Duygu Duman (D Duman)

Scopus Author ID ORCID

Publication Activity (10 Years)

Years Active: 2015-2024
Publications (10 Years): 13

Top Venues

American journal of medical genetics. Part A

Proceedings of the National Academy of Sciences of the United States of America

Balkan medical journal

Journal of the European Academy of Dermatology and Venereology : JEADV

Ankara University

This page only lists publications with an associated author ORCID identifier.

Affiliation History

Ankara University

Turkey

Associate Prof

Publications

Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A 194 (6) (2024)
Duygu Duman, Memoona Ramzan, Asli Subasioglu, Ahmet Mutlu, LéShon Peart, Serhat Seyhan, Shengru Guo, Kadri Ila, Burhan Balta, Mahmut Tayyar Kalcioglu, Güney Bademci, Mustafa Tekin
Identification of novel MYH14 variants in families with autosomal dominant sensorineural hearing loss. American journal of medical genetics. Part A (2024)
Barbara Vona, D A Schwartzbaum, A A Rodriguez, S S Lewis, M B Toosi, P Radhakrishnan, Nazim Bozan, Ramazan Akın, M Doosti, R Manju, Duygu Duman, C J Sineni, Sheela Nampoothiri, E G Karimiani, Henry Houlden, Güney Bademci, Mustafa Tekin, Katta Mohan Girisha, Reza Maroofian, Sofia Douzgou Houge
Biallelic KITLG variants lead to a distinct spectrum of hypomelanosis and sensorineural hearing loss. Journal of the European Academy of Dermatology and Venereology : JEADV 36 (9) (2022)
Güney Bademci, María Lachgar, Mangesh Deokar, Mohammad Faraz Zafeer, Clemer Abad, Muzeyyen Yildirim Baylan, Neil J Ingham, Jing Chen, Claire J Sineni, Nirmal Vadgama, Ioannis Karakikes, Shengru Guo, Duygu Duman, Nitu Singh, Gaurav V Harlalka, Shirish P Jain, Barry A Chioza, Katherina Walz, Karen P Steel, Jamal Nasir, Mustafa Tekin
Mutations in MINAR2 encoding membrane integral NOTCH2-associated receptor 2 cause deafness in humans and mice. Proceedings of the National Academy of Sciences of the United States of America 119 (26) (2022)
Emine Begüm Gencer Öncül, Duygu Duman, Süleyman Aktuna, Mustafa Türker Duman
Whole Mitochondrial Genome Analysis in Turkish Patients with Mitochondrial Diseases Balkan medical journal 39 (2) (2021)
Chong Li, Guney Bademci, Asli Subasioglu, Oscar Diaz-Horta, Yi Zhu, Jiaqi Liu, Timothy Gavin Mitchell, Clemer Abad, Serhat Seyhan, Duygu Duman, Filiz Basak Cengiz, Suna Tokgoz-Yilmaz, Susan H Blanton, Amjad Farooq, Katherina Walz, R Grace Zhai, Mustafa Tekin
Dysfunction of GRAP, encoding the GRB2-related adaptor protein, is linked to sensorineural hearing loss. Proceedings of the National Academy of Sciences of the United States of America 116 (4) (2019)
Kevin T A Booth, Kimia Kahrizi, Mojgan Babanejad, H Daghagh, Güney Bademci, S Arzhangi, D Zareabdollahi, Duygu Duman, Aziz El-Amraoui, Mustafa Tekin, Hossein Najmabadi, Hela Azaiez, Richard J H Smith
Variants in CIB2 cause DFNB48 and not USH1J. Clinical genetics 93 (4) (2018)
Oscar Diaz-Horta, Clemer Abad, Levent Sennaroglu, Joseph Foster, Alexandra DeSmidt, Guney Bademci, Suna Tokgoz-Yilmaz, Duygu Duman, F Basak Cengiz, M'hamed Grati, Suat Fitoz, Xue Z Liu, Amjad Farooq, Faiqa Imtiaz, Benjamin B Currall, Cynthia Casson Morton, Michiru Nishita, Yasuhiro Minami, Zhongmin Lu, Katherina Walz, Mustafa Tekin
ROR1 is essential for proper innervation of auditory hair cells and hearing in humans and mice. Proceedings of the National Academy of Sciences of the United States of America 113 (21) (2016)
Guney Bademci, Joseph Foster, Nejat Mahdieh, Mortaza Bonyadi, Duygu Duman, F Basak Cengiz, Ibis Menendez, Oscar Diaz-Horta, Atefeh Shirkavand, Sirous Zeinali, Asli Subasioglu, Suna Tokgoz-Yilmaz, Fabiola Huesca-Hernandez, Maria de la Luz Arenas-Sordo, Juan Dominguez-Aburto, Edgar Hernandez-Zamora, Paola Montenegro, Rosario Paredes, Germania Moreta, Rodrigo Vinueza, Franklin Villegas, Santiago Mendoza-Benitez, Shengru Guo, Nazim Bozan, Tulay Tos, Armagan Incesulu, Gonca Sennaroglu, Susan H Blanton, Hatice Ozturkmen-Akay, Muzeyyen Yildirim-Baylan, Mustafa Tekin
Comprehensive analysis via exome sequencing uncovers genetic etiology in autosomal recessive nonsyndromic deafness in a large multiethnic cohort. Genetics in medicine : official journal of the American College of Medical Genetics 18 (4) (2015)

Duygu Duman.css-eqlu8i{font-size:small;padding-left:4px;} (D Duman)

Publication Activity (10 Years)

Top Topics

Top Venues

Duygu Duman (D Duman)