EpiSAFARI: sensitive detection of valleys in epigenetic signals for enhancing annotations of functional elements

por Harmanci, Arif, Harmanci, Akdes Serin, Swaminathan, Jyothishmathi, Gopalakrishnan, Vidya
Publicado en Bioinformatics (2019)

Exome Analysis of the Evolutionary Path of Hepatocellular Adenoma-Carcinoma Transition, Vascular Invasion and Brain Dissemination

por Vilarinho, Sílvia, Erson-Omay, Zeynep, Mitchell-Richards, Kisha, Cha, Charles, Nelson-Williams, Carol, Harmancı, Akdes Serin, Yasuno, Katsuhito, Günel, Murat, Taddei, Tamar H.
Publicado en J Hepatol (2017)

METAP1 Mutation Is a Novel Candidate for Autosomal Recessive Intellectual Disability

por Caglayan, Ahmet Okay, Aktar, Fesih, Bilguvar, Kaya, Baranoski, Jacob F., Akgumus, Gozde Tugce, Harmanci, Akdes Serin, Erson-Omay, Emine Zeynep, Yasuno, Katsuhito, Caksen, Huseyin, Gunel, Murat
Publicado en J Hum Genet (2020)

ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features

por Çağlayan, Ahmet Okay, Sezer, Rabia Gonul, Kaymakçalan, Hande, Ulgen, Ege, Yavuz, Taner, Baranoski, Jacob F., Bozaykut, Abdulkadir, Harmanci, Akdes Serin, Yalcin, Yalim, Youngblood, Mark W., Yasuno, Katsuhito, Bilgüvar, Kaya, Gunel, Murat
Publicado en Cold Spring Harb Mol Case Stud (2017)

A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP

por Çağlayan, Ahmet Okay, Tüysüz, Beyhan, Coşkun, Süleyman, Quon, Jennifer, Harmanci, Akdes Serin, Baranoski, Jacob F., Baran, Burçin, Erson-Omay, E. Zeynep, Henegariu, Octavian, Mane, Shrikant M., Bilgüvar, Kaya, Yasuno, Katsuhito, Günel, Murat
Publicado en J Hum Genet (2016)

GENO-15 IDENTIFICATION AND GENOMIC ANALYSIS OF HYPER-MUTATED AND ULTRA-MUTATED GBMS

por Erson-Omay, E. Zeynep, Schultz, Nikolaus, Omay, S. Bulent, Ozduman, Koray, Harmanci, Akdes Serin, Clark, Victoria, Baranoski, Jacob, Gunel, Jennifer Moliterno, Pamir, M. Necmettin, Bilguvar, Kaya, Yasuno, Katsuhito, Vortmeyer, Alexander, Huttner, Anita J., Sander, Chris, Gunel, Murat
Publicado en Neuro Oncol (2015)

NGLY1 Mutation Causes Neuromotor Impairment, Intellectual Disability, and Neuropathy

por Caglayan, Ahmet Okay, Comu, Sinan, Baranoski, Jacob F., Parman, Yesim, Kaymakçalan, Hande, Akgumus, Gozde Tugce, Caglar, Caner, Dolen, Duygu, Omay, E. Zeynep Erson, Harmanci, Akdes Serin, Mishra, Ketu, Freeze, Hudson H., Yasuno, Katsuhito, Bilguvar, Kaya, Gunel, Murat
Publicado en Eur J Med Genet (2014)

Longitudinal analysis of treatment-induced genomic alterations in gliomas

por Erson-Omay, E. Zeynep, Henegariu, Octavian, Omay, S. Bülent, Harmancı, Akdes Serin, Youngblood, Mark W., Mishra-Gorur, Ketu, Li, Jie, Özduman, Koray, Carrión-Grant, Geneive, Clark, Victoria E., Çağlar, Caner, Bakırcıoğlu, Mehmet, Pamir, M. Necmettin, Tabar, Viviane, Vortmeyer, Alexander O., Bilguvar, Kaya, Yasuno, Katsuhito, DeAngelis, Lisa M., Baehring, Joachim M., Moliterno, Jennifer, Günel, Murat
Publicado en Genome Med (2017)

