Severe Phenotype in Patients with X-linked Hydrocephalus Caused by a Missense Mutation in L1CAM by Tüysüz, Beyhan, Ercan-Sençicek, Adife Gülhan, Özer, Emre, Göç, Nükte, Yalçınkaya, Cengiz, Bilguvar, Kaya

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Prevalence and clinical/molecular characteristics of PTEN mutations in Turkish children with autism spectrum disorders and macrocephaly by Kaymakcalan, Hande, Kaya, İlyas, Cevher Binici, Nagihan, Nikerel, Emrah, Özbaran, Burcu, Görkem Aksoy, Mehmet, Erbilgin, Seda, Özyurt, Gonca, Jahan, Noor, Çelik, Didem, Yararbaş, Kanay, Yalçınkaya, Leyla, Köse, Sezen, Durak, Sibel, Ercan‐Sencicek, Adife Gulhan

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Renal involvement in patients with mucolipidosis IIIalpha/beta: Causal relation or co-occurrence? by Tüysüz, Beyhan, Ercan-Sencicek, Adife Gülhan, Canpolat, Nur, Koparır, Asuman, Yılmaz, Saliha, Kılıçaslan, Işın, Gülez, Burcu, Bilguvar, Kaya, Günel, Murat

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YAP/TEAD1 Complex Is a Default Repressor of Cardiac Toll-Like Receptor Genes by Gao, Yunan, Sun, Yan, Ercan-Sencicek, Adife Gulhan, King, Justin S, Akerberg, Brynn N, Ma, Qing, Kontaridis, Maria I, Pu, William T, Lin, Zhiqiang

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Rare deleterious mutations of the gene EFR3A in autism spectrum disorders by Gupta, Abha R, Pirruccello, Michelle, Cheng, Feng, Kang, Hyo Jung, Fernandez, Thomas V, Baskin, Jeremy M, Choi, Murim, Liu, Li, Ercan-Sencicek, Adife Gulhan, Murdoch, John D, Klei, Lambertus, Neale, Benjamin M, Franjic, Daniel, Daly, Mark J, Lifton, Richard P, De Camilli, Pietro, Zhao, Hongyu, Sestan, Nenad, State, Matthew W

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A novel heterozygous deletion within the 3’ region of the PAX6 gene causing isolated aniridia in a large family group by Bayrakli, Fatih, Guney, Ilter, Bayri, Yasar, Ercan-Sencicek, Adife Gulhan, Ceyhan, Dogan, Cankaya, Tufan, Mason, Christopher, Bilguvar, Kaya, Bayrakli, Sengul, Mane, Shrikant M, State, Matthew W, Gunel, Murat

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