The Spectrum of HBB Mutations among 2315 Beta Thalassemia Patients of a Reference Clinic in Tehran-Iran.

Autor: Bazazzadegan N; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Abedini SS; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Azarkeivan A; Blood Transfusion Research Center, High Institute for Research and Education in Transfusion Medicine, Tehran, Iran.; Iranian Blood Transfusion Organization, Thalassemia Clinic, Tehran, Iran., Banihashemi S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Nikzat N; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Neishabury M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

Publikováno v: Hemoglobin [Hemoglobin] 2023 Nov; Vol. 47 (4), pp. 147-151. Date of Electronic Publication: 2023 Aug 07.

Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran.

Autor: Mohseni M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Babanejad M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Booth KT; Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA.; Department of Neurobiology, Harvard Medical School, Boston, Massachusetts, USA., Jamali P; Shahrood Genetic Counseling Center, Welfare Organization, Semnan, Iran., Jalalvand K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Davarnia B; Department of Anatomy and Pathology, Ardabil University of Medical Sciences, Ardabil, Iran., Ardalani F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Khoshaeen A; Mehrgan Genetic Clinic, Sari, Iran., Arzhangi S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Ghodratpour F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Beheshtian M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Jahanshad F; Navid's Institute of Infertility, Tehran, Iran., Otukesh H; Department of Pediatric Neurology, Iran University of Medical Sciences, Tehran, Iran., Bahrami F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Seifati SM; Medical Biotechnology Research Center, Islamic Azad University, Ashkezar, Iran., Bazazzadegan N; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Habibi F; Genetic Counseling Center of Welfare Organization, Rasht, Iran., Behravan H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Mirzaei S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Keshavarzi F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Nikzat N; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Mehrjoo Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Thiele H; Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany., Nothnagel M; Cologne Center for Genomics (CCG), University of Cologne, Cologne, Germany.; University Hospital Cologne, Cologne, Germany., Azaiez H; Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA., Smith RJ; Molecular Otolaryngology and Renal Research Laboratories, Department of Otolaryngology, Carver College of Medicine, University of Iowa, Iowa City, Iowa, USA., Kahrizi K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.

Publikováno v: Clinical genetics [Clin Genet] 2021 Jul; Vol. 100 (1), pp. 59-78. Date of Electronic Publication: 2021 Mar 24.

Association of the Single Nucleotide Polymorphisms rs11556218, rs4778889, rs4072111, and rs1131445 of the Interleukin-16 Gene with Ovarian Cancer.

Autor: Watrowski, Rafał^1,2 (AUTHOR) rafal.watrowski@gmx.at, Schuster, Eva³ (AUTHOR) eva.schuster@meduniwien.ac.at, Van Gorp, Toon^4,5 (AUTHOR) toon.vangorp@uzleuven.be, Hofstetter, Gerda⁶ (AUTHOR) gerda.hofstetter@meduniwien.ac.at, Fischer, Michael B.^7,8 (AUTHOR) michael.b.fischer@meduniwien.ac.at, Mahner, Sven^9,10 (AUTHOR) sven.mahner@med.uni-muenchen.de, Polterauer, Stefan³ (AUTHOR) stefan.polterauer@muv.ac.at, Zeillinger, Robert³ (AUTHOR) robert.zeillinger@muv.ac.at, Obermayr, Eva³ (AUTHOR) eva.obermayr@muv.ac.at

Publikováno v: International Journal of Molecular Sciences. Oct2024, Vol. 25 Issue 19, p10272. 18p.

Novel compound heterozygous variants in MARVELD2 causing autosomal recessive hearing loss in two Chinese families.

Autor: Shi, Xinyu¹ (AUTHOR), Liu, Xiaozhou¹ (AUTHOR), Zong, Yanjun¹ (AUTHOR), Zhao, Zhengdong¹ (AUTHOR), Sun, Yu^1,2,3 (AUTHOR) sunyu@hust.edu.cn

Publikováno v: Molecular Genetics & Genomic Medicine. Aug2024, Vol. 12 Issue 8, p1-8. 8p.

Brief Report of Variants Detected in Hereditary Hearing Loss Cases in Iran over a 3-Year Period.

Autor: Bazazzadegan N; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Vazehan R; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran., Fadaee M; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran., Fattahi Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Abolhassani A; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran., Parsimehr E; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran., Kalhor Z; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran., Faraji Zonooz M; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran., Ahangari F; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran., Dehdahsi S; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran., Samiee F; Genetic Medical Counseling Center, Qazvin, Iran., Jamali P; Shahrood Genetic Counseling Center, Welfare Office, Shahrood, Iran., Habibi H; Genetic Counseling Center, Family Health Clinic, Mobasher Hospital, Hamedan, Iran., Nourizadeh Y; Genetic Counseling Center Welfare Organization, Ilam, Iran., Mahdavi S; Welfare Institution Genetic Office, Tehran, Iran., Beheshtian M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Kariminejad A; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran., Smith RJ; Department of Otolaryngology-Head and Neck Surgery, Molecular Otolaryngology & Renal Research Laboratories, Carver College of Medicine, University of Iowa, Iowa City, IA, USA., Najmabadi H; Kariminejad-Najmabadi Pathology & Genetics Center, Tehran, Iran.

Publikováno v: Iranian journal of public health [Iran J Public Health] 2019 Oct; Vol. 48 (10), pp. 1910-1915.