Prof. HATİCE MERGEN

Publication Network

Journal articles indexed in SCI, SSCI, and AHCI

Investigation of Fibrillar Aggregates Formed by Pathogenic Pre-pro-vasopressin Mutants that Cause ADNDI

Vaizoglu R. D., Erdem B., GÜL M., ACAR C., ÖZDEMİREL H. Ö., SAĞLAR ÖZER E., et al.

JOURNAL OF CLINICAL ENDOCRINOLOGY & METABOLISM , 2024 (SCI-Expanded)

A Novel Bioprotective Strain of <i>Lactiplantibacillus plantarum</i> F2-Physiological, Genetical, and Antimicrobial Characterization

GÜNEŞ ALTUNTAŞ E., Celik A. A., Sevim B., TOK K. C., GÜMÜŞTAŞ M., MERGEN H., et al.

FOODBORNE PATHOGENS AND DISEASE , 2024 (SCI-Expanded)

Researching of resistance to etravirine in some HIV-1 low-level viremia strains by <i>in-silico</i> methods

OFLAZ O., MERGEN H., Demir T.

TURKISH JOURNAL OF BIOCHEMISTRY-TURK BIYOKIMYA DERGISI , vol.48, no.6, pp.653-658, 2024 (SCI-Expanded)

Differential expression of Phlebotomus tobbi Adler, Theodor & Lourie, 1930 (Diptera: Psychodidae) genes under different environmental conditions

Oguz G., Bilgic H. A., KARAASLAN İ. Ç., MERGEN H., Kasap O. E., ALTEN S. B.

Acta Tropica , vol.239, 2023 (SCI-Expanded)

Comparison of ELISA and RIA methods to quantify arginine vasopressin hormone levels in cell culture

Özcan Türkmen M., KARADUMAN T., MERGEN H.

Biologia , vol.78, no.3, pp.887-894, 2023 (SCI-Expanded)

Phosphorus-nitrogen compounds: Part 69—Unsymmetrical dispiro(N/N)cyclotriphosphazenes containing different pendant arms: syntheses, characterization, stereogenism, photophysical and bioactivity studies

CEMALOĞLU R., ASMAFİLİZ N., Çoşut B., Kılıç Z., SABAH B. N., AÇIK L., et al.

Research on Chemical Intermediates , vol.49, 2023 (SCI-Expanded)

Phosphorus-nitrogen compounds. Part 65. Novel diansa-spiro-cyclotetraphosphazenes: synthesis, characterization, bioactivity and electrochemical properties, and dye-sensitized solar cell fabrication studies

Mutlu G., OKUMUŞ A., ELMAS G., Kilic Z., GÜZEL R., SABAH B. N., et al.

NEW JOURNAL OF CHEMISTRY , vol.46, no.38, pp.18384-18401, 2022 (SCI-Expanded)

Design and Development of Gold-Loaded and Boron-Attached Multicore Manganese Ferrite Nanoparticles as a Potential Agent in Biomedical Applications

İÇTEN O., ERDEM TUNÇDEMİR B., MERGEN H.

ACS OMEGA , vol.7, no.23, pp.20195-20203, 2022 (SCI-Expanded) Sustainable Development

Functional analyses of three different mutations in the AVP-NPII gene causing familial neurohypophyseal diabetes insipidus

Turkmen M. O., KARADUMAN T., ERDEM TUNÇDEMİR B., ÜNAL M. A., MERGEN H.

ENDOCRINE , vol.74, no.3, pp.658-665, 2021 (SCI-Expanded) Sustainable Development

Functional analysis of AQP2 mutants found in patients with diabetes insipidus

KARADUMAN T., Ozcan Turkmen M., Ozer E., ERGİN B., SAĞLAM B., ERDEM TUNÇDEMİR B., et al.

BIOLOGIA , vol.76, no.9, pp.2767-2776, 2021 (SCI-Expanded) Sustainable Development

Low Base-Substitution Mutation Rate but High Rate of Slippage Mutations in the Sequence Repeat-Rich Genome ofDictyostelium discoideum

Kucukyildirim S., Behringer M., Sung W., Brock D. A., Doak T. G., MERGEN H., et al.

G3-GENES GENOMES GENETICS , vol.10, no.9, pp.3445-3452, 2020 (SCI-Expanded)

Molecular characterization of an aquaporin-2 mutation causing a severe form of nephrogenic diabetes insipidus

Ozer E., Moeller H. B., Karaduman T., Fenton R. A., MERGEN H.

