Hossein Najmabadi - Publications, H-index & Citations

Hossein Najmabadi

genetics research center

57H指数

479论文数

1.3W被引数

收录论文 102

发表时间

Appreciating diversity: a review of the Iranian genomic landscape 欣赏多样性：伊朗基因组景观的综述

European Journal of Human Genetics

IF4.6

2026-09-08

OAAI

Somayeh Alinaghi; Farzane Zare Ashrafi; Zohreh Elahi; Masoumeh Ghasemi; Hossein Najmabadi; Michael Nothnagel

Expanding the molecular and clinical spectrum of POLR3A-related charcot–marie–tooth disease 扩展POLR3A相关腓骨肌萎缩症的分子和临床谱系

Molecular Biology Reports

IF2.8

2026-08-27

PREAI

Masoumeh Goleyjani Moghadam; Ebrahim Shokouhian; Mohamad Soveyzi; Zohreh Elahi; Shahriar Nafissi; Hossein Najmabadi; Zohreh Fattahi; Kimia Kahrizi

Genetic contributors to premature coronary artery disease identified by whole-exome sequencing 通过全外显子组测序鉴定的早发冠状动脉疾病遗传易感因素

Scientific Reports

IF3.9

2026-07-31

OAAI

Mahsa Tahmasebivand; Kaveh Hosseini; Marzieh Mohseni; Ebrahim Shokouhian; Sanaz Arzhangi; Fatemeh Ghodratpour; Saeed Sadeghian; Mohammadali Boroumand; Fatemeh Shokohizadeh; Elham Rostami; Reza Malekzadeh; Hamidreza Khorram Khorshid; Reza Najafipour; Mohammadreza Akbari; Yasser Riazalhosseini; Hossein Najmabadi; Mark Lathrop; Kimia Kahrizi

Diagnostic Yield of Genome Sequencing in an Iranian Exome-Negative Autosomal-Recessive Intellectual Disability Cohort 基因组测序在伊朗外显子阴性常染色体隐性智力障碍队列中的诊断效能

Human Mutation

IF3.7

2026-07-01

OAAI

Ebrahim Shokouhian; Masoumeh Moslemi; Masoumeh Goleyjani Moghadam; Negar Molaei; Parnian Alagha; Azadeh Reshadmanesh; Sanaz Arzhangi; Fatemeh Ghodratpour; Mert Celik; Ilayda Selcen Kadioglu; Masoud Edizadeh; Mohammad Reza Akbari; Kimia Kahrizi; Hossein Najmabadi

Identification of Two Rare Variants in Iranian Families With Familial Sudden Cardiac Death 鉴定伊朗家族性突发性心脏病患者中的两种罕见变异

International Journal of Genomics

IF1.9

2026-01-01

OAAI

Tahmasebivand, Mahsa; Mehvari, Sepideh; Ghodratpour, Fatemeh; Khoram Khorshid, Hamidreza; Malekzadeh, Reza; Najafipour, Reza; Riazalhosseini, Yasser; Lathrop, Mark; Najmabadi, Hossein; Kahrizi, Kimia

Combining re-evaluation and new exome sequencing to identify novel genetic variants and candidate genes in Iranian families with non-syndromic hearing loss 结合重新评估和新一代外显子测序，以识别伊朗非综合征性听力损失家系中的新型遗传变异和候选基因

Molecular Biology Reports

IF2.8

2025-12-18

PREAI

Raziye Rezvani Rezvandeh; Negar Kazemi; Farzane Zare Ashrafi; Ebrahim Shokouhian; Zahra Bolghanabadi; Mohammad Amin Omrani; Masoud Edizadeh; Kimia Kahrizi; Hossein Najmabadi; Marzieh Mohseni

Biallelic Variant in NRDC Gene in Two Siblings With Developmental Delay and Seizures NRDC基因中的双等位基因变异在两位伴有发育迟缓和癫痫的同胞中

American Journal of Medical Genetics Part A

IF1.7

2025-12-01

PREAI

Fatehi, Fatemeh; Ghorbanoghli, Zeinab; Kooshki, Mahdieh; Najafabadi, Shima Zamanian; Noudehi, Khadijeh; Amooian, Sepideh; Taghiloo, Aidin; Makvand, Mina; Najmabadi, Hossein; Kariminejad, Ariana

