A novel homozygous RIPK4 variant in a family with severe Bartsocas‐Papas syndrome von Dinçer, Tuba, Gümüş, Evren, Toraman, Bayram, Er, İdris, Yildiz, Gokhan, Yüksel, Zafer, Kalay, Ersan

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RIPK4 suppresses the TGF‐β1 signaling pathway in HaCaT cells von Dinçer, Tuba, Boz Er, Asiye Büşra, Er, İdris, Toraman, Bayram, Yildiz, Gokhan, Kalay, Ersan

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Finding underlying genetic mechanisms of two patients with autism spectrum disorder carrying familial apparently balanced chromosomal translocations von Toraman, Bayram, Bilginer, Samiye Çilem, Hesapçıoğlu, Selma Tural, Göker, Zeynep, Soykam, Hüseyin Okan, Ergüner, Bekir, Dinçer, Tuba, Yıldız, Gökhan, Ünsal, Serbülent, Kasap, Burak Kaan, Kandil, Sema, Kalay, Ersan

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Genetically determined plasma trefoil factor-3 levels are causally associated with the risk of ulcerative colitis: a Mendelian randomization study von TORAMAN, Bayram, FİDAN, Sami, YILDIZ, Gökhan

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Mutations in RIPK4 Cause the Autosomal-Recessive Form of Popliteal Pterygium Syndrome von Kalay, Ersan, Sezgin, Orhan, Chellappa, Vasant, Mutlu, Mehmet, Morsy, Heba, Kayserili, Hulya, Kreiger, Elmar, Cansu, Aysegul, Toraman, Bayram, Abdalla, Ebtesam Mohammed, Aslan, Yakup, Pillai, Shiv, Akarsu, Nurten A.

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Investigation of Plasmid Mediated mcr Colistin Resistance Gene in Clinical Enterobacterales Isolates von Ozkaya, Esra, Buruk, Celal Kurtulus, Tosun, Ilknur, Toraman, Bayram, Kaklikkaya, Nese, Aydin, Faruk

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Klinik Enterobacterales İzolatlarında Plazmit Aracılı mcr Kolistin Direnç Geninin Araştırılması von Özkaya, Esra, Buruk, Celal Kurtuluş, Tosun, İlknur, Toraman, Bayram, Kaklıkkaya, Neşe, Aydın, Faruk

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Analysis of centrosome and DNA damage response in PLK4 associated Seckel syndrome von Dinçer, Tuba, Yorgancıoğlu-Budak, Gülden, Ölmez, Akgün, Er, İdris, Dodurga, Yavuz, Özdemir, Özmert Ma, Toraman, Bayram, Yıldırım, Adem, Sabir, Nuran, Akarsu, Nurten A, Semerci, C Nur, Kalay, Ersan

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Two male patients from an extended seven generation Turkish family diagnosed with Renpenning syndrome: identifying the causative mutation and review of the literature von TORAMAN, Bayram, DİNÇER, Tuba, BUDAK, Gülden, BİLGİNER, Cilem, KAYSERİLİ, Hülya, KALAY, Ersan

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HLA-E0101/0103X is Associated with Susceptibility to Pemphigus Vulgaris: A Case-control Study von Altun, Ece, Yayli, Savas, Toraman, Bayram, Arica, Deniz Aksu, Kalay, Ersan, Selcuk, Leyla Baykal, Bahadir, Sevgi

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Novel splice-site and missense mutations in the ALDH1A3 gene underlying autosomal recessive anophthalmia/microphthalmia von Semerci, C Nur, Kalay, Ersan, Yıldırım, Cem, Dinçer, Tuba, Ölmez, Akgün, Toraman, Bayram, Koçyiğit, Ali, Bulgu, Yunus, Okur, Volkan, Şatıroğlu-Tufan, Lale, Akarsu, Nurten A

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CEP152 is a genome maintenance protein disrupted in Seckel syndrome von Kalay, Ersan, Wollnik, Bernd, Yigit, Gökhan, Aslan, Yakup, Brown, Karen E, Pohl, Esther, Bicknell, Louise S, Kayserili, Hülya, Li, Yun, Tüysüz, Beyhan, Nürnberg, Gudrun, Kiess, Wieland, Koegl, Manfred, Baessmann, Ingelore, Buruk, Kurtulus, Toraman, Bayram, Kayipmaz, Saadettin, Kul, Sibel, Ikbal, Mevlit, Turner, Daniel J, Taylor, Martin S, Aerts, Jan, Scott, Carol, Milstein, Karen, Dollfus, Helene, Wieczorek, Dagmar, Brunner, Han G, Hurles, Matthew, Jackson, Andrew P, Rauch, Anita, Nürnberg, Peter, Karagüzel, Ahmet

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Investigation of CYP21A2 mutations in Turkish patients with 21-hydroxylase deficiency and a novel founder mutation von Toraman, Bayram, Ökten, Ayşenur, Kalay, Ersan, Karagüzel, Gülay, Dinçer, Tuba, Açıkgöz, Emel Gül, Karagüzel, Ahmet

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Investigation of Plasmid Mediated mcr Colistin Resistance Gene in Clinical Enterobacterales Isolates von Özkaya, Esra, Buruk, Celal Kurtuluş, Tosun, İlknur, Toraman, Bayram, Kaklıkkaya, Neşe, Aydın, Faruk

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Involvement ofDFNB59 mutations in autosomal recessive nonsyndromic hearing impairment von Collin, Rob W.J., Kalay, Ersan, Oostrik, Jaap, Çaylan, Refik, Wollnik, Bernd, Arslan, Selçuk, den Hollander, Anneke I., Birinci, Yelda, Lichtner, Peter, Strom, Tim M., Toraman, Bayram, Hoefsloot, Lies H., Cremers, Cor W.R.J., Brunner, Han G., Cremers, Frans P.M., Karaguzel, Ahmet, Kremer, Hannie

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Involvement of DFNB59 mutations in autosomal recessive nonsyndromic hearing impairment von Collin, Rob W.J., Kalay, Ersan, Oostrik, Jaap, Çaylan, Refik, Wollnik, Bernd, Arslan, Selçuk, den Hollander, Anneke I., Birinci, Yelda, Lichtner, Peter, Strom, Tim M., Toraman, Bayram, Hoefsloot, Lies H., Cremers, Cor W.R.J., Brunner, Han G., Cremers, Frans P.M., Karaguzel, Ahmet, Kremer, Hannie

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HLA-E0101/0103X is associated with susceptibility to pemphigus vulgaris: a case-control study von Altun, Ece, Yayli, Savas, Toraman, Bayram, Aksu Arica, Deniz, Kalay, Ersan, Baykal Selçuk, Leyla, Bahadir, Sevgi

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Role of parthenolide in paclitaxel-induced oxidative stress injury and impaired reproductive function in rat testicular tissue von Toraman, Emine, Budak, Büşra, Bayram, Cemil, Sezen, Selma, Mokhtare, Behzad, Hacımüftüoğlu, Ahmet

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Parthenolide as a potential analgesic in the treatment of paclitaxel-induced neuropathic pain: the rat modeling von Toraman, Emine, Bayram, Cemil, Sezen, Selma, Özkaraca, Mustafa, Hacımüftüoğlu, Ahmet, Budak, Harun

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Treatment Planning Comparison of Intensity Modulated Arc Therapy and CyberKnife Techniques in Early Stage Glottic Larynx Radiotherapy von ALAY, Serdar, GOKSEL, Evren Ozan, ÖZKAYA TORAMAN, Kübra, OKUTAN, Murat, DEMİR, Bayram

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