Laurence Hubert

2.7k total citations
33 papers, 1.3k citations indexed

About

Laurence Hubert is a scholar working on Molecular Biology, Clinical Biochemistry and Surgery. According to data from OpenAlex, Laurence Hubert has authored 33 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 17 papers in Molecular Biology, 9 papers in Clinical Biochemistry and 7 papers in Surgery. Recurrent topics in Laurence Hubert's work include Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Laurence Hubert is often cited by papers focused on Metabolism and Genetic Disorders (9 papers), Mitochondrial Function and Pathology (7 papers) and Genetics and Neurodevelopmental Disorders (6 papers). Laurence Hubert collaborates with scholars based in France, Netherlands and United States. Laurence Hubert's co-authors include Pascale de Lonlay, Yves de Keyzer, Arnold Münnich, Dominique Chrétien, Nathalie Boddaert, Claude Besmond, Christine Bellanné‐Chantelot, Claudine Junien, Hein te Riele and Vassili Valayannopoulos and has published in prestigious journals such as Journal of Clinical Investigation, PLoS ONE and Brain.

In The Last Decade

Laurence Hubert

33 papers receiving 1.3k citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Laurence Hubert France 21 742 318 226 221 219 33 1.3k
Jean‐François Decaux France 23 981 1.3× 190 0.6× 164 0.7× 139 0.6× 248 1.1× 44 1.7k
M C Glennon United States 13 846 1.1× 91 0.3× 151 0.7× 63 0.3× 223 1.0× 16 1.3k
Reigh-Yi Lin United States 12 469 0.6× 224 0.7× 154 0.7× 46 0.2× 297 1.4× 18 984
Mitsuru Hashiramoto Japan 19 675 0.9× 65 0.2× 130 0.6× 58 0.3× 342 1.6× 44 1.3k
Mark Lal Sweden 17 754 1.0× 98 0.3× 218 1.0× 21 0.1× 129 0.6× 27 1.2k
Camila López‐Crisosto Chile 22 1.2k 1.6× 127 0.4× 54 0.2× 45 0.2× 60 0.3× 35 1.6k
Samira Daniel United States 14 873 1.2× 44 0.1× 168 0.7× 58 0.3× 292 1.3× 16 1.4k
Stéphanie Gobin France 16 432 0.6× 321 1.0× 125 0.6× 61 0.3× 37 0.2× 27 778
Shigeaki Miyabayashi Japan 20 1.0k 1.4× 708 2.2× 102 0.5× 111 0.5× 38 0.2× 62 1.3k
Brigitte Bois-Joyeux France 17 391 0.5× 69 0.2× 123 0.5× 46 0.2× 92 0.4× 45 844

