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About the database ScholarIQanswers from OpenAlex & ORCID
How has Beyhan Tüysüz's publication output changed over time?
ScholarIQpublication output · 2000–2023
Output declined50% over the shown period — from 2 works in 2000 to 1 in 2023.
2
1
2
3
1
1
1
2000200720102013201420152023
What are the most-cited papers on Beyhan Tüysüz?
ScholarIQmost cited works
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
Kaya Bilgüvar, Ali K. Ozturk, Angeliki Louvi, Kenneth Y. Kwan, Murim Choi, Burak Tatli, Dilek Yalnızoğlu, Beyhan Tüysüz, Ahmet Okay Çağlayan, Sarenur Gökben, Hande Kaymakçalan, Tanyeri Barak, Mehmet Bakırcıoğlu, Katsuhito Yasuno, Winson S. Ho, Stephan Sanders, Ying Zhu, Sanem Yılmaz, Alp Di̇nçer, Michele H. Johnson, Richard A. Bronen, Naci Koçer, Hüseyin Per, Shrikant Mane, M. Necmettin Pamir, Cengiz Yalçınkaya, Sefer Kumandaş, Meral Topçu, Meral Özmen, Nenad Šestan, Richard P. Lifton, Matthew W. State, Murat Günel
Nature. 2010499 CitationsOPEN ACCESS
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
Pascale Bomont, L Cavalier, F Blondeau, Christiane Ben Hamida, Samir Belal, Mériem Tazir, Ercan Demir, Haluk Topaloğlu, Rudolf Korinthenberg, Beyhan Tüysüz, P. Landrieu, Fayçal Hentati, Michel Koenig
S137905309. 2000413 Citations
IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy
Philip L. Beales, Elizabeth Bland, Jonathan L. Tobin, Chiara Bacchelli, Beyhan Tüysüz, Josephine Hill, Suzanne Rix, Chad G. Pearson, Masatake Kai, Jane Hartley, Colin A. Johnson, Melita Irving, Nursel Elçioğlu, Mark Winey, Masazumi Tada, Peter Scambler
S137905309. 2007342 CitationsOPEN ACCESS
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2
Ali R. Afzal, Anna Rajab, Christiane Fenske, Michael Oldridge, Navaratnam Elanko, E. Ternes-Pereira, Beyhan Tüysüz, Victoria A. Murday, Michael A. Patton, Andrew O.M. Wilkie, Steven Jeffery
S137905309. 2000306 Citations
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity
Ruxandra Bachmann‐Gagescu, Jennifer C. Dempsey, Ian G. Phelps, Brian J. O’Roak, Dana Knutzen, Tessa Rue, Gisele E. Ishak, Christine R. Isabella, Nicholas T. Gorden, Jonathan Adkins, E A Boyle, Nathan Lacy, Diana R. O’Day, Abdulrahman Alswaid, Radha Ramadevi A, Lokesh Lingappa, Charles Marques Lourenço, Loreto Martorell, Ángeles García‐Cazorla, Hamìt Özyürek, Göknur Haliloğlu, Beyhan Tüysüz, Meral Topçu, P. F. Chance, Melissa A. Parisi, Ian A. Glass, Jay Shendure, Dan Doherty
S112540174. 2015298 CitationsOPEN ACCESS
Related on ScholarIQ
Istanbul University-Cerrahpaşa
Institution
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
Paper
The gene encoding gigaxonin, a new member of the cytoskeletal BTB/kelch repeat family, is mutated in giant axonal neuropathy
Paper
IFT80, which encodes a conserved intraflagellar transport protein, is mutated in Jeune asphyxiating thoracic dystrophy
Paper
Recessive Robinow syndrome, allelic to dominant brachydactyly type B, is caused by mutation of ROR2
Paper
Joubert syndrome: a model for untangling recessive disorders with extreme genetic heterogeneity
Paper