Chloé Quēlin

2.4k total citations
24 papers, 280 citations indexed

About

Chloé Quēlin is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Chloé Quēlin has authored 24 papers receiving a total of 280 indexed citations (citations by other indexed papers that have themselves been cited), including 15 papers in Genetics, 14 papers in Molecular Biology and 9 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in Chloé Quēlin's work include Genomic variations and chromosomal abnormalities (7 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Prenatal Screening and Diagnostics (5 papers). Chloé Quēlin is often cited by papers focused on Genomic variations and chromosomal abnormalities (7 papers), Fetal and Pediatric Neurological Disorders (6 papers) and Prenatal Screening and Diagnostics (5 papers). Chloé Quēlin collaborates with scholars based in France, Australia and Japan. Chloé Quēlin's co-authors include Laurent Pasquier, Sylvie Odent, Sylvie Jaillard, Christèle Dubourg, Josette Lucas, Philippe Loget, Véronique David, Laurence Lœuillet, Mélanie Fradin and Jean‐Marie Rival and has published in prestigious journals such as Human Genetics, European Journal of Human Genetics and Orphanet Journal of Rare Diseases.

In The Last Decade

Chloé Quēlin

21 papers receiving 265 citations

Peers

Chloé Quēlin

GENET

PPCH

SURGE

GENET

Lucie Rochard United States

Özge Özalp Yüreğir Türkiye

Kristen L. Sund United States

N. A. Skryabin Russia

Amal Hashem Saudi Arabia

Kiyoshi Kikkawa Japan

Emma Hobson United Kingdom

Jeannette Hoogeboom Netherlands

Josef Davidsson Sweden

Emma Kivuva United Kingdom

Lucie Rochard United States

Chloé Quēlin

242 ×1.6

183 ×1.3

GENET

77 ×0.9

PPCH

27 ×1.0

SURGE

21 ×1.0

GENET

Citations per year, relative to Chloé Quēlin Chloé Quēlin (= 1×) peers Lucie Rochard

Countries citing papers authored by Chloé Quēlin

Since Specialization

Citations

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

Fields of papers citing papers by Chloé Quēlin

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Chloé Quēlin

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

All Works

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20 of 20 papers shown

Boutaud, Lucile, Chloé Quēlin, Philippe Roth, et al.. (2025). Complete loss of IFT27 function leads to a phenotypic spectrum of fetal lethal ciliopathy associated with altered ciliogenesis. European Journal of Human Genetics. 33(3). 387–392. 2 indexed citations

Dion, Ludivine, Maud Bidet, Chloé Quēlin, et al.. (2024). Optimizing care for MRKH patients: From malformation screening to uterus transplantation eligibility. Acta Obstetricia Et Gynecologica Scandinavica. 104(3). 514–521.

Quēlin, Chloé, et al.. (2024). Expanding the TUBB3‐Related Phenotypic Landscape: Fetal Diagnosis of Novel TUBB3 Variant Linked With Phenotypic Variability Within a Single Family. Prenatal Diagnosis. 45(1). 134–137.

Quēlin, Chloé, Laurent Pasquier, Philippe Loget, et al.. (2023). PHGDH-related microcephalic dwarfism in two fetuses: Expanding the phenotypical spectrum of L-serine biosynthesis defect. European Journal of Medical Genetics. 66(11). 104852–104852.

Kato, Kohji, Frédéric Tran Mau‐Them, Chloé Quēlin, et al.. (2023). Gain-of-function MYCN causes a megalencephaly-polydactyly syndrome manifesting mirror phenotypes of Feingold syndrome. Human Genetics and Genomics Advances. 4(4). 100238–100238. 2 indexed citations

Breton, Sylvain, Marie‐Liesse Piketty, Alexandra Afenjar, et al.. (2022). SATB2-associated syndrome: characterization of skeletal features and of bone fragility in a prospective cohort of 19 patients. Orphanet Journal of Rare Diseases. 17(1). 100–100. 10 indexed citations

Lavillaureix, Alinoë, Philippe Loget, Erika Launay, et al.. (2022). Prenatal phenotype of 22q11 micro-duplications: A systematic review and report on 12 new cases. European Journal of Medical Genetics. 65(2). 104422–104422. 7 indexed citations

Carré, Wilfrid, et al.. (2022). Fetal Description of the Pancreatic Agenesis and Holoprosencephaly Syndrome Associated to a Specific CNOT1 Variant. Pediatric and Developmental Pathology. 25(5). 548–552. 5 indexed citations

Braden, Ruth, Siddharth Srivastava, Gaëtan Lesca, et al.. (2021). Clinical delineation of SETBP1 haploinsufficiency disorder. European Journal of Human Genetics. 29(8). 1198–1205. 17 indexed citations

10.

Fradin, Mélanie, Alinoë Lavillaureix, Sylvie Jaillard, et al.. (2020). ATP7A mutation with occipital horns and distal motor neuropathy: A continuum. European Journal of Medical Genetics. 63(12). 104087–104087. 8 indexed citations

11.

Akloul, Linda, Wilfrid Carré, Chloé Quēlin, et al.. (2019). Targeted panel sequencing establishes the implication of planar cell polarity pathway and involves new candidate genes in neural tube defect disorders. Human Genetics. 138(4). 363–374. 17 indexed citations

12.

Quēlin, Chloé, Philippe Loget, Lucile Boutaud, et al.. (2018). Loss of function IFT27 variants associated with an unclassified lethal fetal ciliopathy with renal agenesis. American Journal of Medical Genetics Part A. 176(7). 1610–1613. 11 indexed citations

13.

Deloison, B., P. Sonigo, A. Millischer, et al.. (2018). Prenatally diagnosed periventricular nodular heterotopia: Further delineation of the imaging phenotype and outcome. European Journal of Medical Genetics. 61(12). 773–782. 12 indexed citations

14.

Bouchghoul, Hanane, Chloé Quēlin, Philippe Loget, et al.. (2018). Fetal cerebral hemorrhage due to X‐linkedGATA1gene mutation. Prenatal Diagnosis. 38(10). 772–778. 7 indexed citations

15.

Pasquier, Laurent, Mélanie Fradin, Dominique Martin‐Coignard, et al.. (2015). Karyotype is not dead (yet)!. European Journal of Medical Genetics. 59(1). 11–15. 31 indexed citations

16.

Dubourg, Christèle, Laurent Pasquier, Sylvie Odent, et al.. (2014). Postnatal diagnosis of 9q interstitial imbalances involving PTCH1, resulting from a familial intrachromosomal insertion. European Journal of Medical Genetics. 57(5). 195–199. 1 indexed citations

17.

Démurger, Florence, Laurent Pasquier, Christèle Dubourg, et al.. (2013). Array-CGH Analysis Suggests Genetic Heterogeneity in Rhombencephalosynapsis. Molecular Syndromology. 4(6). 267–272. 11 indexed citations

18.

Quēlin, Chloé, Yoann Saillour, Isabelle Souville, et al.. (2012). Mosaic DCX deletion causes subcortical band heterotopia in males. Neurogenetics. 13(4). 367–373. 11 indexed citations

19.

Quēlin, Chloé, Yoann Saillour, Karine Poirier, et al.. (2012). Focal polymicrogyria are associated with submicroscopic chromosomal rearrangements detected by CGH microarray analysis. European Journal of Medical Genetics. 55(10). 527–530. 6 indexed citations

20.

Osimani, Sara, Isabelle Husson, Sandrine Passemard, et al.. (2010). Craniosynostosis: A rare complication of pycnodysostosis. European Journal of Medical Genetics. 53(2). 89–92. 20 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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