FF Chehab
Impact in
- Genetics top 5%
- Hemoglobinopathies and Related Disorders
- Genetic Syndromes and Imprinting
- Genomic variations and chromosomal abnormalities
- Hematology top 5%
- Iron Metabolism and Disorders
- Blood groups and transfusion
Papers in
- Genetics 8
- Hemoglobinopathies and Related Disorders 8
- Genetic Syndromes and Imprinting 1
- Neurogenetic and Muscular Disorders Research 1
-
- Iron Metabolism and Disorders 7
- Blood groups and transfusion 1
- Co-authors
- YW Kan (4 shared papers)Aurelio Maggio (2 shared papers)Antonino Giambona (1 shared paper)Jeffrey D. Wall (1 shared paper)V Der Kaloustian (1 shared paper)SS Deeb (1 shared paper)Faye A. Eggerding (1 shared paper)Victoria Cox (1 shared paper)
- Journals
- Blood (6 papers)The Lancet (1 paper)Hemoglobin (1 paper)PubMed (2 papers)
- Partner nations
- United StatesItaly
In The Last Decade
FF Chehab
9 papers receiving 388 citations
Peers
Comparison fields: 5 of 48
- Genetics 267
- Hematology 184
- Pediatrics, Perinatology and Child Health 86
- Genetics 115
- Endocrine and Autonomic Systems 16
Countries citing papers authored by FF Chehab
This map shows the geographic impact of FF Chehab'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 FF Chehab with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites FF Chehab more than expected).
Fields of papers citing papers by FF Chehab
This network shows the impact of papers produced by FF Chehab. 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 FF Chehab. The network helps show where FF Chehab may publish in the future.
Co-authors
The 12 scholars most cited alongside FF Chehab, 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 | 1993 | 148 | |
| 2 | 1987 | 95 | |
| 3 | Uniparental isodisomy for paternal 7p and maternal 7q in a child with growth retardation. | 1994 | 64 |
| 4 | 1990 | 35 | |
| 5 | 2004 | 23 | |
| 6 | 1990 | 19 | |
| 7 | 1989 | 18 | |
| 8 | 1993 | 13 | |
| 9 | 1997 | 10 | |
| 10 | 1990 | 0 |
About FF Chehab
FF Chehab is a scholar working on Genetics, Hematology, Pediatrics, Perinatology and Child Health, Molecular Biology and Endocrine and Autonomic Systems, having authored 10 papers that have together received 425 indexed citations. Recurring topics across this work include Hemoglobinopathies and Related Disorders (8 papers), Iron Metabolism and Disorders (7 papers), Prenatal Screening and Diagnostics (4 papers), Folate and B Vitamins Research (1 paper), Genetic Syndromes and Imprinting (1 paper), Neurogenetic and Muscular Disorders Research (1 paper), DNA and Nucleic Acid Chemistry (1 paper) and Blood groups and transfusion (1 paper). The work is most often cited by research in Genetics (267 citations), Hematology (184 citations), Pediatrics, Perinatology and Child Health (86 citations), Genetics (115 citations) and Endocrine and Autonomic Systems (16 citations). FF Chehab has collaborated with scholars based in United States and Italy. Frequent co-authors include YW Kan, Aurelio Maggio, Antonino Giambona, Jeffrey D. Wall, V Der Kaloustian, SS Deeb, Faye A. Eggerding, Victoria Cox, Charles J. Epstein and Mary E. Norton. Their work appears in journals such as Blood, The Lancet, Hemoglobin and PubMed.
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.