Philippe M. Campeau

11.1k citations

123 papers · 3.3k indexed · h-index 33

Genetics top 2%
- Connective tissue disorders research 20
- Genetics and Neurodevelopmental Disorders 14
- Genomics and Rare Diseases 12
Genetics top 2%
- Connective tissue disorders research 20
- Genetics and Neurodevelopmental Disorders 14
- Genomics and Rare Diseases 12
Cancer Research top 5%
Clinical Biochemistry top 2%
Molecular Biology top 5%
- RNA modifications and cancer 12
Physiology
- Lysosomal Storage Disorders Research 16
Epidemiology
- Trypanosoma species research and implications 12
Cell Biology
- Cellular transport and secretion 10
Immunology and Allergy
- Cell Adhesion Molecules Research 7

Co-authors: Brendan Lee Marc Tischkowitz William D. Foulkes Jacques Galipeau Richard A. Gibbs Moutih Rafei Brian C. Dawson James T. Lu
Cited by: Genetics Cancer Research
Journals: New England Journal of Medicine (1 paper)Proceedings of the National Academy of Sciences (2 papers)Nucleic Acids Research (1 paper)
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

The 25 scholars most cited alongside Philippe M. Campeau, 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 Philippe M. Campeau Line = papers co-authored together Philippe M. Campeau links everyone, so they are left out of the graph.

