Emin KARACA

Tıp Fakültesi, Dahili Tıp Bilimleri Bölümü, Tıbbi Genetik Anabilim Dalı

Research areas: Health Sciences, Medicine, Internal Medicine Sciences, Medical Genetics, Natural Sciences, Life Sciences, Internal Diseases, Fundamental Medical Sciences, Child Health and Diseases, Molecular Biology and Genetics

Publications

Clinical Spectrum of Drug Hypersensitivity Reactions in Systemic Mastocytosis: Drug-Induced Anaphylaxis as a Unique Clinical Presentation (2026)
A Rare Case of Lhermitte Duclos Disease Associated with Somatic PTEN and Germline SUFU Variants (2025)
Identifying a rare mechanism: double parallel trisomy rescue leading to combined segmental and whole-chromosome mosaicism in an IVF-derived embryo (2025)
MALIGNANCY IN FANCONI APLASTIC ANEMIA; SINGLE CENTER EXPERIENCE (2025)
Next Generation Sequence-Based Targeted Somatic Mutation Analysis in Thyroid Nodules with Pathologically Diagnosed as Indeterminate Cytology (2024)
SUFU: A potential novel gene responsible for Lhermitte Duclos disease (2024)
Investigation of the Effect of Vitamin D on Testicular Damage Caused by Cisplatin in Rats (2024)
A Case of Myosin Heavy Chain 9-Related Disorder Following Splenectomy Due to Misdiagnosis of Idiopathic Thrombocytopenic Purpura (2024)
A complex t(15;22;17)(q22;q11.2;q21) variant of APL (2024)
Next generation sequence-based targeted somatic mutation analysis in thyroid nodules with pathologically diagnosed as indeterminate cytology (2024)
Next generation sequence-based targeted somatic mutation analysis in thyroid nodules with pathologically diagnosed as indeterminate cytology (2024)
An Experimental Insight Into the Role of Agomelatine in Renal Ischemia/Reperfusion Injury (2024)
Successful Treatment of a Child with Hemoglobin Hammersmith with Hematopoietic Stem Cell Transplantation (2023)
Clinical and molecular evaluation of MEFV gene variants in the Turkish population: a study by the National Genetics Consortium (2022)
Prenatal diagnosis of a case with tetrasomy 9p confirmed by cytogenetics, FISH, microarray analysis and review (2022)
Complex karyotype with double Philadelphia chromosome and T315I mutation results in blastic phase and extensive extramedullary infiltration in a chronic myeloid leukemia patient (2022)
Clinicopathological characteristics, genetics and prognosis of patients with myeloid sarcoma: a single-center study. (2022)
The Effect of Radiofrequency Waves on Pregnant Mice in Association with Genes Involved in Neuronal Migration (2022)
The Effect of Radiofrequency Waves on Pregnant Mice in Association with Genes Involved in Neuronal Migration (2022)
In vitro fertilization and preimplantation genetic diagnosis outcomes in mosaic Turners syndrome: A retrospective cohort study from a single referral center experience (2022)
Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain Cancer Stem Cells. (2022)
Does MicroRNA Profile Differ in Early Onset Coronary Artery Disease? (2022)
Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain Cancer Stem Cells. (2022)
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (2021)
20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey (2021)
A FOLK HERO İN THE CONTEXT OF ERİC HOBSBAWM'S SOCİAL BANDİT PRİNCİPLES: YADO PASHA (2021)
Eight years of follow-up experience in children with mendelian susceptibility to mycobacterial disease and review of the literature (2021)