Myo-Neuropathy and Congenital Bilateral Cataract Due to a GFER Variant in an Iranian Family Myo-Neuropathy及因GFER变异导致的先天性双侧白内障：一例伊朗家族病例

Current Genetic Medicine Reports

IF1.3

2025-10-08

PREAI

Ghasemi, Aida; Hadei, Seyed Jalaleddin; Salami, Zahra; Saffar, Hiva; Najmabadi, Hossein; Okhovat, Ali Asghar

Pyruvate Kinase Deficiency: An Underdiagnosed Cause of Severe Hemolytic Anemia in Iranian Population: Insights From Whole Exome Sequencing of Four Families and Screening of a Population-Specific Database 丙酮酸激酶缺乏症：伊朗人群中严重溶血性贫血的一个易被忽视的原因——来自四个家庭全外显子测序及特定人群数据库筛查的见解

INTERNATIONAL JOURNAL OF LABORATORY HEMATOLOGY

IF0

2025-09-01

PREAI

Rafat, Milad; Bouraqi, Yassin; Sisakht, Jafar Mehrabi; Azarkeivan, Azita; Najmabadi, Hossein; Neishabury, Maryam

FSCN1 as a Candidate Gene for Syndromic Intellectual Disability? Evidence From a Recurrent Variant in an Iranian Cohort FSCN1作为综合征性智力障碍的候选基因？来自一个伊朗队列中复发性变异的证据

Clinical Genetics

IF2.3

2025-08-25

PREAI

Hossein Najmabadi; Tara Akhtarkhavari; Ebrahim Shokouhian; Sanaz Arzhangi; Kimia Kahrizi

The liver-derived exosomes stimulate insulin gene expression in pancreatic beta cells under condition of insulin resistance

FRONTIERS IN ENDOCRINOLOGY

IF4.6

2023-11-07

OAAI

Mahmoudi-Aznaveh, Azam; Tavoosidana, Gholamreza; Najmabadi, Hossein; Azizi, Zahra; Ardestani, Amin

Prevalence, parameters, and pathogenic mechanisms for splice-altering acceptor variants that disrupt the AG exclusion zone

HUMAN GENETICS AND GENOMICS ADVANCES

IF3.6

2022-10-01

OAAI

Nair, Divya; Li, Dong; Erdogan, Hannah; Yoon, Andrew; Harr, Margaret H.; Bergant, Gaber; Peterlin, Borut; Pusenjak, Marusa Skrjanec; Jayakar, Parul; Pfundt, Rolph; Jansen, Sandra; McWalter, Kirsty; Sidhu, Alpa; Saliganan, Sheila; Agolini, Emanuele; Jacob, Arthur; Pasquier, Jennifer; Arash, Rafii; Kahrizi, Kimia; Najmabadi, Hossein; Ropers, Hans-Hilger; Bhoj, Elizabeth J.

Identification of microRNAs associated with human fragile X syndrome using next-generation sequencing

SCIENTIFIC REPORTS

IF3.9

2022-03-23

OAAI

Anvari, Maryam Sotoudeh; Vasei, Hamed; Najmabadi, Hossein; Badv, Reza Shervin; Golipour, Akram; Mohammadi-Yeganeh, Samira; Salehi, Saeede; Mohamadi, Mahmood; Goodarzynejad, Hamidreza; Mowla, Seyed Javad

ZBTB11 dysfunction: spectrum of brain abnormalities, biochemical signature and cellular consequences

BRAIN

IF11.7

2022-02-01

OAAI

Sumathipala, Dulika; Stromme, Petter; Fattahi, Zohreh; Luders, Torben; Sheng, Ying; Kahrizi, Kimia; Einarsen, Ingunn Holm; Sloan, Jennifer L.; Najmabadi, Hossein; van den Heuvel, Lambert; Wevers, Ron A.; Guerrero-Castillo, Sergio; Morkrid, Lars; Valayannopoulos, Vassili; Backe, Paul Hoff; Venditti, Charles P.; van Karnebeek, Clara D.; Nilsen, Hilde; Frengen, Eirik; Misceo, Doriana

