L. Zahed

690 total citations
31 papers, 495 citations indexed

About

L. Zahed is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, L. Zahed has authored 31 papers receiving a total of 495 indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Genetics, 15 papers in Pediatrics, Perinatology and Child Health and 9 papers in Molecular Biology. Recurrent topics in L. Zahed's work include Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (10 papers) and Chromosomal and Genetic Variations (7 papers). L. Zahed is often cited by papers focused on Prenatal Screening and Diagnostics (15 papers), Genomic variations and chromosomal abnormalities (10 papers) and Chromosomal and Genetic Variations (7 papers). L. Zahed collaborates with scholars based in Lebanon, Canada and United Kingdom. L. Zahed's co-authors include Mona Nabulsi, M. Seoud, Ghazi Zaatari, Rima Slim, Michel Vekemans, Alì Taher, Mohammed Qatanani, Yasuhiko Nishioka, V Der Kaloustian and Hani Tamim and has published in prestigious journals such as Molecular Biology and Evolution, Obstetrics and Gynecology and Journal of Medical Genetics.

In The Last Decade

L. Zahed

30 papers receiving 461 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
L. Zahed Lebanon	14	263	219	151	97	95	31	495
M.‐J. Le Bris France	13	164 0.6×	262 1.2×	95 0.6×	102 1.1×	45 0.5×	21	422
Mahmoud Aarabi United States	11	214 0.8×	207 0.9×	68 0.5×	196 2.0×	34 0.4×	20	541
Stacy Colaco India	11	132 0.5×	183 0.8×	148 1.0×	165 1.7×	99 1.0×	21	556
G. Reza Jalali United Kingdom	13	103 0.4×	132 0.6×	210 1.4×	191 2.0×	41 0.4×	16	456
Sugandhi A. Tharapel United States	10	142 0.5×	215 1.0×	30 0.2×	83 0.9×	26 0.3×	19	337
Catarina Lundin Sweden	11	106 0.4×	98 0.4×	98 0.6×	85 0.9×	13 0.1×	17	287
Svetlana Madjunkova Canada	14	239 0.9×	152 0.7×	198 1.3×	173 1.8×	12 0.1×	33	502
Qun Fang China	15	359 1.4×	152 0.7×	26 0.2×	176 1.8×	36 0.4×	65	582
Emilia Mateu Spain	18	618 2.3×	266 1.2×	373 2.5×	172 1.8×	16 0.2×	36	860
Masood Bazrgar Iran	9	103 0.4×	67 0.3×	112 0.7×	89 0.9×	23 0.2×	26	293

Countries citing papers authored by L. Zahed

Since Specialization

Citations

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

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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-authorship network of co-authors of L. Zahed

This figure shows the co-authorship network connecting the top 25 collaborators of L. Zahed. A scholar is included among the top collaborators of L. Zahed 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 L. Zahed. L. Zahed is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

20 of 20 papers shown

Arabi, Asma, et al.. (2010). Effect of age, gender and calciotropic hormones on the relationship between vitamin D receptor gene polymorphisms and bone mineral density. European Journal of Clinical Nutrition. 64(4). 383–391. 25 indexed citations

Zahed, L., et al.. (2004). A new patient with pure trisomy 4p resulting from isochromosome formation and whole arm translocation. American Journal of Medical Genetics Part A. 128A(1). 60–62. 5 indexed citations

Salameh, Wael, Mahmoud Choucair, Taylor B. Guo, et al.. (2004). Leydig cell hypoplasia due to inactivation of luteinizing hormone receptor by a novel homozygous nonsense truncation mutation in the seventh transmembrane domain. Molecular and Cellular Endocrinology. 229(1-2). 57–64. 16 indexed citations

Zahed, L., et al.. (2004). Ring chromosome 18q and jumping translocation 18p in an adult male with hypergonadotrophic hypogonadism. American Journal of Medical Genetics Part A. 129A(1). 25–28. 10 indexed citations

Zahed, L., Mona Nabulsi, & Hani Tamim. (2002). Attitudes towards prenatal diagnosis and termination of pregnancy among health professionals in Lebanon. Prenatal Diagnosis. 22(10). 880–886. 25 indexed citations

Zahed, L., et al.. (2002). Homologous telomere association of 19q in a female with premature ovarian failure. Clinical Genetics. 62(4). 310–314. 6 indexed citations

Zahed, L., et al.. (2001). Karyotype of amniotic fluid cells at the AUB-MC results on 2000 cases.. PubMed. 48(3). 121–6. 1 indexed citations

Qatanani, Mohammed, Alì Taher, Suzanne Koussa, et al.. (2000). β‐Thalassaemia intermedia in Lebanon. European Journal Of Haematology. 64(4). 237–244. 27 indexed citations

Zahed, L., Mohammed Qatanani, Mona Nabulsi, & Alì Taher. (2000). β-Thalassemia Mutations and Haplotype Analysis in Lebanon. Hemoglobin. 24(4). 269–276. 22 indexed citations

10.

Seoud, M., et al.. (1999). A familial case of recurrent hydatidiform molar pregnancies with biparental genomic contribution. Human Genetics. 105(1-2). 112–115. 83 indexed citations

11.

Zahed, L. & André Mégarbané. (1998). A Cytogenetic Register of Down Syndrome in Lebanon. Public Health Genomics. 1(2). 84–89. 4 indexed citations

12.

Zahed, L., et al.. (1998). Familial complex chromosome rearrangement giving rise to balanced and unbalanced recombination products. American Journal of Medical Genetics. 79(1). 30–34. 20 indexed citations

13.

Zahed, L., et al.. (1997). The Spectrum of Beta-Thalassaemia Mutations in the Lebanon. Human Heredity. 47(5). 241–249. 26 indexed citations

14.

Zahed, L., et al.. (1997). ACCEPTANCE OF FIRST-TRIMESTER PRENATAL DIAGNOSIS FOR THE HAEMOGLOBINOPATHIES IN LEBANON. Prenatal Diagnosis. 17(5). 423–428. 40 indexed citations

15.

Seoud, Muhieddine, Abdelouahed Khalil, Antonio H. Frangieh, et al.. (1995). Recurrent molar pregnancies in a family with extensive intermarriage: Report of a family and review of the literature. Obstetrics and Gynecology. 86(4). 692–695. 30 indexed citations

16.

Nishioka, Yasuhiko, et al.. (1994). Molecular evolution of a Y-chromosomal repetitive sequence family in the genus Mus.. Molecular Biology and Evolution. 11(1). 146–53. 6 indexed citations

17.

Nishioka, Yasuhiko, et al.. (1993). Comparison of mouse Y-chromosomal repetitive sequences isolated from Mus musculus, M. Spicilegus, and M. spretus. Cytogenetic and Genome Research. 64(1). 54–58. 8 indexed citations

18.

Prado, Vânia F., et al.. (1992). Molecular characterization of a mouse Y chromosomal repetitive sequence that detects transcripts in the testis. Cytogenetic and Genome Research. 61(2). 87–90. 27 indexed citations

19.

Zahed, L., M. Murer‐Orlando, & Martin Bobrow. (1989). The application of automated metaphase scanning to direct preparations of chorionic villi. Prenatal Diagnosis. 9(1). 7–17. 2 indexed citations

20.

Murer‐Orlando, M., Maura McGuire, L. Zahed, et al.. (1988). Chromosome banding in direct preparations of chorionic villi. Prenatal Diagnosis. 8(6). 461–469. 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.

Explore authors with similar magnitude of impact