Data and Methodology
This page documents how the ATMP Research Platform is built: the data sources, how publications are identified as ATMP-related, how technology sub-fields are defined, how metrics are computed, and what the known limitations are. Every number on the platform should be interpretable using the information here.
What are ATMPs?
Advanced Therapy Medicinal Products (ATMPs) are a class of medicines for human use defined under EU Regulation 1394/2007 and assessed centrally by the European Medicines Agency (EMA) through its Committee for Advanced Therapies (CAT). There are four statutory categories:
| Category | Abbreviation | Core definition |
|---|---|---|
| Gene Therapy Medicinal Product | GTMP | Contains recombinant nucleic acid that is itself the active therapeutic agent, used to regulate, repair, replace, add, or delete a genetic sequence in human cells |
| Somatic Cell Therapy Medicinal Product | sCTMP | Cells or tissues that have been substantially manipulated, or used in a non-homologous function, to treat, prevent, or diagnose disease |
| Tissue-Engineered Product | TEP | Contains or consists of engineered cells or tissues intended to regenerate, repair, or replace human tissue |
| Combined ATMP | cATMP | An ATMP that also incorporates a medical device as an integral part of the product |
This platform covers research related to all four ATMP categories. The scope extends beyond approved products to include the underlying enabling technologies — CRISPR genome editing, iPSC reprogramming, lentiviral vectors, and similar foundational science. Publications are identified by their MeSH term assignments, not by regulatory approval status.
Publication data
Data source
Publications are retrieved from Dimensions (Digital Science) using the Dimensions Search Language (DSL) API. Dimensions aggregates records from PubMed, Crossref, and other major bibliographic databases, enriched with MeSH assignments, institutional affiliation data, citation counts, funder names, and linked clinical trial records. All publication data was downloaded in May 2026.
Identification strategy
The central challenge in a bibliometric study of ATMPs is defining a principled research boundary. Free-text search is inadequate: the same concept appears under dozens of linguistic variants across journals, years, and languages. This platform uses MeSH (Medical Subject Headings) term classification instead, for three reasons:
- MeSH terms are assigned by trained human indexers at the US National Library of Medicine, providing a consistent controlled vocabulary across all PubMed-indexed literature.
- A publication about "CAR T-cell therapy" and one about "chimeric antigen receptor lymphocytes" will both carry the same MeSH descriptor regardless of how authors phrased their title.
- Dimensions exposes MeSH assignments for all PubMed-indexed publications and supports filtering by canonical descriptor name.
A publication is classified as ATMP-related if Dimensions has assigned to it at least one of the 112 classified ATMP MeSH descriptors described below.
:::note[Query design]
Only canonical DescriptorName values are used in API queries, never MeSH entry terms (synonyms). Dimensions indexes publications by canonical descriptor; querying synonyms is redundant and risks false positives. Each of the 112 descriptors is queried independently and results are deduplicated by Dimensions publication ID.
:::
Country and institutional attribution
Country and institutional affiliation are taken from Dimensions' parsed affiliation records. Each publication can carry multiple country attributions (one per contributing institution). The unit of analysis in all cross-country comparisons is the paper-country pair, not the unique publication:
- A paper co-authored by Swedish and German researchers is counted once for Sweden and once for Germany.
- Author leadership (first-author country) is computed from per-paper affiliation arrays, where author order follows the Dimensions JSON array order reflecting the published byline.
- The global baseline in all Sweden-versus-global comparisons excludes Swedish papers to avoid contaminating the reference distribution with the quantity being compared.
Known limitations
- Affiliation parsing is imperfect. Some affiliations are unresolved or incorrectly attributed, particularly for institutions in countries with non-standard address formats.
- Conference papers and preprints are included if they carry at least one ATMP MeSH term in Dimensions.
- MeSH indexing typically lags six to eighteen months behind publication date. Publications from 2024 onward may be systematically undercounted relative to earlier years.
- MeSH terms are applied only to PubMed-indexed publications. Publications not in PubMed (some engineering and materials science journals, for example) will not appear in this corpus even if scientifically relevant.
ATMP research classification
Vocabulary source
The ATMP classification is built on the MeSH 2026 descriptor vocabulary released by the US National Library of Medicine (31,110 terms), parsed from the NLM XML distribution. Each descriptor record includes a canonical name, hierarchical tree numbers, a scope note (definition), and a list of entry terms (synonyms).
Classification approach
MeSH terms were selected in two passes, followed by explicit exclusion review.
