Kátia M. Rocha

563 total citations
20 papers, 287 citations indexed

About

Kátia M. Rocha is a scholar working on Genetics, Molecular Biology and Genetics. According to data from OpenAlex, Kátia M. Rocha has authored 20 papers receiving a total of 287 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 6 papers in Genetics. Recurrent topics in Kátia M. Rocha's work include Cleft Lip and Palate Research (8 papers), Craniofacial Disorders and Treatments (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Kátia M. Rocha is often cited by papers focused on Cleft Lip and Palate Research (8 papers), Craniofacial Disorders and Treatments (7 papers) and Genomic variations and chromosomal abnormalities (6 papers). Kátia M. Rocha collaborates with scholars based in Brazil, Netherlands and United States. Kátia M. Rocha's co-authors include Maria Rita Passos‐Bueno, Hugo A. Armelin, Nivaldo Alonso, Débora Romeo Bertola, Luciano Abreu Brito, Ana Paula Lepique, Fábio Luís Forti, Diogo Franco, Miriam S. Moraes and Daniela Franco Bueno and has published in prestigious journals such as PLoS ONE, Cancer Research and Journal of Medical Genetics.

In The Last Decade

Kátia M. Rocha

20 papers receiving 281 citations

Peers

Countries citing papers authored by Kátia M. Rocha

Since Specialization

Citations

This map shows the geographic impact of Kátia M. Rocha's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by Kátia M. Rocha with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Kátia M. Rocha more than expected).

Fields of papers citing papers by Kátia M. Rocha

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Kátia M. Rocha. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by Kátia M. Rocha. The network helps show where Kátia M. Rocha may publish in the future.

