What We Offer
Discover our comprehensive range of health & medical services
Health Resources
Comprehensive genetics and genomics health information curated and reviewed by board-certified medical geneticists, genetic counselors, and research scientists to ensure clinical accuracy and relevance. Our resource library covers inherited conditions, genetic testing methodologies, variant interpretation frameworks, and the latest research on gene-disease associations across thousands of conditions documented in OMIM and ClinVar. Patient-accessible explanations are written at multiple reading levels, from introductory overviews for newly diagnosed patients to detailed technical references for clinicians and researchers. All content is reviewed on an annual basis and updated to reflect changes in clinical guidelines and emerging evidence.
Research Database
Access a curated database of peer-reviewed genetic and genomic research publications, open-access clinical trial registries, and preprint archives covering the full spectrum of human genetics from basic molecular biology to translational medicine. Our search and filtering tools allow researchers and clinicians to rapidly identify relevant studies by gene, disease, variant type, population, and study design. We index publications from major genomics journals including Nature Genetics, Genome Research, AJHG, and Genetics in Medicine, with abstracts and key findings summarized for non-specialist readers. PubMed and ClinicalTrials.gov integration provides seamless access to the broader scientific literature alongside our curated content.
Patient Community
Connect with a global community of patients, families, researchers, and clinicians united by their interest in human genetics and genetic conditions — sharing experiences, asking questions, and finding mutual support in our moderated discussion forums. Condition-specific groups allow families affected by rare genetic syndromes to connect with others navigating the same diagnostic journey, clinical decision-making, and advocacy landscape. Our community partners with patient advocacy organizations for over 500 rare genetic conditions to amplify resources, research funding opportunities, and clinical trial recruitment. All community discussions are moderated by trained volunteers and reviewed by clinical advisors to ensure medical information shared is accurate and appropriately contextualized.
Health Assessments
Interactive genetic risk assessment and screening tools that help individuals understand their potential hereditary risk for common conditions and identify whether genetic testing or specialist referral is warranted based on personal and family history. Our family history collection tool generates a structured pedigree and uses validated algorithms to estimate risk levels for hereditary cancer syndromes, cardiac conditions, and metabolic disorders according to published clinical guidelines. Risk assessment outputs are clearly communicated as relative risk levels with actionable guidance on appropriate next steps — from lifestyle modification to genetic counseling consultation. All screening tools are reviewed by clinical geneticists and clearly labeled as screening aids, not diagnostic instruments.
Educational Content
In-depth educational articles, illustrated guides, explainer videos, and infographics covering the full spectrum of human genetics — from foundational concepts like DNA structure and Mendelian inheritance to advanced topics like polygenic risk scores, epigenetics, and somatic mutation in cancer. Our educational content series includes structured learning pathways for specific audiences: a Genetics 101 series for patients newly entering the genetics healthcare system, an Advanced Genomics track for biology students and early-career researchers, and a Clinical Genetics module for healthcare providers expanding their genomics literacy. All multimedia content is produced in collaboration with science communicators, medical illustrators, and clinical reviewers.
Expert Consultations
Schedule telehealth and in-person consultations with board-certified genetic counselors, clinical geneticists, and genomic medicine specialists who can review your test results, assess hereditary risk, and guide clinical decision-making based on the latest evidence and guidelines. Pre-consultation questionnaires and family history collection tools ensure your specialist has comprehensive information before your appointment, maximizing the value of your consultation time. Our provider network includes certified genetic counselors holding CGC credentials, medical geneticists certified by the American Board of Medical Genetics and Genomics, and specialty oncologists with advanced genomics training. Consultations are available for adult genetics, pediatric genetics, prenatal genetics, and oncology genetics.