Muhammad Ayub

Research interests

Publications

• A roadmap to increase diversity in genomic studies

  Nature Medicine · 2022 · https://doi.org/10.1038/s41591-021-01672-4

• Brain charts for the human lifespan

  Nature · 2022 · https://doi.org/10.1038/s41586-022-04554-y

• Suicide, self-harm and suicidal ideation during COVID-19: A systematic review

  Psychiatry Research · 2021 · https://doi.org/10.1016/j.psychres.2021.114228

• An International Adult Guideline for Making Clozapine Titration Safer by Using Six Ancestry-Based Personalized Dosing Titrations, CRP, and Clozapine Levels

  Pharmacopsychiatry · 2021 · https://doi.org/10.1055/a-1625-6388

• Cultural adaptation of cognitive–behavioural therapy

  BJPsych Advances · 2019 · https://doi.org/10.1192/bja.2019.15

• Barriers to using clozapine in treatment-resistant schizophrenia: systematic review

  BJPsych Bulletin · 2018 · https://doi.org/10.1192/bjb.2018.67

• Mapping autosomal recessive intellectual disability: combined microarray and exome sequencing identifies 26 novel candidate genes in 192 consanguineous families

  Molecular Psychiatry · 2017 · https://doi.org/10.1038/mp.2017.60

• Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

  Nature Neuroscience · 2016 · https://doi.org/10.1038/nn.4267

• Correction: Corrigendum: TCTEX1D2 mutations underlie Jeune asphyxiating thoracic dystrophy with impaired retrograde intraflagellar transport

  Nature Communications · 2016 · https://doi.org/10.1038/ncomms11270

• Ethnobotanical survey of medicinally important shrubs and trees of Himalayan region of Azad Jammu and Kashmir, Pakistan

  Journal of Ethnopharmacology · 2015 · https://doi.org/10.1016/j.jep.2015.03.042

• Improved imputation of low-frequency and rare variants using the UK10K haplotype reference panel

  Nature Communications · 2015 · https://doi.org/10.1038/ncomms9111

• Mutation in NSUN2, which Encodes an RNA Methyltransferase, Causes Autosomal-Recessive Intellectual Disability

  The American Journal of Human Genetics · 2012 · https://doi.org/10.1016/j.ajhg.2012.03.023

• Alterations of the CIB2 calcium- and integrin-binding protein cause Usher syndrome type 1J and nonsyndromic deafness DFNB48

  Nature Genetics · 2012 · https://doi.org/10.1038/ng.2426

• The genetic basis of non-syndromic intellectual disability: a review

  Journal of Neurodevelopmental Disorders · 2010 · https://doi.org/10.1007/s11689-010-9055-2

• INPP5E mutations cause primary cilium signaling defects, ciliary instability and ciliopathies in human and mouse

  Nature Genetics · 2009 · https://doi.org/10.1038/ng.427

Current projects

No projects listed.