Philippe M. Campeau

11.1k citations

123 papers · 3.3k indexed · h-index 33

Molecular Biology top 5%
Genetics top 2%
Cancer Research top 5%
Genetics top 2%
Physiology top 5%

Co-authors: Brendan Lee Marc Tischkowitz William D. Foulkes Jacques Galipeau Richard A. Gibbs Moutih Rafei Brian C. Dawson James T. Lu
Topics: Connective tissue disorders research (20 papers)Lysosomal Storage Disorders Research (16 papers)Genetics and Neurodevelopmental Disorders (14 papers)
Cited by: Genetics Cancer Research
Journals: New England Journal of Medicine Proceedings of the National Academy of Sciences Nucleic Acids Research
Partner nations: Canada United States United Kingdom

In The Last Decade

Philippe M. Campeau

108 papers receiving 3.3k citations

Peers

Countries citing papers authored by Philippe M. Campeau

Since Specialization

Citations

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

Fields of papers citing papers by Philippe M. Campeau

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by Philippe M. Campeau. 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 Philippe M. Campeau. The network helps show where Philippe M. Campeau may publish in the future.

Co-authorship network of co-authors of Philippe M. Campeau

This figure shows the co-authorship network connecting the top 25 collaborators of Philippe M. Campeau. A scholar is included among the top collaborators of Philippe M. Campeau 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 Philippe M. Campeau. Philippe M. Campeau 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	Transcriptomic and lipidomic profiling provide novel insight into the pathogenesis of monogenic SGMS2 -related osteoporosis 2025 ·JBMR Plus ·(unknown),Ali Oghabian,Kirsi Määttä,(unknown),Riikka E. Mäkitie,Philippe M. Campeau,Pauline Terhal,Lorenzo D. Botto,Vesa M. Olkkonen,Outi Mäkitie,Minna Pekkinen	0
2	Neurobehavioral profile of individuals with pathogenic variants in CHD3 2025 ·European Journal of Human Genetics ·(unknown),(unknown),(unknown),Inga Sophia Knoth,(unknown),(unknown),(unknown),(unknown),(unknown),Sébastien Jacquemont,David Hessl,Leonard Abbeduto,Evdokia Anagnostou,François V. Bolduc,Randi J. Hagerman,Philippe M. Campeau,Sarah Lippé	0
3	The NuRD component CHD3 promotes BMP signalling during cranial neural crest cell specification 2025 ·EMBO Reports ·(unknown),Joery den Hoed,(unknown),(unknown),(unknown),Philippe M. Campeau,Karen Liu,Simon E. Fisher,Marco Trizzino	0
4	Fibronectin isoforms promote postnatal skeletal development 2024 ·Matrix Biology ·(unknown),Nissan Baratang,(unknown),(unknown),(unknown),(unknown),Kerstin Tiedemann,Philippe M. Campeau,Dieter P. Reinhardt	2
5	Functional studies in yeast confirm the pathogenicity of a new GINS3 Meier–Gorlin syndrome variant 2024 ·Clinical Genetics ·(unknown),Philippe M. Campeau,(unknown),(unknown),(unknown),Fowzan S. Alkuraya,Marta Codina‐Solà,Anna M. Cueto‐González,Hugo Würtele	0
6	An adult patient with Tatton–Brown–Rahman syndrome caused by a novel DNMT3A variant and axonal polyneuropathy 2023 ·American Journal of Medical Genetics Part A ·(unknown),(unknown),Rami Massie,(unknown),Philippe M. Campeau,Serge McGraw,Daniela D’Agostino	1
7	The ATP6V1B2 DDOD/DOORS-Associated p.Arg506* Variant Causes Hyperactivity and Seizures in Mice 2023 ·Genes ·Justine Rousseau,(unknown),(unknown),Thi Tuyet Mai Nguyen,Norbert Fonya Ajeawung,Ann M. Flenniken,Lauryl M. J. Nutter,Igor Vukobradovic,Elsa Rossignol,Philippe M. Campeau	2
8	The Quebec Dental Anomalies Registry: Identifying genes for rare disorders 2023 ·PNAS Nexus ·(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),(unknown),Marie‐Ange Delrue,Matthieu Schmittbuhl,(unknown),Florina Moldovan,Philippe M. Campeau	0
9	Ethanolamine‐phosphate on the second mannose is a preferential bridge for some GPI‐anchored proteins 2022 ·EMBO Reports ·(unknown),(unknown),Akinori Ninomiya,Yoko Takada,Philippe M. Campeau,Taroh Kinoshita,Yoshiko Murakami	11
10	Disruption of exon-bridging interactions between the minor and major spliceosomes results in alternative splicing around minor introns 2021 ·Nucleic Acids Research ·(unknown),(unknown),Stephen Mieruszynski,Karen Doggett,(unknown),(unknown),Alice Abdel Aleem,Justine Rousseau,Cinzia Magnani,Chaim M. Roifman,Philippe M. Campeau,Joan K. Heath,Rahul Kanadia	16
