Claes Möller

Neuroscience · Life Sciences

37h-index5.1kcitations231works0.02yr avg
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Research Topics

Hearing, Cochlea, Tinnitus, Genetics(63), Vestibular and auditory disorders(52), Hearing Loss and Rehabilitation(42), Retinal Development and Disorders(12), Ophthalmology and Eye Disorders(12)

Publications231 total

Deafblindness, Theory of Mind, and Cognitive Functioning in Alström Syndrome and Usher Syndrome Type 2
2025
Usher Syndrome
Audiology Research·2022· 96 citedOpen Access
[Possibilities to diagnose hearing impairment in children].
PubMed·2020
Similarities and Differences in Health, Social Trust, and Financial Situation in People With Usher Syndrome, a Bio-Psychosocial Perspective
Frontiers in Psychology·2020· 14 citedOpen Access
Congenital chloride diarrhea and Pendred syndrome: case report of siblings with two rare recessive disorders of SLC26 family genes
BMC Medical Genetics·2020· 6 citedOpen Access
The lived experiences of work and health of people living with deaf-blindness due to Usher syndrome type 2
International Journal of Qualitative Studies on Health and Well-Being·2020· 12 citedOpen Access
Experiences of work and health in people with Usher Syndrome type 2 : a qualitative study
2020
Life strategies of people with deafblindness due to Usher syndrome type 2a - a qualitative study
International Journal of Qualitative Studies on Health and Well-Being·2019· 35 citedOpen Access
Life Strategies And Facilitating Factors When Having Deafblindness Due To Usher Syndrome Type 2a
2019
Oral therapy for riboflavin transporter deficiency - What is the regimen of choice?
Parkinsonism & Related Disorders·2018· 18 cited
Health, work, social trust, and financial situation in persons with Usher syndrome type 1
Work·2018· 17 citedOpen Access
Headphone listening habits, hearing thresholds and listening levels in Swedish adolescents with severe to profound HL and adolescents with normal hearing
International Journal of Audiology·2018· 21 citedOpen Access
Correction to: The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management
Human Genetics·2018· 3 citedOpen Access
The CAPOS mutation in ATP1A3 alters Na/K-ATPase function and results in auditory neuropathy which has implications for management
Human Genetics·2018· 38 citedOpen Access
An Expanded Multi-Organ Disease Phenotype Associated with Mutations in YARS
Genes·2017· 27 citedOpen Access
Headphone listening habits and hearing thresholds in swedish adolescents
Noise and Health·2017· 56 citedOpen Access
Aspects of learning in deafblindness : opportunities and limitations for persons with Alström syndrome
2017
Functional validation of ABHD12 mutations in the neurodegenerative disease PHARC
Neurobiology of Disease·2016· 44 citedOpen Access
Theory of Mind and Cognitive Function in Adults with Alström or Usher Syndrome
Journal of Visual Impairment & Blindness·2016
The Relationship between Work and Health in Persons with Usher Syndrome Type 2
Journal of Visual Impairment & Blindness·2016· 18 cited
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Frequent Co-authors

William J. Kimberling(12), Lisbeth Tranebjærg(9), Michael D. Weston(7), Berth Danermark(7), Sarah Granberg(6), Mehdi Sadeghi(5), Lars Ödkvist(5), Cor W. R. J. Cremers(4), Richard J. Smith(4), Nanna Dahl Rendtorff(4), Carmen Ayuso(3), Sandra L. H. Davenport(3), Traci Flynn(3), Anette Lohmander(3), William Reardon(3), Kim Kähäri(3), Sophia E. Kramer(3), De Wet Swanepoel(3), Eva Malm(3), Sten Andréasson(3)