Pass 1: Keyword matching. Each descriptor's canonical name and entry terms were searched against a curated set of ATMP-relevant keywords spanning gene therapy, viral vectors, genome editing, CAR and other immune cell therapies, stem cells, tissue engineering, and manufacturing technologies. The first matching keyword category is recorded.
Pass 2: Tree-number matching. Two MeSH sub-trees were identified as wholly ATMP-relevant and all their member descriptors included:
E02.095.260(Gene Therapy, within the MeSH analytical/therapeutic techniques hierarchy)E02.095.465.430(Immunotherapy, Adoptive)
Explicit exclusions. Two descriptors were removed despite triggering keyword matches, because domain review confirmed they are unrelated to ATMPs:
- Cell-Free System (matched "stem cell" in extended entry terms; describes in vitro cell-free translation, not therapy)
- Nevus, Sebaceous of Jadassohn (matched "organoid" in entry terms from clinical literature; describes a congenital skin hamartoma)
Certainty tiers
Both tiers are included in all platform analyses.
What is intentionally excluded
The following categories are not classified as ATMP-related, even where superficial MeSH overlap exists:
| Excluded category | Examples | Reason for exclusion |
|---|---|---|
| Monoclonal antibodies | Rituximab, Pembrolizumab | Recombinant protein biologics, not gene or cell products |
| Small molecule drugs | Imatinib, chemotherapy agents | Chemical medicines with no gene or cell component |
| Conventional vaccines | Inactivated, subunit, live-attenuated | Not substantially manipulated cells; not recombinant nucleic acid as the active agent |
| mRNA/siRNA therapeutics (non-ATMP) | siRNA drugs, antisense oligonucleotides | Classified by EMA as chemical medicinal products |
| Recombinant protein replacement | Factor VIII/IX as infused proteins, growth hormone | Recombinant proteins, not ATMPs |
| Minimally manipulated transplants | Standard bone marrow transplantation without gene modification | Below the substantial manipulation threshold for sCTMP classification |
| Standard blood transfusion | Red cell, platelet, plasma transfusions | Minimal manipulation |
| Checkpoint inhibitors | Anti-PD-1/PD-L1 antibodies | Monoclonal antibodies |
:::tip[Note on mRNA vaccines] The descriptor mRNA Vaccines is included because mRNA-based delivery is central to several ATMP development programmes, even though approved COVID-19 mRNA vaccines are not ATMPs under EU Regulation 1394/2007. Users who wish to exclude general vaccine research should apply additional domain filters. :::
Technology domain classification
Overview
To enable sub-field comparisons, each of the 112 ATMP MeSH terms is assigned to one of eight technology domains organised in two conceptual categories.
Fundamental Technologies cover the core biological mechanisms underlying ATMPs: how genetic material is edited and corrected, how cells are reprogrammed toward therapeutic identities, how therapeutic cargo is delivered into cells and tissues, and how engineered cells are designed to sense and respond to their environment.
Enabling Technologies cover the tools and platforms that support ATMP development without being the therapeutic mechanism themselves: how cells are characterised and quality-controlled, how they are expanded and processed outside the body, how they are tested in model systems before clinical use, and how they are fabricated into final products.
Domains at a glance
| Category | Domain | Scope |
|---|---|---|
| Fundamental | DNA Editing and Tailoring | Precision genome modification tools: CRISPR systems, zinc finger nucleases, TALENs, targeted gene insertion and correction, and analysis of vector integration safety |
| Fundamental | Cell Identity and Fate Reprogramming | Technologies that alter or harness cellular identity: iPSC reprogramming, embryonic stem cells, directed differentiation of progenitor populations into therapeutic cell types, and stem cell self-renewal biology |
| Fundamental | Delivery Systems | Vehicles and strategies for introducing therapeutic material into cells or the body: lentiviral and AAV vectors, oncolytic virotherapy, mRNA delivery, and adoptive cell transfer |
| Fundamental | Sensing and Control Systems | Engineering cells to sense their environment and respond: chimeric antigen receptors (CARs), inducible gene circuits, and immune cell engineering platforms |
| Enabling | Cell Phenotyping | Methods for characterising cell identity, surface markers, purity, and function: receptor profiling, functional assays, and disease-related phenotyping for quality assessment |
| Enabling | Bioprocessing | Technologies for collecting, expanding, and processing therapeutic cells outside the body: leukapheresis, stem cell mobilisation, bioreactors, and ex vivo culture systems |
| Enabling | Preclinical Modelling | Model systems for testing ATMPs before clinical use: organoids, 3D tissue scaffolds, organ-on-chip platforms, and bioartificial organ constructs |
| Enabling | Biofabrication and Manufacturing | Processes for fabricating structured ATMP constructs at scale: bioprinting and the production of cell-seeded tissue products |
Assignment rules
Each MeSH term receives a primary domain assignment. A small number of terms with clear dual relevance also carry a secondary domain assignment (29 terms in total). In platform analyses, a paper's domain membership is determined by the primary assignments of its indexed MeSH terms. A paper indexed under terms spanning multiple domains appears in each of those domains.
