Thank you for your interest in collaborating with FDNA. We invite you to let us know how you would like to collaborate using the form on this page. We will get back to you promptly.
FDNA grants research partners:
- The free use of the core technology powering Face2Gene
- The support of a dedicated research team that will work with your team to draft grant proposals and IRB applications and manuscripts
- Access to tens-of-thousands of curated and annotated data-points
- Full authorship rights
Bibliography (updated as of March, 2017)
Basel-Vanagaite L, Wolf L, Orin M, Larizza L, Gervasini C, Krantz ID, Deardoff MA. Recognition of the Cornelia de Lange syndrome phenotype with facial dysmorphology novel analysis. Clin Genet. 2016 May;89(5):557-63.
Chiu Annie T.G., Zhu Lixing, Gary T.K. Moka, Leung G K.C. , Chowa, C.B. Chung Brian H.Y. (2016) Before and after – Nutritional transformation of dysmorphism in a case of Costello, Eur J Med Genet. 2016 Nov;59(11):573-576.
Gardner OK, Haynes K, Schweitzer D, Johns A, Magee WP, Urata MM, Sanchez-Lara PA. Familial Recurrence of 3MC Syndrome in Consanguineous Families: A Clinical and Molecular Diagnostic Approach With Review of the Literature. Cleft Palate Craniofac J. 2016 Jun 29. DOI: 10.1597/15-151
Gripp KW, Baker L, Telegrafi A, Monaghan KG. The role of objective facial analysis using FDNA in making diagnoses following whole exome analysis. Report of two patients with mutations in the BAF complex genes. Am J Med Genet A. 2016 Apr 26.
Kayembe KT., Kasole LT, Mbuyi-Musanzayi S, Kabamba NL, Katshiez Nawej C, Musa Obadia P, Banza Lubaba Nkulu C, Nemery B, Devriendt K.. 2016, Microtia in Cornelia de Lange syndrome: a case from Democratic Republic of the Congo. Clinical Dysmorpholgy 2016 Oct;25(4):178-8
Lumaka A, Cosemans N, Lulebo Mampasi A, Mubungu G, Mvuama N, Lubala T, Mbuyi-Musanzayi S, Breckpot J, Holvoet M, De Ravel T, Van Buggenhout G, Peeters H, Donnai D, Mutesa L, Verloes A, Lukusa Tshilobo P, Devriendt K.,Facial dysmorphism is influenced by ethnic background of the patient and of the evaluator Clin Genet. 2016 Dec 7.
Lumaka A, Lukoo R, Mubungu G, Lumpala P, Mbayabo G, Mupuala A, Lukusa Tshilobo P, Devriendt K., Williams-Beuren syndrome: pitfalls for diagnosis in limited resources setting. Clinical Case Reports 2016 4(3):294-297.