Laïla Zahed

689 total citations
20 papers, 493 citations indexed

About

Laïla Zahed is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Laïla Zahed has authored 20 papers receiving a total of 493 indexed citations (citations by other indexed papers that have themselves been cited), including 10 papers in Genetics, 4 papers in Molecular Biology and 4 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Laïla Zahed's work include Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Laïla Zahed is often cited by papers focused on Prenatal Screening and Diagnostics (4 papers), Genomic variations and chromosomal abnormalities (3 papers) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (3 papers). Laïla Zahed collaborates with scholars based in Lebanon, Canada and United States. Laïla Zahed's co-authors include Alì Taher, Wael Salameh, Éric Vilain, Stanley F. Nelson, Hane Lee, Mahmoud Choucair, Ziyad Mahfoud, Asma Arabi, Rami Mahfouz and Ghada El‐Hajj Fuleihan and has published in prestigious journals such as The Journal of Clinical Endocrinology & Metabolism, The American Journal of Human Genetics and American Journal of Obstetrics and Gynecology.

In The Last Decade

Laïla Zahed

20 papers receiving 470 citations

Peers

Laïla Zahed

GENET

HEMAT

GENET

PPCH

Cassie Keener United States

Bahadır Batar Türkiye

Ziba Rahimi Iran

Simge Erdem Türkiye

Ronald Honchel United States

Melinda Zsuzsanna Szabó Hungary

Vassiliki Kalotychou Greece

Su Q. Wang United States

Francisca Hudig Netherlands

Shiro Imai Japan

Cassie Keener United States

Laïla Zahed

53 ×0.3

GENET

59 ×0.5

HEMAT

37 ×0.3

GENET

154 ×1.4

69 ×0.9

PPCH

Citations per year, relative to Laïla Zahed Laïla Zahed (= 1×) peers Cassie Keener

Countries citing papers authored by Laïla Zahed

Since Specialization

Citations

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

Fields of papers citing papers by Laïla Zahed

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laïla Zahed

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

All Works

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20 of 20 papers shown

Fiévet, Alice, Dorine Bellanger, Laïla Zahed, et al.. (2019). DNA repair functional analyses of NBN hypomorphic variants associated with NBN‐related infertility. Human Mutation. 41(3). 608–618. 8 indexed citations

Zahed, Laïla, et al.. (2011). Pharmacogenetics of Coumarin Dosing: Prevalence of CYP2C9 and VKORC1 Polymorphisms in the Lebanese Population. Genetic Testing and Molecular Biomarkers. 15(11). 827–830. 18 indexed citations

Zahed, Laïla, et al.. (2011). Prevalence of CYP2C19 polymorphisms in the Lebanese population. Molecular Biology Reports. 38(8). 5449–5452. 31 indexed citations

Arabi, Asma, Laïla Zahed, Ziyad Mahfoud, et al.. (2009). Vitamin D receptor gene polymorphisms modulate the skeletal response to vitamin D supplementation in healthy girls. Bone. 45(6). 1091–1097. 36 indexed citations

Zahed, Laïla, et al.. (2008). Molecular and clinical description of a girl with a 46,X,t(Y;4)(q11.2;p16)/45,X,der(4)t(Y;4)(q11.2;p16) karyotype and a small cryptic 4p subtelomeric deletion. American Journal of Medical Genetics Part A. 146A(7). 893–898. 1 indexed citations

Ormond, Kelly E., et al.. (2007). Outcome of chromosomally abnormal pregnancies in Lebanon: obstetricians' roles during and after prenatal diagnosis. Prenatal Diagnosis. 27(6). 525–534. 13 indexed citations

Zahed, Laïla, Tiziano Pramparo, Chantal Farra, Mohamad A. Mikati, & Orsetta Zuffardi. (2006). A patient with duplication (7)(p22.1pter) characterized by array‐CGH. American Journal of Medical Genetics Part A. 143A(2). 168–171. 8 indexed citations

Mahfouz, Rami, Audrey Sabbagh, Laïla Zahed, et al.. (2006). Apolipoprotein E Gene Polymorphism and Allele Frequencies in the Lebanese Population. Molecular Biology Reports. 33(2). 145–149. 37 indexed citations

Arabi, Asma, et al.. (2006). Regression of Skeletal Manifestations of Hyperparathyroidism with Oral Vitamin D. The Journal of Clinical Endocrinology & Metabolism. 91(7). 2480–2483. 21 indexed citations

10.

Zahed, Laïla, et al.. (2006). Prevalence of factor V Leiden, prothrombin and methylene tetrahydrofolate reductase mutations in women with adverse pregnancy outcomes in Lebanon. American Journal of Obstetrics and Gynecology. 195(4). 1114–1118. 25 indexed citations

11.

Lee, Hane, Laïla Zahed, Mahmoud Choucair, et al.. (2006). Disruption of POF1B Binding to Nonmuscle Actin Filaments Is Associated with Premature Ovarian Failure. The American Journal of Human Genetics. 79(1). 113–119. 91 indexed citations

12.

Sawaya, Raja, Laïla Zahed, & Alì Taher. (2006). Peripheral neuropathy in thalassemia. Annals of Saudi Medicine. 26(5). 358–363. 11 indexed citations

13.

Zahed, Laïla, et al.. (2005). Molecular basis of oculocutaneous albinism type 1 in Lebanese patients. Journal of Human Genetics. 50(6). 317–319. 13 indexed citations

14.

Zahed, Laïla, et al.. (2002). Origin and History of the IVS-I-110 and Codon 39 [beta]-Thalassemia Mutations in the Lebanese Population. Human Biology. 74(6). 837–847. 19 indexed citations

15.

Zahed, Laïla. (2001). The Spectrum of β‐Thalassemia Mutations in the Arab Populations. BioMed Research International. 1(3). 129–132. 73 indexed citations

16.

Kobrynski, Lisa, David Chitayat, Laïla Zahed, et al.. (1993). Trisomy 22 and facioauriculovertebral (Goldenhar) sequence. American Journal of Medical Genetics. 46(1). 68–71. 45 indexed citations

17.

Nishioka, Yutaka, et al.. (1993). Molecular characterization of a mouse Y chromosomal repetitive sequence amplified in distantly related species in the genus Mus. Genome. 36(3). 588–593. 8 indexed citations

18.

Aubry, Muriel, Claude Marineau, Laïla Zahed, et al.. (1992). Cloning of six new genes with zinc finger motifs mapping to short and long arms of human acrocentric chromosome 22 (p and q11.2). Genomics. 13(3). 641–648. 22 indexed citations

19.

Zahed, Laïla & Michel Vekemans. (1991). Use of in Situ Hybridization in Clinical Cytogenetics. Pediatric Pathology. 11(4). 497–505. 2 indexed citations

20.

Zahed, Laïla, M. Murer‐Orlando, & Martin Bobrow. (1988). Cell cycle studies in chorionic villi. Human Genetics. 80(2). 127–134. 11 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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