# Haluk Topaloğlu

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/haluk-topaloglu/

## Facts

| Field | Value |
| --- | --- |
| Citations | 23,171 |
| Field | Muscle Physiology and Disorders |
| h-index | 78 |
| i10-index | 215 |
| Last Known Institution | Yeditepe University |
| OpenAlex ID | https://openalex.org/A5086201681 |
| ORCID iD | https://orcid.org/0000-0002-3545-3830 |
| Works | 510 |

## Researcher papers

- [Nusinersen versus Sham Control in Infantile-Onset Spinal Muscular Atrophy](https://scholariq.org/papers/nusinersen-versus-sham-control-in-infantile-onset-spinal-muscular-atrophy/)
- [Diagnosis and management of spinal muscular atrophy: Part 1: Recommendations for diagnosis, rehabilitation, orthopedic and nutritional care](https://scholariq.org/papers/diagnosis-and-management-of-spinal-muscular-atrophy-part-1-recommendations-for/)
- [The TREAT-NMD DMD Global Database: Analysis of More than 7,000 Duchenne Muscular Dystrophy Mutations](https://scholariq.org/papers/the-treat-nmd-dmd-global-database-analysis-of-more-than-7-000-duchenne-muscular/)
- [Nusinersen initiated in infants during the presymptomatic stage of spinal muscular atrophy: Interim efficacy and safety results from the Phase 2 NURTURE study](https://scholariq.org/papers/nusinersen-initiated-in-infants-during-the-presymptomatic-stage-of-spinal/)
- [Ataluren in patients with nonsense mutation Duchenne muscular dystrophy (ACT DMD): a multicentre, randomised, double-blind, placebo-controlled, phase 3 trial](https://scholariq.org/papers/ataluren-in-patients-with-nonsense-mutation-duchenne-muscular-dystrophy-act-dmd/)
- [The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy](https://scholariq.org/papers/the-gene-encoding-gigaxonin-a-new-member-of-the-cytoskeletal-btb-kelch-repeat/)
- [Use of Whole-Exome Sequencing to Determine the Genetic Basis of Multiple Mitochondrial Respiratory Chain Complex Deficiencies](https://scholariq.org/papers/use-of-whole-exome-sequencing-to-determine-the-genetic-basis-of-multiple/)
- [The myopathic form of coenzyme Q10 deficiency is caused by mutations in the electron-transferring-flavoprotein dehydrogenase (ETFDH) gene](https://scholariq.org/papers/the-myopathic-form-of-coenzyme-q10-deficiency-is-caused-by-mutations-in-the/)
- [Localization of merosin-negative congenital muscular dystrophy to chromosome 6q2 by homozygosity mapping](https://scholariq.org/papers/localization-of-merosin-negative-congenital-muscular-dystrophy-to-chromosome-6q2/)
- [Clinical Outcomes in Duchenne Muscular Dystrophy: A Study of 5345 Patients from the TREAT-NMD DMD Global Database](https://scholariq.org/papers/clinical-outcomes-in-duchenne-muscular-dystrophy-a-study-of-5345-patients-from/)
- [Newborn screening programs for spinal muscular atrophy worldwide: Where we stand and where to go](https://scholariq.org/papers/newborn-screening-programs-for-spinal-muscular-atrophy-worldwide-where-we-stand/)

## Researcher topics

- [Muscle Physiology and Disorders](https://scholariq.org/topics/muscle-physiology-and-disorders/)
- [Neurogenetic and Muscular Disorders Research](https://scholariq.org/topics/neurogenetic-and-muscular-disorders-research/)
- [Mitochondrial Function and Pathology](https://scholariq.org/topics/mitochondrial-function-and-pathology/)
- [Hereditary Neurological Disorders](https://scholariq.org/topics/hereditary-neurological-disorders/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)

## Researcher university

- [Yeditepe University](https://scholariq.org/institutions/yeditepe-university/)

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Source: ScholarIQ — public research metadata, principally OpenAlex. See https://scholariq.org/sources/ for provenance and https://scholariq.org/methodology/ for what these figures mean.