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1. Full Text Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine
by Green, Robert C and Goddard, Katrina A.B and Jarvik, Gail P and Amendola, Laura M and Appelbaum, Paul S and Berg, Jonathan S and Bernhardt, Barbara A and Biesecker, Leslie G and Biswas, Sawona and Blout, Carrie L and Bowling, Kevin M and Brothers, Kyle B and Burke, Wylie and Caga-anan, Charlisse F and Chinnaiyan, Arul M and Chung, Wendy K and Clayton, Ellen W and Cooper, Gregory M and East, Kelly and Evans, James P and Fullerton, Stephanie M and Garraway, Levi A and Garrett, Jeremy R and Gray, Stacy W and Henderson, Gail E and Hindorff, Lucia A and Holm, Ingrid A and Lewis, Michelle Huckaby and Hutter, Carolyn M and Janne, Pasi A and Joffe, Steven and Kaufman, David and Knoppers, Bartha M and Koenig, Barbara A and Krantz, Ian D and Manolio, Teri A and McCullough, Laurence and McEwen, Jean and McGuire, Amy and Muzny, Donna and Myers, Richard M and Nickerson, Deborah A and Ou, Jeffrey and Parsons, Donald W and Petersen, Gloria M and Plon, Sharon E and Rehm, Heidi L and Roberts, J. Scott and Robinson, Dan and Salama, Joseph S and Scollon, Sarah and Sharp, Richard R and Shirts, Brian and Spinner, Nancy B and Tabor, Holly K and Tarczy-Hornoch, Peter and Veenstra, David L and Wagle, Nikhil and Weck, Karen and Wilfond, Benjamin S and Wilhelmsen, Kirk and Wolf, Susan M and Wynn, Julia and Yu, Joon-Ho and Amaral, Michelle and Amendola, Laura and Appelbaum, Paul S and Aronson, Samuel J and Arora, Shubhangi and Azzariti, Danielle R and Barsh, Greg S and Bebin, E.M and Biesecker, Barbara B and Biesecker, Leslie G and Biswas, Sawona and Blout, Carrie L and Bowling, Kevin M and Brothers, Kyle B and Brown, Brian L and Burt, Amber A and Byers, Peter H and Caga-anan, Charlisse F and Calikoglu, Muge G and Carlson, Sara J and Chahin, Nizar and Chinnaiyan, Arul M and Christensen, Kurt D and Chung, Wendy and Cirino, Allison L and Clayton, Ellen and Conlin, Laura K and Cooper, Greg M and Crosslin, David R and Davis, James V and Davis, Kelly and Deardorff, Matthew A and Devkota, Batsal and De Vries, Raymond and Diamond, Pamela and Dorschner, Michael O and ... and the CSER Consortium and CSER Consortium
American journal of human genetics, ISSN 0002-9297, 06/2016, Volume 98, Issue 6, pp. 1051 - 1066
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Evidence-Based Practice | United States | Humans | Clinical Trials as Topic | Cardiovascular Diseases - genetics | Exome - genetics | National Human Genome Research Institute (U.S.) | Polymorphism, Single Nucleotide - genetics | Adult | Biomedical Research | Population Groups | Software | Genome, Human | Genomics - methods | High-Throughput Nucleotide Sequencing - methods | Child | Genetic research | Nucleotide sequencing | Methods | DNA sequencing | Medical diagnosis | Electronic health records | Genomics | Genes | Children & youth | Index Medicus
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2. Climate from tree rings
by Hughes, M. K
1981, ISBN 0521242916, 223
Dendroclimatology
Book
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3. Full Text The clustering of adverse childhood experiences and relationship with inflammation in later childhood and into adolescence
by East, R and Kelly-Irving, M and Howe, L and Bartley, M and Bevilacqua, L and Kelly, Y
Journal of psychosomatic research, ISSN 0022-3999, 06/2020, Volume 133, p. 110010
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4. Full Text Genomic diagnosis for children with intellectual disability and/or developmental delay
by Bowling, Kevin M and Thompson, Michelle L and Amaral, Michelle D and Finnila, Candice R and Hiatt, Susan M and Engel, Krysta L and Cochran, J.Nicholas and Brothers, Kyle B and East, Kelly M and Gray, David E and Kelley, Whitley V and Lamb, Neil E and Lose, Edward J and Rich, Carla A and Simmons, Shirley and Whittle, Jana S and Weaver, Benjamin T and Nesmith, Amy S and Myers, Richard M and Barsh, Gregory S and Bebin, E.Martina and Cooper, Gregory M
Genome medicine, ISSN 1756-994X, 05/2017, Volume 9, Issue 1, pp. 43 - 43
CSER | Intellectual disability | Clinical sequencing | Developmental delay | De novo | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Humans | Child, Preschool | Infant | Male | Developmental Disabilities - genetics | DNA Copy Number Variations | Intellectual Disability - genetics | Exome | Young Adult | Intellectual Disability - diagnosis | Adolescent | Adult | Female | Mutation | Genomics - methods | Child | Developmental Disabilities - diagnosis | Sequence Analysis, DNA - methods | Laboratories | Intellectual disabilities | Genomics | Genes | Genomes | Mitochondrial DNA | Genetic diversity | Research | Consortia | Autism | Genetics | Genetic testing | Children | Diagnosis | Deoxyribonucleic acid--DNA | Index Medicus
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5. Full Text Return of Genomic Results to Research Participants: The Floor, the Ceiling, and the Choices In Between
