Amalia Dutra

Recurrent de novo point mutations in lamin A cause Hutchinson–Gilford progeria syndrome

Laura Scott, Michael Boehnke, Peter Berglund, 2003, Nature.

Turning on and off recurrent balanced cortical activity

Michael Boehnke, Thomas W. Glover, Francis S. Collins, 2022 .

A genomic map of a 6-Mb region at 13q21-q22 implicated in cancer development: identification and characterization of candidate genes

Heli Nevanlinna, Therese Sandberg, Dietrich A. Stephan, 2002, Human Genetics.

Telomere-to-telomere assembly of a complete human X chromosome

Sergey Koren, Adam M. Phillippy, Joel Armstrong, 2019, bioRxiv.

The fusion gene Cbfb-MYH11 blocks myeloid differentiation and predisposes mice to acute myelomonocytic leukaemia

Lisa Garrett, David Bodine, A. Dutra, 1999, Nature Genetics.

A Hexanucleotide Repeat Expansion in C9ORF72 Is the Cause of Chromosome 9p21-Linked ALS-FTD

David Heckerman, Lorne Zinman, Joanne Wuu, 2011, Neuron.

Mutation in the α-Synuclein Gene Identified in Families with Parkinson's Disease

Robert L. Nussbaum, Giuseppe Di Iorio, William G. Johnson, 1997 .