Author/Creator: Arslan, Ahmet - British Library Electronic Legal Deposit Catalogue-Journal Issues and Articles Search Results

Author/Creator Arslan, Ahmet

1. An intrinsic evaluation of the Waterloo spam rankings of the ClueWeb09 and ClueWeb12 datasets. (February 2021)

Authors:: Yılmazel, İbrahim Barış; Arslan, Ahmet
Journal:: Journal of information science
Issue:: Volume 47:Number 1(2021)
Page Start:: 41
Record Type:: Journal Article
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2. Automatic gender determination from 3D digital maxillary tooth plaster models based on the random forest algorithm and discrete cosine transform. (May 2017)

Authors:: Akkoç, Betül; Arslan, Ahmet; Kök, Hatice
Journal:: Computer methods and programs in biomedicine
Issue:: Volume 143(2017)
Page Start:: 59
Record Type:: Journal Article
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3. DeASCIIfication approach to handle diacritics in Turkish information retrieval. Issue 2 (March 2016)

Authors:: Arslan, Ahmet
Journal:: Information processing & management
Issue:: Volume 52:Issue 2(2016:Mar.)
Page Start:: 326
Record Type:: Journal Article
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4. Does the serotonin receptor gene (rs6313 and rs6314) polymorphism have a role in suicidal attempts?. (May 2018)

Authors:: Atan, Yusuf; Akbaba, Murat; Kul, Seval; Tataroğlu, Zekeriya; Temiz, Ebru; Nacarkahya, Gülper; Arslan, Ahmet
Journal:: Journal of forensic and legal medicine
Issue:: Volume 56(2018)
Page Start:: 32
Record Type:: Journal Article
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5. Endothelial NOS gene Glu298Asp polymorphism in preterm neonates with respiratory distress syndrome. Issue 10 (28th January 2013)

Authors:: Demirçubuk, Ayşe G.; Coşkun, M. Yavuz; Demiryürek, Şeniz; Dokuyucu, Recep; Öztuzcu, Serdar; Taviloğlu, Z. Şafak; Arslan, Ahmet; Sivaslı, Ercan
Journal:: Pediatric pulmonology
Issue:: Volume 48:Issue 10(2013:Oct.)
Page Start:: 976
Record Type:: Journal Article
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6. FP400MULTIPLE GNAS1, FGF23, FGFR3 GENES' STRİKİNG MUTATIONS IN CKD PATIENTS WITH SH. NEW BONE DISPLASIA-HEREDİTARY OSTEODISTROPHY AND UGLIFYING HUMAN FACE APPEARANCES. SAGLIKER SYNDROME(SS ). (18th May 2018)

Authors:: Sagliker, Yahya; Demirhan, Osman; Arslan, Ahmet; Sagliker, Hasan Sabit; Bayraktar, Recep; Dogan, Ekrem; Sagliker Ozkaynak, Piril; Paylar, Nuray; Akbal, Eylül; Akbal, Eylül; Ergun, Sercan
Journal:: Nephrology dialysis transplantation
Issue:: Volume 33(2018)Supplement 1
Page Start:: i168
Record Type:: Journal Article
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7. FP400MULTIPLE GNAS1, FGF23, FGFR3 GENES' STRİKİNG MUTATIONS IN CKD PATIENTS WITH SH. NEW BONE DISPLASIA-HEREDİTARY OSTEODISTROPHY AND UGLIFYING HUMAN FACE APPEARANCES. SAGLIKER SYNDROME(SS ). (18th May 2018)

Authors:: Sagliker, Yahya; Demirhan, Osman; Arslan, Ahmet; Sagliker, Hasan Sabit; Bayraktar, Recep; Dogan, Ekrem; Sagliker Ozkaynak, Piril; Paylar, Nuray; Akbal, Eylül; Akbal, Eylül; Ergun, Sercan
Journal:: Nephrology dialysis transplantation
Issue:: Volume 33(2018)Supplement 1
Page Start:: i168
Record Type:: Journal Article
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8. Fresh Ready-mixed Concrete Waste in Construction Projects: A Planning Approach. (2015)

Authors:: Kazaz, Aynur; Ulubeyli, Serdar; Er, Bayram; Arslan, Volkan; Arslan, Ahmet; Atici, Murat
Journal:: Procedia engineering
Issue:: Volume 123(2015)
Page Start:: 268
Record Type:: Journal Article
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9. Gray level co-occurrence and random forest algorithm-based gender determination with maxillary tooth plaster images. (1st June 2016)

Authors:: Akkoç, Betül; Arslan, Ahmet; Kök, Hatice
Journal:: Computers in biology and medicine
Issue:: Volume 73(2016)
Page Start:: 102
Record Type:: Journal Article
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10. Investigation of Distribution of Beta -Thalassemia Hereditary Mutations in Gaziantep and the Surrounding Areas. Issue 4 (2016)

Authors:: Öztuzcu, Serdar; Bay, Ali; Nacarkahya, Gülper; Ulaşlı, Mustafa; Aktekin, Elif; Akbayram, Sinan; Korkmaz, Murat; Taşgül, Füsun; Arslan, Ahmet
Journal:: Journal of clinical and experimental investigations
Issue:: Volume 7:Issue 4(2016)
Page Start:: 265
Record Type:: Journal Article
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