Baylor Genetics is hiring a Senior Director of Product Design. In this role, you’ll lead user-centered design for digital tools that support physicians & lab teams. Join our team & create seamless, intuitive experiences that improve healthcare delivery:

Inclusivity and genetics go hand in hand. Patient-centered care means breaking down barriers, promoting equity, & empowering every individual on their diagnostic odyssey. When patients feel seen, heard, & respected, care becomes that much more impactful. #Inclusivity #Genetics

80% of genes are active in the brain and 40% of genetic conditions affect the CNS. AAP, ACMG, NSGC, and AES recommend WGS/WES for kids with unexplained symptoms. Baylor Genetics offers WGS/WES to support faster diagnosis and better outcomes. Learn more:

Do you know which of following traits was not one of the seven characteristics Gregor Mendel studied in pea plants? Drop your guess in the comments!. A) Seed shape .B) Flower color .C) Leaf size .D) Pod color . #GregorMendel #InheritedTraits

Baylor Genetics is hiring an Associate Clinical Director, Clinical Reporting. Lead data interpretation, lab ops, and cross-functional teams to ensure accurate, impactful reporting. Help shape the future of clinical genomics. Apply now: . #Hiring #JobSearch

Genetic conditions are often labeled as rare, but they affect an estimated 6-8% of the overall population. From inherited cancers to familial heart conditions & metabolic disorders, our genes play a profound role in shaping our health. . #Genetics

People with autism often face additional health challenges. A SPARK study of 42,000+ individuals found 74% have other medical conditions, with 10% having epilepsy. Genetic tests like WGS/WES offer crucial answers for quicker diagnoses. Learn more:

At NW Rare Disease Fair, Susan Capps, VP of Market Access, discussed WGS's growing role in rare disease diagnosis, highlighting the Sunshine Genetics Act for newborn screening, & Washington’s proposal to reimburse rWGS beyond traditional payment. #RareDisease #GenomeSequencing

We are #hiring! As an Eligibility #Specialist, you’ll verify coverage, resolve claim issues & ensure clean submissions. #Apply here: . We’re also seeking a Denials & Appeals Specialist to manage denials & submit appeals. Apply now:

We asked Laura Fuqua, MS, CGC, what affirming care means. Her answer: inclusion builds trust. At Baylor Genetics, we’re committed to equitable access to genetic testing and resources for all. Learn more: . #Inclusivity #GeneticCounseling

Cerebral palsy (CP) is a common motor condition in children, with up to 35% linked to genetic causes. Understanding these genetic factors can help improve care strategies. Learn the impact of WGS on CP diagnosis:

ICYMI: The @AmerAcadPeds now recommends WGS/WES as first-tier tests for kids with certain developmental delays. A big step for access, reimbursement & care. BG leaders weigh in via @GenomeWeb: . #GeneticTesting #Access #Pediatrics.

When every moment counts, rWGS delivers fast, actionable answers. A 2025 JALM study showed it may cut hospital stays by 592 days & save up to $28K per patient. Baylor Genetics adds RNA insights + STR detection to guide care. Learn more: . #GenomeSequencing

How long can cord blood be stored and still remain viable for transplant?. #CordBloodAwarenessMonth.

This Fourth of July, we celebrate the courage, resilience, and unity that define our nation’s journey. Wishing you a joyful and safe #IndependenceDay from all of us at Baylor Genetics! . #JulyFourth

Underlying genetic factors may contribute to drug resistant epilepsy, posing a significant challenge in clinical management. Whole Genome Sequencing can help identify the genetic causes of epilepsy. Learn more: . #GenomeSequencing

Which of the following is a genetic condition currently treated using cord blood stem cells? . A) Sickle cell disease.B) Fanconi anemia.C) Severe combined immunodeficiency (SCID).D) All of the above. #CordBloodAwarenessMonth.

Early insights shape lifelong health. This Cord Blood Awareness Month, learn how GeneAware™ from Baylor Genetics helps families understand genetic risks and plan ahead, including decisions like preserving #CordBlood. Learn more:

In this patient case, Rapid Whole Genome Sequencing delivered actionable results for a 3-day-old infant, who presented with symptoms that prompted an urgent need for a clear diagnosis & prompt intervention. Read the patient case: . #GenomeSequencing

We are seeking out passionate individuals to join our team in shaping the future of genetics. Explore career opportunities that align with your skills & aspirations: . #NowHiring #Genetics