Monia Hammer

751 total citations
12 papers, 213 citations indexed

About

Monia Hammer is a scholar working on Molecular Biology, Cellular and Molecular Neuroscience and Neurology. According to data from OpenAlex, Monia Hammer has authored 12 papers receiving a total of 213 indexed citations (citations by other indexed papers that have themselves been cited), including 6 papers in Molecular Biology, 4 papers in Cellular and Molecular Neuroscience and 4 papers in Neurology. Recurrent topics in Monia Hammer's work include Neurological diseases and metabolism (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Mitochondrial Function and Pathology (3 papers). Monia Hammer is often cited by papers focused on Neurological diseases and metabolism (4 papers), Genetic Neurodegenerative Diseases (4 papers) and Mitochondrial Function and Pathology (3 papers). Monia Hammer collaborates with scholars based in United States, Tunisia and United Kingdom. Monia Hammer's co-authors include Rim Amouri, J. Raphael Gibbs, Fayçal Hentati, Yosr Bouhlal, Celeste Sassi, Sean Chong, Andrew B. Singleton, Anna Sailer, Huaibin Cai and Lucía Schottlaender and has published in prestigious journals such as Scientific Reports, The American Journal of Human Genetics and Alzheimer s & Dementia.

In The Last Decade

Monia Hammer

12 papers receiving 209 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Monia Hammer United States 8 111 71 67 46 43 12 213
Irene Sambri Italy 7 129 1.2× 30 0.4× 155 2.3× 23 0.5× 18 0.4× 9 285
Anneke J.A. Kievit Netherlands 10 139 1.3× 51 0.7× 103 1.5× 108 2.3× 54 1.3× 17 352
Neil Kulkarni United States 4 178 1.6× 54 0.8× 134 2.0× 105 2.3× 25 0.6× 9 306
Florian Harmuth Germany 8 120 1.1× 117 1.6× 16 0.2× 58 1.3× 52 1.2× 11 235
Chiara Reale Italy 11 121 1.1× 113 1.6× 40 0.6× 157 3.4× 87 2.0× 19 320
Shenzhao Lu United States 10 157 1.4× 38 0.5× 43 0.6× 30 0.7× 50 1.2× 16 255
Marie‐France Rioux Canada 6 140 1.3× 117 1.6× 24 0.4× 22 0.5× 48 1.1× 8 270
Taku Arano Japan 5 177 1.6× 64 0.9× 64 1.0× 152 3.3× 26 0.6× 5 314
Anna-Kaisa Anttonen Finland 3 151 1.4× 69 1.0× 128 1.9× 15 0.3× 11 0.3× 3 286

Countries citing papers authored by Monia Hammer

Since Specialization
Citations

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

Fields of papers citing papers by Monia Hammer

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Monia Hammer

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

All Works

12 of 12 papers shown
1.
Guidugli, Lucia, Monia Hammer, Anne Gregor, et al.. (2023). Novel association of Dandy–Walker malformation with CAPN15 variants expands the phenotype of oculogastrointestinal neurodevelopmental syndrome. American Journal of Medical Genetics Part A. 191(11). 2757–2767. 5 indexed citations
2.
Xiromerisiou, Georgia, Thomas Bourinaris, Henry Houlden, et al.. (2021). SORL1 mutation in a Greek family with Parkinson's disease and dementia. Annals of Clinical and Translational Neurology. 8(10). 1961–1969. 4 indexed citations
3.
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
4.
Kobayashi, Erica Sanford, Marilyn C. Jones, Matthew T. Brigger, et al.. (2020). Postmortem diagnosis of PPA2-associated sudden cardiac death from dried blood spot in a neonate presenting with vocal cord paralysis. Molecular Case Studies. 6(5). a005611–a005611. 10 indexed citations
5.
Hammer, Monia, et al.. (2019). Blepharospasm: A genetic screening study in 132 patients. Parkinsonism & Related Disorders. 64. 315–318. 13 indexed citations
6.
Hammer, Monia, Jinhui Ding, Fanny Mochel, et al.. (2017). SLC25A46 Mutations Associated with Autosomal Recessive Cerebellar Ataxia in North African Families. Neurodegenerative Diseases. 17(4-5). 208–212. 23 indexed citations
7.
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
8.
Hammer, Monia, et al.. (2013). Clinical features and molecular genetics of two Tunisian families with abetalipoproteinemia. Journal of Clinical Neuroscience. 21(2). 311–315. 8 indexed citations
9.
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
10.
Hammer, Monia, et al.. (2012). Clinical and Molecular Findings of Ataxia With Oculomotor Apraxia Type 2 (AOA2) in 5 Tunisian Families. Diagnostic Molecular Pathology. 21(4). 241–245. 6 indexed citations
11.
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
12.
Hammer, Monia, et al.. (2010). Spinal Muscular Atrophy Due to Double Gene Conversion Event. International Journal of Neuroscience. 121(2). 107–111. 3 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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