Anna Szekely

9.6k total citations · 1 hit paper
22 papers, 2.3k citations indexed

About

Anna Szekely is a scholar working on Molecular Biology, Genetics and Cancer Research. According to data from OpenAlex, Anna Szekely has authored 22 papers receiving a total of 2.3k indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Molecular Biology, 5 papers in Genetics and 5 papers in Cancer Research. Recurrent topics in Anna Szekely's work include Pluripotent Stem Cells Research (5 papers), CRISPR and Genetic Engineering (4 papers) and Single-cell and spatial transcriptomics (3 papers). Anna Szekely is often cited by papers focused on Pluripotent Stem Cells Research (5 papers), CRISPR and Genetic Engineering (4 papers) and Single-cell and spatial transcriptomics (3 papers). Anna Szekely collaborates with scholars based in United States, Qatar and United Kingdom. Anna Szekely's co-authors include Flora M. Vaccarino, Dean Palejev, Livia Tomasini, Jessica Mariani, Sherman M. Weissman, Gianfilippo Coppola, Mark Gerstein, Alexej Abyzov, Michael Wilson and Katarzyna Chawarska and has published in prestigious journals such as Nature, Science and Cell.

In The Last Decade

Anna Szekely

22 papers receiving 2.2k citations

Hit Papers

align trajectories sort by overperformance

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.

FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders

2015 767 citations Jessica Mariani, Gianfilippo Coppola et al. Cell profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Anna Szekely United States	14	1.8k	470	326	318	293	22	2.3k
Livia Tomasini United States	12	1.5k 0.9×	585 1.2×	332 1.0×	311 1.0×	275 0.9×	16	2.1k
Jessica Mariani United States	12	1.9k 1.1×	534 1.1×	425 1.3×	351 1.1×	545 1.9×	22	2.4k
Dean Palejev United States	10	1.3k 0.7×	336 0.7×	308 0.9×	325 1.0×	287 1.0×	18	1.8k
Steven D. Sheridan United States	22	1.5k 0.9×	736 1.6×	356 1.1×	167 0.5×	245 0.8×	43	2.6k
Nissim Ben‐Arie Israel	20	1.7k 0.9×	348 0.7×	624 1.9×	210 0.7×	409 1.4×	29	3.0k
Cleber A. Trujillo United States	25	1.3k 0.8×	375 0.8×	581 1.8×	356 1.1×	355 1.2×	47	2.1k
Cassiano Carromeu United States	16	1.4k 0.8×	562 1.2×	488 1.5×	228 0.7×	275 0.9×	28	2.0k
Apuã C.M. Paquola United States	18	1.6k 0.9×	298 0.6×	375 1.2×	153 0.5×	263 0.9×	27	2.0k
Alex M. Sykes Australia	14	1.3k 0.7×	204 0.4×	473 1.5×	205 0.6×	500 1.7×	31	2.0k
Le Sun China	14	1.2k 0.7×	194 0.4×	253 0.8×	213 0.7×	357 1.2×	22	1.6k

Countries citing papers authored by Anna Szekely

Since Specialization

Citations

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

Fields of papers citing papers by Anna Szekely

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Anna Szekely

This figure shows the co-authorship network connecting the top 25 collaborators of Anna Szekely. A scholar is included among the top collaborators of Anna Szekely 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 Anna Szekely. Anna Szekely 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

Jang, Yeongjun, Liana Fasching, Taejeong Bae, et al.. (2023). Efficient reconstruction of cell lineage trees for cell ancestry and cancer. Nucleic Acids Research. 51(10). e57–e57. 1 indexed citations

Mariani, Jessica, Anna Szekely, Robert A. King, et al.. (2022). Mispatterning and interneuron deficit in Tourette Syndrome basal ganglia organoids. Molecular Psychiatry. 27(12). 5007–5019. 11 indexed citations

Mariani, Jessica, Anna Szekely, Robert A. King, et al.. (2022). Characterization of human basal ganglia organoids. Molecular Psychiatry. 27(12). 4823–4823. 1 indexed citations

Quraishi, Imran H., Anna Szekely, Anushree C. Shirali, Pramod K. Mistry, & Lawrence J. Hirsch. (2021). Miglustat Therapy for SCARB2 -Associated Action Myoclonus–Renal Failure Syndrome. Neurology Genetics. 7(5). e614–e614. 7 indexed citations

