Kimia Najafi

Publication Activity (10 Years)

Years Active: 2017-2022
Publications (10 Years): 5

Top Topics

Cervical Cancer Screening

Autism Spectrum Disorder

Dna Methylation

Top Venues

Molecular genetics & genomic medicine

Case reports in genetics

American journal of medical genetics. Part A

Scientific reports

This page only lists publications with an associated author ORCID identifier.

Publications

Ariana Kariminejad, Siavash Ghaderi-Sohi, Soheila Gholami, Kimia Najafi, Roxana Kariminejad, Raoul C M Hennekam
5p13 microduplication in a malformed fetus and his unaffected father. American journal of medical genetics. Part A (2022)
Kimia Najafi, Zohreh Mehrjoo, Fariba Ardalani, Siavash Ghaderi-Sohi, Ariana Kariminejad, Roxana Kariminejad, Hossein Najmabadi
Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities. Scientific reports 11 (1) (2021)
Kimia Najafi, Soheila Gholami, Azadeh Moshtagh, Masood Bazrgar, Neda Sadatian, Golemaryam Abbasi, Parvin Rostami, Soheila Khalili, Mojgan Babanejad, Bahareh Nourmohammadi, Negin Faramarzi Garous, Hossein Najmabadi, Roxana Kariminejad
Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases. Molecular genetics & genomic medicine 7 (8) (2019)
Maryam Taghdiri, Atie Kashef, Golemaryam Abbassi, Azadeh Moshtagh, Neda Sadatian, Majid Fardaei, Kimia Najafi, Roxana Kariminejad
Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient. Clinical case reports 7 (6) (2019)
Kimia Najafi, Roxana Kariminejad, Kaveh Hosseini, Azadeh Moshtagh, Gole Maryam Abbassi, Neda Sadatian, Masood Bazrgar, Ariana Kariminejad, Mohamad Hassan Kariminejad
Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis. Case reports in genetics 2017 (2017)