Nadine Jalkh

1.4k total citations
38 papers, 751 citations indexed

About

Nadine Jalkh is a scholar working on Molecular Biology, Genetics and Surgery. According to data from OpenAlex, Nadine Jalkh has authored 38 papers receiving a total of 751 indexed citations (citations by other indexed papers that have themselves been cited), including 23 papers in Molecular Biology, 21 papers in Genetics and 6 papers in Surgery. Recurrent topics in Nadine Jalkh's work include RNA regulation and disease (6 papers), BRCA gene mutations in cancer (5 papers) and Genomics and Rare Diseases (4 papers). Nadine Jalkh is often cited by papers focused on RNA regulation and disease (6 papers), BRCA gene mutations in cancer (5 papers) and Genomics and Rare Diseases (4 papers). Nadine Jalkh collaborates with scholars based in Lebanon, France and United States. Nadine Jalkh's co-authors include Éliane Chouery, André Mégarbané, Valérie Delague, Nabiha Salem, Myrna Medlej‐Hashim, Joelle Abou Ghoch, Sandra Corbani, Diana Rodriguez, Odile Boespflug‐Tanguy and Martin Teichmann and has published in prestigious journals such as Journal of Clinical Oncology, The American Journal of Human Genetics and Journal of Medical Genetics.

In The Last Decade

Nadine Jalkh

36 papers receiving 738 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Nadine Jalkh Lebanon 13 541 238 96 90 51 38 751
Zeynep Coban‐Akdemir United States 18 544 1.0× 396 1.7× 131 1.4× 86 1.0× 48 0.9× 50 965
Jason A. Watts United States 12 862 1.6× 144 0.6× 67 0.7× 87 1.0× 29 0.6× 21 1.0k
Hiroki Ura Japan 12 849 1.6× 160 0.7× 55 0.6× 123 1.4× 40 0.8× 40 989
Joseph A. Wamstad United States 10 1.1k 2.1× 223 0.9× 56 0.6× 132 1.5× 27 0.5× 10 1.3k
Yeran Yang China 13 457 0.8× 80 0.3× 61 0.6× 150 1.7× 27 0.5× 39 622
Alan Lap‐Yin Pang United States 15 349 0.6× 133 0.6× 51 0.5× 161 1.8× 29 0.6× 19 599
Faith H. Barnett United States 11 369 0.7× 304 1.3× 55 0.6× 62 0.7× 31 0.6× 13 665
Christine Vignon France 12 482 0.9× 246 1.0× 53 0.6× 90 1.0× 13 0.3× 24 910
Fulya Taylan Sweden 16 346 0.6× 267 1.1× 60 0.6× 82 0.9× 15 0.3× 43 618
Jens Böse Germany 8 714 1.3× 187 0.8× 87 0.9× 54 0.6× 32 0.6× 8 839

