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Year Number of Results
2003 1
2004 9
2005 2
2006 3
2007 3
2012 1
2013 4
2014 4
2015 2
2016 3
2017 4
2018 2
2019 4
2020 7
2021 9
2022 8
2023 15
2024 20
2025 22

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115 results

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Page 1
Genomic architecture of autism from comprehensive whole-genome sequence annotation.
Trost B, Thiruvahindrapuram B, Chan AJS, Engchuan W, Higginbotham EJ, Howe JL, Loureiro LO, Reuter MS, Roshandel D, Whitney J, Zarrei M, Bookman M, Somerville C, Shaath R, Abdi M, Aliyev E, Patel RV, Nalpathamkalam T, Pellecchia G, Hamdan O, Kaur G, Wang Z, MacDonald JR, Wei J, Sung WWL, Lamoureux S, Hoang N, Selvanayagam T, Deflaux N, Geng M, Ghaffari S, Bates J, Young EJ, Ding Q, Shum C, D'Abate L, Bradley CA, Rutherford A, Aguda V, Apresto B, Chen N, Desai S, Du X, Fong MLY, Pullenayegum S, Samler K, Wang T, Ho K, Paton T, Pereira SL, Herbrick JA, Wintle RF, Fuerth J, Noppornpitak J, Ward H, Magee P, Al Baz A, Kajendirarajah U, Kapadia S, Vlasblom J, Valluri M, Green J, Seifer V, Quirbach M, Rennie O, Kelley E, Masjedi N, Lord C, Szego MJ, Zawati MH, Lang M, Strug LJ, Marshall CR, Costain G, Calli K, Iaboni A, Yusuf A, Ambrozewicz P, Gallagher L, Amaral DG, Brian J, Elsabbagh M, Georgiades S, Messinger DS, Ozonoff S, Sebat J, Sjaarda C, Smith IM, Szatmari P, Zwaigenbaum L, Kushki A, Frazier TW, Vorstman JAS, Fakhro KA, Fernandez BA, Lewis MES, Weksberg R, Fiume M, Yuen RKC, Anagnostou E, Sondheimer N, Glazer D, Hartley DM, Scherer SW. Trost B, et al. Among authors: aliyev e. Cell. 2022 Nov 10;185(23):4409-4427.e18. doi: 10.1016/j.cell.2022.10.009. Cell. 2022. PMID: 36368308 Free PMC article.
Macrophage activation syndrome in patients with systemic juvenile idiopathic arthritis on anti-interleukin-1 or -6 therapy.
Ulu K, Aliyev E, Kılıç Könte E, Tanatar A, Türkmen Ş, Doğantan Ş, Kızıldağ Z, Kasap Demir B, Gezgin Yıldırım D, Otar Yener G, Öztürk K, Baba Ö, Açarı C, Kılbaş G, Taşkın SN, Haşlak F, Çağlayan Ş, Bağlan E, Dundar HA, Başaran Ö, Barut K, Karadağ ŞG, Coşkuner T, Sönmez HE, Yüksel S, Kalyoncu M, Bakkaloğlu SA, Ünsal E, Paç Kısaarslan A, Bilginer Y, Aktay Ayaz N, Kasapçopur Ö, Özen S, Sözeri B. Ulu K, et al. Among authors: aliyev e. Rheumatology (Oxford). 2024 Sep 1;63(SI2):SI167-SI172. doi: 10.1093/rheumatology/keae124. Rheumatology (Oxford). 2024. PMID: 38441301
Cyclophosphamide treatment with a comparison in both pediatric rheumatology and pediatric nephrology practices.
Gezgin Yildirim D, Orulluoglu EY, Yildiz C, Acari C, Dundar HA, Akaci O, Akinci N, Aliyev E, Alpman BN, Altug Gucenmez O, Arslanoglu Aydin E, Atmis B, Avar Aydin PO, Aydin F, Baba O, Baglan E, Bagrul I, Barut K, Basaran O, Bayrakci US, Belder N, Yucel BB, Buyukkaragoz B, Caglayan S, Cakan M, Celikel E, Demir F, Demir S, Demir Yigit Y, Demirkan FG, Dincel N, Dogantan S, Ekici Tekin Z, Genc E, Haslak F, Isguder R, Kara A, Kasap Cuceoglu M, Kaya Akca U, Kisaoglu H, Kisla Ekinci RM, Kızıldag Z, Kurt T, Kucukali B, Leventoglu E, Nalcacioglu H, Yener GO, Ozdel S, Ozdemir Atikel Y, Ozdemir Cicek S, Pektas Leblebiciler S, Serdaroglu E, Sonmez HE, Sunar Yayla EN, Surmeli Doven S, Sahin S, Sener S, Tanatar A, Tanidir M, Taskin SN, Tiryaki B, Tuncez S, Turkucar S, Uzun Kenan B, Yildiz N, Yilmaz K, Tabel Y, Dursun I, Canpolat N, Mir S, Peru H, Topaloglu R, Kaya Gurgoze M, Balat A, Bilginer Y, Celikel Acar B, Sozeri B, Unsal E, Kasapcopur O, Bakkaloglu SA. Gezgin Yildirim D, et al. Among authors: aliyev e. Pediatr Rheumatol Online J. 2025 Mar 11;23(1):24. doi: 10.1186/s12969-025-01080-9. Pediatr Rheumatol Online J. 2025. PMID: 40069880 Free PMC article.
