Akgün Ölmez - Concepedia

Author

Akgün Ölmez

Hacettepe University ORCID

Also Known As

A. Olmez, A. Ölmez, AKGÜN ÖLMEZ, Akgun Olmez, Akgün Olmez, Akgün Ölmez, Ayca Olmez, Olmez, A

Publications

348

Citations

H-Index

Concepts

All Affiliations

Hacettepe University Karadeniz Technical University Denizli Devlet Hastanesi Pamukkale University University of Regensburg

AÖ

About

Akgün Ölmez is an author at Hacettepe University specializing in medicine, pathology, and pediatrics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	5	5	153
2	Pathology	3	3	64
3	Cell Biology	1	1	25
4	Immunology	1	1	13
5	Neurology	1	1	26

Akgün Ölmez

Publications

303

Citations

H-Index

Page 1

	Year	Citations
Novel truncating and missense mutations of the <i>KCC3</i> gene associated with Andermann syndrome G. Uyanık, Nursel Elçioğlu, Johannes Penzien, Neurology	2006	66
Risk of recurrence after drug withdrawal in childhood epilepsy Akgün Ölmez, Ümüt Arslan, Güzide Turanlı, Seizure Substance AbuseChildhood EpilepsyAddictionRebound EffectPediatrics	2008	49
Cyclic Vomiting With Generalized Epileptiform Discharges Responsive to Topiramate Therapy Akgün Ölmez, Gülşen Köse, Güzide Turanlı Pediatric Neurology MedicineTopiramate TherapyAnesthesiology	2006	40
Genotype–phenotype correlation in seven motor neuron disease families with novel <scp><i>ALS2</i></scp> mutations Rosanne Sprute, Hannah Jergas, Akgün Ölmez, American Journal of Medical Genetics Part A	2020	29
Congenital Hydrocephalus as a Rare Association with Ligneous Conjunctivitis and Type I Plasminogen Deficiency Ayşe Tana Aslan, Uğur Özçelik, Deni̇z Doğru, Neuropediatrics Pediatric HydrocephalusOphthalmologyLigneous ConjunctivitisPlasminogen DeficiencyPediatrics	2005	26
Further Clinical and Genetic Characterization of SPG11: Hereditary Spastic Paraplegia with Thin Corpus Callosum Akgün Ölmez, G. Uyanık, Rıza Köksal Özgül, Neuropediatrics	2006	25
Analysis of centrosome and DNA damage response in PLK4 associated Seckel syndrome Tugba Dincer, Gülden Yorgancıoğlu-Budak, Akgün Ölmez, European Journal of Human Genetics ChromatinGenome InstabilityCell DivisionGenetic DisorderGenetics	2017	25
Novel splice-site and missense mutations in the<i>ALDH1A3</i>gene underlying autosomal recessive anophthalmia/microphthalmia C. Nur Semerci, Ersan Kalay, Cem Yıldırım, British Journal of Ophthalmology	2014	19
Alpha-mannosidosis and mutational analysis in a Turkish patient. Akgün Ölmez, Øivind Nilssen, Turgay Coşkun, PubMed Turkish PatientMutational AnalysisGenetic DisorderImmunodeficienciesPathogenesis	2003	13
Serum Selenium Levels in Acute Gastroenteritis of Possible Viral Origin Akgün Ölmez, Kadriye Yurdakök, Turgay Coşkun Journal of Tropical Pediatrics	2004	11

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