Seda Taşır Yılmaz

Author

Seda Taşır Yılmaz

Also Known As

S Taşır‐Yılmaz, S YILMAZ, Seda TAŞIR, Seda Tasir Yilmaz, Seda Tasır Yılmaz, Seda Taşır Yılmaz, Seda Taşır-Yılmaz, Seda Yılmaz

Publications

241

Citations

H-Index

Concepts

All Affiliations

Seda Taşır Yılmaz is an author at Ankara University specializing in medicine, autoimmune disease, and autoimmunity.

#	Concept	H-Index	Publications	Citations
1	Medicine	4	4	203
2	Arts	2	2	172
3	Immunology	2	2	31
4	Allergy	1	1	21
5	Cell Biology	1	1	111

Seda Taşır Yılmaz

Publications

227

Citations

H-Index

Page 1

	Year	Citations
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
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
A founder <i>TMIE </i>mutation is a frequent cause of hearing loss in southeastern Anatolia Aslı Sırmacı, Hatice Akay, Seyra Erbek, Clinical Genetics	2009	24
Behçet's: A Disease or a Syndrome? Answer from an Expression Profiling Study Ali Kemal Oğuz, Seda Taşır Yılmaz, Çağdaş Şahap Oygür, PLoS ONE Disease EtiologyImmunodeficienciesGenetic EpidemiologyImmunologyPathology	2016	21
C-type lectin domain family 12, member A: A common denominator in Behçet’s syndrome and acute gouty arthritis Ali Kemal Oğuz, Seda Taşır Yılmaz, Nejat Akar, Medical Hypotheses InflammationRheumatologyRheumatoid DisorderAutoimmune DiseaseC-type Lectin	2015	10

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