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PLoS Genetics, ISSN 1553-7390, 12/2018, Volume 14, Issue 12, p. e1007752
Journal Article
Genome Medicine, ISSN 1756-994X, 05/2019, Volume 11, Issue 1, pp. 31 - 31
As epigenetic studies become more common and lead to new insights into health and disease, the return of individual epigenetic results to research... 
Epigenetics | ELSI | Return of results | Incidental findings | Epigenetic inheritance | Genetic research | Nervous system | Degeneration | Genetic aspects | Research | Gene expression | Consortia | Validity | Ethics | Researchers | Genomics | Bioethics | Genetics | Genomes | Communication
Journal Article
HUMAN MUTATION, ISSN 1059-7794, 10/2017, Volume 38, Issue 10, pp. 1281 - 1285
Journal Article
Nature biotechnology, ISSN 1087-0156, 03/2019, Volume 37, Issue 4, pp. 480 - 480
In the version of this article initially published, Lena Dolman's second affiliation was given as Wellcome Trust Sanger Institute, Wellcome Genome Campus,... 
Genomics | Genomes | Error correction | Beacons | Cancer
Journal Article
PLoS Biology, ISSN 1544-9173, 12/2015, Volume 13, Issue 12
  In parallel with massive genomic data production, data sharing practices have rapidly expanded over the last decade. To ensure authorized access to data,... 
Federal employees | Researchers | Archives & records | Data integrity | Funding | Objectivity | Information sharing | Genomes | Research centers | Data bases
Journal Article
Human Mutation, ISSN 1059-7794, 2015, Volume 36, Issue 10, pp. 915 - 921
Journal Article
by Hudson, Thomas J and Anderson, Warwick and Aretz, Axel and Barker, Anna D and Bell, Cindy and Bernabé, Rosa R and Bhan, M. K and Calvo, Fabien and Eerola, Iiro and Gerhard, Daniela S and Guttmacher, Alan and Guyer, Mark and Hemsley, Fiona M and Jennings, Jennifer L and Kerr, David and Klatt, Peter and Kolar, Patrik and Kusuda, Jun and Lane, David P and Laplace, Frank and Lu, Youyong and Nettekoven, Gerd and Ozenberger, Brad and Peterson, Jane and Rao, T. S and Remacle, Jacques and Schafer, Alan J and Shibata, Tatsuhiro and Stratton, Michael R and Vockley, Joseph G and Watanabe, Koichi and Yang, Huanming and Yuen, Matthew M. F and Knoppers, Bartha M and Bobrow, Martin and Cambon-Thomsen, Anne and ssler, Lynn G and Dyke, Stephanie O. M and Joly, Yann and Kato, Kazuto and Kennedy, Karen L and Nicolás, Pilar and Parker, Michael J and Rial-Sebbag, Emmanuelle and Romeo-Casabona, Carlos M and Shaw, Kenna M and Wallace, Susan and Wiesner, Georgia L and Zeps, Nikolajs and Lichter, Peter and Biankin, Anew V and Chabannon, Christian and Chin, Lynda and Clément, Bruno and de Alava, Enrique and Degos, Françoise and Ferguson, Martin L and Geary, Peter and Hayes, D. Neil and Johns, Amber L and Kasprzyk, Arek and Nakagawa, Hidewaki and Penny, Robert and Piris, Miguel A and Sarin, Rajiv and Scarpa, Aldo and van de Vijver, Marc and Futreal, P. Anew and Aburatani, Hiroyuki and Bayés, Mónica and Bowtell, David D. L and Campbell, Peter J and Estivill, Xavier and Grimmond, Sean M and Gut, Ivo and Hirst, Martin and López-Otín, Carlos and Majumder, Partha and Marra, Marco and McPherson, John D and Ning, Zemin and Puente, Xose S and Ruan, Yijun and Stunnenberg, Henik G and Swerdlow, Harold and Velculescu, Victor E and Wilson, Richard K and Xue, Hong H and Yang, Liu and Spellman, Paul T and Bader, Gary D and Boutros, Paul C and Flicek, Paul and Getz, Gad and Guigó, Roderic and Guo, Guangwu and Haussler, David and Heath, Simon and Hubbard, Tim J and Jiang, Tao and ... and Int Canc Genome Consortium and International Cancer Genome Consortium and The International Cancer Genome Consortium and Science for Life Laboratory, SciLifeLab and Centra and Proteomik (stängd 20130101) and Skolan för bioteknologi (BIO) and KTH
Nature, ISSN 0028-0836, 2010, Volume 464, Issue 7291, pp. 993 - 998
Journal Article
PLoS Biology, ISSN 1544-9173, 12/2015, Volume 13, Issue 12, p. e1002339
Journal Article
The American Journal of Human Genetics, ISSN 0002-9297, 05/2017, Volume 100, Issue 5, pp. 695 - 705
Journal Article
Genetics in Medicine, ISSN 1098-3600, 2018, Volume 21, Issue 5, pp. 1031 - 1037
Access to detailed variant data is key to inform and verify the interpretation of genomic data. Clinical laboratories can play a significant role in sharing... 
public databases | variants | consent | data sharing | clinical laboratories | GENETICS & HEREDITY | Informed Consent | Public Policy | Genetic Privacy | Laboratories | Consent Forms | Databases, Genetic | Information Dissemination
Journal Article
Cell, ISSN 0092-8674, 11/2016, Volume 167, Issue 5, pp. 1150 - 1154
Journal Article
Trends in Genetics, ISSN 0168-9525, 2016, Volume 32, Issue 10, pp. 591 - 592
Emerging ethical, legal, and social implications (ELSI) scholarship in epigenetics has focused largely on hypothetical issues involving institutional racism,... 
Medical Education | epigenomics | ethics | eugenics | ELSI | genetic discrimination | science communication | epigenetics | GENETICS & HEREDITY | Epigenomics - ethics | Eugenics - trends | Humans | Racism - ethics | Epigenomics - trends | Ethics, Research | Epigenetic inheritance
Journal Article
European Journal of Human Genetics, ISSN 1018-4813, 12/2016, Volume 24, Issue 12, pp. 1676 - 1680
We propose a standard model for a novel data access tier - registered access - to facilitate access to data that cannot be published in open access archives... 
DATABASE | BIOCHEMISTRY & MOLECULAR BIOLOGY | GENETICS & HEREDITY | Databases, Genetic | Security Measures - standards | Security Measures - organization & administration | Access to Information | Information Dissemination | Genomics | Genomes | Research | Data bases | Medicine | Datasets | Consortia | Privacy | Ethics | Researchers | Information sharing | Genetics | Open access
Journal Article
PLoS Genetics, ISSN 1553-7390, 2016, Volume 12, Issue 1, p. e1005772
A systematic way of recording data use conditions that are based on consent permissions as found in the datasets of the main public genome archives (NCBI dbGaP... 
ONTOLOGY | DISEASE | GENETICS & HEREDITY | Genomic Library | Genome | Databases, Nucleic Acid | Health Services Research | Surveys | Genomics | Genetic research | Technology application | Usage | Big data | Studies | Datasets | Codes | Archives & records | Working groups | Consent | Funding | Information sharing | Genomes | Research
Journal Article
Human Mutation, ISSN 1059-7794, 10/2017, Volume 38, Issue 10, pp. 1281 - 1285
The Matchmaker Exchange (MME) connects rare disease clinicians and researchers to facilitate the sharing of data from undiagnosed patients for the purpose of... 
precision medicine | privacy | consent | data sharing | data access | personalized medicine | Consent
Journal Article