Danny Antaki

46.4k total citations
8 papers, 347 citations indexed

About

Danny Antaki is a scholar working on Molecular Biology, Genetics and Infectious Diseases. According to data from OpenAlex, Danny Antaki has authored 8 papers receiving a total of 347 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 6 papers in Genetics and 1 paper in Infectious Diseases. Recurrent topics in Danny Antaki's work include Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Congenital heart defects research (2 papers). Danny Antaki is often cited by papers focused on Genetics and Neurodevelopmental Disorders (3 papers), Genomics and Rare Diseases (2 papers) and Congenital heart defects research (2 papers). Danny Antaki collaborates with scholars based in United States, Spain and Denmark. Danny Antaki's co-authors include Jonathan Sebat, Lilia M. Iakoucheva, Alysson R. Muotri, William M. Brandler, Sébastien Lyonnais, Mattia Mori, Bruce E. Torbett, Yves Mély, Gilles Mirambeau and Adam X. Maihofer and has published in prestigious journals such as Cell, Nature Genetics and Bioinformatics.

In The Last Decade

Danny Antaki

8 papers receiving 345 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Danny Antaki United States 7 189 178 104 35 32 8 347
Garilyn Jentarra United States 10 170 0.9× 144 0.8× 65 0.6× 127 3.6× 29 0.9× 11 406
Arielle N. Valdez‐Sinon United States 8 214 1.1× 104 0.6× 38 0.4× 22 0.6× 44 1.4× 13 347
Shannon Hamilton United States 9 261 1.4× 288 1.6× 246 2.4× 85 2.4× 111 3.5× 11 684
Xiu Xu China 6 92 0.5× 57 0.3× 87 0.8× 4 0.1× 23 0.7× 28 263
Alice K. Min United States 6 315 1.7× 122 0.7× 36 0.3× 17 0.5× 12 0.4× 8 419
Raphaël Faucard France 9 184 1.0× 44 0.2× 16 0.2× 17 0.5× 18 0.6× 11 389
Leon Tejwani United States 8 323 1.7× 102 0.6× 69 0.7× 3 0.1× 31 1.0× 14 492
Lise-Andrée Gobeil Canada 8 271 1.4× 178 1.0× 25 0.2× 59 1.7× 19 0.6× 9 512
Nallur B. Ramachandra India 14 223 1.2× 254 1.4× 56 0.5× 3 0.1× 5 0.2× 54 528
Xing‐Da Ju China 10 234 1.2× 57 0.3× 48 0.5× 3 0.1× 8 0.3× 29 400

Countries citing papers authored by Danny Antaki

Since Specialization
Citations

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

Fields of papers citing papers by Danny Antaki

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Danny Antaki

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

All Works

8 of 8 papers shown
1.
Antaki, Danny, James P. Guevara, Adam X. Maihofer, et al.. (2022). A phenotypic spectrum of autism is attributable to the combined effects of rare variants, polygenic risk and sex. Nature Genetics. 54(9). 1284–1292. 110 indexed citations
2.
Saini, Shubham, Danny Antaki, Celine L. St. Pierre, et al.. (2022). SNPs, short tandem repeats, and structural variants are responsible for differential gene expression across C57BL/6 and C57BL/10 substrains. Cell Genomics. 2(3). 100102–100102. 10 indexed citations
3.
Urresti, Jorge, Pan Zhang, Patricia Moran‐Losada, et al.. (2021). Cortical organoids model early brain development disrupted by 16p11.2 copy number variants in autism. Molecular Psychiatry. 26(12). 7560–7580. 74 indexed citations
4.
Yang, Xiaoxu, Martin W. Breuss, Danny Antaki, et al.. (2021). Developmental and temporal characteristics of clonal sperm mosaicism. Cell. 184(18). 4772–4783.e15. 26 indexed citations
5.
Pagel, Kymberleigh A., Danny Antaki, Matthew Mort, et al.. (2019). Pathogenicity and functional impact of non-frameshifting insertion/deletion variation in the human genome. PLoS Computational Biology. 15(6). e1007112–e1007112. 40 indexed citations
6.
Urresti, Jorge, Patricia Morán Losada, Pan Zhang, et al.. (2019). 84 16P11.2 PATIENT-DERIVED CEREBRAL ORGANOIDS SHOW MIGRATION AND SYNAPTIC DEFECTS. European Neuropsychopharmacology. 29. S106–S106. 1 indexed citations
7.
Antaki, Danny, William M. Brandler, & Jonathan Sebat. (2017). SV2: accurate structural variation genotyping and de novo mutation detection from whole genomes. Bioinformatics. 34(10). 1774–1777. 29 indexed citations
8.
Mori, Mattia, Sébastien Lyonnais, Danny Antaki, et al.. (2015). Nucleocapsid Protein: A Desirable Target for Future Therapies Against HIV-1. Current topics in microbiology and immunology. 389. 53–92. 57 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.

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