Moneef Shoukier
Impact in
Papers in
- Genetics 14
- Genomic variations and chromosomal abnormalities 10
- Genetics and Neurodevelopmental Disorders 6
- Genomics and Rare Diseases 4
- Vascular Anomalies and Treatments 2
- Co-authors
- Leila Chaieb (3 shared papers)Walter Paulus (3 shared papers)Vera Moliadze (3 shared papers)Andrea Antal (3 shared papers)Csaba Poreisz (2 shared papers)Katia Karina Monte-Silva (1 shared paper)Iris Bartels (9 shared papers)Nivethida Thirugnanasambandam (2 shared papers)
- Journals
- Clinical Genetics (4 papers)Neuropediatrics (2 papers)Brain (2 papers)Journal of Medical Genetics (2 papers)Cytogenetic and Genome Research (2 papers)
- Partner nations
- GermanyUnited StatesPoland
In The Last Decade
Moneef Shoukier
42 papers receiving 1.1k citations
Peers
Comparison fields: 5 of 71
- Neurology 216
- Genetics 341
- Cellular and Molecular Neuroscience 181
- Genetics 71
- Developmental Neuroscience 26
Countries citing papers authored by Moneef Shoukier
This map shows the geographic impact of Moneef Shoukier'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 Moneef Shoukier with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Moneef Shoukier more than expected).
Fields of papers citing papers by Moneef Shoukier
This network shows the impact of papers produced by Moneef Shoukier. 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 Moneef Shoukier. The network helps show where Moneef Shoukier may publish in the future.
Co-authors
The 25 scholars most cited alongside Moneef Shoukier, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 42 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 207 | |
| 2 | 2011 | 110 | |
| 3 | 2010 | 103 | |
| 4 | 2018 | 89 | |
| 5 | 2008 | 75 | |
| 6 | 2021 | 65 | |
| 7 | 2012 | 59 | |
| 8 | 2010 | 40 | |
| 9 | 2010 | 34 | |
| 10 | 2013 | 34 | |
| 11 | 2018 | 25 | |
| 12 | 2018 | 25 | |
| 13 | 2011 | 24 | |
| 14 | 2011 | 21 | |
| 15 | 2013 | 19 | |
| 16 | 2010 | 19 | |
| 17 | 2020 | 19 | |
| 18 | 2013 | 15 | |
| 19 | 2012 | 15 | |
| 20 | 2011 | 14 |
About Moneef Shoukier
Moneef Shoukier is a scholar working on Genetics, Neurology, Cellular and Molecular Neuroscience, Genetics and Molecular Biology, having authored 42 papers that have together received 1.1k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (10 papers), Genetics and Neurodevelopmental Disorders (6 papers), Genomics and Rare Diseases (4 papers), Congenital heart defects research (4 papers), Hereditary Neurological Disorders (3 papers), Immunodeficiency and Autoimmune Disorders (2 papers), Vascular Anomalies and Treatments (2 papers) and RNA modifications and cancer (2 papers). The work is most often cited by research in Neurology (216 citations), Genetics (341 citations), Cellular and Molecular Neuroscience (181 citations), Genetics (71 citations) and Developmental Neuroscience (26 citations). Moneef Shoukier has collaborated with scholars based in Germany, United States and Poland. Frequent co-authors include Leila Chaieb, Walter Paulus, Vera Moliadze, Andrea Antal, Csaba Poreisz, Katia Karina Monte-Silva, Iris Bartels, Nivethida Thirugnanasambandam, Harald Ludwig and Michael Andreas Nitsche. Their work appears in journals such as Clinical Genetics, Neuropediatrics, Brain, Journal of Medical Genetics and Cytogenetic and Genome Research.
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.