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Naci Senkal, Istemi Serin, Sacide Pehlivan, Mustafa Pehlivan, Alpay Medetalibeyoglu, Timurhan Cebeci, Hilal Konyaoglu, Yasemin Oyacı, Gozde Yesil Sayın, Ummuhan Isoglu-Alkac, Tufan Tukek & Murat Kose. (2023) The effect of DNA repair gene variants on COVID-19 disease: susceptibility, severity, and clinical course. Nucleosides, Nucleotides & Nucleic Acids 42:8, pages 571-585.
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MK Gupta, AS Kushwah, R Singh & M Banerjee. (2020) Genotypic analysis of XRCC4 and susceptibility to cervical cancer. British Journal of Biomedical Science 77:1, pages 7-12.
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Daniele Campa, Alessandro Martino, Angelica Macauda, Marek Dudziński, Anna Suska, Agnieszka Druzd-Sitek, Marc-Steffen Raab, Victor Moreno, Stefanie Huhn, Aleksandra Butrym, Juan Sainz, Gergely Szombath, Marcin Rymko, Herlander Marques, Fabienne Lesueur, Annette Juul Vangsted, Ulla Vogel, Marcin Kruszewski, Edyta Subocz, Gabriele Buda, Elżbieta Iskierka-Jażdżewska, Rafael Ríos, Maximilian Merz, Ben Schöttker, Grzegorz Mazur, Emeline Perrial, Joaquin Martinez-Lopez, Katja Butterbach, Ramón García Sanz, Hartmut Goldschmidt, Hermann Brenner, Krzysztof Jamroziak, Rui Manuel Reis, Katalin Kadar, Charles Dumontet, Marzena Wątek, Eva Kannik Haastrup, Grzegorz Helbig, Artur Jurczyszyn, Andrés Jerez, Judit Varkonyi, Torben Barington, Norbert Grzasko, Jan Maciej Zaucha, Vibeke Andersen, Daria Zawirska & Federico Canzian. (2019) Genetic polymorphisms in genes of class switch recombination and multiple myeloma risk and survival: an IMMEnSE study. Leukemia & Lymphoma 60:7, pages 1803-1811.
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S. Pehlivan, N. Aydin, A. F. Nursal, M. A. Uysal, M. Pehlivan, A. Tekcan, F. K. Yavuz, U. Sever, H. Yavuzlar, S. Kurnaz, S. Uysal & P. C. Aydin. (2019) Association of XRCC1 and XPD functional gene variants with nicotine dependence and/or schizophrenia: a case-control study and in silico analysis. Psychiatry and Clinical Psychopharmacology 29:1, pages 21-27.
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Sacide Pehlivan, Ahmet Bulent Yazici, Nazan Aydin, Ayse Feyda Nursal, Selin Kurnaz, Ayca Ongel Atar, Ulgen Sever, Zeliha Kincir, Mustafa Pehlivan & Pınar Cetinay Aydin. (2018) Possible association between DNA repair gene variants and cannabis dependence in a Turkish cohort: a pilot study. Psychiatry and Clinical Psychopharmacology 28:4, pages 402-407.
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H. Haydaroglu, S. Oguzkan Balcı, S. Pehlıvan, K. Ozdıllı, E. Gundogan, V. Okan, A. F. Nursal & M. Pehlıvan. (2017) Effect of Cytokine Genes in the Pathogenesis and on the Clinical Parameters for the Treatment of Multiple Myeloma. Immunological Investigations 46:1, pages 10-21.
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Maia van Kan, Kathryn E. Burns & Nuala A. Helsby. (2021) A systematic review of inter-individual differences in the DNA repair processes involved in melphalan monoadduct repair in relation to treatment outcomes. Cancer Chemotherapy and Pharmacology 88:5, pages 755-769.
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Brian Ruis, Amy Molan, Taylor Takasugi & Eric A. Hendrickson. (2020) Absence of XRCC4 and its paralogs in human cells reveal differences in outcomes for DNA repair and V(D)J recombination. DNA Repair 85, pages 102738.
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Sebastian Gonzalez-McQuire, Meletios-Athanassios Dimopoulos, Katja Weisel, Walter Bouwmeester, Roman Hájek, Marco Campioni, Craig Bennison, Weiwei Xu, Krystallia Pantiri, Marja Hensen, Evangelos Terpos & Stefan Knop. (2019) Development of an Initial Conceptual Model of Multiple Myeloma to Support Clinical and Health Economics Decision Making. MDM Policy & Practice 4:1, pages 238146831881425.
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Emily A. Hill, J. Rachel Carr, Chris R. Stokes & G. Hilmar Gudmundsson. (2018) Dynamic changes in outlet glaciers in northern Greenland from 1948 to 2015. The Cryosphere 12:10, pages 3243-3263.
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Nadine Steiger, Kerim H. Nisancioglu, Henning Åkesson, Basile de Fleurian & Faezeh M. Nick. (2018) Simulated retreat of Jakobshavn Isbræ since the Little Ice Age controlled by geometry. The Cryosphere 12:7, pages 2249-2266.
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Sacide Pehlivan, Mehmet Atilla Uysal, Nazan Aydin, Ayse Feyda Nursal, Mustafa Pehlivan, Hazal Yavuzlar, Ulgen Sever, Selin Kurnaz, Fatih Kasım Yavuz, Suna Uysal & Pinar Cetinay Aydin. (2018) XRCC4 rs6869366 polymorphism is associated with susceptibility to both nicotine dependence and/or schizophrenia. Archives of Clinical Psychiatry (São Paulo) 45:3, pages 53-56.
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Pelin Mutlu, Mualla Pınar Elçi, Murat Yıldırım, Oral Nevruz, Ahmet Türker Çetin & Ferit Avcu. (2014) Identification of XRCC1 Arg399Gln and XRCC3 Thr241Met Polymorphisms in a Turkish Population and Their Association with the Risk of Chronic Lymphocytic Leukemia. Indian Journal of Hematology and Blood Transfusion 31:3, pages 332-338.
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Leila Fallahzadeh-Abarghooei, Tahereh Zahedi, Farkhonde Mirabedi & Mostafa Saadat. (2015) Allelic prevalence of intron 3 insertion/deletion genetic polymorphism of DNA double-strand break repair gene XRCC4 in four healthy Iranian populations. Egyptian Journal of Medical Human Genetics 16:3, pages 215-218.
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Sacide PehlivanSibel Oguzkan BalciAli AydenizMustafa PehlivanTugce SeverSavas Gursoy. (2015)
Might There Be a Link Between Intron 3 VNTR Polymorphism in the
XRCC4
DNA Repair Gene and the Etiopathogenesis of Rheumatoid Arthritis?
. Genetic Testing and Molecular Biomarkers 19:1, pages 48-51.
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