Guilherme Lopes Yamamoto

Author

Also Known As

G. Yamamoto, G.L. Yamamoto, Guilherme L Yamamoto, Guilherme L. Yamamoto, Guilherme Lopes Yamamoto, Guilherme Yamamoto, Guilherme L. Yamamoto, Yamamoto, Guilherme L, Yamamoto, Guilherme L., Yamamoto, Guilherme Lopes

118

Publications

2.8K

Citations

H-Index

Concepts

All Affiliations

Universidade de São Paulo Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo Universidade Federal de Minas Gerais Boston Children's Hospital Harvard University

About

Guilherme Lopes Yamamoto is an author at Universidade de São Paulo specializing in genetics, medicine, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	15	18	1.5K
2	Public Health	2	2	299
3	Health Sciences	1	1	48
4	Natural Sciences	1	1	15
5	Biology	1	1	15

Guilherme Lopes Yamamoto

Publications

2.6K

Citations

H-Index

Page 1

	Year	Citations
Somatic Mosaic Activating Mutations in PIK3CA Cause CLOVES Syndrome Kyle C. Kurek, Valerie L. Luks, Ugur M. Ayturk, The American Journal of Human Genetics Genetic DisorderGeneticsPathologyMolecular GeneticsMedicine	2012	519
Exomic variants of an elderly cohort of Brazilians in the ABraOM database Michel Satya Naslavsky, Guilherme Lopes Yamamoto, Tatiana Ferreira de Almeida, Human Mutation Elderly IndividualsAgingGeneticsExomic VariantsGenetic Epidemiology	2017	280
Rare variants in <i>SOS2</i> and <i>LZTR1</i> are associated with Noonan syndrome Guilherme Lopes Yamamoto, Meire Aguena, Monika Goś, Journal of Medical Genetics	2015	237
Bi-allelic CSF1R Mutations Cause Skeletal Dysplasia of Dysosteosclerosis-Pyle Disease Spectrum and Degenerative Encephalopathy with Brain Malformation Long Guo, Débora Romeo Bertola, Asako Takanohashi, The American Journal of Human Genetics Neurodegenerative DiseasesMendelian DisorderDysosteosclerosis-pyle Disease SpectrumBrain MalformationGenetics	2019	125
Discordant congenital Zika syndrome twins show differential in vitro viral susceptibility of neural progenitor cells Luiz C. Caires-Júnior, Ernesto Goulart, Uirá Souto Melo, Nature Communications	2018	124
Whole-genome sequencing of 1,171 elderly admixed individuals from Brazil Michel Satya Naslavsky, Marília O. Scliar, Guilherme Lopes Yamamoto, Nature Communications	2022	116
IHH Gene Mutations Causing Short Stature With Nonspecific Skeletal Abnormalities and Response to Growth Hormone Therapy Gabriela A. Vasques, Mariana F.A. Funari, Frederico Moraes Ferreira, The Journal of Clinical Endocrinology & Metabolism	2017	72
Rare Variants in the Epithelial Cadherin Gene Underlying the Genetic Etiology of Nonsyndromic Cleft Lip with or without Cleft Palate Luciano Abreu Brito, Guilherme Lopes Yamamoto, Soraia Melo, Human Mutation GeneticsGenetic EpidemiologyNonsyndromic Orofacial CleftPathologyMolecular Genetics	2015	69
Autosomal-Recessive Mutations in MESD Cause Osteogenesis Imperfecta Shahida Moosa, Guilherme Lopes Yamamoto, Lutz Garbes, The American Journal of Human Genetics Autosomal-recessive MutationsDevelopmental BiologyMendelian DisorderGenetic DisorderGenetics	2019	63
Further evidence of the importance of <i>RIT1</i> in Noonan syndrome Débora Romeo Bertola, Guilherme Lopes Yamamoto, Tatiana Ferreira de Almeida, American Journal of Medical Genetics Part A Signal TransductionAutoimmune DiseaseShort StatureGenetic DisorderMendelian Disorder	2014	62

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