• 945 Citations
  • 16 h-Index
20052019
If you made any changes in Pure these will be visible here soon.

Fingerprint Dive into the research topics where N. Nagy is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 3 Similar Profiles
Mutation Medicine & Life Sciences
Genes Medicine & Life Sciences
Missense Mutation Medicine & Life Sciences
Pedigree Medicine & Life Sciences
Keratinocytes Medicine & Life Sciences
Skin Medicine & Life Sciences
Cathepsin C Medicine & Life Sciences
Genetic Databases Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Research Output 2005 2019

  • 945 Citations
  • 16 h-Index
  • 57 Article
  • 2 Review article
  • 1 Comment/debate

A novel WDR62 missense mutation in microcephaly with abnormal cortical architecture and review of the literature

Zombor, M., Kalmár, T., Nagy, N., Berényi, M., Telcs, B., Maróti, Z., Brandau, O. & Sztriha, L., Jan 1 2019, In : Journal of Applied Genetics.

Research output: Contribution to journalReview article

Microcephaly
Missense Mutation
Mutation
Lissencephaly
Genes

Brooke-Spiegler Syndrome: Two Patients From a Turkish Family With Multiple Familial Trichoepithelioma

Cakmak Genc, G., Dursun, A., Nagy, N., Celikmakas, A. & Acuner, B., Oct 1 2019, In : The American Journal of dermatopathology. 41, 10, p. 778-780 3 p.

Research output: Contribution to journalArticle

Familial cylindromatosis

Genetic investigation confirmed the clinical phenotype of congenital chloride diarrhea in a Hungarian patient: A case report

Dávid, É., Török, D., Farkas, K., Nagy, N., Horváth, E., Kiss, Z., Oroszlán, G., Balogh, M. & Széll, M., Jan 11 2019, In : BMC Pediatrics. 19, 1, 16.

Research output: Contribution to journalArticle

Genetic Databases
Genetic Testing
Phenotype
Mutation
Chlorides