Mohammad Amin Tabatabaiefar

12PUBLICATIONS
18CO-AUTHORS
Epigenetics (incl. genome methylation and epigenomics)Haematological tumoursGenetic immunologyOrganometallic chemistryPredictive and prognostic markers
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Publications (12)

|Dec 29, 2025
A Truncating Variant in the ERCC6 Gene With Three Different Phenotypes: Significant Effects of Modifier Genes.

Mehdi Khorrami, Erfan Khorram, Mohammad Amin Tabatabaiefar

|Oct 02, 2025
Mono-allelic MUTYH mutation as the likely inherited etiology of hereditary breast cancer in a patient from a multi-cancer family- report of a family and literature review.

Akram Sarmadi, Shaghayegh Haghjooy Javanmard, Mehrdad Zeinalian

|Nov 23, 2024
A Novel Homozygote Pathogenic Variant in the DIAPH1 Gene Associated With Seizures, Cortical Blindness, and Microcephaly Syndrome (SCBMS): Report of a Family and Literature Review.

Emran Esmaeilzadeh, Sajjad Biglari, Meysam Mosallaei

|Oct 25, 2023
A novel de novo frameshift variant in the CHD2 gene related to intellectual and developmental disability, seizures and speech problems.

Atefeh Mir, Yongjun Song, Hane Lee

|Oct 11, 2023
Whole exome sequencing revealed variants in four genes underlying X-linked intellectual disability in four Iranian families: novel deleterious variants and clinical features with the review of literature.

Atefeh Mir, Yongjun Song, Hane Lee

|Jul 27, 2023
A deleterious frameshift insertion mutation in the ZNF142 gene leads to intellectual developmental disorder with impaired speech in three affected siblings: Clinical features and literature review.

Atefeh Mir, Yongjun Song, Hane Lee

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Frequent Collaborators

2 joint publications

Mehdi Khorrami

2 joint publications

Erfan Khorram

2 joint publications

Omid Yaghini

2 joint publications

Majid Kheirollahi