Emin KARACA

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

Araştırma alanları: Sağlık Bilimleri, Tıp, Dahili Tıp Bilimleri, Tıbbi Genetik, Temel Bilimler, Yaşam Bilimleri, İç Hastalıkları, Temel Tıp Bilimleri, Çocuk Sağlığı ve Hastalıkları, Moleküler Biyoloji ve Genetik

Yayınlar

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)
Investigation of the Effect of Vitamin D on Testicular Damage Caused by Cisplatin in Rats (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)
A Case of Myosin Heavy Chain 9-Related Disorder Following Splenectomy Due to Misdiagnosis of Idiopathic Thrombocytopenic Purpura (2024)
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)
A complex t(15;22;17)(q22;q11.2;q21) variant of APL (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)
Does MicroRNA Profile Differ in Early Onset Coronary Artery Disease? (2022)
Propolis Extract Regulates microRNA Expression in Glioblastoma and Brain Cancer Stem Cells. (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)
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)
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)
TYR GENİNDE DELESYON SAPTANAN OKÜLOKÜTANÖZ ALBİNİZMLİ BİR OLGU (2020)
NF1 TÜM GEN DELESYONU SAPTANAN DİSMORFİK BİR NÖROFİBROMATOZİS OLGUSU (2020)
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)
İnterlökin 12 / Interferon gamma yolak bozuklukları ve atipik mikobakteriyel enfeksiyonlara yatkınlık (2019)
TRNT1 DISEASE PRESENTING WITH CONGENITAL HEMOLYTIC ANEMIA AND HYPOGAMMAGLOBULINEMIA (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)
Hangi Diyabet Ne Zaman? (2019)
Konjenital hemolitik anemi ve hipogammaglobulinemi ile prezente olan TRNT1 hastalığı (2019)
Akut Myeloblastik Lösemi’de Kromozomal Yeniden Düzenlemelerin Tespiti: Standart Sitogenetik ve FISH Yöntemleri Arasında Bir Karşılaştırma (2019)
Mikozis fungoideste miR-155 ve miR-34a ekspresyon düzeyi (2019)
Medu¨ller Tı·roid Kanserlı· Tu¨rk Olgularda Genişletilmiş Ret Genı· Mutasyon Spektrumu (2019)
Cytogenetic analysis of miscarriage materials of couples with recurrent pregnancy loss in a tertiary center (2019)
Myelodisplastik Sendrom Tanısında Karyotip ve FISH Analizlerinin Kullanımının Değerlendirilmesi (2019)
Gain of 1q21 locus in a multiple myeloma patient (2019)
Co-occurrences of polymorphic heterochromatin regions of chromosomes and effect on reproductive failure (2019)
Evaluation of 22q11.2 anomalies via two pediatric patients (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)
KML ÖN TANILI OLGULARDA SİTOGENETİK VE FISHSONUÇLARININ DEĞERLENDİRİLMESİ (2018)
Prevalence of Y microdeletions in Turkish azoospermia or oligospermia patients (2018)
Bölüm 3 Nedenleri ve Oluşum Mekanizmaları (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)
Evaluation of the effects of miRNAs in familial Mediterranean fever. (2018)
The role of MikroRNAs in premature cardiovascular disease (2018)
Clinical, Neuroimaging, and Genetic Features of the Patients with L-2-Hydroxyglutaric Aciduria (2018)
Mutation spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations (2017)
Mutation Spectrum of GCK, HNF1A and HNF1B in MODY Patients and 40 Novel Mutations. (2017)
Epidemiological Analysis of L. tropica Strains and Clinical Slides from Syrian and Turkish Patients using Multilocus Microsatellite Typing (MLMT) (2017)
Superoxide dismutase 1 and 2 gene polymorphism in Turkish vitiligo patients (2017)
PRENATAL DIAGNOSIS IN SINGLE GENE DISORDERS: EGEUNIVERSITY EXPERIENCE IN 497 CASES (2017)
MODY Sendromlarından Sorumlu GCK, HNF1A ve HNF1B Genleri Mutasyon Spektrumu ve 40 Yeni Mutasyon (2017)
Bölüm 2: Tıbbi Genetikte Kullanılan Yöntemler (2017)
Tetrasomy Xq in a Primary Infertile Case (2017)
Nörolojik Genetik Hastalıklar (2017)
TIBBİ GENETİĞİN TARİHÇESİ (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)
Mutation Spectrum of GCK, HNF1A and HNF1B in MODY patients and 40 novel mutations (2017)
Tıbbi Genetiğin Tarihçesi (2017)
Evaluation of Immunoglobulin Heavy Chain Region Deletions in CLL (2017)
Evaluation Of Immunoglobulin Heavy Chain Region Deletions In Chronic Lymphocyte Leukemia (2017)
PRENATAL DIAGNOSIS OF A FETUS CARRYING INV (12): CASE REPORT (2017)
Tıbbi Genetiğin Tarihçesi (2017)
The spectrum of HNF1A gene mutations in patients with MODY 3 phenotype and identification of three germline mutations in Turkish population (2017)
Epidemiological analysis of Leishmania tropica strains and giemsa-stained smears from Syrian and Turkish leishmaniasis patients using multilocus microsatellite typing (MLMT) (2017)
Tetrasomy Xq in a Primary Infertile Case (2017)
CHROMOSOMAL MICROARRAY EXPERIENCE OF 94 CASES:INITIATE DIFFICULTIES AND PROGRESSION (2017)
Laboratory Genetic Testing in Clinical Practice 2016 (2017)
PREIMPLANTATION GENETIC DIAGNOSIS FOR T(25)(q37.1q35.1): CASE REPORT (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)
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)
AKUT MYELOİD LÖSEMİ AML ÖN TANILI OLGULARINSİTOGENETİK SONUÇLARININ RETROSPEKTİF OLARAKDEĞERLENDİRİLMESİ (2016)
Transmembrane activator and CAML interactor TACI haplosufficiency in B cell dysfunction in a patient with Smith Magenis syndrome (2016)
Evaluation of preimplantation genetic aneuploidy screening cases at a reference genetics center: 10 years’ experience (2016)
Areview of 20 year experience with prenatal diagnosis records 9297 cases from Turkey (2016)
SCANNING OF PATIENTS WITH CONGENITAL HEART DEFECTS FOR DI GEORGE SYNDROME AND IMMUNODEFICIENCIES WITH ONE BLOOD SAMPLE (2016)
Marker kromozom tesbit edilen olgunun konvansiyonel sitogenetik ve mikroarray ile incelenmesi (2016)
AKUT MYELOİD LÖSEMİ AML ÖN TANILI OLGULARIN FISHTESTLERİNİN ANALİZİ (2016)
MİYELODİSPLASTİK SENDROM MDS ÖN TANILI OLGULARINSİTOGENETİK SONUÇLARININ RETROSPEKTİF OLARAKDEĞERLENDİRİLMESİ (2016)
Clinical Neuroimaging and genetic features of L 2hydroxyglutaric aciduria case series (2016)
PRENATAL DİAGNOSİS PALLISTER KILLIAN SYNDROME MOSAİC TETROSMY 12P (2016)
Evaluation of preimplantation genetic aneuploidy screening cases at a reference genetic center 10 years experience (2016)

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