Hana Zouk

530 total citations
7 papers, 72 citations indexed

About

Hana Zouk is a scholar working on Molecular Biology, Genetics and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Hana Zouk has authored 7 papers receiving a total of 72 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Cardiology and Cardiovascular Medicine. Recurrent topics in Hana Zouk's work include Genomics and Rare Diseases (3 papers), Amino Acid Enzymes and Metabolism (1 paper) and Child Nutrition and Feeding Issues (1 paper). Hana Zouk is often cited by papers focused on Genomics and Rare Diseases (3 papers), Amino Acid Enzymes and Metabolism (1 paper) and Child Nutrition and Feeding Issues (1 paper). Hana Zouk collaborates with scholars based in United States, Jordan and Canada. Hana Zouk's co-authors include Leora Witkowski, Kevin P. Daly, Amy E. Roberts, Daniel Quiat, Kalotina Machini, Christopher Koch, Heidi L. Rehm, Robert C. Green, Jordan W. Smoller and Emma Perez and has published in prestigious journals such as The American Journal of Human Genetics, Genetics in Medicine and Journal of the American Heart Association.

In The Last Decade

Hana Zouk

6 papers receiving 70 citations

Peers

Hana Zouk

GENET

MB

CCM

PHEOH

CR

Kristin Boulier United States

Julie Hathaway Canada

Ziqi Xu United States

Anna Lehman Canada

Karen L. Mohlke United States

Catherine L. Mercer United Kingdom

Lamisse Mansour‐Hendili France

Geoffroy Delplancq France

Nataša Rojnić Putarek Croatia

Bennet Peterson United States

Kristin Boulier United States

Hana Zouk

82 ×1.9

GENET

20 ×1.1

MB

9 ×0.5

CCM

7 ×0.6

PHEOH

10 ×1.3

CR

Citations per year, relative to Hana Zouk Hana Zouk (= 1×) peers Kristin Boulier

Countries citing papers authored by Hana Zouk

Since Specialization

Citations

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

Fields of papers citing papers by Hana Zouk

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hana Zouk

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

All Works

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7 of 7 papers shown

1.

Gold, Nina B., et al.. (2025). O35: A genotype-first approach among adults at risk for treatable monogenic disorders reveals underdiagnosis and incomplete penetrance. Genetics in Medicine Open. 3. 102111–102111. 1 indexed citations

2.

Zoltick, Emilie S., Hana Zouk, Emma Perez, et al.. (2024). Long‐Term Health Outcomes of Individuals With Pseudodeficiency Alleles in IDUA May Inform Newborn Screening Practices for Mucopolysaccharidosis Type I. American Journal of Medical Genetics Part A. 197(4). e63940–e63940.

3.

Gold, Jessica I., Sarina Madhavan, Joseph Park, et al.. (2023). Phenotypes of undiagnosed adults with actionable OTC and GLA variants. Human Genetics and Genomics Advances. 4(4). 100226–100226. 2 indexed citations

4.

Zouk, Hana, Wanfeng Yu, Andrea M. Oza, et al.. (2021). Reanalysis of eMERGE phase III sequence variants in 10,500 participants and infrastructure to support the automated return of knowledge updates. Genetics in Medicine. 24(2). 454–462. 7 indexed citations

5.

Zawatsky, Carrie L. Blout, Nidhi Shah, Kalotina Machini, et al.. (2021). Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization. The American Journal of Human Genetics. 108(12). 2224–2237. 32 indexed citations

6.

Azab, Belal, Muawyah Al Bdour, Tareq Saleh, et al.. (2021). Unique Variant Spectrum in a Jordanian Cohort with Inherited Retinal Dystrophies. Genes. 12(4). 593–593. 3 indexed citations

7.

Quiat, Daniel, Leora Witkowski, Hana Zouk, Kevin P. Daly, & Amy E. Roberts. (2020). Retrospective Analysis of Clinical Genetic Testing in Pediatric Primary Dilated Cardiomyopathy: Testing Outcomes and the Effects of Variant Reclassification. Journal of the American Heart Association. 9(11). e016195–e016195. 27 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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