Full classification table
The table below lists all 112 MeSH terms included in the ATMP research classification, together with their technology category, domain, and research sub-area.
| MeSH Term | Category | Domain | Research Sub-area |
|---|---|---|---|
| CRISPR-Cas Systems | Fundamental | DNA Editing and Tailoring | Sequence editors |
| CRISPR-Associated Protein 9 | Fundamental | DNA Editing and Tailoring | Sequence editors |
| CRISPR-Associated Proteins | Fundamental | DNA Editing and Tailoring | Sequence editors |
| Clustered Regularly Interspaced Short Palindromic Repeats | Fundamental | DNA Editing and Tailoring | Sequence editors |
| Gene Editing | Fundamental | DNA Editing and Tailoring | Sequence editors |
| RNA, Guide, CRISPR-Cas Systems | Fundamental | DNA Editing and Tailoring | Sequence editors |
| Transcription Activator-Like Effector Nucleases | Fundamental | DNA Editing and Tailoring | Sequence editors |
| Zinc Finger Nucleases | Fundamental | DNA Editing and Tailoring | Sequence editors |
| Genetic Therapy | Fundamental | DNA Editing and Tailoring | Sequence editors |
| Targeted Gene Repair | Fundamental | DNA Editing and Tailoring | Gene insertion and correction |
| Gene Transfer, Horizontal | Fundamental | DNA Editing and Tailoring | Genotoxicity and vector integration safety |
| Mutagenesis, Insertional | Fundamental | DNA Editing and Tailoring | Genotoxicity and vector integration safety |
| Epigenome Editing | Fundamental | Cell Identity and Fate Reprogramming | Epigenome and chromatin remodelling |
| Induced Pluripotent Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Embryonic Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Human Embryonic Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Mouse Embryonic Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Pluripotent Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Cellular Reprogramming | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Cellular Reprogramming Techniques | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Octamer Transcription Factor-3 | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Embryonal Carcinoma Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Totipotent Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Regenerative Medicine | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Stem Cell Research | Fundamental | Cell Identity and Fate Reprogramming | Pluripotency and iPSC reprogramming |
| Hematopoietic Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Mesenchymal Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Adult Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Multipotent Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Neural Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Killer Cells, Natural | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Lymphoid Progenitor Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Myeloid Progenitor Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Erythroid Precursor Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Limbal Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Langerhans Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Peripheral Blood Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Adult Germline Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Fetal Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Oogonial Stem Cells | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Acellular Dermis | Fundamental | Cell Identity and Fate Reprogramming | Directed differentiation |
| Cell Self Renewal | Fundamental | Cell Identity and Fate Reprogramming | Stem cell self-renewal and cycle |
| Asymmetric Cell Division | Fundamental | Cell Identity and Fate Reprogramming | Stem cell self-renewal and cycle |
| Proto-Oncogene Proteins c-kit | Fundamental | Cell Identity and Fate Reprogramming | Stem cell self-renewal and cycle |
| Stem Cell Factor | Fundamental | Cell Identity and Fate Reprogramming | Stem cell self-renewal and cycle |
| Stem Cell Niche | Fundamental | Cell Identity and Fate Reprogramming | Stem cell self-renewal and cycle |
| Hematopoietic Cell Growth Factors | Fundamental | Cell Identity and Fate Reprogramming | Stem cell self-renewal and cycle |
| fms-Like Tyrosine Kinase 3 | Fundamental | Cell Identity and Fate Reprogramming | Stem cell self-renewal and cycle |
