A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay by Özkan Kart, Pınar, Citli, Senol, Yildiz, Nihal, Cansu, Ali

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A Rare Duplication in the PLAG1 Gene: A Case of Neonatal Diabetes by Hekimoğlu, Berna, Çitli, Şenol

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IL-17A, MCP-1, CCR-2, and ABCA1 polymorphisms in children with non-alcoholic fatty liver disease by Akbulut, Ulas Emre, Emeksiz, Hamdi Cihan, Citli, Senol, Cebi, Alper Han, Korkmaz, Hatice Ayca Ata, Baki, Gaye

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Importance and usage of chromosomal microarray analysis in diagnosing intellectual disability, global developmental delay, and autism; and discovering new loci for these disorders by Ceylan, Ahmet Cevdet, Citli, Senol, Erdem, Haktan Bagis, Sahin, Ibrahim, Acar Arslan, Elif, Erdogan, Murat

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Combination treatment of bortezomib and epirubicin increases the expression of TNFRSF10 A/B, and induces TRAIL-mediated cell death in colorectal cancer cells by Caldiran, Feyzanur, Berkel, Caglar, Yilmaz, Esra, Kucuk, Burak, Cacan, Aslihan Hatun, Citli, Senol, Canpolat, Emel, Cacan, Ercan

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IL‐17A, MCP‐1, CCR‐2, and ABCA1 polymorphisms in children with non‐alcoholic fatty liver disease by Akbulut, Ulas Emre, Emeksiz, Hamdi Cihan, Citli, Senol, Cebi, Alper Han, Korkmaz, Hatice Ayca Ata, Baki, Gaye

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Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients by Yakici, Nalan, Kreins, Alexandra Y., Catak, Mehmet Cihangir, Babayeva, Royala, Erman, Baran, Kenney, Heather, Gungor, Hatice Eke, Cea, Pablo A., Kawai, Tomoki, Bosticardo, Marita, Delmonte, Ottavia Maria, Adams, Stuart, Fan, Yu-Tong, Pala, Francesca, Turkyilmaz, Ayberk, Howley, Evey, Worth, Austen, Kot, Hakan, Sefer, Asena Pinar, Kara, Altan, Bulutoglu, Alper, Bilgic-Eltan, Sevgi, Altunbas, Melek Yorgun, Bayram Catak, Feyza, Karakus, Ibrahim Serhat, Karatay, Emrah, Tekeoglu, Sidem Didar, Eser, Metin, Albayrak, Davut, Citli, Senol, Kiykim, Ayca, Karakoc-Aydiner, Elif, Ozen, Ahmet, Ghosh, Sujal, Gohlke, Holger, Orhan, Fazil, Notarangelo, Luigi D., Davies, E. Graham, Baris, Safa

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Corrigendum to "Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients" [Clinical Immunology 255 (2023) 109757] by Yakici, Nalan, Kreins, Alexandra Y, Catak, Mehmet Cihangir, Babayeva, Royala, Erman, Baran, Kenney, Heather, Eke-Gungor, Hatice, Cea, Pablo A, Kawai, Tomoki, Bosticardo, Marita, Delmonte, Ottavia Maria, Adams, Stuart, Fan, Yu-Tong, Pala, Francesca, Turkyilmaz, Ayberk, Howley, Evey, Worth, Austen, Kot, Hakan, Sefer, Asena Pinar, Kara, Altan, Bulutoglu, Alper, Bilgic-Eltan, Sevgi, Yorgun Altunbas, Melek, Bayram Catak, Feyza, Karakus, Ibrahim Serhat, Karatay, Emrah, Tekeoglu, Sidem Didar, Eser, Metin, Albayrak, Davut, Citli, Senol, Kiykim, Ayca, Karakoc-Aydiner, Elif, Ozen, Ahmet, Ghosh, Sujal, Gohlke, Holger, Orhan, Fazil, Notarangelo, Luigi D, Davies, E Graham, Baris, Safa

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Prevalence of known mutations in the MEFV gene in a population screening with high rate of carriers by Ozdemir, Oztürk, Sezgin, Ilhan, Kurtulgan, Hande Kucuk, Candan, Ferhan, Koksal, Binnur, Sumer, Haldun, Icagasioglu, Dilara, Uslu, Atilla, Yildiz, Fazilet, Arslan, Sulhattin, Cetinkaya, Selma, Citli, Senol, Oztemur, Zekeriya, Kayatas, Mansur

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ASD with the Bor Syndrome: A Case Report by Yaylaci, Ferhat, Sahbudak, Begum, Citli, Senol, Kilit, Neriman

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Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings by Çitli, Şenol, Serdaroglu, Esra

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A novel INPP4A mutation with pontocerebellar hypoplasia, myoclonic epilepsy, microcephaly, and severe developmental delay by Özkan Kart, Pınar, Citli, Senol, Yildiz, Nihal, Cansu, Ali

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ASD with the Bor Syndrome: A Case Report by Yaylaci, Ferhat, Sahbudak, Begum, Citli, Senol, Kilit, Neriman

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Maternal Germline Mosaicism of a de Novo TUBB2B Mutation Leads to Complex Cortical Dysplasia in Two Siblings by Çitli, Şenol, Serdaroglu, Esra

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