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Andreia Cunha

Senior Editor at Genome Medicine

Latest posts by Andreia Cunha (see all)

  • SRST2: a new tool for genomic epidemiology - 18th December 2014
  • Less talking and more doing: the return of secondary genomic findings to patients - 29th May 2014
  • Call for papers: Genome Medicine announces a new series on Participatory Medicine - 23rd July 2013

SRST2: a new tool for genomic epidemiology

Generic-pink-bacteria-cropped-e1418906299578-150x52

18/12/2014

On Medicine

In this Q&A, Michael Inouye and Kathryn Holt, authors of a Software article recently published in Genome Medicine, tell us about the development of the… Read more »

Less talking and more doing: the return of secondary genomic findings to patients

woman concentrating (Flickr, RelaxingMusic, CC)

29/05/2014

On Medicine

A study published today in Genome Medicine describes a framework for returning ‘secondary’ or ‘incidental’ genomic findings to patients. We take a look… Read more »

Call for papers: Genome Medicine announces a new series on Participatory Medicine

GM logo

23/07/2013

On Medicine

Later this year, Genome Medicine will publish a new thematic series focusing on Participatory Medicine. This article collection will highlight how the… Read more »

Anti-TNF-alpha therapeutics in chronic inflammatory diseases – seeing in the dark

28/06/2013

On Medicine

Multiple diseases are covered by the umbrella of poorly understood etiology coupled to an exaggerated or misguided inflammatory response. At first sight, it… Read more »

In this issue of Genome Medicine: disease in the microbial jungle, a technology for target enrichment, genomics of osteoporosis and chronic lymphocytic leukemia, and more…

GM logo

31/05/2013

On Medicine

The May issue of Genome Medicine features two articles that highlight the role of microbes in human health and disease as part of a recently launched thematic… Read more »

With a little help from your family: advances in non-invasive prenatal diagnosis

Genome Medicine

04/03/2013

On Medicine

Accurate prenatal diagnosis is important to guide pregnancy and birth management, therapeutic strategies, and future family planning, but invasive diagnostic… Read more »

Not a mixed bag: redefining syndromes associated with ASXL gene mutations

GM-logo-1

26/02/2013

On Medicine

Bohring-Opitz syndrome is a clinically heterogeneous developmental condition characterized by feeding difficulties, severe developmental delays, a smaller than… Read more »

Return of incidental genetic findings: guidelines for clinical trials

GM logo 1

30/01/2013

On Medicine

The decrease in cost and increase in efficiency of genome-scale studies means we can enjoy fast-paced generation of genomic data. In the clinic, this growth has… Read more »

miRNA biomarkers in osteosarcoma: crossing a new bridge

GM logo 1

22/01/2013

On Medicine

Osteosarcoma is the most common type of bone tumor, but the lack of good biomarkers to predict the outcome of standard treatment has so far prevented patient… Read more »

Cystic fibrosis modifier genes: the last refuge of the complex

GM logo 1

02/01/2013

On Medicine

Cystic fibrosis is a rare but lethal autosomal recessive disorder caused by mutations in the cystic fibrosis transmembrane conductance regulator (CFTR) gene.… Read more »

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