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

Clinical and genetic heterogeneity of syndromic hearing loss and its non-syndromic hearing loss mimics

综合征性听力损失及其非综合征性听力损失类似症状的临床和遗传异质性

Koparir, Asuman; Carbajal, Paulina Bahena; Zamini, Mina; Naghinejad, Maryam; Najarzadeh Torbati, Paria; Hofrichter, Michaela A H; Tovornik, Stefanie; Koparir, Erkan; Dragicevic Babic, Neda; Rad, Aboulfazl; Owrang, Daniel; Kalay, Irem; Chamanrou, Niloofar; Martínez Völter, Luis Nicolás; Christophersen, Nele; Baranzehi, Tayebeh; Rajati, Mohsen; Loum, Stephen; Kunstmann, Erdmute; Shadab, Madiha; Abbasi, Ansar Ahmed; Doosti, Mohammad; Alidadiani, Neda; Ghaderi, Shahrooz; Haack, Tobias B; Alavi, Shahryar; Doll, Julia; Kremer, Hannie; Kordi-Tamandani, Dor Mohammad; Murphy, David; Mohammad, Rahema; Hebestreit, Helge; Ghayoor Karimiani, Ehsan; Flandin, Sophie; Linares, Paola; Villalobos, Daniel; Houlden, Henry; Galehdari, Hamid; Shehata-Dieler, Wafaa; Maroofian, Reza; Haaf, Thomas; Vona, Barbara

Monoallelic and biallelic KDM5A variants identified in patients with autism spectrum disorder.

在自闭症谱系障碍患者中发现了KDM5A的单等位基因和双等位基因变异。

El Hayek Lauretta, Gogate Ashlesha, Chen Wei-Chen, Kaur Kiran, Zaki Maha S, De Wachter Matthias, Van Schil Kristof, Dublin-Ryan Leeran, Zamani Mina, Bartos Meghan N, Hiatt Susan M, Courdier Cécile, Michaud Vincent, Kenny Janna, Day Michael, Pang Lewis, Nasab Mahya Ebrahimi, Madani Manshadi Seyed Ali, Eslahi Atieh, Rasoul Masoomeh Ale, Sanchez-Mendoza Eduardo Humberto, DeLuca Charles, Marafi Dana, Stevens Servi J C, Ivanovski Ivan, Frey Tanja, Steindl Katharina, Rauch Anita, O'Connor Kaitlyn, Velinov Milen, Shen Xiaoming, Janssen Etienne J M, Sedighzadeh Sahar, Kordi-Tamandani Dor Mohammad, Khajeh Ali, Elshafie Reem M, Bastaki Laila, Misra Vinod K, Firoozfar Zahra, Goldenberg Paula C, Toosi Mehran Beiraghi, Mojarrad Majid, Kavanagh Karl, Koboldt Daniel C, Margot Henri, Hurst Anna C E, Weber Axel, Bergmann Carsten, Houlden Henry, Maroofian Reza, Weis Denisa, Ceulemans Berten, Chahrour Maria H

DOK7 Gene Novel Homozygous Mutation is Related to Fetal Akinesia Deformation Sequence 3

DOK7基因新型纯合突变与胎儿运动不能畸形序列3相关

Komachali, Sajad Rafiee; Keikhaie, Khadije Rezaie; Siahpoosh, Zakieh; Salehi, Mansoor; Tamandani, Dor Mohammad Kordi

Correlation between JAK2, STAT3, and CTLA4 Relative Gene Expressions and Oral Squamous Cell Carcinoma

JAK2、STAT3 和 CTLA4 相对基因表达与口腔鳞状细胞癌的相关性

Kadeh, Hamideh; Baranzehi, Tayebeh; Mollaali, Milad; Maserat, Neda; Shahraki, Mohammad Javad; Kordi-Tamandani, Dor Mohammad

Different Effects of Low-Level Laser Therapy on the Proliferation of HT29 Cells in Culture and Xenograft Models

低强度激光疗法对体外培养和异种移植模型中HT29细胞增殖的不同影响

Malekzadeh Gonabadi, Najmeh; Shamsara, Mehdi; Kordi Tamandani, Dor Mohammad; Shojaei, Sahar; Alavi, Seyed Mehdi

Identification of a TPP1 Q278X Mutation in an Iranian Patient with Neuronal Ceroid Lipofuscinosis 2: Literature Review and Mutations Update

伊朗一名神经元蜡样脂褐质沉积症2型患者中TPP1 Q278X突变的鉴定:文献回顾和突变更新

Baranzehi, Tayebeh; Kordi-Tamandani, Dor Mohammad; Najafi, Maryam; Khajeh, Ali; Schmidts, Miriam

Association of Genetic Polymorphisms in GSTP1, GSTM1, and GSTT1 Genes with Vesicoureteral Reflux Susceptibility in the Children of Southeast Iran

东南伊朗儿童GSTP1、GSTM1和GSTT1基因多态性与膀胱输尿管反流易感性的关联

Shahrokhzadeh, Sima; Soleimani, Azam; Kordi-Tamandani, Dor-Mohammad; Sangtarash, Mohammad Hossein; Nejati, Omid; Taheri, Mohsen

Mimicry and well known genetic friends: molecular diagnosis in an Iranian cohort of suspected Bartter syndrome and proposition of an algorithm for clinical differential diagnosis

模仿与已知的遗传伙伴:伊朗疑似巴特综合征患者队列的分子诊断及临床鉴别诊断算法的提出

Najafi, Maryam; Kordi-Tamandani, Dor Mohammad; Behjati, Farkhondeh; Sadeghi-Bojd, Simin; Bakey, Zeineb; Karimiani, Ehsan Ghayoor; Schüle, Isabel; Azarfar, Anoush; Schmidts, Miriam

Analysis of Polymorphism and Expression Profile of ASIC1 and IL-6 Genes in Patients with Gastric Cancer

胃癌患者ASIC1和IL-6基因多态性和表达谱分析

Heydari-Mehrabadi, Abdulkuddous; Kordi Tamandani, Dor Mohammad; Baranzehi, Taybeh; Hemati, Simin

Contribution of LATS1 and LATS2 promoter methylation in OSCC development

LATS1和LATS2启动子甲基化在口腔鳞状细胞癌发展中的作用

Ladiz, Mohammad Ayoub Rigi; Najafi, Maryam; Kordi-Tamandani, Dor Mohammad