CELLULAR AND MOLECULAR LIFE SCIENCES , vol.77, no.5, pp.953-962, 2020 (SCI-Expanded) Sustainable Development

Evaluation of pharmacochaperone-mediated rescue of mutant V2 receptor proteins

Tuncdemir B., MERGEN H., Ozer E.

EUROPEAN JOURNAL OF PHARMACOLOGY , vol.865, 2019 (SCI-Expanded) Sustainable Development

A Novel Mutation in the AVPR2 Gene Causing Congenital Nephrogenic Diabetes Insipidus

Tayfur A. C., KARADUMAN T., Turkmen M. O., ŞAHİN D., Yilmaz A. C., Buyukkaragoz B., et al.

JOURNAL OF CLINICAL RESEARCH IN PEDIATRIC ENDOCRINOLOGY , vol.10, no.4, pp.350-356, 2018 (SCI-Expanded)

Functional characterization of AVPR2 mutants found in Turkish patients with nephrogenic diabetes insipidus

Erdem B., Schulz A., SAĞLAR ÖZER E., Deniz F., Schoeneberg T., MERGEN H.

ENDOCRINE CONNECTIONS , vol.7, no.1, pp.56-64, 2018 (SCI-Expanded)

Functional characterization of a large deletion in AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish patient

SAĞLAR ÖZER E., Erdem B., Deniz F., MERGEN H.

INTERNATIONAL JOURNAL OF CLINICAL AND EXPERIMENTAL MEDICINE , vol.9, no.8, pp.16199-16205, 2016 (SCI-Expanded) Sustainable Development

AVP-NPII gene mutations and clinical characteristics of the patients with autosomal dominant familial central diabetes insipidus

TURKKAHRAMAN D., Saglar E., Karaduman T., MERGEN H.

PITUITARY , vol.18, no.6, pp.898-904, 2015 (SCI-Expanded) Sustainable Development

Identification of a Novel Deletion in AVP-NPII Gene in a Patient with Central Diabetes Insipidus

DENIZ F., ACAR C., Saglar E., ERDEM B., Karaduman T., YONEM A., et al.

ANNALS OF CLINICAL AND LABORATORY SCIENCE , vol.45, no.5, pp.588-592, 2015 (SCI-Expanded) Sustainable Development

Association of VNTR polymorphisms in DRD4, 5-HTT and DAT1 genes with obesity

UZUN M., Saglar E., Kucukyildirim S., ERDEM B., Unlu H., MERGEN H.

ARCHIVES OF PHYSIOLOGY AND BIOCHEMISTRY , vol.121, no.2, pp.75-79, 2015 (SCI-Expanded) Sustainable Development

Promoter hypermethylation of p16 and APC in gastrointestinal cancer patients

ERDEM B., KUCUKYILDIRIM S., Saglar E., POLAT Z., MERGEN H.

TURKISH JOURNAL OF GASTROENTEROLOGY , vol.25, no.5, pp.512-517, 2014 (SCI-Expanded) Sustainable Development

Assessment of ER Stress and Autophagy Induced by Ionizing Radiation in Both Radiotherapy Patients and Ex Vivo Irradiated Samples

SAĞLAR ÖZER E., Unlu S., Babalioglu I., GÖKÇE Ş. Ç., MERGEN H.

JOURNAL OF BIOCHEMICAL AND MOLECULAR TOXICOLOGY , vol.28, no.9, pp.413-417, 2014 (SCI-Expanded) Sustainable Development

Identification of a Novel Deletion of the AVP-NPII Gene in a Patient with Central Diabetes Insipidus

Deniz F., SAĞLAR ÖZER E., Yonem A., Cagiltay E., Ay A. S., Ozsari L., et al.

ENDOCRINE REVIEWS , vol.35, no.3, 2014 (SCI-Expanded) Sustainable Development

A large deletion of the AVPR2 gene causing severe nephrogenic diabetes insipidus in a Turkish family

Saglar E., DENIZ F., ERDEM B., KARADUMAN T., YONEM A., CAGILTAY E., et al.

ENDOCRINE , vol.46, no.1, pp.148-153, 2014 (SCI-Expanded) Sustainable Development

Evaluation of MUC1, CK20, and hTERT expression in peripheral blood of gastrointestinal cancer patients in search of diagnostic criteria

Kucuyildirim S., ERDEM B., SAGLAR E., POLAT Z., MERGEN H.

TURKISH JOURNAL OF BIOLOGY , vol.38, no.6, pp.848-857, 2014 (SCI-Expanded)

Mutations in the AVPR2, AVP-NPII, and AQP2 genes in Turkish patients with diabetes insipidus.

