Embed

Academic

Authors

Filiz Basak Cengiz

Filiz Basak Cengiz (Filiz Başak Cengiz),Ankara University,Genetics & Genealogy,Anatomy,Molecular Biology

Edit

Filiz Basak Cengiz (Filiz Başak Cengiz)

Ankara University

Publications: 11 | Citations: 60

Fields: Genetics & Genealogy, Anatomy, Molecular Biology

Collaborated with 84 co-authors from 2006 to 2010 | Cited by 358 authors

Cumulative Annual

Sort by:

Publications (11)

BibTeX | RIS | RefWorks Download

A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss (Citations: 2)

, , , , , , , , , , , http://academic.research.microsoft.com/io.ashx?type=5&id=36196397&selfId1=24577097&selfId2=0&maxNumber=12&query=

Journal: American Journal of Human Genetics - AMER J HUM GENET , vol. 86, no. 5, pp. 797-804, 2010

GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf (Citations: 1)

, , , , , , , , ,

Journal: Annals of Human Genetics - ANN HUM GENET , vol. 74, no. 2, pp. 155-164, 2010

Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population

, , , , , , , ,

Journal: Genetic Testing and Molecular Biomarkers - GENET TEST MOL BIOMARK , vol. 14, no. 4, pp. 543-550, 2010

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

, , , , , , , , , , , http://academic.research.microsoft.com/io.ashx?type=5&id=32452444&selfId1=24577097&selfId2=0&maxNumber=12&query=

Journal: International Journal of Pediatric Otorhinolaryngology - INT J PED OTORHINOLARYNGOL , vol. 73, no. 5, pp. 699-705, 2009

A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia

, , , , , , , , ,

Journal: Laryngoscope , pp. NA-NA, 2009

Sort by:

Citations (60 times by 54 publications)

Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome (Citations: 1)

, , , , , , , , , ,

Journal: BMC Medical Genetics - BMC MED GENET , vol. 12, no. 1, pp. 21-11, 2011

Novel NKX2-5 Mutations in Patients With Familial Atrial Septal Defects

, , , , , , , ,

Journal: Pediatric Cardiology - PEDIAT CARDIOL , vol. 32, no. 2, pp. 193-201, 2011

Altered expression of securin (Pttg1) and serpina3n in the auditory system of hearing-impaired Tff3 -deficient mice

, , , , , , , , ,

Journal: Experientia , vol. 68, no. 16, pp. 2739-2749, 2011

491 OUTCOME AND DETERMINANTS OF MORTALITY FOLLOWING DRUG INDUCED LIVER INJURY SECONDARY TO ANTITUBERCULOSIS TREATMENT

, , , , , , ,

Journal: Journal of Hepatology - J HEPATOL , vol. 54, pp. S201-S201, 2011

Fibroblast growth factor signalling: from development to cancer (Citations: 42)

Journal: Nature Reviews Cancer - NAT REV CANCER , vol. 10, no. 2, pp. 116-129, 2010

Comments

Co-authors (84)

Journals (9)

Keywords (26)

Filiz Basak Cengiz (Filiz Başak Cengiz),Ankara University,Genetics & Genealogy,Anatomy,Molecular Biology

Publications (11)

BibTeX | RIS | RefWorks Download

A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss (Citations: 2)

GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf (Citations: 1)

Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population

Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations

A FGF3 mutation associated with differential inner ear malformation, microtia, and microdontia

Citations (60 times by 54 publications)

Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome (Citations: 1)

Novel NKX2-5 Mutations in Patients With Familial Atrial Septal Defects

Altered expression of securin (Pttg1) and serpina3n in the auditory system of hearing-impaired Tff3 -deficient mice

491 OUTCOME AND DETERMINANTS OF MORTALITY FOLLOWING DRUG INDUCED LIVER INJURY SECONDARY TO ANTITUBERCULOSIS TREATMENT

Fibroblast growth factor signalling: from development to cancer (Citations: 42)


	View FAQ about top research areas and Fields of study

Filiz Basak Cengiz (Filiz Başak Cengiz),Ankara University,Genetics & Genealogy,Anatomy,Molecular Biology

Publications (11) BibTeX | RIS | RefWorks Download

A Truncating Mutation in SERPINB6 Is Associated with Autosomal-Recessive Nonsyndromic Sensorineural Hearing Loss (Citations: 2)

GJB2 Mutations in Mongolia: Complex Alleles, Low Frequency, and Reduced Fitness of the Deaf (Citations: 1)

Variable expressivity of FGF3 mutations associated with deafness and LAMM syndrome (Citations: 1)

Fibroblast growth factor signalling: from development to cancer (Citations: 42)

Publications (11)

BibTeX | RIS | RefWorks Download