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Mohammad Amin Tabatabaiefar

Isfahan University of Medical Sciences

19H指数
138论文数
1.2K被引数
收录论文 25
发表时间
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Prevalence of Novel and Recurrent Pathogenic Variants in BRCA Genes in a Cohort of Iranian Hereditary Breast Cancer Patients伊朗遗传性乳腺癌患者队列中BRCA基因新型和复发性致病变异的流行率
errAdvanced Biomedical Research
IF0
err2025-12-01
err0
PREAI
errSarmadi, Akram; Haghjooy Javanmard, Shaghayegh; Zeinalian, Mehrdad; Hosseinzadeh, Majid; Tabatabaiefar, Mohammad Amin
err分享
err收藏
Mono-allelic MUTYH mutation as the likely inherited etiology of hereditary breast cancer in a patient from a multi-cancer family- report of a family and literature review单等位基因MUTYH突变作为来自多癌家族的一名遗传性乳腺癌患者可能的遗传病因——一家系报道及文献复习
errBMC MEDICAL GENOMICS
IF2
err2025-10-01
err0
errOAAI
errSarmadi, Akram; Javanmard, Shaghayegh Haghjooy; Zeinalian, Mehrdad; Hosseinzadeh, Majid; Tabatabaiefar, Mohammad Amin
err分享
err收藏
Contribution of BARD1 gene to male breast cancer- report of a family with different types of cancerBARD1基因对男性乳腺癌的贡献——一个患有不同类型癌症的家族报告
errCurrent Problems in Cancer
IF2.3
err2025-10-01
err0
PREAI
errSarmadi, Akram; Javanmard, Shaghayegh Haghjooy; Zeinalian, Mehrdad; Hosseinzadeh, Majid; Nouri, Zahra; Tabatabaiefar, Mohammad Amin
err分享
err收藏
A Deleterious Frameshift Deletion Variant in Exon 5 of the CYP21A2 Gene Causes Classic Salt-Wasting Congenital Adrenal HyperplasiaCYP21A2基因外显子5中的一个有害移码缺失变异导致经典性盐皮质激素丢失型先天性肾上腺皮质增生症
errCURRENT GENETIC MEDICINE REPORTS
IF0
err2025-09-09
err0
PREAI
errMolavi, Newsha; Aghaei, Shahrzad; Hoseinzadeh, Marziyeh; Khanahmad, Hossein; Hashemipour, Mahin; Tabatabaiefar, Mohammad Amin
err分享
err收藏
Investigating TSHR gene variants in consanguineous families: novel insights into variable expression in familial congenital hypothyroidism在近亲婚配家庭中调查TSHR基因变异：对家族性先天性甲状腺功能减退症中表型变异的新见解
errFRONTIERS IN ENDOCRINOLOGY
IF4.6
err2025-05-05
err0
errOAAI
errNadeali, Zakiye; Mohammadi-Zaniani, Zohreh; Biglari, Sajjad; Molavi, Newsha; Zardoui, Khashayar; Mirfendereski, Sam; Hashemipour, Mahin; Tabatabaiefar, Mohammad Amin; Polychronakos, Constantin
err分享
err收藏
Clinicogenetic characterisation of SLC29A3-related syndromes: a case series, tracing ancestral variants and molecular dynamics simulation
errJOURNAL OF MEDICAL GENETICS
IF3.7
err2025-03-01
err0
PREAI
errBiglari, Sajjad; Shahrooei, Mohammad; Vahidnezhad, Fatemeh; Youssefian, Leila; Ziaee, Vahid; Rezaei, Nima; Moghaddam, Atefeh Sohanforooshan; Sedighzadeh, Sahar; Moravej, Hossein; Safari Foroushani, Parisa; Keivanfar, Majid; Ilkhanipoor, Homa; Hozhabrpour, Amir; Seyedhosseini-Ghaheh, Hooria; Mohammadzadeh, Iraj; Naderi, Majid; Sheikhi Ghayur, Elham; Mansour Samaei, Nader; Dorgaleleh, Saeed; Esmaeilzadeh, Emran; Sherkat, Roya; Khorram Khorshid, Hamid Reza; Tabatabaiefar, Mohammad Amin; Hakonarson, Hakon; Vahidnezhad, Hassan
