日期 影响因子
日期:
2020 年 — 2026 年
2020
2021
2022
2023
2024
2025
2026
影响因子:
–

Recent developments using malononitrile in ultrasound-assisted multicomponent synthesis of heterocycles

近年来，丙二腈在超声辅助多组分合成杂环化合物中的应用取得了进展

期刊:Ultrasonics Sonochemistry
影响因子:9.7
doi:10.1016/j.ultsonch.2023.106741
Javahershenas, Ramin; Nikzat, Sahand
发表日期：2024
文献求助 收藏

Identification of a Novel Variant in CC2D1A Gene Linked to Autosomal Recessive Intellectual Disability 3 in an Iranian Family and Investigating the Structure and Pleiotropic Effects of this Gene

在伊朗一个家族中鉴定出与常染色体隐性遗传智力障碍3型相关的CC2D1A基因新变异，并研究该基因的结构和多效性

期刊:Iranian Journal of Child Neurology
影响因子:0.9
doi:10.22037/ijcn.v18i1.42188
Rashvand, Zahra; Najmabadi, Hossein; Kahrizi, Kimia; Mozhdehipanah, Hossein; Moradi, Mohammad; Estaki, Zohreh; Taherkhani, Khadijeh; Nikzat, Nooshin; Najafipour, Reza; Omrani, Mir Davood
C2D1A
发表日期：2024
文献求助 收藏

Recent advances in the multicomponent synthesis of heterocycles using tetronic acid

利用四氢呋喃酸进行杂环多组分合成的最新进展

期刊:RSC Advances
影响因子:4.6
doi:10.1039/d3ra02505e
Javahershenas, Ramin; Nikzat, Sahand
发表日期：2023
文献求助 收藏

Exome sequencing utility in defining the genetic landscape of hearing loss and novel-gene discovery in Iran

外显子组测序在伊朗听力损失遗传图谱的界定和新基因发现中的应用

期刊:Clinical Genetics
影响因子:2.3
doi:10.1111/cge.13956
Mohseni, Marzieh; Babanejad, Mojgan; Booth, Kevin T; Jamali, Payman; Jalalvand, Khadijeh; Davarnia, Behzad; Ardalani, Fariba; Khoshaeen, Atefeh; Arzhangi, Sanaz; Ghodratpour, Fatemeh; Beheshtian, Maryam; Jahanshad, Faezeh; Otukesh, Hasan; Bahrami, Fatemeh; Seifati, Seyed Morteza; Bazazzadegan, Niloofar; Habibi, Farkhonde; Behravan, Hanieh; Mirzaei, Sepide; Keshavarzi, Fatemeh; Nikzat, Nooshin; Mehrjoo, Zohreh; Thiele, Holger; Nothnagel, Michael; Azaiez, Hela; Smith, Richard J; Kahrizi, Kimia; Najmabadi, Hossein
发表日期：2021
文献求助 收藏

Nutlet micromorphology and character evolution of Lappula species (Boraginaceae) and its systematic implications

紫草科植物拉普拉属（Lappula）小坚果的微观形态和性状演化及其系统学意义

期刊:
影响因子:
doi:10.1186/s40529-021-00325-6
Ebadi, Mostafa; Nikzat, Sedigheh
发表日期：2021
文献求助 收藏

When transcripts matter: delineating between non-syndromic hearing loss DFNB32 and hearing impairment infertile male syndrome (HIIMS)

转录文本的重要性：区分非综合征性听力损失 DFNB32 和听力障碍不育男性综合征 (HIIMS)

期刊:Journal of Human Genetics
影响因子:2.5
doi:10.1038/s10038-020-0740-z
Mohseni, Marzieh; Akbari, Mojdeh; Booth, Kevin T; Babanejad, Mojgan; Azaiez, Hela; Ardalani, Fariba; Arzhangi, Sanaz; Jalalvand, Khadijeh; Nikzat, Nooshin; Ghodratpour, Fatemeh; Jamali, Payman; Adeli, Omid Ali; Habibi, Haleh; Kahrizi, Kimia; Najmabadi, Hossein
多发性硬化症
发表日期：2020
文献求助 收藏

Did the GJB2 35delG mutation originate in Iran?

GJB2 35delG 突变起源于伊朗吗？

期刊:American Journal of Medical Genetics Part A
影响因子:1.7
doi:10.1002/ajmg.a.34225
Norouzi, Vahideh; Azizi, Hiva; Fattahi, Zohreh; Esteghamat, Fatemehsadat; Bazazzadegan, Niloofar; Nishimura, Carla; Nikzat, Nooshin; Jalalvand, Khadijeh; Kahrizi, Kimia; Smith, Richard J H; Najmabadi, Hossein
发表日期：2011
文献求助 收藏

Mutations in TMC1 are a common cause of DFNB7/11 hearing loss in the Iranian population

TMC1基因突变是伊朗人群中DFNB7/11型听力损失的常见原因

期刊:Annals of Otology Rhinology and Laryngology
影响因子:1.2
doi:10.1177/000348941011901207
Hildebrand, Michael S; Kahrizi, Kimia; Bromhead, Catherine J; Shearer, A Eliot; Webster, Jennifer A; Khodaei, Hossein; Abtahi, Rezvan; Bazazzadegan, Niloofar; Babanejad, Mojgan; Nikzat, Nooshin; Kimberling, William J; Stephan, Dietrich; Huygen, Patrick L M; Bahlo, Melanie; Smith, Richard J H; Najmabadi, Hossein
发表日期：2010
文献求助 收藏