Author

Muhammad Iqbal

Islamia University of Bahawalpur

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Same name, identified by ORCID

Biology Disciplines

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Genetic & Genomic Medicine· 2

Signature Assays, Organisms & Methods

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Organism:human· 2 Approach:statistical model· 2 Assay:bulk RNA-seq· 1 Research Focus:differential expression· 1 Research Focus:gene regulatory network inference· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Abolfazl Heidari· 1 shared Ada HamoshiD· 1 shared Aisha Nasir HashmiiD· 1 shared Alan H. BeggsiD· 1 shared Alice PoissoniD· 1 shared André ReisiD· 1 shared Anita M. RauchiD· 1 shared Anna MikhailoviD· 1 shared

Activity by Year

2021-2021 · peak 2/yr

Co-Author Collaboration Network

10 top collaborators · 21 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Abolfazl Heidari

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2 papers

Recent·Most cited

Genetic & Genomic MedicinemedRxivPreprintDec 24, 2021

Autism spectrum disorder trios from consanguineous populations are enriched for rare biallelic variants, identifying 32 new candidate genes

Ricardo Harripaul, Ansa Rabia, Nasim Vasli…·John B. Vincent

3 citations

humanwhole-exome sequencing

Genetic & Genomic MedicineGenetics in MedicinePeer-reviewedMar 3, 2021

Disruption of RFX family transcription factors causes autism, attention-deficit/hyperactivity disorder, intellectual disability, and dysregulated behavior

Holly K. Harris, Tojo Nakayama, Jenny F. Lai…·Timothy W. Yu

The paper identifies RFX3, RFX4, and RFX7 mutations as causes of neurodevelopmental disorders including autism, ADHD, and intellectual disability, and links these genes to ASD risk genes through bioinformatic analysis.

84 citationstop 3%

humanbulk RNA-seq