Didem Ardıçlı

410 total citations
25 papers, 146 citations indexed

About

Didem Ardıçlı is a scholar working on Molecular Biology, Genetics and Psychiatry and Mental health. According to data from OpenAlex, Didem Ardıçlı has authored 25 papers receiving a total of 146 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 6 papers in Psychiatry and Mental health. Recurrent topics in Didem Ardıçlı's work include Muscle Physiology and Disorders (5 papers), Cellular transport and secretion (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Didem Ardıçlı is often cited by papers focused on Muscle Physiology and Disorders (5 papers), Cellular transport and secretion (4 papers) and Genetic Neurodegenerative Diseases (4 papers). Didem Ardıçlı collaborates with scholars based in Türkiye, United Kingdom and Somalia. Didem Ardıçlı's co-authors include Göknur Haliloğlu, Kader Karlı Oğuz, Haluk Topaloğlu, Alev Özön, Nurgün Kandemir, Ayfer Alikaşifoğlu, Rahşan Göçmen, Nazlı Gönç, Meral Topçu and Dilek Yalnızoğlu and has published in prestigious journals such as Journal of Medical Genetics, Epilepsy & Behavior and Molecular Genetics and Metabolism.

In The Last Decade

Didem Ardıçlı

19 papers receiving 144 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Didem Ardıçlı Türkiye 8 50 35 29 24 17 25 146
Erik Lorentzen Sweden 8 52 1.0× 36 1.0× 55 1.9× 11 0.5× 8 0.5× 9 189
Kang-Hsien Fan United States 9 66 1.3× 72 2.1× 14 0.5× 30 1.3× 15 0.9× 23 188
Anna Marcé‐Grau Spain 10 139 2.8× 48 1.4× 25 0.9× 25 1.0× 19 1.1× 19 284
Maura Ruzhnikov United States 9 96 1.9× 73 2.1× 8 0.3× 48 2.0× 8 0.5× 21 213
Zeyu Zhu China 7 41 0.8× 19 0.5× 4 0.1× 12 0.5× 23 1.4× 25 113
Anne Roubergue France 9 125 2.5× 55 1.6× 18 0.6× 20 0.8× 22 1.3× 18 291
Veronica Codoni France 5 95 1.9× 48 1.4× 13 0.4× 10 0.4× 4 0.2× 5 161
Enrico Alfei Italy 11 140 2.8× 160 4.6× 12 0.4× 35 1.5× 7 0.4× 25 333
François Eyskens Belgium 8 72 1.4× 70 2.0× 37 1.3× 6 0.3× 15 0.9× 17 292
Shanice Beerepoot Netherlands 8 100 2.0× 19 0.5× 4 0.1× 20 0.8× 45 2.6× 17 221

