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SPINK5 mutation and FLG gene deletion in an infant with Netherton syndrome

Pediatrics international, 2022-01, Vol.64 (1), p.e15087-n/a

2022

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Jacobsen syndrome: a case report and clinical features of a rare genetic syndrome

Perinatal journal, 2022-12, Vol.30 (3), p.320-325

2022

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Evaluation of TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms in Turkish patients with tuberculosis

Journal of infection and public health, 2017-11, Vol.10 (6), p.774-777

2017

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GST (GSTM1, GSTT1, and GSTP1) polymorphisms in the genetic susceptibility of Turkish patients to cervical cancer

Journal of Gynecologic Oncology, 2010, 21(3), , pp.169-173

2010

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MBL2 Gene Polymorphism and Risk of Vitiligo in Turkish Patients

International journal of human genetics, 2015-06, Vol.15 (3)

Karkucak, Mutlu

2015

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Sudden blastic crisis and additional chromosomal abnormalities during chronic myeloid leukemia in the imatinib era

International journal of clinical oncology, 2009-12, Vol.14 (6), p.545-550

2009

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Investigation of Monnose-Binding Lectin gene Polymorphism in Patients with Erythema Multiforme, Stevens-Johnson Syndrome and Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Overlap Syndrome

Balkan medical journal, 2012-09, Vol.29 (3), p.310-313

2012

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Investigation of GSTP1 (Ile105Val) Gene Polymorphism in Chronic Myeloid Leukaemia Patients

International journal of human genetics, 2012-06, Vol.12 (3)

Karkucak, Mutlu

2012

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XRCC1 Gene Polymorphisms and Risk of Lung Cancer in Turkish Patients

International journal of human genetics, 2012-04, Vol.12 (2)

Karkucak, Mutlu

2012

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GSTT1 and GSTM1 gene polymorphisims in sarcoidosis

Sarcoidosis, vasculitis, and diffuse lung diseases, 2016-10, Vol.33 (3), p.253-257

2016

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Prenatal Diagnosis of De Novo Reciprocal Translocation t(1;12)(q21.3;p11.2) with Trisomy 21 and Sperm FISH Analysis for Increased Aneuploidy Risk

International journal of human genetics, 2010-10, Vol.10 (4)

Karkucak, Mutlu

2010

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Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencing

Annals of medicine (Helsinki), 2019-02, Vol.51 (2), p.141-148

2019

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Omentin serum levels and omentin gene Val109Asp polymorphism in patients with psoriasis

International journal of dermatology, 2014-05, Vol.53 (5), p.601-605

2014

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Investigation of the glutathione S-transferase gene M1/T1 and angiotensin converting enzyme gene I/D polymorphism in type 1 diabetic patients and possible association with diabetic microvascular complications

The European research journal, 2021-09, Vol.7 (5), p.447-456

2021

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Distribution of KRAS and BRAF Mutations in Metastatic Colorectal Cancers in Turkish Patients

Asian Pacific journal of cancer prevention : APJCP, 2016-04, Vol.17 (3), p.1175-1179

2016

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The potential utility of real-time PCR of the 16S-rRNA gene in the diagnosis of neonatal sepsis

Turkish journal of pediatrics, 2019, Vol.61 (4), p.493-499

2019

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Investigation of MEFV gene polymorphisms (G138G and A165A) in adult patients with familial Mediterranean fever

Revista Brasileira de Reumatologia, 2017-11, Vol.57 (6), p.501-506

2017

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Comparison of aneuploidy frequencies between in vitro matured and unstimulated cycles oocytes by metaphase comparative genomic hybridization (mCGH)

Molecular biology reports, 2012-05, Vol.39 (5), p.6187-6191

2012

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Distribution of KRAS and BRAF Mutations in Metastatic Colorectal Cancers in Turkish Patients

Asian Pacific journal of cancer prevention : APJCP, 2016, Vol.17 (3), p.1175-1179

2016

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Oxytocin system social function impacts in children with attention-deficit/hyperactivity disorder

