F.M. Sonmez

431 total citations
13 papers, 86 citations indexed

About

F.M. Sonmez is a scholar working on Pathology and Forensic Medicine, Pediatrics, Perinatology and Child Health and Psychiatry and Mental health. According to data from OpenAlex, F.M. Sonmez has authored 13 papers receiving a total of 86 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Pathology and Forensic Medicine, 3 papers in Pediatrics, Perinatology and Child Health and 3 papers in Psychiatry and Mental health. Recurrent topics in F.M. Sonmez's work include Vitamin D Research Studies (3 papers), Migraine and Headache Studies (2 papers) and Pharmacological Effects and Toxicity Studies (2 papers). F.M. Sonmez is often cited by papers focused on Vitamin D Research Studies (3 papers), Migraine and Headache Studies (2 papers) and Pharmacological Effects and Toxicity Studies (2 papers). F.M. Sonmez collaborates with scholars based in Türkiye, United States and Iran. F.M. Sonmez's co-authors include Orhan Değer, Ayşe Aksoy, Gülay Karagüzel, İncilay Lay, Meral Topçu, Murat Topbaş, Gamze Çan, Halil İbrahim Aydın, Mehmet Namuslu and Haluk Topaloğlu and has published in prestigious journals such as European Journal of Human Genetics, Neurological Research and European Journal of Paediatric Neurology.

In The Last Decade

F.M. Sonmez

11 papers receiving 82 citations

Peers

F.M. Sonmez

PMH

PPCH

PFM

PHYSI

Maja Kopczynska United Kingdom

Janice Brunstrom-Hernandez United States

Zubeda Sheikh United States

Madeline Chadehumbe United States

Payam Tabaee Damavandi Italy

Anna E. Fürtjes United Kingdom

Jean‐Baptiste Le Pichon United States

Nathan Li United States

L. Pierce Clark United States

Swapnil Awasthi Germany

Maja Kopczynska United Kingdom

F.M. Sonmez

24 ×0.6

PMH

11 ×0.4

PPCH

10 ×0.4

PFM

38 ×2.5

PHYSI

21 ×1.8

Citations per year, relative to F.M. Sonmez F.M. Sonmez (= 1×) peers Maja Kopczynska

Countries citing papers authored by F.M. Sonmez

Since Specialization

Citations

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

Fields of papers citing papers by F.M. Sonmez

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by F.M. Sonmez. 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 F.M. Sonmez. The network helps show where F.M. Sonmez may publish in the future.

Co-authorship network of co-authors of F.M. Sonmez

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

All Works

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13 of 13 papers shown

Vona, Barbara, F.M. Sonmez, Thomas Smol, et al.. (2023). Bi-allelic truncating variants in CASP2 underlie a neurodevelopmental disorder with lissencephaly. European Journal of Human Genetics. 32(1). 52–60. 4 indexed citations

Breuss, Martin W., Guoliang Chai, Valentina Stanley, et al.. (2021). Biallelic hypomorphic mutations in HEATR5B, encoding HEAT repeat-containing protein 5B, in a neurological syndrome with pontocerebellar hypoplasia. European Journal of Human Genetics. 29(6). 957–964. 3 indexed citations

Sonmez, F.M., et al.. (2017). Vitamin D status in children with headache: A case-control study. Clinical Nutrition ESPEN. 23. 222–227. 22 indexed citations

Aydın, Halil İbrahim & F.M. Sonmez. (2017). A novel mutation in guanidinoacetate methyltransferase (GAMT) deficiency in two patients associated with epilepsy, developmental delay, hyperactivity, autistic behavior. European Journal of Paediatric Neurology. 21. e125–e125. 1 indexed citations

Sonmez, F.M.. (2016). The Role of the Vitamin D in Neurology: Interrelationships Between Headache, Epilepsy and Vitamin D Deficiency. Journal of Pediatrics & Neonatal Care. 4(2).

Sonmez, F.M., et al.. (2016). Insomnia, parasomnia, and predisposing factors in Turkish school children. Pediatrics International. 58(10). 1014–1022. 10 indexed citations

Sonmez, F.M., et al.. (2015). OP30 – 2317: Vitamin D status in children with headache: A case-control study. European Journal of Paediatric Neurology. 19. S10–S10. 3 indexed citations

Sonmez, F.M., et al.. (2014). Hemihyperplasia-multiple lipomatosis syndrome associated with hydrocephalus.. PubMed. 25(3). 251–5. 1 indexed citations

Sonmez, F.M., et al.. (2013). Phacomatosis pigmentovascularis type IIB associated with Sturge-Weber syndrome: a case report and review of the literature.. PubMed. 24(2). 247–50. 2 indexed citations

10.

Aksoy, Ayşe, et al.. (2011). The effects of antiepileptic drugs on the relationships between leptin levels and bone turnover in prepubertal children with epilepsy. Journal of Pediatric Endocrinology and Metabolism. 24(9-10). 703–8. 28 indexed citations

11.

Serin, Meltem, et al.. (2011). P21.11 A case presented with the clinical features of pseudotumor cerebri and diagnosed as Lyme disease. European Journal of Paediatric Neurology. 15. S119–S119. 2 indexed citations

12.

Lay, İncilay, et al.. (2008). Identification of two novel arylsulfatase A mutations with a polymorphism as a cause of metachromatic leukodystrophy. Neurological Research. 31(1). 60–66. 10 indexed citations

13.

Sonmez, F.M., Esra Baltacıoğlu, Ufuk Çobanoğlu, & Mukaddes Kalyoncu. (2008). A case of plasminogen deficiency associated with hydrocephalus, epilepsy and multiorgan involvement. European Journal of Paediatric Neurology. 12. S35–S35.

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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