Countries citing papers authored by Didem Ardıçlı

Since Specialization
Citations

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

Fields of papers citing papers by Didem Ardıçlı

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Didem Ardıçlı

This figure shows the co-authorship network connecting the top 25 collaborators of Didem Ardıçlı. A scholar is included among the top collaborators of Didem Ardıçlı 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 Didem Ardıçlı. Didem Ardıçlı 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.
Ardıçlı, Didem, et al.. (2025). Clinical features, quality of life, and fatigue in children with myotonic dystrophy type 1: A cross-sectional study. European Journal of Paediatric Neurology. 60. 24–31.
2.
Ardıçlı, Didem, et al.. (2024). Childhood vertigo: A retrospective series of 791 cases. Neurology Asia. 29(1). 229–236.
3.
Yıldız, Yılmaz, Didem Ardıçlı, Rahşan Göçmen, et al.. (2024). Electro-clinical features and long-term outcomes in guanidinoacetate methyltransferase (GAMT) deficiency. European Journal of Paediatric Neurology. 49. 66–72. 2 indexed citations
4.
Akman, Alkım Öden, et al.. (2024). Rare skin manifestation of juvenile dermatomyositis: peri-orbital oedema and facial swelling. Paediatrics and International Child Health. 44(3-4). 141–145.
5.
Kandemir, Nurgün, Doğuş Vurallı, Alev Özön, et al.. (2024). Epidemiology of type 1 diabetes mellitus in children and adolescents: A 50‐year, single‐center experience. Journal of Diabetes. 16(5). e13562–e13562. 12 indexed citations
6.
Ardıçlı, Didem, et al.. (2023). P293 Clinical and genetic spectrum of sarcoglycanopathies in a cohort of Turkish patients with a possible founder variation. Neuromuscular Disorders. 33. S116–S117. 1 indexed citations
7.
Mroczek, Magdalena, Cheryl Longman, Maria Elena Farrugia, et al.. (2022). FXR1-related congenital myopathy: expansion of the clinical and genetic spectrum. Journal of Medical Genetics. 59(11). 1069–1074. 3 indexed citations
8.
Ardıçlı, Didem, et al.. (2022). Evaluation and Management of the First Unprovoked Seizure in Children: Single-Center ExperienceFirst Unprovoked Seizure in Children. Annals of Medical Research. 29(11). 1–1. 1 indexed citations
9.
10.
Ardıçlı, Didem, et al.. (2021). Clinical and laboratory features of children with tremor: a single-center experience. Acta Neurologica Belgica. 122(2). 479–484. 1 indexed citations
11.
Ardıçlı, Didem, et al.. (2021). Unraveling neuronal ceroid lipofuscinosis type 2 (CLN2) disease: A tertiary center experience for determinants of diagnostic delay. European Journal of Paediatric Neurology. 33. 94–98. 5 indexed citations
12.
Yalnızoğlu, Dilek, Didem Ardıçlı, Burçak Bilginer, et al.. (2020). Long-term effects of vagus nerve stimulation in refractory pediatric epilepsy: A single-center experience. Epilepsy & Behavior. 110. 107147–107147. 14 indexed citations
13.
Sárközy, Anna, Mariacristina Scoto, Deborah Ridout, et al.. (2020). Selenoprotein N‐related myopathy: a retrospective natural history study to guide clinical trials. Annals of Clinical and Translational Neurology. 7(11). 2288–2296. 20 indexed citations
14.
Ardıçlı, Didem, et al.. (2019). Dirençli Epilepside Düşük Glisemik İndeksli Diyet Tedavisi: Olgu Sunumu. 47(2). 108–113. 1 indexed citations
15.
Sprute, Rosanne, Didem Ardıçlı, Kader Karlı Oğuz, et al.. (2019). Clinical outcomes of two patients with a novel pathogenic variant in ASNS: response to asparagine supplementation and review of the literature. Human Genome Variation. 6(1). 24–24. 19 indexed citations
16.
Ardıçlı, Didem, Anna Sárközy, Irina Zaharieva, et al.. (2019). A novel case of MSTO1 gene related congenital muscular dystrophy with progressive neurological involvement. Neuromuscular Disorders. 29(6). 448–455. 8 indexed citations
17.
Ardıçlı, Didem, Göknur Haliloğlu, Mehmet Alikaşifoğlu, & Haluk Topaloğlu. (2018). Diagnostic Pathway to Nonsense Mutation Dystrophinopathy: A Tertiary-Center, Retrospective Experience. Neuropediatrics. 50(1). 41–45. 4 indexed citations
18.
Ardıçlı, Didem, Ekim Z. Taşkıran, Can Koşukçu, et al.. (2017). Neonatal-Onset Recurrent Guillain–Barré Syndrome-Like Disease: Clues for Inherited CD59 Deficiency. Neuropediatrics. 48(6). 477–481. 16 indexed citations
19.
Ardıçlı, Didem, Rahşan Göçmen, Beril Talim, et al.. (2016). Congenital mirror movements in a patient with alpha-dystroglycanopathy due to a novel POMK mutation. Neuromuscular Disorders. 27(3). 239–242. 11 indexed citations
20.
Ardıçlı, Didem, et al.. (2016). Reversible Hypertensive Myelopathy—The Spinal Cord Variant of Posterior Reversible Encephalopathy Syndrome. Neuropediatrics. 48(2). 115–118. 3 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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