| Gene Transfer Techniques | Fundamental | Delivery Systems | Viral vector delivery |
| Lentivirus | Fundamental | Delivery Systems | Viral vector delivery |
| Dependovirus | Fundamental | Delivery Systems | Viral vector delivery |
| Gammaretrovirus | Fundamental | Delivery Systems | Viral vector delivery |
| Lentiviruses, Primate | Fundamental | Delivery Systems | Viral vector delivery |
| Immunodeficiency Virus, Feline | Fundamental | Delivery Systems | Viral vector delivery |
| Transduction, Genetic | Fundamental | Delivery Systems | Viral vector delivery |
| Gene Therapy Agents | Fundamental | Delivery Systems | Viral vector delivery |
| Immunotherapy, Adoptive | Fundamental | Delivery Systems | Viral vector delivery |
| Lentivirus Infections | Fundamental | Delivery Systems | Viral vector delivery |
| Lentiviruses, Bovine | Fundamental | Delivery Systems | Viral vector delivery |
| Lentiviruses, Equine | Fundamental | Delivery Systems | Viral vector delivery |
| Lentiviruses, Feline | Fundamental | Delivery Systems | Viral vector delivery |
| Lentiviruses, Ovine-Caprine | Fundamental | Delivery Systems | Viral vector delivery |
| Oncolytic Viruses | Fundamental | Delivery Systems | Oncolytic viral delivery |
| Oncolytic Virotherapy | Fundamental | Delivery Systems | Oncolytic viral delivery |
| mRNA Vaccines | Fundamental | Delivery Systems | Non-viral and mRNA delivery |
| Adoptive Transfer | Fundamental | Delivery Systems | Non-viral and mRNA delivery |
| Blood Vessel Prosthesis | Fundamental | Delivery Systems | Non-viral and mRNA delivery |
| Receptors, Chimeric Antigen | Fundamental | Sensing and Control Systems | Synthetic receptors |
| Blastic Plasmacytoid Dendritic Cell Neoplasm | Fundamental | Sensing and Control Systems | Synthetic receptors |
| Dendritic Cells, Follicular | Fundamental | Sensing and Control Systems | Synthetic receptors |
| Interleukin-12 | Fundamental | Sensing and Control Systems | Inducible gene circuits |
| Antigens, CD34 | Enabling | Cell Phenotyping | Surface marker characterisation |
| Receptors, KIR | Enabling | Cell Phenotyping | Surface marker characterisation |
| Receptors, Natural Killer Cell | Enabling | Cell Phenotyping | Surface marker characterisation |
| Receptors, NK Cell Lectin-Like | Enabling | Cell Phenotyping | Surface marker characterisation |
| NK Cell Lectin-Like Receptor Subfamily A | Enabling | Cell Phenotyping | Surface marker characterisation |
| NK Cell Lectin-Like Receptor Subfamily C | Enabling | Cell Phenotyping | Surface marker characterisation |
| Natural Cytotoxicity Triggering Receptor 1 | Enabling | Cell Phenotyping | Surface marker characterisation |
| Natural Cytotoxicity Triggering Receptor 2 | Enabling | Cell Phenotyping | Surface marker characterisation |
| Natural Cytotoxicity Triggering Receptor 3 | Enabling | Cell Phenotyping | Surface marker characterisation |
| GATA2 Deficiency | Enabling | Cell Phenotyping | Surface marker characterisation |
| Leukemia, Large Granular Lymphocytic | Enabling | Cell Phenotyping | Surface marker characterisation |
| Limbal Stem Cell Deficiency | Enabling | Cell Phenotyping | Surface marker characterisation |
| Colony-Forming Units Assay | Enabling | Cell Phenotyping | Functional cell assays |
| Tumor Stem Cell Assay | Enabling | Cell Phenotyping | Functional cell assays |
| Granzymes | Enabling | Cell Phenotyping | Functional cell assays |
| Neoplastic Stem Cells | Enabling | Cell Phenotyping | Functional cell assays |
| Leukapheresis | Enabling | Bioprocessing | Cell collection and isolation |
| Bone Marrow Purging | Enabling | Bioprocessing | Cell collection and isolation |
| Dendritic Cells | Enabling | Bioprocessing | Ex vivo cell expansion and culture |
| Lymphocytes, Tumor-Infiltrating | Enabling | Bioprocessing | Ex vivo cell expansion and culture |
| Bioreactors | Enabling | Bioprocessing | Ex vivo cell expansion and culture |
| Cytokine-Induced Killer Cells | Enabling | Bioprocessing | Ex vivo cell expansion and culture |
| Killer Cells, Lymphokine-Activated | Enabling | Bioprocessing | Ex vivo cell expansion and culture |
| Mesenchymal Stem Cell Transplantation | Enabling | Bioprocessing | Ex vivo cell expansion and culture |
| Photobioreactors | Enabling | Bioprocessing | Ex vivo cell expansion and culture |
| Hematopoietic Stem Cell Mobilization | Enabling | Bioprocessing | Stem cell mobilisation and harvest |
