E-LIB Suche - Ergebnisse für: Najmabadi, Hossein

1

P483: A comprehensive study of spinal muscular atrophy test..:

Khanbazi, Ali ; Beheshtian, Maryam ; Azad, Maryam...
Genetics in Medicine Open. 2 (2024) - p. 101382 , 2024

Link: https://doi.org/10.1016/..

2

Core myopathy in two siblings with a biallelic variant in t..:

Khoeini, Tara ; Kariminejad, Ariana ; Nilipour, Yalda...
Clinical Case Reports. 12 (2024) 8 - p. , 2024

Link: https://doi.org/10.1002/..

3

Contribution of genetic variants in the development of fami..:

Mehvari, Sepideh ; Karimian Fathi, Nahid ; Saki, Sara...
Clinical Genetics. 105 (2024) 6 - p. 611-619 , 2024

Link: https://doi.org/10.1111/..

4

P292: Contribution of rare variants in the development of f..:

Mehvari, Sepideh ; Fathi, Nahid Karimian ; Asadnezhad, Maryam...
Genetics in Medicine Open. 2 (2024) - p. 101188 , 2024

Link: https://doi.org/10.1016/..

5

The liver-derived exosomes stimulate insulin gene expressio..:

Mahmoudi-Aznaveh, Azam ; Tavoosidana, Gholamreza ; Najmabadi, Hossein..
Frontiers in Endocrinology. 14 (2023) - p. , 2023

Link: https://doi.org/10.3389/..

6

Identification of a homozygous frameshift mutation in the F..:

Jamshidi, Fereshteh ; Shokouhian, Ebrahim ; Mohseni, Marzieh...
Molecular Genetics & Genomic Medicine. 11 (2023) 5 - p. , 2023

Link: https://doi.org/10.1002/..

7

Aberrant phase separation and nucleolar dysfunction in rare..:

Mensah, Martin A. ; Niskanen, Henri ; Magalhaes, Alexandre P....
Nature. , 2023

Link: https://doi.org/10.1038/..

8

The prevalence and phenotypic range associated with biallel..:

Pagnamenta, Alistair T. ; Belles, Rebecca S. ; Salbert, Bonnie Anne...
Clinical Genetics. 104 (2023) 1 - p. 121-126 , 2023

Link: https://doi.org/10.1111/..

9

A biallelic frameshift indel in PPP1R35 as a cause of prima..:

Dawood, Moez ; Akay, Gulsen ; Mitani, Tadahiro...
American Journal of Medical Genetics Part A. 191 (2023) 3 - p. 794-804 , 2023

Link: https://doi.org/10.1002/..

10

Bi‐allelic loss of function variant in the NRCAM gene is as..:

Elahi, Zohreh ; Soveyzi, Mohamad ; Nafissi, Shahriar...
Molecular Genetics & Genomic Medicine. 11 (2023) 4 - p. , 2023

Link: https://doi.org/10.1002/..

11

Discovery of a neuromuscular syndrome caused by biallelic v..:

Nair, Divya ; Li, Dong ; Erdogan, Hannah...
Human Genetics and Genomics Advances. 3 (2022) 4 - p. 100122 , 2022

Link: https://doi.org/10.1016/..

12

Identification of microRNAs associated with human fragile X..:

Sotoudeh Anvari, Maryam ; Vasei, Hamed ; Najmabadi, Hossein...
Scientific Reports. 12 (2022) 1 - p. , 2022

Link: https://doi.org/10.1038/..

13

DNA Banking to Assess Genetic Influences on Schizophrenia:

Sadighi, Gita ; Nazeri Astaneh, Ali ; Najmabadi, Hossein..
Medical Journal of The Islamic Republic of Iran. , 2022

Link: https://doi.org/10.47176..

14

A novel variant of C12orf4 linked to autosomal recessive in..:

Rashvand, Zahra ; Kahrizi, Kimia ; Najmabadi, Hossein..
The Journal of Gene Medicine. 24 (2022) 4 - p. , 2022

Link: https://doi.org/10.1002/..

15

Genetic etiology of hearing loss in Iran:

Babanejad, Mojgan ; Beheshtian, Maryam ; Jamshidi, Fereshteh...
Human Genetics. , 2022

Link: https://doi.org/10.1007/..