Ihsan Khan - University of Science and Technology of China, University of Science and Technology of China

基本信息

Career Trajectory

Bio

Ihsan Khan Currently works at the department of molecular biology and cell biology, University of science and technology of China (USTC). Experience in biochemistry, biotechnology and human genetics. Expertise includes establishing molecular and cellular techniques for identification of human genetic disease as well as find a way to enhance the detection and identification of mutation with acceptable specificities, sensitivities and accuracy.

Research Interests

Papers共 25 篇Author StatisticsCo-AuthorSimilar Experts

By YearBy Citation主题筛选期刊级别筛选合作者筛选合作机构筛选

Novel Biallelic ADCY10 Variants Cause Asthenozoospermia with Excessive Residual Cytoplasm and Hydronephrosis in Humans

Aurang Zeb, Menglei Yang, Nisar Ahmad, Huan Zhang, Wasim Shah,Khalid Khan, Meftah Uddin, Abu Mansoor, Fazal Rahim,Ansar Hussain, Imtiaz Ali,Tanveer Abbas,Muhammad Zubair,Ihsan Khan,Qinghua Shi

Reproductive BioMedicine Online (2024)

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A Homozygous ARMC3 Splicing Variant Causes Asthenozoospermia and Flagellar Disorganization in a Consanguineous Family

Fazal Rahim, Liu Tao,Khalid Khan, Imtiaz Ali, Aurang Zeb,Ihsan Khan,Sobia Dil,Tanveer Abbas,Ansar Hussain,Muhammad Zubair, Huan Zhang, Ma Hui,Muzammil Ahmad Khan,Wasim Shah, Qinghua Shi

CLINICAL GENETICSno. 4 (2024): 437-447

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A Novel Homozygous TSGA10 Missense Variant Causes Acephalic Spermatozoa Syndrome in a Pakistani Family

Khalid Khan,Xiangjun Zhang,Sobia Dil,Ihsan Khan,Ahsanullah Unar,Jingwei Ye,Aurang Zeb,Muhammad Zubair,Wasim Shah, Huan Zhang, Muzammil Ahmad Khan,Limin Wu,Bo Xu,Hui Ma,Zina Wen,Qinghua Shi

BASIC AND CLINICAL ANDROLOGY（2024）

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A Recessive ACTL7A Founder Variant Leads to Male Infertility Due to Acrosome Detachment in Pakistani Pashtuns

Clinical geneticsno. 5 (2023): 564-570

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Cornichon Protein CNIH4 is Not Essential for Mice Gametogenesis and Fertility

Sobia Dil,Jingwei Ye,Hui Ma,Ahsanullah Unar,Ihsan Khan,Asim Ali,Khalid Khan,Yang Menglei,Ao Ma,Basit Shah,Ranjha Khan,Zhiwei Liu,Qinghua Shi

DEVELOPMENTAL BIOLOGY (2023): 15-23

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A Homozygous KASH5 Frameshift Mutation Causes Diminished Ovarian Reserve, Recurrent Miscarriage, and Non-Obstructive Azoospermia in Humans

Xiaoning Hou,Aurang Zeb,Sobia Dil,Jianteng Zhou, Huan Zhang,Baolu Shi,Zubair Muhammad,Ihsan Khan,Qamar Zaman,Wasim Akbar Shah,Xiaohua Jiang,Limin Wu,Hui Ma,Qinghua Shi

FRONTIERS IN ENDOCRINOLOGY（2023）

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M1AP Interacts with the Mammalian ZZS Complex and Promotes Male Meiotic Recombination

Yang Li,Yufan Wu,Ihsan Khan,Jianteng Zhou, Yue Lu,Jingwei Ye, Junyan Liu,Xuefeng Xie,Congyuan Hu,Hanwei Jiang,Suixing Fan, Huan Zhang,Yuanwei Zhang,Xiaohua Jiang,Bo Xu,Hui Ma,Qinghua Shi

EMBO REPORTSno. 2 (2023)

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A Recurrent Homozygous Missense Mutation in CCDC103 Causes Asthenoteratozoospermia Due to Disorganized Dynein Arms

Muhammad Zubair,Ranjha Khan,Ao Ma,Uzma Hameed,Mazhar Khan,Tanveer Abbas,Riaz Ahmad,Jian-Teng Zhou,Wasim Shah,Ansar Hussain,Nisar Ahmed,Ihsan Khan,Khalid Khan,Yuan-Wei Zhang, Huan Zhang,Li-Min Wu,Qing-Hua Shi

Asian Journal of Andrology（2022）

Cited7Views0WOSBibtex

Testis-specific fascin component FSCN3 is dispensable for mouse spermatogenesis and fertility

Haider Ali,Ahsanullah Unar,Sobia Dil,Imtiaz Ali,Khalid Khan,Ihsan Khan,Qinghua Shi

Mol Biol Rep（2022）

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