Countries citing papers authored by Nadine Jalkh

Since Specialization
Citations

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

Fields of papers citing papers by Nadine Jalkh

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Nadine Jalkh

This figure shows the co-authorship network connecting the top 25 collaborators of Nadine Jalkh. A scholar is included among the top collaborators of Nadine Jalkh 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 Nadine Jalkh. Nadine Jalkh 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.
Kourié, Hampig Raphaël, Éliane Chouery, Cybel Mehawej, et al.. (2023). Genetic Polymorphisms Involved in Bladder Cancer: A Global Review. Oncology Reviews. 17. 10603–10603. 3 indexed citations
2.
Kourié, Hampig Raphaël, Nadine Jalkh, Cybel Mehawej, et al.. (2021). Molecular profiling of basal cell carcinomas in young patients. BMC Medical Genomics. 14(1). 187–187. 6 indexed citations
3.
4.
Mehawej, Cybel, et al.. (2020). A homozygous stop gain mutation in BOD1 gene in a Lebanese patient with syndromic intellectual disability. Clinical Genetics. 98(3). 288–292. 4 indexed citations
5.
Jalkh, Nadine, Cybel Mehawej, & Éliane Chouery. (2020). Actionable Exomic Secondary Findings in 280 Lebanese Participants. Frontiers in Genetics. 11. 208–208. 13 indexed citations
6.
Gutierrez‐Rodrigues, Fernanda, Éliane Chouery, Nadine Jalkh, et al.. (2019). A novel homozygous RTEL1 variant in a consanguineous Lebanese family: phenotypic heterogeneity and disease anticipation. Human Genetics. 138(11-12). 1323–1330. 5 indexed citations
7.
Ibrahim, José-Noël, Rania Jounblat, Nadine Jalkh, et al.. (2018). RAC1 expression and role in IL-1β production and oxidative stress generation in familial Mediterranean fever (FMF) patients. European Cytokine Network. 29(4). 127–135. 11 indexed citations
8.
Haidar, Ziyad S., Nadine Jalkh, Sandra Corbani, et al.. (2018). Atypical pyridoxine dependent epilepsy resulting from a new homozygous missense mutation, in ALDH7A1. Seizure. 57. 32–33. 12 indexed citations
9.
Haidar, Ziyad S., Ramzi Temanni, Éliane Chouery, et al.. (2017). Diagnosis implications of the whole genome sequencing in a large Lebanese family with hyaline fibromatosis syndrome. BMC Genetics. 18(1). 3–3. 6 indexed citations
10.
Jalkh, Nadine, Éliane Chouery, Ziyad S. Haidar, et al.. (2017). Next-generation sequencing in familial breast cancer patients from Lebanon. BMC Medical Genomics. 10(1). 8–8. 31 indexed citations
11.
Ghoch, Joelle Abou, Sandra Corbani, Pierre Cacciagli, et al.. (2015). Contribution of copy number variants (CNVs) to congenital, unexplained intellectual and developmental disabilities in Lebanese patients. Molecular Cytogenetics. 8(1). 26–26. 6 indexed citations
12.
Mégarbané, André, Nadine Hanna, Éliane Chouery, et al.. (2012). Marfanoid habitus, inguinal hernia, advanced bone age, and distinctive facial features: A new collagenopathy?. American Journal of Medical Genetics Part A. 158A(5). 1185–1189. 8 indexed citations
13.
Jalkh, Nadine, Éliane Chouery, Nabiha Salem, et al.. (2012). Prevalance of BRCA1 and BRCA2 mutations in familial breast cancer patients in Lebanon. Hereditary Cancer in Clinical Practice. 10(1). 7–7. 40 indexed citations
14.
Bernard, Geneviève, Éliane Chouery, Martine Tétreault, et al.. (2012). Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy p415. The American Journal of Human Genetics. 91(5). 972–972. 1 indexed citations
15.
Bernard, Geneviève, Éliane Chouery, Martine Tétreault, et al.. (2011). Mutations of POLR3A Encoding a Catalytic Subunit of RNA Polymerase Pol III Cause a Recessive Hypomyelinating Leukodystrophy. The American Journal of Human Genetics. 89(3). 415–423. 181 indexed citations
16.
Mégarbané, André, Éliane Chouery, Cécile Mignon‐Ravix, et al.. (2011). Ambiguous genitalia, microcephaly, seizures, bone malformations, and early death: A distinct MCA/MR syndrome. American Journal of Medical Genetics Part A. 155(5). 1147–1151. 2 indexed citations
17.
Chouery, Éliane, Valérie Delague, Nadine Jalkh, et al.. (2010). A whole-genome scan in a large family with leukodystrophy and oligodontia reveals linkage to 10q22. Neurogenetics. 12(1). 73–78. 11 indexed citations
18.
Haddad, Nabila, Éliane Chouery, Nadine Jalkh, et al.. (2010). Molecular Study of Three Lebanese and Syrian Patients with Waardenburg Syndrome and Report of Novel Mutations in the <i>EDNRB</i> and <i>MITF</i> Genes. Molecular Syndromology. 1(4). 169–175. 16 indexed citations
19.
Stora, Samantha, et al.. (2009). A 56-year-old female patient with facio-oculo-acoustico-renal syndrome (FOAR) syndrome. Report on the natural history and of a novel mutation. European Journal of Medical Genetics. 52(5). 341–343. 6 indexed citations
20.
Laurier, Virginie, Corinne Stoetzel, Jean Muller, et al.. (2006). Pitfalls of homozygosity mapping: an extended consanguineous Bardet–Biedl syndrome family with two mutant genes (BBS2, BBS10), three mutations, but no triallelism. European Journal of Human Genetics. 14(11). 1195–1203. 43 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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