Contribution of genetic variants in the development of familial premature coronary artery disease in a cohort of cardiac patients.

Autor: Mehvari S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Karimian Fathi N; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Saki S; Digestive Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran., Asadnezhad M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, 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., Mohseni M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Zare Ashrafi F; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Sadeghian S; Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran., Boroumand M; Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran., Shokohizadeh F; Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran., Rostami E; Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran., Boroumand R; Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran., Najafipour R; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Malekzadeh R; Digestive Disease Research Institute, Tehran University of Medical Sciences, Tehran, Iran., Riazalhosseini Y; McGill Genome Centre, Montreal, Quebec, Canada., Akbari M; Women's College Research Institute, University of Toronto, Toronto, Ontario, Canada., Lathrop M; McGill Genome Centre, Montreal, Quebec, Canada., Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Hosseini K; Tehran Heart Center, Cardiovascular Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran., Kahrizi K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; McGill Genome Centre, Montreal, Quebec, Canada.

Publikováno v: Clinical genetics [Clin Genet] 2024 Jun; Vol. 105 (6), pp. 611-619. Date of Electronic Publication: 2024 Feb 03.

Expanding the Molecular Spectrum of HK1 -Related Charcot-Marie-Tooth Disease, Type 4G; the First Report in Iran.

Autor: Goleyjani Moghadam M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Elahi Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; Kariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran., Soveyzi M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Arzhangi S; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Nafissi S; Iranian Neuromuscular Research Center (INMRC), Tehran University of Medical Sciences, Tehran, Iran.; Department of Neurology, Shariati Hospital, Tehran University of Medical Sciences, Tehran, Iran., Najmabadi H; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; Kariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran., Kahrizi K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Fattahi Z; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran.; Kariminejad - Najmabadi Pathology & Genetics Center, Tehran, Iran.

Publikováno v: Archives of Iranian medicine [Arch Iran Med] 2023 May 01; Vol. 26 (5), pp. 279-284. Date of Electronic Publication: 2023 May 01.

An Extended Iranian Family with Autosomal Dominant Non-syndromic Hearing Loss Associated with A Nonsense Mutation in the DIAPH1 Gene.

Autor: Mohseni M; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Mohammadi Y; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Zare Ashrafi F; 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., Jalalvand K; Genetics Research Center, University of Social Welfare and Rehabilitation Sciences, Tehran, Iran., Arzhangi S; 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., Azizi MH; Associate Professor of Otolaryngology, Academy of Medical Sciences of IR Iran, Tehran, Iran., 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: Archives of Iranian medicine [Arch Iran Med] 2023 Mar 01; Vol. 26 (3), pp. 176-180. Date of Electronic Publication: 2023 Mar 01.

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.

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