Countries citing papers authored by Laurence Hubert

Since Specialization
Citations

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

Fields of papers citing papers by Laurence Hubert

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Laurence Hubert

This figure shows the co-authorship network connecting the top 25 collaborators of Laurence Hubert. A scholar is included among the top collaborators of Laurence Hubert 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 Laurence Hubert. Laurence Hubert 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.
Wang, Huilun, Xiaoqiong Wei, Gerarda Cappuccio, et al.. (2023). Hypomorphic variants of SEL1L-HRD1 ER-associated degradation are associated with neurodevelopmental disorders. Journal of Clinical Investigation. 134(2). 16 indexed citations
2.
Rötig, Agnès, Charles‐Joris Roux, R. Lévy, et al.. (2020). Heterogeneity of PNPT1 neuroimaging: mitochondriopathy, interferonopathy or both?. Journal of Medical Genetics. 59(2). 204–208. 5 indexed citations
3.
Bouchemal, Nadia, Lisa Ouss, Anaïs Brassier, et al.. (2019). Diagnosis and phenotypic assessment of trimethylaminuria, and its treatment with riboflavin: 1H NMR spectroscopy and genetic testing. Orphanet Journal of Rare Diseases. 14(1). 222–222. 9 indexed citations
4.
Münnich, Arnold, Caroline Demily, Valérie Malan, et al.. (2019). Impact of on-site clinical genetics consultations on diagnostic rate in children and young adults with autism spectrum disorder. Molecular Autism. 10(1). 33–33. 26 indexed citations
5.
Cavallin, Mara, Tjitske Kleefstra, Lonneke de Boer, et al.. (2018). Mutations in TBR1 gene leads to cortical malformations and intellectual disability. European Journal of Medical Genetics. 61(12). 759–764. 21 indexed citations
6.
Besmond, Claude, Dominique Valla, Laurence Hubert, et al.. (2017). Mutations in the novel gene FOPV are associated with familial autosomal dominant and non‐familial obliterative portal venopathy. Liver International. 38(2). 358–364. 20 indexed citations
7.
Hully, Marie, Juliette Ropars, Laurence Hubert, et al.. (2016). Mosaicism in ATP1A3-related disorders: not just a theoretical risk. Neurogenetics. 18(1). 23–28. 24 indexed citations
8.
Carré, Aurore, Athanasia Stoupa, Dulanjalee Kariyawasam, et al.. (2016). Mutations in BOREALIN cause thyroid dysgenesis. Human Molecular Genetics. 26(3). ddw419–ddw419. 36 indexed citations
9.
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
10.
Martinelli, Diego, Lorena Travaglini, Christian A. Drouin, et al.. (2013). MEDNIK syndrome: a novel defect of copper metabolism treatable by zinc acetate therapy. Brain. 136(3). 872–881. 102 indexed citations
11.
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
12.
Damaj, Léna, Valérie Serre, Laurence Hubert, et al.. (2013). Aromatic L-Amino Acid Decarboxylase Deficiency Is a Cause of Long-Fasting Hypoglycemia. The Journal of Clinical Endocrinology & Metabolism. 98(11). 4279–4284. 22 indexed citations
13.
Bergounioux, Jean, Anaïs Brassier, Caroline Rambaud, et al.. (2012). Fatal Rhabdomyolysis in 2 Children with LPIN1 Mutations. The Journal of Pediatrics. 160(6). 1052–1054. 42 indexed citations
14.
Barth, M., Valérie Serre, Laurence Hubert, et al.. (2011). Kinetic Analyses Guide the Therapeutic Decision in a Novel Form of Moderate Aromatic Acid Decarboxylase Deficiency. JIMD Reports. 3. 25–32. 20 indexed citations
15.
Keyzer, Yves de, Vassili Valayannopoulos, Jean‐François Benoist, et al.. (2009). Multiple OXPHOS Deficiency in the Liver, Kidney, Heart, and Skeletal Muscle of Patients With Methylmalonic Aciduria and Propionic Aciduria. Pediatric Research. 66(1). 91–95. 121 indexed citations
16.
Zeharia, Avraham, Avraham Shaag, Riekelt H. Houtkooper, et al.. (2009). Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood. The American Journal of Human Genetics. 84(1). 95–95. 2 indexed citations
17.
Zeharia, Avraham, Avraham Shaag, Riekelt H. Houtkooper, et al.. (2008). Mutations in LPIN1 Cause Recurrent Acute Myoglobinuria in Childhood. The American Journal of Human Genetics. 83(4). 489–494. 163 indexed citations
18.
González‐Barroso, M. Mar, Irina Giurgea, Frédéric Bouillaud, et al.. (2008). Mutations in UCP2 in Congenital Hyperinsulinism Reveal a Role for Regulation of Insulin Secretion. PLoS ONE. 3(12). e3850–e3850. 91 indexed citations
19.
Damaj, Léna, Marc Le Lorc’h, Virginie Verkarre, et al.. (2008). Chromosome 11p15 Paternal Isodisomy in Focal Forms of Neonatal Hyperinsulinism. The Journal of Clinical Endocrinology & Metabolism. 93(12). 4941–4947. 59 indexed citations
20.
Pihlanto-Leppälä, Anne, Pertti Marnila, Laurence Hubert, et al.. (1999). The effect of αα-lactalbumin and ββ-lactoglobulin hydrolysates on the metabolic activity of Escherichia coli JM103. Journal of Applied Microbiology. 87(4). 540–545. 48 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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