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Murat Gunel
Murat Gunel
在 yale.edu 的电子邮件经过验证
标题
引用次数
引用次数
年份
De novo mutations revealed by whole-exome sequencing are strongly associated with autism
SJ Sanders, MT Murtha, AR Gupta, JD Murdoch, MJ Raubeson, ...
Nature 485 (7397), 237-241, 2012
23672012
Human hypertension caused by mutations in WNK kinases
FH Wilson, S Disse-Nicodeme, KA Choate, K Ishikawa, ...
Science 293 (5532), 1107-1112, 2001
16742001
Multiple recurrent de novo CNVs, including duplications of the 7q11. 23 Williams syndrome region, are strongly associated with autism
SJ Sanders, AG Ercan-Sencicek, V Hus, R Luo, MT Murtha, ...
Neuron 70 (5), 863-885, 2011
14922011
Sequence Variants in SLITRK1 Are Associated with Tourette's Syndrome
JF Abelson, KY Kwan, BJ O'Roak, DY Baek, AA Stillman, TM Morgan, ...
Science 310 (5746), 317-320, 2005
12362005
Neuroinvasion of SARS-CoV-2 in human and mouse brain
E Song, C Zhang, B Israelow, A Lu-Culligan, AV Prado, S Skriabine, P Lu, ...
The Journal of experimental medicine 218 (3), 2021
9702021
Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO
VE Clark, EZ Erson-Omay, A Serin, J Yin, J Cotney, K Özduman, T Avşar, ...
Science 339 (6123), 1077-1080, 2013
8662013
The genetic basis of Mendelian phenotypes: discoveries, challenges, and opportunities
JX Chong, KJ Buckingham, SN Jhangiani, C Boehm, N Sobreira, ...
The American Journal of Human Genetics 97 (2), 199-215, 2015
7522015
Genome-wide association study identifies susceptibility loci for IgA nephropathy
AG Gharavi, K Kiryluk, M Choi, Y Li, P Hou, J Xie, S Sanna-Cherchi, ...
Nature genetics 43 (4), 321-327, 2011
6812011
Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations
K Bilgüvar, AK Öztürk, A Louvi, KY Kwan, M Choi, B Tatlı, D Yalnızoğlu, ...
Nature 467 (7312), 207-210, 2010
6262010
Molecular cytogenetic analysis and resequencing of contactin associated protein-like 2 in autism spectrum disorders
B Bakkaloglu, BJ O'Roak, A Louvi, AR Gupta, JF Abelson, TM Morgan, ...
The American Journal of Human Genetics 82 (1), 165-173, 2008
6162008
Exome sequencing links corticospinal motor neuron disease to common neurodegenerative disorders
G Novarino, AG Fenstermaker, MS Zaki, M Hofree, JL Silhavy, ...
science 343 (6170), 506-511, 2014
5582014
2-Hydroxyglutarate produced by neomorphic IDH mutations suppresses homologous recombination and induces PARP inhibitor sensitivity
PL Sulkowski, CD Corso, ND Robinson, SE Scanlon, KR Purshouse, ...
Science translational medicine 9 (375), eaal2463, 2017
5352017
Multilocus linkage identifies two new loci for a mendelian form of stroke, cerebral cavernous malformation, at 7p15–13 and 3q25. 2–27
HD Craig, M Günel, O Cepeda, EW Johnson, L Ptacek, GK Steinberg, ...
Human molecular genetics 7 (12), 1851-1858, 1998
3971998
L-histidine decarboxylase and Tourette's syndrome
AG Ercan-Sencicek, AA Stillman, AK Ghosh, K Bilguvar, BJ O'Roak, ...
New England Journal of Medicine 362 (20), 1901-1908, 2010
3692010
Genome-wide association study of intracranial aneurysm identifies three new risk loci
K Yasuno, K Bilguvar, P Bijlenga, SK Low, B Krischek, G Auburger, ...
Nature genetics 42 (5), 420-425, 2010
3602010
The critical role of hemodynamics in the development of cerebral vascular disease: a review
AM Nixon, M Gunel, BE Sumpio
Journal of neurosurgery 112 (6), 1240-1253, 2010
3332010
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
VE Clark, AS Harmancı, H Bai, MW Youngblood, TI Lee, JF Baranoski, ...
Nature genetics 48 (10), 1253-1259, 2016
3222016
Integrated genomic characterization of IDH1-mutant glioma malignant progression
H Bai, AS Harmancı, EZ Erson-Omay, J Li, S Coşkun, M Simon, ...
Nature genetics 48 (1), 59-66, 2016
3202016
Susceptibility loci for intracranial aneurysm in European and Japanese populations
K Bilguvar, K Yasuno, M Niemelä, YM Ruigrok, M Von Und Zu Fraunberg, ...
Nature genetics 40 (12), 1472-1477, 2008
3182008
Inflammation-dependent cerebrospinal fluid hypersecretion by the choroid plexus epithelium in posthemorrhagic hydrocephalus
JK Karimy, J Zhang, DB Kurland, BC Theriault, D Duran, JA Stokum, ...
Nature medicine 23 (8), 997-1003, 2017
3132017
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