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How has Davut Pehli̇van's publication output changed over time?
ScholarIQpublication output · 2010–2024
Output grew0% over the shown period — from 1 works in 2010 to 1 in 2024.
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20102011201320142015201920222024
What are the most-cited papers on Davut Pehli̇van?
ScholarIQmost cited works
Detection of mosaic and population-level structural variants with Sniffles2
Moritz Smolka, Luis F. Paulin, Christopher M. Grochowski, Dominic W. Horner, Medhat Mahmoud, Sairam Behera, Ester Kalef-Ezra, Mira Gandhi, Karl Hong, Davut Pehli̇van, Sonja W. Scholz, Claudia M.B. Carvalho, Christos Proukakis, Fritz J. Sedlazeck
S106963461. 2024461 CitationsOPEN ACCESS
A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases
Shinya Yamamoto, Manish Jaiswal, Wu‐Lin Charng, Tomasz Gambin, Ender Karaca, Ghayda Mirzaa, Wojciech Wiszniewski, Héctor Sandoval, Nele A Haelterman, Bo Xiong, Ke Zhang, Vafa Bayat, Gabriela David, Tongchao Li, Kuchuan Chen, Upasana Gala, Tamar Harel, Davut Pehli̇van, Samantha Penney, Lisenka E.L.M. Vissers, Joep de Ligt, Shalini N. Jhangiani, Ya‐Jing Xie, Stephen H. Tsang, Yeşim Parman, Merve Sivaci, Esra Battaloğlu, Donna M. Muzny, Ying-Wooi Wan, Zhandong Liu, Alexander T. Lin-Moore, Robin D. Clark, Cynthia J. Curry, Nichole Link, Karen L. Schulze, Eric Boerwinkle, William B. Dobyns, Rando Allikmets, Richard A. Gibbs, Rui Chen, James R. Lupski, Michael F. Wangler, Hugo J. Bellen
S110447773. 2014399 CitationsOPEN ACCESS
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease
Ender Karaca, Tamar Harel, Davut Pehli̇van, Shalini N. Jhangiani, Tomasz Gambin, Zeynep Coban‐Akdemir, Claudia Gonzaga‐Jauregui, Serkan Erdin, Yavuz Bayram, Ian M. Campbell, Jill V. Hunter, Mehmed M. Atik, Hilde Van Esch, Bo Yuan, Wojciech Wiszniewski, Sedat Işıkay, Gözde Yeşil, Özge Özalp Yüreğir, Sevcan Tuğ Bozdoğan, Hüseyin Aslan, Hatip Aydın, Tülay Tos, Ayşe Aksoy, Darryl C. De Vivo, Preti Jain, Bilgen Bilge Geçkinli, Özlem Sezer, Davut Gül, Burak Durmaz, Özgür Çoğulu, Ferda Özkınay, Vehap Topçu, Şükrü Candan, Alper Han Çebi, Mevlit Íkbal, Elif Yılmaz Güleç, Alper Gezdirici, Erkan Koparir, Fatma Ekici, Salih Coşkun, Salih Cicek, Kadri Karaer, Asuman Koparır, Mehmet Buğrahan Düz, Emre Kırat, Elif Fenercioğlu, Hakan Ulucan, Mehmet Seven, Tülay Güran, Nursel Elçioğlu, Mahmut Selman Yıldırım, Dilek Aktaş, Mehmet Alikaşifoğlu, Mehmet Türe, Tahsin Yakut, John D. Overton, Adnan Yüksel, Mustafa Özen, Donna M. Muzny, David R. Adams, Eric Boerwinkle, Wendy K. Chung, Richard A. Gibbs, James R. Lupski
Neuron. 2015342 CitationsOPEN ACCESS
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy
Claudia Gonzaga‐Jauregui, Tamar Harel, Tomasz Gambin, Maria Kousi, Laurie B. Griffin, Ludmila Francescatto, Burçak Özeş, Ender Karaca, Shalini N. Jhangiani, Matthew N. Bainbridge, Kim Lawson, Davut Pehli̇van, Yuji Okamoto, Marjorie Withers, Pedro Mancías, Anne Slavotinek, Pamela J. Reitnauer, Meryem Tuba Goksungur, Michael E. Shy, Thomas O. Crawford, Michel Koenig, Jason R. Willer, Brittany N. Flores, Igor Pediaditrakis, Önder Us, Wojciech Wiszniewski, Yeşim Parman, Anthony Antonellis, Donna M. Muzny, Nicholas Katsanis, Esra Battaloglu, Eric Boerwinkle, Richard A. Gibbs, James R. Lupski
S169236886. 2015249 CitationsOPEN ACCESS
Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome
Claudia M.B. Carvalho, Melissa B. Ramocki, Davut Pehli̇van, Luis M. Franco, Claudia Gonzaga‐Jauregui, Ping Fang, Alanna E. McCall, Enikö K. Pivnick, Stacy J. Hines‐Dowell, Laurie H. Seaver, Linda Friehling, Sansan Lee, Rosemarie Smith, Daniela del Gaudio, Marjorie Withers, Pengfei Liu, Sau Wai Cheung, John W. Belmont, Huda Y. Zoghbi, P. J. Hastings, James R. Lupski
S137905309. 2011233 Citations
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Detection of mosaic and population-level structural variants with Sniffles2
Paper
A Drosophila Genetic Resource of Mutants to Study Mechanisms Underlying Human Genetic Diseases
Paper
Genes that Affect Brain Structure and Function Identified by Rare Variant Analyses of Mendelian Neurologic Disease
Paper
Exome Sequence Analysis Suggests that Genetic Burden Contributes to Phenotypic Variability and Complex Neuropathy
Paper
Inverted genomic segments and complex triplication rearrangements are mediated by inverted repeats in the human genome
Paper