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Murat Günel

Active 1995–2025

107
Papers
24,128
Citations
78
h-index
105
i10-index

Citations

Citations per year for Murat Günel1955: 1 citations1987: 1 citations1989: 2 citations1994: 2 citations1995: 1 citations1996: 6 citations1997: 2 citations1998: 12 citations1999: 21 citations2000: 16 citations2001: 15 citations2002: 30 citations2003: 46 citations2004: 48 citations2005: 54 citations2006: 71 citations2007: 82 citations2008: 90 citations2009: 116 citations2010: 125 citations2011: 175 citations2012: 277 citations2013: 335 citations2014: 353 citations2015: 287 citations2016: 246 citations2017: 310 citations2018: 320 citations2019: 815 citations2020: 1,031 citations2021: 1,173 citations2022: 649 citations2023: 467 citations2024: 713 citations2025: 252 citations2026: 12 citations1956–1986: no citations, so these years are not shown1988: no citations, so this year is not shown1990–1993: no citations, so these years are not shown

Citation sources

Countries

World map of the countries and regions citing this authorUnited States: 3,729 citing papers, 29.6% of this breakdownChina: 989 citing papers, 7.9% of this breakdownUnited Kingdom: 924 citing papers, 7.3% of this breakdownGermany: 747 citing papers, 5.9% of this breakdownFrance: 563 citing papers, 4.5% of this breakdownCanada: 515 citing papers, 4.1% of this breakdownItaly: 493 citing papers, 3.9% of this breakdownNetherlands: 420 citing papers, 3.3% of this breakdownJapan: 366 citing papers, 2.9% of this breakdownAustralia: 287 citing papers, 2.3% of this breakdownSwitzerland: 271 citing papers, 2.2% of this breakdownSpain: 242 citing papers, 1.9% of this breakdown
0%29.6%Other 24.2%

Institutions

Fields

  • Biochemistry, Genetics and Molecular Biology42.7%
  • Medicine33.8%
  • Neuroscience14.7%
  • Immunology and Microbiology2.8%
  • Psychology2.2%
  • Nursing0.7%
  • Other3.1%

Topics

  • Genetics and Neurodevelopmental Disorders4.5%
  • Autism Spectrum Disorder Research3.7%
  • Genomics and Rare Diseases3%
  • Genomic variations and chromosomal abnormalities2.7%
  • Glioma Diagnosis and Treatment2.2%
  • Intracranial Aneurysms: Treatment and Complications2.1%
  • Other81.8%

Coauthors

All papers

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  1. 2-Hydroxyglutarate produced by neomorphic IDH mutations suppresses homologous recombination and induces PARP inhibitor sensitivity

    Authors: Parker L. Sulkowski, Christopher D. Corso, Nathaniel D. Robinson, Susan E. Scanlon, Karin Purshouse, Hanwen Bai, Yanfeng Liu, Ranjini K. Sundaram, Denise C. Hegan, Nathan R. Fons, G. Breuer, Yuanbin Song, Ketu Mishra-Gorur, Henk M. De Feyter, Robin A. de Graaf, Yulia V. Surovtseva, Maureen Kachman, Stephanie Halene, Murat Günel, Peter M. Glazer, Ranjit S. Bindra - Science Translational Medicine 2017 cited by 564

  2. De novo mutations revealed by whole-exome sequencing are strongly associated with autism

    Authors: Stephan Sanders, Michael T. Murtha, Abha R. Gupta, John D. Murdoch, Melanie J. Raubeson, A. Jeremy Willsey, A. Gulhan Ercan‐Sencicek, Nicholas M. DiLullo, Neelroop Parikshak, Jason L. Stein, Michael F. Walker, G Ober, Nicole A. Teran, Youeun Song, Paul El-Fishawy, Ryan Murtha, Murim Choi, John D. Overton, Robert Bjornson, Nicholas Carriero, Kyle A. Meyer, Kaya Bilgüvar, Shrikant Mane, Nenad Šestan, Richard P. Lifton, Murat Günel, Kathryn Roeder, Daniel H. Geschwind, Bernie Devlin, Matthew W. State - Nature 2012 cited by 2,183

