Feyza Yilmaz

3.0k total citations
9 papers, 418 citations indexed

About

Feyza Yilmaz is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Feyza Yilmaz has authored 9 papers receiving a total of 418 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Plant Science. Recurrent topics in Feyza Yilmaz's work include Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Feyza Yilmaz is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Chromosomal and Genetic Variations (4 papers) and Genomics and Rare Diseases (3 papers). Feyza Yilmaz collaborates with scholars based in United States, Canada and Austria. Feyza Yilmaz's co-authors include Jin Billy Li, Eric F. Joyce, Ruth B. McCole, Benjamin R. Williams, Jean-Marie Rouillard, Brian J. Beliveau, Yiming Chang, Chamith Y. Fonseka, T. Niroshini Senaratne and Nicholas Apostolopoulos and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and SHILAP Revista de lepidopterología.

In The Last Decade

Feyza Yilmaz

9 papers receiving 416 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Feyza Yilmaz United States	7	319	149	115	31	25	9	418
Yiming Chang United States	5	347 1.1×	132 0.9×	75 0.7×	31 1.0×	19 0.8×	7	433
Marlies E. Oomen United States	7	542 1.7×	170 1.1×	67 0.6×	28 0.9×	24 1.0×	12	590
Huy Q. Nguyen United States	7	448 1.4×	166 1.1×	54 0.5×	21 0.7×	18 0.7×	8	487
Françoise Jaunin Switzerland	8	405 1.3×	131 0.9×	62 0.5×	31 1.0×	17 0.7×	14	477
Sandra S. de Vries Netherlands	3	808 2.5×	134 0.9×	73 0.6×	19 0.6×	43 1.7×	4	839
Susan Gilchrist United Kingdom	6	536 1.7×	133 0.9×	94 0.8×	18 0.6×	13 0.5×	7	559
Angeline Rivkin United States	5	430 1.3×	115 0.8×	48 0.4×	36 1.2×	64 2.6×	7	473
Ting Gang Chew Singapore	12	386 1.2×	87 0.6×	37 0.3×	16 0.5×	10 0.4×	21	471
Mariya Kryzhanovska Switzerland	5	581 1.8×	123 0.8×	69 0.6×	19 0.6×	33 1.3×	5	623
Sedona E. Murphy United States	8	560 1.8×	157 1.1×	56 0.5×	40 1.3×	37 1.5×	9	590

Countries citing papers authored by Feyza Yilmaz

Since Specialization

Citations

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

Fields of papers citing papers by Feyza Yilmaz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Feyza Yilmaz

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

All Works

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9 of 9 papers shown

Jeong, Hyeonsoo, Philip C. Dishuck, DongAhn Yoo, et al.. (2025). Structural polymorphism and diversity of human segmental duplications. Nature Genetics. 57(2). 390–401. 8 indexed citations

Yilmaz, Feyza, Gurusamy Umamaheswaran, Pille Hallast, et al.. (2023). High level of complexity and global diversity of the 3q29 locus revealed by optical mapping and long-read sequencing. Genome Medicine. 15(1). 35–35. 4 indexed citations

Daniš, Daniel, Julius O.B. Jacobsen, Parithi Balachandran, et al.. (2022). SvAnna: efficient and accurate pathogenicity prediction of coding and regulatory structural variants in long-read genome sequencing. Genome Medicine. 14(1). 44–44. 16 indexed citations

Yilmaz, Feyza, David P. Astling, Hung‐Chun Yu, et al.. (2021). Genome-wide analysis of copy number variants and normal facial variation in a large cohort of Bantu Africans. SHILAP Revista de lepidopterología. 3(1). 100082–100082. 2 indexed citations

Yilmaz, Feyza, David P. Astling, Hung‐Chun Yu, et al.. (2021). Genome-wide copy number variations in a large cohort of bantu African children. BMC Medical Genomics. 14(1). 129–129. 7 indexed citations

Mostovoy, Yulia, Feyza Yilmaz, Catherine Chu, et al.. (2021). Genomic regions associated with microdeletion/microduplication syndromes exhibit extreme diversity of structural variation. Genetics. 217(2). 13 indexed citations

Mostovoy, Yulia, Feyza Yilmaz, Steven Pastor, et al.. (2019). The 22q11 low copy repeats are characterized by unprecedented size and structural variability. Genome Research. 29(9). 1389–1401. 28 indexed citations

Melia, Tisha, et al.. (2015). Hepatic Long Intergenic Noncoding RNAs: High Promoter Conservation and Dynamic, Sex-Dependent Transcriptional Regulation by Growth Hormone. Molecular and Cellular Biology. 36(1). 50–69. 26 indexed citations

Beliveau, Brian J., Eric F. Joyce, Nicholas Apostolopoulos, et al.. (2012). Versatile design and synthesis platform for visualizing genomes with Oligopaint FISH probes. Proceedings of the National Academy of Sciences. 109(52). 21301–21306. 314 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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