Ariana Kariminejad

13PUBLICATIONS
74CO-AUTHORS
Gene mappingNeurogeneticsMedical mycologyCancer geneticsDevelopmental genetics (incl. sex determination)
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Publications (13)

|Nov 28, 2025
A Cohort of Iranian Patients With Congenital Myasthenic Syndrome due to Glycosylation Defects.

Mahtab Ramezani, Ali Asghar Okhovat, Yalda Nilipour

|Aug 02, 2025
Expanding the Clinical Phenotype Associated with the NIN Gene; Report of a Patient with Short Stature, Microcephaly and Hearing Loss.

Shima Zamanian Najafabadi, Zeinab Ghorbanoghli, Zhila Ghaderi

|Apr 02, 2025
Biallelic Variant in LYSET Associated With Mucolipidosis II-Like Phenotype.

Ariana Kariminejad, Farzaneh Pouya, Fatemeh Ahangari

|Aug 06, 2024
Core myopathy in two siblings with a biallelic variant in the CACNA1S gene-A case series study.

Tara Khoeini, Ariana Kariminejad, Yalda Nilipour

|Jun 28, 2023
Genomic analyses in Cornelia de Lange Syndrome and related diagnoses: Novel candidate genes, genotype-phenotype correlations and common mechanisms.

Maninder Kaur, Justin Blair, Batsal Devkota

|Mar 10, 2023
The prevalence and phenotypic range associated with biallelic PKDCC variants.

Alistair T Pagnamenta, Rebecca S Belles, Bonnie Anne Salbert

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Frequent Collaborators

3 joint publications

Hossein Najmabadi

2 joint publications

Shahriar Nafissi

1 joint publications

Kimia Kahrizi

1 joint publications

Jennifer Winter