Aslı Sırmacı

1.7k total citations
15 papers, 860 citations indexed

About

Aslı Sırmacı is a scholar working on Sensory Systems, Molecular Biology and Otorhinolaryngology. According to data from OpenAlex, Aslı Sırmacı has authored 15 papers receiving a total of 860 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Sensory Systems, 7 papers in Molecular Biology and 5 papers in Otorhinolaryngology. Recurrent topics in Aslı Sırmacı's work include Hearing, Cochlea, Tinnitus, Genetics (10 papers), Ear Surgery and Otitis Media (5 papers) and Vestibular and auditory disorders (5 papers). Aslı Sırmacı is often cited by papers focused on Hearing, Cochlea, Tinnitus, Genetics (10 papers), Ear Surgery and Otitis Media (5 papers) and Vestibular and auditory disorders (5 papers). Aslı Sırmacı collaborates with scholars based in Türkiye, United States and Iran. Aslı Sırmacı's co-authors include Mustafa Tekin, Duygu Duman, Filiz Başak Cengiz, Hi̇lal Özdağ, Hatice Akay, Yvonne J. K. Edwards, Michail Spiliopoulos, Stephan Züchner, Susan H. Blanton and Suat Fítöz and has published in prestigious journals such as PLoS ONE, The American Journal of Human Genetics and Clinical Genetics.

In The Last Decade

Aslı Sırmacı

15 papers receiving 845 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Aslı Sırmacı Türkiye	14	437	385	262	191	124	15	860
Güney Bademci United States	19	582 1.3×	356 0.9×	331 1.3×	166 0.9×	102 0.8×	63	1.1k
Duygu Duman Türkiye	19	697 1.6×	601 1.6×	303 1.2×	268 1.4×	166 1.3×	42	1.4k
Filiz Başak Cengiz Türkiye	16	408 0.9×	419 1.1×	152 0.6×	186 1.0×	123 1.0×	25	750
Laurence Jonard France	15	379 0.9×	301 0.8×	102 0.4×	135 0.7×	66 0.5×	36	742
Margriet Verstreken Belgium	14	480 1.1×	504 1.3×	70 0.3×	285 1.5×	170 1.4×	24	913
E. Ann Black-Ziegelbein United States	8	488 1.1×	797 2.1×	138 0.5×	233 1.2×	289 2.3×	8	1.0k
Nanna Dahl Rendtorff Denmark	19	487 1.1×	223 0.6×	136 0.5×	109 0.6×	61 0.5×	40	816
P J Willems Belgium	17	611 1.4×	559 1.5×	280 1.1×	264 1.4×	141 1.1×	36	1.3k
Patricia Blanchet France	16	501 1.1×	268 0.7×	245 0.9×	84 0.4×	24 0.2×	47	828
Arthur G. Kristiansen United States	13	199 0.5×	228 0.6×	78 0.3×	121 0.6×	258 2.1×	17	734

Countries citing papers authored by Aslı Sırmacı

Since Specialization

Citations

This map shows the geographic impact of Aslı Sırmacı's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Aslı Sırmacı with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Aslı Sırmacı more than expected).

Fields of papers citing papers by Aslı Sırmacı

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Aslı Sırmacı. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Aslı Sırmacı. The network helps show where Aslı Sırmacı may publish in the future.

Co-authorship network of co-authors of Aslı Sırmacı

This figure shows the co-authorship network connecting the top 25 collaborators of Aslı Sırmacı. A scholar is included among the top collaborators of Aslı Sırmacı based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Aslı Sırmacı. Aslı Sırmacı is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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15 of 15 papers shown

Duman, Duygu, Aslı Sırmacı, Güney Bademci, et al.. (2017). Research of genetic bases of hereditary non-syndromic hearing loss. Türk Pediatri Arşivi. 52(3). 122–132. 7 indexed citations

Diaz‐Horta, Oscar, Duygu Duman, Joseph Foster, et al.. (2012). Whole-Exome Sequencing Efficiently Detects Rare Mutations in Autosomal Recessive Nonsyndromic Hearing Loss. PLoS ONE. 7(11). e50628–e50628. 127 indexed citations

