Bader Almuzzaini

发表

Blood pressure–lowering activity of statins: a systematic literature review and meta-analysis of placebo-randomized controlled trials

S. Padmanabhan, Manal A. Alaamery, J. Alghamdi, 2020, European Journal of Clinical Pharmacology.

Blockade of p38 MAPK overcomes AML stem cell line KG1a resistance to 5-Fluorouridine and the impact on miRNA profiling

S. Matou-Nasri, Bader Almuzzaini, Hamad Al-Eidi, 2022, PloS one.

Identification of the TTC26 Splice Variant in a Novel Complex Ciliopathy Syndrome with Biliary, Renal, Neurological, and Skeletal Manifestations

Muhammad Umair, M. Alfadhel, M. Al-Owain, 2021, Molecular Syndromology.

Identification of Novel Mutations in Colorectal Cancer Patients Using AmpliSeq Comprehensive Cancer Panel

M. Aziz, Saleh A Alghamdi, Bader Almuzzaini, 2021, Journal of personalized medicine.

In β‐actin knockouts, epigenetic reprogramming and rDNA transcription inactivation lead to growth and proliferation defects

A. Ö. Farrants, O. Sangfelt, A. Sarshad, 2016, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Targeted SLC19A3 gene sequencing of 3000 Saudi newborn: a pilot study toward newborn screening

Muhammad Umair, M. Alfadhel, A. Alfares, 2019, Annals of clinical and translational neurology.

Analysis of chronic kidney disease patients by targeted next-generation sequencing identifies novel variants in kidney-related genes

F. Quintana, Adel F. Almutairi, M. Alfadhel, 2022, Frontiers in Genetics.

Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality

S. Yezli, M. Rashid, A. Bouchama, 2021, Genomics.

Herbal melanin induces interleukin-1β secretion and production by human THP-1 monocytes via Toll-like receptor 2 and p38 MAPK activation

A. El-Obeid, S. Matou-Nasri, Bader Almuzzaini, 2021, Experimental and therapeutic medicine.

Identification of Novel Mutations in Colorectal Cancer Patients Using AmpliSeq Comprehensive Cancer Panel

M. Aziz, Saleh A Alghamdi, Bader Almuzzaini, 2021, Journal of personalized medicine.

β‐Actin‐dependent global chromatin organization and gene expression programs control cellular identity

K. Gunsalus, Nizar Drou, A. Ö. Farrants, 2017, FASEB journal : official publication of the Federation of American Societies for Experimental Biology.

Epidemiology of cancer in Saudi Arabia thru 2010–2019: a systematic review with constrained meta-analysis

H. Ahmed, Bassam Ahmed Almutlaq, A. Elasbali, 2020, AIMS public health.

Nuclear Wiskott–Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cells

S. Snapper, Marisa A. P. Baptista, P. Percipalle, 2017, Genome Medicine.

Pancytopenia, Recurrent Infection, Poor Wound Healing, Heterotopia of the Brain Probably Associated with A Candidate Novel de Novo CDC42 Gene Defect: Expanding the Molecular and Phenotypic Spectrum

Bahauddeen M. Alrfaei, Muhammad Umair, M. Alfadhel, 2021, Genes.

Identification of CSF3R Mutations in B-Lineage Acute Lymphoblastic Leukemia Using Comprehensive Cancer Panel and Next-Generation Sequencing

A. Alsultan, M. Rashid, Bader Almuzzaini, 2021, Genes.

Can First-Dose Therapeutic Drug Monitoring Predict the Steady State Area Under the Blood Concentration-Time Curve of Busulfan in Pediatric Patients Undergoing Hematopoietic Stem Cell Transplantation?

A. Alsultan, M. Essa, A. Alsultan, 2022, Frontiers in Pediatrics.

Nuclear myosin 1 contributes to a chromatin landscape compatible with RNA polymerase II transcription activation

A. Ö. Farrants, A. Sarshad, P. Percipalle, 2015, BMC Biology.

Mutated RAP1GDS1 causes a new syndrome of dysmorphic feature, intellectual disability & speech delay

Muhammad Umair, M. Alfadhel, Bader Almuzzaini, 2020, Annals of clinical and translational neurology.

The effect of the VKORC1 promoter variant on warfarin responsiveness in the Saudi WArfarin Pharmacogenetic (SWAP) cohort

M. A. Al Ammari, Bader Almuzzaini, M. Albalwi, 2020, Scientific Reports.

Biallelic variant in DACH1, encoding Dachshund Homolog 1, defines a novel candidate locus for recessive postaxial polydactyly type A.

Muhammad Umair, M. Alfadhel, Q. Alam, 2021, Genomics.

Nuclear Wiskott–Aldrich syndrome protein co-regulates T cell factor 1-mediated transcription in T cells

S. Snapper, Marisa A. P. Baptista, P. Percipalle, 2017, Genome Medicine.

Nuclear myosin 1 contributes to a chromatin landscape compatible with RNA polymerase II transcription activation

A. Ö. Farrants, A. Sarshad, P. Percipalle, 2015, BMC Biology.

Biallelic variants in four genes underlying recessive osteogenesis imperfecta.

O. Mäkitie, W. Ahmad, Muhammad Umair, 2020, European journal of medical genetics.

A classification system for split-hand/ foot malformation (SHFM): A proposal based on 3 pedigrees with WNT10B mutations.

Bader Almuzzaini, M. Albalwi, M. Al-Qattan, 2020, European journal of medical genetics.

Discovery of a novel potentially transforming somatic mutation in CSF2RB gene in breast cancer

Hao Song, M. Rashid, Rizwan Ali, 2021, Cancer medicine.

Interferon-induced transmembrane protein-3 genetic variant rs12252 is associated with COVID-19 mortality

S. Yezli, M. Rashid, Salleh N. Ehaideb, 2021, Genomics.