Aniko Sabo

58.0k total citations
31 papers, 980 citations indexed

About

Aniko Sabo is a scholar working on Genetics, Molecular Biology and Plant Science. According to data from OpenAlex, Aniko Sabo has authored 31 papers receiving a total of 980 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Genetics, 10 papers in Molecular Biology and 5 papers in Plant Science. Recurrent topics in Aniko Sabo's work include Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (6 papers). Aniko Sabo is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Genetics and Neurodevelopmental Disorders (7 papers) and Genomics and Rare Diseases (6 papers). Aniko Sabo collaborates with scholars based in United States, Israel and Brazil. Aniko Sabo's co-authors include Vincent Magrini, Philip Ozersky, Thomas M. Hooton, Christopher S. Reigstad, Chia‐Suei Hung, Elaine R. Mardis, Jian Xu, Jeffrey I. Gordon, Swaine L. Chen and Darin Blasiar and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Nature Communications and Blood.

In The Last Decade

Aniko Sabo

29 papers receiving 958 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Aniko Sabo United States	12	490	446	257	140	113	31	980
Anika Witten Germany	18	533 1.1×	122 0.3×	69 0.3×	71 0.5×	95 0.8×	46	1.2k
Katja Koeppen United States	18	733 1.5×	84 0.2×	84 0.3×	143 1.0×	120 1.1×	34	1.1k
Carsten A. Raabe Germany	16	650 1.3×	164 0.4×	46 0.2×	30 0.2×	100 0.9×	25	803
Donna M. Muzny United States	7	580 1.2×	328 0.7×	42 0.2×	119 0.8×	140 1.2×	8	1.1k
Verena Pfeiffer Germany	17	1.4k 2.9×	894 2.0×	233 0.9×	67 0.5×	635 5.6×	28	2.0k
Yuya NAKAMOTO Japan	14	177 0.4×	146 0.3×	232 0.9×	46 0.3×	38 0.3×	49	842
Antonin Marchais France	17	1.1k 2.2×	247 0.6×	77 0.3×	48 0.3×	249 2.2×	32	1.6k
Romualdas Vaisvila United States	15	1.0k 2.1×	312 0.7×	38 0.1×	25 0.2×	116 1.0×	20	1.2k
Todd A. Gray United States	24	1.4k 2.9×	760 1.7×	32 0.1×	334 2.4×	158 1.4×	38	1.9k
Igor Ruiz de los Mozos United Kingdom	19	1.1k 2.3×	200 0.4×	37 0.1×	58 0.4×	126 1.1×	26	1.4k

Countries citing papers authored by Aniko Sabo

Since Specialization

Citations

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

Fields of papers citing papers by Aniko Sabo

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Aniko Sabo

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

All Works

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20 of 20 papers shown

Chen, Ying, Panpan Liu, Aniko Sabo, & Dongyin Guan. (2025). Human genetic variation determines 24-hour rhythmic gene expression and disease risk. Nature Communications. 16(1). 4270–4270.

Fair, Douglas, Luke Maese, Yueh‐Yun Chi, et al.. (2023). TP53 germline pathogenic variant frequency in anaplastic rhabdomyosarcoma: A Children's Oncology Group report. Pediatric Blood & Cancer. 70(9). e30413–e30413. 4 indexed citations

Li, He, Jeremy M. Schraw, Michael E. Scheurer, et al.. (2023). Identification of USP9X as a leukemia susceptibility gene. Blood Advances. 7(16). 4563–4575. 5 indexed citations

Tosur, Mustafa, Claudia Soler‐Alfonso, Michael M. Khayat, et al.. (2021). Exome sequencing in children with clinically suspected maturity‐onset diabetes of the young. Pediatric Diabetes. 22(7). 960–968. 5 indexed citations

He, Li, Moez Dawood, Michael M. Khayat, et al.. (2021). Exome variant discrepancies due to reference-genome differences. The American Journal of Human Genetics. 108(7). 1239–1250. 31 indexed citations

