日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:

IgG4-Related Disease: Emerging Roles of Novel Genetic Variants, Immune Cell Subsets and Therapeutic Targets

IgG4相关疾病:新型基因变异、免疫细胞亚群和治疗靶点的新兴作用

Tedesco, Louisa; Ali, Syed B; Erman, Baran; Baris, Safa; Pant, Harshita; Hissaria, Pravin; Bilginer, Yelda; Tumes, Damon J; Cildir, Gökhan

Beyond the skin: immunological profiles and infectious complications in ALOX12B-associated autosomal recessive congenital ichthyosis

超越皮肤层面:ALOX12B相关常染色体隐性先天性鱼鳞病的免疫学特征和感染并发症

Sefer, Asena Pinar; Catak, Mehmet Cihangir; An, Isa; Keser Ozturk, Necmiye; Baykal Selcuk, Leyla; Dincer, Oguz Salih; Benamar, Mehdi; Getachew, Feven; Schmitz-Abe, Klaus; Agrawal, Pankaj B; Bayram Catak, Feyza; Erman, Baran; Bilgic Eltan, Sevgi; Karakoc Aydiner, Elif; Ozen, Ahmet; Chatila, Talal; Baris, Safa

LTβR deficiency causes lymph node aplasia and impaired B cell differentiation.

LTβR 缺乏会导致淋巴结发育不全和 B 细胞分化受损

Ransmayr Bernhard, Bal Sevgi Köstel, Thian Marini, Svaton Michael, van de Wetering Cheryl, Hafemeister Christoph, Segarra-Roca Anna, Block Jana, Frohne Alexandra, Krolo Ana, Altunbas Melek Yorgun, Bilgic-Eltan Sevgi, Kıykım Ayça, Aydiner Omer, Kesim Selin, Inanir Sabahat, Karakoc-Aydiner Elif, Ozen Ahmet, Aba Ümran, Çomak Aylin, Tuğcu Gökçen Dilşa, Pazdzior Robert, Huber Bettina, Farlik Matthias, Kubicek Stefan, von Bernuth Horst, Simonitsch-Klupp Ingrid, Rizzi Marta, Halbritter Florian, Tumanov Alexei V, Kraakman Michael J, Metin Ayşe, Castanon Irinka, Erman Baran, Baris Safa, Boztug Kaan

A Novel Homozygous Six Base Pair Deletion Found in the NFATC2 Gene in a Patient with EBV-Associated Lymphoproliferation

在一名EBV相关淋巴增殖症患者的NFATC2基因中发现一种新的纯合六碱基对缺失。

Erman, Baran; Bal, Sevgi Köstel; Aydoğmuş, Çiğdem; Ersoy, Gizem Zengin; Boztug, Kaan

Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye

利用全外显子组测序对临床诊断的先天性免疫缺陷患者进行基因评估:来自土耳其免疫缺陷专科研究中心的研究结果

Erman, Baran; Aba, Umran; Ipsir, Canberk; Pehlivan, Damla; Aytekin, Caner; Cildir, Gökhan; Cicek, Begum; Bozkurt, Ceren; Tekeoglu, Sidem; Kaya, Melisa; Aydogmus, Cigdem; Cipe, Funda; Sucak, Gulsan; Eltan, Sevgi Bilgic; Ozen, Ahmet; Barıs, Safa; Karakoc-Aydiner, Elif; Kıykım, Ayca; Karaatmaca, Betul; Kose, Hulya; Uygun, Dilara Fatma Kocacık; Celmeli, Fatih; Arikoglu, Tugba; Ozcan, Dilek; Keskin, Ozlem; Arık, Elif; Aytekin, Elif Soyak; Cesur, Mahmut; Kucukosmanoglu, Ercan; Kılıc, Mehmet; Yuksek, Mutlu; Bıcakcı, Zafer; Esenboga, Saliha; Ayvaz, Deniz Çagdaş; Sefer, Asena Pınar; Guner, Sukrü Nail; Keles, Sevgi; Reisli, Ismail; Musabak, Ugur; Demirbas, Nazlı Deveci; Haskologlu, Sule; Kilic, Sara Sebnem; Metin, Ayse; Dogu, Figen; Ikinciogulları, Aydan; Tezcan, Ilhan

Correction to: Genetic Evaluation of the Patients with Clinically Diagnosed Inborn Errors of Immunity by Whole Exome Sequencing: Results from a Specialized Research Center for Immunodeficiency in Türkiye

更正:通过全外显子组测序对临床诊断的先天性免疫缺陷患者进行基因评估:来自土耳其免疫缺陷专科研究中心的研究结果

Erman, Baran; Aba, Umran; Ipsir, Canberk; Pehlivan, Damla; Aytekin, Caner; Cildir, Gokhan; Cicek, Begum; Bozkurt, Ceren; Tekeoglu, Sidem; Kaya, Melisa; Aydogmus, Cigdem; Cipe, Funda; Sucak, Gulsan; Eltan, Sevgi Bilgic; Ozen, Ahmet; Barıs, Safa; Karakoc-Aydiner, Elif; Kıykım, Ayca; Karaatmaca, Betul; Kose, Hulya; Uygun, Dilara Fatma Kocacık; Celmeli, Fatih; Arikoglu, Tugba; Ozcan, Dilek; Keskin, Ozlem; Arık, Elif; Aytekin, Elif Soyak; Cesur, Mahmut; Kucukosmanoglu, Ercan; Kılıc, Mehmet; Yuksek, Mutlu; Bıcakcı, Zafer; Esenboga, Saliha; Ayvaz, Deniz Çagdaş; Sefer, Asena Pınar; Guner, Sukrü Nail; Keles, Sevgi; Reisli, Ismail; Musabak, Ugur; Demirbas, Nazlı Deveci; Haskologlu, Sule; Kilic, Sara Sebnem; Metin, Ayse; Dogu, Figen; Ikinciogulları, Aydan; Tezcan, Ilhan