  3. Impaired Amino Acid Transport at the Blood Brain Barrier Is a Cause of Autism Spectrum Disorder

    Authors: Dora C. Tărlungeanu, Elena Deliu, Christoph Dotter, Majdi Kara, Philipp Christoph Janiesch, Mariafrancesca Scalise, Michele Galluccio, Mateja Rybiczka-Tešulov, Emanuela Morelli, Fatma Müjgan Sönmez, Kaya Bilgüvar, Ryuichi Ohgaki, Yoshikatsu Kanai, Anide Johansen, Seham Esharif, Tawfeg Ben‐Omran, Meral Topçu, Avner Schlessinger, Cesare Indiveri, Kent E. Duncan, Ahmet Okay Çağlayan, Murat Günel, Joseph G. Gleeson, Gaia Novarino - Cell 2016 cited by 370

  4. Inflammation-dependent cerebrospinal fluid hypersecretion by the choroid plexus epithelium in posthemorrhagic hydrocephalus

    Authors: Jason K. Karimy, Jinwei Zhang, David B. Kurland, Brianna C. Theriault, Daniel Durán, Jesse A. Stokum, Charuta G. Furey, Xu Zhou, M. Shahid Mansuri, Julio D. Montejo, Alberto Vera, Michael L. DiLuna, Eric Delpire, Seth L. Alper, Murat Günel, Volodymyr Gerzanich, Ruslan Medzhitov, J. Marc Simard, Kristopher T. Kahle - Nature Medicine 2017 cited by 438

  5. The choroid plexus links innate immunity to CSF dysregulation in hydrocephalus

    Authors: Stephanie M. Robert, Benjamin C. Reeves, Emre Kiziltug, Phan Q. Duy, Jason K. Karimy, M. Shahid Mansuri, Arnaud Marlier, Garrett Allington, Ana B.W. Greenberg, Tyrone DeSpenza, Amrita Singh, Xue Zeng, Kedous Y. Mekbib, Adam J. Kundishora, Carol Nelson‐Williams, Le Hao, Jinwei Zhang, TuKiet T. Lam, Rashaun S. Wilson, William E. Butler, Michael L. DiLuna, Philip A. Feinberg, Dorothy P. Schafer, Kiavash Movahedi, Allen Tannenbaum, Sunil Koundal, Xinan Chen, Helene Benveniste, David D. Limbrick, Steven J. Schiff, Bob S. Carter, Murat Günel, J. Marc Simard, Richard P. Lifton, Seth L. Alper, Eric Delpire, Kristopher T. Kahle - Cell 2023 cited by 151

  6. Genomic Analysis of Non- NF2 Meningiomas Reveals Mutations in TRAF7 , KLF4 , AKT1 , and SMO

    Authors: 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 - Science 2013 cited by 904

  7. PD-1 marks dysfunctional regulatory T cells in malignant gliomas

    Authors: Daniel E. Lowther, Brittany A. Goods, Liliana E. Lucca, Benjamin A. Lerner, Khadir Raddassi, David van Dijk, Amanda Hernandez, Xiangguo Duan, Murat Günel, Vlad Coric, Smita Krishnaswamy, J. Christopher Love, David A. Hafler - JCI Insight 2016 cited by 265

  8. Correlations between genomic subgroup and clinical features in a cohort of more than 3000 meningiomas

    Authors: Mark W. Youngblood, Daniel Durán, Julio D. Montejo, Chang Li, Sacit Bulent Omay, Koray Özduman, Amar H. Sheth, Amy Zhao, Evgeniya Tyrtova, Danielle Miyagishima, Elena I. Fomchenko, Christopher S. Hong, Victoria Clark, Maximilien Riche, Matthieu Peyre, Julien Boetto, Sadaf Sohrabi, Sarah Koljaka, Jacob F. Baranoski, James Knight, Hongda Zhu, M. Necmettin Pamir, Timuçin Avşar, Türker Kılıç, Johannes Schramm, Marco Timmer, Roland Goldbrunner, Ye Gong, Yaşar Bayri, Nduka Amankulor, Ronald L. Hamilton, Kaya Bilgüvar, Irina Tikhonova, Patrick Tomak, Anita Hüttner, Matthias Simon, Boris Krischek, Michel Kalamarides, E. Zeynep Erson‐Omay, Jennifer Moliterno, Murat Günel - Journal of neurosurgery 2019 cited by 182

