Recuro's Focus

We leverage science, data, technology and care services to catch illness early and prevent disease.

To keep people healthy and happy for the long term, Recuro built…

A one-stop shop where people can access primary care, behavioral health, and their benefits, all in one place

An innovative care model, built on genomics, to target care, meaningfully reduce cost, and improve care outcomes

Recuro's Proactive

Digital Medical Home™

Ingest Data

Aggregate and analyze data from across the patient’s health journey through our interoperable, API-based platform

Understand Risk

Risk stratify the population to identify actionable and proactive interventions that prevent adverse health events

Tailor Diagnostic & Genomic Tests

Deliver personalized, at-home lab tests, with diagnostic screening and actionable genomics that includes hereditary disease risk and pharmacogenomics (PGx)

Assign Care Team

Introduce a dedicated primary care physicians who quarterbacks the patient’s healthcare journey, collaborating with behavioral health providers, care managers, and the broader care team

Improve Health

Achieve better health for the long term by better identifying risks, catching illness early, and removing barriers to care

Risk Stratification

Powered by the Cleveland Clinic’s Hereditary Risk Tool

Capture genetic disease and prescription risk factors to drive personalized genomics and labs

Identify risk of depression and anxiety, to proactively engage patients for behavioral health care

Understand key lifestyle areas such as sleep, diet, and exercise, to ensure care is holistic based on each patient’s unique needs

Identify the unique ways patients want to experience communications and engagement

Surface food security, loneliness, transportation barriers, and other social determinants to connect patients with the support they need

Genomics & Labs

Prevent Panel

Hereditary Breast and Ovarian Cancer Syndrome (HBOC) – Inceased risk for breast, ovarian, tubal, peritoneal, and other cancers due to mutations.

BRCA1 BRCA2

Lync syndrome (LS) – increased risk for colorectal, endometrial, ovarian, and other cancers associated with mutations in mismatch – repair genes

BRCA1 BRCA2 EPCAM MLH1 MSH2 MSH6 PMS2

Familial hypercholesterolemia (FH) – increased risk for heart disease or stroke due to mutations leading to very high cholesterol levels from an early age

APOB LDLR PCSK9

Coverage of haplotypes related to SSRIs & opioids

CYP2D6 CYP2C19

PGx

ABCB1 ABCG2 AGT CACNA1C CES1 CFTR COMT CYP1A2 CYP2C9 CYP2C19 CYP2D6 CYP3A4 CYP2A5 DRD1 DRD2 DRD3 DYPD F2 F5 GNB3 GRIK4 HTR1A HTR2A HTR2C IFNL3 KCNIP1 LDLR MTHFR NR1H3 OPRM1 RYR1 SLC01B1 SLC6A2 TPMT VKORC1 NAT1 ADRB1 EDN1 GSTA1 UGT2B7 UGT2B10