DUZENLI D., SAGLAR E., DENIZ F., AZAL O., ERDEM B., MERGEN H.

Endocrine , vol.42, no.3, pp.664-9, 2012 (SCI-Expanded) Sustainable Development

Understanding Early Bronze Age social structure through mortuary remains: A pilot aDNA study from Titris Hoyuk, southeastern Turkey

Matney T., ALGAZE G., Dulik M. C., ERDAL Ö. D., ERDAL Y. S., Gokcumen O., et al.

INTERNATIONAL JOURNAL OF OSTEOARCHAEOLOGY , vol.22, no.3, pp.338-351, 2012 (SSCI)

Investigation of Serotonin Transporter Gene Promoter (5-HTTLPR) and Intron 2 (Variable Number of Tandem Repeats) Polymorphisms with Suicidal Behavior in a Turkish Population

AKAR T., Sayin A., Bakkaloglu Z., Cabuk D. K., KÜÇÜKYILDIRIM ÇELİK S., Demirel B., et al.

DNA AND CELL BIOLOGY , vol.29, no.8, pp.429-434, 2010 (SCI-Expanded) Sustainable Development

A Prospective Study of Serotonin Transporter Gene Promoter (5-HTT Gene Linked Polymorphic Region) and Intron 2 (Variable Number of Tandem Repeats) Polymorphisms as Predictors of Trauma Response to Mild Physical Injury

Sayin A., KÜÇÜKYILDIRIM ÇELİK S., AKAR T., Bakkaloglu Z., DEMİRCAN A., Kurtoglu G., et al.

DNA AND CELL BIOLOGY , vol.29, no.2, pp.71-77, 2010 (SCI-Expanded)

Lack of association between the serotonin transporter and tryptophan hydroxylase gene polymorphisms and completed suicide

Mergen H., Demirel B., Akar T., Senol E.

PSYCHIATRIC GENETICS , vol.16, no.2, pp.53, 2006 (SCI-Expanded) Sustainable Development

Molecular scanning for mutations in the insulin receptor substrate-1 (Irs-1) gene in Turkish with type 2 diabetes mellitus

Orkunoglu Suer F. E., MERGEN H., Bolu E., Ozata M.

Endocrine Journal , vol.52, no.5, pp.593-598, 2005 (SCI-Expanded)

Effect of alpha-gene numbers on the expression of beta-thalassemia intermedia, beta-thalassemia and (delta beta)(0)-thalassemia traits

Altay C., Oner C., Oner R., Gumruk F., Mergen H., Gurgey A.

HUMAN HEREDITY , vol.48, no.3, pp.121-125, 1998 (SCI-Expanded)

Hb H disease with homozygosity for red cell G6PD deficiency in a Turkish female

Oner C., Oner R., Birben E., Balkan H., Gumruk F., Gurgey A., et al.

HEMOGLOBIN , vol.22, no.2, pp.157-160, 1998 (SCI-Expanded)

Coexistence of Hb Lepore-Boston-Washington (delta 87Gln-beta-IVS-II-8) with alpha-thalassemia [alpha(-5NT)alpha/alpha alpha]

Oner C., Oner R., Balkan H., Gumruk F., Gurgey A.

HEMOGLOBIN , vol.22, no.3, pp.273-276, 1998 (SCI-Expanded)

Articles Published in Other Journals

CHEMICAL CHAPERONE EFFECTS ON ARGININE-VASOPRESSIN RECEPTOR 2 MUTANTS

ERDEM TUNÇDEMİR B., KARADUMAN T., ÖZCAN TÜRKMEN M., Şahin D., MERGEN H., SAĞLAR ÖZER E.

Hacettepe Journal of Biology and Chemistry , vol.50, no.1, pp.37-43, 2022 (Peer-Reviewed Journal)

Screening For Mutations In The Coding Regions Of PSEN1 Gene, 16-17 Exons Of APP Gene And APOE Genotyping In Patients With Alzheimer’s Disease

KARADUMAN T., Eroğlu E., SAĞLAR ÖZER E., ERDEM TUNÇDEMİR B., MERGEN H.

Türk Doğa ve Fen Dergisi , vol.9, no.9, pp.35-41, 2020 (Peer-Reviewed Journal)

Lipoid proteinosis and epilepsy: Molecular analysis

TECELLİOĞLU M., KAMIŞLI Ö., ACAR C., MERGEN H., SÖZEN M. M., KARADUMAN T., et al.

Annals of Medical research , vol.26, no.4, pp.744-747, 2019 (Peer-Reviewed Journal)

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