20-year experience on prenatal diagnosis in a reference university medical genetics center in Turkey (2021)
Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure (2020)
Akut miyeloid lösemi (AML) hastalarında sitogenetik, moleküler sitogenetik, moleküler genetik ve klinik sonuçların retrospektif analizi; tek merkezden 4 yıllık veri analizi (2020)
Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure. (2020)
Çocukluk çağı akut lenfoblastik lösemide FISH yöntemi ile kromozomal yeniden düzenlenmelerin tespiti (2020)
TYR GENİNDE DELESYON SAPTANAN OKÜLOKÜTANÖZ ALBİNİZMLİ BİR OLGU (2020)
NF1 TÜM GEN DELESYONU SAPTANAN DİSMORFİK BİR NÖROFİBROMATOZİS OLGUSU (2020)
Mikozis fungoideste miR-155 ve miR-34a ekspresyon düzeyi (2019)
Hangi Diyabet Ne Zaman? (2019)
Correction to: Evaluation of the effects of miRNAs in familial Mediterranean fever (2019)
INTERLEUKIN-12/INTERFERON-GAMMA PATHWAY DISORDERS AND PREDISPOSITION TO ATYPICAL MYCOBACTERIAL INFECTIONS (2019)
Akut Myeloblastik Lösemi’de Kromozomal Yeniden Düzenlemelerin Tespiti: Standart Sitogenetik ve FISH Yöntemleri Arasında Bir Karşılaştırma (2019)
Konjenital hemolitik anemi ve hipogammaglobulinemi ile prezente olan TRNT1 hastalığı (2019)
Medu¨ller Tı·roid Kanserlı· Tu¨rk Olgularda Genişletilmiş Ret Genı· Mutasyon Spektrumu (2019)
TRNT1 DISEASE PRESENTING WITH CONGENITAL HEMOLYTIC ANEMIA AND HYPOGAMMAGLOBULINEMIA (2019)
İnterlökin 12 / Interferon gamma yolak bozuklukları ve atipik mikobakteriyel enfeksiyonlara yatkınlık (2019)
Gain of 1q21 locus in a multiple myeloma patient (2019)
Evaluation of 22q11.2 anomalies via two pediatric patients (2019)
Myelodisplastik Sendrom Tanısında Karyotip ve FISH Analizlerinin Kullanımının Değerlendirilmesi (2019)
Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure (2019)
Cytogenetic analysis of miscarriage materials of couples with recurrent pregnancy loss in a tertiary center (2019)
Cytogenetic analysis of miscarriage materials of couples with recurrent pregnancy loss at a high-volume tertiary center (2019)
MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome (2018)
MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome (2018)
PRENATAL DÖNEMDE TANI ALAN NADİR BİR OLGU: NON-MOZAİK TETRAZOMİ 9P (2018)
Bölüm 3 Nedenleri ve Oluşum Mekanizmaları (2018)
The role of MikroRNAs in premature cardiovascular disease (2018)
Prevalence of Y microdeletions in Turkish azoospermia or oligospermia patients (2018)
KML ÖN TANILI OLGULARDA SİTOGENETİK VE FISHSONUÇLARININ DEĞERLENDİRİLMESİ (2018)
Evaluation of the effects of miRNAs in familial Mediterranean fever. (2018)
Clinical, Neuroimaging, and Genetic Features of the Patients with L-2-Hydroxyglutaric Aciduria (2018)
Evaluation of Immunoglobulin Heavy Chain Region Deletions in CLL (2017)
Bölüm 2: Tıbbi Genetikte Kullanılan Yöntemler (2017)
Evaluation Of Immunoglobulin Heavy Chain Region Deletions In Chronic Lymphocyte Leukemia (2017)
Mutation Spectrum of GCK, HNF1A and HNF1B in MODY Patients and 40 Novel Mutations. (2017)
TIBBİ GENETİĞİN TARİHÇESİ (2017)
Tıbbi Genetiğin Tarihçesi (2017)
PRENATAL DIAGNOSIS OF A FETUS CARRYING INV (12): CASE REPORT (2017)
Tetrasomy Xq in a Primary Infertile Case (2017)
Nörolojik Genetik Hastalıklar (2017)
