Kátia M. Rocha - Concepedia

Author

Kátia M. Rocha

Also Known As

Beatriz Burin, K M Rocha, K.M. Rocha, Katia M. Rocha, Katia M. da Rocha, Katia Maria Rocha, Katia Maria da Rocha, Katia Rocha, Kátia M Rocha, Kátia M. Rocha

Publications

559

Citations

H-Index

Concepts

All Affiliations

Universidade de São Paulo Hospital das Clínicas da Faculdade de Medicina da Universidade de São Paulo Radboud University Medical Center Radboud University Nijmegen Universidade Estadual de Campinas (UNICAMP)

About

Kátia M. Rocha is an author at Universidade de São Paulo specializing in medicine, genetics, and pathology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	6	6	187
2	Health Sciences	1	1	68
3	Biostatistics	1	1	12
4	Cell Biology	1	1	17
5	Molecular Genetics	1	1	21

Kátia M. Rocha

Publications

510

Citations

H-Index

Page 1

	Year	Citations
Overlapping SETBP1 gain-of-function mutations in Schinzel-Giedion syndrome and hematologic malignancies Rocío Acuña‐Hidalgo, Pelagia Derizioti, Marloes Steehouwer, PLoS Genetics Setbp1 StabilityMixed-phenotype Acute LeukemiaGeneticsPathologyDisease Gene Identification	2017	68
Genetic contribution for non‐syndromic cleft lip with or without cleft palate (NS CL/P) in different regions of Brazil and implications for association studies Luciano Abreu Brito, Lucas Alvizi Cruz, Kátia M. Rocha, American Journal of Medical Genetics Part A	2011	53
Schinzel–Giedion syndrome in two Brazilian patients: Report of a novel mutation in <i>SETBP1</i> and literature review of the clinical features Ellaine Dóris Fernandes Carvalho, Rachel Sayuri Honjo, Monize Lazar Magalhães, American Journal of Medical Genetics Part A	2015	51
IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population Luciano Abreu Brito, Camila Fernandes Silva Bassi, Cibele Masotti, American Journal of Medical Genetics Part A	2012	48
Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil Luciano Abreu Brito, Lívia Máris Ribeiro Paranaiba, Camila Fernandes Silva Bassi, Birth Defects Research Part A Clinical and Molecular Teratology	2012	47
High frequency of submicroscopic chromosomal imbalances in patients with syndromic craniosynostosis detected by a combined approach of microsatellite segregation analysis, multiplex ligation-dependent probe amplification and array-based comparative genome hybridisation Fernanda Sarquis Jehee, Ana Cristina Victorino Krepischi, Kátia M. Rocha, Journal of Medical Genetics Developmental BiologyMendelian DisorderGenetic DisorderGeneticsSyndromic Craniosynostosis	2008	41
Fibroblast Growth Factor 2 Restrains Ras-Driven Proliferation of Malignant Cells by Triggering RhoA-Mediated Senescence Érico T. Costa, Fábio Luís Forti, Tatiana G.F. Matos, Cancer Research	2008	36
c-Myc protein is stabilized by fibroblast growth factor 2 and destabilized by ACTH to control cell cycle in mouse Y1 adrenocortical cells Ana Paula Lepique, Miriam S. Moraes, Kátia M. Rocha, Journal of Molecular Endocrinology	2004	33
Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy Danielle P. Moreira, Karina Griesi‐Oliveira, A.L. Bossolani-Martins, PLoS ONE Additional CnvsGeneticsGenetic EpidemiologyHuman PolymorphismPathology	2014	28
Novel mutations in<i>IRF6</i>in nonsyndromic cleft lip with or without cleft palate: When should<i>IRF6</i>mutational screening be done? Fernanda Sarquis Jehee, Beatriz A. Burin, Kátia M. Rocha, American Journal of Medical Genetics Part A Developmental AnomalyCleft LipDevelopmental BiologyNonsyndromic Cleft LipGenetic Disorder	2009	21

Page 1