Haltrich I, Pikó H, Pamjav H, Somogyi A, Völgyi A, David D, Beke A, Garamvölgyi Z, Kiss E, Karcagi V, Fekete G. Complex X chromosome rearrangement associated with multiorgan autoimmunity. Molecular Cytogenetics 8:1, 2015​ DOI: 10.1186/s13039-015-0152-5
​
David D, Almeida LS, Maggi M, Araújo C, Imreh S, Valentini G, Fekete G, Haltrich I. Clinical Severity of PGK1 Deficiency Due To a Novel p. E120K Substitution Is Exacerbated by Co-inheritance of a Subclinical Translocation t (3; 14)(q26. 33; q12), Disrupting NUBPL Gene. Journal of Inherited Metabolic Disease 23:55-65, 2015. DOI 10.1007/8904_2015_427
​
David D, Marques B, Ferreira C, Araújo C, Vieira L, Soares G, Dias D, Pinto M. Co-segregation of trichorhinophalangeal syndrome with a t(8;13)(q23.3;q21.31) familial translocation that appears to increase TRPS1 gene expression. Human Genetics, 132:1287-99, 2013. DOI 10.1007/s00439-013-1333-0
David D, Marques B, Ferreira C, Vieira P, Corona-Rivera A, Ferreira JC, van Bokhoven H. Characterization of two ectrodactyly-associated translocation breakpoints separated by 2.5Mb on chromosome 2q14.1-q14.2. European Journal of Human Genetics, 17:1024-1033, 2009. DOI 10.1038/ejhg.2009.2
David D, Cardoso J, Marques B, Marques R, Silva ED, Santos H, Boavida MG. Molecular characterization of a familial translocation implicates disruption of HDAC9 and possible position effect on TGFB2 in the pathogenesis of Peters’ anomaly. Genomics, 81:489-503, 2003. DOI 10.1016/S0888-7543(03)00046-6
​
Kutsche K, Yntema H, Brandt A, Jantke I, Nothwang HG, Orth U, Boavida MG, David D, Chelly J, Fryns JP, Moraine C, Ropers HH, Hamel BCJ, van Bokhoven H, Gal A. Mutations in ARHGEF6, encoding a guanine nucleotide exchange factor for Rho GTPases, in patients with X-linked mental retardation. Nature Genetics 26:247-250, 2000. DOI10.1038/80002
​