Houda Hamdi‐Rozé

488 total citations
14 papers, 228 citations indexed

About

Houda Hamdi‐Rozé is a scholar working on Molecular Biology, Genetics and Hematology. According to data from OpenAlex, Houda Hamdi‐Rozé has authored 14 papers receiving a total of 228 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 7 papers in Genetics and 6 papers in Hematology. Recurrent topics in Houda Hamdi‐Rozé's work include Hemoglobinopathies and Related Disorders (6 papers), Iron Metabolism and Disorders (6 papers) and Hedgehog Signaling Pathway Studies (4 papers). Houda Hamdi‐Rozé is often cited by papers focused on Hemoglobinopathies and Related Disorders (6 papers), Iron Metabolism and Disorders (6 papers) and Hedgehog Signaling Pathway Studies (4 papers). Houda Hamdi‐Rozé collaborates with scholars based in France, United Kingdom and Netherlands. Houda Hamdi‐Rozé's co-authors include Edouard Bardou‐Jacquet, Valérie Dupé, Christèle Dubourg, Linda Akloul, Véronique David, Sylvie Odent, Wilfrid Carré, Hal Drakesmith, Dorine W. Swinkels and Hanka Venselaar and has published in prestigious journals such as PLoS ONE, The Journal of Clinical Endocrinology & Metabolism and Journal of Hepatology.

In The Last Decade

Houda Hamdi‐Rozé

14 papers receiving 226 citations

Peers

Houda Hamdi‐Rozé

HEMAT

GENET

Jessica Goodman United States

Amy J. Lambert United States

Lea Shalmon Israel

Valeh Hadavi Iran

Flavia Guillem France

Chiara Castronovo Italy

Priscila Ferreira Slepicka United States

Astrīda Krūmiņa Latvia

Gordon J. Hildick-Smith United States

Mylène Béri‐Dexheimer France

Jessica Goodman United States

Houda Hamdi‐Rozé

65 ×0.6

97 ×1.3

HEMAT

43 ×0.6

GENET

88 ×1.3

GENET

64 ×1.1

Citations per year, relative to Houda Hamdi‐Rozé Houda Hamdi‐Rozé (= 1×) peers Jessica Goodman

Countries citing papers authored by Houda Hamdi‐Rozé

Since Specialization

Citations

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

Fields of papers citing papers by Houda Hamdi‐Rozé

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Houda Hamdi‐Rozé. 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 Houda Hamdi‐Rozé. The network helps show where Houda Hamdi‐Rozé may publish in the future.

Co-authorship network of co-authors of Houda Hamdi‐Rozé

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

All Works

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14 of 14 papers shown

Hamdi‐Rozé, Houda, Séverine Cunat, V. Loustaud‐Ratti, et al.. (2021). A simple clinical score to promote and enhance ferroportin disease screening. Journal of Hepatology. 76(3). 568–576. 5 indexed citations

Bardou‐Jacquet, Edouard, Houda Hamdi‐Rozé, Anita Paisant, et al.. (2021). Non-invasive diagnosis and follow-up of hyperferritinaemia. Clinics and Research in Hepatology and Gastroenterology. 46(1). 101762–101762. 1 indexed citations

Hamdi‐Rozé, Houda, Leslie Ratié, Wilfrid Carré, et al.. (2020). Disrupted Hypothalamo-Pituitary Axis in Association With Reduced SHH Underlies the Pathogenesis of NOTCH-Deficiency. The Journal of Clinical Endocrinology & Metabolism. 105(9). e3183–e3196. 9 indexed citations

Bardou‐Jacquet, Edouard, et al.. (2019). Twenty Years of Ferroportin Disease: A Review or An Update of Published Clinical, Biochemical, Molecular, and Functional Features. Pharmaceuticals. 12(3). 132–132. 36 indexed citations

Akloul, Linda, Wilfrid Carré, Chloé Quēlin, et al.. (2019). Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders. Human Genetics. 138(4). 363–374. 17 indexed citations

Deugnier, Yves, Jeff Morçet, Fabrice Lainé, et al.. (2018). Reduced phenotypic expression in genetic hemochromatosis with time: Role of exposure to non-genetic modifiers. Journal of Hepatology. 70(1). 118–125. 16 indexed citations

Hamdi‐Rozé, Houda, Martine Ropert, Lénaı̈ck Détivaud, et al.. (2018). Variable expressivity of HJV related hemochromatosis: “Juvenile” hemochromatosis?. Blood Cells Molecules and Diseases. 74. 30–33. 10 indexed citations

Ricordel, Charles, Alexandra Lespagnol, Francisco Llamas‐Gutierrez, et al.. (2017). Mutational Landscape of DDR2 Gene in Lung Squamous Cell Carcinoma Using Next-generation Sequencing. Clinical Lung Cancer. 19(2). 163–169.e4. 8 indexed citations

Hamdi‐Rozé, Houda, et al.. (2016). Regulation of downstream neuronal genes by proneural transcription factors during initial neurogenesis in the vertebrate brain. Neural Development. 11(1). 22–22. 14 indexed citations

10.

Jaillard, Sylvie, Linda Akloul, Houda Hamdi‐Rozé, et al.. (2016). Array-CGH diagnosis in ovarian failure: identification of new molecular actors for ovarian physiology. Journal of Ovarian Research. 9(1). 63–63. 26 indexed citations

11.

Hamdi‐Rozé, Houda, Caroline Le Lan, V. Loustaud‐Ratti, et al.. (2016). Rare HFE variants are the most frequent cause of hemochromatosis in non‐c282y homozygous patients with hemochromatosis. American Journal of Hematology. 91(12). 1202–1205. 13 indexed citations

12.

Dubourg, Christèle, Wilfrid Carré, Sophie Rose, et al.. (2016). Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing. Clinical Genetics. 89(6). 659–668. 26 indexed citations

13.

Tayrac, Marie de, Christèle Dubourg, Sophie Rose, et al.. (2015). Homozygous STIL Mutation Causes Holoprosencephaly and Microcephaly in Two Siblings. PLoS ONE. 10(2). e0117418–e0117418. 28 indexed citations

14.

Hamdi‐Rozé, Houda, et al.. (2014). Notch signaling and proneural genes work together to control the neural building blocks for the initial scaffold in the hypothalamus. Frontiers in Neuroanatomy. 8. 140–140. 19 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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