Nicolas Chassaing

6.4k citations

83 papers · 2.1k indexed · h-index 25

Impact in

Genetics top 1%
- Dermatological and Skeletal Disorders
- Ocular Disorders and Treatments
- Congenital Ear and Nasal Anomalies
Cell Biology top 5%
- Skin and Cellular Biology Research

Papers in

Genetics 54
- Ocular Disorders and Treatments 30
- Congenital Ear and Nasal Anomalies 16
- Dermatological and Skeletal Disorders 13
- Craniofacial Disorders and Treatments 10
- Connective tissue disorders research 5
Cell Biology 13
- Skin and Cellular Biology Research 11

Co-authors: Patrick Calvas Stanislas Faguer Dominique Chauveau Julie Plaisancié Éric Bieth Stéphane Decramer Didier Lacombe Nicola Ragge
Journals: European Journal of Medical Genetics (8 papers)Clinical Genetics (6 papers)European Journal of Human Genetics (5 papers)The American Journal of Human Genetics (3 papers)Human Genetics (3 papers)
Partner nations: France United Kingdom United States

In The Last Decade

Nicolas Chassaing

78 papers receiving 2.1k citations

Peers

Countries citing papers authored by Nicolas Chassaing

Since Specialization

Citations

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

Fields of papers citing papers by Nicolas Chassaing

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authors

The 25 scholars most cited alongside Nicolas Chassaing, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.