  9. The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities

    Authors: Jessica X. Chong, Kati J. Buckingham, Shalini N. Jhangiani, Corinne D. Boehm, Nara Sobreira, Joshua D. Smith, Tanya M. Harrell, Margaret J. McMillin, Wojciech Wiszniewski, Tomasz Gambin, Zeynep H. Coban Akdemir, Kimberly F. Doheny, Alan F. Scott, Dimitri Avramopoulos, Aravinda Chakravarti, Julie Hoover‐Fong, Debra Mathews, P. Dane Witmer, Hua Ling, Kurt N. Hetrick, Lee Watkins, Karynne Patterson, Frédéric Reinier, Elizabeth Blue, Donna M. Muzny, Martin Kircher, Kaya Bilgüvar, Francesc López‐Giráldez, V. Reid Sutton, Holly K. Tabor, Suzanne M. Leal, Murat Günel, Shrikant Mane, Richard A. Gibbs, Eric Boerwinkle, Ada Hamosh, Jay Shendure, James R. Lupski, Richard P. Lifton, David Valle, Deborah A. Nickerson, Michael J. Bamshad - The American Journal of Human Genetics 2015 cited by 688

  10. AAV-mediated direct in vivo CRISPR screen identifies functional suppressors in glioblastoma

    Authors: Ryan D. Chow, Christopher D. Guzman, Guangchuan Wang, Florian Schmidt, Mark W. Youngblood, Lupeng Ye, Youssef Errami, Matthew B. Dong, Michael A. Q. Martinez, Sensen Zhang, Paul Renauer, Kaya Bilgüvar, Murat Günel, Phillip A. Sharp, Feng Zhang, Randall J. Platt, Sidi Chen - Nature Neuroscience 2017 cited by 247

  11. Human Hypertension Caused by Mutations in WNK Kinases

    Authors: Frederick H. Wilson, Sandra Disse-Nicodème, Keith A. Choate, Kazuhiko Ishikawa, Carol Nelson‐Williams, Isabelle Desitter, Murat Günel, David V. Milford, Graham Lipkin, Jean‐Michel Achard, Morgan Feely, Bertrand Dussol, Yvon Berland, Robert J. Unwin, Haim Mayan, David B. Simon, Zvi Farfel, Xavier Jeunemaı̂tre, Richard P. Lifton - Science 2001 cited by 1,490

  12. Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas

    Authors: Victoria Clark, Akdes Serin Harmancı, Hanwen Bai, Mark W. Youngblood, Tong Ihn Lee, Jacob F. Baranoski, A. Gulhan Ercan‐Sencicek, Brian J. Abraham, Abraham S. Weintraub, Denes Hnisz, Matthias Simon, Boris Krischek, E. Zeynep Erson‐Omay, Octavian Henegariu, Geneive Carrión-Grant, Ketu Mishra-Gorur, Daniel Durán, Johanna Goldmann, Johannes Schramm, Roland Goldbrunner, Joseph M. Piepmeier, Alexander O. Vortmeyer, Jennifer Moliterno Günel, Kaya Bilgüvar, Katsuhito Yasuno, Richard A. Young, Murat Günel - Nature Genetics 2016 cited by 357

  13. Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus

    Authors: Sheng Chih Jin, Weilai Dong, Adam J. Kundishora, Shreyas Panchagnula, Andrés Moreno-De-Luca, Charuta G. Furey, August Allocco, Rebecca L. Walker, Carol Nelson‐Williams, Hannah Smith, Ashley Dunbar, Sierra Conine, Qiongshi Lu, Xue Zeng, Michael C. Sierant, James Knight, William Sullivan, Phan Q. Duy, Tyrone DeSpenza, Benjamin C. Reeves, Jason K. Karimy, Arnaud Marlier, Christopher Castaldi, Irina R. Tikhonova, Boyang Li, Helena Pérez‐Peña, James R. Broach, Edith Mbabazi Kabachelor, Peter Ssenyonga, Christine Hehnly, Ge Li, Boris Keren, Andrew T. Timberlake, June Goto, Francesco T. Mangano, James M. Johnston, William E. Butler, Benjamin C. Warf, Edward R. Smith, Steven J. Schiff, David D. Limbrick, Gregory G. Heuer, Eric M. Jackson, Bermans J. Iskandar, Shrikant Mane, Shozeb Haider, Bülent Güçlü, Yaşar Bayri, Yener Şahin, Charles C. Duncan, Michael L.J. Apuzzo, Michael L. DiLuna, Ellen J. Hoffman, Nenad Šestan, Laura R. Ment, Seth L. Alper, Kaya Bilgüvar, Daniel H. Geschwind, Murat Günel, Richard P. Lifton, Kristopher T. Kahle - Nature Medicine 2020 cited by 164

  14. Multiple Recurrent De Novo CNVs, Including Duplications of the 7q11.23 Williams Syndrome Region, Are Strongly Associated with Autism

    Authors: 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 - Neuron 2011 cited by 1,292

