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

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

#	Title	Journal	Authors	Indexed citations
1	Copy number variations in a Brazilian cohort with autism spectrum disorders highlight the contribution of cell adhesion genes	Clinical Genetics	Claudia Ismania Samogy Costa, Mehdi Zarrei et al.	16
2	Congenital limb deficiency: Genetic investigation of 44 individuals presenting mainly longitudinal defects in isolated or syndromic forms	Clinical Genetics	Guilherme Lopes Yamamoto, José Ricardo Magliocco Ceroni et al.	2
3	Congenital chromoanagenesis in the routine postnatal chromosomal microarray analyses	American Journal of Medical Genetics Part A	Alexander A.L. Jorge, Lucilene Arilho Ribeiro et al.	2
4	Cytogenetically visible inversions are formed by multiple molecular mechanisms	Human Mutation	Maria Pettersson, Christopher M. Grochowski et al.	11
5	Insight into the mechanisms and consequences of recurrent telomere capture associated with a sub-telomeric deletion	Chromosome Research	Ana Cristina Victorino Krepischi, Angela Maria Vianna‐Morgante et al.	4
6	Genomic imbalances pinpoint potential oncogenes and tumor suppressors in Wilms tumors	Molecular Cytogenetics	Ana Cristina Victorino Krepischi, Mariana Maschietto et al.	40
7	Interstitial 1q21.1 Microdeletion Is Associated with Severe Skeletal Anomalies, Dysmorphic Face and Moderate Intellectual Disability	Molecular Syndromology	Roseli Maria Zechi‐Ceide, Nancy Mizue Kokitsu‐Nakata et al.	18
8	Do Copy Number Changes in CACNA2D2, CACNA2D3, and CACNA1D Constitute a Predisposing Risk Factor for Alzheimer’s Disease?	Frontiers in Genetics	Cláudia Kimie Suemoto, Carlos Augusto Pasqualucci et al.	15
9	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	Claudia M.B. Carvalho, Shivakumar Vasanth et al.	39
10	A familial case with interstitial 2q36 deletion: Variable phenotypic expression in full and mosaic state	European Journal of Medical Genetics	Érika L. Freitas, Susan Gribble et al.	4
11	Germline DNA copy number variation in familial and early-onset breast cancer	Breast Cancer Research	Ana Cristina Victorino Krepischi, Maria Isabel Achatz et al.	67
12	Nonrecurrent MECP2 duplications mediated by genomic architecture-driven DNA breaks and break-induced replication repair	Genome Research	Marijke Bauters, Hilde Van Esch et al.	92
13	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	Fernanda Sarquis Jehee, Ana Cristina Victorino Krepischi et al.	26
14	Chromosomal Instability in MYH - and APC -Mutant Adenomatous Polyps	Cancer Research	Joana Cardoso, Renée X. de Menezes et al.	45
15	Spectrum of genetic changes in gastro-esophageal cancer cell lines determined by an integrated molecular cytogenetic approach	Cancer Genetics and Cytogenetics	Carla Rosenberg, Eric Geelen et al.	17
16	Differentially Painting Human Chromosome Arms with Combined Binary Ratio-labeling Fluorescence In Situ Hybridization	Genome Research	J. Wiegant, Vladimir Bezrookove et al.	50
17	Comparative genomic hybridization with lissamine- and fluorescein-labeled nucleotides	Cytometry	Carla Rosenberg, R.P.M. van Gijlswijk et al.	9
18	Chromosomal gains and losses in marginal zone B-cell lymphoma detected by comparative genomic hybridization	Blood	Judith Dierlamm, Carla Rosenberg et al.	1
19	The karyotype of the brown mussel Perna perna (L.) (Bivalvia: Mytilidae).		Cláudia Maria Jacobi, Carla Rosenberg et al.	4
20	Normal male carriers of the Martin-Bell syndrome gene: implications for genetic counseling	Revista brasileira de genetica	Carla Rosenberg, Angela Maria Vianna‐Morgante et al.	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.

Explore authors with similar magnitude of impact