--- type: "firecrawl-provider" description: "NIH RePORTER research funding database via the public, keyless api.reporter.nih.gov v2 API: search NIH and other HHS-funded research projects by text, principal investigator, organization, state, fiscal year, agency and activity code; read one project with abstract, investigators, program officers, costs and study section; and list the PubMed IDs of publications linked to a project." use_when: "NIH RePORTER research funding database via the public, keyless api.reporter.nih.gov v2 API: search NIH and other HHS-funded research projects by text, principal investigator, organization, state, fiscal year, agency and activity code; read one project with abstract, investigators, program officers, costs and study section; and list the PubMed IDs of publications linked to a project." categories: "Health" capabilities: 3 credits_per_call: 5 --- # NIH RePORTER on Firecrawl Alexandria NIH RePORTER research funding database via the public, keyless api.reporter.nih.gov v2 API: search NIH and other HHS-funded research projects by text, principal investigator, organization, state, fiscal year, agency and activity code; read one project with abstract, investigators, program officers, costs and study section; and list the PubMed IDs of publications linked to a project. - Categories: Health - Category index: [Health category](https://firecrawl.dev/alexandria/agents/categories/health) - Provider key: `reporter-nih-gov` - Access: Firecrawl credits - Cost: 5 credits per call ## More - [Human guide](https://firecrawl.dev/app/alexandria/reporter-nih-gov) - [OpenAPI spec](https://firecrawl.dev/alexandria/agents/providers/reporter-nih-gov/openapi.json) ## Capabilities - [Project](https://firecrawl.dev/alexandria/agents/providers/reporter-nih-gov/research-grants/project): One project record by application id, full project number or RePORTER URL: title, abstract, public health relevance, RCDC terms, PIs with profile ids, program officers, organization with UEI and location, institute, award amount with direct/indirect costs and per-institute funding, budget and project dates, opportunity number and study section. - [Publications](https://firecrawl.dev/alexandria/agents/providers/reporter-nih-gov/research-grants/publications): PubMed IDs of publications that acknowledge a core project (POST /v2/publications/search), newest first, with the citing application id. A known project without linked papers returns an empty list; an unknown core project number is not_found. - [Search projects](https://firecrawl.dev/alexandria/agents/providers/reporter-nih-gov/research-grants/search_projects): Search funded research projects (POST /v2/projects/search). Combine free text over titles, abstracts and terms with PI name or profile id, organization, state, fiscal years, agencies and activity codes. Returns one page of project-year records with PIs, organization, administering institute, award amount and dates, plus the total and next_offset. ## 1. Choose this provider when NIH RePORTER research funding database via the public, keyless api.reporter.nih.gov v2 API: search NIH and other HHS-funded research projects by text, principal investigator, organization, state, fiscal year, agency and activity code; read one project with abstract, investigators, program officers, costs and study section; and list the PubMed IDs of publications linked to a project. ## 2. Minimal request Call `POST https://api.firecrawl.dev/v2/scrape` with `{ alexandria: { provider, capability, options } }`. For a batch, send `{ alexandria: [...] }` with up to 10 calls. ```json { "provider": "reporter-nih-gov", "capability": "research-grants/project", "options": { "appl_id": 11171443 } } ``` ## 3. Add provider options Use only the options needed for the task: - `appl_id` (number): Application id from search_projects, e.g. 11171443. Example: `10` - `project_num` (string): Full project number, e.g. 5P01CA244114-05. Returns the parent record (not a subproject); when several fiscal-year records share the number, the latest one with a warning. Pattern: ^\s*[A-Za-z0-9-]+\s*$. Example: `` - `url` (string): A RePORTER project page, e.g. https://reporter.nih.gov/project-details/11171443. Example: `` ## 4. Request through your preferred interface ### JavaScript ```javascript const result = await firecrawl.scrape({ alexandria: { provider: "reporter-nih-gov", capability: "research-grants/project", options: { appl_id: 11171443, }, }, }); ``` ### Python ```python result = firecrawl.scrape_alexandria({ "provider": "reporter-nih-gov", "capability": "research-grants/project", "options": { "appl_id": 11171443 } }) ``` ### cURL ```sh curl https://api.firecrawl.dev/v2/scrape \ -H "Authorization: Bearer $FIRECRAWL_API_KEY" \ -H "Content-Type: application/json" \ -d '{ "alexandria": { "provider": "reporter-nih-gov", "capability": "research-grants/project", "options": { "appl_id": 11171443 } } }' ``` ### CLI ```sh firecrawl scrape 'reporter-nih-gov/research-grants/project' \ --options '{"appl_id":11171443}' ``` ### MCP Call the FCX MCP retrieve tool with this object: ```json { "provider": "reporter-nih-gov", "capability": "research-grants/project", "options": { "appl_id": 11171443 } } ``` Ask for only the returned fields needed by the task. ## 5. Full request shape ```json { "provider": "reporter-nih-gov", "capability": "research-grants/project", "options": { "appl_id": 11171443 } } ``` ## 6. Response data The response includes `success`, `provider`, `capability`, `creditsCost` and `data`. This example shows the provider payload in `data`: ```json { "abstract": "Abstract (Overall):\nPancreatic Ductal Adenocarcinoma (PDAC) is a deadly disease whose mechanisms of development remain\nincompletely understood. Evidence suggests that pancreatic cancers may arise from acinar cells undergoing a\nprocess called acinar to ductal metaplasia (ADM) or from ductal cells to give rise to Pancreatic Intraepithelial\nNeoplasias (PanINs). How mutations or combinations of mutations promote PDAC development and the role of\ninflammation in the process still remains unclear. Moreover, interactions between immune cells, cancer-\nassociated fibroblasts (CAFs) and cancer cells can promote PDAC development and progression, but much\nremains to be learned about how signaling between cells in the tumor microenvironment (TME) affects the stem\ncell compartment (`stemness') thought to underlie PDAC development and promotes immune evasion. Thus,\nmultiple questions about fundamental mechanisms governing PDAC development persist.\nTo address these challenges, our superb and highly interactive team will identify genetic and stromal (immune\ncells and CAFs) interactions and pathways that regulate the inception and progression of PDAC using innovative\nmouse models and human tissue-based approaches. We propose three Projects to address the following overall\naims:\n1. Identify the originating cell(s) and deconstruct genetic pathways underlying PDAC initiation\n2. Discover immune signals that cross-talk with epithelial cells and CAFs to promote pancreas cancer\ndevelopment and stemness\n3. Investigate the impact of tumor genetics on PDAC immunobiology and response to macrophage-targeted\nimmunotherapy\nEffort on these projects will be organized through an Administrative and Biostatistics Core (A) and empowered\nby two Research Cores, focused on human tissue procurement (Core B), and use of high-dimensional imaging\nto measure cell and signaling interactions in tissues (CODEX; Core C).\nThe participating investigators on this P01 lead teams that have collaborated productively for years and have\ngenerated compelling preliminary data that support the potential for unraveling the genetic and immune signaling\nmechanisms underlying PDAC development, and developing new immunotherapeutic strategies for PDAC,\nwhich has proven frustratingly resistant to immuno-based therapies.\nOur studies should broadly impact pancreas cancer biology and importantly, elucidate the reciprocal interactions\nbetween immune and non-immune compartments (epithelial, CAFs) in shaping the tumor microenvironment\nduring disease evolution. accelerate discovery of novel diagnostic or preventive strategies for early-stage\ndisease, or therapeutics for advanced PDAC.", "activity_code": "P01", "agency": { "abbreviation": "NCI", "code": "CA", "name": "National Cancer Institute" }, "agency_code": "NIH", "appl_id": 11171443, "award_amount": 2023000, "award_notice_date": "2025-08-20", "contact_pi_name": "KIM, SEUNG K", "core_project_num": "P01CA244114", "date_added": "2025-08-23", "fiscal_year": 