Near-complete Middle Eastern genomes refine autozygosity and enhance disease-causing and population-specific variant discovery.
Ghorbani M, Moosa S, Siddig Z, Farhad R, Naeem H, Harvey WT, Mastrorosa FK, Munson KM, Mohamad Razali R, Aliyev E, Diboun I, Abouelhassan R, Tauro M, Hassan S, Mathew R, Al Hashmi M, Mathew LS, Wang K, Salhab AR, Vempalli FR, El Khouly A; Qatar Genome Program Research Consortium; Alazwani I, Tomei S, Fakhro KA, Satti A, Benini R, Rhie A, Eichler EE, Mokrab Y. Ghorbani M, et al. Among authors: aliyev e. Nat Genet. 2025 May;57(5):1119-1131. doi: 10.1038/s41588-025-02173-7. Epub 2025 May 5. Nat Genet. 2025. PMID: 40325133 Free PMC article.
Ritscher-Schinzel syndrome can be characterized as an endosomal recyclinopathy.
Kato K, Nishio Y, McMillan KJ, Al-Maraghi A, Kroes HY, Abdel-Hamid MS, Jones E, Shaw S, Yoshida A, Otsuji S, Murofushi Y, Aamer W, Bhat AA, AlRayahi J, Al-Shabeeb Akil AS, Aliyev E, van Binsbergen E, Janssen EJ, Mehrin KM, Oishi H, Kobayashi R, Horii T, Hatada I, Saito A, Hattori M, Kawano Y, Lewis PA, Heesom KJ, Takarada T, Sawamoto K, Matsushita M, Ogi T, Butkovic R, Danson C, Wilkinson KA, Fakhro KA, Zaki MS, Saitoh S, Cullen PJ. Kato K, et al. Among authors: aliyev e. Sci Transl Med. 2025 Jul 2;17(805):eadt2426. doi: 10.1126/scitranslmed.adt2426. Epub 2025 Jul 2. Sci Transl Med. 2025. PMID: 40601774
Mapping the genetic landscape of treatable inherited metabolic disorders in a large Middle Eastern biobank.
Devadoss Gandhi G, Aliyev E, Syed N, Vempalli FR, Saad C, Mbarek H, Al-Saei O, Al-Maraghi A, Abdi M, Krishnamoorthy N, Badii R; Qatar Genome Program Research Consortium; Akil AA, Ben-Omran T, Fakhro KA. Devadoss Gandhi G, et al. Among authors: aliyev e. Genet Med. 2024 Dec;26(12):101268. doi: 10.1016/j.gim.2024.101268. Epub 2024 Sep 14. Genet Med. 2024. PMID: 39286960 Free article.
Evaluation of pediatric rheumatologists' approach to rituximab use: a questionnaire study.
Sunar Yayla EN, Gezgin Yıldırım D, Adıgüzel Dündar H, Adrovic A, Akbörü EG, Aktay Ayaz N, Aliyev E, Avar Aydın PÖ, Aydın F, Baba Ö, Bağlan E, Bora Makay B, Bozkaya Yücel B, Çakan M, Çelikel E, Demir F, Demir S, Demirkan FG, Ekici Tekin Z, Esmeray Şenol P, Guliyeva V, Güngörer V, İşgüder R, Kalyoncu M, Karadağ ŞG, Kısaoğlu H, Kışla Ekinci RM, Kızıldağ Z, Kurt T, Özdel S, Özdemir Çiçek S, Öztürk K, Polat MC, Sezer M, Sönmez HE, Sözeri B, Şener S, Taşkın SN, Türkuçar S, Ünsal E, Yıldız Ç, Bakkaloğlu SA. Sunar Yayla EN, et al. Among authors: aliyev e. Eur J Pediatr. 2024 Sep;183(9):3959-3968. doi: 10.1007/s00431-024-05654-9. Epub 2024 Jun 26. Eur J Pediatr. 2024. PMID: 38926187
Exploring gastrointestinal manifestations in childhood onset systemic lupus erythematosus - Insights from a multicenter study.
Sönmez HE, Batu ED, İşgüder R, Şahin N, Aliyev E, Aslan E, Çoban S, Güngörer V, Karadağ ŞG, Karaçayır N, Kısaoğlu H, Yekedüz Bülbül A, Garip S, Karalı Y, Ayduran S, Demir S, Kaya Akça Ü, Başaran Ö, Şahin S, Kasap B, Kilic SS, Kışla Ekinci RM, Kısaarslan AP, Kalyoncu M, Bakkaloğlu S, Yüksel S, Aktay Ayaz N, Çelikel Acar B, Sözeri B, Kasapçopur Ö, Ünsal E, Özen S. Sönmez HE, et al. Among authors: aliyev e. Lupus. 2024 Oct;33(12):1358-1364. doi: 10.1177/09612033241279071. Epub 2024 Aug 26. Lupus. 2024. PMID: 39186467
115 results