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

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

Sort: Min cites: Since: Top N: Style:

14 of 14 papers shown

#	Work	Indexed citations
1	A simple clinical score to promote and enhance ferroportin disease screening 2021 ·Journal of Hepatology ·(unknown), Houda Hamdi‐Rozé, Séverine Cunat, V. Loustaud‐Ratti, Xavier Causse, Si Nafa Si Ahmed, Bernard Drénou, Christophe Bureau, Gilles Pelletier, Caroline de Kerguenec, Nathalie Ganne‐Carrié, S. Durupt, Fabrice Lainé, Olivier Loréal, Martine Ropert, Lénaı̈ck Détivaud, Jeff Morçet, Patricia Aguilar‐Martinez, Yves Deugnier, Edouard Bardou‐Jacquet	5
2	Non-invasive diagnosis and follow-up of hyperferritinaemia 2021 ·Clinics and Research in Hepatology and Gastroenterology ·Edouard Bardou‐Jacquet, Houda Hamdi‐Rozé, Anita Paisant, (unknown), Marc Bourlière, Nathalie Ganne‐Carrié, Victor de Lédinghen, Christophe Bureau	1
3	Disrupted Hypothalamo-Pituitary Axis in Association With Reduced SHH Underlies the Pathogenesis of NOTCH-Deficiency 2020 ·The Journal of Clinical Endocrinology & Metabolism ·Houda Hamdi‐Rozé, (unknown), (unknown), (unknown), Leslie Ratié, (unknown), Wilfrid Carré, (unknown), Sylvie Odent, Christèle Dubourg, Véronique David, Marie de Tayrac, Valérie Dupé	9
4	Twenty Years of Ferroportin Disease: A Review or An Update of Published Clinical, Biochemical, Molecular, and Functional Features 2019 ·Pharmaceuticals ·(unknown), (unknown), Edouard Bardou‐Jacquet, Hanka Venselaar, Houda Hamdi‐Rozé, Hal Drakesmith, Dorine W. Swinkels	36
5	Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders 2019 ·Human Genetics ·(unknown), Linda Akloul, Wilfrid Carré, Chloé Quēlin, Hubert Journel, Laurent Pasquier, Mélanie Fradin, Sylvie Odent, Houda Hamdi‐Rozé, Erwan Watrin, Valérie Dupé, Christèle Dubourg, Véronique David	17
6	Reduced phenotypic expression in genetic hemochromatosis with time: Role of exposure to non-genetic modifiers 2018 ·Journal of Hepatology ·Yves Deugnier, Jeff Morçet, Fabrice Lainé, Houda Hamdi‐Rozé, (unknown), Dominique Guyader, Romain Moirand, Edouard Bardou‐Jacquet	16
7	Variable expressivity of HJV related hemochromatosis: “Juvenile” hemochromatosis? 2018 ·Blood Cells Molecules and Diseases ·Houda Hamdi‐Rozé, (unknown), Martine Ropert, Lénaı̈ck Détivaud, (unknown), Dominique Simon, Gilles Pelletier, Yves Deugnier, Véronique David, Edouard Bardou‐Jacquet	10
8	Mutational Landscape of DDR2 Gene in Lung Squamous Cell Carcinoma Using Next-generation Sequencing 2017 ·Clinical Lung Cancer ·Charles Ricordel, Alexandra Lespagnol, Francisco Llamas‐Gutierrez, Marie de Tayrac, M. Kerjouan, Alice Fiévet, Houda Hamdi‐Rozé, (unknown), B. Desrues, Jean Mosser, H. Léna	8
9	Regulation of downstream neuronal genes by proneural transcription factors during initial neurogenesis in the vertebrate brain 2016 ·Neural Development ·(unknown), Houda Hamdi‐Rozé, (unknown), Véronique David, Valérie Dupé	14
10	Array-CGH diagnosis in ovarian failure: identification of new molecular actors for ovarian physiology 2016 ·Journal of Ovarian Research ·Sylvie Jaillard, Linda Akloul, (unknown), Houda Hamdi‐Rozé, Christèle Dubourg, Sylvie Odent, (unknown), Nathalie Dejucq‐Rainsford, Marc‐Antoine Belaud‐Rotureau, Célia Ravel	26
11	Rare HFE variants are the most frequent cause of hemochromatosis in non‐c282y homozygous patients with hemochromatosis 2016 ·American Journal of Hematology ·Houda Hamdi‐Rozé, (unknown), (unknown), Caroline Le Lan, V. Loustaud‐Ratti, Xavier Causse, Olivier Loréal, Yves Deugnier, Pierre Brissot, Anne‐Marie Jouanolle, Edouard Bardou‐Jacquet	13
12	Complex mode of inheritance in holoprosencephaly revealed by whole exome sequencing 2016 ·Clinical Genetics ·(unknown), Christèle Dubourg, Wilfrid Carré, Sophie Rose, (unknown), Linda Akloul, Houda Hamdi‐Rozé, Géraldine Viot, (unknown), P. Darnault, (unknown), Valérie Dupé, Véronique David	26
13	Homozygous STIL Mutation Causes Holoprosencephaly and Microcephaly in Two Siblings 2015 ·PLoS ONE ·(unknown), Marie de Tayrac, Christèle Dubourg, Sophie Rose, Wilfrid Carré, Houda Hamdi‐Rozé, Marie‐Claude Babron, Linda Akloul, (unknown), Sylvie Odent, Valérie Dupé, Régis Giet, Véronique David	28
14	Notch signaling and proneural genes work together to control the neural building blocks for the initial scaffold in the hypothalamus 2014 ·Frontiers in Neuroanatomy ·(unknown), Houda Hamdi‐Rozé, (unknown)	19

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.

Explore authors with similar magnitude of impact