2025, "funding": { "arra_funded": false, "award_type": "5", "budget_end": "2027-07-31", "budget_start": "2025-08-01", "cfda_code": "93.396", "covid_response": [], "direct_cost": 1283733, "ic_fundings": [ { "abbreviation": "NCI", "code": "CA", "direct_cost": 1283733, "fiscal_year": 2025, "indirect_cost": 739267, "name": "National Cancer Institute", "total_cost": 2023000 } ], "indirect_cost": 739267, "is_new": false, "opportunity_number": "PAR-20-077" }, "funding_mechanism": "Non-SBIR/STTR", "is_active": true, "observed_at_ms": 1791417600000, "organization": { "city": "STANFORD", "congressional_district": "CA-16", "country": "UNITED STATES", "department": "ANATOMY/CELL BIOLOGY", "duns": "009214214", "ipf_code": "8046501", "latitude": 37.426852, "longitude": -122.17047, "name": "STANFORD UNIVERSITY", "state": "CA", "type": "SCHOOLS OF MEDICINE", "uei": "HJD6G4D6TJY5", "zipcode": "943052004" }, "principal_investigators": [ { "first_name": "LAURA", "full_name": "LAURA D ATTARDI", "is_contact_pi": false, "last_name": "ATTARDI", "middle_name": "D", "profile_id": 1885021, "title": "PROFESSOR" }, { "first_name": "Seung", "full_name": "Seung K Kim", "is_contact_pi": true, "last_name": "Kim", "middle_name": "K", "profile_id": 1927492, "title": "PROFESSOR" } ], "program_officers": [ { "first_name": "NATALIA", "full_name": "NATALIA MERCER", "last_name": "MERCER" } ], "project_end_date": "2027-07-31", "project_num": "5P01CA244114-05", "project_start_date": "2021-08-01", "public_health_relevance": "Project Narrative (Overall):\nThis P01 application from investigators at Stanford University seeks to discover, apply, and translate science\nabout pancreatic cancer (PDAC), with the ultimate goal of improving care for patients with this disease. To\naddress fundamental, persistent questions about the biology of PDAC, we have assembled a superb,\ninteractive team of productive collaborators to lead our Projects and Research Cores that will identify genetic,\nimmune cell, and cancer-associated fibroblasts based interactions and pathways that regulate the inception\nand progression of PDAC. Advances from studies proposed here could broadly impact pancreas cancer\nbiology and drive translational efforts in PDAC.", "spending_categories": [], "study_section": { "code": "ZCA1", "name": "ZCA1-RPRB-H(J1)P" }, "subproject_id": null, "terms": [ "Acceleration", "Acinar Cell", "Address", "Affect", "Amplifiers", "Biology", "Biostatistics Core", "Cancer Biology", "Carcinoma", "Cell Compartmentation", "Cell Ontogeny", "Cells", "Chronic", "Collaborations", "Conceptions", "Data", "Data Analyses", "Data Set", "Dedications", "Dependence", "Detection", "Development", "Disease", "Duct (organ) structure", "Ductal Epithelial Cell", "Epithelial Cells", "Epithelium", "Evolution", "Fibroblasts", "Frustration", "Generations", "Genetic", "Genetically Engineered Mouse", "Genotype", "Goals", "Human", "Image", "Imaging technology", "Immune", "Immune Evasion", "Immune response", "Immune signaling", "Immunobiology", "Immunotherapeutic agent", "Immunotherapy", "Infiltration", "Inflammation", "Inflammatory", "Investigation", "KRAS2 gene", "Lead", "Learning", "Macrophage", "Malignant Neoplasms", "Malignant neoplasm of pancreas", "Measures", "Metaplasia", "Molecular", "Mus", "Mutation", "Neoplasm Metastasis", "Pancreas", "Pancreatic Ductal Adenocarcinoma", "Pancreatic Intraepithelial Neoplasia", "Pathway interactions", "Patient Care", "Preparation", "Prevention strategy", "Process", "Productivity", "Research", "Research Personnel", "Resistance", "Resource Sharing", "Resources", "Risk", "Role", "Science", "Shapes", "Signal Transduction", "Therapeutic", "Tissue Procurements", "Tissues", "Translating", "Universities", "Work", "cancer cell", "candidate identification", "cell type", "diagnostic strategy", "driver mutation", "empowerment", "genetic resource", "high dimensionality", "human tissue", "immunoregulation", "improved", "indexing", "infrastructure development", "innovation", "lymph nodes", "medical schools", "member", "mouse model", "novel", "novel diagnostics", "pancreas development", "pancreatic cancer patients", "pancreatic ductal adenocarcinoma model", "programs", "response", "search engine", "stem cells", "stemness", "targeted