| Hematopoietic Stem Cell Transplantation | Enabling | Bioprocessing | Stem cell mobilisation and harvest |
| Cord Blood Stem Cell Transplantation | Enabling | Bioprocessing | Stem cell mobilisation and harvest |
| Peripheral Blood Stem Cell Transplantation | Enabling | Bioprocessing | Stem cell mobilisation and harvest |
| Stem Cell Transplantation | Enabling | Bioprocessing | Stem cell mobilisation and harvest |
| Organoids | Enabling | Preclinical Modelling | 3D culture and organoid models |
| Tissue Engineering | Enabling | Preclinical Modelling | 3D culture and organoid models |
| Microphysiological Systems | Enabling | Preclinical Modelling | Organ-on-chip and microphysiological systems |
| Bioartificial Organs | Enabling | Preclinical Modelling | Bioartificial organ models |
| Liver, Artificial | Enabling | Preclinical Modelling | Bioartificial organ models |
| Skin, Artificial | Enabling | Preclinical Modelling | Bioartificial organ models |
| Tissue Scaffolds | Enabling | Preclinical Modelling | Biomaterial characterisation in model systems |
| Biocompatible Materials | Enabling | Preclinical Modelling | Biomaterial characterisation in model systems |
| Decellularized Extracellular Matrix | Enabling | Preclinical Modelling | Biomaterial characterisation in model systems |
| Bioprinting | Enabling | Biofabrication and Manufacturing | Biofabrication and bioprinting |
Citation metrics
Raw citation counts
Citation counts are sourced from Dimensions and represent the total number of forward citations each publication has received from other works in the Dimensions database as of May 2026. Self-citations are not excluded.
Relative Citation Ratio (RCR)
The Relative Citation Ratio (Hutchins et al., 2016, PLOS Biology) is a field- and time-normalised citation metric from the NIH iCite database. An RCR of 1.0 means a paper has been cited at the same rate as the average paper in the same field and year; values above 1.0 indicate above-average citation impact within the field.
iCite computes RCR by comparing each paper's citation rate against the co-citation network of papers it most closely resembles, adjusting for both research field and publication year. This makes RCR more informative than raw citation counts for cross-field comparisons, where citation norms vary substantially.
:::note[RCR coverage] Approximately 93% of ATMP publications through 2022 have an RCR value. Publications from 2023 onward are largely excluded because iCite requires at least two years of citation accumulation to compute a stable rate. iCite data was joined to the ATMP corpus via DOI. Papers with a missing or zero RCR are excluded from all RCR-based analyses. :::
Science and commercial potential scores
Two scores derived from citation network analysis estimate the future impact trajectory of publications. Both come from the dataset published by Masclans et al. (2025), which provides pre-computed scores for tens of millions of publications.
:::note[Interpretation] Both scores are probabilistic estimates of future behaviour based on structural position in citation networks at the time of scoring. They reflect relative indicators, not precise predictions. Papers without a score are excluded from the respective analysis. :::
Altmetric coverage
Source
Altmetric data is retrieved from the Altmetric Details API (Altmetric.com / Digital Science) for all ATMP publications with a DOI. Coverage depends on Altmetric having indexed the publication. Data was downloaded in May 2026. For details on the data schema, see the Altmetric Explorer API documentation.
Coverage types
| Type | What it measures |
|---|---|
| News | Mentions in journalism and press outlets tracked by Altmetric |
| Blogs | Mentions in researcher, science communication, and institutional blogs |
| Patents | Patent filings or grants that cite the publication as prior art (via USPTO, EPO, WIPO, and national offices) |
| Policy documents | Government policy documents and reports that cite the publication |
| Clinical guidelines | Clinical practice guidelines and evidence summaries that cite the publication |
| Clinical trials | Registered clinical trials (ClinicalTrials.gov and WHO ICTRP) linked to the publication |
Patent jurisdiction classification
Patent citations are grouped by filing office to allow regional comparison.
