Florence Habarou

1.4k total citations
23 papers, 727 citations indexed

About

Florence Habarou is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Florence Habarou has authored 23 papers receiving a total of 727 indexed citations (citations by other indexed papers that have themselves been cited), including 11 papers in Molecular Biology, 11 papers in Clinical Biochemistry and 5 papers in Surgery. Recurrent topics in Florence Habarou's work include Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (6 papers) and Cancer, Hypoxia, and Metabolism (3 papers). Florence Habarou is often cited by papers focused on Metabolism and Genetic Disorders (11 papers), Mitochondrial Function and Pathology (6 papers) and Cancer, Hypoxia, and Metabolism (3 papers). Florence Habarou collaborates with scholars based in France, United States and United Kingdom. Florence Habarou's co-authors include Chris Ottolenghi, Pascale de Lonlay, Nathalie Boddaert, Anaïs Brassier, Vassili Valayannopoulos, Valérie Barbier, Asmaa Mamoune, Jean‐Paul Bonnefont, Audrey Boutron and Yamina Hamel and has published in prestigious journals such as Cancer Research, Scientific Reports and The American Journal of Human Genetics.

In The Last Decade

Florence Habarou

22 papers receiving 716 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Florence Habarou France 16 372 250 134 124 101 23 727
Leighton R. James United States 19 472 1.3× 136 0.5× 103 0.8× 51 0.4× 104 1.0× 38 961
Shanti Balasubramaniam Australia 17 487 1.3× 248 1.0× 114 0.9× 38 0.3× 42 0.4× 39 926
Andrea Hodgkinson United Kingdom 15 264 0.7× 144 0.6× 55 0.4× 47 0.4× 58 0.6× 28 702
Bridget Ford United States 11 410 1.1× 174 0.7× 72 0.5× 45 0.4× 59 0.6× 15 728
Raffaello Roesel United States 13 216 0.6× 162 0.6× 71 0.5× 34 0.3× 50 0.5× 43 527
Regine Schroeder Germany 16 414 1.1× 80 0.3× 64 0.5× 76 0.6× 62 0.6× 21 912
Adrienne Laskowski Australia 14 868 2.3× 537 2.1× 122 0.9× 61 0.5× 36 0.4× 23 1.4k
Anne‐Frédérique Dessein France 12 362 1.0× 150 0.6× 46 0.3× 50 0.4× 44 0.4× 33 686
Bertrand Toutain France 21 444 1.2× 53 0.2× 80 0.6× 81 0.7× 72 0.7× 42 951
Olga Rafikova United States 22 421 1.1× 42 0.2× 127 0.9× 98 0.8× 107 1.1× 56 1.1k

