Jamal Ghoumid
Impact in
-
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Genetic and Kidney Cyst Diseases
- Genomics and Rare Diseases
Papers in
-
- Congenital heart defects research 6
- RNA modifications and cancer 6
- Renal and related cancers 4
- RNA Research and Splicing 4
- Genetics 17
- Genetics and Neurodevelopmental Disorders 7
- Genomic variations and chromosomal abnormalities 4
- Genomics and Rare Diseases 3
- Co-authors
- Sylvie Manouvrier‐Hanu (11 shared papers)Florence Petit (8 shared papers)Muriel Holder‐Espinasse (5 shared papers)Thomas Smol (17 shared papers)Anne‐Sophie Jourdain (5 shared papers)Audrey Briand‐Suleau (4 shared papers)Irina Giurgea (4 shared papers)Fabienne Escande (4 shared papers)
- Journals
- European Journal of Human Genetics (5 papers)European Journal of Medical Genetics (5 papers)Human Molecular Genetics (3 papers)Genetics in Medicine (3 papers)Frontiers in Genetics (2 papers)
- Partner nations
- FranceUnited StatesUnited Kingdom
In The Last Decade
Jamal Ghoumid
28 papers receiving 374 citations
Peers
Comparison fields: 5 of 60
- Genetics 155
- Developmental Biology 12
- Molecular Biology 200
- Nephrology 17
- Cell Biology 30
Countries citing papers authored by Jamal Ghoumid
This map shows the geographic impact of Jamal Ghoumid'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 Jamal Ghoumid with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Jamal Ghoumid more than expected).
Fields of papers citing papers by Jamal Ghoumid
This network shows the impact of papers produced by Jamal Ghoumid. 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 Jamal Ghoumid. The network helps show where Jamal Ghoumid may publish in the future.
Co-authors
The 25 scholars most cited alongside Jamal Ghoumid, 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 34 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2013 | 42 | |
| 2 | 2017 | 39 | |
| 3 | 2015 | 37 | |
| 4 | 2018 | 31 | |
| 5 | 2019 | 30 | |
| 6 | 2013 | 27 | |
| 7 | 2017 | 26 | |
| 8 | 2015 | 24 | |
| 9 | 2016 | 17 | |
| 10 | 2020 | 12 | |
| 11 | 2021 | 12 | |
| 12 | 2019 | 10 | |
| 13 | 2017 | 10 | |
| 14 | 2021 | 10 | |
| 15 | 2019 | 9 | |
| 16 | 2009 | 9 | |
| 17 | 2011 | 7 | |
| 18 | 2021 | 6 | |
| 19 | 2022 | 5 | |
| 20 | 2024 | 3 |
About Jamal Ghoumid
Jamal Ghoumid is a scholar working on Molecular Biology, Genetics, Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Surgery, having authored 34 papers that have together received 379 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (7 papers), Congenital heart defects research (6 papers), RNA modifications and cancer (6 papers), Renal and related cancers (4 papers), Genomic variations and chromosomal abnormalities (4 papers), RNA Research and Splicing (4 papers), Metabolism and Genetic Disorders (3 papers) and Genomics and Rare Diseases (3 papers). The work is most often cited by research in Genetics (155 citations), Developmental Biology (12 citations), Molecular Biology (200 citations), Nephrology (17 citations) and Cell Biology (30 citations). Jamal Ghoumid has collaborated with scholars based in France, United States and United Kingdom. Frequent co-authors include Sylvie Manouvrier‐Hanu, Florence Petit, Muriel Holder‐Espinasse, Thomas Smol, Anne‐Sophie Jourdain, Audrey Briand‐Suleau, Irina Giurgea, Fabienne Escande, Nicole Porchet and Clémence Vanlerberghe. Their work appears in journals such as European Journal of Human Genetics, European Journal of Medical Genetics, Human Molecular Genetics, Genetics in Medicine and Frontiers in 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.