• 543 Citations
  • 14 h-Index
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Fingerprint Dive into the research topics where K. Komlósi is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 19 Similar Profiles
Mutation Medicine & Life Sciences
Carnitine Medicine & Life Sciences
Genes Medicine & Life Sciences
Mitochondrial DNA Medicine & Life Sciences
Esters Medicine & Life Sciences
Phenotype Medicine & Life Sciences
Alleles Medicine & Life Sciences
Hearing Loss Medicine & Life Sciences

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Research Output 2001 2019

  • 543 Citations
  • 14 h-Index
  • 54 Article
  • 2 Chapter
  • 2 Comment/debate

Heterotopic ossifications and Charcot joints: Congenital insensitivity to pain with anhidrosis (CIPA) and a novel NTRK1 gene mutation

Gucev, Z., Tasic, V., Bogevska, I., Laban, N., Saveski, A., Polenakovic, M., Plaseska-Karanfilska, D., Komlósi, K., Winter, J., Schweiger, S., Nishimura, G., Spranger, J. & Bartsch, O., Jan 1 2019, (Accepted/In press) In : European Journal of Medical Genetics.

Research output: Contribution to journalArticle

Neurogenic Arthropathy
Hereditary Sensory and Autonomic Neuropathies
Heterotopic Ossification

Age-Related Hearing Impairment Associated NAT2, GRM7, GRHL2 Susceptibility Gene Polymorphisms and Haplotypes in Roma and Hungarian Populations

Matyas, P., Postyeni, E., Komlósi, K., Szalai, R., Bene, J., Magyari, L., Melegh, B. & Hadzsiev, K., Feb 17 2018, (Accepted/In press) In : Pathology and Oncology Research. p. 1-7 7 p.

Research output: Contribution to journalArticle

Hearing Loss

Small supernumerary marker chromosome 15 and a ring chromosome 15 associated with a 15q26.3 deletion excluding the IGF1R gene

Szabó, A., Czakó, M., Hadzsiev, K., Duga, B., Bánfai, Z., Komlósi, K. & Melegh, B., Feb 1 2018, In : American Journal of Medical Genetics, Part A. 176, 2, p. 443-449 7 p.

Research output: Contribution to journalArticle

Ring Chromosomes
Chromosomes, Human, Pair 15
Genetic Markers