Fasching, Liana, Yeongjun Jang, Simone Tomasi, et al.. (2021). Early developmental asymmetries in cell lineage trees in living individuals. Science. 371(6535). 1245–1248. 35 indexed citations

Schaefer, Sara M., Anna Szekely, Jeremy J. Moeller, & Sule Tinaz. (2018). Hereditary spastic paraplegia presenting as limb dystonia with a rare SPG7 mutation. Neurology Clinical Practice. 8(6). e49–e50. 7 indexed citations

Mariani, Jessica, Gianfilippo Coppola, Ping Zhang, et al.. (2015). FOXG1-Dependent Dysregulation of GABA/Glutamate Neuron Differentiation in Autism Spectrum Disorders. Cell. 162(2). 375–390. 767 indexed citations breakdown →

Moghimi, Narges, Bahman Jabbari, & Anna Szekely. (2013). Primary dystonias and genetic disorders with dystonia as clinical feature of the disease. European Journal of Paediatric Neurology. 18(1). 79–105. 11 indexed citations

Zhang, Ying, Vincent Schulz, Brian D. Reed, et al.. (2013). Functional genomic screen of human stem cell differentiation reveals pathways involved in neurodevelopment and neurodegeneration. Proceedings of the National Academy of Sciences. 110(30). 12361–12366. 20 indexed citations

10.

Charos, Alexandra, Brian D. Reed, Debasish Raha, et al.. (2012). A highly integrated and complex PPARGC1A transcription factor binding network in HepG2 cells. Genome Research. 22(9). 1668–1679. 63 indexed citations

11.

Abyzov, Alexej, Jessica Mariani, Dean Palejev, et al.. (2012). Somatic copy number mosaicism in human skin revealed by induced pluripotent stem cells. Nature. 492(7429). 438–442. 270 indexed citations

12.

Mariani, Jessica, Maria Vittoria Simonini, Dean Palejev, et al.. (2012). Modeling human cortical development in vitro using induced pluripotent stem cells. Proceedings of the National Academy of Sciences. 109(31). 12770–12775. 378 indexed citations

13.

Vaccarino, Flora M., Hanna E. Stevens, Arif Kocabas, et al.. (2011). Induced pluripotent stem cells: A new tool to confront the challenge of neuropsychiatric disorders. Neuropharmacology. 60(7-8). 1355–1363. 32 indexed citations

14.

Vaccarino, Flora M., Alexander E. Urban, Hanna E. Stevens, et al.. (2011). Annual Research Review: The promise of stem cell research for neuropsychiatric disorders. Journal of Child Psychology and Psychiatry. 52(4). 504–516. 29 indexed citations

15.

Wu, Jia Qian, Lukas Habegger, Parinya Noisa, et al.. (2010). Dynamic transcriptomes during neural differentiation of human embryonic stem cells revealed by short, long, and paired-end sequencing. Proceedings of the National Academy of Sciences. 107(11). 5254–5259. 150 indexed citations

16.

Reed, Brian D., Alexandra Charos, Anna Szekely, Sherman M. Weissman, & M Snyder. (2008). Genome-Wide Occupancy of SREBP1 and Its Partners NFY and SP1 Reveals Novel Functional Roles and Combinatorial Regulation of Distinct Classes of Genes. PLoS Genetics. 4(7). e1000133–e1000133. 172 indexed citations

17.

Héjjas, Krisztina, Judit Vas, József Topál, et al.. (2007). Association of polymorphisms in the dopamine D4 receptor gene and the activity‐impulsivity endophenotype in dogs. Animal Genetics. 38(6). 629–633. 83 indexed citations

18.

Li, Peining, Manjunath Nimmakayalu, Mazin Β. Qumsiyeh, et al.. (2006). Karyotype–phenotype insights from 11q14.1‐q23.2 interstitial deletions:FZD4haploinsufficiency and exudative vitreoretinopathy in a patient with a complex chromosome rearrangement. American Journal of Medical Genetics Part A. 140A(24). 2721–2729. 26 indexed citations

19.

Szekely, Anna, Franziska Bleichert, Astrid Nümann, et al.. (2005). Werner Protein Protects Nonproliferating Cells from Oxidative DNA Damage. Molecular and Cellular Biology. 25(23). 10492–10506. 80 indexed citations

20.

Szekely, Anna, et al.. (2000). Werner protein recruits DNA polymerase δ to the nucleolus. Proceedings of the National Academy of Sciences. 97(21). 11365–11370. 102 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