Murat Günel

26.6k citations

135 papers · 6.6k indexed · 1 hit paper · h-index 43

Impact in

Neurology top 0.2%
- Intracranial Aneurysms: Treatment and Complications
- Vascular Malformations Diagnosis and Treatment
- Intracerebral and Subarachnoid Hemorrhage Research
- Traumatic Brain Injury and Neurovascular Disturbances
Molecular Biology top 5%
- Ion Transport and Channel Regulation

Papers in

Neurology 59
- Intracranial Aneurysms: Treatment and Complications 40
- Vascular Malformations Diagnosis and Treatment 33
- Intracerebral and Subarachnoid Hemorrhage Research 26
Genetics 15
- Glioma Diagnosis and Treatment 10
- Connective tissue disorders research 9

Co-authors: Richard P. Lifton Kaya Bilgüvar Issam A. Awad Carol Nelson‐Williams Angeliki Louvi Michael L. DiLuna Bauer E. Sumpio Alexander Nixon
Journals: Neurosurgery (17 papers)Proceedings of the National Academy of Sciences (9 papers)Journal of neurosurgery (7 papers)The American Journal of Human Genetics (5 papers)Stroke (5 papers)
Partner nations: United States Türkiye United Kingdom

In The Last Decade

Murat Günel

131 papers receiving 6.5k citations

Hit Papers

align trajectories log scale

Human Hypertension Caused by Mutations in WNK Kinases 2001 · 1.1k citations

Peers

Countries citing papers authored by Murat Günel

Since Specialization

Citations

This map shows the geographic impact of Murat Günel's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Murat Günel with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Murat Günel more than expected).

Fields of papers citing papers by Murat Günel

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Murat Günel. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Murat Günel. The network helps show where Murat Günel may publish in the future.

