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R

Reza Shervin Badv

children's medical center
H指数:17
被引数:893

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Inherited metabolic disorder-related genes and mutation spectrum in Iranians: an 11-year analysis using next-generation sequencing and sanger sequencing

伊朗人遗传代谢病相关基因及突变谱：一项基于下一代测序和Sanger测序的11年分析

Orphanet Journal of Rare Diseases
IF3.5
2026-10-020
OAAI
Parnian Alagha; Negar Molaei; Maryam Beheshtian; Fatemeh Ahangari; Shima Dehdahsi; Mahsa Fadaee; Mehri Ashki; Zhila Ghaderi; Zohreh Elahi; Raheleh Vazehan; Maryam Mozaffarpour Nouri; Parishad Saei; Khadijeh Noudehi; Fatemeh Fatehi; Shima Zamanian Najafabadi; Fariba Afroozan; Banafsheh Salmani; Mahdieh kooshki; Armita Ghaderi; Zohreh Vahidi; Mina Makvand; Atiyeh Ahmadpour; Mahsa Tahmasebivand; Elmira Shiuokhi; Saeed Talebi; Reza Shervin Badv; Babak Zamani; Farhad Mahvelati-Shamsabadi; Bahram Haghi Ashtiani; Payam Sarraf; Haleh Habibi; Afshin Fayyazi; Ali Asghar Okhovat; Mahmoud Reza Ashrafi; Farzad Fatehi; Parvaneh Karimzadeh; Shahriar Nafissi; Kimia Kahrizi; Ariana Kariminejad; Hossein Najmabadi
Clinical, genetic, neuroimaging, and severity spectrum of peroxisomal disorders in Iran: a multicenter cohort study

伊朗过氧化物酶体障碍的临床、遗传、神经影像及严重程度谱：一项多中心队列研究

Orphanet Journal of Rare Diseases
IF3.5
2026-08-120
OA
Golazin Shahbodagh Khan; Narges Mashayekhi; Shiva Bayat; Mehran Beiraghi Toosi; Sareh Hosseinpour; Neda Pak; Danielle Dircks; Zahra Rezaei; Reza Shervin Badv; Gholam Reza Zamani; Mahmoud Mohammadi; Mojtaba Movahednia; Parvaneh Karimzadeh; Reza Maroofian; Michael C. Kruer; Ehsan Ghayoor Karimiani; Masoud Garshasbi; Mahmoud Reza Ashrafi; Morteza Heidari; Ali Reza Tavasoli
A programmed decline in ribosome levels governs human early neurodevelopment

