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Melo, Uirá Souto
47
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Online (47)
Mediatypes
Articles (Online) (21)
OpenAccess-fulltext (26)
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1
TAD boundary deletion causes PITX2-related cardiac electric..:
Baudic, Manon
;
Murata, Hiroshige
;
Bosada, Fernanda M.
...
Nature Communications. 15 (2024) 1 - p. , 2024
Link:
https://doi.org/10.1038/..
?
2
AML with complex karyotype: extreme genomic complexity reve..:
Klever, Marius-Konstantin
;
Sträng, Eric
;
Hetzel, Sara
...
Blood Advances. 7 (2023) 21 - p. 6520-6531 , 2023
Link:
https://doi.org/10.1182/..
?
3
Author Correction: Enhancer hijacking at the ARHGAP36 locus..:
Melo, Uirá Souto
;
Jatzlau, Jerome
;
Prada-Medina, Cesar A.
...
Nature Communications. 14 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
4
Enhancer hijacking at the ARHGAP36 locus is associated with..:
Melo, Uirá Souto
;
Jatzlau, Jerome
;
Prada-Medina, Cesar A.
...
Nature Communications. 14 (2023) 1 - p. , 2023
Link:
https://doi.org/10.1038/..
?
5
Integration of Hi-C with short and long-read genome sequenc..:
Schöpflin, Robert
;
Melo, Uirá Souto
;
Moeinzadeh, Hossein
...
Nature Communications. 13 (2022) 1 - p. , 2022
Link:
https://doi.org/10.1038/..
?
6
Non-coding deletion induces 3D chromatin remodelling and PI..:
Baudic, Manon
;
Murata, Hiroshigue
;
Bosada, Fernanda
...
Archives of Cardiovascular Diseases Supplements. 14 (2022) 2 - p. 209 , 2022
Link:
https://doi.org/10.1016/..
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7
Biallelic UBE4A loss-of-function variants cause intellectua..:
Melo, Uirá Souto
;
Bonner, Devon
;
Kent Lloyd, Kevin C.
...
Genetics in Medicine. 23 (2021) 4 - p. 661-668 , 2021
Link:
https://doi.org/10.1038/..
?
8
Diagnostic Yield of Whole Genome Sequencing After Nondiagno..:
Palmer, Elizabeth Emma
;
Sachdev, Rani
;
Macintosh, Rebecca
...
Neurology. 96 (2021) 13 - p. , 2021
Link:
https://doi.org/10.1212/..
?
9
Complete lung agenesis caused by complex genomic rearrangem..:
Melo, Uirá Souto
;
Piard, Juliette
;
Fischer-Zirnsak, Björn
...
Human Genetics. 140 (2021) 10 - p. 1459-1469 , 2021
Link:
https://doi.org/10.1007/..
?
10
Discordant congenital Zika syndrome twins show differential..:
Caires-Júnior, Luiz Carlos
;
Goulart, Ernesto
;
Melo, Uirá Souto
...
Nature Communications. 9 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1038/..
?
11
Publisher Correction: Discordant congenital Zika syndrome t..:
Caires-Júnior, Luiz Carlos
;
Goulart, Ernesto
;
Melo, Uirá Souto
...
Nature Communications. 9 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1038/..
?
12
A fast method to reprogram and CRISPR/Cas9 gene editing fro..:
Melo, Uirá Souto
;
de Souza Leite, Felipe
;
Costa, Silvia
..
Stem Cell Research. 31 (2018) - p. 52-54 , 2018
Link:
https://doi.org/10.1016/..
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13
Origin and age of the causative mutations in KLC2, IMPA1, M..:
de Farias, Allysson Allan
;
Nunes, Kelly
;
Lemes, Renan Barbosa
...
Scientific Reports. 8 (2018) 1 - p. , 2018
Link:
https://doi.org/10.1038/..
?
14
A novel complex neurological phenotype due to a homozygous ..:
Gurgel-Giannetti, Juliana
;
Lynch, David S
;
Paiva, Anderson Rodrigues Brandão de
...
Brain. 141 (2018) 8 - p. 2289-2298 , 2018
Link:
https://doi.org/10.1093/..
?
15
Waardenburg syndrome: Novel mutations in a large Brazilian ..:
Bocángel, Magnolia Astrid Pretell
;
Melo, Uirá Souto
;
Alves, Leandro Ucela
...
European Journal of Medical Genetics. 61 (2018) 6 - p. 348-354 , 2018
Link:
https://doi.org/10.1016/..
1-15