Carla Rosenberg

11.7k total citations · 2 hit papers
183 papers, 5.7k citations indexed

About

Carla Rosenberg is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Carla Rosenberg has authored 183 papers receiving a total of 5.7k indexed citations (citations by other indexed papers that have themselves been cited), including 128 papers in Genetics, 91 papers in Molecular Biology and 30 papers in Plant Science. Recurrent topics in Carla Rosenberg's work include Genomic variations and chromosomal abnormalities (103 papers), Congenital heart defects research (32 papers) and Genetics and Neurodevelopmental Disorders (29 papers). Carla Rosenberg is often cited by papers focused on Genomic variations and chromosomal abnormalities (103 papers), Congenital heart defects research (32 papers) and Genetics and Neurodevelopmental Disorders (29 papers). Carla Rosenberg collaborates with scholars based in Brazil, Netherlands and United States. Carla Rosenberg's co-authors include Ana Cristina Victorino Krepischi, Hans J. Tanke, Gail Stetten, Angela Maria Vianna‐Morgante, Károly Szuhai, Craig Montell, Paul D. Wes, Andreas Jeromin, J Chevesich and J. Wiegant and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Genetics and Journal of Clinical Oncology.

In The Last Decade

Carla Rosenberg

183 papers receiving 5.6k citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Mutations in the APC tumour suppressor gene cause chromosomal instability

2001 545 citations Riccardo Fodde, Carla Rosenberg et al. profile →
TRPC1, a human homolog of a Drosophila store-operated channel.

1995 522 citations Carla Rosenberg et al. profile →

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
Carla Rosenberg Brazil	38	2.8k	2.3k	789	736	731	183	5.7k
J.-M. Lalouel United States	26	3.3k 1.2×	2.9k 1.2×	604 0.8×	687 0.9×	485 0.7×	99	7.4k
Mireille Claustres France	46	4.3k 1.5×	1.8k 0.8×	427 0.5×	255 0.3×	516 0.7×	221	8.2k
Marcella Devoto Italy	45	2.7k 1.0×	1.8k 0.8×	1.1k 1.5×	303 0.4×	492 0.7×	161	6.6k
Leonidas Tsiokas United States	31	3.3k 1.2×	2.3k 1.0×	172 0.2×	930 1.3×	507 0.7×	49	4.7k
Hirotomo Saitsu Japan	43	4.2k 1.5×	2.8k 1.2×	774 1.0×	353 0.5×	369 0.5×	430	7.7k
Tom Glaser United States	31	5.9k 2.1×	1.8k 0.7×	563 0.7×	231 0.3×	293 0.4×	51	7.7k
Marco Seri Italy	38	2.3k 0.8×	1.4k 0.6×	1.1k 1.4×	279 0.4×	262 0.4×	193	5.3k
Baoli Yang United States	39	3.9k 1.4×	1.4k 0.6×	380 0.5×	218 0.3×	376 0.5×	84	6.1k
M. Graziella Persico Italy	41	4.4k 1.6×	949 0.4×	453 0.6×	205 0.3×	722 1.0×	69	6.4k
Lee S. Weinstein United States	55	5.4k 1.9×	3.7k 1.6×	1.4k 1.8×	382 0.5×	557 0.8×	184	10.4k

Countries citing papers authored by Carla Rosenberg

Since Specialization

Citations

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

Fields of papers citing papers by Carla Rosenberg

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Carla Rosenberg

This figure shows the co-authorship network connecting the top 25 collaborators of Carla Rosenberg. A scholar is included among the top collaborators of Carla Rosenberg 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 Carla Rosenberg. Carla Rosenberg is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Costa, Claudia Ismania Samogy, Mehdi Zarrei, Eloisa De Sá Moreira, et al.. (2021). Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes. Clinical Genetics. 101(1). 134–141. 16 indexed citations

Yamamoto, Guilherme Lopes, José Ricardo Magliocco Ceroni, Rachel Sayuri Honjo, et al.. (2021). Congenital limb deficiency: Genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms. Clinical Genetics. 100(5). 615–623. 2 indexed citations

Jorge, Alexander A.L., Lucilene Arilho Ribeiro, Fernando Kok, et al.. (2021). Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses. American Journal of Medical Genetics Part A. 185(8). 2335–2344. 2 indexed citations