| Jurisdiction group | Patent offices included |
|---|---|
| United States | USPTO (United States Patent and Trademark Office) |
| Europe (EPO) | EPO (European Patent Office, covers multi-country European filings) |
| International (PCT) | WIPO PCT international applications |
| China | CNIPA (China National Intellectual Property Administration) |
| Japan | JPO (Japan Patent Office) |
| South Korea | KIPO (Korean Intellectual Property Office) |
| Rest of Europe | All other European national patent offices, including the Swedish Patent and Registration Office (PRV) |
| Rest of World | All remaining national and regional offices |
:::note[Sweden is additive] Swedish patents (PRV filings) are counted in both the "Rest of Europe" group and a dedicated Sweden column. This is intentional: it allows Sweden to be compared against its regional peer group without needing to subtract Swedish contributions from the group total. :::
Policy and guideline source classification
242 unique policy document sources and 997 unique guideline sources were manually classified by geographic scope using known institutional identity and web search. Each source was assigned to one of the following categories, with a certainty level (high or medium):
| Classification | Scope | Coverage |
|---|---|---|
| International | WHO, UN, OECD, ICH, and other supranational bodies | 235 / 242 policy sources at high certainty; 933 / 997 guideline sources at high certainty |
| EU and Regional | EMA, European Commission, ECDC, and EU-level bodies | Included in both classification tables |
| National | National health ministries, regulatory agencies, and government health bodies | Includes Sweden; SE column uses Altmetric's reported location field |
Clinical trials
Source
Clinical trial metadata is retrieved from Dimensions via the clinical trials endpoint, drawing on ClinicalTrials.gov and WHO ICTRP registrations. Dimensions links publications to registered trials via citation and metadata matching.
Dimensions identifies links through two mechanisms: explicit citation of a trial registration number in the publication text, and algorithmic matching on shared identifiers and metadata. A single trial can be linked to multiple publications, and a single publication can be linked to multiple trials.
Phase classification
| Stage | Included phases |
|---|---|
| Early | Phase 1 and Phase 1/2 |
| Mid | Phase 2 and Phase 2/3 |
| Late | Phase 3, Phase 3/4, and Phase 4 |
| Not Reported | Phase not specified or listed as N/A in the registry |
Translation rate
The translation rate for a publication group is defined as: the number of publications linked to at least one registered clinical trial, divided by the total number of publications in the group. Trial geography is based on the country of the registering organisation; a single trial can be attributed to multiple countries.
Funder information
Source
Funder names are extracted from Dimensions publication metadata. Each publication can carry multiple funder records. The ATMP corpus contains 6,092 unique funder name strings.
Classification
| Category | Description |
|---|---|
| Swedish public | Swedish public research councils and grant agencies: Vetenskapsrådet (VR), FORMAS, FORTE, MISTRA, Vinnova |
| EU public | EU-level funding bodies: Horizon 2020, Horizon Europe, ERC, Marie Curie Actions |
| Foreign public | Public research councils and government agencies outside Sweden and the EU |
| Corporate | Private companies and industry funders |
| Foundation | Private philanthropic foundations, e.g., Wellcome Trust, Gates Foundation |
| Unknown | Funder string not matched to any classified entity |
:::note[Coverage limitation] Of the 6,092 unique funder strings, 252 have been explicitly classified. The long tail of funders with 15 or fewer papers is intentionally left as unknown. Classification is concentrated in high-volume funders that account for the majority of funded publications. Dimensions funder strings often differ from assumed short forms (for example, "Wellcome Trust Ltd" rather than "Wellcome Trust"), meaning some known funders may be missed due to name variation. :::
Sample restrictions
The following exclusions apply consistently across all platform analyses:
- Publications with a missing year are excluded from time-series analysis.
- Publications with a missing or zero
compotscore are excluded from commercial potential analysis. - Publications with a missing or zero RCR value are excluded from scientific quality analysis.
- Publications without a
scipotmatch are excluded from science potential analysis. - Records with a missing country code are excluded from country-level comparisons.
- The global baseline in all Sweden-versus-global comparisons excludes Swedish papers to avoid contaminating the reference distribution.
Platform
This platform is built with Observable Framework and Apache DuckDB. Charts use Observable Plot. Data queries run in a DuckDB instance (in-browser WASM for local use; remote server for the live deployment).
How to cite
ATMP Research Platform (2026). Descriptive analysis of global ATMP research output and Sweden's position in the global ecosystem. Developed in support of the VR/VINNOVA Excellence Clusters for Groundbreaking Technologies proposal. Stockholm: Stockholm School of Economics. Analysis: Yotam Sofer, House of Innovation.
Data sources
Dimensions (publications, citations, clinical trials, funder data) · Altmetric Details API (patent, policy, guideline, news, and blog mention events) · NIH iCite (Relative Citation Ratio) · MeSH 2026 descriptor vocabulary (US National Library of Medicine) · Masclans et al. (2025), Zenodo (commercial and science potential scores).