The Essential Role of Centrosomal NDE1 in Human Cerebral Cortex Neurogenesis
Bakircioglu, Mehmet, Carvalho, Ofélia P., Khurshid, Maryam, Cox, James J., Tuysuz, Beyhan, Barak, Tanyeri, Yilmaz, Saliha, Caglayan, Okay, Dincer, Alp, Nicholas, Adeline K., Quarrell, Oliver, Springell, Kelly, Karbani, Gulshan, Malik, Saghira, Gannon, Caroline, Sheridan, Eamonn, Crosier, Moira, Lisgo, Steve N., Lindsay, Susan, Bilguvar, Kaya, Gergely, Fanni, Gunel, Murat, Woods, C. Geoffrey
Published in American journal of human genetics (13.05.2011)
Published in American journal of human genetics (13.05.2011)
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Journal Article
P1485: PKM AND PKR EXPRESSION DURING HEMATOPOIESIS AND ERYTHROPOIESIS
Tsai, Erin, Rivadeneyra, Leonardo, Yilmaz, Saliha, Dang, Lenny, Wind‐Rotolo, Megan
Published in HemaSphere (08.08.2023)
Published in HemaSphere (08.08.2023)
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Journal Article
Evaluation of Exudative Pleural Effusions: A Multicenter, Prospective, Observational Study
Ak, Guntulu, Metintas, Selma, Taskın, Ayse Naz, Uzel Sener, Melahat, Soyler, Yasemin, Yilmaz, Meltem, Turna, Akif, Akin Kabalak, Pınar, Bilaceroglu, Semra, Koksal, Deniz, Yilmaz Demirci, Nilgun, Sogukpinar, Ozlem, Boga, Sibel, Ercelik, Merve, Karadeniz, Gulistan, Polat, Gulru, Guldaval, Filiz, Aka Akturk, Ulku, Yilmaz, Senay, Ogan, Nalan, Yilmaz, Saliha, Esendagli, Dorina, Caglayan, Benan, Zeybek, Arife, Durmus Kocak, Nagihan, Mutlu, Pinar, Atinkaya Baytemir, Cansel, Sarbay, Ismail, Yilmaz, Ulku, Metintas, Muzaffer
Published in Lung (01.12.2022)
Published in Lung (01.12.2022)
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Journal Article
Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO
Clark, Victoria E., Erson-Omay, E. Zeynep, Serin, Akdes, Yin, Jun, Cotney, Justin, Özduman, Koray, Avşar, Timuçin, Li, Jie, Murray, Phillip B., Henegariu, Octavian, Yilmaz, Saliha, Günel, Jennifer Moliterno, Carrión-Grant, Geneive, Yılmaz, Baran, Grady, Conor, Tanrıkulu, Bahattin, Bakırcıoǧlu, Mehmet, Kaymakçalan, Hande, Caglayan, Ahmet Okay, Sencar, Leman, Ceyhun, Emre, Atik, A. Fatih, Bayri, Yaşar, Bai, Hanwen, Kolb, Luis E., Hebert, Ryan M., Omay, S. Bulent, Mishra-Gorur, Ketu, Choi, Murim, Overton, John D., Holland, Eric C., Mane, Shrikant, State, Matthew W., Bilgüvar, Kaya, Baehring, Joachim M., Gutin, Philip H., Piepmeier, Joseph M., Vortmeyer, Alexander, Brennan, Cameron W., Pamir, M. Necmettin, Kılıç, Türker, Lifton, Richard P., Noonan, James P., Yasuno, Katsuhito, Günel, Murat
Published in Science (American Association for the Advancement of Science) (01.03.2013)
Published in Science (American Association for the Advancement of Science) (01.03.2013)
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Journal Article
Regional Genetic Heterogeneity Among Patients with Pyruvate Kinase Deficiency
Bianchi, Paola, Fermo, Elisa, Kuo, Kevin H.M., Pospíšilová, Dagmar, Glenthoej, Andreas, Lander, Carl, Van Beers, Eduard J., Glader, Bertil, Vives Corrons, Joan-Lluis, Eber, Stefan W, Yan, Yan, McGee, Bryan, Ford, Janet H, Yilmaz, Saliha, Grace, Rachael F.
