FDNA and Microsoft Collaborate to Enhance Genomics Technology Through AI
FDNA and Microsoft Genomics are working together to integrate the most advanced Artificial Intelligence solutions to support clinical genomics. Read more
FDNA and Face2Gene Featured at ESHG
A flock of researchers from around the globe shared their findings in dysmorphology and molecular genetics at this year’s Read more
Redefining Phenotyping for Clinical Advancements and Variant Prioritization
FDNA’s CEO, Dekel Gelbman, joined two distinguished members of the genetics community—Dr. John Carey (University of Utah) and Dr. Christine Read more
Happening at HIMMS: Precision Medicine Through Next-Generation Phenotyping—A Customer’s Journey
HIMSS Conference, Microsoft booth Thursday, March 7 3:40 PM PST Las Vegas, Nevada As over 40,000 health IT professionals, Read more
FDNA Announces Genomics Collaborative® at a Global Innovation Summit
English | Spanish In a packed auditorium at Mexico City’s CENTRO University, FDNA’s Senior Director of Marketing, Jeff Daniels, announced Read more
NIH offering $190 million to research somatic gene editing
The National Institutes of Health (NIH) recently launched a program to accelerate the transition of genome editing into clinical applications. Read more
2017 Year in Review
At FDNA, we’re making precision medicine a reality by crowdsourcing knowledge and integrating next-generation phenotyping (NGP) technologies into every patient Read more
Drug Delivery Partnership: Precision Medicine Drives Discovery, Development and Commercialization in Pharma
In an era of breakthrough advancements in healthcare, it is hard to believe that 90% of blockbuster medicines are only Read more
Skin Disorders Discoveries in the Year of Discovery
December Discoveries – Skin Disorders As part of FDNA’s Year of Discovery, FDNA collaborated with the National Foundation for Ectodermal Read more
Dexter’s Journey with Ectodermal Dysplasia
Photo from the National Foundation for Ectodermal Dysplasias (NFED) website. FDNA focused on skin disorders in December for the Year of Read more
Improving the Molecular Diagnostic Yield: Using Artificial Intelligence to Deliver Precision Phenomics
Genetic sequencing is becoming a more popular diagnostic tool; however, even with all the advancements, it only reaches a diagnosis Read more
Skeletal Dysplasia Discoveries in the Year of Discovery
October Discoveries – Skeletal Dysplasias As part of FDNA’s Year of Discovery, FDNA collaborated with the Little People of America, Read more
Craniosynostoses and Craniofacial Conditions Discoveries in the Year of Discovery
September Discoveries – Craniosynostoses and Craniofacial Conditions FDNA collaborated with the World Craniofacial Foundation, sponsored by Blueprint Genetics, to promote Read more
Seizure and Epilepsy-related Disorders Discoveries in the Year of Discovery
November Discoveries – Seizure and Epilepsy-related Conditions As a part of FDNA’s Year of Discovery, FDNA collaborated with the C.U.R.E: Read more
Baraitser-Winter Syndrome Facial Analysis Discoveries in the Year of Discovery
Lissencephalies and Other Brain Malformations FDNA collaborated with the American Brain Foundation, sponsored by Fabric Genomics, to promote awareness of Read more
Marfan Syndrome Facial Analysis Discoveries in the Year of Discovery
Spotlight On Congenital Heart Defect Syndromes, Aortopathies, and other Inherited Heart Conditions As part of FDNA’s Year of Discovery, GeneDx Read more
Morgan’s Story
“Morgan is so expressive. She smiles and she lights up the room. She just loves watching what’s happening and Read more
FDNA Presents Rare Disease Technologies at the 2017 Precision Medicine Summit at Boston Children’s Hospital
The Division of Genetics and Genomics Department of Medicine at Boston Children’s Hospital will present their exciting new Fall Precision Read more
Disorder: The Rare Disease Film Festival
Disorder: The Rare Disease Film Festival will be held October 2 & 3, 2017 in Boston, MA. This is a new event Read more
Izzy’s Journey with 22q and CHD
FDNA focused on congenital heart defect syndromes, aortopathies and other inherited heart conditions in July for the Year of Discovery. We are uniting Read more