Human CARMIL2 deficiency underlies a broader immunological and clinical phenotype than CD28 deficiency

人类 CARMIL2 缺陷所导致的免疫学和临床表型比 CD28 缺陷更为广泛。

Lévy, Romain; Gothe, Florian; Momenilandi, Mana; Magg, Thomas; Materna, Marie; Peters, Philipp; Raedler, Johannes; Philippot, Quentin; Rack-Hoch, Anita Lena; Langlais, David; Bourgey, Mathieu; Lanz, Anna-Lisa; Ogishi, Masato; Rosain, Jérémie; Martin, Emmanuel; Latour, Sylvain; Vladikine, Natasha; Distefano, Marco; Khan, Taushif; Rapaport, Franck; Schulz, Marian S; Holzer, Ursula; Fasth, Anders; Sogkas, Georgios; Speckmann, Carsten; Troilo, Arianna; Bigley, Venetia; Roppelt, Anna; Dinur-Schejter, Yael; Toker, Ori; Bronken Martinsen, Karen Helene; Sherkat, Roya; Somekh, Ido; Somech, Raz; Shouval, Dror S; Kühl, Jörn-Sven; Ip, Winnie; McDermott, Elizabeth M; Cliffe, Lucy; Ozen, Ahmet; Baris, Safa; Rangarajan, Hemalatha G; Jouanguy, Emmanuelle; Puel, Anne; Bustamante, Jacinta; Alyanakian, Marie-Alexandra; Fusaro, Mathieu; Wang, Yi; Kong, Xiao-Fei; Cobat, Aurélie; Boutboul, David; Castelle, Martin; Aguilar, Claire; Hermine, Olivier; Cheminant, Morgane; Suarez, Felipe; Yildiran, Alisan; Bousfiha, Aziz; Al-Mousa, Hamoud; Alsohime, Fahad; Cagdas, Deniz; Abraham, Roshini S; Knutsen, Alan P; Fevang, Borre; Bhattad, Sagar; Kiykim, Ayca; Erman, Baran; Arikoglu, Tugba; Unal, Ekrem; Kumar, Ashish; Geier, Christoph B; Baumann, Ulrich; Neven, Bénédicte; Rohlfs, Meino; Walz, Christoph; Abel, Laurent; Malissen, Bernard; Marr, Nico; Klein, Christoph; Casanova, Jean-Laurent; Hauck, Fabian; Béziat, Vivien

Corrigendum to "Expanding the clinical and immunological phenotypes of PAX1-deficient SCID and CID patients" [Clinical Immunology 255 (2023) 109757]

对“扩展 PAX1 缺陷型 SCID 和 CID 患者的临床和免疫表型”的更正 [临床免疫学 255 (2023) 109757]

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

Extended clinical and immunological phenotype and transplant outcome in CD27 and CD70 deficiency

CD27 和 CD70 缺陷患者的扩展临床和免疫表型及移植结果

Ghosh, Sujal; Köstel Bal, Sevgi; Edwards, Emily S J; Pillay, Bethany; Jiménez Heredia, Raúl; Erol Cipe, Funda; Rao, Geetha; Salzer, Elisabeth; Zoghi, Samaneh; Abolhassani, Hassan; Momen, Tooba; Gostick, Emma; Price, David A; Zhang, Yu; Oler, Andrew J; Gonzaga-Jauregui, Claudia; Erman, Baran; Metin, Ayse; Ilhan, Inci; Haskologlu, Sule; Islamoglu, Candan; Baskin, Kubra; Ceylaner, Serdar; Yilmaz, Ebru; Unal, Ekrem; Karakukcu, Musa; Berghuis, Dagmar; Cole, Theresa; Gupta, Aditya K; Hauck, Fabian; Kogler, Hubert; Hoepelman, Andy I M; Baris, Safa; Karakoc-Aydiner, Elif; Ozen, Ahmet; Kager, Leo; Holzinger, Dirk; Paulussen, Michael; Krüger, Renate; Meisel, Roland; Oommen, Prasad T; Morris, Emma; Neven, Benedicte; Worth, Austen; van Montfrans, Joris; Fraaij, Pieter L A; Choo, Sharon; Dogu, Figen; Davies, E Graham; Burns, Siobhan; Dückers, Gregor; Becker, Ruy Perez; von Bernuth, Horst; Latour, Sylvain; Faraci, Maura; Gattorno, Marco; Su, Helen C; Pan-Hammarström, Qiang; Hammarström, Lennart; Lenardo, Michael J; Ma, Cindy S; Niehues, Tim; Aghamohammadi, Asghar; Rezaei, Nima; Ikinciogullari, Aydan; Tangye, Stuart G; Lankester, Arjan C; Boztug, Kaan

Genetic Screening of the Patients with Primary Immunodeficiency by Whole-Exome Sequencing

利用全外显子组测序对原发性免疫缺陷患者进行基因筛查

Erman, Baran; Çipe, Funda