err分享
err收藏
Filaggrinopathies—FLG/FLG2: Diagnostic Complexities and Immunotherapy丝聚蛋白病—FLG/FLG2：诊断复杂性及免疫治疗
errJournal of Investigative Dermatology
IF5.7
err2025-02-07
err0
PREAI
errZahra Nouri; Sajjad Biglari; Mohammad Amin Tabatabaiefar; Fatemeh Vahidnezhad; Amir Hozhabrpour; Michael E. March; David J. Margolis; Johann E. Gudjonsson; Hakon Hakonarson; Hassan Vahidnezhad
err分享
err收藏
Monogenic etiologies of persistent human papillomavirus infections: A comprehensive systematic review
errGENETICS IN MEDICINE
IF6.2
err2024-02-01
err1
PREAI
errBiglari, Sajjad; Moghaddam, Atefeh Sohanforooshan; Tabatabaiefar, Mohammad Amin; Sherkat, Roya; Saeidian, Amir Hossein; Vahidnezhad, Fatemeh; Tsoi, Lam C.; Gudjonsson, Johann E.; Hakonarson, Hakon; Casanova, Jean -Laurent; Beziat, Vivien; Jouanguy, Emmanuelle; Vahidnezhad, Hassan
err分享
err收藏
The Importance of SNPs at miRNA Binding Sites as Biomarkers of Gastric and Colorectal Cancers: A Systematic Review
errJOURNAL OF PERSONALIZED MEDICINE
IF3
err2022-03-14
err20
errOAAI
errHajibabaie, Fatemeh; Abedpoor, Navid; Assareh, Nazanin; Tabatabaiefar, Mohammad Amin; Shariati, Laleh; Zarrabi, Ali
err分享
err收藏
Predicting deleterious missense genetic variants via integrative supervised nonnegative matrix tri-factorization
errSCIENTIFIC REPORTS
IF3.9
err2021-12-09
err0
errOAAI
errArani, Asieh Amousoltani; Sehhati, Mohammadreza; Tabatabaiefar, Mohammad Amin
err分享
err收藏
WRN Germline Mutation Is the Likely Inherited Etiology of Various Cancer Types in One Iranian Family
errFRONTIERS IN ONCOLOGY
IF3.3
err2021-06-07
err1
errOAAI
errNorouzi, Mahnaz; Shafiei, Mohammad; Abdollahi, Zeinab; Miar, Paniz; Galehdari, Hamid; Emami, Mohammad Hasan; Zeinalian, Mehrdad; Tabatabaiefar, Mohammad Amin
err分享
err收藏
Genetic variant effect prediction by supervised nonnegative matrix tri-factorization
errMOLECULAR OMICS
IF2.4
err2021-01-01
err2
PREAI
errArani, Asieh Amousoltani; Sehhati, Mohammadreza; Tabatabaiefar, Mohammad Amin
err分享
err收藏
Upregulation ofMTOR,RPS6KB1, andEIF4EBP1in the whole blood samples of Iranian patients with multiple sclerosis compared to healthy controls
errMETABOLIC BRAIN DISEASE
IF3.5
err2020-08-18
err7
PREAI
errAkbarian, Fahimeh; Tabatabaiefar, Mohammad Amin; Shaygannejad, Vahid; Shahpouri, Mohammad Mahdi; Badihian, Negin; Sajjadi, Roshanak; Dabiri, Arezou; Jalilian, Nazanin; Noori-Daloii, Mohammad Reza
err分享
err收藏
Clinical and molecular assessment of 13 Iranian families with Wolfram syndrome
errENDOCRINE
IF2.9