Co-authorship network of co-authors of Kátia M. Rocha

This figure shows the co-authorship network connecting the top 25 collaborators of Kátia M. Rocha. A scholar is included among the top collaborators of Kátia M. Rocha based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Kátia M. Rocha. Kátia M. Rocha is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Newborn Screening for 5q Spinal Muscular Atrophy: Comparisons between Real-Time PCR Methodologies and Cost Estimations for Future Implementation Programs 2021 ·International Journal of Neonatal Screening ·(unknown), Frederico Monfardini, Naila Cristina Vilaça Lourenço, Kátia M. Rocha, (unknown), Rita C.M. Pavanello, Mayana Zatz	7
2	Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH) 2016 ·Research in autism spectrum disorders ·Eloísa S. Moreira, Isabela Mayá Wayhs Silva, Naila Cristina Vilaça Lourenço, (unknown), (unknown), (unknown), Karina Griesi‐Oliveira, Monize Lazar, Silvia Souza da Costa, Michel Satya Naslavsky, Kátia M. Rocha, Meire Aguena, Agnes Cristina Fett‐Conte, Mayana Zatz, Carla Rosenberg, Elaine Cristina Zachi, Débora Romeo Bertola, (unknown), Maria Rita Passos‐Bueno	7
3	Schinzel–Giedion syndrome in two Brazilian patients: Report of a novel mutation in SETBP1 and literature review of the clinical features 2015 ·American Journal of Medical Genetics Part A ·(unknown), Rachel Sayuri Honjo, (unknown), Guilherme Lopes Yamamoto, Kátia M. Rocha, Michel Satya Naslavsky, Mayana Zatz, Maria Rita Passos‐Bueno, Chong Ae Kim, Débora Romeo Bertola	22
4	Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy 2014 ·PLoS ONE ·(unknown), Karina Griesi‐Oliveira, (unknown), Naila Cristina Vilaça Lourenço, (unknown), Kátia M. Rocha, Eloísa S. Moreira, (unknown), (unknown), Débora Romeo Bertola, (unknown), Tiago R. Magalhães, Agnes Cristina Fett‐Conte, Maria Rita Passos‐Bueno	19
5	Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome 2013 ·PLoS ONE ·Erika Yeh, Roberto D. Fanganiello, Daniele Yumi Sunaga, Xueyan Zhou, (unknown), Kátia M. Rocha, Nivaldo Alonso, Hamilton Matushita, Yingli Wang, Ethylin Wang Jabs, Maria Rita Passos‐Bueno	11
6	Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil 2012 ·Birth Defects Research Part A Clinical and Molecular Teratology ·Luciano Abreu Brito, Lívia Máris Ribeiro Paranaiba, (unknown), Cibele Masotti, (unknown), David Schlesinger, Kátia M. Rocha, (unknown), (unknown), Nivaldo Alonso, Diogo Franco, Elizabete Bagordakis Pinto, Hercílio Martelli Júnior, Diogo Meyer, Ricardo D. Coletta, Maria Rita Passos‐Bueno	34
7	IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population 2012 ·American Journal of Medical Genetics Part A ·Luciano Abreu Brito, (unknown), Cibele Masotti, (unknown), Kátia M. Rocha, David Schlesinger, Daniela Franco Bueno, (unknown), (unknown), Débora Romeo Bertola, Diogo Meyer, Diogo Franco, Nivaldo Alonso, Maria Rita Passos‐Bueno	31
8	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 2011 ·American Journal of Medical Genetics Part A ·Luciano Abreu Brito, (unknown), Kátia M. Rocha, (unknown), (unknown), Daniela Franco Bueno, Meire Aguena, Débora Romeo Bertola, Diogo Franco, André Monteiro Costa, Nivaldo Alonso, Paulo Alberto Otto, Maria Rita Passos‐Bueno	27
9	FGFR2 Mutation Confers a Less Drastic Gain of Function in Mesenchymal Stem Cells Than in Fibroblasts 2011 ·Stem Cell Reviews and Reports ·Erika Yeh, (unknown), (unknown), Roberto D. Fanganiello, Nivaldo Alonso, Hamilton Matushita, Kátia M. Rocha, Maria Rita Passos‐Bueno	9
10	Mandibulofacial dysostosis, severe lower eyelid coloboma, cleft palate, and alopecia: A new distinct form of mandibulofacial dysostosis or a severe form of Johnson–McMillin syndrome? 2010 ·American Journal of Medical Genetics Part A ·Roseli Maria Zechi‐Ceide, Maria Leine Guion‐Almeida, Fernanda Sarquis Jehee, Kátia M. Rocha, (unknown)	3
11	Saethre-Chotzen Syndrome, Pro136His TWIST Mutation, Hearing Loss, and External and Middle Ear Structural Anomalies: Report on a Brazilian Family 2010 ·The Cleft Palate-Craniofacial Journal ·Dionísia Aparecida Cusin Lamônica, Luciana Paula Maximino, Mariza Ribeiro Feniman, (unknown), (unknown), Dagma Venturini Marques Abramides, Maria Rita Passos‐Bueno, Kátia M. Rocha, Antônio Richieri‐Costa	7
12	Novel mutations inIRF6in nonsyndromic cleft lip with or without cleft palate: When shouldIRF6mutational screening be done? 2009 ·American Journal of Medical Genetics Part A ·Fernanda Sarquis Jehee, (unknown), Kátia M. Rocha, Roseli Maria Zechi‐Ceide, Daniela Franco Bueno, Luciano Abreu Brito, Josiane Souza, Gabriela Ferraz Leal, Antônio Richieri‐Costa, Nivaldo Alonso, Paulo Alberto Otto, Maria Rita Passos‐Bueno	14
13	Fibroblast Growth Factor 2 Restrains Ras-Driven Proliferation of Malignant Cells by Triggering RhoA-Mediated Senescence 2008 ·Cancer Research ·Érico T. Costa, Fábio Luís Forti, (unknown), Alexandre Dermargos, (unknown), Jacqueline Salotti, Kátia M. Rocha, Paula Fontes Asprino, (unknown), Marianna M. Koga, Hugo A. Armelin	17
14	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 2008 ·Journal of Medical Genetics ·Fernanda Sarquis Jehee, Ana Cristina Victorino Krepischi, Kátia M. Rocha, Denise P. Cavalcanti, Chong Ae Kim, Débora Romeo Bertola, Luís Garcia Alonso, Carla S. D’Angelo, Juliana F. Mazzeu, Guy Froyen, Dorien Lugtenberg, Angela Maria Vianna‐Morgante, Carla Rosenberg, Maria Rita Passos‐Bueno	26
15	c-Ki-ras oncogene amplification and FGF2 signaling pathways in the mouse Y1 adrenocortical cell line 2006 ·Anais da Academia Brasileira de Ciências ·Fábio Luís Forti, Érico T. Costa, Kátia M. Rocha, Miriam S. Moraes, Hugo A. Armelin	1
16	Molecular Mechanisms of Cell Cycle Control in the Mouse Y1 Adrenal Cell Line 2004 ·Endocrine Research ·Érico T. Costa, Fábio Luís Forti, Kátia M. Rocha, Miriam S. Moraes, Hugo A. Armelin	7
17	c-Myc protein is stabilized by fibroblast growth factor 2 and destabilized by ACTH to control cell cycle in mouse Y1 adrenocortical cells 2004 ·Journal of Molecular Endocrinology ·Ana Paula Lepique, Miriam S. Moraes, Kátia M. Rocha, (unknown), Glaucia N. M. Hajj, Telma T. Schwindt, Hugo A. Armelin	22
18	Deconstructing the molecular mechanisms of cell cycle control in a mouse adrenocortical cell line: Roles of ACTH 2003 ·Microscopy Research and Technique ·Kátia M. Rocha, Fábio Luís Forti, Ana Paula Lepique, Hugo A. Armelin	21
19	Centro de Estudos do Genoma Humano: 2001 ·Revista Neurociências ·Alessandra Splendore, Kátia M. Rocha, (unknown), Maria Rita Passos‐Bueno, Mayana Zatz	1
20	Isolamento de clones revertentes normais a partir de celulas balb/3t3 transformadas com o oncogene humano ej-ras 1994 ·Kátia M. Rocha, Hugo A. Armelin	1

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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