Pauline Marzin

462 total citations
14 papers, 120 citations indexed

About

Pauline Marzin is a scholar working on Genetics, Molecular Biology and Oncology. According to data from OpenAlex, Pauline Marzin has authored 14 papers receiving a total of 120 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Genetics, 6 papers in Molecular Biology and 4 papers in Oncology. Recurrent topics in Pauline Marzin's work include Connective tissue disorders research (4 papers), Genetic Syndromes and Imprinting (2 papers) and Bone health and treatments (2 papers). Pauline Marzin is often cited by papers focused on Connective tissue disorders research (4 papers), Genetic Syndromes and Imprinting (2 papers) and Bone health and treatments (2 papers). Pauline Marzin collaborates with scholars based in France, United Kingdom and Portugal. Pauline Marzin's co-authors include Valérie Cormier‐Daire, Kimberly A. Aldinger, Boris Keren, Jean‐Luc Alessandri, Sophie Rondeau, Delphine Héron, Bertrand Isidor, William B. Dobyns, Caroline Michot and Geneviève Baujat and has published in prestigious journals such as International Journal of Molecular Sciences, Journal of Medical Genetics and Genetics in Medicine.

In The Last Decade

Pauline Marzin

11 papers receiving 120 citations

Peers

Pauline Marzin

GENET

RHEUM

ONCOL

PPCH

Bruna Lucheze Freire Brazil

Kévin Yauy France

Tossaporn Seeherunvong United States

Mehmet Tekman United Kingdom

Francesca Chiappe Italy

Wagner Antonio da Rosa Baratela Brazil

Houda Karmous‐Benailly France

Guillaume Jedraszak France

Michael Kessler United States

Desislava Nesheva Bulgaria

Bruna Lucheze Freire Brazil

Pauline Marzin

133 ×1.7

GENET

128 ×2.1

8 ×0.5

RHEUM

16 ×1.0

ONCOL

34 ×2.3

PPCH

Citations per year, relative to Pauline Marzin Pauline Marzin (= 1×) peers Bruna Lucheze Freire

Countries citing papers authored by Pauline Marzin

Since Specialization

Citations

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

Fields of papers citing papers by Pauline Marzin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Pauline Marzin

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

All Works

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14 of 14 papers shown

Marzin, Pauline, et al.. (2025). Rare features in Feingold syndrome type 1. European Journal of Medical Genetics. 78. 105049–105049.

Siquier-Pernet, Karine, Pauline Marzin, Christine Bôle‐Feysot, et al.. (2024). LSM7 variants involving key amino acids for LSM complex function cause a neurodevelopmental disorder with leukodystrophy and cerebellar atrophy. Human Genetics and Genomics Advances. 6(1). 100372–100372.

Güleç, Elif Yılmaz, Pauline Marzin, Céline Huber, & Valérie Cormier‐Daire. (2023). An intermediate phenotype in IDH related enchondromatosis spectrum. European Journal of Medical Genetics. 66(3). 104697–104697. 1 indexed citations

Marzin, Pauline, Sophie Rondeau, Jean‐Luc Alessandri, et al.. (2023). Weill-Marchesani syndrome: natural history and genotype-phenotype correlations from 18 news cases and review of literature. Journal of Medical Genetics. 61(2). 109–116. 7 indexed citations

Plaisancié, Julie, Jelena Martinović, Sandra Whalen, et al.. (2023). Clinical, genetic and biochemical signatures of RBP4-related ocular malformations. Journal of Medical Genetics. 61(1). 84–92. 2 indexed citations

Marzin, Pauline & Valérie Cormier‐Daire. (2021). Enfermedades óseas constitucionales. 56(2). 1–13.

Khirani, Sonia, Lucie Griffon, Geneviève Baujat, et al.. (2021). Sleep‐disordered breathing and its management in children with rare skeletal dysplasias. American Journal of Medical Genetics Part A. 185(7). 2108–2118. 2 indexed citations

Velasco, Guillaume, Damien Ulveling, Sophie Rondeau, et al.. (2021). Interplay between Histone and DNA Methylation Seen through Comparative Methylomes in Rare Mendelian Disorders. International Journal of Molecular Sciences. 22(7). 3735–3735. 8 indexed citations

Marzin, Pauline, Briac Thierry, Caroline Michot, et al.. (2020). Geleophysic and acromicric dysplasias: natural history, genotype–phenotype correlations, and management guidelines from 38 cases. Genetics in Medicine. 23(2). 331–340. 20 indexed citations

10.

Marzin, Pauline & Valérie Cormier‐Daire. (2020). New perspectives on the treatment of skeletal dysplasia. Therapeutic Advances in Endocrinology and Metabolism. 11. 2389824592–2389824592. 29 indexed citations

11.

Marzin, Pauline, Geneviève Baujat, D. Gensburger, et al.. (2019). Heterozygous FGFR1 mutation may be responsible for an incomplete form of osteoglophonic dysplasia, characterized only by radiolucent bone lesions and teeth retentions. European Journal of Medical Genetics. 63(2). 103729–103729. 7 indexed citations

12.

Ader, Flavie, Solveig Heide, Pauline Marzin, et al.. (2019). A 14q distal chromoanagenesis elucidated by whole genome sequencing. European Journal of Medical Genetics. 63(4). 103776–103776. 3 indexed citations

13.

Marzin, Pauline, Kimberly A. Aldinger, Jean‐Luc Alessandri, et al.. (2019). SETD2 related overgrowth syndrome: Presentation of four new patients and review of the literature. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 181(4). 509–518. 24 indexed citations

14.

Heide, Solveig, Matthieu Egloff, Pauline Marzin, et al.. (2017). Potential selection of genetically balanced spermatozoa based on the hypo-osmotic swelling test in chromosomal rearrangement carriers. Reproductive BioMedicine Online. 35(4). 372–378. 17 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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