Vieira TP - Search Results

1

Genome Sequencing in an Individual Presenting with 22q11.2 Deletion Syndrome and Juvenile Idiopathic Arthritis.

de Oliveira-Sobrinho RP, Appenzeller S, Holanda IP, Heleno JL, Jorente J, On Behalf Of The Rare Genomes Project Consortium, Vieira TP, Steiner CE. de Oliveira-Sobrinho RP, et al. Among authors: vieira tp. Genes (Basel). 2024 Apr 19;15(4):513. doi: 10.3390/genes15040513. Genes (Basel). 2024. PMID: 38674447 Free PMC article.

2

Clinical, cytogenetic, and molecular characterization of six patients with ring chromosomes 22, including one with concomitant 22q11.2 deletion.

Guilherme RS, Soares KC, Simioni M, Vieira TP, Gil-da-Silva-Lopes VL, Kim CA, Brunoni D, Spinner NB, Conlin LK, Christofolini DM, Kulikowski LD, Steiner CE, Melaragno MI. Guilherme RS, et al. Among authors: vieira tp. Am J Med Genet A. 2014 Jul;164A(7):1659-65. doi: 10.1002/ajmg.a.36512. Epub 2014 Apr 3. Am J Med Genet A. 2014. PMID: 24700634 Review.

3

Tetrasomy 3q26.32-q29 due to a supernumerary marker chromosome in a child with pigmentary mosaicism of Ito.

Cunha KS, Simioni M, Vieira TP, Gil-da-Silva-Lopes VL, Puzzi MB, Steiner CE. Cunha KS, et al. Among authors: vieira tp. Genet Mol Biol. 2016 Mar;39(1):35-9. doi: 10.1590/1678-4685-GMB-2015-0033. Genet Mol Biol. 2016. PMID: 27007896 Free PMC article.

4

Phenotype comparison among individuals with developmental delay/intellectual disability with or without genomic imbalances.

de Souza LC, Dos Santos AP, Sgardioli IC, Viguetti-Campos NL, Marques Prota JR, de Oliveira-Sobrinho RP, Vieira TP, Gil-da-Silva-Lopes VL. de Souza LC, et al. Among authors: vieira tp. J Intellect Disabil Res. 2019 Nov;63(11):1379-1389. doi: 10.1111/jir.12615. Epub 2019 Mar 21. J Intellect Disabil Res. 2019. PMID: 30900361

5

Dual Molecular Diagnoses of Recessive Disorders in a Child from Consanguineous Parents: Case Report and Literature Review.

Correia-Costa GR, Dos Santos AM, de Leeuw N, Rigatto SZP, Belangero VMS, Steiner CE, Gil-da-Silva-Lopes VL, Vieira TP. Correia-Costa GR, et al. Among authors: vieira tp. Genes (Basel). 2022 Dec 16;13(12):2377. doi: 10.3390/genes13122377. Genes (Basel). 2022. PMID: 36553645 Free PMC article. Review.

6

SATB2-Associated Syndrome Due to a c.715C>T:p(Arg239*) Variant in Adulthood: Natural History and Literature Review.

Copelli MM, Pairet E, Atique-Tacla M, Vieira TP, Appenzeller S, Helaers R, Vikkula M, Gil-da-Silva-Lopes VL. Copelli MM, et al. Among authors: vieira tp. Genes (Basel). 2023 Apr 8;14(4):882. doi: 10.3390/genes14040882. Genes (Basel). 2023. PMID: 37107640 Free PMC article. Review.

7

Rare 15q21.1q22.31 Duplication Due to a Familial Chromosomal Insertion and Diagnostic Investigation in a Carrier of Balanced Chromosomal Rearrangement and Intellectual Disability.

Nascimento CG, Prota JRM, Sgardioli IC, Spineli-Silva S, Campos NLV, Gil-da-Silva-Lopes VL, Vieira TP. Nascimento CG, et al. Among authors: vieira tp. Genes (Basel). 2023 Apr 9;14(4):885. doi: 10.3390/genes14040885. Genes (Basel). 2023. PMID: 37107643 Free PMC article.

8

Variants in KMT2A in Three Individuals with Previous Suspicion of 22q11.2 Deletion Syndrome.

Silveira HG, Steiner CE, Toccoli G, Angeloni LL, Heleno JL, Spineli-Silva S, Dos Santos AM, Vieira TP, Melaragno MI, Gil-da-Silva-Lopes VL. Silveira HG, et al. Among authors: vieira tp. Genes (Basel). 2024 Feb 6;15(2):211. doi: 10.3390/genes15020211. Genes (Basel). 2024. PMID: 38397201 Free PMC article.

9

22q11.2 Deletion Syndrome: Influence of Parental Origin on Clinical Heterogeneity.

de Wallau MB, Xavier AC, Moreno CA, Kim CA, Mendes EL, Ribeiro EM, Oliveira A, Félix TM, Fett-Conte AC, Bonadia LC, Correia-Costa GR, Monlleó IL, Gil-da-Silva-Lopes VL, Vieira TP. de Wallau MB, et al. Among authors: vieira tp. Genes (Basel). 2024 Apr 21;15(4):518. doi: 10.3390/genes15040518. Genes (Basel). 2024. PMID: 38674452 Free PMC article.

10

Microdeletion 1p32p31 Presenting with Moyamoya Disease and Incomplete Hippocampal Inversion.

Pires de Oliveira-Sobrinho R, Bispo LM, Heleno JL, Rojas Ayala FR, Reis F, Vieira TP, Steiner CE. Pires de Oliveira-Sobrinho R, et al. Among authors: vieira tp. Mol Syndromol. 2024 Jun;15(3):225-231. doi: 10.1159/000535240. Epub 2024 Jan 15. Mol Syndromol. 2024. PMID: 38841325 Free PMC article.

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