Haluk Topaloğlu

23.3k citations
326 papers · 18.1k · 7 hit papers · h-index 69

Impact in

  • Genetics top 0.1%
    • Neurogenetic and Muscular Disorders Research
    • Genomics and Rare Diseases
    • Metabolism and Genetic Disorders

Papers in

    • Neurogenetic and Muscular Disorders Research 69
    • Genomics and Rare Diseases 25
    • Muscle Physiology and Disorders 149
    • Mitochondrial Function and Pathology 10

Haluk Topaloğlu

314 papers receiving 17.3k citations

Haluk Topaloğlu's Hit Papers

European Academy of Neurology/Peripheral Nerve Society Guideline on diagnosis and treatment of Guillain–Barré syndrome 2023 · 103 citations
1030+3+7Years since publication5001k1.5k

Peers

Haluk Topaloğlu
Comparison fields: 5 of 141
  • Genetics 3.9k
  • Clinical Biochemistry 737
  • Molecular Biology 8.3k
  • Cellular and Molecular Neuroscience 1.8k
  • Neurology 1.5k
Replace Caroline A. Sewry with:
Caroline A. Sewry United Kingdom
Hans Scheffer Netherlands
Claudio Bruno Italy
Klaus Zerres Germany
Michel Fardeau France
Thomas O. Crawford United States
Brunhilde Wirth Germany
Janbernd Kirschner Germany
Monique M. Ryan Australia
Kathryn J. Swoboda United States
Haluk Topaloğlu relative to Caroline A. Sewry United Kingdom Caroline A. Sewry's profile →
Citations per field
00.5×2×2.8×
Caroline A. Sewry · 1×
Citations per year

Countries citing papers authored by Haluk Topaloğlu

Since Specialization
Citations

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

Fields of papers citing papers by Haluk Topaloğlu

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Haluk Topaloğlu, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Haluk Topaloğlu Line = papers co-authored together Haluk Topaloğlu links everyone, so they are left out of the graph.

All Works

20 of 20 papers shown

Showing the 20 most-cited of 326 papers — load more, or switch the sort, to bring in the rest.

#Work
1
Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy
Hit paper breakdown →
20171803
2
Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care
Hit paper breakdown →
2017766
3 2001609
4
The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations
Hit paper breakdown →
2015574
5 1995538
6
Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study
Hit paper breakdown →
2019498
7 2017370
8 2007359
9 2000351
10
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision
Hit paper breakdown →
2021339
11 2014316
12
European Academy of Neurology/Peripheral Nerve Society guideline on diagnosis and treatment of chronic inflammatory demyelinating polyradiculoneuropathy: Report of a joint Task Force—Second revision
Hit paper breakdown →
2021313
13 2001289
14 2007274
15 2014265
16 2013243
17 2000241
18 2004238
19 2011218
20 2009215

About Haluk Topaloğlu

Haluk Topaloğlu is a scholar working on Genetics, Molecular Biology, Cellular and Molecular Neuroscience, Clinical Biochemistry and Neurology, having authored 326 papers that have together received 18.1k indexed citations. Recurring topics across this work include Muscle Physiology and Disorders (149 papers), Neurogenetic and Muscular Disorders Research (69 papers), Hereditary Neurological Disorders (40 papers), Genomics and Rare Diseases (25 papers), Metabolism and Genetic Disorders (23 papers), Genetic Neurodegenerative Diseases (15 papers), Peripheral Neuropathies and Disorders (10 papers) and Mitochondrial Function and Pathology (10 papers). The work is most often cited by research in Genetics (3.9k citations), Clinical Biochemistry (737 citations), Molecular Biology (8.3k citations), Cellular and Molecular Neuroscience (1.8k citations) and Neurology (1.5k citations). Haluk Topaloğlu has collaborated with scholars based in Türkiye, Germany and France. Frequent co-authors include Beril Talim, Pascale Guicheney, Francesco Muntoni, Göknur Haliloğlu, Thomas Voit, Corinne Cruaud, Fernando M. S. Tomé, Luciano Merlini, Anne Helbling-Leclerc and Michel Fardeau. Their work appears in journals such as Neuromuscular Disorders, Neuropediatrics, Neurology, The American Journal of Human Genetics and European Journal of Paediatric Neurology.

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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