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  1. 1
    Network for Pancreatic Organ Donors with Diabetes (nPOD): developing a tissue biobank for type 1 diabetes

    Network for Pancreatic Organ Donors with Diabetes (nPOD): developing a tissue biobank for type 1 diabetes by Martha Campbell‐Thompson, Clive Wasserfall, John S. Kaddis, Anastasia Albanese-O’Neill, Teodora Staeva, Concepcion R. Nierras, Jayne Moraski, Patrick Rowe, Roberto Gianani, George S. Eisenbarth, James M. Crawford, Desmond Schatz, Alberto Pugliese, Mark A. Atkinson

    Published 2012
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  2. 2
    Next-Generation Sequencing for Infectious Disease Diagnosis and Management

    Next-Generation Sequencing for Infectious Disease Diagnosis and Management by Martina I. Lefterova, Carlos J. Suarez, Niaz Banaei, Benjamin A. Pinsky

    Published 2015
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  3. 3
    Cell Line and DNA Biobank From Patients Affected by Genetic Diseases

    Cell Line and DNA Biobank From Patients Affected by Genetic Diseases by Mirella Filocamo, Raffaella Mazzotti, Fabio Corsolini, Marina Stroppiano, Giorgia Stroppiana, Serena Grossi, Susanna Lualdi, Barbara Tappino, Federica Lanza, Sara Galotto, Roberta Biancheri

    Published 2014
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  4. 4
    Nordic biological specimen banks as basis for studies of cancer causes and control – more than 2 million sample donors, 25 million person years and 100 000 prospective cancers

    Nordic biological specimen banks as basis for studies of cancer causes and control – more than 2 million sample donors, 25 million person years and 100 000 prospective cancers by ­Eero Pukkala, Aage Andersen, Göran Berglund, Randi E. Gislefoss, Vilmundur Guðnason, Göran Hallmans, Egil Jellum, Pekka Jousilahti, Paul Knekt, Pentti Koskela, Pentti Kyyrönen, Per Lenner, Tapio Luostarinen, Arthur Löve, Helga M. Ögmundsdóttir, Pär Stattin, Leena Tenkanen, Laufey Tryggvadóttír, Jarmo Virtamo, Göran Wadell, Anders Widell, Matti Lehtinen, Joakim Dillner

    Published 2007
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  5. 5
    Public and Biobank Participant Attitudes toward Genetic Research Participation and Data Sharing

    Public and Biobank Participant Attitudes toward Genetic Research Participation and Data Sharing by Amy A. Lemke, W.A. Wolf, Jeni Hebert‐Beirne, Maureen E. Smith

    Published 2010
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  6. 6
    Canary Prostate Active Surveillance Study: Design of a Multi-institutional Active Surveillance Cohort and Biorepository

    Canary Prostate Active Surveillance Study: Design of a Multi-institutional Active Surveillance Cohort and Biorepository by Lisa F. Newcomb, James D. Brooks, Peter R. Carroll, Ziding Feng, Martin Gleave, Peter S. Nelson, Ian M. Thompson, Daniel W. Lin

    Published 2009
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  7. 7
    Creating a global rare disease patient registry linked to a rare diseases biorepository database: Rare Disease-HUB (RD-HUB)

    Creating a global rare disease patient registry linked to a rare diseases biorepository database: Rare Disease-HUB (RD-HUB) by Yaffa Rubinstein, Stephen C. Groft, Ronald Bartek, Kyle Brown, Ronald Christensen, Elaine Collier, Amy Farber, Jennifer Farmer, John H. Ferguson, Christopher B. Forrest, Nicole C. Lockhart, Kate R. McCurdy, Helen Moore, Geraldine B. Pollen, Rachel Richesson, Vanessa Rangel Miller, Sara Chandros Hull, Jim Vaught

    Published 2010
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  8. 8
    “Collection of a lifetime: A practical approach to developing a longitudinal collection of women's healthcare biological samples”

    “Collection of a lifetime: A practical approach to developing a longitudinal collection of women's healthcare biological samples” by Mark K. Santillan, Kimberly K. Leslie, Wendy S. Hamilton, Brenda Boese, Monika Ahuja, Stephen K. Hunter, Donna A. Santillan

    Published 2014
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  9. 9
    The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases

    The EuroBioBank Network: 10 years of hands-on experience of collaborative, transnational biobanking for rare diseases by Marina Mora, C. Angelini, Fabrizia Bignami, Anne-Mary Bodin, Marco Crimi, Jeanne Hélène di Donato, Alex E. Felice, Cécile Jaeger, Veronika Karcagi, Yann LeCam, Stephen Lynn, Marija Meznarič, Maurizio Moggio, Lucía Monaco, Luisa Politano, Manuel Posada de la Paz, Safaa Saker, Peter Schneiderat, Monica Ensini, Barbara Garavaglia, David Gurwitz, Diana Johnson, Francesco Muntoni, Jack Puymirat, Mojgan Reza, Thomas Voit, Chiara Baldo, F. Dagna Bricarelli, Stefano Goldwurm, Giuseppe Merla, Elena Pegoraro, Alessandra Renieri, Kurt Zatloukal, Mirella Filocamo, Hanns Lochmüller

