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X
Yamamoto, Guilherme Lopes
2079  Ergebnisse:
Personensuche X
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1

Genetic variation in NOTCH1 is associated with overweight a..:

Silva Barcelos, Estevão Carlos ; Naslavsky, Michel Satya ; Fernandes, Izadora Silveira...
Scientific Reports.  14 (2024)  1 - p. , 2024
Link: https://doi.org/10.1038/..
 
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2

Clinical Characterization and Underlying Genetic Findings i..:

Tolezano, Giovanna Cantini ; Bastos, Giovanna Civitate ; da Costa, Silvia Souza...
Molecular Neurobiology.  61 (2024)  8 - p. 5230-5247 , 2024
Link: https://doi.org/10.1007/..
 
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3

Low‐pass whole genome sequencing as a cost‐effective altern..:

Mazzonetto, Patricia C. ; Villela, Darine ; Krepischi, Ana C. V....
American Journal of Medical Genetics Part A.  , 2024
Link: https://doi.org/10.1002/..
 
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4

A Benchmark of In-House Homologous Recombination Repair Def..:

Guarischi-Sousa, Rodrigo ; Kroll, José Eduardo ; Bonaldi, Adriano...
Diagnostics.  13 (2023)  21 - p. 3293 , 2023
Link: https://doi.org/10.3390/..
 
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5

A dopamine receptor D2 genetic polymorphism associated with..:

Marques, Julia Hatagami ; Talib, Leda Leme ; Hortêncio, Lucas...
Brazilian Journal of Psychiatry.  , 2023
Link: https://doi.org/10.47626..
 
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6

Burden of Rare Copy Number Variants in Microcephaly: A Braz..:

Tolezano, Giovanna Cantini ; Bastos, Giovanna Civitate ; da Costa, Silvia Souza...
Journal of Autism and Developmental Disorders.  54 (2022)  3 - p. 1181-1212 , 2022
Link: https://doi.org/10.1007/..
 
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7

Twenty‐year follow‐up of the facial phenotype of Brazilian ..:

Castro, Matheus Augusto Araújo ; dos Santos, Juliana Heather Vedovato ; Honjo, Rachel Sayuri...
American Journal of Medical Genetics Part A.  185 (2021)  12 - p. 3916-3923 , 2021
Link: https://doi.org/10.1002/..
 
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8

Atypical, severe hypertrophic cardiomyopathy in a newborn p..:

Pires, Lucas Vieira Lacerda ; Bordim, Renata de Almeida ; Maciel, Maria Beatriz Rabelo...
American Journal of Medical Genetics Part A.  185 (2021)  10 - p. 3099-3103 , 2021
Link: https://doi.org/10.1002/..
 
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9

Congenital limb deficiency: Genetic investigation of 44 ind..:

da Rocha, Letícia Alves ; Pires, Lucas Vieira Lacerda ; Yamamoto, Guilherme Lopes...
Clinical Genetics.  100 (2021)  5 - p. 615-623 , 2021
Link: https://doi.org/10.1111/..
 
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10

Meta‐Analyses Support Previous and Novel Autism Candidate G..:

da Silva Montenegro, Eduarda Morgana ; Costa, Claudia Samogy ; Campos, Gabriele...
Autism Research.  13 (2019)  2 - p. 199-206 , 2019
Link: https://doi.org/10.1002/..
 
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11

Mutation analysis of SLC26A4 (Pendrin) gene in a Brazilian ..:

Nonose, Renata Watanabe ; Lezirovitz, Karina ; de Mello Auricchio, Maria Teresa Balester...
BMC Medical Genetics.  19 (2018)  1 - p. , 2018
Link: https://doi.org/10.1186/..
 
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12

Actin cytoskeleton dynamics in stem cells from autistic ind..:

Griesi-Oliveira, Karina ; Suzuki, Angela May ; Alves, Aline Yasuda...
Scientific Reports.  8 (2018)  1 - p. , 2018
Link: https://doi.org/10.1038/..
 
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13

Natural history of 39 patients with Achondroplasia:

Ceroni, Jose Ricardo Magliocco ; Soares, Diogo Cordeiro de Queiroz ; Testai, Larissa de Cássia...
Clinics.  73 (2018)  - p. e324 , 2018
Link: https://doi.org/10.6061/..
 
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14

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/..
 
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15

Diagnosis of Atelosteogenesis Type I suggested by Fetal Ult..:

Meira, Joanna Goes Castro ; Sarno, Manoel Alfredo Curvelo ; Faria, Ágatha Cristhina Oliveira...
Revista Brasileira de Ginecologia e Obstetrícia / RBGO Gynecology and Obstetrics.  40 (2018)  9 - p. 570-576 , 2018
Link: https://doi.org/10.1055/..
 
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