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Akdes Serin Harmanci
Akdes Serin Harmanci
Assistant Professor, Baylor College of Medicine
Verified email at bcm.edu
Title
Cited by
Cited by
Year
Genomic Analysis of Non-NF2 Meningiomas Reveals Mutations in TRAF7, KLF4, AKT1, and SMO
VE Clark, EZ Erson-Omay, A Serin, J Yin, J Cotney, K Özduman, T Avşar, ...
Science 339 (6123), 1077-1080, 2013
8382013
Recurrent somatic mutations in POLR2A define a distinct subset of meningiomas
VE Clark, AS Harmancı, H Bai, MW Youngblood, TI Lee, JF Baranoski, ...
Nature genetics 48 (10), 1253-1259, 2016
3142016
Integrated genomic characterization of IDH1-mutant glioma malignant progression
H Bai, AS Harmancı, EZ Erson-Omay, J Li, S Coşkun, M Simon, ...
Nature genetics 48 (1), 59-66, 2016
3062016
Integrated genomic analyses of de novo pathways underlying atypical meningiomas
AS Harmancı, MW Youngblood, VE Clark, S Coşkun, O Henegariu, ...
Nature communications 8 (1), 14433, 2017
197*2017
Mitochondrial-associated cell death mechanisms are reset to an embryonic-like state in aged donor-derived iPS cells harboring chromosomal aberrations
A Prigione, AM Hossini, B Lichtner, A Serin, B Fauler, M Megges, R Lurz, ...
PloS one 6 (11), e27352, 2011
1222011
Somatic POLE mutations cause an ultramutated giant cell high-grade glioma subtype with better prognosis
EZ Erson-Omay, AO Çağlayan, N Schultz, N Weinhold, SB Omay, ...
Neuro-oncology 17 (10), 1356-1364, 2015
1202015
CaSpER identifies and visualizes CNV events by integrative analysis of single-cell or bulk RNA-sequencing data
A Serin Harmanci, AO Harmanci, X Zhou
Nature communications 11 (1), 89, 2020
1162020
NGLY1 mutation causes neuromotor impairment, intellectual disability, and neuropathy
AO Caglayan, S Comu, JF Baranoski, Y Parman, H Kaymakçalan, ...
European journal of medical genetics 58 (1), 39-43, 2015
962015
Debi: Discovering differentially expressed biclusters using a frequent itemset approach
A Serin, M Vingron
Algorithms for Molecular Biology 6, 1-12, 2011
852011
Paediatric hepatocellular carcinoma due to somatic CTNNB1 and NFE2L2 mutations in the setting of inherited bi-allelic ABCB11 mutations
S Vilarinho, EZ Erson-Omay, AS Harmanci, R Morotti, G Carrion-Grant, ...
Journal of hepatology 61 (5), 1178-1183, 2014
482014
Multiple approaches converge on three biological subtypes of meningioma and extract new insights from published studies
JC Bayley, CC Hadley, AO Harmanci, AS Harmanci, TJ Klisch, AJ Patel
Science advances 8 (5), eabm6247, 2022
382022
ALPK3 gene mutation in a patient with congenital cardiomyopathy and dysmorphic features
AO Çağlayan, RG Sezer, H Kaymakçalan, E Ulgen, T Yavuz, ...
Molecular Case Studies 3 (5), a001859, 2017
262017
Patient-derived orthotopic xenograft (PDOX) mouse models of primary and recurrent meningioma
H Zhang, L Qi, Y Du, LF Huang, FK Braun, M Kogiso, Y Zhao, C Li, ...
Cancers 12 (6), 1478, 2020
252020
Longitudinal analysis of treatment-induced genomic alterations in gliomas
EZ Erson-Omay, O Henegariu, SB Omay, AS Harmancı, MW Youngblood, ...
Genome medicine 9, 1-10, 2017
252017
Hypermitotic meningiomas harbor DNA methylation subgroups with distinct biological and clinical features
A Choudhury, WC Chen, CHG Lucas, JC Bayley, AS Harmanci, ...
Neuro-oncology 25 (3), 520-530, 2023
242023
PPIL4 is essential for brain angiogenesis and implicated in intracranial aneurysms in humans
T Barak, E Ristori, AG Ercan-Sencicek, DF Miyagishima, ...
Nature medicine 27 (12), 2165-2175, 2021
232021
Remote neuronal activity drives glioma progression through SEMA4F
E Huang-Hobbs, YT Cheng, Y Ko, E Luna-Figueroa, B Lozzi, KR Taylor, ...
Nature 619 (7971), 844-850, 2023
222023
Glioma epileptiform activity and progression are driven by IGSF3-mediated potassium dysregulation
RN Curry, I Aiba, J Meyer, B Lozzi, Y Ko, MF McDonald, A Rosenbaum, ...
Neuron 111 (5), 682-695. e9, 2023
212023
A patient with a novel homozygous missense mutation in FTO and concomitant nonsense mutation in CETP
AO Çağlayan, B Tüysüz, S Coşkun, J Quon, AS Harmancı, JF Baranoski, ...
Journal of human genetics 61 (5), 395-403, 2016
172016
Single-cell RNA sequencing reveals immunosuppressive myeloid cell diversity during malignant progression in a murine model of glioma
S Rajendran, Y Hu, A Canella, C Peterson, A Gross, M Cam, M Nazzaro, ...
Cell Reports 42 (3), 2023
162023
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