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.


112
MeSH terms classified as ATMP-related
8
Technology domains covering the ATMP landscape
31,110
Total terms in MeSH 2026 vocabulary
6,092
Unique funder name strings in the corpus

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:

  1. 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.
  2. 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.
  3. 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:

Known limitations


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:

Explicit exclusions. Two descriptors were removed despite triggering keyword matches, because domain review confirmed they are unrelated to ATMPs:

Certainty tiers

51 terms
Certain ATMP
Unambiguous ATMP concepts with no plausible non-ATMP interpretation. Examples: CRISPR-Cas Systems, Receptors Chimeric Antigen, Induced Pluripotent Stem Cells, Oncolytic Virotherapy.
61 terms
Edge Cases
Concepts with substantial ATMP overlap but also broader scientific use. Examples: Stem Cells, Lentivirus, Tissue Engineering, Bioreactors. Included by default; may be refined after expert validation.

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.

Commercial potential score (compot)
Estimates the likelihood that a publication will be cited in a patent, based on the citation structure of papers with known patent-citation histories. Continuous scale approximately 0 to 1. Source: Masclans et al. (2025) v3. Coverage: approximately 60–70% of ATMP publications.
Science potential score (scipot)
Estimates future scientific citation impact using citation network position. Source: Masclans et al. (2025) v2. Matched to 469,564 ATMP publications in this corpus (range: 0.002–0.998). Uses a different dataset release than compot.

:::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:


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

Platform citation
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).