Gingras, Marie‐Claude, Aniko Sabo, Maria Cardenas, et al.. (2021). Sequencing of a central nervous system tumor demonstrates cancer transmission in an organ transplant. Life Science Alliance. 4(9). e202000941–e202000941. 2 indexed citations

Chen, Chun‐An, Rituraj Pal, Jiani Yin, et al.. (2020). Combination of whole exome sequencing and animal modeling identifies TMPRSS9 as a candidate gene for autism spectrum disorder. Human Molecular Genetics. 29(3). 459–470. 4 indexed citations

Murdock, David R., Yunyun Jiang, Michael F. Wangler, et al.. (2019). Xia–Gibbs syndrome in adulthood: a case report with insight into the natural history of the condition. Molecular Case Studies. 5(3). a003608–a003608. 13 indexed citations

Sabo, Aniko, Shannon Dugan‐Perez, V. Saroja Voruganti, et al.. (2017). Exome sequencing reveals novel genetic loci influencing obesity‐related traits in Hispanic children. Obesity. 25(7). 1270–1276. 10 indexed citations

10.

Lindstrand, Anna, Stephan Frangakis, Claudia M.B. Carvalho, et al.. (2016). Copy-Number Variation Contributes to the Mutational Load of Bardet-Biedl Syndrome. The American Journal of Human Genetics. 99(2). 318–336. 91 indexed citations

11.

Davis, Erica E., Aniko Sabo, Marjan M. Weiss, et al.. (2015). A t(5;16) translocation is the likely driver of a syndrome with ambiguous genitalia, facial dysmorphism, intellectual disability, and speech delay. Molecular Case Studies. 2(2). a000703–a000703. 1 indexed citations

12.

Sheehan, Vivien, Jacy R. Crosby, Aniko Sabo, et al.. (2014). Whole Exome Sequencing Identifies Novel Genes for Fetal Hemoglobin Response to Hydroxyurea in Children with Sickle Cell Anemia. PLoS ONE. 9(10). e110740–e110740. 28 indexed citations

13.

Lindstrand, Anna, Erica E. Davis, Claudia M.B. Carvalho, et al.. (2014). Recurrent CNVs and SNVs at the NPHP1 Locus Contribute Pathogenic Alleles to Bardet-Biedl Syndrome. The American Journal of Human Genetics. 94(5). 745–754. 64 indexed citations

14.

Sheehan, Vivien, Jacy R. Crosby, Aniko Sabo, et al.. (2013). FOXO3 Variants Are Associated With Lower Fetal Hemoglobin Levels In Children With Sickle Cell Disease. Blood. 122(21). 778–778. 2 indexed citations

15.

Sheehan, Vivien, Thad A. Howard, Aniko Sabo, et al.. (2012). Genetic Predictors of Hemoglobin F Response to Hydroxyurea in Sickle Cell Anemia. Blood. 120(21). 241–241. 6 indexed citations

16.

Schaaf, Christian P., Aniko Sabo, Yasunari Sakai, et al.. (2011). Oligogenic heterozygosity in individuals with high-functioning autism spectrum disorders. Human Molecular Genetics. 20(17). 3366–3375. 111 indexed citations

17.

Gijavanekar, Charul, Feng Chen, Catherine Putonti, et al.. (2011). PCR detection of nearly any dengue virus strain using a highly sensitive primer ‘cocktail’. FEBS Journal. 278(10). 1676–1687. 13 indexed citations

18.

Xing, Jinchuan, W. Scott Watkins, Ya Hu, et al.. (2010). Genetic diversity in India and the inference of Eurasian population expansion. Genome biology. 11(11). R113–R113. 54 indexed citations

19.

Chen, Swaine L., Chia‐Suei Hung, Jian Xu, et al.. (2006). Identification of genes subject to positive selection in uropathogenic strains of Escherichia coli : A comparative genomics approach. Proceedings of the National Academy of Sciences. 103(15). 5977–5982. 441 indexed citations

20.

Sabo, Aniko, et al.. (2002). Phylogenetic relationships of a distinct species of globodera from portugal and two punctodera species.. PubMed. 34(3). 263–6. 8 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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