Perrine Pennamen

1.2k citations

15 papers · 637 indexed · 1 hit paper · h-index 9

Co-authors: Caroline Rooryck Aurélie Bedel Sandrine Dabernat François Moreau‐Gaudry Veronique Guyonnet‐Dupérat Jean‐Marc Blouin Jérôme Toutain Grégoire Cullot
Topics: melanin and skin pigmentation (6 papers)RNA regulation and disease (4 papers)Genomic variations and chromosomal abnormalities (3 papers)
Cited by: Business and International Management Aging Cell Biology
Journals: Nature Communications British Journal of Ophthalmology Genetics in Medicine
Partner nations: France Germany United Kingdom

In The Last Decade

Perrine Pennamen

15 papers receiving 629 citations

Hit Papers

align trajectories

What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncations

2019 310 citations Grégoire Cullot, Julian Boutin et al. Nature Communications profile →

Peers

Countries citing papers authored by Perrine Pennamen

Since Specialization

Citations

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

Fields of papers citing papers by Perrine Pennamen

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Perrine Pennamen

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

All Works

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15 of 15 papers shown

#	Work	Indexed citations
1	Cell cycle arrest and p53 prevent ON-target megabase-scale rearrangements induced by CRISPR-Cas9 2023 ·Nature Communications ·Grégoire Cullot,Julian Boutin,(unknown),(unknown),(unknown),David Cappellen,(unknown),Perrine Pennamen,Julie Bouron,Samuel Amintas,(unknown),Isabelle Moranvillier,Elodie Laharanne,Jean‐Philippe Merlio,Veronique Guyonnet‐Dupérat,Jean‐Marc Blouin,Emmanuel Richard,Sandrine Dabernat,François Moreau‐Gaudry,Aurélie Bedel	16
2	Evidence of mosaicism in SPAST variant carriers in four French families 2021 ·European Journal of Human Genetics ·(unknown),Cyril Goizet,(unknown),William Camu,Christel Depienne,Bénédicte Héron,(unknown),Marine Guillaud-Bataille,Perrine Pennamen,Caroline Rooryck,Clarisse Scherer‐Gagou,(unknown),Giovanni Stévanin,Eric Leguern,Guillaume Banneau	2
3	CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells 2021 ·Nature Communications ·Julian Boutin,(unknown),David Cappellen,(unknown),Jérôme Toutain,Perrine Pennamen,Julie Bouron,Caroline Rooryck,Jean‐Philippe Merlio,Isabelle Lamrissi‐Garcia,Grégoire Cullot,Samuel Amintas,Veronique Guyonnet‐Dupérat,Cécile Ged,Jean‐Marc Blouin,Élodie Richard,Sandrine Dabernat,François Moreau‐Gaudry,Aurélie Bedel	50
4	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
5	BLOC1S5 pathogenic variants cause a new type of Hermansky–Pudlak syndrome 2020 ·Genetics in Medicine ·Perrine Pennamen,Linh Le,Angèle Tingaud‐Sequeira,Mathieu Fiore,Anne Bauters,(unknown),(unknown),Jean‐Claude Bordet,Claudio Plaisant,(unknown),Vincent Michaud,Aurélien Trimouille,Didier Lacombe,Eulalie Lasseaux,Cédric Delevoye,(unknown),Bruno Delobel,Michael S. Marks,Benoı̂t Arveiler	55
6	Dopachrome tautomerase variants in patients with oculocutaneous albinism 2020 ·Genetics in Medicine ·Perrine Pennamen,Angèle Tingaud‐Sequeira,Iveta Gažová,Margaret Keighren,Lisa McKie,Sandrine Marlin,(unknown),Josseline Kaplan,Cédric Delevoye,Didier Lacombe,Claudio Plaisant,Vincent Michaud,Eulalie Lasseaux,Sophie Javerzat,Ian J. Jackson,Benoı̂t Arveiler	36
7	Clinical and molecular findings of FRMD7 related congenital nystagmus as adifferential diagnosis of ocular albinism 2019 ·Ophthalmic Genetics ·Vincent Michaud,Sabine Defoort‐Dhellemmes,Isabelle Drumare,Perrine Pennamen,Claudio Plaisant,Eulalie Lasseaux,Benoı̂t Arveiler	1
