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Shahriar Nafissi

neuromuscular research center
H指数:33
被引数:3,460

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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
Generalizable lower-limb muscle MRI segmentation and quantification on heterogeneous multisite datasets

多中心异构数据集中下肢肌肉MRI分割与量化

Scientific Reports
IF3.9
2026-09-030
OAAI
Jose Verdu-Diaz; Carla Bolano-Diaz; Alejandro Gonzalez Chamorro; Sam Fitzsimmons; Longdan Hao; Stephen Wandera; Sipho Ndlovu; Joel Mannion; Holly Borland; Goknur Selen Kocak; Alicia Alonso-Jiménez; Daniele Amore; Andrea Barp; Jorge A. Bevilacqua; Kristl G. Claeys; Michele Giovanni Croce; Matteo Garibaldi; Teresa Gerhalter; Shona Haston; Gema Iglesias Escalera; Anna Kostera-Pruszczyk; Peter Krkoska; Sergei Kurbatov; Lea Leonardis; Sushan Luo; Anne Marie Childs; Mauro Monforte; Shahriar Nafissi; Atchayaram Nalini; Hanna Palahuta; Anna Pichiecchio; Benjamín Pizarro-Galleguillos; Stefano Carlo Previtali; Ricard Rojas-García; Jin-Hong Shin; Elena Stebbings; Nicol C. Voermans; Jodi Warman-Chardon; Edmar Zanoteli; Kieren Hollingsworth; Michela Guglieri; Chiara Marini Bettolo; Volker Straub; Giorgio Tasca; Jaume Bacardit; Jordi Díaz-Manera
Expanding the genetic and clinical landscapes of hereditary spastic paraplegia (HSP): a cohort study of 103 families

扩展遗传性痉挛性截瘫（HSP）的遗传和临床景观：103个家庭的队列研究

Orphanet Journal of Rare Diseases
IF3.5
2026-05-120
OAAI
Atefeh Davarzani; Moez Ravanbod; Aida Ghasemi; Mahsa Mohammadi; Mohammad Rohani; Shahriar Nafissi; Payman Jamali; Hossein Najmabadi; Farzad Fatehi; Shahryar Alavi; Zahra Firoozfar; Fariba Zemorshidi; Mohammad Reza Habibi-Kavashkohie; Afagh Alavi
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
RABENOSYN separation-of-function mutations uncouple endosomal recycling from lysosomal degradation, causing a distinct Mendelian disorder
HUMAN MOLECULAR GENETICS
IF3.2
2022-06-020
OA
Paul, Franziska; Ng, Calista; Mohamad Sahari, Umar Bin; Nafissi, Shahriar; Nilipoor, Yalda; Tavasoli, Ali Reza; Bonnard, Carine; Wong, Pui-Mun; Nabavizadeh, Nasrinsadat; Altunoglu, Umut; Estiar, Mehrdad A.; Majoie, Charles B.; Lee, Hane; Nelson, Stanley F.; Gan-Or, Ziv; Rouleau, Guy A.; Van Veldhoven, Paul P.; Massie, Rami; Hennekam, Raoul C.; Kariminejad, Ariana; Reversade, Bruno
Clinical and genetic spectrum of a large cohort of patients with δ-sarcoglycan muscular dystrophy
BRAIN
IF11.7
2021-09-1316
OAAI
Alonso-Perez, Jorge; Gonzalez-Quereda, Lidia; Bruno, Claudio; Panicucci, Chiara; Alavi, Afagh; Nafissi, Shahriar; Nilipour, Yalda; Zanoteli, Edmar; de Augusto Isihi, Lucas Michielon; Melegh, Bela; Hadzsiev, Kinga; Muelas, Nuria; Vilchez, Juan J.; Dourado, Mario Emilio; Kadem, Naz; Kutluk, Gultekin; Umair, Muhammad; Younus, Muhammad; Pegorano, Elena; Bello, Luca; Crawford, Thomas O.; Suarez-Calvet, Xavier; Topf, Ana; Guglieri, Michela; Marini-Bettolo, Chiara; Gallano, Pia; Straub, Volker; Diaz-Manera, Jordi

研究方向

暂未获取到该数据
A
Afagh Alavi
H 指数:18论文数:92被引数:860
F
Farzad Fatehi
H 指数:23论文数:230被引数:2,211
E
Elahe Elahi
H 指数:31论文数:131被引数:3,306
H
Hosein Shamshiri
H 指数:11论文数:25被引数:344
A
Ali Asghar Okhovat
H 指数:11论文数:63被引数:587
A
Aida Ghasemi
H 指数:4论文数:27被引数:94
Y
Yalda Nilipour
H 指数:16论文数:91被引数:1,039
V
Volker Straub
H 指数:101论文数:962被引数:3.4万
A
Ana Töpf
H 指数:39论文数:256被引数:6,037
A
Ariana Kariminejad
H 指数:35论文数:178被引数:4,398