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Magnetic resonance spectroscopic correlates of progression free and overall survival in "glioblastoma, IDH-wildtype, WHO grade-4"

Frontiers in neuroscience, 2023-06, Vol.17, p.1149292-1149292

2023

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Angiogenesis, Invasion, and Metastasis Characteristics of Hepatocellular Carcinoma

Journal of gastrointestinal cancer, 2017-09, Vol.48 (3), p.256-259

2017

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Evaluation of AlphaFold structure-based protein stability prediction on missense variations in cancer

Frontiers in genetics, 2023-02, Vol.14, p.1052383

2023

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BRAFV600E mutation in Turkish patients with papillary thyroid cancer: strong correlation with indicators of tumor aggressiveness

Endocrine, 2012-10, Vol.42 (2), p.404-410

2012

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Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene

Journal of human genetics, 2015-12, Vol.60 (12), p.763-768

2015

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"Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports"

BMC medical genetics, 2017-10, Vol.18 (1), p.114-8, Article 114

2017

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BRAF(V600E) mutation in Turkish patients with papillary thyroid cancer: strong correlation with indicators of tumor aggressiveness

Endocrine, 2012-10, Vol.42 (2), p.404

2012

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Identification of homozygous deletions at chromosome 16q23 in Aflatoxin B1 exposed hepatocellular carcinoma

Oncogene, 2001-08, Vol.20 (37), p.5232-5238

2001

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Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate

European journal of human genetics : EJHG, 2016-01, Vol.24 (1), p.51-58

2016

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Reprogramming of Replicative Senescence in Hepatocellular Carcinoma-Derived Cells

Proceedings of the National Academy of Sciences - PNAS, 2006-02, Vol.103 (7), p.2178-2183

2006

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Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas

Journal of neurosurgery, 2018-04, Vol.128 (4), p.1102-1114

2018

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PTPRD is homozygously deleted and epigenetically downregulated in human hepatocellular carcinomas

Omics (Larchmont, N.Y.), 2015-04, Vol.19 (4), p.220-229

2015

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STUB1 polyadenylation signal variant AACAAA does not affect polyadenylation but decreases STUB1 translation causing SCAR16

Human mutation, 2018-10, Vol.39 (10), p.1344-1348

2018

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Identification of IDH and TERTp mutations using dynamic susceptibility contrast MRI with deep learning in 162 gliomas

European journal of radiology, 2024-01, Vol.170, p.111257-111257, Article 111257

2024

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Noninvasive amino acid turnover predicts human embryo aneuploidy

Gynecological endocrinology, 2022-06, Vol.38 (6), p.461-466

2022

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Type I IFN–related NETosis in ataxia telangiectasia and Artemis deficiency

Journal of allergy and clinical immunology, 2018-07, Vol.142 (1), p.246-257

2018

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Mutations and Copy Number Alterations in IDH Wild-Type Glioblastomas Are Shaped by Different Oncogenic Mechanisms

Biomedicines, 2020-12, Vol.8 (12), p.574

2020

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Identification of IDH and TERTp mutation status using 1 H-MRS in 112 hemispheric diffuse gliomas

Journal of magnetic resonance imaging, 2020-06, Vol.51 (6), p.1799-1809

2020

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Postmortem genetic testing in sudden cardiac death: To be or not to be?

Journal of biotechnology, 2018-08, Vol.280, p.S19-S19

2018

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mESAdb: microRNA expression and sequence analysis database

Nucleic acids research, 2011-01, Vol.39 (Database issue), p.D170-D180

2011

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Identification of IDH and TERTp mutation status using 1H‐MRS in 112 hemispheric diffuse gliomas

Journal of magnetic resonance imaging, 2020-06, Vol.51 (6), p.1799-1809

2020

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NECESSITY FOR A CUSTOMIZED NGS PANEL FOR ACCURATE DIAGNOSIS AND TARGETED THERAPIES IN PEDIATRIC GLIAL TUMORS

Hematology, Transfusion and Cell Therapy, 2021-11, Vol.43, p.S29-S29

2021

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Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

BMC medical genomics, 2021-02, Vol.14 (1), p.54-14, Article 54

2021

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Optimizing the Personalized Care for the Management of Rectal Cancer: A Consensus Statement

The Turkish Journal of Gastroenterology, 2022-08, Vol.33 (8), p.627-663

2022

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Genetic Analysis of MEFV Gene Pyrin Domain in Patients With Behcet’s Disease

Mediators of Inflammation, 2006-01, Vol.2006 (3), p.229-232

2006

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Magnetic resonance spectroscopic correlates of progression free and overall survival in "glioblastoma, IDH-wildtype, WHO grade-4"

Angiogenesis, Invasion, and Metastasis Characteristics of Hepatocellular Carcinoma

Evaluation of AlphaFold structure-based protein stability prediction on missense variations in cancer

BRAFV600E mutation in Turkish patients with papillary thyroid cancer: strong correlation with indicators of tumor aggressiveness

Hereditary spastic paraplegia with recessive trait caused by mutation in KLC4 gene

"Homozygous, and compound heterozygous mutation in 3 Turkish family with Jervell and Lange-Nielsen syndrome: case reports"

BRAF(V600E) mutation in Turkish patients with papillary thyroid cancer: strong correlation with indicators of tumor aggressiveness

Identification of homozygous deletions at chromosome 16q23 in Aflatoxin B1 exposed hepatocellular carcinoma

Chromosome 22q12.1 microdeletions: confirmation of the MN1 gene as a candidate gene for cleft palate

Reprogramming of Replicative Senescence in Hepatocellular Carcinoma-Derived Cells

Use of telomerase promoter mutations to mark specific molecular subsets with reciprocal clinical behavior in IDH mutant and IDH wild-type diffuse gliomas

PTPRD is homozygously deleted and epigenetically downregulated in human hepatocellular carcinomas

STUB1 polyadenylation signal variant AACAAA does not affect polyadenylation but decreases STUB1 translation causing SCAR16

Identification of IDH and TERTp mutations using dynamic susceptibility contrast MRI with deep learning in 162 gliomas

Noninvasive amino acid turnover predicts human embryo aneuploidy

Type I IFN–related NETosis in ataxia telangiectasia and Artemis deficiency

Mutations and Copy Number Alterations in IDH Wild-Type Glioblastomas Are Shaped by Different Oncogenic Mechanisms

Identification of IDH and TERTp mutation status using 1 H-MRS in 112 hemispheric diffuse gliomas

Postmortem genetic testing in sudden cardiac death: To be or not to be?

mESAdb: microRNA expression and sequence analysis database

Identification of IDH and TERTp mutation status using 1H‐MRS in 112 hemispheric diffuse gliomas

NECESSITY FOR A CUSTOMIZED NGS PANEL FOR ACCURATE DIAGNOSIS AND TARGETED THERAPIES IN PEDIATRIC GLIAL TUMORS

Sequential filtering for clinically relevant variants as a method for clinical interpretation of whole exome sequencing findings in glioma

Optimizing the Personalized Care for the Management of Rectal Cancer: A Consensus Statement

Genetic Analysis of MEFV Gene Pyrin Domain in Patients With Behcet’s Disease

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