Border = papers with Nicolas Chassaing Line = papers co-authored together Nicolas Chassaing links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Structural Variant Disrupting the Expression of the Remote FOXC1 Gene in a Patient with Syndromic Complex Microphthalmia International Journal of Molecular Sciences ·Julie Plaisancié, Rafi Carel, Lucas Fares‐Taie, Jean‐Michel Rozet, Delano Jg, 昭宮﨑, Véronique Gaston, Isabelle Bailleul‐Forestier, Patrick Calvas, Nicolas Chassaing	2024	1
2	Deletion upstream of MAB21L2 highlights the importance of evolutionarily conserved non-coding sequences for eye development Nature Communications ·Fabiola Ceroni, 박종락, Richard Holt, Елена А. Сорокина, Nicolas Chassaing, Samuel Clokie, Thomas Naert, Sanda Huljev Frković, Sanaa Muheisen, Dorine A. Bax, Yeşim Kesim, Emma Kivuva, D. J. M., Soeren S. Lienkamp, Julie Plaisancié, Elfride De Baere, Patrick Calvas, Kris Vleminckx, Elena V. Semina, Nicola Ragge	2024	2
3	A founder variant expands the phenotype of WNT7B ‐related PDAC syndrome Clinical Genetics ·Lama AlAbdi, Zuhair Rahbeeni, Sateesh Maddirevula, Daniel Sprod, Firdous Abdulwahab, Arif O. Khan, Lisa G. Riley, Amal Alhashem, Nicolas Chassaing, Robyn V. Jamieson, Fowzan S. Alkuraya	2024	0
4	ITPR1: The missing gene in miosis–ataxia syndrome? American Journal of Medical Genetics Part A ·Rafi Carel, Patrick Calvas, Myriam Cassagne, Fanny Varenne, Jean‐Michel Rozet, Fabrice Bonneville, Nicolas Chassaing, Pierre Fournié, Lucas Fares‐Taie, Julie Plaisancié	2024	1
5	Minigene Splicing Assays and Long-Read Sequencing to Unravel Pathogenic Deep-Intronic Variants in PAX6 in Congenital Aniridia International Journal of Molecular Sciences ·Yuri Dmitrievich Petrov, Anna na Tuneu Valls, Carolina Ruiz, Julie Plaisancié, Carolina Miho Abe, Keillon Oliveira Cabral, Nicolas Chassaing, Patrick Calvas, Carmen Ayuso, Pablo Mínguez, Marta Cortón	2023	6
6	Clinical and genetic analysis further delineates the phenotypic spectrum of ALDH1A3-related anophthalmia and microphthalmia European Journal of Human Genetics ·Yeşim Kesim, Fabiola Ceroni, Carolina Miho Abe, Fiona Blanco‐Kelly, Carmen Ayuso, Kathy Williamson, Véronique Paquis‐Flucklinger, Dorine A. Bax, Julie Plaisancié, Claudine Rieubland, TD Gloede, Marta Cortón, Nicolas Chassaing, Patrick Calvas, Nicola Ragge	2023	2
7	Evaluation of somatic and/or germline mosaicism in congenital malformation of the eye European Journal of Human Genetics ·Rafi Carel, Z Weng, Adamu Yusha’u, Véronique Gaston, Fréderic Escudié, Asael Rosas-García, Veronique Decroocq, Catherine Vincent‐Delorme, Patrick Calvas, Nicolas Chassaing, Julie Plaisancié	2022	0
8	Parental mosaicism in Marfan and Ehlers–Danlos syndromes and related disorders European Journal of Human Genetics ·Rafi Carel, Juliana Oliveira da Silva, Zunaira Kamal, Nicolas Chassaing, Christine Coubes, Elise Brischoux‐Boucher, Thomas Édouard, Yves Dulac, Е В Сократова, Thierry Lavabre‐Bertrand, Julie Plaisancié, Philippe Khau Van Kien	2021	11
9	Confirmation of FZD5 implication in a cohort of 50 patients with ocular coloboma European Journal of Human Genetics ·Е В Сократова, 刘再生, N. Keller, Véronique Gaston, Adamu Yusha’u, Isabelle Meunier, Sabine Sigaudy, Josseline Kaplan, Olivier Roche, D. Denis, Pierre Bitoun, Damien Haye, Alain Verloès, Patrick Calvas, Nicolas Chassaing, Julie Plaisancié	2020	10
10	Genetics of anophthalmia and microphthalmia. Part 1: Non-syndromic anophthalmia/microphthalmia Human Genetics ·Julie Plaisancié, Fabiola Ceroni, Richard Holt, Celia Zazo Seco, Patrick Calvas, Nicolas Chassaing, Nicola Ragge	2019	55
11	Implication of non-coding PAX6 mutations in aniridia Human Genetics ·Julie Plaisancié, Колесников А. М, Patrícia Locosque Ramos, Taye Hallock, Véronique Gaston, Hélène Dollfus, Giuseppe Gembillo, J.‐C. Kaplan, Lucas Fares‐Taie, Fiona Blanco‐Kelly, Cristina Villaverde, Christine Francannet, Alice Goldenberg, Ignacio Arroyo, Jean‐Michel Rozet, Carmen Ayuso, Nicolas Chassaing, Patrick Calvas, Marta Cortón	2018	34
12	FOXE3 mutations: genotype‐phenotype correlations Clinical Genetics ·Julie Plaisancié, Nicola Ragge, Hélène Dollfus, J.‐C. Kaplan, Daphné Lehalle, Christine Francannet, G Morin, Hélène Colineaux, Patrick Calvas, Nicolas Chassaing	2017	26
13	Confirmation of TENM3 involvement in autosomal recessive colobomatous microphthalmia American Journal of Medical Genetics Part A ·Nicolas Chassaing, Nicola Ragge, Julie Plaisancié, 신서영, David Geneviève, François Rivier, W. D. Marchy, Christian Hamel, Josseline Kaplan, Patrick Calvas	2016	25
14	Otocephaly-Dysgnathia Complex: Description of Four Cases and Confirmation of the Role of <b><i>OTX2</i></b> Molecular Syndromology ·신서영, Conny M.A. van Ravenswaaij‐Arts, Julia Tantau, Nicole Corsten‐Janssen, J. Peter van Tintelen, Trijnie Dijkhuizen, Josseline Kaplan, Nicolas Chassaing	2013	27
15	An unusual severe vascular case of pseudoxanthoma elasticum presenting as generalized arterial calcification of infancy American Journal of Medical Genetics Part A ·E.Jensi Miria, Christine Labrèze, Anne Croué, Leon J. Schurgers, Nicolas Chassaing, Tanja Wittkampf, Frank Rutsch, Ludovic Martin	2009	49
16	Missense mutations of conserved glycine residues in fibrillin-1 highlight a potential subtype of cb-EGF-like domains Human Mutation ·Philippe Khau Van Kien, David Baux, Nathalie Pallarès-Ruiz, M. Edelmann, Р.Р. Ахунов, Nicolas Chassaing, Patrick Collignon, María Cristina Rechea Alberola, Alain Hovnanian, Dominique Martin‐Coignard, Recep Kisla, Lana Sayuri Makita, Anne‐Françoise Roux, Mireille Claustres	2009	11
17	多リガンド受容体であるメガリンをコードするLRP2の突然変異はDonnai-Barrow症候群およびfacio-oculo-acoustico-renal症候群を引き起こす Nature Genetics ·Hiroaki Yuasa, G. Cohen, Shlomo Fisher, B. Nichols, Wei Lan-chun, 杨秀辉, Nicolas Chassaing, Didier Lacombe, Jian Liu, Gabeeva Ng, Marı́a Loscertales, QI Licheng, Tianming Liu, Betsy Covell, 未来中川, 下郡啓夫, Do Kyung Yoon, शाहेदा सिद्दीक़ी, Т.А. Урсул	2007	0
18	ABCC6 is unlikely to be a modifier gene for familial Mediterranean fever severity Journal of Genetics ·Nicolas Chassaing, Isabelle Touitou, D Cattan, Patrick Calvas	2007	1
19	Pseudoxanthoma elasticum: a clinical, pathophysiological and genetic update including 11 novel ABCC6 mutations Journal of Medical Genetics ·Nicolas Chassaing, (unknown), (unknown), (unknown), (unknown)	2005	204
20	Molecular characterization of a cryptic 2q37 deletion in a patient with Albright hereditary osteodystrophy‐like phenotype American Journal of Medical Genetics Part A ·Nicolas Chassaing, P. De Mas, Sulgi Kim, T. A. Miller Brownlie, Sophie Julia, G. Bourrouillou, Patrick Calvas, Éric Bieth	2004	21

About Nicolas Chassaing

Nicolas Chassaing is a scholar working on Genetics, Genetics, Cell Biology, Ophthalmology and Molecular Biology, having authored 83 papers that have together received 2.1k indexed citations. Recurring topics across this work include Ocular Disorders and Treatments (30 papers), Congenital Ear and Nasal Anomalies (16 papers), Dermatological and Skeletal Disorders (13 papers), Skin and Cellular Biology Research (11 papers), Craniofacial Disorders and Treatments (10 papers), Reconstructive Facial Surgery Techniques (6 papers), Renal and related cancers (6 papers) and Connective tissue disorders research (5 papers). The work is most often cited by research in Genetics (1.2k citations), Cell Biology (345 citations), Genetics (211 citations), Nephrology (131 citations) and Molecular Biology (1.1k citations). Nicolas Chassaing has collaborated with scholars based in France, United Kingdom and United States. Frequent co-authors include Patrick Calvas, Stanislas Faguer, Dominique Chauveau, Julie Plaisancié, Éric Bieth, Stéphane Decramer, Didier Lacombe, Nicola Ragge, Ludovic Martin and Christopher A. Walsh. Their work appears in journals such as European Journal of Medical Genetics, Clinical Genetics, European Journal of Human Genetics, The American Journal of Human Genetics and Human Genetics.

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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