Nilay Güneş

458 total citations
25 papers, 126 citations indexed

About

Nilay Güneş is a scholar working on Genetics, Molecular Biology and Rheumatology. According to data from OpenAlex, Nilay Güneş has authored 25 papers receiving a total of 126 indexed citations (citations by other indexed papers that have themselves been cited), including 14 papers in Genetics, 12 papers in Molecular Biology and 7 papers in Rheumatology. Recurrent topics in Nilay Güneş's work include Connective tissue disorders research (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Bone and Dental Protein Studies (3 papers). Nilay Güneş is often cited by papers focused on Connective tissue disorders research (7 papers), Genomic variations and chromosomal abnormalities (4 papers) and Bone and Dental Protein Studies (3 papers). Nilay Güneş collaborates with scholars based in Türkiye, United States and Germany. Nilay Güneş's co-authors include Beyhan Tüysüz, Gözde Yeşil, Zehra Oya Uyguner, Güven Toksoy, Firdevs Baş, Fulya Taylan, Zehra Yavaş Abalı, Outi Mäkitie, Timur Yıldırım and Şükran Poyrazoğlu and has published in prestigious journals such as The Journal of Pediatrics, Gene and Bone.

In The Last Decade

Nilay Güneş

21 papers receiving 125 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nilay Güneş Türkiye 7 79 68 23 22 16 25 126
Maha Faden Saudi Arabia 6 93 1.2× 100 1.5× 20 0.9× 22 1.0× 12 0.8× 9 178
Arnaud Chignon Canada 7 76 1.0× 44 0.6× 11 0.5× 15 0.7× 26 1.6× 9 172
Celeste Owen Canada 7 118 1.5× 28 0.4× 23 1.0× 18 0.8× 14 0.9× 8 180
Alison Colley Australia 3 115 1.5× 91 1.3× 68 3.0× 13 0.6× 6 0.4× 4 178
Shefali Rajpopat United Kingdom 5 53 0.7× 34 0.5× 74 3.2× 8 0.4× 15 0.9× 7 175
Aleksandra Ivovic United States 6 43 0.5× 90 1.3× 30 1.3× 87 4.0× 11 0.7× 8 150
Ana Krolo Austria 7 62 0.8× 32 0.5× 9 0.4× 13 0.6× 14 0.9× 11 143
Edyta Rohmann Germany 5 128 1.6× 49 0.7× 16 0.7× 6 0.3× 13 0.8× 5 149
Kim Jenny United States 4 188 2.4× 160 2.4× 10 0.4× 13 0.6× 10 0.6× 6 265
Maja Sukalo Germany 6 146 1.8× 44 0.6× 44 1.9× 8 0.4× 7 0.4× 12 191

Countries citing papers authored by Nilay Güneş

Since Specialization
Citations

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

Fields of papers citing papers by Nilay Güneş

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nilay Güneş

This figure shows the co-authorship network connecting the top 25 collaborators of Nilay Güneş. A scholar is included among the top collaborators of Nilay Güneş 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 Nilay Güneş. Nilay Güneş 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.
2.
Güneş, Nilay, et al.. (2023). Phenotypic and Molecular Spectrum of a Turkish Cohort with Hereditary Multiple Osteochondromas. Turkish Archives of Pediatrics. 58(4). 376–381. 1 indexed citations
3.
Güneş, Nilay, et al.. (2023). Effects of Long-Term Pamidronate Treatment on Bone Density and Fracture Rate in 65 Osteogenesis Imperfecta Patients. Turkish Archives of Pediatrics. 56(5). 474–478. 1 indexed citations
4.
Güneş, Nilay, et al.. (2023). The Clinical and Molecular Spectrum of Trichorhinophalangeal Syndrome Types I and II in a Turkish Cohort Involving 22 Patients. Turkish Archives of Pediatrics. 58(1). 98–104. 2 indexed citations
5.
Güneş, Nilay, et al.. (2022). Early Diagnostic Signs and the Natural History of Typical Findings in Cohen Syndrome. The Journal of Pediatrics. 252. 93–100. 5 indexed citations
6.
Uyguner, Zehra Oya, et al.. (2022). Long‐term follow‐up findings in a Turkish girl with osteogenesis imperfecta type XX caused by a homozygous MESD variant. American Journal of Medical Genetics Part A. 188(5). 1639–1646. 4 indexed citations
7.
Tüysüz, Beyhan, Güven Toksoy, Nilay Güneş, et al.. (2021). Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants. Bone. 155. 116293–116293. 14 indexed citations
8.
9.
Ocak, Süheyla, et al.. (2021). Neurofibromatosis Type 1 in Children: A Single-Center Experience. Turkish Archives of Pediatrics. 56(4). 339–343.
10.
Altunoğlu, Umut, Kıvanç Çefle, Ercan Mıhçı, et al.. (2021). Skeletal and molecular findings in 51 Cleidocranial dysplasia patients from Turkey. American Journal of Medical Genetics Part A. 185(8). 2488–2495. 9 indexed citations
11.
12.
Toksoy, Güven, Şahin Avcı, Nilay Güneş, et al.. (2020). Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey. Molecular Syndromology. 11(4). 183–196. 6 indexed citations
13.
Fischer‐Zirnsak, Björn, Rainer Koenig, Nilay Güneş, et al.. (2019). SOPH syndrome in three affected individuals showing similarities with progeroid cutis laxa conditions in early infancy. Journal of Human Genetics. 64(7). 609–616. 9 indexed citations
14.
Tüysüz, Beyhan, Güven Toksoy, Nilay Güneş, et al.. (2019). Mutation spectrum and pivotal features for differential diagnosis of Mucopolysaccharidosis IVA patients with severe and attenuated phenotype. Gene. 704. 59–67. 6 indexed citations
15.
Güneş, Nilay, Tufan Kutlu, Gonca Topuzlu Tekant, et al.. (2019). Congenital generalized lipodystrophy: The evaluation of clinical follow-up findings in a series of five patients with type 1 and two patients with type 4. European Journal of Medical Genetics. 63(4). 103819–103819. 9 indexed citations
16.
Güneş, Nilay, et al.. (2018). Longitudinal Follow-Up of Two Patients with Dysspondyloenchondromatosis due to Novel Heterozygous Mutations in <b><i>COL2A1</i></b>. Molecular Syndromology. 9(3). 134–140. 2 indexed citations
17.
Güneş, Nilay, et al.. (2018). A Novel Mutation of KIF11 in a Child with 22q11.2 Deletion Syndrome Associated with MCLMR. Molecular Syndromology. 9(5). 266–270. 4 indexed citations
18.
Türkmen, Seval, Malte Spielmann, Nilay Güneş, et al.. (2017). A Novel de novo FZD2 Mutation in a Patient with Autosomal Dominant Omodysplasia. Molecular Syndromology. 8(6). 318–324. 10 indexed citations
19.
Taylan, Fulya, Zehra Yavaş Abalı, Nilay Güneş, et al.. (2017). Two novel mutations in XYLT2 cause spondyloocular syndrome. American Journal of Medical Genetics Part A. 173(12). 3195–3200. 20 indexed citations
20.
Güneş, Nilay, Filiz Başak Cengiz, Duygu Duman, et al.. (2014). Branchio-oculo-facial syndrome in a newborn caused by a novel TFAP2A mutation.. PubMed. 25(1). 41–7. 4 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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