Published in Blood (02.11.2023)
Published in Blood (02.11.2023)
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Journal Article
Spondyloepimetaphyseal dysplasia Pakistani type: Expansion of the phenotype
Tüysüz, Beyhan, Yılmaz, Saliha, Gül, Ece, Kolb, Luis, Bilguvar, Kaya, Evliyaoğlu, Olcay, Günel, Murat
Published in American journal of medical genetics. Part A (01.06.2013)
Published in American journal of medical genetics. Part A (01.06.2013)
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Journal Article
Hidden Permissions on Android: A Permission-Based Android Mobile Privacy Risk Model
Yilmaz, Saliha, Davis, Mastaneh
Published in European Conference on Cyber Warfare and Security (01.06.2023)
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Published in European Conference on Cyber Warfare and Security (01.06.2023)
Conference Proceeding
Hyperandrogenism and Skeletal Dysplasia: Evaluation of 7 Patients with PAPSS2 Gene Mutation
Alkaya, Dilek Uludag, Yilmaz, Saliha, Evliyaoglu, Olcay, Bilguvar, Kaya, Gunel, Murat, Tuysuz, Beyhan
Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
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Published in Journal of clinical research in pediatric endocrinology (01.06.2017)
Journal Article
Genotype–phenotype investigation of 35 patients from 11 unrelated families with camptodactyly–arthropathy–coxa vara–pericarditis (CACP) syndrome
Yilmaz, Saliha, Uludağ Alkaya, Dilek, Kasapçopur, Özgür, Barut, Kenan, Akdemir, Ekin S., Celen, Cemre, Youngblood, Mark W., Yasuno, Katsuhito, Bilguvar, Kaya, Günel, Murat, Tüysüz, Beyhan
Published in Molecular genetics & genomic medicine (01.03.2018)
Published in Molecular genetics & genomic medicine (01.03.2018)
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Journal Article
Retrospective evaluation of patients with organizing pneumonia: is cryptogenic organizing pneumonia different from secondary organizing pneumonia?
Yılmaz, Saliha, Akıncı Özyürek, Berna, Erdoğan, Yurdanur, Cirit Koçer, Burcu, Demirağ, Funda, Dadalı, Yeliz, Büyükyaylacı Özden, Sertaç
Published in Tüberküloz ve toraks (01.03.2017)
Published in Tüberküloz ve toraks (01.03.2017)
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Journal Article
Investigation of low-dose ritonavir on human peripheral blood mononuclear cells using gene expression whole genome microarrays
Yilmaz, Saliha, Boffito, Marta, Collot-Teixeira, Sophie, De Lorenzo, Ferruccio, Waters, Laura, Fletcher, Carl, Back, David, Pozniak, Anton, Gazzard, Brian, McGregor, John Louis
Published in Genomics (San Diego, Calif.) (01.07.2010)
Published in Genomics (San Diego, Calif.) (01.07.2010)
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Journal Article
Gene–disease relationship discovery based on model-driven data integration and database view definition
Yilmaz, S., Jonveaux, P., Bicep, C., Pierron, L., Smaïl-Tabbone, M., Devignes, M.D.
Published in Bioinformatics (15.01.2009)
Published in Bioinformatics (15.01.2009)
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Journal Article
Gene Expression Signature in Peripheral Blood Cells Detects Intracranial Aneurysm
Yilmaz, Saliha, Bijlenga, Philippe, Rashid, Mamunur, Collot-Teixeira, Sophie, Brocheton, Jessy, Proust, Carole, Rotival, Maxime, Risselada, Roelof, Summers, Paul, Blasco, J., Singh, J., Waterworth, Alan, Ebeling, Christian, Friedrich, Christoph, Frangi, A. F., Macho, J. J., Byrne, J., Sturkenboom, M. C.J.M., Schaller, K., Cambien, Francois, Gunel, Murat, McGregor, John Louis
Published in Neurosurgery (01.08.2010)
Published in Neurosurgery (01.08.2010)
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Journal Article
Deleterious mutations in exon 1 of MECP2 in Rett syndrome
Quenard, Aline, Yilmaz, Saliha, Fontaine, Hervé, Bienvenu, Thierry, Moncla, Anne, des Portes, Vincent, Rivier, François, Mathieu, Michèle, Raux, Grégory, Jonveaux, Philippe, Philippe, Christophe
Published in European journal of medical genetics (01.07.2006)
Published in European journal of medical genetics (01.07.2006)
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Journal Article
Screening of subtle copy number changes in Aicardi syndrome patients with a high resolution X chromosome array-CGH
Yilmaz, Saliha, Fontaine, Hervé, Brochet, Karène, Grégoire, Marie-José, Devignes, Marie-Dominique, Schaff, Jean-Luc, Philippe, Christophe, Nemos, Christophe, McGregor, John Louis, Jonveaux, Philippe
Published in European journal of medical genetics (01.09.2007)
Published in European journal of medical genetics (01.09.2007)
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Journal Article
Recessive LAMC3 mutations cause malformations of occipital cortical development
Barak, Tanyeri, Kwan, Kenneth Y, Louvi, Angeliki, Demirbilek, Veysi, Saygı, Serap, Tüysüz, Beyhan, Choi, Murim, Boyacı, Hüseyin, Doerschner, Katja, Zhu, Ying, Kaymakçalan, Hande, Yılmaz, Saliha, Bakırcıoğlu, Mehmet, Çağlayan, Ahmet Okay, Öztürk, Ali Kemal, Yasuno, Katsuhito, Brunken, William J, Atalar, Ergin, Yalçınkaya, Cengiz, Dinçer, Alp, Bronen, Richard A, Mane, Shrikant, Özçelik, Tayfun, Lifton, Richard P, Šestan, Nenad, Bilgüvar, Kaya, Günel, Murat
Published in Nature genetics (01.06.2011)
Published in Nature genetics (01.06.2011)
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Journal Article
Self-esteem in Turkish diabetic children
Pek, Hatice, Yildirim, Zerrin, Akdovan, Tülin, Yilmaz, Saliha
Published in Journal of pediatric nursing (01.08.2002)
Published in Journal of pediatric nursing (01.08.2002)
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Journal Article