Fanny Morice‐Picard

5.1k total citations
67 papers, 1.3k citations indexed

About

Fanny Morice‐Picard is a scholar working on Molecular Biology, Cell Biology and Genetics. According to data from OpenAlex, Fanny Morice‐Picard has authored 67 papers receiving a total of 1.3k indexed citations (citations by other indexed papers that have themselves been cited), including 41 papers in Molecular Biology, 35 papers in Cell Biology and 16 papers in Genetics. Recurrent topics in Fanny Morice‐Picard's work include melanin and skin pigmentation (20 papers), RNA regulation and disease (14 papers) and Skin and Cellular Biology Research (13 papers). Fanny Morice‐Picard is often cited by papers focused on melanin and skin pigmentation (20 papers), RNA regulation and disease (14 papers) and Skin and Cellular Biology Research (13 papers). Fanny Morice‐Picard collaborates with scholars based in France, Japan and United Kingdom. Fanny Morice‐Picard's co-authors include Benoı̂t Arveiler, Alain Taı̈eb, Didier Lacombe, Eulalie Lasseaux, Khaled Ezzedine, Caroline Rooryck, Muriel Cario, F. Boralévi, Claudio Plaisant and Vincent Michaud and has published in prestigious journals such as Nature Communications, Nature Genetics and Blood.

In The Last Decade

Fanny Morice‐Picard

65 papers receiving 1.3k citations

Peers

Countries citing papers authored by Fanny Morice‐Picard

Since Specialization

Citations

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

Fields of papers citing papers by Fanny Morice‐Picard

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Fanny Morice‐Picard. 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 Fanny Morice‐Picard. The network helps show where Fanny Morice‐Picard may publish in the future.

Co-authorship network of co-authors of Fanny Morice‐Picard

This figure shows the co-authorship network connecting the top 25 collaborators of Fanny Morice‐Picard. A scholar is included among the top collaborators of Fanny Morice‐Picard 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 Fanny Morice‐Picard. Fanny Morice‐Picard 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

