# Hanns Lochmüller

**Type:** Researchers  
**Canonical URL:** https://scholariq.org/researchers/hanns-lochmuller/

## Facts

| Field | Value |
| --- | --- |
| Citations | 39,384 |
| Field | Muscle Physiology and Disorders |
| h-index | 101 |
| i10-index | 549 |
| Last Known Institution | University of Ottawa |
| OpenAlex ID | https://openalex.org/A5062908694 |
| ORCID iD | 0000-0003-2324-8001 |
| Works | 1,557 |

## Researcher papers

Showing 12 of 14.

- [The Human Phenotype Ontology in 2017](https://scholariq.org/papers/the-human-phenotype-ontology-in-2017/)
- [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/)
- [Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources](https://scholariq.org/papers/expansion-of-the-human-phenotype-ontology-hpo-knowledge-base-and-resources/)
- [Prevalence, incidence and carrier frequency of 5q–linked spinal muscular atrophy – a literature review](https://scholariq.org/papers/prevalence-incidence-and-carrier-frequency-of-5q-linked-spinal-muscular-atrophy/)
- [International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases](https://scholariq.org/papers/international-cooperation-to-enable-the-diagnosis-of-all-rare-genetic-diseases/)
- [Mutations in dynamin 2 cause dominant centronuclear myopathy](https://scholariq.org/papers/mutations-in-dynamin-2-cause-dominant-centronuclear-myopathy/)
- [Radiation Dose and Second Cancer Risk in Patients Treated for Cancer of the Cervix](https://scholariq.org/papers/radiation-dose-and-second-cancer-risk-in-patients-treated-for-cancer-of-the/)
- [Mildly affected patients with spinal muscular atrophy are partially protected by an increased SMN2 copy number](https://scholariq.org/papers/mildly-affected-patients-with-spinal-muscular-atrophy-are-partially-protected-by/)
- [The route of administration is a major determinant of the transduction efficiency of rat tissues by adenoviral recombinants.](https://scholariq.org/papers/the-route-of-administration-is-a-major-determinant-of-the-transduction/)
- [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/)
- [Life expectancy at birth in Duchenne muscular dystrophy: a systematic review and meta-analysis](https://scholariq.org/papers/life-expectancy-at-birth-in-duchenne-muscular-dystrophy-a-systematic-review-and/)
- [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/)

## 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/)
- [Myasthenia Gravis and Thymoma](https://scholariq.org/topics/myasthenia-gravis-and-thymoma/)
- [Genetic Neurodegenerative Diseases](https://scholariq.org/topics/genetic-neurodegenerative-diseases/)
- [Cardiomyopathy and Myosin Studies](https://scholariq.org/topics/cardiomyopathy-and-myosin-studies/)

## Researcher university

- [University of Ottawa](https://scholariq.org/institutions/university-of-ottawa/)

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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.