Mutation Spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations (2017)
MODY Sendromlarından Sorumlu GCK, HNF1A ve HNF1B Genleri Mutasyon Spektrumu ve 40 Yeni Mutasyon (2017)
PRADER-WILLI VE ANGELMAN SENDROMU’NDA METİLASYON VE FISH SONUÇLARININ DEĞERLENDİRİLMESİ (2017)
Mutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations. May 27–30, 2017, Copenhagen, Denmark. (2017)
MODY Sendromlarından Sorumlu GCK, HNF1A VE HNF1B Genleri Mutasyon Spektrumu ve 40 Yeni Mutasyon (2017)
Analysis of GCK gene in 79 MODY type 2 patients: A multicenter Turkish study mutation profile and description of twenty novel mutation (2017)
MODY Sendromlarından Sorumlu GCK, HNF1A ve HNF1B Genleri Mutasyon Spektrumu ve 40 Yeni Mutasyon (2017)
Mutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations (2017)
PRENATAL DIAGNOSIS IN SINGLE GENE DISORDERS: EGEUNIVERSITY EXPERIENCE IN 497 CASES (2017)
Superoxide dismutase 1 and 2 gene polymorphism in Turkish vitiligo patients (2017)
Epidemiological Analysis of L. tropica Strains and Clinical Slides from Syrian and Turkish Patients using Multilocus Microsatellite Typing (MLMT) (2017)
Tıbbi Genetiğin Tarihçesi (2017)
Tetrasomy Xq in a Primary Infertile Case (2017)
CHROMOSOMAL MICROARRAY EXPERIENCE OF 94 CASES:INITIATE DIFFICULTIES AND PROGRESSION (2017)
Diagnostic Role of MicroRNA Expression Profile in the Prenatal Amniotic Fluid Samples of Pregnant Women with Down Syndrome (2017)
SUPEROXIDE DISMUTASE 1 AND 2 GENE POLYMORPHISM IN TURKISH VITILIGO PATIENTS (2017)
Laboratory Genetic Testing in Clinical Practice 2016 (2017)
PREIMPLANTATION GENETIC DIAGNOSIS FOR T(25)(q37.1q35.1): CASE REPORT (2017)
Epidemiological analysis of Leishmania tropica strains and giemsa-stained smears from Syrian and Turkish leishmaniasis patients using multilocus microsatellite typing (MLMT) (2017)
The spectrum of HNF1A gene mutations in patients with MODY 3 phenotype and identification of three germline mutations in Turkish population (2017)
The spectrum of HNF1A gene mutations in patients with MODY 3 phenotype and identification of three novel germline mutations in Turkish Population (2017)
Analysis of the GCK gene in 79 MODY type 2 patients: A multicenter Turkish study, mutation profile and description of twenty novel mutations (2017)
Transmembrane activator and CAML interactor TACI haplosufficiency in B cell dysfunction in a patient with Smith Magenis syndrome (2016)
Evaluation of the miRNA profiling and effectiveness of the propolis on B cell acute lymphoblastic leukemia cell line (2016)
Metabolik Hastalıklar ve Genetiği (2016)
Nörolojik Hastalıklar ve Genetiği (2016)
Konjenital kalp hastalıklı bebeklerde tek tüp kan örneği ile Di George sendromu ve immün yetmezlik taraması (2016)
MİYELODİSPLASTİK SENDROM MDS ÖN TANILI OLGULARINSİTOGENETİK SONUÇLARININ RETROSPEKTİF OLARAKDEĞERLENDİRİLMESİ (2016)
Clinical Neuroimaging and genetic features of L 2hydroxyglutaric aciduria case series (2016)
Evaluation of preimplantation genetic aneuploidy screening cases at a reference genetics center: 10 years’ experience (2016)
Konjenital kalp hastalıklı bebeklerde tek tüp kan örneği ile di george sendromu ve immun yetmezlik taraması (2016)
Metabolik Hastalıklar ve Genetiği (2016)
Evaluation of preimplantation genetic aneuploidy screening cases at a reference genetic center 10 years experience (2016)