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Expression of epigenetic pathway related genes in association with PD-L1, ER/PgR and MLH1 in endometrial carcinoma

PloS one, 2022-02, Vol.17 (2), p.e0264014

2022

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KAT6A amplifications are associated with shorter progression-free survival and overall survival in patients with endometrial serous carcinoma

PloS one, 2020-09, Vol.15 (9), p.e0238477-e0238477

2020

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Low level ALK FISH positive results should be approached with caution and confirmed by an orthogonal method

Translational lung cancer research, 2023-07, Vol.12 (7), p.1361-1363

Toruner, Gokce A.

2023

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Relapsed NPM1 mutated acute myeloid leukemia with PDGFRA rearrangement

Blood, 2019-01, Vol.133 (2), p.181-181

2019

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MicroRNA expression changes in association with changes in interleukin-1ß/interleukin10 ratios produced by monocytes in autism spectrum disorders: their association with neuropsychiatric symptoms and comorbid conditions (observational study)

Journal of neuroinflammation, 2017-11, Vol.14 (1), p.229-229, Article 229

2017

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Evolution of Genetic Techniques: Past, Present, and Beyond

BioMed research international, 2015-01, Vol.2015 (2015), p.1-7

2015

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MicroRNA expression changes in association with changes in interleukin-1β/interleukin10 ratios produced by monocytes in autism spectrum disorders: their association with neuropsychiatric symptoms and comorbid conditions (observational study)

Journal of neuroinflammation, 2017-11, Vol.14

2017

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Immunological characterization and transcription profiling of peripheral blood (PB) monocytes in children with autism spectrum disorders (ASD) and specific polysaccharide antibody deficiency (SPAD): case study

Journal of neuroinflammation, 2012-01, Vol.9 (1), p.4-4, Article 4

2012

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Genomic aberrations involving 12p/ETV6 are highly prevalent in blastic plasmacytoid dendritic cell neoplasms and might represent early clonal events

Leukemia research, 2018-10, Vol.73, p.86-94

2018

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Myeloid neoplasm with <10% blasts and t(3;5)(q25.1;q34)/NPM::MLF1: A classification dilemma

American journal of hematology, 2024-09, Vol.99 (9), p.1827-1829

2024

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Analytical and clinical performance of chromosomal microarrays compared with FISH panel and conventional karyotyping in patients with chronic lymphocytic leukemia

Leukemia research, 2021-09, Vol.108, p.106616-106616, Article 106616

2021

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Children with autism spectrum disorders (ASD) who exhibit chronic gastrointestinal (GI) symptoms and marked fluctuation of behavioral symptoms exhibit distinct innate immune abnormalities and transcriptional profiles of peripheral blood (PB) monocytes

Journal of neuroimmunology, 2011-09, Vol.238 (1), p.73-80

2011

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A Lactotransferrin Single Nucleotide Polymorphism Demonstrates Biological Activity That Can Reduce Susceptibility to Caries

Infection and Immunity, 2013-05, Vol.81 (5), p.1596-1605

2013

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Serum microRNAs in ASD: Association With Monocyte Cytokine Profiles and Mitochondrial Respiration

Frontiers in psychiatry, 2019-09, Vol.10, p.614-614

2019

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Optical genome mapping improves the accuracy of classification, risk stratification, and personalized treatment strategies for patients with acute myeloid leukemia

American journal of hematology, 2024-10, Vol.99 (10), p.1959-1968

2024

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Myeloid neoplasms with 8q24/MYC rearrangement are frequently associated with myelodysplasia, complex karyotype, TP53 alterations, and inferior survival

British journal of haematology, 2022-08, Vol.198 (3), p.604-608

2022

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Recurrent Somatic Copy Number Alterations and Their Association with Oncogene Expression Levels in High-Grade Ovarian Serous Carcinoma

Life (Basel, Switzerland), 2023-11, Vol.13 (11), p.2192

2023

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3′CBFB deletion in CBFB-rearranged acute myeloid leukemia retains morphological features associated with inv(16), but patients have higher risk of relapse and may require stem cell transplant

Annals of hematology, 2022-04, Vol.101 (4), p.847-854

2022

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Clinical Testing for Mismatch Repair in Neoplasms Using Multiple Laboratory Methods

Cancers, 2022-09, Vol.14 (19), p.4550

2022

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Clonal cytogenetic abnormalities in donor-derived cells after sex mismatched allogeneic stem cell transplantation

