L. Zahed
Impact in
-
- Prenatal Screening and Diagnostics
- Genetics top 10%
- Hemoglobinopathies and Related Disorders
- Genomic variations and chromosomal abnormalities
- Genetic Syndromes and Imprinting
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
Papers in
- Genetics 17
- Genomic variations and chromosomal abnormalities 10
- Hemoglobinopathies and Related Disorders 4
-
- Prenatal Screening and Diagnostics 15
- Ethics and Legal Issues in Pediatric Healthcare 3
- Co-authors
- Mona Nabulsi (4 shared papers)M. Seoud (2 shared papers)Ghazi Zaatari (2 shared papers)Rima Slim (2 shared papers)Michel Vekemans (3 shared papers)Alì Taher (2 shared papers)Mohammed Qatanani (2 shared papers)Yasuhiko Nishioka (3 shared papers)
- Journals
- Prenatal Diagnosis (7 papers)Human Genetics (2 papers)Cytogenetic and Genome Research (2 papers)European Journal of Clinical Nutrition (1 paper)Journal of Medical Genetics (1 paper)
- Partner nations
- LebanonCanadaUnited Kingdom
In The Last Decade
L. Zahed
30 papers receiving 461 citations
Peers
Comparison fields: 5 of 52
- Pediatrics, Perinatology and Child Health 263
- Genetics 95
- Genetics 219
- Hematology 76
- Reproductive Medicine 49
Countries citing papers authored by L. Zahed
This map shows the geographic impact of L. Zahed'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 L. Zahed with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites L. Zahed more than expected).
Fields of papers citing papers by L. Zahed
This network shows the impact of papers produced by L. Zahed. 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 L. Zahed. The network helps show where L. Zahed may publish in the future.
Co-authors
The 25 scholars most cited alongside L. Zahed, 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 31 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1999 | 83 | |
| 2 | 1997 | 40 | |
| 3 | 1995 | 30 | |
| 4 | 1999 | 29 | |
| 5 | 2000 | 27 | |
| 6 | 1992 | 27 | |
| 7 | 1997 | 26 | |
| 8 | 2002 | 25 | |
| 9 | 2010 | 25 | |
| 10 | 1999 | 25 | |
| 11 | 2001 | 24 | |
| 12 | 2000 | 22 | |
| 13 | 1998 | 20 | |
| 14 | 2004 | 16 | |
| 15 | 1992 | 13 | |
| 16 | 2004 | 10 | |
| 17 | 1993 | 8 | |
| 18 | 1994 | 6 | |
| 19 | 2002 | 6 | |
| 20 | 1989 | 6 |
About L. Zahed
L. Zahed is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Plant Science and Genetics, having authored 31 papers that have together received 495 indexed citations. Recurring topics across this work include Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (10 papers), Chromosomal and Genetic Variations (7 papers), Hemoglobinopathies and Related Disorders (4 papers), Ethics and Legal Issues in Pediatric Healthcare (3 papers), Iron Metabolism and Disorders (3 papers), Gestational Trophoblastic Disease Studies (3 papers) and Congenital Anomalies and Fetal Surgery (3 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (263 citations), Genetics (95 citations), Genetics (219 citations), Hematology (76 citations) and Reproductive Medicine (49 citations). L. Zahed has collaborated with scholars based in Lebanon, Canada and United Kingdom. Frequent co-authors include Mona Nabulsi, M. Seoud, Ghazi Zaatari, Rima Slim, Michel Vekemans, Alì Taher, Mohammed Qatanani, Yasuhiko Nishioka, Julie M. Old and V Der Kaloustian. Their work appears in journals such as Prenatal Diagnosis, Human Genetics, Cytogenetic and Genome Research, European Journal of Clinical Nutrition and Journal of Medical 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.