  15. Integrated genomic characterization of IDH1-mutant glioma malignant progression

    Authors: 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 - Nature Genetics 2015 cited by 350

  16. Associations of meningioma molecular subgroup and tumor recurrence

    Authors: Mark W. Youngblood, Danielle Miyagishima, Lan Jin, Trisha Gupte, Chang Li, Daniel Durán, Julio D. Montejo, Amy Zhao, Amar H. Sheth, Evgeniya Tyrtova, Koray Özduman, F. Iacoangeli, Matthieu Peyre, Julien Boetto, Matthew Pease, Timuçin Avşar, Anita Hüttner, Kaya Bilgüvar, Türker Kılıç, M. Necmettin Pamir, Nduka Amankulor, Michel Kalamarides, E. Zeynep Erson‐Omay, Murat Günel, Jennifer Moliterno - Neuro-Oncology 2020 cited by 179

  17. Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy

    Authors: Sattar Khoshkhoo, Yilan Wang, Yasmine Chahine, E. Zeynep Erson‐Omay, Stephanie M. Robert, Emre Kiziltug, Eyiyemisi C. Damisah, Carol Nelson‐Williams, Guangya Zhu, Wenna Kong, August Yue Huang, Edward Stronge, H. Westley Phillips, Brian H. Chhouk, Sara Bizzotto, Ming Hui Chen, Thiuni N. Adikari, Zimeng Ye, Tom Witkowski, Dulcie Lai, Nadine Lee, Julie Lokan, Ingrid E. Scheffer, Samuel F. Berkovic, Shozeb Haider, Michael S. Hildebrand, Edward Yang, Murat Günel, Richard P. Lifton, R. Mark Richardson, Ingmar Blümcke, Sanda Alexandrescu, Anita Hüttner, Erin L. Heinzen, Jidong Zhu, Annapurna Poduri, Nihal DeLanerolle, Dennis D. Spencer, Eunjung Alice Lee, Christopher A. Walsh, Kristopher T. Kahle - JAMA Neurology 2023 cited by 74

  18. Exome Sequencing Links Corticospinal Motor Neuron Disease to Common Neurodegenerative Disorders

    Authors: Gaia Novarino, Ali G. Fenstermaker, Maha S. Zaki, Matan Hofree, Jennifer L. Silhavy, Andrew Heiberg, Mostafa Abdellateef, Başak Rosti, Eric Scott, Lobna Mansour, Amira Masri, Hülya Kayserili, Jumana Y. Al‐Aama, Ghada M. H. Abdel‐Salam, Ariana Karminejad, Majdi Kara, Bülent Kara, Bita Bozorgmehri, Tawfeg Ben‐Omran, Faezeh Mojahedi, Iman G. Mahmoud, Naïma Bouslam, Ahmed Bouhouche, Ali Benomar, Sylvain Hanein, Laure Raymond, Sylvie Forlani, Massimo Mascaro, Laila Selim, Nabil Shehata, Nasir Al‐Allawi, Parayil Sankaran Bindu, Matloob Azam, Murat Günel, Ahmet Okay Çağlayan, Kaya Bilgüvar, Aslıhan Tolun, Mahmoud Y. Issa, Jana Schroth, Emily Spencer, Rasim Özgür Rosti, Naiara Akizu, Keith K. Vaux, Anide Johansen, Alice A. Koh, Hisham Megahed, Alexandra Dürr, Alexis Brice, Giovanni Stévanin, Stacy Gabriel, Trey Ideker, Joseph G. Gleeson - Science 2014 cited by 548

  19. CLP1 Founder Mutation Links tRNA Splicing and Maturation to Cerebellar Development and Neurodegeneration

    Authors: Ashleigh E. Schaffer, Veerle Rc Eggens, Ahmet Okay Çağlayan, Miriam S. Reuter, Eric Scott, Nicole G. Coufal, Jennifer L. Silhavy, Yuanchao Xue, Hülya Kayserili, Katsuhito Yasuno, Rasim Özgür Rosti, Mostafa Abdellateef, Caner Çağlar, Paul R. Kasher, J. Leonie Cazemier, Marian A. J. Weterman, Vincent Cantagrel, Na Cai, Christiane Zweier, Umut Altunoğlu, N. Bilge Satkin, Fesih Aktar, Beyhan Tüysüz, Cengiz Yalçınkaya, Hüseyîn Çaksen, Kaya Bilgüvar, Xiang‐Dong Fu, Christopher R. Trotta, Stacey Gabriel, André Reis, Murat Günel, Frank Baas, Joseph G. Gleeson - Cell 2014 cited by 284

