PubRank

Murat Günel

Author PubWeight™ 48.00‹?›

Top papers

Rank Title Journal Year PubWeight™‹?›
1 De novo mutations revealed by whole-exome sequencing are strongly associated with autism. Nature 2012 13.61
2 Multiple recurrent de novo CNVs, including duplications of the 7q11.23 Williams syndrome region, are strongly associated with autism. Neuron 2011 10.61
3 Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations. Nature 2010 6.26
4 Genomic analysis of non-NF2 meningiomas reveals mutations in TRAF7, KLF4, AKT1, and SMO. Science 2013 3.45
5 Rare copy number variants in tourette syndrome disrupt genes in histaminergic pathways and overlap with autism. Biol Psychiatry 2011 2.28
6 Susceptibility loci for intracranial aneurysm in European and Japanese populations. Nat Genet 2008 1.90
7 Recessive LAMC3 mutations cause malformations of occipital cortical development. Nat Genet 2011 1.89
8 Genome-wide association study of intracranial aneurysm identifies three new risk loci. Nat Genet 2010 1.86
9 Loss of cerebral cavernous malformation 3 (Ccm3) in neuroglia leads to CCM and vascular pathology. Proc Natl Acad Sci U S A 2011 1.23
10 Common variant near the endothelin receptor type A (EDNRA) gene is associated with intracranial aneurysm risk. Proc Natl Acad Sci U S A 2011 1.08
11 Vessel wall magnetic resonance imaging identifies the site of rupture in patients with multiple intracranial aneurysms: proof of principle. Neurosurgery 2013 1.06
12 Expression of structural proteins and angiogenic factors in normal arterial and unruptured and ruptured aneurysm walls. Neurosurgery 2005 1.01
13 Ccm3, a gene associated with cerebral cavernous malformations, is required for neuronal migration. Development 2014 0.88
14 Autosomal recessive spastic tetraplegia caused by AP4M1 and AP4B1 gene mutation: expansion of the facial and neuroimaging features. Am J Med Genet A 2014 0.86
15 Intracranial aneurysm risk locus 5q23.2 is associated with elevated systolic blood pressure. PLoS Genet 2012 0.85
16 Expression of integrins in cerebral arteriovenous and cavernous malformations. Neurosurgery 2006 0.83
17 Spondyloepimetaphyseal dysplasia Pakistani type: expansion of the phenotype. Am J Med Genet A 2013 0.79
18 A step toward customizing radiosurgical care for arteriovenous malformations. World Neurosurg 2012 0.75
19 Primary hypertrophic osteoarthropathy caused by homozygous deletion in HPGD gene in a family: changing clinical and radiological findings with long-term follow-up. Rheumatol Int 2014 0.75
20 Spondyloepimetaphyseal dysplasia with joint laxity, leptodactylic type: longitudinal observation of radiographic findings in a child heterozygous for a KIF22 mutation. Pediatr Radiol 2014 0.75