Kimia Najafi

5p13 microduplication in a malformed fetus and his unaffected father

R. Hennekam, A. Kariminejad, S. Ghaderi-sohi, 2022, American journal of medical genetics. Part A.

Chromosomal aberrations in pregnancy and fetal loss: Insight on the effect of consanguinity, review of 1625 cases

H. Najmabadi, R. Kariminejad, M. Bazrgar, 2019, Molecular genetics & genomic medicine.

Familial Case of Pelizaeus-Merzbacher Disorder Detected by Oligoarray Comparative Genomic Hybridization: Genotype-to-Phenotype Diagnosis

A. Kariminejad, K. Hosseini, R. Kariminejad, 2017, Case reports in genetics.

Loss-of-function variants of SETD5 cause intellectual disability and the core phenotype of microdeletion 3p25.3 syndrome

T. Wieland, T. Strom, A. Schlessinger, 2014, European Journal of Human Genetics.

Identifying the causes of recurrent pregnancy loss in consanguineous couples using whole exome sequencing on the products of miscarriage with no chromosomal abnormalities

A. Kariminejad, H. Najmabadi, S. Ghaderi-sohi, 2021, Scientific Reports.

A Report on 167 Cases of Array-Based Comparative Genomic Hybridization: Comparison with Previous Techniques

A. Kariminejad, H. Najmabadi, F. Behjati, 2012 .

Kaufman Oculo-cerebro-facial Syndrome in a child with small and absent terminal phalanges and absent nails

R. Gibbs, R. Hennekam, A. Dionne‐Laporte, 2016, Journal of Human Genetics.

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

M. Fardaei, R. Kariminejad, Maryam Taghdiri, 2019, Clinical case reports.

Further delineation of the phenotype caused by a novel large homozygous deletion of GRID2 gene in an adult patient

M. Fardaei, R. Kariminejad, Maryam Taghdiri, 2019, Clinical case reports.