Public Health Genomics Knowledge Base - CDC

A database of published scientific literature, CDC resources, and other materials that address the translation of genomic discoveries into improved health care and disease prevention.

An international database on ethical, legal and social issues in human genetics.


Database of Health Economics and Genomics Studies - Health Economics Research Centre (Oxford)

A database of health economics and genomics studies which is updated quarterly.


Journals Series and Special Editions

Science Magazine

Genotype to Phenotype - September 2019

Lancet Series

Genomic Medicine - August 2019

Journal of Genetic Counseling Special Issue

Exploring the Exome - April 2019

Cell Special Edition

Unraveling the Human Genome - March 2019

Genetics & Genomic Medicine around the World

Invited Commentaries


Other resources

Notable Accomplishments in Genomic Medicine

A list of interesting advances in genomic medicine since 2011.


Relevant Articles & Reviews 

Krebs K, Milani L. Translating pharmacogenomics into clinical decisions: do not let the perfect be the enemy of the good. Human Genomics. 2019;13(1):39.

Pasquier L, Isidor B, Rial-Sebbag E, Odent S, Minguet G, Moutel G. Population genetic screening: current issues in a European country. European Journal of Human Genetics. 2019;27(9):1321-3.

Sirugo G, Williams SM, Tishkoff SA. The Missing Diversity in Human Genetic Studies. Cell. 2019;177(1):26-31.

Zebrowski AM, Ellis DE, Barg FK, Sperber NR, Bernhardt BA, Denny JC, et al. Qualitative study of system-level factors related to genomic implementation. Genet Med. 2018. [Pub ahead of print]

Carrieri D, Howard HC, Benjamin C, Clarke AJ, Dheensa S, Doheny S, et al. Recontacting patients in clinical genetics services: recommendations of the European Society of Human Genetics. European Journal of Human Genetics. 2018. [Epub ahead of print]

Jusaku Minari,  Kyle B. Brothers and Michael Morrison. Tensions in ethics and policy created by National Precision Medicine Programs. Human Genomics (2018) 12:22.

W. Mazzucco, R. Pastorino, T. Lagerberg, M. Colotto, E. d’Andrea, C. Marotta, C. Marzuillo, P. Villari, A. Federici, W. Ricciardi, S. Boccia; Current state of genomic policies in healthcare among EU member states: results of a survey of chief medical officers, European Journal of Public Health, Volume 27, Issue 5, 1 October 2017, Pages 931–937.

Haeusermann T, Greshake B, Blasimme A, Irdam D, Richards M, et al. (2017) Open sharing of genomic data: Who does it and why? PLOS ONE 12(5): e0177158. 

Dubow, Talitha and Sonja Marjanovic. Population-scale sequencing and the future of genomic medicine: Learning from past and present efforts. Santa Monica, CA: RAND Corporation, 2016.

Messner DA, Al Naber J, Koay P, et al. Barriers to clinical adoption of next generation sequencing: Perspectives of a policy Delphi panel. Applied & Translational Genomics. 2016;10:19-24.

Manolio TA, Abramowicz M, Al-Mulla F, et al. Global Implementation of Genomic Medicine: We Are Not Alone. Science Translational Medicine. 2015;7(290):290ps13.

Korf BR, Berry AB, Limson M, Marian AJ, Murray MF, O’Rourke PP, et al. Framework for development of physician competencies in genomic medicine: report of the Competencies Working Group of the Inter-Society Coordinating Committee for Physician Education in Genomics. Genetics In Medicine. 2014;16:804.

Yim, S.-H., & Chung, Y.-J. Introduction to International Ethical Standards Related to Genetics and Genomics. Genomics & Informatics, (2013) 11(4), 218–223.