Celeste Sassi

4.6k total citations
13 papers, 281 citations indexed

About

Celeste Sassi is a scholar working on Physiology, Neurology and Neurology. According to data from OpenAlex, Celeste Sassi has authored 13 papers receiving a total of 281 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Physiology, 6 papers in Neurology and 6 papers in Neurology. Recurrent topics in Celeste Sassi's work include Alzheimer's disease research and treatments (5 papers), Amyotrophic Lateral Sclerosis Research (4 papers) and Neurological diseases and metabolism (3 papers). Celeste Sassi is often cited by papers focused on Alzheimer's disease research and treatments (5 papers), Amyotrophic Lateral Sclerosis Research (4 papers) and Neurological diseases and metabolism (3 papers). Celeste Sassi collaborates with scholars based in United States, Germany and United Kingdom. Celeste Sassi's co-authors include J. Raphael Gibbs, Monia Hammer, Sean Chong, Rim Amouri, Yosr Bouhlal, Fayçal Hentati, Andrew B. Singleton, Anna Sailer, Huaibin Cai and Lucía Schottlaender and has published in prestigious journals such as PLoS ONE, Neurology and Scientific Reports.

In The Last Decade

Celeste Sassi

13 papers receiving 276 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Celeste Sassi United States	9	138	129	70	64	61	13	281
Neil Kulkarni United States	4	134 1.0×	178 1.4×	25 0.4×	54 0.8×	105 1.7×	9	306
Manuela Tan United Kingdom	10	134 1.0×	57 0.4×	72 1.0×	57 0.9×	221 3.6×	17	337
Holly Stefen Australia	10	112 0.8×	146 1.1×	74 1.1×	106 1.7×	25 0.4×	20	335
Francesco Scalabrì Italy	9	57 0.4×	227 1.8×	43 0.6×	71 1.1×	29 0.5×	11	324
Shamiram Melhem Netherlands	12	102 0.7×	113 0.9×	69 1.0×	53 0.8×	107 1.8×	16	256
Tsz Hang Wong Netherlands	10	145 1.1×	146 1.1×	70 1.0×	37 0.6×	127 2.1×	13	308
Niko-Petteri Nykänen United States	8	215 1.6×	185 1.4×	102 1.5×	91 1.4×	170 2.8×	14	436
Yefei Cai United States	5	241 1.7×	162 1.3×	201 2.9×	44 0.7×	32 0.5×	5	439
Linda Rousseau United States	7	155 1.1×	105 0.8×	82 1.2×	63 1.0×	173 2.8×	7	325
Uladzislau Rudakou Canada	9	66 0.5×	55 0.4×	41 0.6×	51 0.8×	122 2.0×	9	208

Countries citing papers authored by Celeste Sassi

Since Specialization

Citations

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

Fields of papers citing papers by Celeste Sassi

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Celeste Sassi

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

All Works

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13 of 13 papers shown

1.

Sassi, Celeste, Rosa Capozzo, Monia Hammer, et al.. (2021). Exploring dementia and neuronal ceroid lipofuscinosis genes in 100 FTD-like patients from 6 towns and rural villages on the Adriatic Sea cost of Apulia. Scientific Reports. 11(1). 6353–6353. 7 indexed citations

2.

Yildirim, Ferah, Marco Foddis, Susanne Müller, et al.. (2021). Shared and oppositely regulated transcriptomic signatures in Huntington's disease and brain ischemia confirm known and unveil novel potential neuroprotective genes. Neurobiology of Aging. 104. 122.e1–122.e17. 4 indexed citations

3.

Foddis, Marco, Susanne Müller, Manuel Holtgrewe, et al.. (2020). Investigating APOE, APP-Aβ metabolism genes and Alzheimer’s disease GWAS hits in brain small vessel ischemic disease. Scientific Reports. 10(1). 7103–7103. 14 indexed citations

4.

Foddis, Marco, Katarzyna Winek, Susanne Mueller, et al.. (2019). An exploratory investigation of brain collateral circulation plasticity after cerebral ischemia in two experimental C57BL/6 mouse models. Journal of Cerebral Blood Flow & Metabolism. 40(2). 276–287. 10 indexed citations

5.

Crespo‐Garcia, Sergio, Nadine Reichhart, Sergej Skosyrski, et al.. (2018). Individual and temporal variability of the retina after chronic bilateral common carotid artery occlusion (BCCAO). PLoS ONE. 13(3). e0193961–e0193961. 15 indexed citations

6.

Capozzo, Rosa, Celeste Sassi, Monia Hammer, et al.. (2017). Clinical and genetic analyses of familial and sporadic frontotemporal dementia patients in Southern Italy. Alzheimer s & Dementia. 13(8). 858–869. 19 indexed citations

7.

Sassi, Celeste, Rosa Capozzo, J. Raphael Gibbs, et al.. (2016). A Novel Splice-Acceptor Site Mutation in GRN (c.709-2 A>T) Causes Frontotemporal Dementia Spectrum in a Large Family from Southern Italy. Journal of Alzheimer s Disease. 53(2). 475–485. 10 indexed citations

8.

Capozzo, Rosa, Celeste Sassi, Chiara Zecca, et al.. (2015). A Novel Splice Site Mutation in GRN (p.A237fs [A>T]) in a Large Italian Family With FTD From The Apulia-FTD Registry (P2.160). Neurology. 84(14_supplement). 1 indexed citations

9.

Capozzo, Rosa, Celeste Sassi, Chiara Zecca, et al.. (2015). A Novel Splice Site Mutation in GRN (p.A237fs [A>T]) in a Large Italian Family With FTD From The Apulia-FTD Registry (P2.160). 84. 1 indexed citations

10.

Sassi, Celeste, Rita Guerreiro, J. Raphael Gibbs, et al.. (2014). Investigating the role of rare coding variability in Mendelian dementia genes ( APP , PSEN1 , PSEN2 , GRN , MAPT , and PRNP ) in late-onset Alzheimer's disease. Neurobiology of Aging. 35(12). 2881.e1–2881.e6. 55 indexed citations

11.

Sassi, Celeste, Rita Guerreiro, J. Raphael Gibbs, et al.. (2014). Exome sequencing identifies 2 novel presenilin 1 mutations (p.L166V and p.S230R) in British early-onset Alzheimer's disease. Neurobiology of Aging. 35(10). 2422.e13–2422.e16. 30 indexed citations

12.

Hammer, Monia, Lucía Schottlaender, J. Raphael Gibbs, et al.. (2013). Mutations in GBA2 Cause Autosomal-Recessive Cerebellar Ataxia with Spasticity. The American Journal of Human Genetics. 92(2). 245–251. 93 indexed citations

13.

Hammer, Monia, J. Raphael Gibbs, Sean Chong, et al.. (2012). Exome sequencing: an efficient diagnostic tool for complex neurodegenerative disorders. European Journal of Neurology. 20(3). 486–492. 22 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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