Arnaud Molin

1.2k total citations
31 papers, 497 citations indexed

About

Arnaud Molin is a scholar working on Genetics, Pathology and Forensic Medicine and Molecular Biology. According to data from OpenAlex, Arnaud Molin has authored 31 papers receiving a total of 497 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 14 papers in Pathology and Forensic Medicine and 12 papers in Molecular Biology. Recurrent topics in Arnaud Molin's work include Vitamin D Research Studies (13 papers), Genetic Syndromes and Imprinting (7 papers) and Genomics and Rare Diseases (6 papers). Arnaud Molin is often cited by papers focused on Vitamin D Research Studies (13 papers), Genetic Syndromes and Imprinting (7 papers) and Genomics and Rare Diseases (6 papers). Arnaud Molin collaborates with scholars based in France, United States and Canada. Arnaud Molin's co-authors include Nicolas Richard, Nadia Coudray, Marie‐Laure Kottler, Martin Kaufmann, Glenville Jones, Justine Bacchetta, Harald Jüppner, Marie-Laure Kottler, Karl P. Schlingmann and John C. Gallagher and has published in prestigious journals such as Proceedings of the National Academy of Sciences, Journal of Clinical Investigation and Nature Communications.

In The Last Decade

Arnaud Molin

29 papers receiving 490 citations

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
Arnaud Molin France 12 258 157 139 107 101 31 497
Seong Min Lee United States 16 490 1.9× 213 1.4× 210 1.5× 151 1.4× 104 1.0× 26 703
Christine Kimmel‐Jehan United States 6 241 0.9× 87 0.6× 99 0.7× 79 0.7× 89 0.9× 8 355
Tsunesuke Shimotsuji Japan 12 185 0.7× 80 0.5× 82 0.6× 71 0.7× 76 0.8× 31 466
Jürgen Merke Germany 10 201 0.8× 145 0.9× 89 0.6× 97 0.9× 259 2.6× 11 458
Julia Höbaus Austria 9 216 0.8× 85 0.5× 107 0.8× 79 0.7× 52 0.5× 11 360
Ann Marie Hynes United Kingdom 12 127 0.5× 190 1.2× 259 1.9× 47 0.4× 155 1.5× 14 518
Fumie Saji Japan 10 153 0.6× 199 1.3× 127 0.9× 121 1.1× 422 4.2× 21 523
Adel B. Korkor United States 9 136 0.5× 107 0.7× 83 0.6× 74 0.7× 289 2.9× 14 459
Myriam Cloutier Canada 8 79 0.3× 87 0.6× 74 0.5× 53 0.5× 255 2.5× 9 386
Lyman W. Whitlatch United States 8 426 1.7× 187 1.2× 80 0.6× 101 0.9× 14 0.1× 9 526

