Saliha Yılmaz

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 · 850 citations · Full text

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 · 159 citations · Full text

Recessive LAMC3 mutations cause malformations of occipital cortical development

Tanyeri Barak, Kenneth Y. Kwan, Angeliki Louvi et al. · Nature Genetics · 2011 · 113 citations · Full text

Developmental Anomaly, Developmental Biology, Brain Development +7

Deleterious mutations in exon 1 of MECP2 in Rett syndrome

Aline Quenard, Saliha Yılmaz, Hervé Fontaine et al. · European Journal of Medical Genetics · 2005 · 34 citations

Genome Instability, Exon 1, Genetic Disorder +5

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

Saliha Yılmaz, Dilek Uludağ Alkaya, Özgür Kasapçopur et al. · Molecular Genetics & Genomic Medicine · 2018 · 32 citations · Full text