  20. De Novo Mutation in Genes Regulating Neural Stem Cell Fate in Human Congenital Hydrocephalus

    Authors: Charuta G. Furey, Jungmin Choi, Sheng Chih Jin, Xue Zeng, Andrew T. Timberlake, Carol Nelson‐Williams, M. Shahid Mansuri, Qiongshi Lu, Daniel Durán, Shreyas Panchagnula, August Allocco, Jason K. Karimy, Arjun Khanna, Jonathan Gaillard, Tyrone DeSpenza, Prince Antwi, Erin Loring, William E. Butler, Edward R. Smith, Benjamin C. Warf, Jennifer M. Strahle, David D. Limbrick, Phillip B. Storm, Gregory G. Heuer, Eric M. Jackson, Bermans J. Iskandar, James M. Johnston, Irina Tikhonova, Christopher Castaldi, Francesc López‐Giráldez, Robert Bjornson, James Knight, Kaya Bilgüvar, Shrikant Mane, Seth L. Alper, Shozeb Haider, Bülent Güçlü, Yaşar Bayri, Yener Şahin, Michael L.J. Apuzzo, Charles C. Duncan, Michael L. DiLuna, Murat Günel, Richard P. Lifton, Kristopher T. Kahle - Neuron 2018 cited by 162

  21. Integrated genomic analyses of de novo pathways underlying atypical meningiomas

    Authors: Akdes Serin Harmancı, Mark W. Youngblood, Victoria Clark, Süleyman Coşkun, Octavian Henegariu, Daniel Durán, E. Zeynep Erson‐Omay, Leon D. Kaulen, Tong Ihn Lee, Brian J. Abraham, Matthias Simon, Boris Krischek, Marco Timmer, Roland Goldbrunner, Sacit Bulent Omay, Jacob F. Baranoski, Burçin Baran, Geneive Carrión-Grant, Hanwen Bai, Ketu Mishra-Gorur, Johannes Schramm, Jennifer Moliterno, Alexander O. Vortmeyer, Kaya Bilgüvar, Katsuhito Yasuno, Richard A. Young, Murat Günel - Nature Communications 2017 cited by 217

  22. Insights into genetics, human biology and disease gleaned from family based genomic studies

    Authors: Jennifer E. Posey, Anne O’Donnell‐Luria, Jessica X. Chong, Tamar Harel, Shalini N. Jhangiani, Zeynep H. Coban Akdemir, Steven Buyske, Davut Pehli̇van, Claudia M.B. Carvalho, Samantha Baxter, Nara Sobreira, Pengfei Liu, Nan Wu, Jill A. Rosenfeld, Sushant Kumar, Dimitri Avramopoulos, Janson J. White, Kimberly F. Doheny, P. Dane Witmer, Corinne D. Boehm, V. Reid Sutton, Donna M. Muzny, Eric Boerwinkle, Murat Günel, Deborah A. Nickerson, Shrikant Mane, Daniel G. MacArthur, Richard A. Gibbs, Ada Hamosh, Richard P. Lifton, Tara C. Matise, Heidi L. Rehm, Mark Gerstein, Michael J. Bamshad, David Valle, James R. Lupski - Genetics in Medicine 2019 cited by 211

  23. Genome-wide association study identifies susceptibility loci for IgA nephropathy

    Authors: 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 - Nature Genetics 2011 cited by 624

  24. PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans

    Authors: Tanyeri Barak, Emma Ristori, A. Gulhan Ercan‐Sencicek, Danielle Miyagishima, Carol Nelson‐Williams, Weilai Dong, Sheng Chih Jin, Andrew Prendergast, William Armero, Octavian Henegariu, E. Zeynep Erson‐Omay, Akdes Serin Harmancı, Mikhael Guy, Batur Gültekin, Deniz Kılıç, Devendra K. Rai, Nükte Göç, Stephanie Marie Aguilera, Burcu Gülez, Selin Altınok, Kent Ozcan, Yanki Yarman, Süleyman Coşkun, Emily Sempou, Engin Deniz, Jared Hintzen, Andy Cox, Elena I. Fomchenko, Su Woong Jung, Ali K. Ozturk, Angeliki Louvi, Kaya Bilgüvar, E. Sander Connolly, Mustafa K. Khokha, Kristopher T. Kahle, Katsuhito Yasuno, Richard P. Lifton, Ketu Mishra-Gorur, Stefania Nicoli, Murat Günel - Nature Medicine 2021 cited by 61