Armağan İncesulu - Concepedia

Author

Armağan İncesulu

Also Known As

A Incesulu, A İncesulu, A. Incesulu, A. İncesulu, Armagan Incesulu, Armagan S. İncesulu, Armagan İncesulu, Armağan Incesulu, Armağan İncesulu, Armaḡan İncesulu

100

Publications

2.6K

Citations

H-Index

Concepts

All Affiliations

Eskişehir Osmangazi University Ankara University University of Miami Dr. John T. Macdonald Foundation Social Security Children's Hospital

Aİ

About

Armağan İncesulu is an author at Eskişehir Osmangazi University specializing in medicine, hearing loss, and genetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	16	18	749
2	Arts	12	12	1.1K
3	Health Sciences	6	6	279
4	Social Sciences	3	3	160
5	Public Health	2	2	91

Armağan İncesulu

Publications

Citations

H-Index

Page 1

	Year	Citations
GJB2 Mutations and Degree of Hearing Loss: A Multicenter Study Rikkert L. Snoeckx, P.L.M. Huygen, Delphine Feldmann, The American Journal of Human Genetics Genetic DisorderGeneticsAudiologyGenetic EpidemiologyGjb2 Mutations	2005	551
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort Güney Bademci, Joseph Foster, Nejat Mahdieh, Genetics in Medicine Mendelian DisorderGenetic DisorderGeneticsGenetic EpidemiologyAudiology	2015	158
Children With Cochlear Implants: Parental Perspective Armağan İncesulu, M. Vural, Ünsal Erkam Otology & Neurotology	2003	135
Correlation of Acoustic Threshold Measures and Spiral Ganglion Cell Survival in Severe to Profound Sensorineural Hearing Loss: Implications for Cochlear Implantation Armağan İncesulu, Joseph B. Nadol Annals of Otology Rhinology & Laryngology Hearing HealthTemporal Bone StudySocial SciencesBetter Residual HearingNoise	1998	110
Frequency of mtDNA A1555G and A7445G mutations among children with prelingual deafness in Turkey Mustafa Tekin, Türker Duman, G Boğoçlu, European Journal of Pediatrics Genetic TestingMtdna A1555gGenetic DisorderGeneticsPediatrics	2003	65
Spectrum of GJB2 mutations in Turkey comprises both Caucasian and Oriental variants: Roles of parental consanguinity and assortative mating Mustafa Tekin, Türker Duman, G Boğoçlu, Human Mutation GeneticsGenetic EpidemiologyGjb2 MutationsGenetic AnalysisMendelian Disorder	2003	65
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations Aslı Sırmacı, Duygu Duman, Hatice Akay, International Journal of Pediatric Otorhinolaryngology Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiology	2009	61
Cochlear implantation in cases with incomplete partition type III (X-linked anomaly) Armağan İncesulu, Baki Adapınar, Cem Keçik European Archives of Oto-Rhino-Laryngology Health SciencesX-linked AnomalyAudiologyNeurotologyHuman Hearing	2008	59
A novel missense mutation in a C2 domain ofOTOF results in autosomal recessive auditory neuropathy Mustafa Tekin, Duygu Akçayöz, Armağan İncesulu American Journal of Medical Genetics Part A	2005	55
Investigation of the Presence of Biofilms in Chronic Suppurative Otitis Media, Nonsuppurative Otitis Media, and Chronic Otitis Media with Cholesteatoma by Scanning Electron Microscopy Ercan Kaya, İlknur Dağ, Armağan İncesulu, The Scientific World JOURNAL	2013	55

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