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Mingroni-Netto, Regina C
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1

Generation of four induced pluripotent stem cells lines fro..:

Kobayashi, Gerson S. ; Vieira-Silva, Gleiciele A. ; Varella-Branco, Elisa...
Stem Cell Research.  71 (2023)  - p. 103181 , 2023
Link: https://doi.org/10.1016/..
 
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2

Frequency and origin of the c.2090T>G p.(Leu697Trp) MYO3A v..:

Bueno, André S. ; Nunes, Kelly ; Dias, Alex M. M....
European Journal of Human Genetics.  30 (2021)  1 - p. 13-21 , 2021
Link: https://doi.org/10.1038/..
 
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3

A rare genomic duplication in 2p14 underlies autosomal domi..:

Oiticica, Jeanne ; Mingroni-Netto, Regina C ; Bento, Ricardo F...
Human Molecular Genetics.  29 (2020)  9 - p. 1520-1536 , 2020
Link: https://doi.org/10.1093/..
 
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4

Characterization of a novel MYO3A missense mutation associa..:

Dantas, Vitor G. L. ; Raval, Manmeet H. ; Ballesteros, Angela...
Scientific Reports.  8 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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5

Inbreeding estimates in human populations: Applying new app..:

Lemes, Renan B. ; Nunes, Kelly ; Carnavalli, Juliana E. P....
PLOS ONE.  13 (2018)  4 - p. e0196360 , 2018
Link: https://doi.org/10.1371/..
 
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6

A Cell Junctional Protein Network Associated with Connexin-..:

Batissoco, Ana C. ; Salazar-Silva, Rodrigo ; Oiticica, Jeanne...
International Journal of Molecular Sciences.  19 (2018)  9 - p. 2535 , 2018
Link: https://doi.org/10.3390/..
 
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7

Santos syndrome is caused by mutation in the WNT7A gene:

Alves, Leandro U ; Santos, Silvana ; Musso, Camila M...
Journal of Human Genetics.  62 (2017)  12 - p. 1073-1078 , 2017
Link: https://doi.org/10.1038/..
 
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8

Patients with a Kabuki syndrome phenotype demonstrate DNA m..:

Sobreira, Nara ; Brucato, Martha ; Zhang, Li...
European Journal of Human Genetics.  25 (2017)  12 - p. 1335-1344 , 2017
Link: https://doi.org/10.1038/..
 
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9

A new HLA-C∗02 null allele described in quilombo remnants s..:

Nunes, Kelly ; Torres, Margareth A. ; Piovezan, Bruno Z....
Human Immunology.  76 (2015)  - p. 140 , 2015
Link: https://doi.org/10.1016/..
 
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10

A novel KCNQ4 mutation and a private IMMP2L-DOCK4 duplicati..:

Uehara, Daniela T ; Freitas, Érika L ; Alves, Leandro U...
Human Genome Variation.  2 (2015)  1 - p. , 2015
Link: https://doi.org/10.1038/..
 
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11

Deletion of the entire POU4F3 gene in a familial case of au..:

Freitas, Érika L. ; Oiticica, Jeanne ; Silva, Amanda G....
European Journal of Medical Genetics.  57 (2014)  4 - p. 125-128 , 2014
Link: https://doi.org/10.1016/..
 
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12

Multivariate meta-analysis of the association of G-protein ..:

Pereira, Tiago V. ; Kimura, Lilian ; Suwazono, Yasushi...
Molecular Biology Reports.  41 (2014)  5 - p. 3113-3125 , 2014
Link: https://doi.org/10.1007/..
 
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13

Aberrant transcript produced by a splice donor site deletio..:

Lezirovitz, Karina ; Batissoco, Ana C. ; Lima, Fernanda T....
Gene.  511 (2012)  2 - p. 280-284 , 2012
Link: https://doi.org/10.1016/..
 
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14

ADRB2 and LEPR Gene Polymorphisms: Synergistic Effects on t..:

Pereira, Tiago V. ; Mingroni-Netto, Regina C. ; Yamada, Yoshiji
Obesity.  19 (2011)  7 - p. 1523-1527 , 2011
Link: https://doi.org/10.1038/..
 
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15

A note on the use of the generalized odds ratio in meta-ana..:

Pereira, Tiago V ; Mingroni-Netto, Regina C
BMC Research Notes.  4 (2011)  1 - p. , 2011
Link: https://doi.org/10.1186/..
 
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