11	Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males 2021 ·Human Genetics ·Hans‐Jürgen Kreienkamp,Matias Wagner,Heike Weigand,(unknown),Marie McDonald,Boris Keren,Cyril Mignot,Julie Gauthier,(unknown),Jacques L. Michaud,(unknown),Rosemarie Smith,Ulrike Löbel,Maja Hempel,Christian Kubisch,Jonas Denecke,Philippe M. Campeau,Jennifer Bain,Davor Lessel	13
12	Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome 2020 ·SHILAP Revista de lepidopterología ·Emma Wakeling,Meriel McEntagart,(unknown),Charles Shaw‐Smith,Karen Stals,Matthew N. Wakeling,Angela Barnicoat,Clare Beesley,Andrea Hanson‐Kahn,Mary K. Kukolich,David A. Stevenson,Philippe M. Campeau,Sian Ellard,Sarah H. Elsea,Xiang-Jiao Yang,Richard Caswell	11
13	PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations 2020 ·Clinical Genetics ·(unknown),Rauan Kaiyrzhanov,Reza Maroofian,Thi Tuyet Mai Nguyen,Kamran Salayev,(unknown),Wendy K. Chung,Jill A. Madden,Chanika Phornphutkul,Pankaj B. Agrawal,Henry Houlden,Philippe M. Campeau	6
14	Disrupted minor intron splicing is prevalent in Mendelian disorders 2020 ·Molecular Genetics & Genomic Medicine ·(unknown),(unknown),Philippe M. Campeau,Rahul Kanadia	8
15	MYSM1 maintains ribosomal protein gene expression in hematopoietic stem cells to prevent hematopoietic dysfunction 2020 ·JCI Insight ·Jad I. Belle,(unknown),(unknown),Jessica C. Petrov,Yun Lin,(unknown),Thi Tuyet Mai Nguyen,(unknown),Philippe M. Campeau,Uta Behrends,Theresa Brunet,Gloria Leszinski,Philippe Gros,David Langlais,Anastasia Nijnik	14
16	Genetic Burden Contributing to Extremely Low or High Bone Mineral Density in a Senior Male Population From the Osteoporotic Fractures in Men Study (MrOS) 2019 ·JBMR Plus ·Shan Chen,Mahim Jain,Shalini N. Jhangiani,Zeynep Coban‐Akdemir,Philippe M. Campeau,Robert F. Klein,Carrie M. Nielson,Hongzheng Dai,Donna M. Muzny,Eric Boerwinkle,Richard A. Gibbs,Eric Orwoll,James R. Lupski,Jennifer E. Posey,Brendan Lee	1
17	Clinical variability in inherited glycosylphosphatidylinositol deficiency disorders 2018 ·Clinical Genetics ·(unknown),Thi Tuyet Mai Nguyen,Nissan Baratang,(unknown),Philippe M. Campeau	61
18	Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with “corner fractures” 2018 ·Bone ·Alice Costantini,Helena Valta,Nissan Baratang,Patrick Yap,Débora Romeo Bertola,Guilherme Lopes Yamamoto,Chong Ae Kim,Jiani Chen,Klaas J. Wierenga,Elizabeth A. Fanning,Luis A. Escobar,Kirsty McWalter,Heather M. McLaughlin,Rebecca Willaert,Amber Begtrup,Jessica J. Alm,Dieter P. Reinhardt,Outi Mäkitie,Philippe M. Campeau	12
19	Selective Inhibition of CCR2 Expressing Lymphomyeloid Cells in Experimental Autoimmune Encephalomyelitis by a GM-CSF-MCP1 Fusokine 2009 ·The Journal of Immunology ·Moutih Rafei,Philippe M. Campeau,Jian Wu,Elena Birman,Kathy Forner,Marie‐Noëlle Boivin,Jacques Galipeau	14
20	Mesenchymal Stromal Cells Ameliorate Experimental Autoimmune Encephalomyelitis by Inhibiting CD4 Th17 T Cells in a CC Chemokine Ligand 2-Dependent Manner 2009 ·The Journal of Immunology ·Moutih Rafei,Philippe M. Campeau,Adriana Aguilar‐Mahecha,Marguerite Buchanan,Patrick Williams,Elena Birman,Shala Yuan,Yoon Kow Young,Marie‐Noëlle Boivin,Kathy Forner,Mark Basik,Jacques Galipeau	296

About Philippe M. Campeau

Philippe M. Campeau is a scholar working on Genetics, Immunology and Allergy and Cell Biology, having authored 123 papers that have together received 3.3k indexed citations. Recurring topics across this work include Connective tissue disorders research (20 papers), Lysosomal Storage Disorders Research (16 papers) and Genetics and Neurodevelopmental Disorders (14 papers). The work is most often cited by research in Genetics (412 citations), Genetics (1.0k citations) and Cancer Research (466 citations). Philippe M. Campeau has collaborated with scholars based in Canada, United States and United Kingdom. Frequent co-authors include Brendan Lee, Marc Tischkowitz, William D. Foulkes, Jacques Galipeau, Richard A. Gibbs, Moutih Rafei, Brian C. Dawson, James T. Lu, Sandesh C.S. Nagamani and Marie‐Noëlle Boivin. Their work appears in journals such as New England Journal of Medicine, Proceedings of the National Academy of Sciences and Nucleic Acids Research.

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