treatment", "tool", "translational impact", "tumor", "tumor microenvironment" ], "title": "Pancreatic Cancer Development: Genetic and Immune Regulation", "url": "https://reporter.nih.gov/project-details/11171443" } ``` ## API reference-derived contract The following capability contract is generated from the same normalized Alexandria API reference exposed in the API spec. ### Project - Capability: `research-grants/project` - Description: One project record by application id, full project number or RePORTER URL: title, abstract, public health relevance, RCDC terms, PIs with profile ids, program officers, organization with UEI and location, institute, award amount with direct/indirect costs and per-institute funding, budget and project dates, opportunity number and study section. - Instructions: Read the abstract and funding detail of a grant found with search_projects, or resolve a pasted reporter.nih.gov project link. - Cost: 5 credits per call - Capability file: [Project](https://firecrawl.dev/alexandria/agents/providers/reporter-nih-gov/research-grants/project) Accepted options: - `appl_id` (number): Application id from search_projects, e.g. 11171443. Example: `10` - `project_num` (string): Full project number, e.g. 5P01CA244114-05. Returns the parent record (not a subproject); when several fiscal-year records share the number, the latest one with a warning. Pattern: ^\s*[A-Za-z0-9-]+\s*$. Example: `` - `url` (string): A RePORTER project page, e.g. https://reporter.nih.gov/project-details/11171443. Example: `` Response schema example: ```json { "abstract": "Abstract (Overall):\nPancreatic Ductal Adenocarcinoma (PDAC) is a deadly disease whose mechanisms of development remain\nincompletely understood. Evidence suggests that pancreatic cancers may arise from acinar cells undergoing a\nprocess called acinar to ductal metaplasia (ADM) or from ductal cells to give rise to Pancreatic Intraepithelial\nNeoplasias (PanINs). How mutations or combinations of mutations promote PDAC development and the role of\ninflammation in the process still remains unclear. Moreover, interactions between immune cells, cancer-\nassociated fibroblasts (CAFs) and cancer cells can promote PDAC development and progression, but much\nremains to be learned about how signaling between cells in the tumor microenvironment (TME) affects the stem\ncell compartment (`stemness') thought to underlie PDAC development and promotes immune evasion. Thus,\nmultiple questions about fundamental mechanisms governing PDAC development persist.\nTo address these challenges, our superb and highly interactive team will identify genetic and stromal (immune\ncells and CAFs) interactions and pathways that regulate the inception and progression of PDAC using innovative\nmouse models and human tissue-based approaches. We propose three Projects to address the following overall\naims:\n1. Identify the originating cell(s) and deconstruct genetic pathways underlying PDAC initiation\n2. Discover immune signals that cross-talk with epithelial cells and CAFs to promote pancreas cancer\ndevelopment and stemness\n3. Investigate the impact of tumor genetics on PDAC immunobiology and response to macrophage-targeted\nimmunotherapy\nEffort on these projects will be organized through an Administrative and Biostatistics Core (A) and empowered\nby two Research Cores, focused on human tissue procurement (Core B), and use of high-dimensional imaging\nto measure cell and signaling interactions in tissues (CODEX; Core C).\nThe participating investigators on this P01 lead teams that have collaborated productively for years and have\ngenerated compelling preliminary data that support the potential for unraveling the genetic and immune signaling\nmechanisms underlying PDAC development, and developing new immunotherapeutic strategies for PDAC,\nwhich has proven frustratingly resistant to immuno-based therapies.