Julien Marcadier

770 total citations
15 papers, 417 citations indexed

About

Julien Marcadier is a scholar working on Molecular Biology, Genetics and Pathology and Forensic Medicine. According to data from OpenAlex, Julien Marcadier has authored 15 papers receiving a total of 417 indexed citations (citations by other indexed papers that have themselves been cited), including 9 papers in Molecular Biology, 7 papers in Genetics and 2 papers in Pathology and Forensic Medicine. Recurrent topics in Julien Marcadier's work include Mitochondrial Function and Pathology (3 papers), RNA modifications and cancer (3 papers) and Vitamin D Research Studies (2 papers). Julien Marcadier is often cited by papers focused on Mitochondrial Function and Pathology (3 papers), RNA modifications and cancer (3 papers) and Vitamin D Research Studies (2 papers). Julien Marcadier collaborates with scholars based in Canada, United States and Netherlands. Julien Marcadier's co-authors include Christopher E. Pearson, Zhigang Yang, David Chitayat, Rachel Lau, Duane L. Guernsey, Haiyan Jiang, Andrew Orr, Marie‐Pierre Dubé, Sylvie Provost and Michael T. Geraghty and has published in prestigious journals such as New England Journal of Medicine, Journal of Biological Chemistry and PLoS ONE.

In The Last Decade

Julien Marcadier

15 papers receiving 392 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Julien Marcadier Canada	11	210	119	78	66	51	15	417
Martin Krenn Austria	13	135 0.6×	60 0.5×	86 1.1×	12 0.2×	21 0.4×	36	394
Matthias Klaften Germany	13	255 1.2×	115 1.0×	12 0.2×	26 0.4×	35 0.7×	22	460
Fabiana D’Esposito Italy	10	277 1.3×	68 0.6×	31 0.4×	11 0.2×	98 1.9×	62	451
Yukihiko Kohda Japan	10	214 1.0×	20 0.2×	109 1.4×	17 0.3×	20 0.4×	14	474
Minyan Zhu China	13	212 1.0×	30 0.3×	56 0.7×	23 0.3×	22 0.4×	32	386
Kazuro Sugishita Japan	13	291 1.4×	22 0.2×	65 0.8×	19 0.3×	21 0.4×	23	514
Chunyu Tian China	10	165 0.8×	24 0.2×	64 0.8×	63 1.0×	121 2.4×	17	366
Yoichi Wada Japan	13	209 1.0×	39 0.3×	74 0.9×	8 0.1×	13 0.3×	27	372
Shi Ma China	14	235 1.1×	49 0.4×	21 0.3×	26 0.4×	108 2.1×	31	429
Sari Kiuru Finland	14	466 2.2×	269 2.3×	24 0.3×	39 0.6×	39 0.8×	18	642

Countries citing papers authored by Julien Marcadier

Since Specialization

Citations

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

Fields of papers citing papers by Julien Marcadier

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Julien Marcadier

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

All Works

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15 of 15 papers shown

Marcadier, Julien, et al.. (2022). Psychosis and autism without functional regression in a patient with Kleefstra syndrome. Psychiatric Genetics. 33(1). 34–36. 3 indexed citations

Banerjee, Ronadip R., Tara Spence, Stuart J. Frank, et al.. (2021). Very Low Vitamin D in a Patient With a Novel Pathogenic Variant in the GC Gene That Encodes Vitamin D-Binding Protein. Journal of the Endocrine Society. 5(9). bvab104–bvab104. 6 indexed citations

Christian, Susan, Patricia Birch, Laura Zahavich, et al.. (2021). Development and Evaluation of Decision Aids to Guide Families’ Predictive Testing Choices for Children at Risk for Arrhythmia or Cardiomyopathy. Canadian Journal of Cardiology. 37(10). 1586–1592. 8 indexed citations

Greenway, Steven C., et al.. (2021). Early Death of 2 Siblings Related to Mutations in LMOD2, a Recently Discovered Cause of Neonatal Dilated Cardiomyopathy. CJC Open. 3(10). 1300–1302. 10 indexed citations

Balcı, Tuğçe B., Jennifer M. Kalish, Elaine H. Zackai, et al.. (2020). Tatton‐Brown‐Rahman syndrome: Six individuals with novel features. American Journal of Medical Genetics Part A. 182(4). 673–680. 14 indexed citations

Henderson, Clark M., Susan L. Fink, Bob Argiropoulos, et al.. (2019). Vitamin D–Binding Protein Deficiency and Homozygous Deletion of the GC Gene. New England Journal of Medicine. 380(12). 1150–1157. 38 indexed citations

Lim, Rachel, Stefan J. Marciniak, Julien Marcadier, Doris M. Rassl, & Patrick Mitchell. (2018). Time Is of the Essence: A Young Man with Recurrent Pneumothorax and Cavitating Lung Lesions. Annals of the American Thoracic Society. 15(8). 988–991. 3 indexed citations

Smith, Amanda, Skye McBride, Julien Marcadier, et al.. (2016). Severe Neonatal Presentation of Mitochondrial Citrate Carrier (SLC25A1) Deficiency. JIMD Reports. 30. 73–79. 16 indexed citations

Marcadier, Julien, Alan J. Mears, Elizabeth A. Woods, et al.. (2015). A novel mutation in two Hmong families broadens the range of STRA6‐related malformations to include contractures and camptodactyly. American Journal of Medical Genetics Part A. 170(1). 11–18. 14 indexed citations

10.

Marcadier, Julien, Margaret Boland, C. Ronald Scott, et al.. (2014). Congenital sucrase–isomaltase deficiency: identification of a common Inuit founder mutation. Canadian Medical Association Journal. 187(2). 102–107. 29 indexed citations

11.

Marcadier, Julien, Amanda M. Smith, Daniela Pohl, et al.. (2013). Mutations in ALDH6A1 encoding methylmalonate semialdehyde dehydrogenase are associated with dysmyelination and transient methylmalonic aciduria. Orphanet Journal of Rare Diseases. 8(1). 98–98. 31 indexed citations

12.

Orr, Andrew, Marie‐Pierre Dubé, Juan Carlos Zenteno, et al.. (2011). Mutations in a novel serine protease PRSS56 in families with nanophthalmos.. PubMed. 17. 1850–61. 43 indexed citations

13.

Orr, Andrew, Marie‐Pierre Dubé, Julien Marcadier, et al.. (2007). Mutations in the UBIAD1 Gene, Encoding a Potential Prenyltransferase, Are Causal for Schnyder Crystalline Corneal Dystrophy. PLoS ONE. 2(8). e685–e685. 110 indexed citations

14.

Marcadier, Julien & Christopher E. Pearson. (2003). Fidelity of Primate Cell Repair of a Double-strand Break within a (CTG)·(CAG) Tract. Journal of Biological Chemistry. 278(36). 33848–33856. 30 indexed citations

15.

Yang, Zhigang, Rachel Lau, Julien Marcadier, David Chitayat, & Christopher E. Pearson. (2003). Replication Inhibitors Modulate Instability of an Expanded Trinucleotide Repeat at the Myotonic Dystrophy Type 1 Disease Locus in Human Cells. The American Journal of Human Genetics. 73(5). 1092–1105. 62 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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