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Research article

First published 2021-07

ASPM is a Novel Candidate Gene Associated with Colorectal Cancer Cell Growth

Qian Yang, Mingming Qi, Yongyu Chen [...]

DNA and Cell Biology

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Other

First published 2010-6

Mutation Analysis of the ASPM Gene in 18 Pakistani Families With Autosomal Recessive Primary Microcephaly

Rizwana Kousar, Hira Nawaz, Maryam Khurshid [...]

Journal of Child Neurology

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Research article

First published 2016-7

The Impact of rs3762271 and rs930557 Polymorphisms of ASPM and MCPH1 Genes on the Anatomy and Function of the Brain

Joanna Pierzak-Sominka, Karolina Skonieczna-Żydecka, Jacek Rudnicki [...]

Biological Research For Nursing

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Research article

First published 2024-5

Genetic Microcephaly in a Saudi Population: Unique Spectrum of Affected Genes Including a Novel One

Muhammad Talal Alrifai, Yousof Alrumayyan, Duaa Baarmah [...]

Journal of Child Neurology

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Review article

First published 2005-04

Topical Review: Cortical Malformation and Pediatric Epilepsy: A Molecular Genetic Approach

Ganeshwaran H. Mochida

Journal of Child Neurology

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Review article

First published 2004-03

Topical Review: Cortical Malformation and Pediatric Epilepsy: A Molecular Genetic Approach

Ganeshwaran H. Mochida

Journal of Child Neurology

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Research article

First published 2022-01

A Two-Base Pair Deletion in IQ Repeats in ASPM Underlies Microcephaly in a Pakistani Family

Syeda Farwa Naqvi, Rana Muhammad Kamran Shabbir, Aslıhan Tolun [...]

Genetic Testing and Molecular Biomarkers

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Research article

First published 2018-03

Identification of a Novel Nonsense ASPM Mutation in a Large Consanguineous Pakistani Family Using Targeted Next-Generation Sequencing

Amjad Khan, Rongrong Wang, Shirui Han [...]

Genetic Testing and Molecular Biomarkers

Open access

Research article

First published 2023-6

Integrated Analysis of Transcriptome Changes in Osteoarthritis: Gene Expression,Pathways and Alternative Splicing

Congming Li, Pengli Wei, Lei Wang [...]

CARTILAGE

Free access

Research article

First published 2018-2

Whole-exome sequencing to identify novel mutations of nevoid basal cell carcinoma syndrome in a Chinese population

Nanhang Lu, Jinzeng Wang, Bijun Zhu [...]

Cancer Biomarkers

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