\nOur studies should broadly impact pancreas cancer biology and importantly, elucidate the reciprocal interactions\nbetween immune and non-immune compartments (epithelial, CAFs) in shaping the tumor microenvironment\nduring disease evolution. accelerate discovery of novel diagnostic or preventive strategies for early-stage\ndisease, or therapeutics for advanced PDAC.", "activity_code": "P01", "agency": { "abbreviation": "NCI", "code": "CA", "name": "National Cancer Institute" }, "agency_code": "NIH", "appl_id": 11171443, "award_amount": 2023000, "award_notice_date": "2025-08-20", "contact_pi_name": "KIM, SEUNG K", "core_project_num": "P01CA244114", "date_added": "2025-08-23", "fiscal_year": 2025, "funding": { "arra_funded": false, "award_type": "5", "budget_end": "2027-07-31", "budget_start": "2025-08-01", "cfda_code": "93.396", "covid_response": [], "direct_cost": 1283733, "ic_fundings": [ { "abbreviation": "NCI", "code": "CA", "direct_cost": 1283733, "fiscal_year": 2025, "indirect_cost": 739267, "name": "National Cancer Institute", "total_cost": 2023000 } ], "indirect_cost": 739267, "is_new": false, "opportunity_number": "PAR-20-077" }, "funding_mechanism": "Non-SBIR/STTR", "is_active": true, "observed_at_ms": 1791417600000, "organization": { "city": "STANFORD", "congressional_district": "CA-16", "country": "UNITED STATES", "department": "ANATOMY/CELL BIOLOGY", "duns": "009214214", "ipf_code": "8046501", "latitude": 37.426852, "longitude": -122.17047, "name": "STANFORD UNIVERSITY", "state": "CA", "type": "SCHOOLS OF MEDICINE", "uei": "HJD6G4D6TJY5", "zipcode": "943052004" }, "principal_investigators": [ { "first_name": "LAURA", "full_name": "LAURA D ATTARDI", "is_contact_pi": false, "last_name": "ATTARDI", "middle_name": "D", "profile_id": 1885021, "title": "PROFESSOR" }, { "first_name": "Seung", "full_name": "Seung K Kim", "is_contact_pi": true, "last_name": "Kim", "middle_name": "K", "profile_id": 1927492, "title": "PROFESSOR" } ], "program_officers": [ { "first_name": "NATALIA", "full_name": "NATALIA MERCER", "last_name": "MERCER" } ], "project_end_date": "2027-07-31", "project_num": "5P01CA244114-05", "project_start_date": "2021-08-01", "public_health_relevance": "Project Narrative (Overall):\nThis P01 application from investigators at Stanford University seeks to discover, apply, and translate science\nabout pancreatic cancer (PDAC), with the ultimate goal of improving care for patients with this disease. To\naddress fundamental, persistent questions about the biology of PDAC, we have assembled a superb,\ninteractive team of productive collaborators to lead our Projects and Research Cores that will identify genetic,\nimmune cell, and cancer-associated fibroblasts based interactions and pathways that regulate the inception\nand progression of PDAC. Advances from studies proposed here could broadly impact pancreas cancer\nbiology and drive translational efforts in PDAC.", "spending_categories": [], "study_section": { "code": "ZCA1", "name": "ZCA1-RPRB-H(J1)P" }, "subproject_id": null, "terms": [ "Acceleration", "Acinar Cell", "Address", "Affect", "Amplifiers", "Biology", "Biostatistics Core", "Cancer Biology", "Carcinoma", "Cell Compartmentation", "Cell Ontogeny", "Cells", "Chronic", "Collaborations", "Conceptions", "Data", "Data Analyses", "Data Set", "Dedications", "Dependence", "Detection", "Development", "Disease", "Duct (organ) structure", "Ductal Epithelial Cell", "Epithelial Cells", "Epithelium", "Evolution", "Fibroblasts", "Frustration", "Generations", "Genetic", "Genetically Engineered Mouse", "Genotype", "Goals", "Human", "Image", "Imaging technology", "Immune", "Immune Evasion", "Immune response", "Immune signaling", "Immunobiology", "Immunotherapeutic agent", "Immunotherapy", "Infiltration", "Inflammation", "Inflammatory", "Investigation", "KRAS2 gene", "Lead", "Learning", "Macrophage", "Malignant Neoplasms", "Malignant neoplasm of pancreas", "Measures", "Metaplasia", "Molecular", "Mus", "Mutation", "Neoplasm Metastasis", "Pancreas", "Pancreatic Ductal Adenocarcinoma", "Pancreatic Intraepithelial Neoplasia", "Pathway interactions", "Patient Care", "Preparation", "Prevention strategy", "Process", "Productivity", "Research", "Research Personnel", "Resistance", "Resource Sharing", "Resources", "Risk", "Role", "Science", "Shapes", "Signal Transduction", "Therapeutic", "Tissue Procurements", "Tissues", "Translating", "Universities", "Work", "cancer cell", "candidate identification", "cell type", "diagnostic strategy", "driver mutation", "empowerment", "genetic resource", "high dimensionality", "human tissue", "immunoregulation", "improved", "indexing", "infrastructure development", "innovation", "lymph