ScholarIQanswers from OpenAlex & ORCID
Murat Günel
ResearcherPublications, citations & collaboration network
Murat Günel is a researcher indexed in ScholarIQ from OpenAlex & ORCID.
How many works does Murat Günel have?
ScholarIQindexed works
Murat Günel has 343 works in the ScholarIQ index. The count is the OpenAlex total, not the number of papers listed on this page.
How many citations does Murat Günel have?
ScholarIQcitation count
Murat Günel has 27,169 citations in the OpenAlex counts ScholarIQ stores.
What is the h-index of Murat Günel?
ScholarIQh-index
Murat Günel has an h-index of 78 in OpenAlex.
What is the i10-index of Murat Günel?
ScholarIQi10-index
Murat Günel has an i10-index of 174 in OpenAlex.
What is the ORCID of Murat Günel?
ScholarIQorcid
The ORCID for Murat Günel is on the source record.
What is the OpenAlex record for Murat Günel?
ScholarIQopenalex
The OpenAlex for Murat Günel is on the source record.
What are the most-cited papers on Murat Günel?
ScholarIQmost cited works
Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism
Stephan Sanders, A. Gulhan Ercan‐Sencicek, Vanessa Hus, Rui Luo, Michael T. Murtha, Daniel Moreno‐De‐Luca, Su H. Chu, Michael Moreau, Abha R. Gupta, Susanne Thomson, Christopher E. Mason, Kaya Bilgüvar, Patrícia B. S. Celestino-Soper, Murim Choi, Emily L. Crawford, Lea K. Davis, Nicole R. Davis Wright, Rahul M. Dhodapkar, Michael DiCola, Nicholas M. DiLullo, Thomas Fernandez, Vikram Fielding‐Singh, Daniel O. Fishman, Stephanie Frahm, Rouben Garagaloyan, Gerald Goh, Sindhuja Kammela, Lambertus Klei, Jennifer K. Lowe, Sabata C. Lund, Anna D. McGrew, Kyle A. Meyer, William J. Moffat, John D. Murdoch, Brian J. O’Roak, G Ober, Rebecca S. Pottenger, Melanie J. Raubeson, Youeun Song, Qi Wang, Brian L. Yaspan, Timothy W. Yu, Ilana R. Yurkiewicz, Arthur L. Beaudet, Rita M. Cantor, Martin Curland, Dorothy E. Grice, Murat Günel, Richard P. Lifton, Shrikant Mane, Donna M. Martin, Chad A. Shaw, Michael Sheldon, Jay A. Tischfield, Christopher A. Walsh, Eric M. Morrow, David H. Ledbetter, Éric Fombonne, Catherine Lord, Christa Lese Martin, Andrew I. Brooks, James S. Sutcliffe, Edwin H. Cook, Daniel H. Geschwind, Kathryn Roeder, Bernie Devlin, Matthew W. State
Genomic Analysis of Non- <i>NF2</i> Meningiomas Reveals Mutations in <i>TRAF7</i> , <i>KLF4</i> , <i>AKT1</i> , and <i>SMO</i>
Victoria Clark, E. Zeynep Erson‐Omay, Akdes Serin, Jun Yin, Justin Cotney, Koray Özduman, Timuçin Avşar, Jie Li, Phillip B. Murray, Octavian Henegariu, Saliha Yılmaz, Jennifer Moliterno Günel, Geneive Carrión-Grant, Baran Yılmaz, Conor Grady, Bahattin Tanrıkulu, Mehmet Bakırcıoğlu, Hande Kaymakçalan, Ahmet Okay Çağlayan, Leman Sencar, Emre Ceyhun, Ahmet Atik, Yaşar Bayri, Hanwen Bai, Luis Kolb, Ryan Hebert, Sacit Bulent Omay, Ketu Mishra-Gorur, Murim Choi, John D. Overton, Eric C. Holland, Shrikant Mane, Matthew W. State, Kaya Bilgüvar, Joachim M. Baehring, Philip H. Gutin, Joseph M. Piepmeier, Alexander O. Vortmeyer, Cameron Brennan, M. Necmettin Pamir, Türker Kılıç, Richard P. Lifton, James P. Noonan, Katsuhito Yasuno, Murat Günel
Genome-wide association study identifies susceptibility loci for IgA nephropathy
Ali G. Gharavi, Krzysztof Kiryluk, Murim Choi, Yifu Li, Ping Hou, Jingyuan Xie, Simone Sanna‐Cherchi, Clara J. Men, Bruce A. Julian, Robert Wyatt, Jan Novák, John Cijiang He, Haiyan Wang, Jicheng Lv, Li Zhu, Weiming Wang, Zhaohui Wang, Kasuhito Yasuno, Murat Günel, Shrikant Mane, Sheila Umlauf, Irina Tikhonova, Isabel Beerman, Silvana Savoldi, Riccardo Magistroni, Gian Marco Ghiggeri, Monica Bodria, Francesca Lugani, Pietro Ravani, Claudio Ponticelli, Landino Allegri, Giuliano Boscutti, Giovanni M. Frascà, Alessandro Amore, Licia Peruzzi, Rosanna Coppo, Claudia Izzi, Battista Fabio Viola, E. Prati, Maurizio Salvadori, Renzo Mignani, Loreto Gesualdo, Francesca Bertinetto, Paola Mesiano, Antonio Amoroso, Francesco Scolari, Nan Chen, Hong Zhang, Richard P. Lifton
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
Integrated genomic characterization of IDH1-mutant glioma malignant progression
Hanwen Bai, Akdes Serin Harmancı, E. Zeynep Erson‐Omay, Jie Li, Süleyman Coşkun, Matthias Simon, Boris Krischek, Koray Özduman, Sacit Bulent Omay, Eric A. Sorensen, Şevin Turcan, Mehmet Bakırcığlu, Geneive Carrión-Grant, Phillip B. Murray, Victoria Clark, A. Gulhan Ercan‐Sencicek, James Knight, Leman Sencar, Selin Altınok, Leon D. Kaulen, Burcu Gülez, Marco Timmer, Johannes Schramm, Ketu Mishra-Gorur, Octavian Henegariu, Jennifer Moliterno, Angeliki Louvi, Timothy A. Chan, Stacey Tannheimer, M. Necmettin Pamir, Alexander O. Vortmeyer, Kaya Bilgüvar, Katsuhito Yasuno, Murat Günel