Genome-wide association study of early liveweight traits in fat-tailed Akkaraman lambs von Cinar, Mehmet Ulas, Arslan, Korhan, Sohel, Md Mahmodul Hasan, Bayram, Davut, Piel, Lindsay M. W, White, Stephen N, Daldaban, Fadime, Aksel, Esma Gamze, Akyüz, Bilal

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Genome-wide association study of early liveweight traits in fat-tailed Akkaraman lambs von Mehmet Ulas Cinar, Korhan Arslan, Md Mahmodul Hasan Sohel, Davut Bayram, Lindsay M. W. Piel, Stephen N. White, Fadime Daldaban, Esma Gamze Aksel, Bilal Akyüz

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Allelic frequency of kappa-casein, growth hormone and prolactin gene in holstein, brown swiss and simmental cattle breeds in turkey von AKYUZ B, ARSLAN K, BAYRAM D, ISCAN KM

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Polimeraz zincir reaksiyonu (PZR) ile sığırlardaki freemartinismus sendromunun tanısı von AKYÜZ, Bilal, BAYRAM, Davut, GÜRBULAK, Kutlay

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Diagnosis of Freemartinism Syndrome by Polymerase Chain Reaction (PCR) in Cattle von AKYÜZ, Bilal, BAYRAM, Davut, GÜRBULAK, Kutlay

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Farklı Besi Program ve Sürelerindeki Saf Morkaraman ve Kıvırcık X Morkaraman Fı Kuzuların Besi Performansı,Kesim ve Karkas Özellikleri: I- Vücut Ölçüleri von BAYRAM, Davut, ODABAŞIOĞLU, Fuat

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Zavot ırkı sığırlarda karkas özellikleri ve karkas parçalamanın ekonomik yönü von Savaş, AKÇAY, SARIÖZKAN

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Morkaraman ve Kıvırcık X Morkaraman (G1) melezi kuzularda büyüme, besi performansı, kesim ve karkas özelliklerinin araştırılması von BAYRAM, Davut, KÜÇÜK, Mürsel, YILMAZ, Orhan

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A Study on Growth, Fattening Performance and Carcass Characteristics of Morkaraman and Kıvırcık x Morkaraman Crosses (B1) Lambs von KÜÇÜK, Mürsel, BAYRAM, Davut, YILMAZ, Orhan

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Effects of some factors on gestation length in Hamdani, Morkaraman and Karakul sheep von BAYRAM, Davut, YILMAZ, Orhan

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Phenotypic expansion illuminates multilocus pathogenic variation von Karaca, Ender, Posey, Jennifer E., Coban Akdemir, Zeynep, Pehlivan, Davut, Harel, Tamar, Jhangiani, Shalini N., Bayram, Yavuz, Song, Xiaofei, Bahrambeigi, Vahid, Yuregir, Ozge Ozalp, Bozdogan, Sevcan, Yesil, Gozde, Isikay, Sedat, Muzny, Donna, Gibbs, Richard A., Lupski, James R.

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An Open-Source Hypersonic Solver for Non-equilibrium Flows von Davut Vatansever, Bayram Çelik

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Molecular etiology of arthrogryposis in multiple families of mostly Turkish origin von Bayram, Yavuz, Karaca, Ender, Coban Akdemir, Zeynep, Yilmaz, Elif Ozdamar, Tayfun, Gulsen Akay, Aydin, Hatip, Torun, Deniz, Bozdogan, Sevcan Tug, Gezdirici, Alper, Isikay, Sedat, Atik, Mehmed M, Gambin, Tomasz, Harel, Tamar, El-Hattab, Ayman W, Charng, Wu-Lin, Pehlivan, Davut, Jhangiani, Shalini N, Muzny, Donna M, Karaman, Ali, Celik, Tamer, Yuregir, Ozge Ozalp, Yildirim, Timur, Bayhan, Ilhan A, Boerwinkle, Eric, Gibbs, Richard A, Elcioglu, Nursel, Tuysuz, Beyhan, Lupski, James R

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Exome Sequencing of a Primary Ovarian Insufficiency Cohort Reveals Common Molecular Etiologies for a Spectrum of Disease von Jolly, Angad, Bayram, Yavuz, Turan, Serap, Aycan, Zehra, Tos, Tulay, Abali, Zehra Yavas, Hacihamdioglu, Bulent, Coban Akdemir, Zeynep Hande, Hijazi, Hadia, Bas, Serpil, Atay, Zeynep, Guran, Tulay, Abali, Saygin, Bas, Firdevs, Darendeliler, Feyza, Colombo, Roberto, Barakat, Tahsin Stefan, Rinne, Tuula, White, Janson J, Yesil, Gozde, Gezdirici, Alper, Gulec, Elif Yilmaz, Karaca, Ender, Pehlivan, Davut, Jhangiani, Shalini N, Muzny, Donna M, Poyrazoglu, Sukran, Bereket, Abdullah, Gibbs, Richard A, Posey, Jennifer E, Lupski, James R

