Fulya Taylan

1.8k total citations
43 papers, 618 citations indexed

About

Fulya Taylan is a scholar working on Molecular Biology, Genetics and Oncology. According to data from OpenAlex, Fulya Taylan has authored 43 papers receiving a total of 618 indexed citations (citations by other indexed papers that have themselves been cited), including 24 papers in Molecular Biology, 23 papers in Genetics and 8 papers in Oncology. Recurrent topics in Fulya Taylan's work include Connective tissue disorders research (10 papers), Genomics and Rare Diseases (6 papers) and Bone health and treatments (6 papers). Fulya Taylan is often cited by papers focused on Connective tissue disorders research (10 papers), Genomics and Rare Diseases (6 papers) and Bone health and treatments (6 papers). Fulya Taylan collaborates with scholars based in Sweden, Finland and United States. Fulya Taylan's co-authors include Outi Mäkitie, Ann Nordgren, Anders Kämpe, Magnus Nordenskjöld, Alice Costantini, Anna Lindstrand, Riikka E. Mäkitie, Giedré Grigelioniené, Minna Pekkinen and Maria Bradley and has published in prestigious journals such as Journal of Biological Chemistry, Nature Medicine and SHILAP Revista de lepidopterología.

In The Last Decade

Fulya Taylan

39 papers receiving 614 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Fulya Taylan Sweden 16 346 267 89 82 66 43 618
Jawahir Y. Mohamed Saudi Arabia 15 512 1.5× 239 0.9× 23 0.3× 62 0.8× 34 0.5× 20 849
Dana Fuchs‐Telem Israel 15 424 1.2× 153 0.6× 34 0.4× 49 0.6× 32 0.5× 20 728
Lydia Greenlees United States 10 268 0.8× 44 0.2× 44 0.5× 113 1.4× 69 1.0× 16 480
Tomoko Uehara Japan 14 358 1.0× 275 1.0× 29 0.3× 34 0.4× 52 0.8× 79 733
Lindsay B. Alcaraz France 12 204 0.6× 68 0.3× 42 0.5× 79 1.0× 89 1.3× 15 484
Terri L. Young United States 16 371 1.1× 171 0.6× 27 0.3× 36 0.4× 88 1.3× 20 870
Iris Augustin Germany 11 526 1.5× 62 0.2× 43 0.5× 82 1.0× 128 1.9× 16 756
Michiko Tojo Japan 14 236 0.7× 70 0.3× 50 0.6× 21 0.3× 48 0.7× 20 480
Zeynep Coban‐Akdemir United States 18 544 1.6× 396 1.5× 53 0.6× 86 1.0× 51 0.8× 50 965
Lucie Dupuis Canada 13 243 0.7× 335 1.3× 88 1.0× 51 0.6× 44 0.7× 28 554

