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Author Details

Murat Gunel
Yale School of Medicine
1993
193
60
Richard Andrew Taylor (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
35901838Cross-platform analysis reveals cellular and molecular landscape of glioblastoma invasion.Neuro Oncol2023
37805627Super-enhancer hijacking drives ectopic expression of hedgehog pathway ligands in meningiomas.Nat Commun2023
37978175Mutation of key signaling regulators of cerebrovascular development in vein of Galen malformations.Nat Commun2023
37126322Contribution of Somatic Ras/Raf/Mitogen-Activated Protein Kinase Variants in the Hippocampus in Drug-Resistant Mesial Temporal Lobe Epilepsy.JAMA Neurol2023
36993588Genetic dysregulation of an endothelial Ras signaling network in vein of Galen malformations.bioRxiv2023
37287582The clinical and genomic features of seizures in meningiomas.Neurooncol Adv2023
37043537Pleiotropic role of TRAF7 in skull-base meningiomas and congenital heart disease.Proc Natl Acad Sci U S A2023
37243565A systematic review and individual participant data meta-analysis of gonadal steroid hormone receptors in meningioma.J Neurosurg2023
37243548Clinical and genomic differences in supratentorial versus infratentorial NF2 mutant meningiomas.J Neurosurg2023
36880509Vascular steal and associated intratumoral aneurysms in highly vascular brain tumors: illustrative case.J Neurosurg Case Lessons2023
36879130Multiomic analyses implicate a neurodevelopmental program in the pathogenesis of cerebral arachnoid cysts.Nat Med2023
36399134Biallelic PRMT7 pathogenic variants are associated with a recognizable syndromic neurodevelopmental disorder with short stature, obesity, and craniofacial and digital abnormalities.Genet Med2023
36803604The choroid plexus links innate immunity to CSF dysregulation in hydrocephalus.Cell2023
36418843Hormone therapies in meningioma-where are we?J Neurooncol2023
34846640The integrated multiomic diagnosis of sporadic meningiomas: a review of its clinical implications.J Neurooncol2022
35481623Mutation spectrum of congenital heart disease in a consanguineous Turkish population.Mol Genet Genomic Med2022
35803280Interferon-γ resistance and immune evasion in glioma develop via Notch-regulated co-evolution of malignant and immune cells.Dev Cell2022
35698142Correction: Genomic profiling of sporadic multiple meningiomas.BMC Med Genomics2022
35568945Genomic profiling of sporadic multiple meningiomas.BMC Med Genomics2022
34967924Correction to: The integrated multiomic diagnosis of sporadic meningiomas: a review of its clinical implications.J Neurooncol2022
35338243Biallelic BICD2 variant is a novel candidate for Cohen-like syndrome.J Hum Genet2022
34709661Genetically Determined Low-Density Lipoprotein Cholesterol and Risk of Subarachnoid Hemorrhage.Ann Neurol2022
32764695METAP1 mutation is a novel candidate for autosomal recessive intellectual disability.J Hum Genet2021
33788846Clinical characteristics and outcomes for 7,995 patients with SARS-CoV-2 infection.PLoS One2021
33585216A Quantitative Assessment of Pre-Operative MRI Reports in Glioma Patients: Report Metrics and IDH Prediction Ability.Front Oncol2021
33914067Targeting the CSF1/CSF1R axis is a potential treatment strategy for malignant meningiomas.Neuro Oncol2021
34887573PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans.Nat Med2021
34426522The genetic structure of the Turkish population reveals high levels of variation and admixture.Proc Natl Acad Sci U S A2021
34350560Type of bony involvement predicts genomic subgroup in sphenoid wing meningiomas.J Neurooncol2021
34125151DIAPH1 Variants in Non-East Asian Patients With Sporadic Moyamoya Disease.JAMA Neurol2021
33433624Neuroinvasion of SARS-CoV-2 in human and mouse brain.J Exp Med2021
33393633Spatially Resolved and Quantitative Analysis of the Immunological Landscape in Human Meningiomas.J Neuropathol Exp Neurol2021
33481259Exome sequencing identifies SLIT2 variants in primary CNS lymphoma.Br J Haematol2021
33440997Genetically Determined Smoking Behavior and Risk of Nontraumatic Subarachnoid Hemorrhage.Stroke2021