Countries citing papers authored by Arnaud Molin

Since Specialization
Citations

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

Fields of papers citing papers by Arnaud Molin

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Arnaud Molin

This figure shows the co-authorship network connecting the top 25 collaborators of Arnaud Molin. A scholar is included among the top collaborators of Arnaud Molin 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 Arnaud Molin. Arnaud Molin 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.
Romanet, Pauline, et al.. (2025). Chapter 5: The roles of genetics in primary hyperparathyroidism. Annales d Endocrinologie. 86(1). 101694–101694. 3 indexed citations
2.
3.
Molin, Arnaud, et al.. (2025). Clinical evidence for independent regulation of vitamin D by intestinal CYP24A1. Journal of Clinical Investigation. 135(8). 1 indexed citations
4.
Molin, Arnaud, et al.. (2024). Skeletal growth is enhanced by a shared role for SOX8 and SOX9 in promoting reserve chondrocyte commitment to columnar proliferation. Proceedings of the National Academy of Sciences. 121(8). e2316969121–e2316969121. 9 indexed citations
5.
Dubourg, Laurence, Arnaud Molin, Roland Chapurlat, et al.. (2023). Reassuring Data on the Cardiovascular Risk in Adults With X-linked Hypophosphatemia Receiving Conventional Therapy. The Journal of Clinical Endocrinology & Metabolism. 109(2). e488–e494. 5 indexed citations
6.
Colson, Cindy, et al.. (2023). Phenotypic and genotypic characterization of 1q21.1 copy number variants: A report of 34 new individuals and literature review. American Journal of Medical Genetics Part A. 194(3). e63457–e63457. 6 indexed citations
7.
Bacchetta, Justine, Thomas Édouard, Gilles Laverny, et al.. (2022). Vitamin D and calcium intakes in general pediatric populations: A French expert consensus paper. Archives de Pédiatrie. 29(4). 312–325. 41 indexed citations
8.
Harambat, Jérôme, Anya Rothenbühler, Juliane Léger, et al.. (2022). Genotype-phenotype Description of Vitamin D–dependent Rickets 1A: CYP27B1 p.(Ala129Thr) Variant Induces a Milder Disease. The Journal of Clinical Endocrinology & Metabolism. 108(4). 812–826. 2 indexed citations
9.
Bertholet‐Thomas, Aurélia, Aurélie Portefaix, C. Dhelens, et al.. (2022). Fluconazole in hypercalciuric patients with increased 1,25(OH)2D levels: the prospective, randomized, placebo-controlled, double-blind FLUCOLITH trial. Trials. 23(1). 499–499. 2 indexed citations
10.
11.
Molin, Arnaud, Sandrine Lemoine, Martin Kaufmann, et al.. (2021). Overlapping Phenotypes Associated With CYP24A1, SLC34A1, and SLC34A3 Mutations: A Cohort Study of Patients With Hypersensitivity to Vitamin D. Frontiers in Endocrinology. 12. 736240–736240. 15 indexed citations
12.
Rovito, Daniela, Anna Y. Belorusova, Elvire Guiot, et al.. (2020). Cytosolic sequestration of the vitamin D receptor as a therapeutic option for vitamin D-induced hypercalcemia. Nature Communications. 11(1). 6249–6249. 22 indexed citations
13.
Wiedemann, Arnaud, Arnaud Molin, G. Weryha, et al.. (2020). Prolonged 25-OH Vitamin D Deficiency Does Not Impair Bone Mineral Density in Adult Patients With Vitamin D 25-Hydroxylase Deficiency (CYP2R1). Calcified Tissue International. 107(2). 191–194. 4 indexed citations
14.
Colson, Cindy, Matthieu Décamp, Nicolas Gruchy, et al.. (2019). High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B. Bone. 123. 145–152. 18 indexed citations
15.
Hureaux, Marguerite, Arnaud Molin, Emmanuel Spaggiari, et al.. (2018). Prenatal hyperechogenic kidneys in three cases of infantile hypercalcemia associated with SLC34A1 mutations. Pediatric Nephrology. 33(10). 1723–1729. 16 indexed citations
16.
Molin, Arnaud, et al.. (2017). Calcium pyrophosphate deposition disease revealing a hypersensitivity to vitamin D. Joint Bone Spine. 84(3). 349–351. 4 indexed citations
17.
Molin, Arnaud, François Feillet, Arnaud Wiedemann, et al.. (2016). Two French Families with Vitamin D Dependency Rickets Type 1B Harbor Homozygous Recessive Expression Of CYP2R1 Mutations L99P and G42_L46DEL INSR. 86. 1 indexed citations
18.
Molin, Arnaud, Martin Kaufmann, J.-C. Souberbielle, et al.. (2015). CYP24A1Mutations in a Cohort of Hypercalcemic Patients: Evidence for a Recessive Trait. The Journal of Clinical Endocrinology & Metabolism. 100(10). E1343–E1352. 97 indexed citations
19.
Richard, Nicolas, et al.. (2013). PaternalGNASMutations Lead to Severe Intrauterine Growth Retardation (IUGR) and Provide Evidence for a Role of XLαs in Fetal Development. The Journal of Clinical Endocrinology & Metabolism. 98(9). E1549–E1556. 56 indexed citations
20.
Molin, Arnaud, G. Benoist, Corinne Jeanne‐Pasquier, et al.. (2013). 12q21 Microdeletion in a fetus with Meckel syndrome involving CEP290/MKS4. European Journal of Medical Genetics. 56(10). 580–583. 11 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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