A novel variant of C12orf4 linked to autosomal recessive intellectual disability type 66 with phenotype expansion 与常染色体隐性遗传智力障碍66型相关的C12orf4的新变体，具有表型扩展

JOURNAL OF GENE MEDICINE

IF2.2

2022-01-31

PREAI

Rashvand, Zahra; Kahrizi, Kimia; Najmabadi, Hossein; Najafipour, Reza; Omrani, Mir Davood

Genetic etiology of hearing loss in Iran

HUMAN GENETICS

IF3.6

2022-01-20

PREAI

Babanejad, Mojgan; Beheshtian, Maryam; Jamshidi, Fereshteh; Mohseni, Marzieh; Booth, Kevin T.; Kahrizi, Kimia; Najmabadi, Hossein

SARS-CoV-2 outbreak in Iran: The dynamics of the epidemic and evidence on two independent introductions

TRANSBOUNDARY AND EMERGING DISEASES

IF3

2021-05-22

OAAI

Fattahi, Zohreh; Mohseni, Marzieh; Jalalvand, Khadijeh; Aghakhani Moghadam, Fatemeh; Ghaziasadi, Azam; Keshavarzi, Fatemeh; Yavarian, Jila; Jafarpour, Ali; Mortazavi, Seyedeh Elham; Ghodratpour, Fatemeh; Behravan, Hanieh; Khazeni, Mohammad; Momeni, Seyed Amir; Jahanzad, Issa; Moradi, Abdolvahab; Tabarraei, Alijan; Azimi, Sadegh Ali; Kord, Ebrahim; Hashemi-Shahri, Seyed Mohammad; Azaran, Azarakhsh; Yousefi, Farid; Mokhames, Zakiye; Soleimani, Alireza; Ghafari, Shokouh; Ziaee, Masood; Habibzadeh, Shahram; Jeddi, Farhad; Hadadi, Azar; Abdollahi, Alireza; Kaydani, Gholam Abbas; Soltani, Saber; Mokhtari-Azad, Talat; Najafipour, Reza; Malekzadeh, Reza; Kahrizi, Kimia; Jazayeri, Seyed Mohammad; Najmabadi, Hossein

Discovery of a neuromuscular syndrome caused by biallelic variants in ASCC3

HUMAN GENETICS AND GENOMICS ADVANCES

IF3.6

2021-04-01

OAAI

Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities

SCIENTIFIC REPORTS

IF3.9

2021-03-26

OAAI

Najafi, Kimia; Mehrjoo, Zohreh; Ardalani, Fariba; Ghaderi-Sohi, Siavash; Kariminejad, Ariana; Kariminejad, Roxana; Najmabadi, Hossein

POLRMT mutations impair mitochondrial transcription causing neurological disease

NATURE COMMUNICATIONS

IF15.7

2021-02-18

OAAI

Olahova, Monika; Peter, Bradley; Szilagyi, Zsolt; Diaz-Maldonado, Hector; Singh, Meenakshi; Sommerville, Ewen W.; Blakely, Emma L.; Collier, Jack J.; Hoberg, Emily; Stranecky, Viktor; Hartmannova, Hana; Bleyer, Anthony J.; McBride, Kim L.; Bowden, Sasigarn A.; Korandova, Zuzana; Pecinova, Alena; Ropers, Hans-Hilger; Kahrizi, Kimia; Najmabadi, Hossein; Tarnopolsky, Mark A.; Brady, Lauren I.; Weaver, K. Nicole; Prada, Carlos E.; Ounap, Katrin; Wojcik, Monica H.; Pajusalu, Sander; Syeda, Safoora B.; Pais, Lynn; Estrella, Elicia A.; Bruels, Christine C.; Kunkel, Louis M.; Kang, Peter B.; Bonnen, Penelope E.; Mracek, Tomas; Kmoch, Stanislav; Gorman, Grainne S.; Falkenberg, Maria; Gustafsson, Claes M.; Taylor, Robert W.

研究方向