Monica Castro Varela

Author

Also Known As

M Varela, M. Castro Varela, M. Varela, M.C. Varela, Monica C Varela, Monica C. Varela, Monica Castro Varela, Mônica Varela, Varela, Monica

Publications

1.4K

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 São Paulo Universidade Federal de Minas Gerais Institute of Human Genetics

About

Monica Castro Varela is an author at Universidade de São Paulo specializing in medicine, genetics, and neurogenetics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	8	8	801
2	Molecular Genetics	2	2	456
3	Neurology	2	2	138
4	Social Sciences	1	1	16
5	Diagnostic Sciences	1	1	11

Monica Castro Varela

Publications

1.4K

Citations

H-Index

Page 1

	Year	Citations
Microdeletion encompassing MAPT at chromosome 17q21.3 is associated with developmental delay and learning disability Charles Shaw‐Smith, Alan Pittman, Lionel Willatt, Nature Genetics ChromatinDevelopmental BiologyCytogeneticsGenetic DisorderGenetics	2006	371
Whole-genome array-CGH screening in undiagnosed syndromic patients: old syndromes revisited and new alterations Ana Cristina Victorino Krepischi, Angela Maria Vianna‐Morgante, Fernanda Sarquis Jehee, Cytogenetic and Genome Research	2006	125
Prader-Willi-like phenotype: investigation of 1p36 deletion in 41 patients with delayed psychomotor development, hypotonia, obesity and/or hyperphagia, learning disabilities and behavioral problems Carla S. D’Angelo, José Albino da Paz, Chong Ae Kim, European Journal of Medical Genetics PsychiatryGenetic DisorderMedicineBehavioral ProblemsNeuropsychiatry	2006	122
Phenotypic variability in Angelman syndrome: comparison among different deletion classes and between deletion and UPD subjects Monica Castro Varela, Fernando Kok, Paulo Alberto Otto, European Journal of Human Genetics PsychiatryAngelman SyndromeUpd SubjectsNeurogeneticsMedicine	2004	114
A new case of interstitial 6q16.2 deletion in a patient with Prader–Willi-like phenotype and investigation of SIM1 gene deletion in 87 patients with syndromic obesity Monica Castro Varela, Alex Y. Simoes-Sato, Chong Ae Kim, European Journal of Medical Genetics New CaseGenetic DisorderGeneticsSim1 Gene DeletionPathology	2006	85
Paternal UPD15: Further genetic and clinical studies in four Angelman syndrome patients Cíntia Fridman, Monica Castro Varela, Fernando Kok, American Journal of Medical Genetics	2000	78
Preferential induction of chromosome 1 multibranched figures and whole-arm deletions in a human pro-B cell line treated with 5-azacytidine or 5-azadeoxycytidine R. Hernandez, A. Frady, X.-Y. Zhang, Cytogenetic and Genome Research	1997	64
Angelman syndrome associated with oculocutaneous albinism due to an intragenic deletion of the <i>P</i> gene Cíntia Fridman, Naoko Hosomi, Monica Castro Varela, American Journal of Medical Genetics Part A	2003	50
Chromosomal microarray analysis in the genetic evaluation of 279 patients with syndromic obesity Carla S. D’Angelo, Monica Castro Varela, Cláudia Irene Emílio de Castro, Molecular Cytogenetics	2018	48
A 17q21.31 microdeletion encompassing the <i>MAPT </i>gene in a mentally impaired patient Monica Castro Varela, Ana Cristina Victorino Krepischi, José Albino da Paz, Cytogenetic and Genome Research	2006	47

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