Hanadi Kazkaz

3.6k total citations · 1 hit paper
17 papers, 459 citations indexed

About

Hanadi Kazkaz is a scholar working on Genetics, Surgery and Cardiology and Cardiovascular Medicine. According to data from OpenAlex, Hanadi Kazkaz has authored 17 papers receiving a total of 459 indexed citations (citations by other indexed papers that have themselves been cited), including 13 papers in Genetics, 10 papers in Surgery and 3 papers in Cardiology and Cardiovascular Medicine. Recurrent topics in Hanadi Kazkaz's work include Connective tissue disorders research (13 papers), Hip disorders and treatments (6 papers) and Dermatological and Skeletal Disorders (4 papers). Hanadi Kazkaz is often cited by papers focused on Connective tissue disorders research (13 papers), Hip disorders and treatments (6 papers) and Dermatological and Skeletal Disorders (4 papers). Hanadi Kazkaz collaborates with scholars based in United Kingdom, Canada and United States. Hanadi Kazkaz's co-authors include Rodney Grahame, Brad T. Tinkle, Marco Castori, Helen Cohen, Howard P. Levy, Britta Berglund, L. Cardozo, Heleni Mastoroudes, Sushma Srikrishna and Ilias Giarenis and has published in prestigious journals such as SHILAP Revista de lepidopterología, Journal of the American College of Cardiology and American Journal of Respiratory and Critical Care Medicine.

In The Last Decade

Hanadi Kazkaz

14 papers receiving 444 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history

2017 317 citations Brad T. Tinkle, Marco Castori et al. American Journal of Medical Genetics Part C Seminars in Medical Genetics profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Hanadi Kazkaz United Kingdom	7	386	136	115	59	52	17	459
Saihu Mao China	19	190 0.5×	858 6.3×	81 0.7×	70 1.2×	16 0.3×	79	981
Cheryl S. Reid United States	11	321 0.8×	152 1.1×	18 0.2×	89 1.5×	43 0.8×	18	483
M L Martínez-Frías Spain	10	152 0.4×	140 1.0×	48 0.4×	113 1.9×	22 0.4×	20	459
D. Franceschini Italy	11	203 0.5×	117 0.9×	32 0.3×	133 2.3×	12 0.2×	25	402
Vladimir Kenis Russia	8	73 0.2×	74 0.5×	48 0.4×	69 1.2×	32 0.6×	111	272
Odile Boute France	13	222 0.6×	129 0.9×	42 0.4×	162 2.7×	18 0.3×	31	471
Douglas L. Vander Woude United States	7	300 0.8×	178 1.3×	13 0.1×	227 3.8×	54 1.0×	8	558
Lílian Maria José Albano Brazil	14	133 0.3×	63 0.5×	37 0.3×	265 4.5×	59 1.1×	32	456
Margo Whiteford United Kingdom	11	193 0.5×	49 0.4×	58 0.5×	194 3.3×	18 0.3×	15	398
Diana Carli Italy	14	272 0.7×	124 0.9×	25 0.2×	279 4.7×	42 0.8×	51	599

Countries citing papers authored by Hanadi Kazkaz

Since Specialization

Citations

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

Fields of papers citing papers by Hanadi Kazkaz

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Hanadi Kazkaz

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

All Works

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17 of 17 papers shown

Kazkaz, Hanadi, et al.. (2025). PERSISTENT CHALLENGES OF ANOMALOUS LEFT MAIN CORONARY ARTERY AND BICUSPID AORTIC VALVE AFTER MINIMALLY INVASIVE CARDIAC SURGERY. Journal of the American College of Cardiology. 85(12). 4479–4479.

Kazkaz, Hanadi, et al.. (2025). A Balancing Act of Appropriate Treatment: Methicillin-resistant Staphylococcus Aureus (MRSA) Bacteremia With Microscopic Polyangiitis (MPA) Vasculitis. American Journal of Respiratory and Critical Care Medicine. 211(Supplement_1). A5777–A5777.

