Mari Rossi

740 total citations
7 papers, 257 citations indexed

About

Mari Rossi is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Mari Rossi has authored 7 papers receiving a total of 257 indexed citations (citations by other indexed papers that have themselves been cited), including 5 papers in Genetics, 3 papers in Pathology and Forensic Medicine and 2 papers in Molecular Biology. Recurrent topics in Mari Rossi's work include Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic factors in colorectal cancer (3 papers). Mari Rossi is often cited by papers focused on Genomics and Rare Diseases (5 papers), Genomic variations and chromosomal abnormalities (4 papers) and Genetic factors in colorectal cancer (3 papers). Mari Rossi collaborates with scholars based in United States, United Kingdom and Germany. Mari Rossi's co-authors include Kelly D. Farwell Hagman, Sha Tang, Zöe Powis, Dima El‐Khechen, Deepali N. Shinde, Kelly Radtke, Erica D. Smith, Mary Helen Black, Katherine L. Helbig and Wendy Alcaraz and has published in prestigious journals such as Journal of Medical Genetics, Human Mutation and Genetics in Medicine.

In The Last Decade

Mari Rossi

7 papers receiving 256 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Mari Rossi United States 6 177 101 37 30 27 7 257
Dima El‐Khechen United States 8 208 1.2× 125 1.2× 49 1.3× 20 0.7× 24 0.9× 10 294
María Isabel Álvarez‐Mora Spain 11 210 1.2× 170 1.7× 96 2.6× 24 0.8× 7 0.3× 34 303
Elena Beristain Spain 11 220 1.2× 161 1.6× 77 2.1× 42 1.4× 35 1.3× 18 284
Mariana Moysés‐Oliveira Brazil 11 206 1.2× 130 1.3× 29 0.8× 17 0.6× 7 0.3× 45 300
Alisdair McNeill United Kingdom 6 93 0.5× 152 1.5× 21 0.6× 14 0.5× 29 1.1× 13 218
Vamsee Pillalamarri United States 9 222 1.3× 204 2.0× 22 0.6× 40 1.3× 9 0.3× 10 388
Claudia Ciaccio Italy 11 221 1.2× 184 1.8× 66 1.8× 23 0.8× 8 0.3× 30 347
Avinash M. Veerappa India 10 112 0.6× 148 1.5× 17 0.5× 25 0.8× 12 0.4× 27 280
Sébastien Moutton France 12 211 1.2× 212 2.1× 26 0.7× 15 0.5× 10 0.4× 17 367
Lauren Grote United States 6 88 0.5× 105 1.0× 11 0.3× 13 0.4× 24 0.9× 7 186

Countries citing papers authored by Mari Rossi

Since Specialization
Citations

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

Fields of papers citing papers by Mari Rossi

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Mari Rossi

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

All Works

7 of 7 papers shown
1.
Towne, Meghan C., Mari Rossi, Jennifer M. Huang, et al.. (2022). Diagnostic testing laboratories are valuable partners for disease gene discovery: 5‐year experience with GeneMatcher. Human Mutation. 43(6). 772–781. 4 indexed citations
2.
Smith, Erica D., Kirsten Blanco, Samin A. Sajan, et al.. (2019). A retrospective review of multiple findings in diagnostic exome sequencing: halF.A.re distinct and halF.A.re overlapping diagnoses. Genetics in Medicine. 21(10). 2199–2207. 61 indexed citations
3.
Park, Joohyun, Mari Rossi, Maren Rautenberg, et al.. (2019). De novo variants in SLC12A6 cause sporadic early-onset progressive sensorimotor neuropathy. Journal of Medical Genetics. 57(4). 283–288. 10 indexed citations
4.
Rossi, Mari, Dima El‐Khechen, Mary Helen Black, et al.. (2017). Outcomes of Diagnostic Exome Sequencing in Patients With Diagnosed or Suspected Autism Spectrum Disorders. Pediatric Neurology. 70. 34–43.e2. 64 indexed citations
5.
Smith, Erica D., Kelly Radtke, Mari Rossi, et al.. (2017). Classification of Genes: Standardized Clinical Validity Assessment of Gene-Disease Associations Aids Diagnostic Exome Analysis and Reclassifications. Human Mutation. 38(5). 600–608. 68 indexed citations
6.
Hagman, Kelly D. Farwell, Deepali N. Shinde, Cameron Mroske, et al.. (2016). Candidate-gene criteria for clinical reporting: diagnostic exome sequencing identifies altered candidate genes among 8% of patients with undiagnosed diseases. Genetics in Medicine. 19(2). 224–235. 34 indexed citations
7.
Rossi, Mari, Helena Kilpinen, Mikko Muona, et al.. (2013). Allele-specific regulation of DISC1 expression by miR-135b-5p. European Journal of Human Genetics. 22(6). 840–843. 16 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

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2026