Milad Gholami

7PUBLICATIONS
13CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Developmental genetics (incl. sex determination)Infant and child healthApplied immunology (incl. antibody engineering, xenotransplantation and t-cell therapies)Psychosocial aspects of childbirth and perinatal mental health
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Publications (7)

|Jul 23, 2026
CRISPR/Cas9-Engineered HEK293T Cellular Model Harboring the Pathogenic CDKL5 c.172A>T Variant Recapitulates Core Molecular Phenotypes of CDKL5 Deficiency Disorder.

|Jul 01, 2026
Expanding the Phenotype and Genotype Spectrum of a Novel Mutation in Hypomyelinating Leukodystrophy-5 With a Review of the Literature on 42 Cases.

|Feb 09, 2026
Identification of Novel Mutation in the ABCA12 Gene Causing Harlequin Ichthyosis.

Nadia Soltani, Zahra Bayati, Mohsen Soosanabadi

|Jan 29, 2022
Novel insertion mutation in the PLA2G6 gene in an Iranian family with infantile neuroaxonal dystrophy.

Dorsa Rostampour, Mohammad Reza Zolfaghari, Milad Gholami

|Jan 25, 2022
The effect of Ccnb1ip1 insulator on monoclonal antibody expression in Chinese hamster ovary cells.

Azam Rahimpour, Es'hagh Pourmaleki, Forough Shams

|Dec 06, 2021
Differential expression of Hsa-miR-517a/b in placental tissue may contribute to the pathogenesis of preeclampsia

Mona Amin-Beidokhti, Hossein Sadeghi, Reihaneh Pirjani

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Frequent Collaborators

2 joint publications

Hossein Sadeghi

2 joint publications

Latif Gachkar

2 joint publications

Reza Mirfakhraie

2 joint publications

Jafar Amani