#	Work	Indexed citations
1	A postzygotic GNA13 variant upregulates the RHOA/ROCK pathway and alters melanocyte function in a mosaic skin hypopigmentation syndrome 2025 ·Nature Communications ·(unknown), (unknown), Paul Kuentz, Rachida Tacine, Marie Vincent, S. Barbarot, Fanny Morice‐Picard, F. Boralévi, (unknown), J. Mazereeuw‐Hautier, Yannis Duffourd, Laurence Faivre, Arthur Sorlin, P. Vabres, Jérôme Delon	2
2	Dyadic adjustment of persons with albinism and their significant other: A Bayesian mediation model of the Actor-Partner Interdependence (APIMeM) 2025 ·Social Science & Medicine ·(unknown), (unknown), Fanny Morice‐Picard, S. Hadj‐Rabia, Benoı̂t Arveiler, Bruno Quintard	1
3	French national protocol for the management of congenital ichthyosis 2024 ·Annales de Dermatologie et de Vénéréologie ·(unknown), (unknown), C. Chiavérini, (unknown), Fanny Morice‐Picard, Hélène Texier, I. Dreyfus, (unknown), S. Mallet, Christine Bodemer, Judith Fischer, Nathalie Jonca, J. Mazereeuw‐Hautier	0
4	Prenatal diagnosis for neurofibromatosis type 1 and the pitfalls of germline mosaics 2024 ·npj Genomic Medicine ·(unknown), Dominique Vidaud, (unknown), (unknown), (unknown), (unknown), (unknown), Ingrid Laurendeau, (unknown), (unknown), Benoît Funalot, P. Wolkenstein, Michel Vidaud, Alice Goldenberg, Fanny Morice‐Picard, Djihad Hadjadj, Béatrice Parfait, Éric Pasmant	2
5	Hypohidrotic ectodermal dysplasia in a family: expanding spectrum of LEF1-related disorders 2024 ·Clinical and Experimental Dermatology ·Mohd Ali Hassan, Fanny Morice‐Picard, (unknown), (unknown), (unknown), (unknown)	0
6	Genomic mutation landscape of skin cancers from DNA repair-deficient xeroderma pigmentosum patients 2023 ·Nature Communications ·Andrey A. Yurchenko, (unknown), Tirzah Braz Petta Lajus, Hiva Fassihi, Alan R. Lehmann, Chikako Nishigori, Jinxin Wang, Ismaël Padioleau, Konstantin Gunbin, (unknown), Fanny Morice‐Picard, (unknown), Caroline Robert, Patricia Kannouche, Carlos Frederico Martins Menck, Alain Sarasin, Sergey I. Nikolaev	28
7	Unsuspected consequences of synonymous and missense variants in OCA2 can be detected in blood cell RNA samples of patients with albinism 2023 ·Pigment Cell & Melanoma Research ·Vincent Michaud, Angèle Tingaud‐Sequeira, (unknown), Eulalie Lasseaux, Claudio Plaisant, S. Hadj‐Rabia, Sandra Whalen, Dominique Bonneau, Anne Dieux‐Coëslier, Fanny Morice‐Picard, (unknown), Benoı̂t Arveiler, Sophie Javerzat	4
8	A novel pathogenic variant in the FZD6 gene causes recessive nail dysplasia in a Moroccan family 2023 ·Clinical and Experimental Dermatology ·(unknown), (unknown), Eulalie Lasseaux, Isabelle Creveaux, C. Léauté‐Labrèze, F. Boralévi, Fanny Morice‐Picard	1
9	Oculo-Cutaneous Albinism Type 4 (OCA4): Phenotype-Genotype Correlation 2022 ·Genes ·(unknown), Fanny Morice‐Picard, Eulalie Lasseaux, Matthieu P. Robert, (unknown), Vincent Michaud, Stéphanie Leclerc‐Mercier, Dominique Brémond‐Gignac, Benoı̂t Arveiler, S. Hadj‐Rabia	6
10	ARP-T1-associated Bazex–Dupré–Christol syndrome is an inherited basal cell cancer with ciliary defects characteristic of ciliopathies 2021 ·Communications Biology ·Hyun‐Sook Park, (unknown), (unknown), (unknown), Daniel Bachmann, Markus Plomann, Fanny Morice‐Picard, P. Vabres, Asma Smahi, Marcel Huber, Christine Pich-Bavastro, Daniel Hohl	6
11	Management of albinism: French guidelines for diagnosis and care 2021 ·Journal of the European Academy of Dermatology and Venereology ·(unknown), Fanny Morice‐Picard, Dominique Brémond‐Gignac, (unknown), (unknown), Stéphanie Leclerc‐Mercier, (unknown), Josseline Kaplan, (unknown), Benoı̂t Arveiler, Alain Taı̈eb, S. Hadj‐Rabia	11
12	A new case with Hermansky-Pudlak syndrome type 9, a rare cause of syndromic albinism with severe defect of platelets dense bodies 2020 ·Platelets ·Vincent Michaud, Mathieu Fiore, (unknown), (unknown), Jean‐Claude Bordet, Claudio Plaisant, Eulalie Lasseaux, Fanny Morice‐Picard, Benoı̂t Arveiler	8
13	Novel variants in the BLOC1S3 gene in patients presenting a mild form of Hermansky–Pudlak syndrome 2020 ·Pigment Cell & Melanoma Research ·Perrine Pennamen, Angèle Tingaud‐Sequeira, Vincent Michaud, Fanny Morice‐Picard, Claudio Plaisant, (unknown), Fabienne Giuliano, Saba Azarnoush, Yline Capri, Carolina Reato Marçon, Didier Lacombe, Eulalie Lasseaux, Benoı̂t Arveiler	7
14	Xeroderma pigmentosum in South Africa: Evidence for a prevalent founder effect 2019 ·British Journal of Dermatology ·(unknown), Fanny Morice‐Picard, Hamid Rezvani, Frédéric Austerlitz, François Cartault, Alain Sarasin, Mike Sathekge, Alain Taı̈eb, Cécile Ged	9
15	Pigmentation abnormalities in nucleotide excision repair disorders: Evidence and hypotheses 2018 ·Pigment Cell & Melanoma Research ·(unknown), S. Trompezinski, Muriel Cario, Fanny Morice‐Picard, Cécile Ged, Marie‐Laure Jullié, Alain Taı̈eb, Hamid Rezvani	5
16	Epidermolysis bullosa simplex generalized severe induces a T helper 17 response and is improved by apremilast treatment 2018 ·British Journal of Dermatology ·E. Castela, Meri K. Tulić, Aurore Rozières, E. Bourrat, Jean‐François Nicolas, Jean Kanitakis, P. Vabres, D. Bessis, J. Mazereeuw‐Hautier, Fanny Morice‐Picard, David Baty, F. Bérard, J.‐P. Lacour, Thierry Passeron, C. Chiavérini	38
17	Mild form of oculocutaneous albinism type 1: phenotypic analysis of compound heterozygous patients with the R402Q variant of the TYR gene 2018 ·British Journal of Ophthalmology ·(unknown), Eulalie Lasseaux, (unknown), Christian Hamel, Sabine Defoort‐Dhellemmes, Isabelle Drumare, Xavier Zanlonghi, Hélène Dollfus, (unknown), Dominique Bonneau, Jean‐François Korobelnik, Claudio Plaisant, Vincent Michaud, Perrine Pennamen, Caroline Rooryck, Fanny Morice‐Picard, (unknown), Benoı̂t Arveiler	26
18	Lessons of a day hospital: Comprehensive assessment of patients with albinism in a European setting 2017 ·Pigment Cell & Melanoma Research ·(unknown), Eulalie Lasseaux, Khaled Ezzedine, C. Léauté‐Labrèze, F. Boralévi, (unknown), (unknown), (unknown), Benoı̂t Arveiler, Alain Taı̈eb, Fanny Morice‐Picard	26
19	Hypertrophic neuropathy in Noonan syndrome with multiple lentigines 2016 ·American Journal of Medical Genetics Part A ·(unknown), Guilhem Solé, Fanny Morice‐Picard, Alain Taı̈eb	9
20	STXBP1-related encephalopathy presenting as infantile spasms and generalized tremor in three patients 2011 ·Epilepsia ·Cyril Mignot, Marie‐Laure Moutard, Oriane Trouillard, Isabelle Gourfinkel‐An, Aurélia Jacquette, Benoı̂t Arveiler, Fanny Morice‐Picard, Didier Lacombe, Catherine Chiron, Dorothée Ville, Perrine Charles, Eric Leguern, Christel Depienne, Delphine Héron	76

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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