Douglas P. Clark
Research Subjects
Research Interests
Douglas P. Clark has a total of 33 co-authors. Here are the top co-authors by number of shared publications:
- William C. Faquin
Department of Pathology Massachusetts General Hospital and Harvard Medical School Boston Massachusetts USA
11 shared publications David A. Elliott
Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21287, USA
2 shared publicationsAndrea B. Kelly
Rose Li and Associates, Inc, Bethesda, Maryland
1 shared publicationClaire Zhu
Division of Cancer Prevention, National Cancer Institute, Bethesda, Maryland
1 shared publicationDaniel F. Hayes
University of Michigan Comprehensive Cancer Center, Ann Arbor, Michigan
1 shared publicationDaniel J. Coleman
<!--label omitted: 1-->Department of Pathology, The Johns Hopkins University School of Medicine, Baltimore, Maryland 21205,1 and
1 shared publication
Latest Publications
- Open Access
- 22 March 2011
- Published by Wiley in Cancer Cytopathology
- Vol. 119 (2) , 92-102
Biospecimen reporting for improved study quality (BRISQ)
Human biospecimens are subjected to collection, processing, and storage that can significantly alter their molecular composition and consistency. These biospecimen preanalytical factors, in turn, influence experimental outcomes and the ability to reproduce scientific results. Currently, the extent and type of information specific to the biospecimen preanalytical conditions reported in scientific publications and regulatory submissions varies widely. To improve the quality of research that uses human tissues, it is crucial that information on the handling of biospecimens be reported in a thorough, accurate, and standardized manner. The Biospecimen Reporting for Improved Study Quality (BRISQ) recommendations outlined herein are intended to apply to any study in which human biospecimens are used. The purpose of reporting these details is to supply others, from researchers to regulators, with more consistent and standardized information to better evaluate, interpret, compare, and reproduce the experimental results. The BRISQ guidelines are proposed as an important and timely resource tool to strengthen communication and publications on biospecimen‐related research and to help reassure patient contributors and the advocacy community that their contributions are valued and respected. Cancer (Cancer Cytopathol) 2011. Published 2011 by the American Cancer Society.
- 22 March 2011
- Published by Wiley in Cancer Cytopathology
- Vol. 119 (2) , 92-102
Open AccessBiospecimen reporting for improved study quality (BRISQ)
Human biospecimens are subjected to collection, processing, and storage that can significantly alter their molecular composition and consistency. These biospecimen preanalytical factors, in turn, influence experimental outcomes and the ability to reproduce scientific results. Currently, the extent and type of information specific to the biospecimen preanalytical conditions reported in scientific publications and regulatory submissions varies widely. To improve the quality of research that uses human tissues, it is crucial that information on the handling of biospecimens be reported in a thorough, accurate, and standardized manner. The Biospecimen Reporting for Improved Study Quality (BRISQ) recommendations outlined herein are intended to apply to any study in which human biospecimens are used. The purpose of reporting these details is to supply others, from researchers to regulators, with more consistent and standardized information to better evaluate, interpret, compare, and reproduce the experimental results. The BRISQ guidelines are proposed as an important and timely resource tool to strengthen communication and publications on biospecimen‐related research and to help reassure patient contributors and the advocacy community that their contributions are valued and respected. Cancer (Cancer Cytopathol) 2011. Published 2011 by the American Cancer Society.
- 17 March 2010
- Published by Springer Nature
- p. 109-124
Cystic Lesions of the Thyroid
- 17 March 2010
- Published by Springer Nature
- p. 69-92
Follicular Lesions
- 17 March 2010
- Published by Springer Nature
- p. 55-67
Colloid-Predominant Lesions
- 17 March 2010
- Published by Springer Nature
- p. 33-53
Inflammatory Lesions and Lymphoma
- 17 March 2010
- Published by Springer Nature
- p. 9-22
How to Perform and Process a Thyroid FNA
- 17 March 2010
- Published by Springer Nature
- p. 167-181
Undifferentiated (Anaplastic) Carcinoma and Secondary Tumors
- 17 March 2010
- Published by Springer Nature
- p. 167-181
Undifferentiated (Anaplastic) Carcinoma and Secondary Tumors