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European Journal of Human Genetics, ISSN 1018-4813, 11/2018, Volume 26, Issue 11, pp. 1566 - 1571
Clinical application of whole-exome and whole-genome sequencing (WES and WGS) has led to an increasing interest in how it could drive healthcare decisions. As... 
GENOMICS | BIOCHEMISTRY & MOLECULAR BIOLOGY | DISEASE | GENETICS & HEREDITY | PEDIATRIC NEUROLOGY | UTILITY | SUSPECTED MONOGENIC DISORDERS | NEXT-GENERATION | CHILDREN | Costs | Next-generation sequencing | Medical innovations | Medical records | Genomes | Diagnosis | Patients | Genetic screening
Journal Article
European journal of human genetics, ISSN 1018-4813, 2015, Volume 23, Issue 9, pp. 1142 - 1150
Journal Article
Journal of Heredity, ISSN 0022-1503, 2009, Volume 100, Issue 6, pp. 659 - 674
Journal Article
by Haussler, David and O'Brien, Stephen J and Ryder, Oliver A and Keith Barker, F and Clamp, Michele and Crawford, Andrew J and Hanner, Robert and Hanotte, Olivier and Johnson, Warren E and McGuire, Jimmy A and Miller, Webb and Murphy, Robert W and Murphy, William J and Sheldon, Frederick H and Sinervo, Barry and Venkatesh, Byrappa and Wiley, Edward O and Allendorf, Fred W and Amato, George and Scott Baker, C and Bauer, Aaron and Beja-Pereira, Albano and Bermingham, Eldredge and Bernardi, Giacomo and Bonvicino, Cibele R and Brenner, Sydney and Burke, Terry and Cracraft, Joel and Diekhans, Mark and Edwards, Scott and Ericson, Per G. P and Estes, James and Fjelsda, Jon and Flesness, Nate and Gamble, Tony and Gaubert, Philippe and Graphodatsky, Alexander S and Marshall Graves, Jennifer A and Green, Eric D and Green, Richard E and Hackett, Shannon and Hebert, Paul and Helgen, Kristofer M and Joseph, Leo and Kessing, Bailey and Kingsley, David M and Lewin, Harris A and Luikart, Gordon and Martelli, Paolo and Moreira, Miguel A. M and Nguyen, Ngan and Ortí, Guillermo and Pike, Brian L and Rawson, David Michael and Schuster, Stephan C and Seuánez, Héctor N and Bradley Shaffer, H and Springer, Mark S and Stuart, Joshua Michael and Sumner, Joanna and Teeling, Emma and Vrijenhoek, Robert C and Ward, Robert D and Warren, Wesley C and Wayne, Robert and Williams, Terrie M and Wolfe, Nathan D and Zhang, Ya-Ping and Marshall Graves, Jennifer A and Springer, Mark and Williams, Terrie and Wolfe, Nathan and Edwards, Scott V and Orti, Guillermo and Rawson, David M and Felsenfeld, Adam and Seuánez, Héctor N and Stuart, Joshua M and Turner, Steve
Journal of Heredity, ISSN 0022-1503, 11/2009, Volume 100, Issue 6, pp. 659 - 674
The human genome project has been recently complemented by whole-genome assessment sequence of 32 mammals and 24 nonmammalian vertebrate species suitable for... 
Comparative genomics | Molecular evolution | Species conservation | Ancestral state reconstruction | G10K | Vertebrate biology
Journal Article
Personalized Medicine, ISSN 1741-0541, 07/2013, Volume 10, Issue 5, pp. 473 - 484
The scope of next-generation DNA sequencing (NGS) is transitioning from research to diagnostics (and beyond), but the conditions for routine clinical... 
service model | genome diagnostics | reimbursement | informed consent | big data | next-generation sequencing | AUTISM SPECTRUM DISORDERS | MEDICINE | IDENTIFICATION | PRIMARY-CARE | DE-NOVO MUTATIONS | GENETICS | ELECTRONIC HEALTH RECORDS | DNA | DISEASE | PERSONAL GENOMES | PHARMACOLOGY & PHARMACY | DNA methylation | Genetics | Costs | Quality standards | Genomes | Technological change
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 11/2018, Volume 26, Issue 11, p. 1566
Clinical application of whole-exome and whole-genome sequencing (WES and WGS) has led to an increasing interest in how it could drive healthcare decisions. As... 
Journal Article
European journal of human genetics : EJHG, ISSN 1018-4813, 09/2015, Volume 23, Issue 9, pp. 1142 - 1150
Journal Article
Journal Article