Pettersson, Maria, Christopher M. Grochowski, Josephine Wincent, et al.. (2020). Cytogenetically visible inversions are formed by multiple molecular mechanisms. Human Mutation. 41(11). 1979–1998. 11 indexed citations

Krepischi, Ana Cristina Victorino, et al.. (2018). Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion. Chromosome Research. 26(3). 191–198. 4 indexed citations

Krepischi, Ana Cristina Victorino, Mariana Maschietto, Elisa Napolitano Ferreira, et al.. (2016). Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors. Molecular Cytogenetics. 9(1). 20–20. 40 indexed citations

Zechi‐Ceide, Roseli Maria, Nancy Mizue Kokitsu‐Nakata, Siulan Vendramini‐Pittoli, et al.. (2016). Interstitial 1q21.1 Microdeletion Is Associated with Severe Skeletal Anomalies, Dysmorphic Face and Moderate Intellectual Disability. Molecular Syndromology. 7(6). 344–348. 18 indexed citations

Suemoto, Cláudia Kimie, et al.. (2016). Do Copy Number Changes in CACNA2D2, CACNA2D3, and CACNA1D Constitute a Predisposing Risk Factor for Alzheimer’s Disease?. Frontiers in Genetics. 7. 107–107. 15 indexed citations

Carvalho, Claudia M.B., Shivakumar Vasanth, Marwan Shinawi, et al.. (2014). Dosage Changes of a Segment at 17p13.1 Lead to Intellectual Disability and Microcephaly as a Result of Complex Genetic Interaction of Multiple Genes. The American Journal of Human Genetics. 95(5). 565–578. 39 indexed citations

10.

Freitas, Érika L., Susan Gribble, Milena Simioni, et al.. (2012). A familial case with interstitial 2q36 deletion: Variable phenotypic expression in full and mosaic state. European Journal of Medical Genetics. 55(11). 660–665. 4 indexed citations

11.

Krepischi, Ana Cristina Victorino, Maria Isabel Achatz, Érika Maria Monteiro Santos, et al.. (2012). Germline DNA copy number variation in familial and early-onset breast cancer. Breast Cancer Research. 14(1). R24–R24. 67 indexed citations

12.

Bauters, Marijke, Hilde Van Esch, Michael J. Friez, et al.. (2008). Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair. Genome Research. 18(6). 847–858. 92 indexed citations

13.

Jehee, Fernanda Sarquis, Ana Cristina Victorino Krepischi, Kátia M. Rocha, et al.. (2008). 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. Journal of Medical Genetics. 45(7). 447–450. 26 indexed citations

14.

Cardoso, Joana, Renée X. de Menezes, Monique E. van Leerdam, et al.. (2006). Chromosomal Instability in MYH - and APC -Mutant Adenomatous Polyps. Cancer Research. 66(5). 2514–2519. 45 indexed citations

15.

Rosenberg, Carla, Eric Geelen, Marije IJszenga, et al.. (2002). Spectrum of genetic changes in gastro-esophageal cancer cell lines determined by an integrated molecular cytogenetic approach. Cancer Genetics and Cytogenetics. 135(1). 35–41. 17 indexed citations

16.

Wiegant, J., Vladimir Bezrookove, Carla Rosenberg, et al.. (2000). Differentially Painting Human Chromosome Arms with Combined Binary Ratio-labeling Fluorescence In Situ Hybridization. Genome Research. 10(6). 861–865. 50 indexed citations

17.

Rosenberg, Carla, R.P.M. van Gijlswijk, J. Wiegant, et al.. (1998). Comparative genomic hybridization with lissamine- and fluorescein-labeled nucleotides. Cytometry. 32(4). 337–341. 9 indexed citations

18.

Dierlamm, Judith, Carla Rosenberg, Michel Stul, et al.. (1996). Chromosomal gains and losses in marginal zone B-cell lymphoma detected by comparative genomic hybridization. Blood. 1 indexed citations

19.

Jacobi, Cláudia Maria, Carla Rosenberg, & Angela Maria Vianna‐Morgante. (1990). The karyotype of the brown mussel Perna perna (L.) (Bivalvia: Mytilidae).. 13(4). 669–673. 4 indexed citations

20.

Rosenberg, Carla, et al.. (1988). Normal male carriers of the Martin-Bell syndrome gene: implications for genetic counseling. Revista brasileira de genetica. 11(3). 769–781. 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.

Explore authors with similar magnitude of impact