Philip Holmgren

562 total citations
5 papers, 174 citations indexed

About

Philip Holmgren is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, Philip Holmgren has authored 5 papers receiving a total of 174 indexed citations (citations by other indexed papers that have themselves been cited), including 3 papers in Molecular Biology, 3 papers in Genetics and 1 paper in Pediatrics, Perinatology and Child Health. Recurrent topics in Philip Holmgren's work include Genetics and Neurodevelopmental Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Philip Holmgren is often cited by papers focused on Genetics and Neurodevelopmental Disorders (2 papers), Genomic variations and chromosomal abnormalities (2 papers) and Glycosylation and Glycoproteins Research (1 paper). Philip Holmgren collaborates with scholars based in Belgium, Netherlands and Australia. Philip Holmgren's co-authors include Arvid Suls, Sarah Weckhuysen, Peter De Jonghe, D. Goossens, Rudy Van Coster, Kristien Verhaert, Albena Jordanova, Anna Jansen, Jurgen Del‐Favero and Simone C. Yendle and has published in prestigious journals such as Neurology, Scientific Reports and Prenatal Diagnosis.

In The Last Decade

Philip Holmgren

5 papers receiving 174 citations

Peers

Countries citing papers authored by Philip Holmgren

Since Specialization

Citations

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

Fields of papers citing papers by Philip Holmgren

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Philip Holmgren

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

All Works

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5 of 5 papers shown

#	Work	Indexed citations
1	Improved selection of zebrafish CRISPR editing by early next-generation sequencing based genotyping 2023 ·Scientific Reports ·(unknown), Benjamin Vandendriessche, Charlotte Claes, (unknown), Maaike Alaerts, Philip Holmgren, (unknown), Dirk J. Snyders, Bart Loeys, Dorien Schepers	5
2	Improving Care And Research Electronic Data Trust Antwerp (iCAREdata): a research database of linked data on out-of-hours primary care 2016 ·BMC Research Notes ·Annelies Colliers, Stefaan Bartholomeeusen, Roy Remmen, Samuel Coenen, B. Michiels, Hilde Bastiaens, Paul Van Royen, Véronique Verhoeven, Philip Holmgren, (unknown), Hilde Philips	24
3	Detection of a case of chronic myeloid leukaemia with deletions at the t(9;22) translocation breakpoints by a genome-wide non-invasive prenatal test 2016 ·Prenatal Diagnosis ·Katrien Janssens, Kathleen Deiteren, Anke Verlinden, Liesbeth Rooms, Sigri Beckers, Philip Holmgren, Katrien Vermeulen, Marie‐Berthe Maes, Geert Mortier, Bettina Blaumeiser	6
4	Duplications of 17q12 can cause familial fever-related epilepsy syndromes 2013 ·Neurology ·Katia Hardies, Sarah Weckhuysen, Elke Peeters, Philip Holmgren, Hilde Van Esch, Peter De Jonghe, Wim Van Paesschen, Arvid Suls	17
5	Clinical spectrum of early-onset epileptic encephalopathies associated with STXBP1 mutations 2010 ·Neurology ·Liesbet Deprez, Sarah Weckhuysen, Philip Holmgren, Arvid Suls, (unknown), D. Goossens, Jurgen Del‐Favero, Anna Jansen, Kristien Verhaert, Liesbet Lagae, Albena Jordanova, Rudy Van Coster, Simone C. Yendle, Samuel F. Berkovic, Ingrid E. Scheffer, Berten Ceulemans, Peter De Jonghe	122

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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