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Mahdieh, Nejat
126
results:
Search for persons
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Format
Online (126)
Mediatypes
Articles (Online) (80)
Bookchapter (Online) (4)
OpenAccess-fulltext (42)
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english (120)
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1
De novo copy number variations in candidate genomic regions..:
Bui, Hoa Thi Phuong
;
Huy Do, Duong
;
Ly, Ha Thi Thanh
...
PLOS ONE. 19 (2024) 3 - p. e0290936 , 2024
Link:
https://doi.org/10.1371/..
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2
Evaluation of the presence of integrons, sul and smqnr gene..:
Mokhtari Bibalan, Maryam
;
Mojtahedi, Ali
;
Mahdieh, Nejat
...
Indian Journal of Medical Microbiology. 49 (2024) - p. 100612 , 2024
Link:
https://doi.org/10.1016/..
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3
The genetic basis of early-onset hereditary ataxia in Iran:..:
Mahdieh, Nejat
;
Heidari, Morteza
;
Rezaei, Zahra
...
Human Genomics. 18 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1186/..
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4
Comparative exploration of mammalian deafness gene homologu..:
Sutton, Daniel C.
;
Andrews, Jonathan C.
;
Dolezal, Dylan M.
...
PLOS ONE. 19 (2024) 2 - p. e0297846 , 2024
Link:
https://doi.org/10.1371/..
?
5
The importance of variant reinterpretation in inherited car..:
Fernandez-Falgueras, Anna
;
Coll, Monica
;
Iglesias, Anna
...
PLOS ONE. 19 (2024) 5 - p. e0297914 , 2024
Link:
https://doi.org/10.1371/..
?
6
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/..
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7
The TTN p. Tyr4418Ter mutation causes cardiomyopathy in hum..:
Sun, Wenqiang
;
Liu, Xiaohui
;
Song, Laichun
...
PLOS ONE. 19 (2024) 2 - p. e0296802 , 2024
Link:
https://doi.org/10.1371/..
?
8
Pancreatitis as a Main Consequence of APOC2-Related Hypertr..:
Rabbani, Bahareh
;
Moghadam, Mohadeseh Aghli
;
Esmaeili, Shiva
...
International Journal of Genomics. 2024 (2024) - p. 1-13 , 2024
Link:
https://doi.org/10.1155/..
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9
4-aminopyridine improves evoked potentials and ambulation i..:
Eguibar, Jose R.
;
Cortes, Carmen
;
Hernandez, Victor H.
...
PLOS ONE. 19 (2024) 3 - p. e0298208 , 2024
Link:
https://doi.org/10.1371/..
?
10
Gene mutations as a non-invasive measure of adult cochlear ..:
Cottrell, Justin
;
Dixon, Peter
;
Cao, Xingshan
...
PLOS ONE. 18 (2023) 9 - p. e0291600 , 2023
Link:
https://doi.org/10.1371/..
?
11
Whole exome data prioritization unveils the hidden weight o..:
Quarantani, Gioia
;
Sorgente, Anna
;
Alfano, Massimo
...
PLOS ONE. 18 (2023) 8 - p. e0288336 , 2023
Link:
https://doi.org/10.1371/..
?
12
Genome sequencing identifies coding and non-coding variants..:
Ramzan, Memoona
;
Duman, Duygu
;
Hendricks, LeShon Chere Peart
...
Journal of Human Genetics. 68 (2023) 10 - p. 657-669 , 2023
Link:
https://doi.org/10.1038/..
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13
A novel splice-site FHOD3 founder variant is a common cause..:
Vodnjov, Nina
;
Toplišek, Janez
;
Maver, Aleš
...
PLOS ONE. 18 (2023) 12 - p. e0294969 , 2023
Link:
https://doi.org/10.1371/..
?
14
Fastidious Bacterial Pathogens in Replaced Heart Valves: Th..:
Aghamohammad, Shadi
;
Amirjamshidi, Narges
;
Shams Nosrati, Mohammad Sadegh
...
Multidisciplinary Cardiovascular Annals. 14 (2023) 1 - p. , 2023
Link:
https://doi.org/10.5812/..
?
15
Identification of candidate genes for developmental colour ..:
Nijboer, Tanja C. W.
;
Hessel, Ellen V. S.
;
van Haaften, Gijs W.
...
PLOS ONE. 18 (2023) 9 - p. e0290013 , 2023
Link:
https://doi.org/10.1371/..
1-15