程序性核糖体水平下降调控人类早期神经发育

Nature Cell Biology
IF19.1
2025-08-040
OA
Chunyang Ni; Yudong Wei; Barbara Vona; Dayea Park; Yulei Wei; Daniel A. Schmitz; Yi Ding; Masahiro Sakurai; Emily Ballard; Leijie Li; Yan Liu; Ashwani Kumar; Chao Xing; Shenlu Qin; Sangin Kim; Martina Foglizzo; Jianchao Zhao; Hyung-Goo Kim; Cumhur Ekmekci; Ehsan Ghayoor Karimiani; Shima Imannezhad; Fatemeh Eghbal; Reza Shervin Badv; Eva Maria Christina Schwaibold; Mohammadreza Dehghani; Mohammad Yahya Vahidi Mehrjardi; Zahra Metanat; Hosein Eslamiyeh; Ebtissal Khouj; Saleh Mohammed Nasser Alhajj; Aziza Chedrawi; Khushnooda Ramzan; Jamil A. Hashmi; Majed M. Alluqmani; Sulman Basit; Danai Veltra; Nikolaos M. Marinakis; Georgios Niotakis; Pelagia Vorgia; Christalena Sofocleous; Hane Lee; Won Chan Jeong; Muhammad Umair; Muhammad Bilal; César Augusto Pinheiro Ferreira Alves; Matthew Sieber; Michael Kruer; Henry Houlden; Fowzan S. Alkuraya; Elton Zeqiraj; Roger A. Greenberg; Can Cenik; Leqian Yu; Reza Maroofian; Jun Wu; Michael Buszczak
Homozygous variants in WDR83OS lead to a neurodevelopmental disorder with hypercholanemia
AMERICAN JOURNAL OF HUMAN GENETICS
IF8.1
2024-11-010
PRE
Barish, Scott; Lin, Sheng-Jia; Maroofian, Reza; Gezdirici, Alper; Alhebby, Hamoud; Trimouille, Aurelien; Waberski, Marta Biderman; Mitani, Tadahiro; Huber, Ilka; Tveten, Kristian; Holla, Oystein L.; Busk, Oyvind L.; Houlden, Henry; Karimiani, Ehsan Ghayoor; Toosi, Mehran Beiraghi; Badv, Reza Shervin; Torbati, Paria Najarzadeh; Eghbal, Fatemeh; Akhondian, Javad; Al Safar, Ayat; Alswaid, Abdulrahman; Zifarelli, Giovanni; Bauer, Peter; Marafi, Dana; Fatih, Jawid M.; Huang, Kevin; Petree, Cassidy; Calame, Daniel G.; von der Lippe, Charlotte; Alkuraya, Fowzan S.; Wali, Sami; Lupski, James R.; Varshney, Gaurav K.; Posey, Jennifer E.; Pehlivan, Davut
The genetic basis of early-onset hereditary ataxia in Iran: results of a national registry of a heterogeneous population
HUMAN GENOMICS
IF4.3
2024-04-032
OAAI
Mahdieh, Nejat; Heidari, Morteza; Rezaei, Zahra; Tavasoli, Ali Reza; Hosseinpour, Sareh; Rasulinejad, Maryam; Dehnavi, Ali Zare; Akbari, Masoud Ghahvechi; Badv, Reza Shervin; Vafaei, Elahe; Mohebbi, Ali; Mohammadi, Pouria; Hosseiny, Seyyed Mohammad Mahdi; Azizimalamiri, Reza; Nikkhah, Ali; Pourbakhtyaran, Elham; Rohani, Mohammad; Khanbanha, Narges; Nikbakht, Sedigheh; Movahedinia, Mojtaba; Karimi, Parviz; Ghabeli, Homa; Hosseini, Seyed Ahmad; Rashidi, Fatemeh Sadat; Garshasbi, Masoud; Kashani, Morteza Rezvani; Ghiasvand, Noor M.; Zuchner, Stephan; Synofzik, Matthis; Ashrafi, Mahmoud Reza
The First Report of Iranian Registry of Patients with Spinal Muscular Atrophy
JOURNAL OF NEUROMUSCULAR DISEASES
IF3.4
2023-03-075
PRE
