ScholarIQanswers from OpenAlex & ORCID
Beyhan Tüysüz
ResearcherPublications, citations & collaboration network
Beyhan Tüysüz is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Beyhan Tüysüz have?
ScholarIQindexed works
Beyhan Tüysüz has 258 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Beyhan Tüysüz have?
ScholarIQcitation count
Beyhan Tüysüz has 7,745 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Beyhan Tüysüz?
ScholarIQh-index
Beyhan Tüysüz has an h-index of 44 in OpenAlex.
What is the i10-index of Beyhan Tüysüz?
ScholarIQi10-index
Beyhan Tüysüz has an i10-index of 105 in OpenAlex.
What is the ORCID of Beyhan Tüysüz?
ScholarIQorcid
The ORCID for Beyhan Tüysüz is on the source record.
What is the OpenAlex record for Beyhan Tüysüz?
ScholarIQopenalex
The OpenAlex for Beyhan Tüysüz is on the source record.
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
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
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
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
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