Dima El‐Khechen
Impact in
- Genetics top 10%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
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- Autism Spectrum Disorder Research
Papers in
- Genetics 8
- Genomics and Rare Diseases 6
- Genomic variations and chromosomal abnormalities 4
- Genetics and Neurodevelopmental Disorders 1
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- Congenital heart defects research 2
- Hedgehog Signaling Pathway Studies 1
- Co-authors
- Kelly D. Farwell Hagman (5 shared papers)Sha Tang (4 shared papers)Mari Rossi (3 shared papers)Zöe Powis (3 shared papers)Mary Helen Black (1 shared paper)Deepali N. Shinde (2 shared papers)Kelly Radtke (2 shared papers)Erica D. Smith (2 shared papers)
- Journals
- Genetics in Medicine (2 papers)European Journal of Medical Genetics (1 paper)Neurology (1 paper)Pediatric Neurology (1 paper)European Journal of Human Genetics (1 paper)
- Partner nations
- United StatesIsraelAustralia
In The Last Decade
Dima El‐Khechen
10 papers receiving 300 citations
Peers
Comparison fields: 5 of 43
- Genetics 191
- Cognitive Neuroscience 42
- Molecular Biology 105
- Reproductive Medicine 11
- Pediatrics, Perinatology and Child Health 22
Countries citing papers authored by Dima El‐Khechen
This map shows the geographic impact of Dima El‐Khechen'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 Dima El‐Khechen with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Dima El‐Khechen more than expected).
Fields of papers citing papers by Dima El‐Khechen
This network shows the impact of papers produced by Dima El‐Khechen. 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 Dima El‐Khechen. The network helps show where Dima El‐Khechen may publish in the future.
Co-authors
The 25 scholars most cited alongside Dima El‐Khechen, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 73 | |
| 2 | 2017 | 64 | |
| 3 | 2012 | 45 | |
| 4 | 2016 | 35 | |
| 5 | 2010 | 27 | |
| 6 | 2009 | 17 | |
| 7 | 2018 | 14 | |
| 8 | 2015 | 12 | |
| 9 | 2010 | 8 | |
| 10 | 2021 | 7 |
About Dima El‐Khechen
Dima El‐Khechen is a scholar working on Genetics, Molecular Biology, Pathology and Forensic Medicine, Cellular and Molecular Neuroscience and Surgery, having authored 10 papers that have together received 302 indexed citations. Recurring topics across this work include Genomics and Rare Diseases (6 papers), Genomic variations and chromosomal abnormalities (4 papers), Genetic factors in colorectal cancer (2 papers), Congenital heart defects research (2 papers), Genetics and Neurodevelopmental Disorders (1 paper), Congenital Anomalies and Fetal Surgery (1 paper), Hedgehog Signaling Pathway Studies (1 paper) and Prenatal Screening and Diagnostics (1 paper). The work is most often cited by research in Genetics (191 citations), Cognitive Neuroscience (42 citations), Molecular Biology (105 citations), Reproductive Medicine (11 citations) and Pediatrics, Perinatology and Child Health (22 citations). Dima El‐Khechen has collaborated with scholars based in United States, Israel and Australia. Frequent co-authors include Kelly D. Farwell Hagman, Sha Tang, Mari Rossi, Zöe Powis, Mary Helen Black, Deepali N. Shinde, Kelly Radtke, Erica D. Smith, Katherine L. Helbig and Luis Escobar. Their work appears in journals such as Genetics in Medicine, European Journal of Medical Genetics, Neurology, Pediatric Neurology and European Journal of Human Genetics.
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.