News & Publications
FDNA Inc. Launches New Face2Gene Suite of Phenotyping Apps to Aid in Identification and Evaluation of Rare and Ultra-rare Genetic Disorders.
October 18, 2016
New suite of phenotyping apps to be launched at the American Society of Human Genetics Annual Meeting
FDNA and Centogene Announce First Grant of Molecular Testing Under the Face2Gene Unknown Forum Grant Program at the American Society of Human Genetics (ASHG) Annual Meeting
October 17, 2016
Collaboration between FDNA, the developer of the Face2Gene Suite and CENTOGENE, worldwide leader in genetic diagnostics, enabled the first grant of molecular testing for a patient with an unknown genetic disorder. The collaboration extends beyond financial support and includes the successful integration of Face2Gene LABS API with CENTOGENE’s bioinformatics pipeline to improve variant prioritization and […]
Familial Recurrence of 3MC Syndrome in Consanguineous Families: A Clinical and Molecular Diagnostic Approach With Review of the Literature.
June 29, 2016
Gardner OK, Haynes K, Schweitzer D, Johns A, Magee WP, Urata MM, Sanchez-Lara PA.; Cleft Palate-Craniofac Journal. 2016 Jun 29.
July 14, 2016
LEUVEN, Belgium — July 14, 2016 — Diploid today announces an update of InHelix, its software for CNV analysis in rare disease diagnostics. InHelix now integrates with Face2Gene, a software platform that facilitates detection of facial dysmorphic features from facial photos. The integration between the two apps allows clinicians to directly access and use dysmorphic […]
March 14, 2016
Grant available exclusively for cases uploaded through the Face2Gene Online Unknown Forum FDNA Inc. (Boston, MA) announced a new grant program for patients with an unknown diagnosis. Under this grant, FDNA will sponsor for genetic testing to be performed for patients with cases uploaded through the Face2Gene Online Unknown Forum. The announcement was made at […]
March 7, 2016
Call for Research Proposals Issued at the American College of Medical Genetics and Genomics (ACMG) Annual Meeting 2016 FDNA Inc. (Boston, MA) issued today a call to geneticists to submit research proposals to the third cycle of the GIVE A FACE TO A SYNDROME research program. The announcement coincides with the American College of Medical […]
October 5, 2015
Call for Research Proposals issued at the American Association of Human Genetics annual meeting ASHG2015 Boston, MA (PRweb) October 5th, 2015 – FDNA, a pioneer in computer-aided dysmorphology analysis, invites geneticists from around the world to join the second cycle of the “GIVE A FACE TO A SYNDROME” research program. The date of the release […]
FDNA to Launch Face2Gene Team Edition at ESHG 2015, Save Time, Collaborate and Share Knowledge when Evaluating Rare Disease Patients
May 28, 2015
Designed for teams and genetics departments, Face2Gene streamlines case and workflow management NEW YORK, May 28, 2015 /PRNewswire/ –FDNA® the pioneer in computer-aided dysmorphology analysis will launch Face2Gene Team Edition at the European Society of Human Genetics conference in Glasgow, Scotland on June 6-9, 2015. This newest addition to the Face2Gene family, powered by FDNA […]
October 2, 2016
Chiu Annie T.G., Zhu Lixing, Gary T.K. Moka, Leung G K.C. , Chowa, C.B. Chung Brian H.Y. (2016) Eur J Med Genet. 2016 Nov;59(11):573-576. doi: 10.1016/j.ejmg.2016.10.001
May 22, 2016
S. Douzgou, S. Banka The face of the developmental disorders of chromatin remodeling. P11.026B Presented at the European Society of Human Genetics (ESHG) 2016 Annual Meeting in Barcelona Spain.
May 22, 2016
M. A. Mensah, N. Hajjir, N. Ehmke, F. Alisch, C. Ott, R. Flöttmann, M. Spielmann, A. Thorwarth, D. Korinth, P. N. Robinson, S. Köhler, T. Zemojtel, P. Lorini, K. Dathe, S. Dölken, M. Schülke-Gerstenfeld, S. Mundlos, L. Graul-Neumann, D. Horn, P. M. Krawitz Image analysis of patients with dysmorphic facial features boosts diagnostic yield in […]