All Works

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20 of 20 papers shown

#	Work
1	Transcriptomic and lipidomic profiling provide novel insight into the pathogenesis of monogenic SGMS2 -related osteoporosis JBMR Plus ·Sandra Pihlström,Ali Oghabian,Kirsi Määttä,Jelmer Legebeke,Riikka E. Mäkitie,Philippe M. Campeau,Pauline Terhal,Lorenzo D. Botto,Vesa M. Olkkonen,Outi Mäkitie,Minna Pekkinen	2025	0
2	Neurobehavioral profile of individuals with pathogenic variants in CHD3 European Journal of Human Genetics ·Anca Ionescu,Emmanuelle Mazur-Lainé,Mélodie Proteau-Lemieux,Inga Sophia Knoth,Keely Vachon,Kerri Whitlock,Hazel Maridith Barlahan Biag,Nazim Rabouhi,Hendrikus J. van Heesbeen,Sébastien Jacquemont,David Hessl,Leonard Abbeduto,Evdokia Anagnostou,François V. Bolduc,Randi J. Hagerman,Philippe M. Campeau,Sarah Lippé	2025	0
3	The NuRD component CHD3 promotes BMP signalling during cranial neural crest cell specification EMBO Reports ·Zoe H. Mitchell,Joery den Hoed,Willemijn Claassen,Martina Demurtas,Laura Deelen,Philippe M. Campeau,Karen Liu,Simon E. Fisher,Marco Trizzino	2025	0
4	Fibronectin isoforms promote postnatal skeletal development Matrix Biology ·Neha E. H. Dinesh,Nissan Baratang,Justine Rosseau,Ronit Mohapatra,Ling Jesse Li,Ramshaa Mahalingam,Kerstin Tiedemann,Philippe M. Campeau,Dieter P. Reinhardt	2024	2
5	Functional studies in yeast confirm the pathogenicity of a new GINS3 Meier–Gorlin syndrome variant Clinical Genetics ·Yosra Mehrjoo,Philippe M. Campeau,Lama Al Abdi,Abdullah Aldowaish,Omar Abouyousef,Fowzan S. Alkuraya,Marta Codina‐Solà,Anna M. Cueto‐González,Hugo Würtele	2024	0
6	An adult patient with Tatton–Brown–Rahman syndrome caused by a novel DNMT3A variant and axonal polyneuropathy American Journal of Medical Genetics Part A ·Al-alya Alsabah,Mohammed Alsalmi,Rami Massie,Marie‐Claude Bilodeau,Philippe M. Campeau,Serge McGraw,Daniela D’Agostino	2023	1
7	The ATP6V1B2 DDOD/DOORS-Associated p.Arg506* Variant Causes Hyperactivity and Seizures in Mice Genes ·Justine Rousseau,Samuel Boris Tene Tadoum,Marisol Lavertu Jolin,Thi Tuyet Mai Nguyen,Norbert Fonya Ajeawung,Ann M. Flenniken,Lauryl M. J. Nutter,Igor Vukobradovic,Elsa Rossignol,Philippe M. Campeau	2023	2
8	The Quebec Dental Anomalies Registry: Identifying genes for rare disorders PNAS Nexus ·Madeleine S Wredenhagen,Andee Goldstein,Hélène Mathieu,Valancy Miranda,Burcin Morali,Jacinthe Santerre,Catalina Maftei,Marie‐Ange Delrue,Matthieu Schmittbuhl,Duy Dat Vu,Florina Moldovan,Philippe M. Campeau	2023	0
9	Ethanolamine‐phosphate on the second mannose is a preferential bridge for some GPI‐anchored proteins EMBO Reports ·Mizuki Ishida,Yuta Maki,Akinori Ninomiya,Yoko Takada,Philippe M. Campeau,Taroh Kinoshita,Yoshiko Murakami	2022	11
10	Disruption of exon-bridging interactions between the minor and major spliceosomes results in alternative splicing around minor introns Nucleic Acids Research ·Anouk Olthof,Alisa K. White,Stephen Mieruszynski,Karen Doggett,Madisen F. Lee,Almahdi Chakroun,Alice Abdel Aleem,Justine Rousseau,Cinzia Magnani,Chaim M. Roifman,Philippe M. Campeau,Joan K. Heath,Rahul Kanadia	2021	16
11	Variant-specific effects define the phenotypic spectrum of HNRNPH2-associated neurodevelopmental disorders in males Human Genetics ·Hans‐Jürgen Kreienkamp,Matias Wagner,Heike Weigand,Allyn McConkie-Rossell,Marie McDonald,Boris Keren,Cyril Mignot,Julie Gauthier,Jean‐François Soucy,Jacques L. Michaud,Meghan Dumas,Rosemarie Smith,Ulrike Löbel,Maja Hempel,Christian Kubisch,Jonas Denecke,Philippe M. Campeau,Jennifer Bain,Davor Lessel	2021	13
12	Missense substitutions at a conserved 14-3-3 binding site in HDAC4 cause a novel intellectual disability syndrome SHILAP Revista de lepidopterología ·Emma Wakeling,Meriel McEntagart,Michael Bruccoleri,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	2020	11
13	PIGH deficiency can be associated with severe neurodevelopmental and skeletal manifestations Clinical Genetics ·Camille Tremblay‐Laganière,Rauan Kaiyrzhanov,Reza Maroofian,Thi Tuyet Mai Nguyen,Kamran Salayev,Ilana Chilton,Wendy K. Chung,Jill A. Madden,Chanika Phornphutkul,Pankaj B. Agrawal,Henry Houlden,Philippe M. Campeau	2020	6
14	Disrupted minor intron splicing is prevalent in Mendelian disorders Molecular Genetics & Genomic Medicine ·Anouk Olthof,Jeffrey S. Rasmussen,Philippe M. Campeau,Rahul Kanadia	2020	8
15	MYSM1 maintains ribosomal protein gene expression in hematopoietic stem cells to prevent hematopoietic dysfunction JCI Insight ·Jad I. Belle,HanChen Wang,Amanda Fiore,Jessica C. Petrov,Yun Lin,Chu-Han Feng,Thi Tuyet Mai Nguyen,Jacky Tung,Philippe M. Campeau,Uta Behrends,Theresa Brunet,Gloria Leszinski,Philippe Gros,David Langlais,Anastasia Nijnik	2020	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) 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	2019	1
17	Clinical variability in inherited glycosylphosphatidylinositol deficiency disorders Clinical Genetics ·Kara Bellai‐Dussault,Thi Tuyet Mai Nguyen,Nissan Baratang,Daniel A. Jimenez‐Cruz,Philippe M. Campeau	2018	61
18	Novel fibronectin mutations and expansion of the phenotype in spondylometaphyseal dysplasia with “corner fractures” 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	2018	12
19	Selective Inhibition of CCR2 Expressing Lymphomyeloid Cells in Experimental Autoimmune Encephalomyelitis by a GM-CSF-MCP1 Fusokine The Journal of Immunology ·Moutih Rafei,Philippe M. Campeau,Jian Wu,Elena Birman,Kathy Forner,Marie‐Noëlle Boivin,Jacques Galipeau	2009	14
20	Mesenchymal Stromal Cells Ameliorate Experimental Autoimmune Encephalomyelitis by Inhibiting CD4 Th17 T Cells in a CC Chemokine Ligand 2-Dependent Manner 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	2009	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), Genetics and Neurodevelopmental Disorders (14 papers), Genomics and Rare Diseases (12 papers), RNA modifications and cancer (12 papers), Trypanosoma species research and implications (12 papers), Cellular transport and secretion (10 papers) and Cell Adhesion Molecules Research (7 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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