Integrated genomic analyses of de novo pathways underlying atypical meningiomas

por Harmancı, Akdes Serin, Youngblood, Mark W., Clark, Victoria E., Coşkun, Süleyman, Henegariu, Octavian, Duran, Daniel, Erson-Omay, E. Zeynep, Kaulen, Leon D., Lee, Tong Ihn, Abraham, Brian J., Simon, Matthias, Krischek, Boris, Timmer, Marco, Goldbrunner, Roland, Omay, S. Bülent, Baranoski, Jacob, Baran, Burçin, Carrión-Grant, Geneive, Bai, Hanwen, Mishra-Gorur, Ketu, Schramm, Johannes, Moliterno, Jennifer, Vortmeyer, Alexander O., Bilgüvar, Kaya, Yasuno, Katsuhito, Young, Richard A., Günel, Murat
Publicado en Nat Commun (2017)

Author Correction: Integrated genomic analyses of de novo pathways underlying atypical meningiomas

por Harmancı, Akdes Serin, Youngblood, Mark W., Clark, Victoria E., Coşkun, Süleyman, Henegariu, Octavian, Duran, Daniel, Erson-Omay, E. Zeynep, Kaulen, Leon D., Lee, Tong Ihn, Abraham, Brian J., Simon, Matthias, Krischek, Boris, Timmer, Marco, Goldbrunner, Roland, Omay, S. Bülent, Baranoski, Jacob, Baran, Burçin, Carrión-Grant, Geneive, Bai, Hanwen, Mishra-Gorur, Ketu, Schramm, Johannes, Moliterno, Jennifer, Vortmeyer, Alexander O., Bilgüvar, Kaya, Yasuno, Katsuhito, Young, Richard A., Günel, Murat
Publicado en Nat Commun (2018)

Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas

por Clark, Victoria E, Harmancı, Akdes Serin, Bai, Hanwen, Youngblood, Mark W, Lee, Tong Ihn, Baranoski, Jacob F, Ercan-Sencicek, A Gulhan, Abraham, Brian J, Weintraub, Abraham S, Hnisz, Denes, Simon, Matthias, Krischek, Boris, Erson-Omay, E Zeynep, Henegariu, Octavian, Carrión-Grant, Geneive, Mishra-Gorur, Ketu, Durán, Daniel, Goldmann, Johanna E, Schramm, Johannes, Goldbrunner, Roland, Piepmeier, Joseph M, Vortmeyer, Alexander O, Günel, Jennifer Moliterno, Bilgüvar, Kaya, Yasuno, Katsuhito, Young, Richard A, Günel, Murat
Publicado en Nat Genet (2016)

Integrated genomic characterization of IDH1-mutant glioma malignant progression

por Bai, Hanwen, Harmanci, Akdes Serin, Erson-Omay, E Zeynep, Li, Jie, Coşkun, Süleyman, Simon, Matthias, Krischek, Boris, Özduman, Koray, Omay, S Bülent, Sorensen, Eric A, Turcan, Şevin, Bakırcığlu, Mehmet, Carrión-Grant, Geneive, Murray, Phillip B, Clark, Victoria E, Ercan-Sencicek, A Gulhan, Knight, James, Sencar, Leman, Altınok, Selin, Kaulen, Leon D, Gülez, Burcu, Timmer, Marco, Schramm, Johannes, Mishra-Gorur, Ketu, Henegariu, Octavian, Moliterno, Jennifer, Louvi, Angeliki, Chan, Timothy A, Tannheimer, Stacey L, Pamir, M Necmettin, Vortmeyer, Alexander O, Bilguvar, Kaya, Yasuno, Katsuhito, Günel, Murat
Publicado en Nat Genet (2015)