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Filiz Başak Cengiz

Observed names: F B 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, Filiz Başak Cengiz
OpenAlex ID: A5111794615
Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss
2012 · Oscar Diaz-Horta, Duygu Duman, et al. · PLoS ONE · 155
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Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort
2015 · Guney Bademci, Joseph Foster, et al. · Genetics in Medicine · 150
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Spectrum of DNA variants for non-syndromic deafness in a large cohort from multiple continents
2016 · Denise Yan, Demet Tekin, et al. · Human Genetics · 130
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Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia
2007 · Mustafa Tekin, Burcu Öztürk Hişmi, et al. · The American Journal of Human Genetics · 111
Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey
2010 · Duygu Duman, Asli Sirmaci, et al. · Genetic Testing and Molecular Biomarkers · 87
FAM65B is a membrane-associated protein of hair cell stereocilia required for hearing
2014 · Oscar Diaz-Horta, Asli Subasioglu-Uzak, et al. · Proceedings of the National Academy of Sciences · 79
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A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss
2010 · Aslı Sırmacı, Seyra Erbek, et al. · The American Journal of Human Genetics · 71
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SLITRK6 mutations cause myopia and deafness in humans and mice
2013 · Mustafa Tekin, Barry A. Chioza, et al. · Journal of Clinical Investigation · 69
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ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice
2016 · Oscar Diaz-Horta, Clemer Abad, et al. · Proceedings of the National Academy of Sciences · 65
Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations
2009 · Aslı Sırmacı, Duygu Duman, et al. · International Journal of Pediatric Otorhinolaryngology · 62
GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf
2010 · Mustafa Tekin, Xia‐Juan Xia, et al. · Annals of Human Genetics · 58
Familial neonatal Marfan syndrome due to parental mosaicism of a missense mutation in the FBN1 gene
2007 · Mustafa Tekin, Filiz Başak Cengiz, et al. · American Journal of Medical Genetics Part A · 57
Variations in Multiple Syndromic Deafness Genes Mimic Non-syndromic Hearing Loss
2016 · G. Bademci, F. B. Cengiz, et al. · Scientific Reports · 54
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Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population
2010 · F. Basak Cengiz, Duygu Duman, et al. · Genetic Testing and Molecular Biomarkers · 46
FOXF2 is required for cochlear development in humans and mice
2018 · Guney Bademci, Clemer Abad, et al. · Human Molecular Genetics · 34
MPZL2 is a novel gene associated with autosomal recessive nonsyndromic moderate hearing loss
2018 · Guney Bademci, Clemer Abad, et al. · Human Genetics · 34
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The Effect of p.Arg25Cys Alteration in NKX2-5 on Conotruncal Heart Anomalies: Mutation or Polymorphism?
2007 · M. İ. Akçaboy, F. B. Cengiz, et al. · Pediatric Cardiology · 33
Identification of Copy Number Variants Through Whole-Exome Sequencing in Autosomal Recessive Nonsyndromic Hearing Loss
2014 · Guney Bademci, Oscar Diaz-Horta, et al. · Genetic Testing and Molecular Biomarkers · 31
Dominant deafness–onychodystrophy syndrome caused by an ATP 6V1B2 mutation
2017 · Ibis Menendez, Claudia Carranza, et al. · Clinical Case Reports · 30
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SLC26A4 mutations are associated with a specific inner ear malformation
2007 · Suat Fitoz, Levent Sennaroğlu, et al. · International Journal of Pediatric Otorhinolaryngology · 30
A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia
2009 · Reinhard Ramsebner, Martin Ludwig, et al. · The Laryngoscope · 27
Novel pathogenic variants underlie SLC26A4 -related hearing loss in a multiethnic cohort
2017 · Filiz Basak Cengiz, Rasim Yilmazer, et al. · International Journal of Pediatric Otorhinolaryngology · 26
Analysis of NPHS2 mutations in Turkish steroid-resistant nephrotic syndrome patients
2006 · Z. Birsin Özçakar, F. Başak Cengiz, et al. · Pediatric Nephrology · 26
Identification of candidate gene FAM183A and novel pathogenic variants in known genes: High genetic heterogeneity for autosomal recessive intellectual disability
2018 · Megan McSherry, Katherine E. Masih, et al. · PLoS ONE · 25
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Targeted Resequencing of Deafness Genes Reveals a FounderMYO15AVariant in Northeastern Brazil
2016 · Gabrielle N. Manzoli, Guney Bademci, et al. · Annals of Human Genetics · 23
Works count: 40
Citation count: 1,631
H-index: 24
I10-index: 31
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