Hubert de Verneuil

6.8k citations

145 papers · 5.1k indexed · h-index 43

Molecular Biology top 2%
Pediatrics, Perinatology and Child Health top 0.5%
Genetics top 5%
Rheumatology top 1%
Hematology top 2%

Co-authors: Y Nordmann Bernard Grandchamp Cécile Ged Frédéric Mazurier François Moreau‐Gaudry Jean‐Charles Deybach Sylvie Mader Pierre Chambon
Topics: Porphyrin Metabolism and Disorders (94 papers)Neonatal Health and Biochemistry (62 papers)Heme Oxygenase-1 and Carbon Monoxide (50 papers)
Cited by: Pediatrics, Perinatology and Child Health Molecular Biology Hematology
Journals: Nature Science Proceedings of the National Academy of Sciences
Partner nations: France United States Spain

In The Last Decade

Hubert de Verneuil

142 papers receiving 5.0k citations

Peers

Countries citing papers authored by Hubert de Verneuil

Since Specialization

Citations

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

Fields of papers citing papers by Hubert de Verneuil

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Hubert de Verneuil. 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 Hubert de Verneuil. The network helps show where Hubert de Verneuil may publish in the future.

Co-authorship network of co-authors of Hubert de Verneuil

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

All Works

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20 of 20 papers shown

#	Work	Indexed citations
1	Missense UROS mutations causing congenital erythropoietic porphyria reduce UROS homeostasis that can be rescued by proteasome inhibition 2017 ·Human Molecular Genetics ·Jean‐Marc Blouin,Ganeko Bernardo‐Seisdedos,(unknown),(unknown),Cécile Ged,Magalie Lalanne,Arantza Sanz-Parra,(unknown),Hubert de Verneuil,Óscar Millet,Emmanuel Richard	19
2	Effect of tyrosine kinase inhibitors on stemness in normal and chronic myeloid leukemia cells 2016 ·Leukemia ·(unknown),F-X Mahon,Isabelle Lamrissi‐Garcia,Isabelle Moranvillier,François Béliveau,Bruno Cardinaud,Sandrine Dabernat,Hubert de Verneuil,François Moreau‐Gaudry,Aurélie Bedel	11
3	Hepatoerythropoietic Porphyria Caused by a Novel Homoallelic Mutation in Uroporphyrinogen Decarboxylase Gene in Egyptian Patients 2015 ·Folia Biologica ·(unknown),Ivan Mikula,Eva Richard,Vladimı́r Saudek,Hubert de Verneuil,Pavel Martásek	3
4	In vivo gene transfer targeting in pancreatic adenocarcinoma with cell surface antigens 2012 ·Molecular Cancer ·M. Lafitte,Benoı̂t Rousseau,Isabelle Moranvillier,(unknown),Evelyne Peuchant,Veronique Guyonnet‐Dupérat,Aurélie Bedel,Pierre Dubus,Hubert de Verneuil,François Moreau‐Gaudry,Sandrine Dabernat	16
5	XPC silencing in normal human keratinocytes triggers metabolic alterations through NOX-1 activation-mediated reactive oxygen species 2010 ·Biochimica et Biophysica Acta (BBA) - Bioenergetics ·Hamid Rezvani,Rodrigue Rossignol,Nsrein Ali,Giovanni Bénard,Xiuwei Tang,Hee Seung Yang,Thomas Jouary,Hubert de Verneuil,Alain Taı̈eb,Arianna L. Kim,Frédéric Mazurier	45
6	XPC silencing in normal human keratinocytes triggers metabolic alterations that drive the formation of squamous cell carcinomas 2010 ·Journal of Clinical Investigation ·Hamid Rezvani,Arianna L. Kim,Rodrigue Rossignol,Nsrein Ali,(unknown),Walid Mahfouf,Nadège Bellancé,Alain Taı̈eb,Hubert de Verneuil,Frédéric Mazurier,David R. Bickers	67
7	Modeling of congenital erythropoietic porphyria by RNA interference: a new tool for preclinical gene therapy evaluation 2010 ·The Journal of Gene Medicine ·Élodie Richard,Magalie Lalanne,Isabelle Lamrissi‐Garcia,Veronique Guyonnet‐Dupérat,Emmanuel Richard,Vincent Pitard,Frédéric Mazurier,François Moreau‐Gaudry,Cécile Ged,Hubert de Verneuil	6
8	Hypoxia-inducible factor-1α regulates the expression of nucleotide excision repair proteins in keratinocytes 2009 ·Nucleic Acids Research ·Hamid Rezvani,Walid Mahfouf,Nsrein Ali,Cécile Chemin,Cécile Ged,Arianna L. Kim,Hubert de Verneuil,Alain Taı̈eb,David R. Bickers,Frédéric Mazurier	51
9	Effective Gene Therapy of Mice with Congenital Erythropoietic Porphyria Is Facilitated by a Survival Advantage of Corrected Erythroid Cells 2008 ·The American Journal of Human Genetics ·Élodie Richard,François Moreau‐Gaudry,Magalie Lalanne,Isabelle Lamrissi‐Garcia,Muriel Cario,Veronique Guyonnet‐Dupérat,Laurence Taine,Cécile Ged,Hubert de Verneuil	37
