Letícia E. Sewaybricker

Author

Universidade Estadual de Campinas (UNICAMP)ORCID

Also Known As

L.E. Sewaybricker, LETICIA E. SEWAYBRICKER, LETICIA ESPOSITO SEWAYBRICKER, LETÍCIA ESPOSITO SEWAYBRICKER, Leticia E Sewaybricker, Leticia E. Sewaybricker, Leticia Esposito Sewaybricker, Leticia Sewaybricker, Letícia E. Sewaybricker, Letícia Esposito Sewaybricker

Publications

378

Citations

H-Index

Concepts

All Affiliations

Universidade Estadual de Campinas (UNICAMP)University of Washington Hospital de Clínicas da Unicamp

About

Letícia E. Sewaybricker is an author at Universidade Estadual de Campinas (UNICAMP) specializing in medicine, pathology, and inherited metabolic disease.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	3	3	61
2	Public Health	2	2	41
3	Social Sciences	1	1	20
4	Cognitive Science	1	1	20
5	Diabetes	1	1	22

Letícia E. Sewaybricker

Publications

273

Citations

H-Index

Page 1

	Year	Citations
Hyperprolactinemia in Children and Adolescents with Use of Risperidone: Clinical and Molecular Genetics Aspects Amilton dos Santos Júnior, Taciane Barbosa Henriques, Maricilda Palandi de Mello, Journal of Child and Adolescent Psychopharmacology	2015	56
Initial evidence for hypothalamic gliosis in children with obesity by quantitative T2 MRI and implications for blood oxygen‐level dependent response to glucose ingestion Letícia E. Sewaybricker, Ellen A. Schur, Susan J. Melhorn, Pediatric Obesity	2018	42
Clinical and Laboratorial Features That May Differentiate 46,XY DSD due to Partial Androgen Insensitivity and 5<i>α</i>-Reductase Type 2 Deficiency Nélio Neves Veiga-Junior, Pedro Augusto Rodrigues Medaets, Reginaldo José Petroli, International Journal of Endocrinology	2011	29
Pharmacogenetics of Risperidone and Cardiovascular Risk in Children and Adolescents Amilton dos Santos Júnior, Taciane Barbosa Henriques, Maricilda Palandi de Mello, International Journal of Endocrinology	2016	23
Clinical application of <scp>ACMG‐AMP</scp> guidelines in <i><scp>HNF1A</scp></i> and <i><scp>GCK</scp></i> variants in a cohort of <scp>MODY</scp> families Lucas Santos de Santana, Lílian Araújo Caetano, Aline Dantas Costa‐Riquetto, Clinical Genetics Hnf1a -ModyGeneticsGenetic EpidemiologyPathologyClinical Genetics	2017	22
Salience network connectivity is reduced by a meal and influenced by genetic background and hypothalamic gliosis Letícia E. Sewaybricker, Susan J. Melhorn, Mary K. Askren, International Journal of Obesity Neurobiological MechanismCognitive ScienceNeurophysiologyNeuroanatomyBehavioral Neuroscience	2019	20
46,XX DSD and Antley-Bixler syndrome due to novel mutations in the cytochrome P450 oxidoreductase gene Guilherme Guaragna‐Filho, Carla Cristina Telles de Sousa Castro, Rodrigo Ribeiro De Carvalho, Arquivos Brasileiros de Endocrinologia & Metabologia GeneticsPathologyGynecologyMolecular GeneticsDisease Gene Identification	2012	19
Greater radiologic evidence of hypothalamic gliosis predicts adiposity gain in children at risk for obesity Letícia E. Sewaybricker, Sarah Kee, Susan J. Melhorn, Obesity	2021	18
Neonatal screening: 9% of children with filter paper thyroid-stimulating hormone levels between 5 and 10 μIU/mL have congenital hypothyroidism Flávia Corrêa Christensen‐Adad, Carolina Taddeo Mendes-dos-Santos, Maura Mikie Fukujima Goto, Jornal de Pediatria	2017	12
Klinefelter syndrome: an unusual diagnosis in pediatric patients Bruna J. Tincani, Bruno R. Mascagni, Roberto Damian Pacheco Pinto, Jornal de Pediatria	2012	11

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