    Published 2014
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  10. 10
    Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium

    Confronting real time ethical, legal, and social issues in the Electronic Medical Records and Genomics (eMERGE) Consortium by Ellen Wright Clayton, Maureen E. Smith, Stephanie M. Fullerton, Wylie Burke, Catherine A. McCarty, Barbara A. Koenig, Amy L. McGuire, Laura M. Beskow, Lynn G. Dressler, Amy A. Lemke, Erin M. Ramos, Laura Lyman Rodriguez

    Published 2010
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  11. 11
    Two large‐scale surveys on community attitudes toward an opt‐out biobank

    Two large‐scale surveys on community attitudes toward an opt‐out biobank by Kyle B. Brothers, Daniel R. Morrison, Ellen Wright Clayton

    Published 2011
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  12. 12
    The Adult Netherlands Twin Register: Twenty-Five Years of Survey and Biological Data Collection

    The Adult Netherlands Twin Register: Twenty-Five Years of Survey and Biological Data Collection by Gonneke Willemsen, Jacqueline M. Vink, Abdel Abdellaoui, Anouk den Braber, Jenny H. D. A. van Beek, Harmen H. M. Draisma, Jenny van Dongen, Dennis van ‘t Ent, Lot M. Geels, René van Lien, Lannie Ligthart, Mathijs Kattenberg, Hamdi Mbarek, Marleen H. M. de Moor, Melanie Neijts, René Pool, N. Stroo, Cornelis Kluft, H. Eka D. Suchiman, P. Eline Slagboom, Eco J. C. de Geus, Dorret I. Boomsma

    Published 2013
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  13. 13
    The ethical use of existing samples for genome research

    The ethical use of existing samples for genome research by Oliver F. Bathe, Amy L. McGuire

    Published 2009
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  14. 14
    Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records

    Assessing the accuracy of observer-reported ancestry in a biorepository linked to electronic medical records by Logan Dumitrescu, Marylyn D. Ritchie, Kristin Brown‐Gentry, Jill M. Pulley, Melissa Basford, Joshua C. Denny, Jorge R. Oksenberg, Dan M. Roden, Jonathan L. Haines, Dana C. Crawford

    Published 2010
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  15. 15
    The biobank of the Norwegian mother and child cohort Study: A resource for the next 100 years

    The biobank of the Norwegian mother and child cohort Study: A resource for the next 100 years by Kjersti S. Rønningen, Liv Paltiel, Helle Margrete Meltzer, R. Nordhagen, Kari Kveim Lie, Ragnhild Hovengen, Margaretha Haugen, Wenche Nystad, Per Magnus, Jane A. Hoppin

    Published 2006
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  16. 16
    Biobanking past, present and future

    Biobanking past, present and future by Yvonne G. De Souza, John S. Greenspan

    Published 2012
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  17. 17
    Intentions to Donate to a Biobank in a National Sample of African Americans

    Intentions to Donate to a Biobank in a National Sample of African Americans by Jasmine A. McDonald, Susan T. Vadaparampil, Deborah J. Bowen, Gayenell Magwood, Jihad S. Obeid, Melanie Jefferson, Richard Drake, Mulugeta Gebregziabher, Chanita Hughes Halbert

    Published 2014
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  18. 18
    The procurement, storage, and quality assurance of frozen blood and tissue biospecimens in pathology, biorepository, and biobank settings

    The procurement, storage, and quality assurance of frozen blood and tissue biospecimens in pathology, biorepository, and biobank settings by Maryam Shabihkhani, Gregory M. Lucey, Bowen Wei, Sergey Mareninov, Jerry J. Lou, Harry V. Vinters, Elyse J. Singer, Timothy F. Cloughesy, William H. Yong

    Published 2014
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  19. 19
    Biobanking in microbiology: From sample collection to epidemiology, diagnosis and research

    Biobanking in microbiology: From sample collection to epidemiology, diagnosis and research by Paolo De Paoli

    Published 2005
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  20. 20
    The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository

    The beliefs, motivations, and expectations of parents who have enrolled their children in a genetic biorepository by Erin D. Harris, Sonja I. Ziniel, Jonathan G. Amatruda, Catherine Clinton, Sarah Savage, Patrick L. Taylor, Noelle Huntington, Robert C. Green, Ingrid A. Holm

    Published 2012
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