Murat Günel

1995–2025 年に発表

107
論文数
24,128
被引用数
78
h 指数
105
i10 指数

被引用数

Murat Günel の年別被引用数1955 年: 被引用 1 件1987 年: 被引用 1 件1989 年: 被引用 2 件1994 年: 被引用 2 件1995 年: 被引用 1 件1996 年: 被引用 6 件1997 年: 被引用 2 件1998 年: 被引用 12 件1999 年: 被引用 21 件2000 年: 被引用 16 件2001 年: 被引用 15 件2002 年: 被引用 30 件2003 年: 被引用 46 件2004 年: 被引用 48 件2005 年: 被引用 54 件2006 年: 被引用 71 件2007 年: 被引用 82 件2008 年: 被引用 90 件2009 年: 被引用 116 件2010 年: 被引用 125 件2011 年: 被引用 175 件2012 年: 被引用 277 件2013 年: 被引用 335 件2014 年: 被引用 353 件2015 年: 被引用 287 件2016 年: 被引用 246 件2017 年: 被引用 310 件2018 年: 被引用 320 件2019 年: 被引用 815 件2020 年: 被引用 1,031 件2021 年: 被引用 1,173 件2022 年: 被引用 649 件2023 年: 被引用 467 件2024 年: 被引用 713 件2025 年: 被引用 252 件2026 年: 被引用 12 件1956〜1986 年は被引用が無いため表示していません1988 年は被引用が無いため表示していません1990〜1993 年は被引用が無いため表示していません

引用元

国・地域

この著者を引用した国・地域の世界地図アメリカ合衆国: 引用元論文 3,729 件、この内訳の 29.6%中国: 引用元論文 989 件、この内訳の 7.9%イギリス: 引用元論文 924 件、この内訳の 7.3%ドイツ: 引用元論文 747 件、この内訳の 5.9%フランス: 引用元論文 563 件、この内訳の 4.5%カナダ: 引用元論文 515 件、この内訳の 4.1%イタリア: 引用元論文 493 件、この内訳の 3.9%オランダ: 引用元論文 420 件、この内訳の 3.3%日本: 引用元論文 366 件、この内訳の 2.9%オーストラリア: 引用元論文 287 件、この内訳の 2.3%スイス: 引用元論文 271 件、この内訳の 2.2%スペイン: 引用元論文 242 件、この内訳の 1.9%
0%29.6%その他 24.2%

分野

  • Biochemistry, Genetics and Molecular Biology42.7%
  • Medicine33.8%
  • Neuroscience14.7%
  • Immunology and Microbiology2.8%
  • Psychology2.2%
  • Nursing0.7%
  • その他3.1%

トピック

  • 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%
  • その他81.8%

共著者

全論文

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

    著者: , , , , , , , , , , , , , , , , , , , , - Science Translational Medicine 2017 被引用: 564

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature 2012 被引用: 2,183

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , - Cell 2016 被引用: 370

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

    著者: , , , , , , , , , , , , , , , , , , - Nature Medicine 2017 被引用: 438

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Bob S. Carter, Murat Günel, J. Marc Simard, Richard P. Lifton, Seth L. Alper, Eric Delpire, Kristopher T. Kahle - Cell 2023 被引用: 151

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 904

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

    著者: , , , , , , , , , , , , - JCI Insight 2016 被引用: 265

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 182

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 688

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

    著者: , , , , , , , , , , , , , , , , - Nature Neuroscience 2017 被引用: 247

  11. Human Hypertension Caused by Mutations in WNK Kinases

    著者: , , , , , , , , , , , , , , , , , , - Science 2001 被引用: 1,490

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Genetics 2016 被引用: 357

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 164

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 1,292

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Alexander O. Vortmeyer, Kaya Bilgüvar, Katsuhito Yasuno, Murat Günel - Nature Genetics 2015 被引用: 350

  16. Associations of meningioma molecular subgroup and tumor recurrence

    著者: , , , , , , , , , , , , , , , , , , , , , , , , - Neuro-Oncology 2020 被引用: 179

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 74

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 548

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Murat Günel, Frank Baas, Joseph G. Gleeson - Cell 2014 被引用: 284

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 162

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , - Nature Communications 2017 被引用: 217

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , Tara C. Matise, Heidi L. Rehm, Mark Gerstein, Michael J. Bamshad, David Valle, James R. Lupski - Genetics in Medicine 2019 被引用: 211

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 624

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

    著者: , , , , , , , , , , , , , , , , , , , , , , , , , , , , , , 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 被引用: 61