Dina Manaa

1.4k total citations · 1 hit paper
2 papers, 793 citations indexed

About

Dina Manaa is a scholar working on Cognitive Neuroscience, Oncology and Epidemiology. According to data from OpenAlex, Dina Manaa has authored 2 papers receiving a total of 793 indexed citations (citations by other indexed papers that have themselves been cited), including 1 paper in Cognitive Neuroscience, 1 paper in Oncology and 1 paper in Epidemiology. Recurrent topics in Dina Manaa's work include Pancreatic and Hepatic Oncology Research (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Cancer Genomics and Diagnostics (1 paper). Dina Manaa is often cited by papers focused on Pancreatic and Hepatic Oncology Research (1 paper), Genomic variations and chromosomal abnormalities (1 paper) and Cancer Genomics and Diagnostics (1 paper). Dina Manaa collaborates with scholars based in United States and Sweden. Dina Manaa's co-authors include Pamela Sklar, Christina M. Hultman, Trent Gaugler, Joseph D. Buxbaum, Milind Mahajan, Jennifer Reichert, Abraham Reichenberg, Sven Sandin, Lambertus Klei and Oscar Svantesson and has published in prestigious journals such as Nature Genetics and Molecular Case Studies.

In The Last Decade

Dina Manaa

2 papers receiving 778 citations

Hit Papers

Most genetic risk for autism resides with common variation 2014 2026 2018 2022 2014 250 500 750

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Dina Manaa United States 2 563 501 270 100 77 2 793
Corneliu Bodea United States 4 563 1.0× 514 1.0× 284 1.1× 100 1.0× 77 1.0× 5 809
Barbara Manzi Italy 13 633 1.1× 516 1.0× 284 1.1× 197 2.0× 67 0.9× 17 979
Simona Trillo Italy 10 648 1.2× 472 0.9× 208 0.8× 212 2.1× 113 1.5× 12 904
Karola Rehnström Finland 14 256 0.5× 432 0.9× 257 1.0× 62 0.6× 56 0.7× 21 760
Michael Duyzend United States 8 336 0.6× 383 0.8× 276 1.0× 58 0.6× 51 0.7× 16 673
Catarina Correia Portugal 12 352 0.6× 331 0.7× 173 0.6× 116 1.2× 49 0.6× 18 639
Toshirou Sugiyama Japan 9 448 0.8× 288 0.6× 244 0.9× 133 1.3× 70 0.9× 11 933
Beth Rosen‐Sheidley United States 7 659 1.2× 505 1.0× 155 0.6× 113 1.1× 147 1.9× 8 831
Andreas G. Chiocchetti Germany 17 284 0.5× 335 0.7× 474 1.8× 101 1.0× 125 1.6× 50 983
Qiong Xu China 13 352 0.6× 263 0.5× 189 0.7× 90 0.9× 120 1.6× 42 580

Countries citing papers authored by Dina Manaa

Since Specialization
Citations

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

Fields of papers citing papers by Dina Manaa

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Dina Manaa

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

All Works

2 of 2 papers shown
1.
Wrzeszczyński, Kazimierz O., Sadia Rahman, Mayu O. Frank, et al.. (2019). Identification of targetable BRAF ΔN486_P490 variant by whole-genome sequencing leading to dabrafenib-induced remission of a BRAF-mutant pancreatic adenocarcinoma. Molecular Case Studies. 5(6). a004424–a004424. 19 indexed citations
2.
Gaugler, Trent, Lambertus Klei, Stephan Sanders, et al.. (2014). Most genetic risk for autism resides with common variation. Nature Genetics. 46(8). 881–885. 774 indexed citations breakdown →

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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