nodes", "medical schools", "member", "mouse model", "novel", "novel diagnostics", "pancreas development", "pancreatic cancer patients", "pancreatic ductal adenocarcinoma model", "programs", "response", "search engine", "stem cells", "stemness", "targeted treatment", "tool", "translational impact", "tumor", "tumor microenvironment" ], "title": "Pancreatic Cancer Development: Genetic and Immune Regulation", "url": "https://reporter.nih.gov/project-details/11171443" } ``` ### Publications - Capability: `research-grants/publications` - Description: PubMed IDs of publications that acknowledge a core project (POST /v2/publications/search), newest first, with the citing application id. A known project without linked papers returns an empty list; an unknown core project number is not_found. - Instructions: List the papers a grant produced; fetch their titles and abstracts from PubMed with the PMIDs. - Cost: 5 credits per call - Capability file: [Publications](https://firecrawl.dev/alexandria/agents/providers/reporter-nih-gov/research-grants/publications) Accepted options: - `core_project_num` (string, required): Core project number, e.g. P01CA244114. A full project number such as 5P01CA244114-05 is reduced to its core. Pattern: ^\s*[A-Za-z0-9-]+\s*$. Example: `` - `limit` (number): limit Example: `25` - `offset` (number): Rows to skip; pass next_offset from the previous page. RePORTER pages no further than offset 9,999. Example: `0` Response schema example: ```json { "core_project_num": "P01CA244114", "limit": 5, "next_offset": 5, "observed_at_ms": 1791417600000, "offset": 0, "publications": [ { "appl_id": 11171443, "core_project_num": "P01CA244114", "pmid": 41811433, "pubmed_url": "https://pubmed.ncbi.nlm.nih.gov/41811433/" }, { "appl_id": 11171443, "core_project_num": "P01CA244114", "pmid": 41726948, "pubmed_url": "https://pubmed.ncbi.nlm.nih.gov/41726948/" }, { "appl_id": 11171443, "core_project_num": "P01CA244114", "pmid": 41529696, "pubmed_url": "https://pubmed.ncbi.nlm.nih.gov/41529696/" }, { "appl_id": 11171443, "core_project_num": "P01CA244114", "pmid": 41372415, "pubmed_url": "https://pubmed.ncbi.nlm.nih.gov/41372415/" }, { "appl_id": 11171443, "core_project_num": "P01CA244114", "pmid": 41292779, "pubmed_url": "https://pubmed.ncbi.nlm.nih.gov/41292779/" } ], "total": 16 } ``` ### Search projects - Capability: `research-grants/search_projects` - Description: Search funded research projects (POST /v2/projects/search). Combine free text over titles, abstracts and terms with PI name or profile id, organization, state, fiscal years, agencies and activity codes. Returns one page of project-year records with PIs, organization, administering institute, award amount and dates, plus the total and next_offset. - Instructions: Find NIH grants for a topic, a researcher or an institution; get appl_id for project and core_project_num for publications. - Cost: 5 credits per call - Capability file: [Search projects](https://firecrawl.dev/alexandria/agents/providers/reporter-nih-gov/research-grants/search_projects) Accepted options: - `activity_codes` (string[]): NIH activity codes, e.g. ["R01", "R21", "P01"]. Example: `[]` - `agencies` (string[]): Administering or funding institute/agency abbreviations, e.g. ["NCI", "NIGMS", "AHRQ"]. Example: `[]` - `exclude_subprojects` (boolean): Drop the component subprojects of multi-project awards (P01, U54, ...) and keep their parent records. Example: `false` - `fiscal_years` (number[]): Federal fiscal years of the award records, e.g. [2024, 2025]. Example: `[]` - `limit` (number): Projects per page. Example: `10` - `offset` (number): Rows to skip; pass next_offset from the previous page with the same criteria. RePORTER pages no further than offset 14,999. Example: `0` - `org_name` (string): Funded organization name; RePORTER matches it as a prefix/wildcard ("Stanford" also matches "Stanford Research Institute") unless org_name_exact is true. Example: `` - `org_name_exact` (boolean): Match org_name exactly as RePORTER spells it, e.g. "STANFORD UNIVERSITY". Requires org_name. Example: `false` - `org_states` (string[]): Organization state or territory codes, e.g. ["CA", "MA"]. Example: `[]` - `pi_name` (string): Principal investigator name, partial match on any name part, e.g. "Seung