Countries citing papers authored by Florence Habarou

Since Specialization
Citations

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

Fields of papers citing papers by Florence Habarou

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Florence Habarou

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

All Works

20 of 20 papers shown
1.
Vasse, Marc, et al.. (2023). Prognostic value of cellular population data in patients with COVID-19. Informatics in Medicine Unlocked. 38. 101207–101207. 1 indexed citations
2.
Vasse, Marc, et al.. (2020). Interest of the cellular population data analysis as an aid in the early diagnosis of SARS‐CoV‐2 infection. International Journal of Laboratory Hematology. 43(1). 116–122. 18 indexed citations
3.
Habarou, Florence, et al.. (2019). Detection of monoclonal B-lymphocytosis: interest of cellular population data and CytoDiff™ analysis. Clinical Chemistry and Laboratory Medicine (CCLM). 58(3). e83–e86.
4.
Buffet, Alexandre, Aurélie Morin, Luis-Jaime Castro-Vega, et al.. (2018). Germline Mutations in the Mitochondrial 2-Oxoglutarate/Malate Carrier SLC25A11 Gene Confer a Predisposition to Metastatic Paragangliomas. Cancer Research. 78(8). 1914–1922. 99 indexed citations
5.
Babdor, Joël, Michaël Dussiot, Nicolas Goudin, et al.. (2018). Impaired Transferrin Receptor Palmitoylation and Recycling in Neurodegeneration with Brain Iron Accumulation. The American Journal of Human Genetics. 102(2). 266–277. 71 indexed citations
6.
Bruneel, Arnaud, Florence Habarou, Tanya Stojkovic, et al.. (2017). Two-dimensional electrophoresis highlights haptoglobin beta chain as an additional biomarker of congenital disorders of glycosylation. Clinica Chimica Acta. 470. 70–74. 14 indexed citations
7.
Lebigot, Élise, Pauline Gaignard, Imen Dorboz, et al.. (2017). Impact of mutations within the [Fe-S] cluster or the lipoic acid biosynthesis pathways on mitochondrial protein expression profiles in fibroblasts from patients. Molecular Genetics and Metabolism. 122(3). 85–94. 40 indexed citations
8.
Habarou, Florence, Nadia Bahi‐Buisson, Élise Lebigot, et al.. (2017). Ketone Bodies as a Possible Adjuvant to Ketogenic Diet in PDHc Deficiency but Not in GLUT1 Deficiency. JIMD Reports. 38. 53–59. 6 indexed citations
9.
Barbier, Valérie, Célina Roda, Anaïs Brassier, et al.. (2017). Autism spectrum disorders in propionic acidemia patients. Journal of Inherited Metabolic Disease. 41(4). 623–629. 27 indexed citations
10.
Hardonnière, Kévin, Elise F. Saunier, Anthony Lemarié, et al.. (2016). The environmental carcinogen benzo[a]pyrene induces a Warburg-like metabolic reprogramming dependent on NHE1 and associated with cell survival. Scientific Reports. 6(1). 30776–30776. 55 indexed citations
11.
Brassier, Anaïs, Vassili Valayannopoulos, Nadia Bahi‐Buisson, et al.. (2015). Two new cases of serine deficiency disorders treated with l-serine. European Journal of Paediatric Neurology. 20(1). 53–60. 29 indexed citations
12.
Pontoizeau, Clément, Florence Habarou, Anaïs Brassier, et al.. (2015). Hyperprolinemia in Type 2 Glutaric Aciduria and MADD-Like Profiles. JIMD Reports. 27. 39–45. 6 indexed citations
13.
Brassier, Anaïs, Stéphanie Gobin, Vassili Valayannopoulos, et al.. (2015). Long-term outcomes in Ornithine Transcarbamylase deficiency: a series of 90 patients. Orphanet Journal of Rare Diseases. 10(1). 60 indexed citations
14.
Hamel, Yamina, Asmaa Mamoune, François‐Xavier Mauvais, et al.. (2015). Acute rhabdomyolysis and inflammation. Journal of Inherited Metabolic Disease. 38(4). 621–628. 49 indexed citations
15.
Habarou, Florence, Anaïs Brassier, Marlène Rio, et al.. (2014). Pyruvate carboxylase deficiency: An underestimated cause of lactic acidosis. Molecular Genetics and Metabolism Reports. 2. 25–31. 17 indexed citations
16.
Mamoune, Asmaa, Michel Bahuau, Yamina Hamel, et al.. (2014). A Thermolabile Aldolase A Mutant Causes Fever-Induced Recurrent Rhabdomyolysis without Hemolytic Anemia. PLoS Genetics. 10(11). e1004711–e1004711. 20 indexed citations
17.
Nizon, Mathilde, Audrey Boutron, Nathalie Boddaert, et al.. (2014). Leukoencephalopathy with cysts and hyperglycinemia may result from NFU1 deficiency. Mitochondrion. 15. 59–64. 32 indexed citations
18.
Boutron, Audrey, Florence Habarou, Christine Barnérias, et al.. (2013). Mutations in human lipoyltransferase gene LIPT1cause a Leigh disease with secondary deficiency for pyruvate and alpha-ketoglutarate dehydrogenase. Orphanet Journal of Rare Diseases. 8(1). 192–192. 69 indexed citations
19.
Nizon, Mathilde, Chris Ottolenghi, Vassili Valayannopoulos, et al.. (2013). Long-term neurological outcome of a cohort of 80 patients with classical organic acidurias. Orphanet Journal of Rare Diseases. 8(1). 148–148. 62 indexed citations
20.
Bruneel, Arnaud, Willy Morelle, Florence Habarou, et al.. (2008). Two dimensional gel electrophoresis of apolipoprotein C‐III and MALDI‐TOF MS are complementary techniques for the study of combined defects in N‐ and mucin type O‐glycan biosynthesis. PROTEOMICS - CLINICAL APPLICATIONS. 2(12). 1670–1674. 5 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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