Tülay Tos

1.2k total citations
16 papers, 112 citations indexed

About

Tülay Tos is a scholar working on Pediatrics, Perinatology and Child Health, Genetics and Molecular Biology. According to data from OpenAlex, Tülay Tos has authored 16 papers receiving a total of 112 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Pediatrics, Perinatology and Child Health, 6 papers in Genetics and 4 papers in Molecular Biology. Recurrent topics in Tülay Tos's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Down syndrome and intellectual disability research (2 papers). Tülay Tos is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (4 papers) and Down syndrome and intellectual disability research (2 papers). Tülay Tos collaborates with scholars based in Türkiye, United States and France. Tülay Tos's co-authors include Beyhan Tüysüz, Hugo J. Bellen, Marjorie Withers, Ghayda Mirzaa, Priya S. Shah, Sedat Işıkay, James R. Lupski, Hyung-Lok Chung, Robin D. Clark and Ganeshwaran H. Mochida and has published in prestigious journals such as Developmental Cell, Current Opinion in Biotechnology and European Journal of Ophthalmology.

In The Last Decade

Tülay Tos

15 papers receiving 109 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Tülay Tos Türkiye	5	45	28	27	15	14	16	112
Elena Velasco Spain	5	44 1.0×	14 0.5×	26 1.0×	25 1.7×	9 0.6×	20	146
Rossana Sanchez Russo United States	8	52 1.2×	10 0.4×	44 1.6×	13 0.9×	7 0.5×	23	150
Bilgen Bilge Geçkinli Türkiye	7	74 1.6×	42 1.5×	54 2.0×	18 1.2×		18	151
Kelly M. Schiabor Barrett United States	7	46 1.0×	6 0.2×	27 1.0×	6 0.4×	2 0.1×	14	126
Sina Zoghi Iran	7	65 1.4×	9 0.3×	37 1.4×	14 0.9×	4 0.3×	48	152
Angad Jolly United States	3	41 0.9×	22 0.8×	17 0.6×	15 1.0×		6	80
Domena Tu Canada	8	93 2.1×	15 0.5×	25 0.9×	20 1.3×	3 0.2×	13	184
Dana Knutzen United States	7	48 1.1×	15 0.5×	39 1.4×	18 1.2×	2 0.1×	9	174
Justin W. Myrick United States	6	72 1.6×	11 0.4×	70 2.6×	47 3.1×	4 0.3×	8	215
Elena S. Gusareva Belgium	10	110 2.4×	7 0.3×	130 4.8×	5 0.3×	8 0.6×	23	255

Countries citing papers authored by Tülay Tos

Since Specialization

Citations

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

Fields of papers citing papers by Tülay Tos

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Tülay Tos

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

All Works

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16 of 16 papers shown

Çelik, Özge, et al.. (2021). Prenatal differential diagnosis of fibular agenesis, tibial campomelia and oligosyndactyly. Clinical Dysmorphology. 30(3). 147–149. 2 indexed citations

Link, Nichole, Hyung-Lok Chung, Angad Jolly, et al.. (2019). Mutations in ANKLE2, a ZIKA Virus Target, Disrupt an Asymmetric Cell Division Pathway in Drosophila Neuroblasts to Cause Microcephaly. Developmental Cell. 51(6). 713–729.e6. 66 indexed citations

Link, Nichole, Hyung-Lok Chung, Angad Jolly, et al.. (2019). Ankle2, a Target of Zika Virus, Controls Asymmetric Cell Division of Neuroblasts and Uncovers a Novel Microcephaly Pathway. SSRN Electronic Journal. 1 indexed citations

Dinç, Gülser Şenses, et al.. (2019). Mothers of 0–3‐year‐old children with Down syndrome: Effects on quality of life. Pediatrics International. 61(9). 865–871. 14 indexed citations

Tos, Tülay, et al.. (2015). A familial case of Coffin-Lowry syndrome caused by RPS6KA3 C.898C>T mutation associated with multiple abnormal brain imaging findings.. PubMed. 26(1). 47–52. 6 indexed citations

Tos, Tülay, et al.. (2014). Down Sendromlu Hastaların Demografik ve Klinik Özelliklerinin Değerlendirilmesi: Tek Merkez Deneyimi. Turkish Journal of Pediatric Disease. 8(2). 71–74.

Tos, Tülay, et al.. (2014). Partial monosomy 8q and partial trisomy 9q due to the maternal translocation t(8;9(q24.3;q34.1): a case report.. PubMed. 25(1). 35–9. 1 indexed citations

Tos, Tülay, et al.. (2014). Evaluation of Demographic and Clinical Features of Patients with Down Syndrome: Single Center Experience. Turkish Journal of Pediatric Disease. 1 indexed citations

Tos, Tülay, et al.. (2014). De novo interstitial deletion of 9q32-34.1 with mental retardation, developmental delay, epilepsy, and cortical dysplasia: a case report.. PubMed. 25(2). 197–201. 1 indexed citations

10.

Karaman, Ali̇ & Tülay Tos. (2013). De Novo Three-Way Chromosome Translocation [46,XX,t(1;20;4) (p32;q12;q32)] in a Patient with Developmental Delay: A Case Report. Turkish Journal of Pediatric Disease. 7. 7–10. 2 indexed citations

11.

Çekmez, Yasemin, et al.. (2013). Pentalogy of Cantrell diagnosed in the first trimester of pregnancy. International Journal of Case Reports and Images. 5(3). 215–215. 2 indexed citations

12.

Şen, Emine, et al.. (2013). Increased Central Corneal Thickness in Patients with Turner Syndrome. European Journal of Ophthalmology. 24(3). 309–313. 6 indexed citations

13.

Karaman, Ali̇, et al.. (2011). Genetic alterations in benign, preneoplastic and malignant breast lesions. Current Opinion in Biotechnology. 22. S102–S103. 1 indexed citations

14.

Zorlu, Pelin, et al.. (2009). A rare subtelomeric deletion syndrome: Wolf Hirschhorn syndrome.. PubMed. 25(3). 299–303. 2 indexed citations

15.

Tos, Tülay, et al.. (2006). Neu-Laxova syndrome: A terrible phenotypic appearance caused by an undefined genetic alteration. 3 indexed citations

16.

Yı́ldı́rı́m, Mustafa, Mevlit Íkbal, Tülay Tos, et al.. (2005). Genotoxicity of Thallium-201 in Patients with Angina Pectoris Undergoing Myocardial Perfusion Study. The Tohoku Journal of Experimental Medicine. 206(4). 299–304. 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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