err2019-07-16
err3
PREAI
errSobhani, Maryam; Tabatabaiefar, Mohammad Amin; Ghafouri-Fard, Soudeh; Rajab, Asadollah; Mozafarpour, Sarah; Nasrniya, Samaneh; Kajbafzadeh, Abdol-Mohammad; Noori-Daloii, Mohammad Reza
err分享
err收藏
Homozygosity mapping and direct sequencing identify a novel pathogenic variant in the CISD2 gene in an Iranian Wolfram syndrome family
errACTA DIABETOLOGICA
IF2.9
err2019-07-15
err9
PREAI
errPourreza, Mohammad Reza; Sobhani, Maryam; Rahimi, Azadeh; Aramideh, Mehdi; Kajbafzadeh, Abdol-Mohammad; Noori-Daloii, Mohammad Reza; Tabatabaiefar, Mohammad Amin
err分享
err收藏
A novel pathogenic variant in the MARVELD2 gene causes autosomal recessive non-syndromic hearing loss in an Iranian family
errGENOMICS
IF3
err2019-07-01
err8
errOAAI
errTaghipour-Sheshdeh, Afsaneh; Nemati-Zargaran, Fatemeh; Zarepour, Narges; Tahmasebi, Parisa; Saki, Nader; Tabatabaiefar, Mohammad Amin; Mohammadi-Asl, Javad; Hashemzadeh-Chaleshtori, Morteza
err分享
err收藏
Engineered zinc-finger nuclease to generate site-directed modification in the KLF1 gene for fetal hemoglobin induction
errJOURNAL OF CELLULAR BIOCHEMISTRY
IF2.8
err2018-12-16
err7
PREAI
errShariati, Laleh; Modarressi, Mohammad Hossein; Tabatabaiefar, Mohammad Amin; Kouhpayeh, Shirin; Hejazi, Zahra; Shahbazi, Mansoureh; Sabzehei, Faezeh; Salehi, Mansoor; Khanahmad, Hossein
err分享
err收藏
Molecular genetic study of glutaric aciduria, type I: Identification of a novel mutation
errJOURNAL OF CELLULAR BIOCHEMISTRY
IF2.8
err2018-09-11
err6
PREAI
errShadmehri, Azam Ahmadi; Fattahi, Najmeh; Pourreza, Mohammad Reza; Koohiyan, Mahboobeh; Zarifi, Shahnaz; Darbouy, Mojtaba; Sharifi, Reza; Bazzaz, Javad Tavakkoly; Tabatabaiefar, Mohammad Amin
err分享
err收藏
Inducing indel mutation in the SOX6 gene by zinc finger nuclease for gamma reactivation: An approach towards gene therapy of beta thalassemia
errJOURNAL OF CELLULAR BIOCHEMISTRY
IF2.8
err2017-11-30
err22
PREAI
errSadeghi, Mehran Modares; Shariati, Laleh; Hejazi, Zahra; Shahbazi, Mansoureh; Tabatabaiefar, Mohammad Amin; Khanahmad, Hossein
err分享
err收藏
A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a large Iranian kindred
errJOURNAL OF DERMATOLOGICAL SCIENCE
IF4
err2017-10-01
err2
errOAAI
errMohammadi-asl, Javad; Pourreza, Mohammad Reza; Mohammadi, Aliasgar; Eskandari, Ameneh; Mozafar-Jalali, Sima; Tabatabaiefar, Mohammad Amin
err分享
err收藏

研究方向

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合作学者
合作期刊
H
Håkon Håkonarson
H 指数: 177 · 论文数: 1.5K
D
David J. Margolis
H 指数: 100 · 论文数: 589
A
Ali Zarrabi
H 指数: 81 · 论文数: 445
J
Jóhann E. Guðjónsson
H 指数: 80 · 论文数: 595
C
Constantin Polychronakos
H 指数: 61 · 论文数: 253
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