Mehmet Bakırcıoğlu

Genomic Analysis of Non- <i>NF2</i> Meningiomas Reveals Mutations in <i>TRAF7</i> , <i>KLF4</i> , <i>AKT1</i> , and <i>SMO</i>

Victoria Clark, E. Zeynep Erson‐Omay, Akdes Serin et al. · Science · 2013 · 887 citations · Full text

Medicine, Genetics, Oncology +16

Whole-exome sequencing identifies recessive WDR62 mutations in severe brain malformations

Kaya Bilgüvar, Ali K. Ozturk, Angeliki Louvi et al. · Nature · 2010 · 496 citations · Full text

Life Sciences, Genetics, Molecular Genetics +14

Recessive loss of function of the neuronal ubiquitin hydrolase UCHL1 leads to early-onset progressive neurodegeneration

Kaya Bilgüvar, Navneet K. Tyagi, Çiğdem Özkara et al. · Proceedings of the National Academy of Sciences · 2013 · 190 citations · Full text

Life Sciences, Genetics, Neuroscience +17

The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis

Mehmet Bakırcıoğlu, Ofélia P. Carvalho, Maryam Khurshid et al. · The American Journal of Human Genetics · 2011 · 163 citations · Full text

Life Sciences, Genetics, Neuroscience +17

Common variant near the endothelin receptor type A ( <i>EDNRA</i> ) gene is associated with intracranial aneurysm risk

Katsuhito Yasuno, Mehmet Bakırcıoğlu, Siew‐Kee Low et al. · Proceedings of the National Academy of Sciences · 2011 · 122 citations · Full text

Life Sciences, Genetics, Molecular Genetics +17