Co-authors

The 25 scholars most cited alongside Murat Günel, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Murat Günel Line = papers co-authored together Murat Günel links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Characterizing Stroke Clots Using Single‐Cell Sequencing Journal of the American Heart Association ·Daniela Renedo, Tanyeri Barak, Jonathan H. DeLong, Julián Acosta, Nanthiya Sujijantarat, Andrew B. Koo, Cyprien Rivier, Santiago Clocchiatti‐Tuozzo, Shufan Huo, Joseph Antonios, James Giles, Guido J. Falcone, Kevin N. Sheth, Ryan Hebert, Murat Günel, Lauren Sansing, Dhasakumar Navaratnam, Charles Matouk	2025	0
2	Impact of Social Determinants of Health on Outcomes of Nontraumatic Subarachnoid Hemorrhage Journal of the American Heart Association ·Daniela Renedo, Cyprien Rivier, Andrew B. Koo, Santiago Clocchiatti‐Tuozzo, Shufan Huo, Nanthiya Sujijantarat, Victor M Torres Lopez, Ryan Hebert, Lee H. Schwamm, Adam de Havenon, Murat Günel, Charles Matouk, Guido J. Falcone, Kevin N. Sheth	2025	0
3	Biallelic BICD2 variant is a novel candidate for Cohen-like syndrome Journal of Human Genetics ·Ahmet Okay Çağlayan, Beyhan Tüysüz, Ece Gül, Dilek Uludağ Alkaya, Cengiz Yalçınkaya, Joseph G. Gleeson, Kaya Bilgüvar, Murat Günel	2022	2
4	The genetic structure of the Turkish population reveals high levels of variation and admixture Proceedings of the National Academy of Sciences ·Meltem Ece Kars, A. Nazlı Başak, Onur Emre Onat, Kaya Bilgüvar, Jungmin Choi, Yuval Itan, Caner Çağlar, Robin Palvadeau, Jean‐Laurent Casanova, D.N. Cooper, Peter D. Stenson, Alper Yavuz, Hakan Buluş, Murat Günel, Jeffrey M. Friedman, Tayfun Özçelık	2021	47
5	METAP1 mutation is a novel candidate for autosomal recessive intellectual disability Journal of Human Genetics ·Ahmet Okay Çağlayan, Fesih Aktar, Kaya Bilgüvar, Jacob F. Baranoski, Gozde Akgumus, Akdes Serin Harmancı, Emine Zeynep Erson-Omay, Katsuhito Yasuno, Hüseyîn Çaksen, Murat Günel	2020	1
6	De novo MYH9 mutation in congenital scalp hemangioma Molecular Case Studies ·Elena I. Fomchenko, Daniel Durán, Sheng Chih Jin, Weilai Dong, E. Zeynep Erson‐Omay, Prince Antwi, August Allocco, Jonathan Gaillard, Anita Hüttner, Murat Günel, Michael L. DiLuna, Kristopher T. Kahle	2018	7
7	Inflammation-dependent cerebrospinal fluid hypersecretion by the choroid plexus epithelium in posthemorrhagic hydrocephalus Nature Medicine ·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	2017	253
8	Exome analysis of the evolutionary path of hepatocellular adenoma-carcinoma transition, vascular invasion and brain dissemination Journal of Hepatology ·Sílvia Vilarinho, E. Zeynep Erson‐Omay, Kisha Mitchell-Richards, Charles Cha, Carol Nelson‐Williams, Akdes Serin Harmancı, Katsuhito Yasuno, Murat Günel, Tamar H. Taddei	2017	8
9	Digenic mutations of human OCRL paralogs in Dent’s disease type 2 associated with Chiari I malformation Human Genome Variation ·Daniel Durán, Sheng Chih Jin, Tyrone DeSpenza, Carol Nelson‐Williams, Andrea G. Cogal, Elizabeth W. Abrash, Peter C. Harris, John C. Lieske, Serena Shimshak, Shrikant Mane, Kaya Bilgüvar, Michael L. DiLuna, Murat Günel, Richard P. Lifton, Kristopher T. Kahle	2016	9
10	A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP Journal of Human Genetics ·Ahmet Okay Çağlayan, Beyhan Tüysüz, Süleyman Coşkun, Jennifer L. Quon, Akdes Serin Harmancı, Jacob F. Baranoski, Burçin Baran, E. Zeynep Erson‐Omay, Octavian Henegariu, Shrikant Mane, Kaya Bilgüvar, Katsuhito Yasuno, Murat Günel	2016	13
11	Spondyloepimetaphyseal dysplasia Pakistani type: Expansion of the phenotype American Journal of Medical Genetics Part A ·Beyhan Tüysüz, Saliha Yılmaz, Ece Gül, Luis Kolb, Kaya Bilgüvar, Olcay Evliyaoğlu, Murat Günel	2013	16
12	Vessel Wall Magnetic Resonance Imaging Identifies the Site of Rupture in Patients With Multiple Intracranial Aneurysms Neurosurgery ·Charles Matouk, Daniel M. Mandell, Murat Günel, Ketan R. Bulsara, Ajay Malhotra, Ryan Hebert, Michele H. Johnson, David J. Mikulis, Frank J. Minja	2012	173
13	Loss of cerebral cavernous malformation 3 ( Ccm3 ) in neuroglia leads to CCM and vascular pathology Proceedings of the National Academy of Sciences ·Angeliki Louvi, Leiling Chen, Aimee Two, Haifeng Zhang, Min Wang, Murat Günel	2011	81
14	Complications from cervical intra-arterial heroin injection: Figure 1 BMJ Case Reports ·Michael L. DiLuna, Mohamad Bydon, Murat Günel, Michele H. Johnson	2009	1
15	COL4A1 Mutation in Preterm Intraventricular Hemorrhage The Journal of Pediatrics ·Kaya Bilgüvar, Michael L. DiLuna, Matthew J. Bizzarro, Yaşar Bayri, Karen Schneider, Richard P. Lifton, Murat Günel, Laura R. Ment	2009	47
16	PDCD10, THE GENE MUTATED IN CEREBRAL CAVERNOUS MALFORMATION 3, IS EXPRESSED IN THE NEUROVASCULAR UNIT Neurosurgery ·Gamze Tanrιöver, Arianne Boylan, Michael L. DiLuna, Katie L. Pricola, Angeliki Louvi, Murat Günel	2008	30
17	KRIT1/Cerebral Cavernous Malformation 1 Protein Localizes to Vascular Endothelium, Astrocytes, and Pyramidal Cells of the Adult Human Cerebral Cortex Neurosurgery ·Ozlem Guzeloglu‐Kayisli, (unknown), Jennifer Voorhees, Güven Lüleci, Richard P. Lifton, Murat Günel	2004	48
18	Clinicopathological Review: Giant Intraventricular Cavernous Malformation Neurosurgery ·Richard C. E. Anderson, E. Sander Connolly, Koray Özduman, Maxwell Laurans, Murat Günel, Alexander G. Khandji, Phyllis L. Faust, Michael B. Sisti	2003	22
19	Human Hypertension Caused by Mutations in WNK Kinases Science ·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 Hit paper breakdown →	2001	1114
20	Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15-13 and 3q25.2-27 Human Molecular Genetics ·Holly Duncan Craig, Murat Günel, Obed M. Cepeda, Eric W. Johnson, Louis J. Ptáček, Gary K. Steinberg, Christopher S. Ogilvy, Michel J. Berg, Steve Crawford, R. Michael Scott, Elisabeth Steichen‐Gersdorf, R.A. Sabroe, Claire Kennedy, Gabrielle Mettler, M Beis, Alan Fryer, Issam A. Awad, Richard P. Lifton	1998	253

About Murat Günel

Murat Günel is a scholar working on Neurology, Genetics, Genetics, Health Informatics and Rheumatology, having authored 135 papers that have together received 6.6k indexed citations. Recurring topics across this work include Intracranial Aneurysms: Treatment and Complications (40 papers), Vascular Malformations Diagnosis and Treatment (33 papers), Intracerebral and Subarachnoid Hemorrhage Research (26 papers), Meningioma and schwannoma management (14 papers), Glioma Diagnosis and Treatment (10 papers), Connective tissue disorders research (9 papers), Fetal and Pediatric Neurological Disorders (8 papers) and Moyamoya disease diagnosis and treatment (8 papers). The work is most often cited by research in Neurology (2.6k citations), Neurology (320 citations), Molecular Biology (2.5k citations), Genetics (982 citations) and Cellular and Molecular Neuroscience (563 citations). Murat Günel has collaborated with scholars based in United States, Türkiye and United Kingdom. Frequent co-authors include Richard P. Lifton, Kaya Bilgüvar, Issam A. Awad, Carol Nelson‐Williams, Angeliki Louvi, Michael L. DiLuna, Bauer E. Sumpio, Alexander Nixon, Isabelle Desitter and Bertrand Dussol. Their work appears in journals such as Neurosurgery, Proceedings of the National Academy of Sciences, Journal of neurosurgery, The American Journal of Human Genetics and Stroke.

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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