Cancer genetics, 2021-11, Vol.258-259, p.120-130

2021

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MET Expression Level in Lung Adenocarcinoma Loosely Correlates with MET Copy Number Gain/Amplification and Is a Poor Predictor of Patient Outcome

Cancers, 2022-05, Vol.14 (10), p.2433

2022

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Clinical impact of 5ʹMYC or 3ʹMYC gain/loss detected by FISH in patients with aggressive B-cell lymphomas

Cancer genetics, 2023-04, Vol.272-273, p.1-8

2023

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MTAP and p16 IHC as Markers for CDKN2A/B Loss in Meningiomas

Cancers, 2024-09, Vol.16 (19), p.3299

2024

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Optical Genome Mapping Helps to Identify BCR::JAK2 Rearrangement Arising from Cryptic Complex Chromosomal Aberrations: A Case Report and Literature Review

Genes, 2023-12, Vol.14 (12), p.2188

2023

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PPP1R7 Is a Novel Translocation Partner of CBFB via t(2;16)(q37;q22) in Acute Myeloid Leukemia

Genes, 2022-07, Vol.13 (8), p.1367

2022

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Expression of epigenetic pathway related genes in association with PD-L1, ER/PgR and MLH1 in endometrial carcinoma

KAT6A amplifications are associated with shorter progression-free survival and overall survival in patients with endometrial serous carcinoma

Low level ALK FISH positive results should be approached with caution and confirmed by an orthogonal method

Relapsed NPM1 mutated acute myeloid leukemia with PDGFRA rearrangement

MicroRNA expression changes in association with changes in interleukin-1ß/interleukin10 ratios produced by monocytes in autism spectrum disorders: their association with neuropsychiatric symptoms and comorbid conditions (observational study)

Evolution of Genetic Techniques: Past, Present, and Beyond

MicroRNA expression changes in association with changes in interleukin-1β/interleukin10 ratios produced by monocytes in autism spectrum disorders: their association with neuropsychiatric symptoms and comorbid conditions (observational study)

Immunological characterization and transcription profiling of peripheral blood (PB) monocytes in children with autism spectrum disorders (ASD) and specific polysaccharide antibody deficiency (SPAD): case study

Genomic aberrations involving 12p/ETV6 are highly prevalent in blastic plasmacytoid dendritic cell neoplasms and might represent early clonal events

Myeloid neoplasm with <10% blasts and t(3;5)(q25.1;q34)/NPM::MLF1: A classification dilemma

Analytical and clinical performance of chromosomal microarrays compared with FISH panel and conventional karyotyping in patients with chronic lymphocytic leukemia

Children with autism spectrum disorders (ASD) who exhibit chronic gastrointestinal (GI) symptoms and marked fluctuation of behavioral symptoms exhibit distinct innate immune abnormalities and transcriptional profiles of peripheral blood (PB) monocytes

A Lactotransferrin Single Nucleotide Polymorphism Demonstrates Biological Activity That Can Reduce Susceptibility to Caries

Serum microRNAs in ASD: Association With Monocyte Cytokine Profiles and Mitochondrial Respiration

Optical genome mapping improves the accuracy of classification, risk stratification, and personalized treatment strategies for patients with acute myeloid leukemia

Myeloid neoplasms with 8q24/MYC rearrangement are frequently associated with myelodysplasia, complex karyotype, TP53 alterations, and inferior survival

Recurrent Somatic Copy Number Alterations and Their Association with Oncogene Expression Levels in High-Grade Ovarian Serous Carcinoma

3′CBFB deletion in CBFB-rearranged acute myeloid leukemia retains morphological features associated with inv(16), but patients have higher risk of relapse and may require stem cell transplant

Clinical Testing for Mismatch Repair in Neoplasms Using Multiple Laboratory Methods

Clonal cytogenetic abnormalities in donor-derived cells after sex mismatched allogeneic stem cell transplantation

MET Expression Level in Lung Adenocarcinoma Loosely Correlates with MET Copy Number Gain/Amplification and Is a Poor Predictor of Patient Outcome

Clinical impact of 5ʹMYC or 3ʹMYC gain/loss detected by FISH in patients with aggressive B-cell lymphomas

MTAP and p16 IHC as Markers for CDKN2A/B Loss in Meningiomas

Optical Genome Mapping Helps to Identify BCR::JAK2 Rearrangement Arising from Cryptic Complex Chromosomal Aberrations: A Case Report and Literature Review

PPP1R7 Is a Novel Translocation Partner of CBFB via t(2;16)(q37;q22) in Acute Myeloid Leukemia

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