Pober, et al.. (2010). Deletions of Xp provide evidence for the role of holocytochrome C‐type synthase (HCCS) in congenital diaphragmatic hernia. American Journal of Medical Genetics Part A. 152A(6). 1588–1590. 14 indexed citations
8.
Shinawi, Marwan, Christian P. Schaaf, Samarth Bhatt, et al.. (2009). A small recurrent deletion within 15q13.3 is associated with a range of neurodevelopmental phenotypes. Nature Genetics. 41(12). 1269–1271. 141 indexed citations
9.
El‐Hattab, Ayman W., Teresa A. Smolarek, Elizabeth K. Schorry, et al.. (2009). Redefined genomic architecture in 15q24 directed by patient deletion/duplication breakpoint mapping. Human Genetics. 126(4). 589–602. 56 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