Chantal Farra

483 total citations
38 papers, 341 citations indexed

About

Chantal Farra is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Chantal Farra has authored 38 papers receiving a total of 341 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Genetics, 10 papers in Molecular Biology and 8 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Chantal Farra's work include Hemoglobinopathies and Related Disorders (6 papers), Cystic Fibrosis Research Advances (5 papers) and Prenatal Screening and Diagnostics (5 papers). Chantal Farra is often cited by papers focused on Hemoglobinopathies and Related Disorders (6 papers), Cystic Fibrosis Research Advances (5 papers) and Prenatal Screening and Diagnostics (5 papers). Chantal Farra collaborates with scholars based in Lebanon, United States and France. Chantal Farra's co-authors include Johnny Awwad, Pascale Salameh, Khalid Yunis, Nadine Yazbeck, Pablo Lapunzina, José A. Caparrós‐Martín, Víctor L. Ruiz‐Pérez, Mona Aglan, Samar Muwakkit and Miguel R. Abboud and has published in prestigious journals such as SHILAP Revista de lepidopterología, Blood and Human Reproduction.

In The Last Decade

Chantal Farra

36 papers receiving 325 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name h Career Trend Papers Cites
Chantal Farra Lebanon 12 127 93 75 74 71 38 341
Celia D. Delozier United States 9 154 1.2× 81 0.9× 65 0.9× 23 0.3× 90 1.3× 14 312
A. Romeu Spain 14 44 0.3× 95 1.0× 70 0.9× 46 0.6× 69 1.0× 29 568
R RUNIC United States 8 46 0.4× 74 0.8× 38 0.5× 22 0.3× 104 1.5× 13 488
Rabea Wagener Germany 8 57 0.4× 22 0.2× 21 0.3× 36 0.5× 64 0.9× 26 236
Eva Svarch Cuba 10 49 0.4× 61 0.7× 104 1.4× 118 1.6× 69 1.0× 46 257
Akiou Okumura Japan 10 50 0.4× 41 0.4× 13 0.2× 11 0.1× 41 0.6× 38 312
Frank Meloni United States 10 37 0.3× 20 0.2× 139 1.9× 98 1.3× 50 0.7× 17 370
F. C. de Waal Netherlands 9 26 0.2× 34 0.4× 124 1.7× 39 0.5× 130 1.8× 23 332
Hagit Daum Israel 12 141 1.1× 172 1.8× 9 0.1× 11 0.1× 87 1.2× 39 420
Lauren Weintraub United States 11 52 0.4× 25 0.3× 17 0.2× 40 0.5× 118 1.7× 28 408

Countries citing papers authored by Chantal Farra

Since Specialization
Citations

This map shows the geographic impact of Chantal Farra'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 Chantal Farra with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Chantal Farra more than expected).

Fields of papers citing papers by Chantal Farra

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Chantal Farra. 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 Chantal Farra. The network helps show where Chantal Farra may publish in the future.

Co-authorship network of co-authors of Chantal Farra

This figure shows the co-authorship network connecting the top 25 collaborators of Chantal Farra. A scholar is included among the top collaborators of Chantal Farra based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with Chantal Farra. Chantal Farra is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