10	Retroviral Coexpression of IFN-α and IFN-γ Genes and Inhibitory Effects in Chronic Myeloid Leukemia Cells 2000 ·Journal of Interferon & Cytokine Research ·Cécile Ged,Hubert de Verneuil,Josy Reiffers,(unknown),Stéphanie Salesse,(unknown)	2
11	Increased incidence of HFE C282Y mutations in patients with iron overload and hepatocellular carcinoma developed in non-cirrhotic liver 2000 ·Journal of Hepatology ·Jean‐Frédéric Blanc,Victor de Lédinghen,Pierre–Henri Bernard,Hubert de Verneuil,María Winnock,Brigitte Le Bail,Jacques Carles,Jean Saric,Charles Balabaud,Paulette Bioulac‐Sage	55
12	A Novel Immunodeficient Mouse Model-RAG2 gamma Cytokine Receptor Chain Double Mutants-Requiring Exogenous Cytokine Administration for Human Hematopoietic Stem Cell Engraftment Common 1999 ·Journal of Interferon & Cytokine Research ·Frédéric Mazurier,Antonio Fontanellas,Stéphanie Salesse,Laurence Taine,(unknown),François Moreau‐Gaudry,Josy Reiffers,Bruno Péault,James P. Di Santo,Hubert de Verneuil	94
13	Rapid analysis and efficient selection of human transduced primitive hematopoietic cells using the humanized S65T green fluorescent protein 1998 ·Gene Therapy ·Frédéric Mazurier,François Moreau‐Gaudry,Véronique Maguer‐Satta,Stéphanie Salesse,(unknown),Cécile Ged,Françis Belloc,Francis Lacombe,F-X Mahon,Josy Reiffers,Hubert de Verneuil	15
14	Hepatic uroporphyrinogen decarboxylase activity in porphyria cutanea tarda patients: The influence of virus C infection 1998 ·Hepatology ·(unknown),Antonio Fontanellas,(unknown),(unknown),Victor de Lédinghen,Patrice Couzigou,Hubert de Verneuil,Rafael Enrı́quez de Salamanca	45
15	Expansion and methylation status at FRAXE can be detected on EcoRI blots used for FRAXA diagnosis: analysis of four FRAXE families with mild mental retardation in males. 1996 ·PubMed ·Valérie Biancalana,Laurence Taine,J. Bouix,(unknown),Alain Chauvin,Hubert de Verneuil,Samantha J.L. Knight,Claude Stoll,Didier Lacombe,Jean‐Louis Mandel	24
16	Identification of Two NewMutations in CongenitalErythropoietic Porphyria 1995 ·European Journal of Human Genetics ·(unknown),Cécile Ged,(unknown),François Moreau‐Gaudry,(unknown),P.N. Meissner,Edward D. Sturrock,Hubert de Verneuil	19
17	Heterogeneity of mutations in the uroporphyrinogen III synthase gene in congenital erythropoietic porphyria 1992 ·Human Genetics ·(unknown),Vasco Da Silva,Jean‐Charles Deybach,Y Nordmann,Bernard Grandchamp,Hubert de Verneuil	42
18	Human Erythropoietic Protoporphyria: Two point mutations in the ferrochelatase gene 1991 ·Biochemical and Biophysical Research Communications ·J. Lamoril,(unknown),Hubert de Verneuil,Bernard Grandchamp,Y Nordmann,Jean‐Charles Deybach	102
19	Sequential activation of genes for heme pathway enzymes during erythroid differentiation of mouse Friend virus-transformed erythroleukemia cells 1991 ·Biochimica et Biophysica Acta (BBA) - Gene Structure and Expression ·Hiroyoshi Fujita,Masayuki Yamamoto,Takashi Yamagami,Norio Hayashi,(unknown),Hubert de Verneuil,Takeo Yoshinaga,Shigeki Shibahara,Richard I. Morimoto,Shigeru Sassa	52
20	Porphyria cutanea tarda and HLA-linked hemochromatosis 1987 ·Gastroenterology ·Carole Beaumont,R Fauchet,(unknown),Hubert de Verneuil,M. Guéguen,Y Nordmann	2

About Hubert de Verneuil

Hubert de Verneuil is a scholar working on Pediatrics, Perinatology and Child Health, Clinical Biochemistry and Molecular Biology, having authored 145 papers that have together received 5.1k indexed citations. Recurring topics across this work include Porphyrin Metabolism and Disorders (94 papers), Neonatal Health and Biochemistry (62 papers) and Heme Oxygenase-1 and Carbon Monoxide (50 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.3k citations), Molecular Biology (3.8k citations) and Hematology (480 citations). Hubert de Verneuil has collaborated with scholars based in France, United States and Spain. Frequent co-authors include Y Nordmann, Bernard Grandchamp, Cécile Ged, Frédéric Mazurier, François Moreau‐Gaudry, Jean‐Charles Deybach, Sylvie Mader, Pierre Chambon, Vijay Kumar and Alain Taı̈eb. Their work appears in journals such as Nature, Science and Proceedings of the National Academy of Sciences.

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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