Murat Gunel
Title
Cited by
Cited by
Year
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
17722012
Human hypertension caused by mutations in WNK kinases
FH Wilson, S Disse-Nicodeme, KA Choate, K Ishikawa, ...
Science 293 (5532), 1107-1112, 2001
13962001
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
11562011
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
10852005
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
5392008
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
5162010
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
4762013
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
4742015
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
4572011
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
3892014
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
3461998
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
2812010
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
2802010
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
2582008
A founder mutation as a cause of cerebral cavernous malformation in Hispanic Americans
M Günel, IA Awad, K Finberg, JA Anson, GK Steinberg, HH Batjer, ...
New England Journal of Medicine 334 (15), 946-951, 1996
2571996
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), 2017
2102017
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
2102010
Mapping a gene causing cerebral cavernous malformation to 7q11. 2-q21
M Günel, IA Awad, J Anson, RP Lifton
Proceedings of the National Academy of Sciences 92 (14), 6620-6624, 1995
1971995
Hypertension, age, and location predict rupture of small intracranial aneurysms
BV Nahed, ML DiLuna, T Morgan, E Ocal, AA Hawkins, K Ozduman, ...
Neurosurgery 57 (4), 676-683, 2005
1792005
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
1772016
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