Kazkaz, Hanadi, Nelly Ninis, Peter C. Rowe, et al.. (2024). The Spider; A Multisystemic Symptom Impact Tool for People with Hypermobility-Related Disorders. Initial Validation in Adolescents. SHILAP Revista de lepidopterología. 12. 200098–200098. 2 indexed citations

Vandersteen, Anthony M., Ruwan Weerakkody, David Parry, et al.. (2023). Genetic complexity of diagnostically unresolved Ehlers-Danlos syndrome. Journal of Medical Genetics. 61(3). 232–238. 7 indexed citations

Kazkaz, Hanadi & Rodney Grahame. (2022). The rheumatological heritable disorders of connective tissue. Medicine. 50(3). 189–193. 2 indexed citations

Ghali, Neeti, Duncan Baker, Jessica Bowen, et al.. (2020). Classical-like Ehlers–Danlos syndrome: a clinical description of 20 newly identified individuals with evidence of tissue fragility. Genetics in Medicine. 22(10). 1576–1582. 17 indexed citations

Mehta, Puja, et al.. (2020). SAT0515 COMPLEX HYPERMOBILITY EHLERS-DANLOS SYNDROME (HEDS): MAPPING THE PATIENT'S JOURNEY OVER 40 MONTHS IN A TERTIARY REFERRAL CENTRE. Annals of the Rheumatic Diseases. 79. 1213–1214. 1 indexed citations

Brady, Angela F., F. Michael Pope, Anthony Vandersteen, et al.. (2020). Arterial complications in classical Ehlers-Danlos syndrome: a case series. Journal of Medical Genetics. 57(11). 769–776. 8 indexed citations

Wright, Sarah, Puja Mehta, Juliet W. L. Parry, & Hanadi Kazkaz. (2020). OP0200 PATIENTS WITH HYPERMOBILITY RELATED DISORDERS HAVE A SIGNIFICANT NUMBER OF ORTHOPAEDIC INTERVENTIONS ON MULTIPLE SITES AND AT A YOUNG AGE: DATA FROM A TERTIARY REFERRAL CENTRE. Annals of the Rheumatic Diseases. 79. 125–125. 4 indexed citations

10.

Wright, Sarah, Puja Mehta, Anisur Rahman, & Hanadi Kazkaz. (2020). P118 Orthopaedic surgical interventions in a cohort of patients with hypermobility related disorders, compared with chronic pain syndrome patients in a tertiary referral centre. Lara D. Veeken. 59(Supplement_2). 1 indexed citations

11.

Kazkaz, Hanadi, et al.. (2018). 82. Not just another hypermobile patient: Noonan syndrome diagnosed in late adulthood in the rheumatology clinic. Rheumatology Advances in Practice. 2(suppl_1). 1 indexed citations

12.

Kazkaz, Hanadi & Rodney Grahame. (2018). The rheumatological heritable disorders of connective tissue. Medicine. 46(4). 256–260. 3 indexed citations

13.

Tinkle, Brad T., Marco Castori, Britta Berglund, et al.. (2017). Hypermobile Ehlers–Danlos syndrome (a.k.a. Ehlers–Danlos syndrome Type III and Ehlers–Danlos syndrome hypermobility type): Clinical description and natural history. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 175(1). 48–69. 317 indexed citations breakdown →

14.

Weerakkody, Ruwan, Jana Vandrovcová, Michael Mueller, et al.. (2016). Targeted next-generation sequencing makes new molecular diagnoses and expands genotype–phenotype relationship in Ehlers–Danlos syndrome. Genetics in Medicine. 18(11). 1119–1127. 45 indexed citations

15.

Mastoroudes, Heleni, Ilias Giarenis, L. Cardozo, et al.. (2013). Lower urinary tract symptoms in women with benign joint hypermobility syndrome: a case–control study. International Urogynecology Journal. 24(9). 1553–1558. 19 indexed citations

16.

Smith, Matthew D., et al.. (2012). Stress urinary incontinence as the presenting complaint of benign joint hypermobility syndrome. JRSM Short Reports. 3(9). 1–3. 5 indexed citations

17.

Mastoroudes, Heleni, Ilias Giarenis, L. Cardozo, et al.. (2012). Prolapse and sexual function in women with benign joint hypermobility syndrome. BJOG An International Journal of Obstetrics & Gynaecology. 120(2). 187–192. 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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