8	CRISPR-Cas9 genome editing induces megabase-scale chromosomal truncationsbreakdown → 2019 ·Nature Communications ·Grégoire Cullot,Julian Boutin,Jérôme Toutain,(unknown),Perrine Pennamen,Caroline Rooryck,Martin Teichmann,Emilie Rousseau,Isabelle Lamrissi‐Garcia,Veronique Guyonnet‐Dupérat,(unknown),Magalie Lalanne,Valérie Prouzet‐Mauleon,Béatrice Turcq,Cécile Ged,Jean‐Marc Blouin,Emmanuel Richard,Sandrine Dabernat,François Moreau‐Gaudry,Aurélie Bedel	310
9	PADDAS syndrome associated with hair dysplasia caused by a de novo missense variant of PUM1 2019 ·American Journal of Medical Genetics Part A ·(unknown),Fanny Morice‐Picard,Perrine Pennamen,Benoı̂t Arveiler,Patricia Fergelot,Cyril Goizet,(unknown),Didier Lacombe,Claudio Plaisant,(unknown),Caroline Rooryck,Eulalie Lasseaux,Aurélien Trimouille	5
10	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
11	An in-frame deletion in BICD2 associated with a non-progressive form of SMALED 2018 ·Clinical Neurology and Neurosurgery ·Aurélien Trimouille,Émilie Obre,Guillaume Banneau,Alexandra Dürr,Giovanni Stévanin,Fabienne Clot,Perrine Pennamen,(unknown),(unknown),Marie Rouanet,(unknown),Guilhem Solé,Stéphane Mathis,Cyril Goizet	7
12	Molecular characterization of a series of 990 index patients with albinism 2018 ·Pigment Cell & Melanoma Research ·Eulalie Lasseaux,Claudio Plaisant,Vincent Michaud,Perrine Pennamen,Aurélien Trimouille,(unknown),(unknown),Didier Lacombe,Caroline Rooryck,Fanny Morice‐Picard,Benoı̂t Arveiler	98
13	Deletion in 2q35 excluding the IHH gene leads to fetal severe limb anomalies and suggests a disruption of chromatin architecture 2018 ·European Journal of Human Genetics ·Aurélien Trimouille,Angèle Tingaud‐Sequeira,Perrine Pennamen,Gwenaëlle André,Julie Bouron,(unknown),Patricia Fergelot,Didier Lacombe,Benoı̂t Arveiler,Caroline Rooryck	3
14	Interest of chromosomal microarray analysis in the prenatal diagnosis of fetal intrauterine growth restriction 2018 ·Prenatal Diagnosis ·S. Brun,Perrine Pennamen,Aurélien Mattuizzi,(unknown),Marie‐Laure Vuillaume,Didier Lacombe,Benoı̂t Arveiler,Jérôme Toutain,Caroline Rooryck	9
15	Balanced complex chromosome rearrangement in male infertility: case report and literature review 2014 ·Andrologia ·Huong Minh Nguyen,Fréderic Morel,Perrine Pennamen,Philippe Parent,Nathalie Douet‐Guilbert,M.‐J. Le Bris,Audrey Basinko,Sylvie Roche,Marc De Braekeleer,Aurore Perrin	12

About Perrine Pennamen

Perrine Pennamen is a scholar working on Business and International Management, Developmental Biology and Cell Biology, having authored 15 papers that have together received 637 indexed citations. Recurring topics across this work include melanin and skin pigmentation (6 papers), RNA regulation and disease (4 papers) and Genomic variations and chromosomal abnormalities (3 papers). The work is most often cited by research in Business and International Management (38 citations), Aging (32 citations) and Cell Biology (203 citations). Perrine Pennamen has collaborated with scholars based in France, Germany and United Kingdom. Frequent co-authors include Caroline Rooryck, Aurélie Bedel, Sandrine Dabernat, François Moreau‐Gaudry, Veronique Guyonnet‐Dupérat, Jean‐Marc Blouin, Jérôme Toutain, Grégoire Cullot, Julian Boutin and Isabelle Lamrissi‐Garcia. Their work appears in journals such as Nature Communications, British Journal of Ophthalmology and Genetics in Medicine.

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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