Countries citing papers authored by Fulya Taylan

Since Specialization
Citations

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

Fields of papers citing papers by Fulya Taylan

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Fulya Taylan

This figure shows the co-authorship network connecting the top 25 collaborators of Fulya Taylan. A scholar is included among the top collaborators of Fulya Taylan 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 Fulya Taylan. Fulya Taylan 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
1.
Eisfeldt, Jesper, Kassahun Desalegn Bilcha, Carl‐Fredrik Wahlgren, et al.. (2024). Uncommon Variants in FLG2 and NOD2 Are Associated with Atopic Dermatitis in the Ethiopian Population. SHILAP Revista de lepidopterología. 4(4). 100284–100284. 2 indexed citations
2.
Delgado-Vega, A M, Fulya Taylan, Kristina Lagerstedt‐Robinson, et al.. (2024). Occurrence of cancer in Marfan syndrome: Report of two patients with neuroblastoma and review of the literature. American Journal of Medical Genetics Part A. 194(12). e63812–e63812.
3.
Palmer, Elizabeth E., A M Delgado-Vega, N Roberts, et al.. (2024). Equity in action: The Diagnostic Working Group of The Undiagnosed Diseases Network International. npj Genomic Medicine. 9(1). 1 indexed citations
4.
Tettamanti, Giorgio, et al.. (2024). Cancer Risk in Patients With Muscular Dystrophy and Myotonic Dystrophy. Neurology. 103(8). e209883–e209883. 1 indexed citations
5.
Ewans, Lisa, Fulya Taylan, Lorenzo D. Botto, et al.. (2023). International Undiagnosed Diseases Programs (UDPs): components and outcomes. Orphanet Journal of Rare Diseases. 18(1). 348–348. 3 indexed citations
6.
Lagerstedt‐Robinson, Kristina, Fulya Taylan, Bianca Tesi, et al.. (2023). Register-based and genetic studies of Prader-Willi syndrome show a high frequency of gonadal tumors and a possible mechanism for tumorigenesis through imprinting relaxation. Frontiers in Medicine. 10. 1172565–1172565.
7.
Laurell, Tobias, Anna Lindstrand, Helena Malmgren, et al.. (2022). Detection of germline mosaicism in fathers of children with intellectual disability syndromes caused by de novo variants. Molecular Genetics & Genomic Medicine. 10(4). e1880–e1880. 10 indexed citations
8.
Taylan, Fulya, Symeon Tournis, Jesper Eisfeldt, et al.. (2022). Mosaic Deletions of Known Genes Explain Skeletal Dysplasias With High and Low Bone Mass. JBMR Plus. 6(8). e10660–e10660.
9.
Costantini, Alice, Helena Valta, Anne‐Maarit Suomi, Outi Mäkitie, & Fulya Taylan. (2021). Oligogenic Inheritance of Monoallelic TRIP11, FKBP10, NEK1, TBX5, and NBAS Variants Leading to a Phenotype Similar to Odontochondrodysplasia. Frontiers in Genetics. 12. 680838–680838. 7 indexed citations
10.
Sahlén, Pelin, Jesper Eisfeldt, Ankit Srivastava, et al.. (2020). Chromatin interactions in differentiating keratinocytes reveal novel atopic dermatitis– and psoriasis-associated genes. Journal of Allergy and Clinical Immunology. 147(5). 1742–1752. 21 indexed citations
11.
Malmgren, B., et al.. (2020). Mutations in COL1A1/A2 and CREB3L1 are associated with oligodontia in osteogenesis imperfecta. Orphanet Journal of Rare Diseases. 15(1). 80–80. 19 indexed citations
12.
Taylan, Fulya, Inger Nennesmo, Göran Annerén, et al.. (2019). Early activating somatic PIK3CA mutations promote ectopic muscle development and upper limb overgrowth. Clinical Genetics. 96(2). 118–125. 9 indexed citations
13.
Öfverholm, Ingegerd, Vasilios Zachariadis, Fulya Taylan, et al.. (2019). Overexpression of chromatin remodeling and tyrosine kinase genes in iAMP21-positive acute lymphoblastic leukemia. Leukemia & lymphoma. 61(3). 604–613. 5 indexed citations
14.
Grigelioniené, Giedré, Hiroshi Suzuki, Fulya Taylan, et al.. (2019). Gain-of-function mutation of microRNA-140 in human skeletal dysplasia. Nature Medicine. 25(4). 583–590. 70 indexed citations
15.
Kvarnung, Malin, Mansoureh Shahsavani, Fulya Taylan, et al.. (2019). Ataxia in Patients With Bi-Allelic NFASC Mutations and Absence of Full-Length NF186. Frontiers in Genetics. 10. 896–896. 5 indexed citations
16.
Costantini, Alice, Sini Skarp, Anders Kämpe, et al.. (2018). Rare Copy Number Variants in Array-Based Comparative Genomic Hybridization in Early-Onset Skeletal Fragility. Frontiers in Endocrinology. 9. 380–380. 24 indexed citations
17.
Costantini, Alice, et al.. (2018). A novel frameshift deletion in PLS3 causing severe primary osteoporosis. Journal of Human Genetics. 63(8). 923–926. 17 indexed citations
18.
Kämpe, Anders, Alice Costantini, Riikka E. Mäkitie, et al.. (2017). PLS3 sequencing in childhood-onset primary osteoporosis identifies two novel disease-causing variants. Osteoporosis International. 28(10). 3023–3032. 34 indexed citations
19.
Mäkitie, Riikka E., Anders Kämpe, Fulya Taylan, & Outi Mäkitie. (2017). Recent Discoveries in Monogenic Disorders of Childhood Bone Fragility. Current Osteoporosis Reports. 15(4). 303–310. 17 indexed citations
20.
Perk, Yıldız, et al.. (2012). A novel mutation in the interleukin-1 receptor antagonist associated with intrauterine disease onset. Clinical Immunology. 145(1). 77–81. 40 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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