SomatiCA: Identifying, Characterizing and Quantifying Somatic Copy Number Aberrations from Cancer Genome Sequencing Data

por Chen, Mengjie, Gunel, Murat, Zhao, Hongyu
Publicado 2013

Functional Synergy between Cholecystokinin Receptors CCKAR and CCKBR in Mammalian Brain Development

por Nishimura, Sayoko, Bilgüvar, Kaya, Ishigame, Keiko, Sestan, Nenad, Günel, Murat, Louvi, Angeliki
Publicado 2015

A Quantitative Assessment of Pre-Operative MRI Reports in Glioma Patients: Report Metrics and IDH Prediction Ability

por Cao, Hang, Erson-Omay, E. Zeynep, Günel, Murat, Moliterno, Jennifer, Fulbright, Robert K.
Publicado 2021

Biallelic BICD2 Variant is a Novel Candidate for Cohen-Like Syndrome

por Caglayan, Ahmet Okay, Tuysuz, Beyhan, Gül, Ece, Alkaya, Dilek Uludag, Yalcinkaya, Cengiz, Gleeson, Joseph G., Bilguvar, Kaya, Gunel, Murat
Publicado 2022

9p24 triplication in syndromic hydrocephalus with diffuse villous hyperplasia of the choroid plexus

por Furey, Charuta, Antwi, Prince, Duran, Daniel, Timberlake, Andrew T., Nelson-Williams, Carol, Matouk, Charles C., DiLuna, Michael L., Günel, Murat, Kahle, Kristopher T.
Publicado 2018

Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (CACP) syndrome

por Yilmaz, Saliha, Uludağ Alkaya, Dilek, Kasapçopur, Özgür, Barut, Kenan, Akdemir, Ekin S., Celen, Cemre, Youngblood, Mark W., Yasuno, Katsuhito, Bilguvar, Kaya, Günel, Murat, Tüysüz, Beyhan
Publicado 2018

METAP1 Mutation Is a Novel Candidate for Autosomal Recessive Intellectual Disability

por Caglayan, Ahmet Okay, Aktar, Fesih, Bilguvar, Kaya, Baranoski, Jacob F., Akgumus, Gozde Tugce, Harmanci, Akdes Serin, Erson-Omay, Emine Zeynep, Yasuno, Katsuhito, Caksen, Huseyin, Gunel, Murat
Publicado 2020

The integrated multiomic diagnosis of sporadic meningiomas: a review of its clinical implications

por Robert, Stephanie M., Vetsa, Shaurey, Nadar, Arushii, Vasandani, Sagar, Youngblood, Mark W., Gorelick, Evan, Jin, Lan, Marianayagam, Neelan, Erson-Omay, E Zeynep, Günel, Murat, Moliterno, Jennifer
Publicado 2021

Correction to: The integrated multiomic diagnosis of sporadic meningiomas: a review of its clinical implications

por Robert, Stephanie M., Vetsa, Shaurey, Nadar, Arushii, Vasandani, Sagar, Youngblood, Mark W., Gorelick, Evan, Jin, Lan, Marianayagam, Neelan, Erson-Omay, E Zeynep, Günel, Murat, Moliterno, Jennifer
Publicado 2021

Functional differences between PD-1(+) and PD-1(-) CD4(+) effector T cells in healthy donors and patients with glioblastoma multiforme

por Goods, Brittany A., Hernandez, Amanda L., Lowther, Daniel E., Lucca, Liliana E., Lerner, Benjamin A., Gunel, Murat, Raddassi, Khadir, Coric, Vlad, Hafler, David A., Love, J. Christopher
Publicado 2017

Disruptions in asymmetric centrosome inheritance and WDR62-Aurora kinase B interactions in primary microcephaly

por Sgourdou, Paraskevi, Mishra-Gorur, Ketu, Saotome, Ichiko, Henagariu, Octavian, Tuysuz, Beyhan, Campos, Cynthia, Ishigame, Keiko, Giannikou, Krinio, Quon, Jennifer L., Sestan, Nenad, Caglayan, Ahmet O., Gunel, Murat, Louvi, Angeliki
Publicado 2017

