• 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.

  • 17 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: Article

Neurogenic Arthropathy
Hereditary Sensory and Autonomic Neuropathies
Heterotopic Ossification
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., febr. 1 2018, In : American Journal of Medical Genetics, Part A. 176, 2, p. 443-449 7 p.

Research output: Article

Ring Chromosomes
Chromosomes, Human, Pair 15
Genetic Markers