Filiz Başak Cengiz - Concepedia

Author

Filiz Başak Cengiz

Also Known As

F B Cengiz, F Cengiz, F. B. Cengiz, F. Basak Cengiz, F. Başak Cengiz, F.Basak Cengiz, Filiz B Cengiz, Filiz B. Cengiz, Filiz Basak Cengiz, Filiz Başak Cengiz

Publications

1.7K

Citations

H-Index

Concepts

All Affiliations

Ankara University University of Miami Dr. John T. Macdonald Foundation Eskişehir Osmangazi University Hacettepe University

About

Filiz Başak Cengiz is an author at Ankara University specializing in medicine, genetics, and hearing loss.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	18	20	1.2K
2	Arts	10	10	773
3	Public Health	3	3	186
4	Biology	2	2	41
5	Health Sciences	1	1	41

Filiz Başak Cengiz

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
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
Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss Oscar Diaz‐Horta, Duygu Duman, Joseph Foster, PLoS ONE GeneticsPathologyArnshl GenesDisease Gene IdentificationGenomics	2012	155
Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents Denise Yan, Demet Tekin, Güney Bademci, Human Genetics Allelic VariantMultiple ContinentsMendelian DisorderGenetic DisorderGenetics	2016	136
Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia Mustafa Tekin, Burcu Öztürk Hişmi, Suat Fítöz, The American Journal of Human Genetics Homozygous MutationsDevelopmental BiologySyndromic Deafness CharacterizedMendelian DisorderGenetic Disorder	2007	111
Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey Duygu Duman, Filiz Başak Cengiz, Hi̇lal Özdağ, Genetic Testing and Molecular Biomarkers Nonsyndromic DeafnessMendelian DisorderGenetic DisorderMedicineGenetics	2010	90
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing Oscar Diaz‐Horta, Asli Subasioglu-Uzak, M’hamed Grati, Proceedings of the National Academy of Sciences	2014	79
A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss Aslı Sırmacı, Seyra Erbek, Justin Price, The American Journal of Human Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsAudiology	2010	72
SLITRK6 mutations cause myopia and deafness in humans and mice Mustafa Tekin, Barry A. Chioza, Yoshifumi Matsumoto, Journal of Clinical Investigation Knockout MouseDevelopmental BiologyMolecular NeuroscienceHigh MyopiaSevere Myopia	2013	66
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice Oscar Diaz‐Horta, Clemer Abad, Levent Sennaroğlu, Proceedings of the National Academy of Sciences	2016	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

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