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Global transcriptional disturbances underlie Cornelia de Lange syndrome and related phenotypes von Yuan, Bo, Pehlivan, Davut, Karaca, Ender, Patel, Nisha, Charng, Wu-Lin, Gambin, Tomasz, Gonzaga-Jauregui, Claudia, Sutton, V Reid, Yesil, Gozde, Bozdogan, Sevcan Tug, Tos, Tulay, Koparir, Asuman, Koparir, Erkan, Beck, Christine R, Gu, Shen, Aslan, Huseyin, Yuregir, Ozge Ozalp, Al Rubeaan, Khalid, Alnaqeb, Dhekra, Alshammari, Muneera J, Bayram, Yavuz, Atik, Mehmed M, Aydin, Hatip, Geckinli, B Bilge, Seven, Mehmet, Ulucan, Hakan, Fenercioglu, Elif, Ozen, Mustafa, Jhangiani, Shalini, Muzny, Donna M, Boerwinkle, Eric, Tuysuz, Beyhan, Alkuraya, Fowzan S, Gibbs, Richard A, Lupski, James R

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Whole-Exome Sequencing Identifies Homozygous GPR161 Mutation in a Family with Pituitary Stalk Interruption Syndrome von Karaca, Ender, Buyukkaya, Ramazan, Pehlivan, Davut, Charng, Wu-Lin, Yaykasli, Kursat O, Bayram, Yavuz, Gambin, Tomasz, Withers, Marjorie, Atik, Mehmed M, Arslanoglu, Ilknur, Bolu, Semih, Erdin, Serkan, Buyukkaya, Ayla, Yaykasli, Emine, Jhangiani, Shalini N, Muzny, Donna M, Gibbs, Richard A, Lupski, James R

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REST Final-Exon-Truncating Mutations Cause Hereditary Gingival Fibromatosis von Bayram, Yavuz, White, Janson J., Elcioglu, Nursel, Cho, Megan T., Zadeh, Neda, Gedikbasi, Asuman, Palanduz, Sukru, Ozturk, Sukru, Cefle, Kivanc, Kasapcopur, Ozgur, Coban Akdemir, Zeynep, Pehlivan, Davut, Begtrup, Amber, Carvalho, Claudia M.B., Paine, Ingrid Sophie, Mentes, Ali, Bektas-Kayhan, Kivanc, Karaca, Ender, Jhangiani, Shalini N., Muzny, Donna M., Gibbs, Richard A., Lupski, James R.

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Monoallelic and Biallelic Variants in EMC1 Identified in Individuals with Global Developmental Delay, Hypotonia, Scoliosis, and Cerebellar Atrophy von Harel, Tamar, Yesil, Gozde, Bayram, Yavuz, Coban-Akdemir, Zeynep, Charng, Wu-Lin, Karaca, Ender, Al Asmari, Ali, Eldomery, Mohammad K., Hunter, Jill V., Jhangiani, Shalini N., Rosenfeld, Jill A., Pehlivan, Davut, El-Hattab, Ayman W., Saleh, Mohammed A., LeDuc, Charles A., Muzny, Donna, Boerwinkle, Eric, Gibbs, Richard A., Chung, Wendy K., Yang, Yaping, Belmont, John W., Lupski, James R.

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Developmental genomics of limb malformations: Allelic series in association with gene dosage effects contribute to the clinical variability von Duan, Ruizhi, Hijazi, Hadia, Gulec, Elif Yilmaz, Eker, Hatice Koçak, Costa, Silvia R., Sahin, Yavuz, Ocak, Zeynep, Isikay, Sedat, Ozalp, Ozge, Bozdogan, Sevcan, Aslan, Huseyin, Elcioglu, Nursel, Bertola, Débora R., Gezdirici, Alper, Du, Haowei, Fatih, Jawid M., Grochowski, Christopher M., Akay, Gulsen, Jhangiani, Shalini N., Karaca, Ender, Gu, Shen, Coban-Akdemir, Zeynep, Posey, Jennifer E., Bayram, Yavuz, Sutton, V. Reid, Carvalho, Claudia M.B., Pehlivan, Davut, Gibbs, Richard A., Lupski, James R.

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