Cindy Colson

722 total citations
13 papers, 131 citations indexed

About

Cindy Colson is a scholar working on Molecular Biology, Genetics and Clinical Biochemistry. According to data from OpenAlex, Cindy Colson has authored 13 papers receiving a total of 131 indexed citations (citations by other indexed papers that have themselves been cited), including 12 papers in Molecular Biology, 7 papers in Genetics and 3 papers in Clinical Biochemistry. Recurrent topics in Cindy Colson's work include Genomics and Rare Diseases (4 papers), Genetic Syndromes and Imprinting (3 papers) and Metabolism and Genetic Disorders (3 papers). Cindy Colson is often cited by papers focused on Genomics and Rare Diseases (4 papers), Genetic Syndromes and Imprinting (3 papers) and Metabolism and Genetic Disorders (3 papers). Cindy Colson collaborates with scholars based in France, Belgium and United States. Cindy Colson's co-authors include Marie‐Laure Kottler, Nicolas Richard, Arnaud Molin, Virginie Grybek, Agnès Linglart, Stéphanie Maupetit‐Mehouas, Harald Jüppner, Marion Gérard, Hervé Mittre and Anne‐Claire Bréhin and has published in prestigious journals such as Nature Communications, The Journal of Clinical Endocrinology & Metabolism and Journal of Bone and Mineral Research.

In The Last Decade

Cindy Colson

12 papers receiving 129 citations

Peers

Countries citing papers authored by Cindy Colson

Since Specialization

Citations

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

Fields of papers citing papers by Cindy Colson

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Cindy Colson

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

All Works

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13 of 13 papers shown

#	Work	Indexed citations
1	Genome sequencing identifies RMND1 as a strong candidate gene for severe prenatal kidney failure mimicking renal tubular dysgenesis associated with hyporeninism 2025 ·Pediatric Nephrology ·(unknown), (unknown), Christelle Arrondel, Giulia Barcia, Zahra Assouline, Olivier Gribouval, Diana Wellesley, Victoria Harrison, Pierre Marijon, Cindy Colson, (unknown), Marie-Claire Gübler, Corinne Antignac, Agnès Rötig, Laurence Heidet	1
2	Expanded phenotypic spectrum of UDP‐glucose‐6‐dehydrogenase recessive neurodevelopmental disorder: Two novel descriptions with or without epileptic encephalopathy 2024 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), (unknown), Perrine Brunelle, C. Thuillier, Clémence Vanlerberghe, Roseline Caumes, Cindy Colson, Emilie Ait‐Yahya, Jamal Ghoumid, Thomas Smol	1
3	Primary Failure of Dental Eruption Due to Variants Parathyroid Hormone Receptor 1: Retrospective Study and Proposal of Guidelines Treatment 2024 ·Journal of Craniofacial Surgery ·(unknown), (unknown), (unknown), Cindy Colson, Clémence Vanlerberghe, (unknown), G. Raoul, (unknown), Joël Ferri	0
4	Phenotypic and genotypic characterization of 1q21.1 copy number variants: A report of 34 new individuals and literature review 2023 ·American Journal of Medical Genetics Part A ·(unknown), (unknown), Cindy Colson, (unknown), Arnaud Molin, Marion Gérard, Nicolas Gruchy	6
5	Joint involvement in Noonan syndrome. A retrospective paediatric descriptive study 2021 ·Joint Bone Spine ·(unknown), Thomas Édouard, Séverine Audebert‐Bellanger, (unknown), (unknown), Cindy Colson, (unknown), Sylvaine Poignant, Alain Saraux, Valérie Devauchelle‐Pensec	3
6	Evolutionary conserved NSL complex/BRD4 axis controls transcription activation via histone acetylation 2020 ·Nature Communications ·(unknown), Bilal N. Sheikh, M. Felicia Basilicata, Marie Vincent, Mathilde Nizon, Cindy Colson, Matthew Bird, James E. Bradner, (unknown), Michael Boutros, Asifa Akhtar	20
7	Expanding the Spectrum of Neurological Manifestations in Cutis Laxa, Autosomal Recessive, Type IIIA 2020 ·Neuropediatrics ·(unknown), Marie Thibaud, Nathalie Aladjidi, P. Bessou, (unknown), Cindy Colson, Caroline Espil‐Taris, Cyril Goizet, Marie Husson, Fanny Morice‐Picard, Annachiara De Sandre‐Giovannoli, Jean‐Michel Pedespan	2
8	Unusual clinical description of adult with Timothy syndrome, carrier of a new heterozygote mutation of CACNA1C 2019 ·European Journal of Medical Genetics ·Cindy Colson, Hervé Mittre, Adeline Busson, Antoine Leenhardt, Isabelle Denjoy, (unknown), (unknown)	10
9	High frequency of paternal iso or heterodisomy at chromosome 20 associated with sporadic pseudohypoparathyroidism 1B 2019 ·Bone ·Cindy Colson, Matthieu Décamp, Nicolas Gruchy, Nadia Coudray, Céline Ballandonne, (unknown), Arnaud Molin, Hervé Mittre, (unknown), Harald Jüppner, Marie‐Laure Kottler, Nicolas Richard	18
10	Maternal Transmission Ratio Distortion of GNAS Loss-of-Function Mutations 2019 ·Journal of Bone and Mineral Research ·(unknown), Arnaud Molin, Cindy Colson, Nadia Coudray, (unknown), Hervé Mittre, Marion Gérard, Élise Schaefer, Alice Goldenberg, Justine Bacchetta, Sylvie Odent, Sophie Naudion, Bénédicte Demeer, Laurence Faivre, Nicolas Gruchy, Marie-Laure Kottler, Nicolas Richard	9
11	SF1 and spleen development: new heterozygous mutation, literature review and consequences for NR5A1‐mutated patient's management 2016 ·Clinical Genetics ·Cindy Colson, Évelyne Aubry, Maryse Cartigny, (unknown), (unknown), Xavier Leroy, (unknown), Caroline Lefèvre, R. Besson, Martine Cools, Anne‐Françoise Spinoit, C. Sultan, Sylvie Manouvrier, Pascal Philibert, Jamal Ghoumid	16
12	Multiple congenital anomalies in two boys with mutation in HCFC1 and cobalamin disorder 2015 ·European Journal of Medical Genetics ·Marion Gérard, Gilles Morin, A. Bourillon, Cindy Colson, Sophie Mathieu, Daniel Rabier, Thierry Billette de Villemeur, H. Ogier de Baulny, Jean François Benoist	21
13	Loss of Methylation at GNAS Exon A/B Is Associated With Increased Intrauterine Growth 2015 ·The Journal of Clinical Endocrinology & Metabolism ·Anne‐Claire Bréhin, Cindy Colson, Stéphanie Maupetit‐Mehouas, Virginie Grybek, Nicolas Richard, Agnès Linglart, Marie‐Laure Kottler, Harald Jüppner	24

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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