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Leila Youssefian
103
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Online (103)
Mediatypes
Articles (Online) (52)
OpenAccess-fulltext (51)
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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
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/..
?
3
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/..
?
4
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/..
?
5
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/..
?
6
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/..
?
7
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/..
?
8
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/..
?
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
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/..
?
11
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/..
?
12
Evaluation of neurodevelopmental symptoms in 10 cases of ne..:
Salik, Deborah
;
Hadj‐Rabia, Smail
;
Hohl, Daniel
...
Pediatric Dermatology. 39 (2022) 4 - p. 590-593 , 2022
Link:
https://doi.org/10.1111/..
?
13
ENPP1 variants in patients with GACI and PXE expand the cli..:
Ralph, Douglas
;
Nitschke, Yvonne
;
Levine, Michael A.
...
PLOS Genetics. 18 (2022) 4 - p. e1010192 , 2022
Link:
https://doi.org/10.1371/..
?
14
Whole-transcriptome sequencing–based concomitant detection ..:
Saeidian, Amir Hossein
;
Youssefian, Leila
;
Huang, Charles Y.
...
JCI Insight. 7 (2022) 8 - p. , 2022
Link:
https://doi.org/10.1172/..
?
15
Pathomechanisms of epidermolysis bullosa: Beyond structural..:
Harvey, Nailah
;
Youssefian, Leila
;
Saeidian, Amir Hossein
..
Matrix Biology. 110 (2022) - p. 91-105 , 2022
Link:
https://doi.org/10.1016/..
1-15