Sırmacı, Aslı, Yvonne J. K. Edwards, Hatice Akay, & Mustafa Tekin. (2012). Challenges in Whole Exome Sequencing: An Example from Hereditary Deafness. PLoS ONE. 7(2). e32000–e32000. 40 indexed citations

Arenas‐Sordo, María de la Luz, et al.. (2012). Unique spectrum of GJB2 mutations in Mexico. International Journal of Pediatric Otorhinolaryngology. 76(11). 1678–1680. 16 indexed citations

Diaz‐Horta, Oscar, Aslı Sırmacı, Dan Doherty, et al.. (2012). GPSM2 mutations in Chudley–McCullough syndrome. American Journal of Medical Genetics Part A. 158A(11). 2972–2973. 17 indexed citations

Sırmacı, Aslı, Michail Spiliopoulos, Francesco Brancati, et al.. (2011). Mutations in ANKRD11 Cause KBG Syndrome, Characterized by Intellectual Disability, Skeletal Malformations, and Macrodontia. The American Journal of Human Genetics. 89(2). 289–294. 170 indexed citations

Duman, Duygu, Aslı Sırmacı, Filiz Başak Cengiz, Hi̇lal Özdağ, & Mustafa Tekin. (2010). Screening of 38 Genes Identifies Mutations in 62% of Families with Nonsyndromic Deafness in Turkey. Genetic Testing and Molecular Biomarkers. 15(1-2). 29–33. 71 indexed citations

Cengiz, Filiz Başak, Duygu Duman, Aslı Sırmacı, et al.. (2010). Recurrent and Private MYO15A Mutations Are Associated with Deafness in the Turkish Population. Genetic Testing and Molecular Biomarkers. 14(4). 543–550. 38 indexed citations

Sırmacı, Aslı, Tom Walsh, Hatice Akay, et al.. (2010). MASP1 Mutations in Patients with Facial, Umbilical, Coccygeal, and Auditory Findings of Carnevale, Malpuech, OSA, and Michels Syndromes. The American Journal of Human Genetics. 87(5). 679–686. 106 indexed citations

10.

Sırmacı, Aslı, et al.. (2009). Homozygous mutations in the 15-hydroxyprostaglandin dehydrogenase gene in patients with primary hypertrophic osteoarthropathy. Rheumatology International. 30(1). 39–43. 34 indexed citations

11.

Tekin, Mustafa, et al.. (2009). A complexTFAP2Aallele is associated with branchio‐oculo‐facial syndrome and inner ear malformation in a deaf child. American Journal of Medical Genetics Part A. 149A(3). 427–430. 34 indexed citations

12.

Sırmacı, Aslı, Duygu Duman, Hatice Akay, et al.. (2009). Mutations in TMC1 contribute significantly to nonsyndromic autosomal recessive sensorineural hearing loss: A report of five novel mutations. International Journal of Pediatric Otorhinolaryngology. 73(5). 699–705. 50 indexed citations

13.

Sırmacı, Aslı, Seyra Erbek, Armağan İncesulu, et al.. (2009). A founder TMIE mutation is a frequent cause of hearing loss in southeastern Anatolia. Clinical Genetics. 75(6). 562–567. 15 indexed citations

14.

Tekin, Mustafa, Burcu Öztürk Hişmi, Suat Fítöz, et al.. (2007). Homozygous Mutations in Fibroblast Growth Factor 3 Are Associated with a New Form of Syndromic Deafness Characterized by Inner Ear Agenesis, Microtia, and Microdontia. The American Journal of Human Genetics. 80(2). 338–344. 86 indexed citations

15.

Sırmacı, Aslı, Duygu Duman, & Mustafa Tekin. (2006). The c.IVS1+1G>A mutation intheGJB2 gene is prevalent and large deletions involving theGJB6 gene are not present in the Turkish population. Journal of Genetics. 85(3). 213–216. 49 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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