K Kim" or "Attardi". Example: `` - `pi_profile_id` (number): RePORTER PI profile id from a previous result: every project of exactly that investigator. Example: `10` - `sort` (string): sort Example: `relevance` - `sort_order` (string): Applies to every sort except relevance. Example: `desc` - `text` (string): Words searched in project titles, abstracts and RCDC terms. All words must match by default; wrap a phrase in double quotes for an exact match. Example: `` - `text_fields` (string[]): Limit the text search to these fields (default all three). Requires text. Example: `[]` - `text_operator` (string): How text words combine: and (all words), or (any word), advanced (RePORTER boolean syntax). Requires text. Example: `and` Response schema example: ```json { "limit": 3, "next_offset": 3, "observed_at_ms": 1791417600000, "offset": 0, "projects": [ { "activity_code": "P30", "agency": { "abbreviation": "NIDDK", "code": "DK", "name": "National Institute of Diabetes and Digestive and Kidney Diseases" }, "appl_id": 10889124, "award_amount": 1967401, "award_notice_date": "2024-06-25", "contact_pi_name": "KIM, SEUNG K", "core_project_num": "P30DK116074", "fiscal_year": 2024, "funding_mechanism": "Research Centers", "is_active": false, "organization": { "city": "STANFORD", "country": "UNITED STATES", "department": "INTERNAL MEDICINE/MEDICINE", "name": "STANFORD UNIVERSITY", "state": "CA", "uei": "HJD6G4D6TJY5" }, "principal_investigators": [ { "first_name": "Seung", "full_name": "Seung K Kim", "is_contact_pi": true, "last_name": "Kim", "middle_name": "K", "profile_id": 1927492, "title": "PROFESSOR" } ], "project_end_date": "2027-06-30", "project_num": "5P30DK116074-08", "project_start_date": "2017-09-15", "subproject_id": null, "title": "Stanford Diabetes Research Center", "url": "https://reporter.nih.gov/project-details/10889124" }, { "activity_code": "P01", "agency": { "abbreviation": "NCI", "code": "CA", "name": "National Cancer Institute" }, "appl_id": 10927287, "award_amount": 1921851, "award_notice_date": "2024-08-16", "contact_pi_name": "KIM, SEUNG K", "core_project_num": "P01CA244114", "fiscal_year": 2024, "funding_mechanism": "Non-SBIR/STTR", "is_active": false, "organization": { "city": "STANFORD", "country": "UNITED STATES", "department": "ANATOMY/CELL BIOLOGY", "name": "STANFORD UNIVERSITY", "state": "CA", "uei": "HJD6G4D6TJY5" }, "principal_investigators": [ { "first_name": "LAURA", "full_name": "LAURA D ATTARDI", "is_contact_pi": false, "last_name": "ATTARDI", "middle_name": "D", "profile_id": 1885021, "title": "PROFESSOR" }, { "first_name": "Seung", "full_name": "Seung K Kim", "is_contact_pi": true, "last_name": "Kim", "middle_name": "K", "profile_id": 1927492, "title": "PROFESSOR" } ], "project_end_date": "2026-07-31", "project_num": "5P01CA244114-04", "project_start_date": "2021-08-01", "subproject_id": null, "title": "Pancreatic Cancer Development: Genetic and Immune Regulation", "url": "https://reporter.nih.gov/project-details/10927287" }, { "activity_code": "R01", "agency": { "abbreviation": "NIDDK", "code": "DK", "name": "National Institute of Diabetes and Digestive and Kidney Diseases" }, "appl_id": 10884197, "award_amount": 596230, "award_notice_date": "2024-05-31", "contact_pi_name": "KIM, SEUNG K", "core_project_num": "R01DK128932", "fiscal_year": 2024, "funding_mechanism": "Non-SBIR/STTR", "is_active": false, "organization": { "city": "STANFORD", "country": "UNITED STATES", "department": "ANATOMY/CELL BIOLOGY", "name": "STANFORD UNIVERSITY", "state": "CA", "uei": "HJD6G4D6TJY5" }, "principal_investigators": [ { "first_name": "Trish", "full_name": "Trish Berger", "is_contact_pi": false, "last_name": "Berger", "middle_name": null, "profile_id": 7933870, "title": null }, { "first_name": "Seung", "full_name": "Seung K Kim", "is_contact_pi": true, "last_name": "Kim", "middle_name": "K", "profile_id": 1927492, "title": "PROFESSOR" } ], "project_end_date": "2025-05-31", "project_num": "5R01DK128932-04", "project_start_date": "2021-06-01", "subproject_id": null, "title": "Genetic and physiologic regulation of pig islet development and function", "url": "https://reporter.nih.gov/project-details/10884197" } ], "search_url": "https://reporter.nih.gov/search/lq4S1AYEfUS3OQ1MyxUl8w/projects", "total": 9 } ```