20 of 20 papers shown
1.
Yammine, Tony, et al.. (2023). Novel SCN9A variant associated with congenital insensitivity to pain. Molecular Biology Reports. 50(7). 6293–6298. 1 indexed citations
2.
Massaad, Elie, et al.. (2022). FISH analyses for 1p and 19q status on gliomas: Reporting an 8 years' experience from a tertiary care center in the Middle East. Annals of Diagnostic Pathology. 57. 151899–151899. 4 indexed citations
3.
Farra, Chantal, Raafat Alameddine, Johnny Awwad, et al.. (2019). BRCA mutation screening and patterns among high-risk Lebanese subjects. Hereditary Cancer in Clinical Practice. 17(1). 4–4. 16 indexed citations
4.
Massaad, Elie, Hala Tfayli, Johnny Awwad, Mona Nabulsi, & Chantal Farra. (2018). Char Syndrome a novel mutation and new insights: A clinical report. European Journal of Medical Genetics. 62(12). 103607–103607. 1 indexed citations
5.
Farra, Chantal, et al.. (2017). A novel cystic fibrosis gene mutation c.2490insT in a Palestinian patient: A case report and review of the literature. Annals of Thoracic Medicine. 12(4). 290–290. 1 indexed citations
6.
Farra, Chantal, et al.. (2015). Incidence of Alpha-Globin Gene Defect in the Lebanese Population: A Pilot Study. BioMed Research International. 2015. 1–3. 8 indexed citations
7.
Valencia, Eulalia, et al.. (2015). Ellis-van Creveld Syndrome: Mutations Uncovered in Lebanese Families. SHILAP Revista de lepidopterología. 2015. 1–4. 2 indexed citations
8.
Al‐Haddad, Christiane, et al.. (2014). Genotype/Phenotype Correlation in Primary Congenital Glaucoma Patients in the Lebanese Population: A Pilot Study. Ophthalmic Genetics. 37(1). 1–6. 20 indexed citations
9.
Caparrós‐Martín, José A., Eulalia Valencia, Verónica Pulido, et al.. (2013). Clinical and molecular analysis in families with autosomal recessive osteogenesis imperfecta identifies mutations in five genes and suggests genotype–phenotype correlations. American Journal of Medical Genetics Part A. 161(6). 1354–1369. 46 indexed citations
10.
Awwad, Johnny, et al.. (2013). Idiopathic premature ovarian failure: What is the most suitable ovarian stimulation protocol?. Scopus. 2 indexed citations
11.
Boulos, Fouad, Chantal Farra, Ayman Tawil, et al.. (2013). Changing frequency of equivocal HER-2/neu scores and factors predictive of negative HER 2/neu fluorescent in situ hybridisation in invasive carcinomas of the breast. Journal of Clinical Pathology. 67(3). 204–209.
12.
Awwad, Johnny, et al.. (2012). An investigational ovarian stimulation protocol increased significantly the psychological burden in women with premature ovarian failure. Acta Obstetricia Et Gynecologica Scandinavica. 91(11). 1273–1278. 2 indexed citations
13.
Awwad, Johnny, et al.. (2012). Fever in women may interfere with follicular development during controlled ovarian stimulation. International Journal of Hyperthermia. 28(8). 742–746. 8 indexed citations
14.
Muwakkit, Samar, Raya Saab, Rami Mahfouz, et al.. (2012). Implementation of an intensive risk‐stratified treatment protocol for children and adolescents with acute lymphoblastic leukemia in Lebanon. American Journal of Hematology. 87(7). 678–683. 14 indexed citations
15.
Farra, Chantal, et al.. (2012). Genetics of autoimmune thyroid disease in the Lebanese population. Journal of Community Genetics. 3(4). 259–264. 12 indexed citations
16.
Charafeddine, Khalil M., et al.. (2010). Essential thrombocythemia with myelofibrosis transformed into acute myeloid leukemia with der(1;15)(q10;q10): case report and literature review. Cancer Genetics and Cytogenetics. 200(1). 28–33. 1 indexed citations
17.
Farra, Chantal, Rita Menassa, Johnny Awwad, et al.. (2010). Mutational spectrum of cystic fibrosis in the Lebanese population. Journal of Cystic Fibrosis. 9(6). 406–410. 36 indexed citations
18.
Abboud, Miguel R., et al.. (2008). Familial infantile pyknocytosis in association with pulmonary hypertension. Pediatric Blood & Cancer. 51(2). 290–292. 7 indexed citations
19.
Farra, Chantal, et al.. (2008). Acceptance of preimplantation genetic diagnosis for β‐thalassemia in Lebanese women with previously affected children. Prenatal Diagnosis. 28(9). 828–832. 16 indexed citations
20.
Farra, Chantal, et al.. (2008). Cystic fibrosis: A new mutation in the Lebanese population. Journal of Cystic Fibrosis. 7(5). 429–432. 5 indexed citations

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.

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