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How has Dilek Uludağ Alkaya's publication output changed over time?
ScholarIQpublication output · 2017–2023
Output grew100% over the shown period — from 1 works in 2017 to 2 in 2023.
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1
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2
201720182019202020212023
What are the most-cited papers on Dilek Uludağ Alkaya?
ScholarIQmost cited works
Epidemiology and survival of childhood cancer in Turkey
Rejin Kebudi, Dilek Uludağ Alkaya
Pediatric Blood & Cancer. 202039 Citations
Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (<scp>CACP</scp>) syndrome
Saliha Yılmaz, Dilek Uludağ Alkaya, Özgür Kasapçopur, Kenan Barut, Ekin Su Akdemir, Cemre Celen, Mark W. Youngblood, Katsuhito Yasuno, Kaya Bilgüvar, Murat Günel, Beyhan Tüysüz
Molecular Genetics & Genomic Medicine. 201838 CitationsOPEN ACCESS
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy
Nicolas Chatron, Felicitas Becker, Heba Morsy, Miriam Schmidts, Katia Hardies, Beyhan Tüysüz, Sandra Roselli, Maryam Najafi, Dilek Uludağ Alkaya, Farah Ashrafzadeh, Amira Nabil, Tarek Omar, Reza Maroofian, Ehsan Ghayoor Karimiani, Haytham Hussien, Fernando Kok, Luiza Ramos, Nilay Güneş, Kaya Bilgüvar, Audrey Labalme, Eudéline Alix, Damien Sanlaville, Julitta de Bellescize, Anne‐Lise Poulat, Ingo Helbig, Sarah von Spiczak, Stéphanie Baulac, Nina Barišić, Rudi Balling, Hande Çağlayan, Dana Craiu, Renzo Guerrini, Karl Martin Klein, Carla Marini, Hiltrud Muhle, Felix Rosenow, José M. Serratosa, Katalin Štěrbová, Yvonne Weber, Ali‐Reza Moslemi, Holger Lerche, Patrick May, Gaëtan Lesca, Sarah Weckhuysen, Homa Tajsharghi
Brain. 202032 CitationsOPEN ACCESS
Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey
Güven Toksoy, Dilek Uludağ Alkaya, Г. Г. Багирова, Şahin Avcı, Agharza Aghayev, Nilay Güneş, Umut Altunoğlu, Yasemin Alanay, Seher Başaran, Ezgi Gizem Berkay, Birsen Karaman, Tiraje Çelkan, Hilmi Apak, Hülya Kayserili, Beyhan Tüysüz, Zehra Oya Uyguner
S150607185. 202027 CitationsOPEN ACCESS
Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants
Beyhan Tüysüz, Leyla Elkanova, Dilek Uludağ Alkaya, Çağrı Güleç, Güven Toksoy, Nilay Güneş, Hakan Yazan, Asuman Bayhan, Timur Yıldırım, Gözde Yeşil, Zehra Oya Uyguner
Bone. 202127 Citations
Related on ScholarIQ
Istanbul University-Cerrahpaşa
Institution
Epidemiology and survival of childhood cancer in Turkey
Paper
Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (<scp>CACP</scp>) syndrome
Paper
Bi-allelic GAD1 variants cause a neonatal onset syndromic developmental and epileptic encephalopathy
Paper
Clinical and Molecular Characterization of Fanconi Anemia Patients in Turkey
Paper
Osteogenesis imperfecta in 140 Turkish families: Molecular spectrum and, comparison of long-term clinical outcome of those with COL1A1/A2 and biallelic variants
Paper