E-LIB Suche - Ergebnisse für: Hassan Vahidnezhad

1

Monogenic etiologies of persistent human papillomavirus inf..:

Biglari, Sajjad ; Moghaddam, Atefeh Sohanforooshan ; Tabatabaiefar, Mohammad Amin...
Genetics in Medicine. 26 (2024) 2 - p. 101028 , 2024

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

2

Secondary ACMG and non-ACMG genetic findings in a multiethn..:

Saeidian, Amir Hossein ; March, Michael E. ; Youssefian, Leila...
Genetics in Medicine. , 2024

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

3

P244: DNA repair-related heritable photosensitivity syndrom..:

Vahidnezhad, Hassan ; Hozhabrpour, Amir ; Youssefian, Leila.
Genetics in Medicine Open. 2 (2024) - p. 101140 , 2024

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

4

RARS1‐related hypomyelinating leukodystrophy‐9 (HLD‐9) in t..:

Biglari, Sajjad ; Vahidnezhad, Hassan ; Tabatabaiefar, Mohammad Amin..
Molecular Genetics & Genomic Medicine. 12 (2024) 4 - p. , 2024

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

5

DNA repair-related heritable photosensitivity syndromes: Mu..:

Hozhabrpour, Amir ; Mojbafan, Marzieh ; Palizban, Fahimeh...
DNA Repair. 136 (2024) - p. 103633 , 2024

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

6

P756: Monogenic etiologies of persistent human papillomavir..:

Youssefian, Leila ; Biglari, Sajjad ; Moghaddam, Atefeh Sohanforooshan...
Genetics in Medicine Open. 2 (2024) - p. 101660 , 2024

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

7

A comprehensive study of mutation and phenotypic heterogene..:

Hosseinpour, Sareh ; Razmara, Ehsan ; Heidari, Morteza...
Brain and Development. 46 (2024) 4 - p. 167-179 , 2024

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

8

Whole-Transcriptome Sequencing–Based Profiling of the Cutan..:

Youssefian, Leila ; Saeidian, Amir Hossein ; Saffarian, Zahra...
JID Innovations. 4 (2024) 4 - p. 100278 , 2024

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

9

Whole transcriptome–based skin virome profiling in typical ..:

Saeidian, Amir Hossein ; Youssefian, Leila ; Naji, Mahtab...
JCI Insight. 8 (2023) 5 - p. , 2023

Link: https://doi.org/10.1172/..

10

Correction: Phenotype and genotype heterogeneity of PLA2G6-..:

Dehnavi, Ali Zare ; Bemanalizadeh, Maryam ; Kahani, Seyyed Mohammad...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

11

Phenotype and genotype heterogeneity of PLA2G6-associated n..:

Dehnavi, Ali Zare ; Bemanalizadeh, Maryam ; Kahani, Seyyed Mohammad...
Orphanet Journal of Rare Diseases. 18 (2023) 1 - p. , 2023

Link: https://doi.org/10.1186/..

12

Interpretation of genomic sequence variants in heritable sk..:

Uitto, Jouni ; Saeidian, Amir Hossein ; Youssefian, Leila.
Journal of the American Academy of Dermatology. 89 (2023) 3 - p. 569-576 , 2023

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

13

P671: Whole-transcriptome-based skin virome profiling in ty..:

Vahidnezhad, Hassan ; Youssefian, Leila ; Saeidian, Amir Hossein...
Genetics in Medicine Open. 1 (2023) 1 - p. 100736 , 2023

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

14

P366: Loss-of-function EGFR mutation in Bartter syndrome wi..:

Youssefian, Leila ; Vahidnezhad, Hassan ; Uitto, Jouni...
Genetics in Medicine Open. 1 (2023) 1 - p. 100394 , 2023

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

15

Inherited ichthyosis as a paradigm of rare skin disorders: ..:

Park, Jason S. ; Saeidian, Amir Hossein ; Youssefian, Leila...
Journal of the American Academy of Dermatology. 89 (2023) 6 - p. 1215-1226 , 2023

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