Fahed Halal
Impact in
- Developmental Biology top 5%
- Congenital limb and hand anomalies
- Genetics top 5%
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Genomics and Rare Diseases
- Genetic Syndromes and Imprinting
- Craniofacial Disorders and Treatments
Papers in
- Genetics 21
- Neurogenetic and Muscular Disorders Research 4
- Congenital Ear and Nasal Anomalies 4
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- Congenital heart defects research 4
- Protein Tyrosine Phosphatases 3
- Co-authors
- John M. Opitz (16 shared papers)F. Clarke Fraser (2 shared papers)John M. Optiz (1 shared paper)Vazken M. Der Kaloustian (4 shared papers)James F. Reynolds (5 shared papers)Stephen R. Williams (1 shared paper)Gordon C. Gowans (1 shared paper)R. Ellen Magenis (1 shared paper)
- Journals
- American Journal of Medical Genetics (37 papers)Archives of Disease in Childhood (1 paper)European Journal of Human Genetics (1 paper)PEDIATRICS (1 paper)The American Journal of Human Genetics (1 paper)
- Partner nations
- CanadaUnited StatesGermany
In The Last Decade
Fahed Halal
49 papers receiving 1.2k citations
Peers
Comparison fields: 5 of 90
- Developmental Biology 87
- Genetics 591
- Genetics 109
- Urology 57
- Pediatrics, Perinatology and Child Health 162
Countries citing papers authored by Fahed Halal
This map shows the geographic impact of Fahed Halal'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 Fahed Halal with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Fahed Halal more than expected).
Fields of papers citing papers by Fahed Halal
This network shows the impact of papers produced by Fahed Halal. 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 Fahed Halal. The network helps show where Fahed Halal may publish in the future.
Co-authors
The 25 scholars most cited alongside Fahed Halal, 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 51 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2010 | 233 | |
| 2 | 1980 | 193 | |
| 3 | 1989 | 67 | |
| 4 | 1983 | 64 | |
| 5 | 2013 | 62 | |
| 6 | 1984 | 47 | |
| 7 | 1978 | 46 | |
| 8 | 1983 | 34 | |
| 9 | 1982 | 34 | |
| 10 | 1980 | 32 | |
| 11 | 1988 | 31 | |
| 12 | 1991 | 30 | |
| 13 | 1986 | 30 | |
| 14 | 1981 | 28 | |
| 15 | 1979 | 25 | |
| 16 | 1978 | 25 | |
| 17 | 1983 | 21 | |
| 18 | 1979 | 20 | |
| 19 | Severe disseminated lung disease and bronchiectasis probably due to Mycoplasma pneumoniae. | 1977 | 20 |
| 20 | 1990 | 19 |
About Fahed Halal
Fahed Halal is a scholar working on Genetics, Molecular Biology, Developmental Biology, Surgery and Urology, having authored 51 papers that have together received 1.3k indexed citations. Recurring topics across this work include Congenital limb and hand anomalies (11 papers), Urological Disorders and Treatments (8 papers), Congenital heart defects research (4 papers), Neurogenetic and Muscular Disorders Research (4 papers), Congenital Ear and Nasal Anomalies (4 papers), Protein Tyrosine Phosphatases (3 papers), Congenital Anomalies and Fetal Surgery (3 papers) and Prenatal Screening and Diagnostics (3 papers). The work is most often cited by research in Developmental Biology (87 citations), Genetics (591 citations), Genetics (109 citations), Urology (57 citations) and Pediatrics, Perinatology and Child Health (162 citations). Fahed Halal has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include John M. Opitz, F. Clarke Fraser, John M. Optiz, Vazken M. Der Kaloustian, James F. Reynolds, Stephen R. Williams, Gordon C. Gowans, R. Ellen Magenis, Micheala A. Aldred and Sarah H. Elsea. Their work appears in journals such as American Journal of Medical Genetics, Archives of Disease in Childhood, European Journal of Human Genetics, PEDIATRICS and The American 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.