Olivier Pichon

1.8k citations

30 papers · 576 indexed · h-index 13

Co-authors: Cédric Le Caignec Albert David Bertrand Isidor Stéphane Bezieau Richard Redon Valérie Cormier‐Daire Martine Le Merrer Pierre Lindenbaum
Topics: Genomic variations and chromosomal abnormalities (9 papers)Congenital heart defects research (7 papers)Genetics and Neurodevelopmental Disorders (5 papers)
Cited by: Developmental Biology Genetics Molecular Biology
Journals: Nature Genetics Blood International Journal of Molecular Sciences
Partner nations: France United States Switzerland

In The Last Decade

Olivier Pichon

29 papers receiving 566 citations

Peers

Countries citing papers authored by Olivier Pichon

Since Specialization

Citations

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

Fields of papers citing papers by Olivier Pichon

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Olivier Pichon

This figure shows the co-authorship network connecting the top 25 collaborators of Olivier Pichon. A scholar is included among the top collaborators of Olivier Pichon 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 Olivier Pichon. Olivier Pichon 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	Optical Genome Mapping Combined with High-Throughput Sequencing Is Effective for the Diagnostic and Prognostic Genomic Classification of Acute Myeloid Leukemia and Myelodysplastic Neoplasms 2023 ·Blood ·Yannick Le Bris,(unknown),Catherine Godon,Olivier Pichon,Pierre Péterlin,Alice Garnier,Patrice Chevallier,(unknown),Marion Eveillard,Marie C. Béné,Olivier Theisen,(unknown)	0
2	Rare and de novo duplications containing TCF20 are associated with a neurodevelopmental disorder 2021 ·Clinical Genetics ·Jonathan Lévy,(unknown),Anna Maruani,(unknown),Céline Dupont,Séverine Drunat,(unknown),(unknown),Richard Delorme,(unknown),Bertrand Isidor,Olivier Pichon,Kamran Moradkhani,Alain Verloès,Anne‐Claude Tabet	8
3	Novel interstitial 2q12.3q13 microdeletion predisposes to developmental delay and behavioral problems 2021 ·Neurogenetics ·(unknown),Marion Gérard,(unknown),Olivier Pichon,(unknown),(unknown),Madeleine Joubert,Stéphane Bezieau,Claire Bénéteau	1
4	Structural abnormalities of chromosome 8 and fetoplacental discrepancy: A second case report and review of fetal phenotype of 8p inverted duplication deletion syndrome 2020 ·European Journal of Medical Genetics ·(unknown),(unknown),Kamran Moradkhani,Olivier Pichon,Sébastien Richard,Madeleine Joubert,Stéphane Bezieau	1
5	Whole genome copy number analysis in search of new prognostic biomarkers in first line treatment of mantle cell lymphoma. A study by the LYSA group 2020 ·Hematological Oncology ·Yannick Le Bris,Florence Magrangeas,Philippe Moreau,David Chiron,Catherine Guérin‐Charbonnel,Olivier Theisen,Olivier Pichon,Danielle Canioni,Barbara Burroni,Hervé Maisonneuve,Catherine Thiéblemont,Lucie Obéric,Emmanuel Gyan,Catherine Pellat‐Deceunynck,Olivier Hermine,Marie‐Hélène Delfau‐Larue,Benoît Tessoulin,Marie C. Béné,Stéphane Minvielle,Steven Le Gouill	8
6	Fryns type mesomelic dysplasia of the upper limbs caused by inverted duplications of the HOXD gene cluster 2019 ·European Journal of Human Genetics ·Cédric Le Caignec,Olivier Pichon,(unknown),(unknown),C. Bonnard,Pierre Lindenbaum,Richard Redon,Caroline Schluth‐Bolard,(unknown),Pierre‐Antoine Rollat‐Farnier,(unknown),Marie‐Laure Vuillaume,Damien Sanlaville,Denis Duboule,André Mégarbané,Annick Toutain	10
7	Pseudodicentric Chromosome Originating from Autosomes 9 and 21 in a Male Patient with Oligozoospermia 2019 ·Cytogenetic and Genome Research ·(unknown),Elena J. Tucker,(unknown),Erika Launay,(unknown),(unknown),(unknown),Linda Akloul,Claire Bénéteau,(unknown),(unknown),Olivier Pichon,Célia Ravel,Sylvie Odent,Marc‐Antoine Belaud‐Rotureau,Sylvie Jaillard	3
8	A de novo 2q37.2 deletion encompassing AGAP1 and SH3BP4 in a patient with autism and intellectual disability 2018 ·European Journal of Medical Genetics ·Mathilde Pacault,Mathilde Nizon,Olivier Pichon,Marie Vincent,Cédric Le Caignec,Bertrand Isidor	11
9	Familial autosomal dominant severe ankyloglossia with tooth abnormalities 2018 ·American Journal of Medical Genetics Part A ·(unknown),Roman Hossein Khonsari,Pierre Corre,(unknown),Cécile Boscher,Mathilde Nizon,Olivier Pichon,Albert David,Cédric Le Caignec,Hélios Bertin,Bertrand Isidor	6