Mansouri, Vahid; Heidari, Morteza; Bemanalizadeh, Maryam; Azizimalamiri, Reza; Nafissi, Shahriar; Akbari, Masood Ghahvechi; Barzegar, Mohammad; Moayedi, Ali Reza; Badv, Reza Shervin; Mohamadi, Mahmood; Tavasoli, Ali Reza; Amirsalari, Susan; Khajeh, Ali; Inaloo, Soroor; Fatehi, Farzad; Hosseinpour, Sareh; Babaei, Meisam; Hosseini, Seyed Ahmad; Hosseiny, Seyyed Mohammad Mahdi; Fayyazi, Afshin; Hosseini, Firoozeh; Toosi, Mehran Beiraghi; Khosroshahi, Nahid; Ghabeli, Homa; Biglari, Habibeh Nejad; Kakhki, Simin Khayatzadeh; Mirlohi, Seyed Hossein; Bidabadi, Elham; Mohammadi, Bahram; Omrani, Abdolmajid; Sedighi, Mostafa; Vafaee-Shahi, Mohammad; Rasulinezhad, Maryam; Hoseini, Seyyed Mohamad; Movahedinia, Mojtaba; Rezaei, Zahra; Karimi, Parviz; Farshadmoghadam, Hossein; Anvari, Saeed; Yaghini, Omid; Nasiri, Jafar; Zamani, Gholamreza; Ashrafi, Mahmoud Reza
Biallelic variants in OGDH encoding oxoglutarate dehydrogenase lead to a neurodevelopmental disorder characterized by global developmental delay, movement disorder, and metabolic abnormalities
GENETICS IN MEDICINE
IF6.2
2023-02-016
OAAI
Whittle, Ella F.; Chilian, Madison; Karimiani, Ehsan Ghayoor; Progri, Helga; Buhas, Daniela; Kose, Melis; Ganetzky, Rebecca D.; Toosi, Mehran Beiraghi; Torbati, Paria Najarzadeh; Badv, Reza Shervin; Shelihan, Ivan; Yang, Hui; Elloumi, Houda Zghal; Lee, Sukyeong; Jamshidi, Yalda; Pittman, Alan M.; Houlden, Henry; Ignatius, Erika; Rahman, Shamima; Maroofian, Reza; Yoon, Wan Hee; Carrol, Christopher J.
Molecular characterization of a large cohort of mucopolysaccharidosis patients: Iran Mucopolysaccharidosis RE-diagnosis study (IMPRESsion)
HUMAN MUTATION
IF3.7
2022-02-034
OA
Ghaffari, Saeed R.; Rafati, Maryam; Shadnoush, Mahdi; Pourbabaee, Shokooh; Aghighi, Mohammad; Mirab Samiee, Siamak; Kermanchi, Jamshid; Alaei, Mohammad R.; Salehpour, Shadab; Amirkashani, Davoud; Setoodeh, Aria; Sarkhail, Peymaneh; Badv, Reza Shervin; Aminzadeh, Majid; Shiva, Siamak; Eshraghi, Peyman; Moravej, Hossein; Hashemipour, Mahin; Rostampour, Noushin; Hamidieh, Amir Ali; Shamsian, Bibi Shahin; Shams, Sedigheh; Zamanfar, Daniel; Ebrahimi, Ayoub; Otadi, Ali; Tara, Seyedeh Zahra; Barati, Zeinab; Fakhri, Laya; Hoseini, Azadeh; Amiri, Hosna; Ramandi, Somayeh; Mostofinezhad, Niusha; Kani, Zahra Pahlevani; Mohammadyari, Elham; Khosravi, Mahsa; Saadati, Masoome; Hoseininasab, Fatemeh; Khorram Khorshid, Hamid Reza; Modaberisaber, Younes
Clinical and imaging outcomes after intrathecal injection of umbilical cord tissue mesenchymal stem cells in cerebral palsy: a randomized double-blind sham-controlled clinical trial
STEM CELL RESEARCH & THERAPY
IF7.3
2021-08-0626
OAAI
Amanat, Man; Majmaa, Anahita; Zarrabi, Morteza; Nouri, Masoumeh; Akbari, Masood Ghahvechi; Moaiedi, Ali Reza; Ghaemi, Omid; Zamani, Fatemeh; Najafi, Sharif; Badv, Reza Shervin; Vosough, Massoud; Hamidieh, Amir Ali; Salehi, Mona; Montazerlotfelahi, Hadi; Tavasoli, Ali Reza; Heidari, Morteza; Mohebi, Hossein; Fatemi, Ali; Garakani, Amir; Ashrafi, Mahmoud Reza

研究方向

暂未获取到该数据
M
Mahmoud Reza Ashrafi
H 指数:26论文数:275被引数:2,673
M
Morteza Heidari
H 指数:15论文数:118被引数:696
A
Ali Reza Tavasoli
H 指数:18论文数:179被引数:1,196
M
Mahmoud Mohammadi
H 指数:14论文数:74被引数:494
S
Sareh Hosseinpour
H 指数:9论文数:52被引数:212
H
Henry Houlden
H 指数:120论文数:1,507被引数:6.4万
R
Reza Maroofian
H 指数:40论文数:319被引数:5,871
A
Ali Rashidi‐Nezhad
H 指数:10论文数:35被引数:281
E
Ehsan Ghayoor Karimiani
H 指数:27论文数:152被引数:2,523
S
Seyed Ahmad Hosseini
H 指数:15论文数:65被引数:559