32553282Molecular genetics of meningiomas.Handb Clin Neurol2020
32025832A quantitative model based on clinically relevant MRI features differentiates lower grade gliomas and glioblastoma.Eur Radiol2020
31820119Loss of UGP2 in brain leads to a severe epileptic encephalopathy, emphasizing that bi-allelic isoform-specific start-loss mutations of essential genes can cause genetic diseases.Acta Neuropathol2020
33276341Clinical and genomic factors associated with seizures in meningiomas.J Neurosurg2020
33077954Exome sequencing implicates genetic disruption of prenatal neuro-gliogenesis in sporadic congenital hydrocephalus.Nat Med2020
32743602Clinical Characteristics and Outcomes for 7,995 Patients with SARS-CoV-2 Infection.medRxiv2020
32739502Genomic alterations in Turcot syndrome: Insights from whole exome sequencing.J Neurol Sci2020
32935108Neuroinvasion of SARS-CoV-2 in human and mouse brain.bioRxiv2020
32152743Correction to: A quantitative model based on clinically relevant MRI features differentiates lower grade gliomas and glioblastoma.Eur Radiol2020
32277781Genetically Elevated LDL Associates with Lower Risk of Intracerebral Hemorrhage.Ann Neurol2020
30487245MAB21L1 loss of function causes a syndromic neurodevelopmental disorder with distinctive <i>c</i>erebellar, <i>o</i>cular, cranio<i>f</i>acial and <i>g</i>enital features (COFG syndrome).J Med Genet2019
31616254Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in <i>ATP1A3</i>.Front Cell Neurosci2019
30911252Serum Prolidase Enzyme Activity Level: Not a Predictive Biomarker for Epilepsy.Eurasian J Med2019
30578106Mutations in Chromatin Modifier and Ephrin Signaling Genes in Vein of Galen Malformation.Neuron2019
28621624Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas.J Neurosurg2018
30178464Loss of Protocadherin-12 Leads to Diencephalic-Mesencephalic Junction Dysplasia Syndrome.Ann Neurol2018
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Collaborators

Kaya Bilguvar
Acibadem Mehmet Ali Aydinlar University
Co-authored papers 79
Richard P Lifton
The Rockefeller University
Co-authored papers 52
Shrikant Mane
Yale School of Medicine
Co-authored papers 32
Ahmet Okay Caglayan
Yale School of Medicine
Co-authored papers 27
Matthew W State
UCSF Weill Institute for Neurosciences, University of California san francisco
Co-authored papers 21
Beyhan T??ys??z
Istanbul University-Cerrahpasa
Co-authored papers 19
Joseph G Gleeson
University of California
Co-authored papers 16
Mark W Youngblood
Co-authored papers 16
Akdes Serin Harmanci
Co-authored papers 15
Maha S Zaki
Human Genetics and Genome Research Institute, National Research Centre
Co-authored papers 12
Nenad Sestan
Yale School of Medicine
Co-authored papers 12
Rasim O Rosti
University of Virginia
Co-authored papers 12
Jennifer L Silhavy
University of California
Co-authored papers 9
Seth L Alper
Beth Israel Deaconess Medical Center RN380F
Co-authored papers 9
Stacey Gabriel
Broad Institute of MIT and Harvard
Co-authored papers 9
H??lya Kayserili
Istanbul University
Co-authored papers 8
Christopher E Mason
Feil Family Brain and Mind Research Institute.
Co-authored papers 8
Eric Scott
Rady Children's Institute for Genomic Medicine, University of California
Co-authored papers 8
Declan McGuone
Smilow Cancer Hospital
Co-authored papers 7
Jana Schroth
University of California
Co-authored papers 7
Alexander O Vortmeyer
Indiana University School of Medicine
Co-authored papers 7
Christopher Castaldi
Yale Center for Genome Analysis, Yale School of Medicine
Co-authored papers 7
Shozeb Haider
Co-authored papers 7
Stephan J Sanders
Co-authored papers 6
Tawfeg Ben-Omran
Hamad Medical Corporation.
Co-authored papers 6
Basak Rosti
Howard Hughes Medical Institute, The Rockefeller University
Co-authored papers 6
Naiara Akizu
University of Pennsylvania
Co-authored papers 6
Neil C Chi
University of California San Diego
Co-authored papers 5
Daniel H Geschwind
University of California los angeles
Co-authored papers 5
William B Dobyns
University of Minnesota
Co-authored papers 5
Release 1.2