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, Belgium and Antigua and Barbuda. Kátia M. Rocha's co-authors include Maria Rita Passos‐Bueno, Hugo A. Armelin, Nivaldo Alonso, Débora Romeo Bertola, Luciano Abreu Brito, Fábio Luís Forti, Ana Paula Lepique, 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

Author Peers

Peers are selected by citation overlap in the author's most active subfields. citations · hero ref

Author Last Decade Papers Cites
Kátia M. Rocha 198 136 45 28 25 20 287
Erica H. Gerkes 203 1.0× 221 1.6× 43 1.0× 37 1.3× 14 0.6× 14 386
Anand Saggar 231 1.2× 280 2.1× 26 0.6× 12 0.4× 16 0.6× 15 415
Tiffany Busa 163 0.8× 174 1.3× 28 0.6× 44 1.6× 13 0.5× 27 312
Ruolan Guo 120 0.6× 158 1.2× 28 0.6× 31 1.1× 48 1.9× 41 332
R.K. Track 121 0.6× 145 1.1× 24 0.5× 11 0.4× 22 0.9× 6 263
Annabella Marozza 108 0.5× 163 1.2× 34 0.8× 14 0.5× 20 0.8× 11 287
Elga Fabia Belligni 179 0.9× 114 0.8× 15 0.3× 46 1.6× 10 0.4× 16 256
Irén Haltrich 93 0.5× 103 0.8× 16 0.4× 15 0.5× 25 1.0× 33 239
Ana Medeira 159 0.8× 176 1.3× 13 0.3× 59 2.1× 13 0.5× 17 300
Outi Kuismin 106 0.5× 118 0.9× 15 0.3× 14 0.5× 40 1.6× 35 253

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

20 of 20 papers shown
1.
Monfardini, Frederico, et al.. (2021). Newborn Screening for 5q Spinal Muscular Atrophy: Comparisons between Real-Time PCR Methodologies and Cost Estimations for Future Implementation Programs. International Journal of Neonatal Screening. 7(3). 53–53. 7 indexed citations
2.
Moreira, Eloísa S., Isabela Mayá Wayhs Silva, Naila Cristina Vilaça Lourenço, et al.. (2016). Detection of small copy number variations (CNVs) in autism spectrum disorder (ASD) by custom array comparative genomic hybridization (aCGH). Research in autism spectrum disorders. 23. 145–151. 7 indexed citations
3.
Honjo, Rachel Sayuri, Guilherme Lopes Yamamoto, Kátia M. Rocha, et al.. (2015). Schinzel–Giedion syndrome in two Brazilian patients: Report of a novel mutation in SETBP1 and literature review of the clinical features. American Journal of Medical Genetics Part A. 167(5). 1039–1046. 22 indexed citations
4.
Griesi‐Oliveira, Karina, Naila Cristina Vilaça Lourenço, Kátia M. Rocha, et al.. (2014). Investigation of 15q11-q13, 16p11.2 and 22q13 CNVs in Autism Spectrum Disorder Brazilian Individuals with and without Epilepsy. PLoS ONE. 9(9). e107705–e107705. 19 indexed citations
5.
Yeh, Erika, Roberto D. Fanganiello, Daniele Yumi Sunaga, et al.. (2013). Novel Molecular Pathways Elicited by Mutant FGFR2 May Account for Brain Abnormalities in Apert Syndrome. PLoS ONE. 8(4). e60439–e60439. 11 indexed citations
6.
Brito, Luciano Abreu, Cibele Masotti, Kátia M. Rocha, et al.. (2012). IRF6 is a risk factor for nonsyndromic cleft lip in the Brazilian population. American Journal of Medical Genetics Part A. 158A(9). 2170–2175. 31 indexed citations
7.
Brito, Luciano Abreu, Lívia Máris Ribeiro Paranaiba, Cibele Masotti, et al.. (2012). Region 8q24 is a susceptibility locus for nonsyndromic oral clefting in Brazil. Birth Defects Research Part A Clinical and Molecular Teratology. 94(6). 464–468. 34 indexed citations
8.
Yeh, Erika, Roberto D. Fanganiello, Nivaldo Alonso, et al.. (2011). FGFR2 Mutation Confers a Less Drastic Gain of Function in Mesenchymal Stem Cells Than in Fibroblasts. Stem Cell Reviews and Reports. 8(3). 685–695. 9 indexed citations
9.
Brito, Luciano Abreu, Kátia M. Rocha, Daniela Franco Bueno, et al.. (2011). 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. American Journal of Medical Genetics Part A. 155(7). 1581–1587. 27 indexed citations
10.
Zechi‐Ceide, Roseli Maria, et al.. (2010). 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?. American Journal of Medical Genetics Part A. 152A(7). 1838–1840. 3 indexed citations
11.
Lamônica, Dionísia Aparecida Cusin, Luciana Paula Maximino, Mariza Ribeiro Feniman, et al.. (2010). Saethre-Chotzen Syndrome, Pro136His TWIST Mutation, Hearing Loss, and External and Middle Ear Structural Anomalies: Report on a Brazilian Family. The Cleft Palate-Craniofacial Journal. 47(5). 548–552. 7 indexed citations
12.
Jehee, Fernanda Sarquis, Kátia M. Rocha, Roseli Maria Zechi‐Ceide, et al.. (2009). Novel mutations inIRF6in nonsyndromic cleft lip with or without cleft palate: When shouldIRF6mutational screening be done?. American Journal of Medical Genetics Part A. 149A(6). 1319–1322. 14 indexed citations
13.
Costa, Érico T., Fábio Luís Forti, Alexandre Dermargos, et al.. (2008). Fibroblast Growth Factor 2 Restrains Ras-Driven Proliferation of Malignant Cells by Triggering RhoA-Mediated Senescence. Cancer Research. 68(15). 6215–6223. 17 indexed citations
14.
15.
Forti, Fábio Luís, Érico T. Costa, Kátia M. Rocha, Miriam S. Moraes, & Hugo A. Armelin. (2006). c-Ki-ras oncogene amplification and FGF2 signaling pathways in the mouse Y1 adrenocortical cell line. Anais da Academia Brasileira de Ciências. 78(2). 231–239. 1 indexed citations
16.
Costa, Érico T., Fábio Luís Forti, Kátia M. Rocha, Miriam S. Moraes, & Hugo A. Armelin. (2004). Molecular Mechanisms of Cell Cycle Control in the Mouse Y1 Adrenal Cell Line. Endocrine Research. 30(4). 503–509. 7 indexed citations
17.
Lepique, Ana Paula, Miriam S. Moraes, Kátia M. Rocha, et al.. (2004). c-Myc protein is stabilized by fibroblast growth factor 2 and destabilized by ACTH to control cell cycle in mouse Y1 adrenocortical cells. Journal of Molecular Endocrinology. 33(3). 623–638. 22 indexed citations
18.
Rocha, Kátia M., Fábio Luís Forti, Ana Paula Lepique, & Hugo A. Armelin. (2003). Deconstructing the molecular mechanisms of cell cycle control in a mouse adrenocortical cell line: Roles of ACTH. Microscopy Research and Technique. 61(3). 268–274. 21 indexed citations
19.
Splendore, Alessandra, et al.. (2001). Centro de Estudos do Genoma Humano:. Revista Neurociências. 20(2). 194–199. 1 indexed citations
20.
Rocha, Kátia M. & Hugo A. Armelin. (1994). Isolamento de clones revertentes normais a partir de celulas balb/3t3 transformadas com o oncogene humano ej-ras. 1 indexed citations

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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