10	Autosomal insertional translocation mimicking an X-linked mode of inheritance 2012 ·European Journal of Medical Genetics ·(unknown),Olivier Pichon,(unknown),(unknown),Yves Sznajer,Albert David,Cédric Le Caignec	4
11	Wilms’ tumor in patients with 9q22.3 microdeletion syndrome suggests a role for PTCH1 in nephroblastomas 2012 ·European Journal of Human Genetics ·Bertrand Isidor,Franck Bourdeaut,(unknown),Ghislaine Plessis,(unknown),Caroline Kannengiesser,Sylvie Rossignol,Olivier Pichon,(unknown),Dominique Martin‐Coignard,Maria Piccione,Albert David,Olivier Delattre,Marc Jeanpierre,Nicolas Sévenet,Cédric Le Caignec	19
12	De novo duplication and deletions at 7q in a three‐generation family 2012 ·American Journal of Medical Genetics Part A ·Bertrand Isidor,Olaya Villa,Olivier Pichon,(unknown),(unknown),Pierre Boisseau,(unknown),Cédric Le Caignec	1
13	Truncating mutations in the last exon of NOTCH2 cause a rare skeletal disorder with osteoporosis 2011 ·Nature Genetics ·Bertrand Isidor,Pierre Lindenbaum,Olivier Pichon,Stéphane Bezieau,Christian Dina,Sébastien Jacquemont,Dominique Martin‐Coignard,Christel Thauvin‐Robinet,Martine Le Merrer,Jean‐Louis Mandel,Albert David,Laurence Faivre,Valérie Cormier‐Daire,Richard Redon,Cédric Le Caignec	148
14	Serpentine fibula-polycystic kidney syndrome caused by truncating mutations in NOTCH2 2011 ·Human Mutation ·Bertrand Isidor,Martine Le Merrer,G. Ulrich Exner,Olivier Pichon,(unknown),Anne Guiochon‐Mantel,Albert David,Valérie Cormier‐Daire,Cédric Le Caignec	28
15	Mesomelia-Synostoses Syndrome Results from Deletion of SULF1 and SLCO5A1 Genes at 8q13 2010 ·The American Journal of Human Genetics ·Bertrand Isidor,Olivier Pichon,Richard Redon,Debra Day‐Salvatore,Antoine Hamel,(unknown),Maria Bitner‐Glindzicz,Dominique Heymann,Lena Kjellén,Cornelia Kraus,Jules G. Leroy,Geert Mortier,Anita Rauch,Alain Verloès,Albert David,Cédric Le Caignec	31
16	Identification of two novel mutations in Shh long-range regulator associated with familial pre-axial polydactyly 2010 ·Clinical Genetics ·Juliette Albuisson,Bertrand Isidor,Marion Giraud,Olivier Pichon,(unknown),A. David,Cédric Le Caignec,Stéphane Bezieau	44
17	Familial acampomelic form of campomelic dysplasia caused by a 960 kb deletion upstream of SOX9 2009 ·American Journal of Medical Genetics Part A ·(unknown),Olivier Pichon,Antoine Hamel,Yves Héloury,Laurence Michel‐Calemard,Yves Morel,Albert David,Cédric Le Caignec	50
18	Deletion of the CUL4B gene in a boy with mental retardation, minor facial anomalies, short stature, hypogonadism, and ataxia 2009 ·American Journal of Medical Genetics Part A ·Bertrand Isidor,Olivier Pichon,S. Baron,Albert David,Cédric Le Caignec	39
19	Congenital skin pedicles with or without amniotic band sequence: Extending the human phenotype resembling mouse disorganization 2009 ·American Journal of Medical Genetics Part A ·Bertrand Isidor,Geneviève Baujat,C. Le Caignec,Olivier Pichon,Dominique Martin‐Coignard,Annick Toutain,A. David	10
20	A 8.26 Mb deletion in 6q16 and a 4.95 Mb deletion in 20p12 including JAG1 and BMP2 in a patient with Alagille syndrome and Wolff–Parkinson–White syndrome 2008 ·European Journal of Medical Genetics ·Laurianne Le Gloan,Olivier Pichon,Bertrand Isidor,(unknown),Jean‐Marie Rival,Albert David,Cédric Le Caignec	16

About Olivier Pichon

Olivier Pichon is a scholar working on Developmental Biology, Genetics and Molecular Biology, having authored 30 papers that have together received 576 indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (9 papers), Congenital heart defects research (7 papers) and Genetics and Neurodevelopmental Disorders (5 papers). The work is most often cited by research in Developmental Biology (51 citations), Genetics (258 citations) and Molecular Biology (416 citations). Olivier Pichon has collaborated with scholars based in France, United States and Switzerland. Frequent co-authors include Cédric Le Caignec, Albert David, Bertrand Isidor, Stéphane Bezieau, Richard Redon, Valérie Cormier‐Daire, Martine Le Merrer, Pierre Lindenbaum, Dominique Martin‐Coignard and Christian Dina. Their work appears in journals such as Nature Genetics, Blood and International Journal of Molecular Sciences.

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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