S.S. Takeno

657 total citations
22 papers, 403 citations indexed

About

S.S. Takeno is a scholar working on Genetics, Plant Science and Molecular Biology. According to data from OpenAlex, S.S. Takeno has authored 22 papers receiving a total of 403 indexed citations (citations by other indexed papers that have themselves been cited), including 22 papers in Genetics, 11 papers in Plant Science and 8 papers in Molecular Biology. Recurrent topics in S.S. Takeno's work include Genomic variations and chromosomal abnormalities (21 papers), Chromosomal and Genetic Variations (11 papers) and Cholangiocarcinoma and Gallbladder Cancer Studies (5 papers). S.S. Takeno is often cited by papers focused on Genomic variations and chromosomal abnormalities (21 papers), Chromosomal and Genetic Variations (11 papers) and Cholangiocarcinoma and Gallbladder Cancer Studies (5 papers). S.S. Takeno collaborates with scholars based in Brazil, Germany and United States. S.S. Takeno's co-authors include Maria Isabel Melaragno, Roberta Santos Guilherme, Mariana Ferreira Leal, Rommel Mário Rodríguez Burbano, Leslie Domenici Kulikowski, Paulo Pimentel de Assumpção, Marı́lia de Arruda Cardoso Smith, Danielle Queiroz Calcagno, Renata Pellegrino and André Salim Khayat and has published in prestigious journals such as Gene, Journal of Intellectual Disability Research and Cytogenetic and Genome Research.

In The Last Decade

S.S. Takeno

22 papers receiving 345 citations

Peers

Countries citing papers authored by S.S. Takeno

Since Specialization

Citations

This map shows the geographic impact of S.S. Takeno'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 S.S. Takeno with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites S.S. Takeno more than expected).

Fields of papers citing papers by S.S. Takeno

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by S.S. Takeno. 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 S.S. Takeno. The network helps show where S.S. Takeno may publish in the future.