American journal of medical genetics. Part B, Neuropsychiatric genetics, 2015-10, Vol.168B (7), p.609-616

2015

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A polymorphism in ERAP1 is associated with susceptibility to ankylosing spondylitis in a Turkish population

Rheumatology international, 2013-11, Vol.33 (11), p.2851-2858

2013

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Corrigendum to “Effect of cyclin D1 (CCND1) gene polymorphism on tumor formation and behavior in patients with prolactinoma” [Gene 509 (2012) 158–163]

Gene, 2014-04, Vol.539 (2), p.284-284

2014

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The rare cause of recurrent fever in adults: PFAPA syndrome

Clinical Case Studies and Reports, 2018, Vol.1 (2)

2018

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Qualitative and quantitative evaluation of the BCR-ABL fusion gene in chronic myelogenous leukemia by flourescence in situ hybridization and molecular genetic methods

Genetic testing and molecular biomarkers, 2015-10, Vol.19 (10), p.584-588

2015

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SPINK5 mutation and FLG gene deletion in an infant with Netherton syndrome

Jacobsen syndrome: a case report and clinical features of a rare genetic syndrome

Evaluation of TNF-alpha gene (G308A) and MBL2 gene codon 54 polymorphisms in Turkish patients with tuberculosis

GST (GSTM1, GSTT1, and GSTP1) polymorphisms in the genetic susceptibility of Turkish patients to cervical cancer

MBL2 Gene Polymorphism and Risk of Vitiligo in Turkish Patients

Sudden blastic crisis and additional chromosomal abnormalities during chronic myeloid leukemia in the imatinib era

Investigation of Monnose-Binding Lectin gene Polymorphism in Patients with Erythema Multiforme, Stevens-Johnson Syndrome and Stevens-Johnson Syndrome/Toxic Epidermal Necrolysis Overlap Syndrome

Investigation of GSTP1 (Ile105Val) Gene Polymorphism in Chronic Myeloid Leukaemia Patients

XRCC1 Gene Polymorphisms and Risk of Lung Cancer in Turkish Patients

GSTT1 and GSTM1 gene polymorphisims in sarcoidosis

Prenatal Diagnosis of De Novo Reciprocal Translocation t(1;12)(q21.3;p11.2) with Trisomy 21 and Sperm FISH Analysis for Increased Aneuploidy Risk

Identification of novel variants in ten patients with Hermansky-Pudlak syndrome by high-throughput sequencing

Omentin serum levels and omentin gene Val109Asp polymorphism in patients with psoriasis

Investigation of the glutathione S-transferase gene M1/T1 and angiotensin converting enzyme gene I/D polymorphism in type 1 diabetic patients and possible association with diabetic microvascular complications

Distribution of KRAS and BRAF Mutations in Metastatic Colorectal Cancers in Turkish Patients

Ten New Cases of Hermansky-Pudlak Syndrome in the Iberian Peninsula: Identification of Novel Genetic Variants in HPS3, HPS4, HPS6 and DTNBP1 Associated with Significant Clinical Complications

The potential utility of real-time PCR of the 16S-rRNA gene in the diagnosis of neonatal sepsis

Investigation of MEFV gene polymorphisms (G138G and A165A) in adult patients with familial Mediterranean fever

Comparison of aneuploidy frequencies between in vitro matured and unstimulated cycles oocytes by metaphase comparative genomic hybridization (mCGH)

Distribution of KRAS and BRAF Mutations in Metastatic Colorectal Cancers in Turkish Patients

Oxytocin system social function impacts in children with attention-deficit/hyperactivity disorder

A polymorphism in ERAP1 is associated with susceptibility to ankylosing spondylitis in a Turkish population

Corrigendum to “Effect of cyclin D1 (CCND1) gene polymorphism on tumor formation and behavior in patients with prolactinoma” [Gene 509 (2012) 158–163]

The rare cause of recurrent fever in adults: PFAPA syndrome

Qualitative and quantitative evaluation of the BCR-ABL fusion gene in chronic myelogenous leukemia by flourescence in situ hybridization and molecular genetic methods

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