Mutation spectrum of congenital heart disease in a consanguineous Turkish population

por Dong, Weilai, Kaymakcalan, Hande, Jin, Sheng Chih, Diab, Nicholas S., Tanıdır, Cansaran, Yalcin, Ali Seyfi Yalim, Ercan‐Sencicek, A. Gulhan, Mane, Shrikant, Gunel, Murat, Lifton, Richard P., Bilguvar, Kaya, Brueckner, Martina
Publicado 2022

ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features

por Çağlayan, Ahmet Okay, Sezer, Rabia Gonul, Kaymakçalan, Hande, Ulgen, Ege, Yavuz, Taner, Baranoski, Jacob F., Bozaykut, Abdulkadir, Harmanci, Akdes Serin, Yalcin, Yalim, Youngblood, Mark W., Yasuno, Katsuhito, Bilgüvar, Kaya, Gunel, Murat
Publicado 2017

De novo MYH9 mutation in congenital scalp hemangioma

por Fomchenko, Elena I., Duran, Daniel, Jin, Sheng Chih, Dong, Weilai, Erson-Omay, E. Zeynep, Antwi, Prince, Allocco, August, Gaillard, Jonathan R., Huttner, Anita, Gunel, Murat, DiLuna, Michael L., Kahle, Kristopher T.
Publicado 2018

A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP

por Çağlayan, Ahmet Okay, Tüysüz, Beyhan, Coşkun, Süleyman, Quon, Jennifer, Harmanci, Akdes Serin, Baranoski, Jacob F., Baran, Burçin, Erson-Omay, E. Zeynep, Henegariu, Octavian, Mane, Shrikant M., Bilgüvar, Kaya, Yasuno, Katsuhito, Günel, Murat
Publicado 2016

The clinical and genomic features of seizures in meningiomas

por Dincer, Alper, Jalal, Muhammad I, Gupte, Trisha P, Vetsa, Shaurey, Vasandani, Sagar, Yalcin, Kanat, Marianayagam, Neelan, Blondin, Nicholas, Corbin, Zachary, McGuone, Declan, Fulbright, Robert K, Erson-Omay, Zeynep, Günel, Murat, Moliterno, Jennifer
Publicado 2023

Vascular steal and associated intratumoral aneurysms in highly vascular brain tumors: illustrative case

por Hong, Christopher S., Marianayagam, Neelan J., Morales-Valero, Saul F., Barak, Tanyeri, Tabor, Joanna K., O’Brien, Joseph, Huttner, Anita, Baehring, Joachim, Gunel, Murat, Erson-Omay, E. Zeynep, Fulbright, Robert K., Matouk, Charles C., Moliterno, Jennifer
Publicado 2023

Genomic profiling of sporadic multiple meningiomas

por Erson-Omay, E. Zeynep, Vetsa, Shaurey, Vasandani, Sagar, Barak, Tanyeri, Nadar, Arushii, Marianayanam, Neelan, Yalcin, Kanat, Miyagishima, Danielle, Aguilera, Stephanie Marie, Robert, Stephanie, Mishra-Gorur, Ketu, Fulbright, Robert K., McGuone, Declan, Günel, Murat, Moliterno, Jennifer
Publicado 2022

Correction: Genomic profiling of sporadic multiple meningiomas

por Erson-Omay, E. Zeynep, Vetsa, Shaurey, Vasandani, Sagar, Barak, Tanyeri, Nadar, Arushii, Marianayagam, Neelan J., Yalcin, Kanat, Miyagishima, Danielle, Aguilera, Stephanie Marie, Robert, Stephanie, Mishra-Gorur, Ketu, Fulbright, Robert K., McGuone, Declan, Günel, Murat, Moliterno, Jennifer
Publicado 2022

Recessive Inheritance of Congenital Hydrocephalus With Other Structural Brain Abnormalities Caused by Compound Heterozygous Mutations in ATP1A3

por Allocco, August A., Jin, Sheng Chih, Duy, Phan Q., Furey, Charuta G., Zeng, Xue, Dong, Weilai, Nelson-Williams, Carol, Karimy, Jason K., DeSpenza, Tyrone, Hao, Le T., Reeves, Benjamin, Haider, Shozeb, Gunel, Murat, Lifton, Richard P., Kahle, Kristopher T.
Publicado 2019