Co-authorship network of co-authors of S.S. Takeno

This figure shows the co-authorship network connecting the top 25 collaborators of S.S. Takeno. A scholar is included among the top collaborators of S.S. Takeno 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 S.S. Takeno. S.S. Takeno 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	Duplication 9p and their implication to phenotype 2014 ·BMC Medical Genetics ·Roberta Santos Guilherme, Vera Ayres Meloni, Ana Beatriz Alvarez Pérez, (unknown), (unknown), (unknown), S.S. Takeno, Leslie Domenici Kulikowski, Maria Isabel Melaragno	40
2	Trisomy 1q32 and monosomy 11q25 associated with congenital heart defect: cytogenomic delineation and patient fourteen years follow-up 2014 ·Molecular Cytogenetics ·Vera Ayres Meloni, S.S. Takeno, (unknown), Cláudia Berlim de Mello, Maria Isabel Melaragno, Leslie Domenici Kulikowski	2
3	Congenital Adrenal Hyperplasia, Ovarian Failure and Ehlers-Danlos Syndrome due to a 6p Deletion 2014 ·Sexual Development ·Mariana Moysés‐Oliveira, (unknown), S.S. Takeno, (unknown), Tânia A.S.S. Bachega, Débora Romeo Bertola, Maria Isabel Melaragno	1
4	Cytogenomic delineation and clinical follow‐up of two siblings with an 8.5 Mb 6q24.2‐q25.2 deletion inherited from a paternal insertion 2014 ·American Journal of Medical Genetics Part A ·Vera Ayres Meloni, Roberta Santos Guilherme, Mariana Moysés‐Oliveira, (unknown), S.S. Takeno, Nara Sobreira, (unknown), Cláudia Berlim de Mello, Maria Isabel Melaragno	5
5	A Complex Chromosome Rearrangement Involving Four Chromosomes, Nine Breakpoints and a Cryptic 0.6-Mb Deletion in a Boy with Cerebellar Hypoplasia and Defects in Skull Ossification 2013 ·Cytogenetic and Genome Research ·Roberta Santos Guilherme, Mirlene Cecília Soares Pinho Cernach, (unknown), S.S. Takeno, (unknown), (unknown), Samarth Bhatt, Thomas Liehr, Maria Isabel Melaragno	17
6	First Report of a Small Supernumerary der(8;14) Marker Chromosome 2013 ·Cytogenetic and Genome Research ·Roberta Santos Guilherme, (unknown), Ana Beatriz Alvarez Pérez, S.S. Takeno, (unknown), Leslie Domenici Kulikowski, Elisabeth Klein, Ahmed B. Hamid, Thomas Liehr, Maria Isabel Melaragno	1
7	Cytogenomic characterization of an unexpected 17.6Mb 9p deletion associated to a 14.8Mb 20p duplication in a dysmorphic patient with multiple congenital anomalies presenting a normal G-banding karyotype 2012 ·Gene ·(unknown), Flávia Piazzon, (unknown), S.S. Takeno, Denise Maria Christofolini, Leslie Domenici Kulikowski, Décio Brunoni, Maria Isabel Melaragno	4
8	Marfan syndrome with a complex chromosomal rearrangement including deletion of the FBN1 gene 2012 ·Molecular Cytogenetics ·(unknown), (unknown), S.S. Takeno, (unknown), (unknown), Roberta Santos Guilherme, Cláudia Berlim de Mello, Maria Isabel Melaragno, Ana Beatriz Alvarez Pérez	18
9	Twenty-year cytogenetic and molecular follow-up of a patient with ring chromosome 15: a case report 2012 ·Journal of Medical Case Reports ·Roberta Santos Guilherme, (unknown), S.S. Takeno, Renata Pellegrino, Décio Brunoni, Leslie Domenici Kulikowski, Maria Isabel Melaragno	20
10	Different Conformation of Two Supernumerary 18p Isochromosomes, One with a Concomitant Partial 18q Trisomy 2012 ·Cytogenetic and Genome Research ·(unknown), (unknown), S.S. Takeno, (unknown), Chong Ae Kim, Ana Beatriz Alvarez Pérez, Leslie Domenici Kulikowski, Maria Isabel Melaragno	2
11	Autistic disorder phenotype associated to a complex 15q intrachromosomal rearrangement 2012 ·American Journal of Medical Genetics Part B Neuropsychiatric Genetics ·Denise Maria Christofolini, Vera Ayres Meloni, Marco A. Ramos, Mariana Moysés‐Oliveira, Cláudia Berlim de Mello, Renata Pellegrino, S.S. Takeno, Maria Isabel Melaragno	1
12	Interstitial 4q Deletion and Isodicentric Y-Chromosome in a Patient with Dysmorphic Features 2012 ·Molecular Syndromology ·(unknown), (unknown), (unknown), Ana Beatriz Alvarez Pérez, (unknown), S.S. Takeno, Maria Isabel Melaragno	3
13	Clinical, Cytogenetic and Molecular Study in a Case of r(3) with 3p Deletion and Review of the Literature 2011 ·Cytogenetic and Genome Research ·Roberta Santos Guilherme, (unknown), Renata Pellegrino, Denise Maria Christofolini, S.S. Takeno, (unknown), Leslie Domenici Kulikowski, Maria Isabel Melaragno	5
14	Mechanisms of ring chromosome formation, ring instability and clinical consequences 2011 ·BMC Medical Genetics ·Roberta Santos Guilherme, (unknown), Chong Ae Kim, Renata Pellegrino, S.S. Takeno, Nancy B. Spinner, Laura K. Conlin, Denise Maria Christofolini, Leslie Domenici Kulikowski, Maria Isabel Melaragno	100
15	Genomic alterations in diffuse-type gastric cancer as shown by high-resolution comparative genomic hybridization 2009 ·Cancer Genetics and Cytogenetics ·S.S. Takeno, Mariana Ferreira Leal, (unknown), Mônica Vannucci Nunes Lipay, André Salim Khayat, Paulo Pimentel de Assumpção, Rommel Mário Rodríguez Burbano, Marı́lia de Arruda Cardoso Smith	15
16	Aneuploidy of chromosome 8 detected by fluorescence in situ hybridisation in ACP01 cell line gastric adenocarcinoma 2006 ·Clinical and Experimental Medicine ·(unknown), (unknown), Mariana Ferreira Leal, S.S. Takeno, Paulo Pimentel de Assumpção, Eleonidas Moura Lima, André Salim Khayat, Elizabeth Chen, Marı́lia de Arruda Cardoso Smith, Rommel Mário Rodríguez Burbano	17
17	C-MYC locus amplification as metastasis predictor in intestinal-type gastric adenocarcinomas: CGH study in Brazil. 2006 ·PubMed ·Rommel Mário Rodríguez Burbano, Paulo Pimentel de Assumpção, Mariana Ferreira Leal, Danielle Queiroz Calcagno, (unknown), André Salim Khayat, S.S. Takeno, Elizabeth Chen, Marı́lia de Arruda Cardoso Smith	52
18	Numerical aberrations of chromosome 8 detected by conventional cytogenetics and fluorescence in situ hybridization in individuals from northern Brazil with gastric adenocarcinoma 2006 ·Cancer Genetics and Cytogenetics ·Paulo Pimentel de Assumpção, Geraldo Ishak, Elizabeth Chen, S.S. Takeno, Mariana Ferreira Leal, (unknown), Danielle Queiroz Calcagno, André Salim Khayat, Sâmia Demachki, Marı́lia de Arruda Cardoso Smith, Rommel Mário Rodríguez Burbano	27
19	Aneuploidy of chromosome 8 and C-MYC amplification in individuals from northern Brazil with gastric adenocarcinoma. 2006 ·PubMed ·Danielle Queiroz Calcagno, Mariana Ferreira Leal, S.S. Takeno, Paulo Pimentel de Assumpção, Sâmia Demachki, Marı́lia de Arruda Cardoso Smith, Rommel Mário Rodríguez Burbano	47
20	Duplication 4p and deletion 4p (Wolf–Hirschhorn syndrome) due to complementary gametes from a 3:1 segregation of a maternal balanced t(4;13)(p16;q11) translocation 2004 ·American Journal of Medical Genetics Part A ·S.S. Takeno, (unknown), Joyce Andrade, Marı́lia de Arruda Cardoso Smith, Décio Brunoni, Maria Isabel Melaragno	5

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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