by Jarvik, Gail P and Amendola, Laura M and Berg, Jonathan S and Brothers, Kyle and Clayton, Ellen W and Chung, Wendy and Evans, Barbara J and Evans, James P and Fullerton, Stephanie M and Gallego, Carlos J and Garrison, Nanibaa’ A and Gray, Stacy W and Holm, Ingrid A and Kullo, Iftikhar J and Lehmann, Lisa Soleymani and McCarty, Cathy and Prows, Cynthia A and Rehm, Heidi L and Sharp, Richard R and Salama, Joseph and Sanderson, Saskia and Van Driest, Sara L and Williams, Marc S and Wolf, Susan M and Wolf, Wendy A and Harley, John and Myers, Melanie and Namjou, Bahram and Vinks, Sander and Connolly, John and Keating, Brendan and Gerhard, Glenn and Sundaresan, Agnes and Tromp, Gerard and Crosslin, David and Leppig, Kathy and Wicklund, Cathy and Chute, Christopher and Lynch, John and De Andrade, Mariza and Heit, John and McCormick, Jen and Brilliant, Murray and Kitchner, Terrie and Ritchie, Marylyn and Böttinger, Erwin and Peter, Inga and Persell, Stephen and Rasmussen-Torvik, Laura and McGregor, Tracy and Roden, Dan and Antommaria, Armand and Chiavacci, Rosetta and Faucett, Andy and Ledbetter, David and Williams, Janet and Hartzler, Andrea and Vitek, Carolyn R. Rohrer and Frost, Norm and Ferryman, Kadija and Horowitz, Carol and Rhodes, Rosamond and Zinberg, Randi and Aufox, Sharon and Pan, Vivian and Long, Rochelle and Ramos, Erin and Odgis, Jackie and Wise, Anastasia and Hull, Sara and Gitlin, Jonathan and Green, Robert and Metterville, Danielle and McGuire, Amy and Kong, Sek Won and Trinidad, Sue and Veenstra, David and Roche, Myra and Skinner, Debra and Raspberry, Kelly and O’Daniel, Julianne and Parsons, Will and Eng, Christine and Hilsenbeck, Susan and Karavite, Dean and Conlin, Laura and Spinner, Nancy and Krantz, Ian and Falk, Marni and Santani, Avni and Dechene, Elizabeth and Dulik, Matthew and Bernhardt, Barbara and Schuetze, Scott and Everett, Jessica and Gornick, Michele Caroline and Wilfond, Ben and Tabor, Holly and Lemke, Amy A and Richards, Sue and ... and eMERGE Act-ROR Committee and CERC Committee and CSER Act-ROR Working Group and CERC Comm and CSER Act-ROR Working Grp and eMERGE Act-ROR Comm
American journal of human genetics, ISSN 0002-9297, 06/2014, Volume 94, Issue 6, pp. 818 - 826
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Biomedical Research - ethics | Genetics, Medical - ethics | Patient Access to Records - ethics | Genetic Privacy | Humans | Societies, Scientific | Population Groups | High-Throughput Nucleotide Sequencing | Disclosure | Genome, Human | Genomics - ethics | Genetic research | Research | Nucleotide sequencing | Population genetics | DNA sequencing | Health care industry | Morality | Mutation | Genomics | Medical ethics | Index Medicus
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6. Full Text The Clinical Sequencing Evidence-Generating Research Consortium: Integrating Genomic Sequencing in Diverse and Medically Underserved Populations
by Amendola, Laura M and Berg, Jonathan S and Horowitz, Carol R and Angelo, Frank and Bensen, Jeannette T and Biesecker, Barbara B and Biesecker, Leslie G and Cooper, Gregory M and East, Kelly and Filipski, Kelly and Fullerton, Stephanie M and Gelb, Bruce D and Goddard, Katrina A.B and Hailu, Benyam and Hart, Ragan and Hassmiller-Lich, Kristen and Joseph, Galen and Kenny, Eimear E and Koenig, Barbara A and Knight, Sara and Kwok, Pui-Yan and Lewis, Katie L and McGuire, Amy L and Norton, Mary E and Ou, Jeffrey and Parsons, Donald W and Powell, Bradford C and Risch, Neil and Robinson, Mimsie and Rini, Christine and Scollon, Sarah and Slavotinek, Anne M and Veenstra, David L and Wasserstein, Melissa P and Wilfond, Benjamin S and Hindorff, Lucia A and Plon, Sharon E and Jarvik, Gail P and CSER consortium and CSER Consortium
American journal of human genetics, ISSN 0002-9297, 09/2018, Volume 103, Issue 3, pp. 319 - 327
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Cost-Benefit Analysis - methods | Exome - genetics | Phenotype | Delivery of Health Care - methods | United States | Europe | Humans | National Human Genome Research Institute (U.S.) | Adult | Whole Genome Sequencing - methods | Genomics - methods | Genome, Human - genetics | Genetic research | Research | Nucleotide sequencing | Human genome | Finance | DNA sequencing | Index Medicus
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7. Full Text Targetable GOPC-ROS1 Gene Fusion Identified in a Case of Lethal Oral Mucosal Melanoma
by East, Ellen and Plouffe, Komal and Harms, Kelly and Patel, Rajiv and McHugh, Jonathan and Tomlins, Scott and Udager, Aaron
American journal of clinical pathology, ISSN 0002-9173, 09/2018, Volume 150, Issue suppl_1, pp. S45 - S46
Tyrosine | Carcinoma | Transcription | Exons | Mucosa | Melanoma | Metastasis | Radiation therapy | Ribonucleic acid--RNA | Kinases | Gene fusion | Metastases | Chemotherapy | Biopsy | Chromosome 8 | Head and neck | Mutation | Protein-tyrosine kinase | DNA sequencing
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8. Full Text Living with diabetes and disadvantage: A qualitative, geographical case study
by Power, Tamara and Kelly, Ray and Usher, Kim and East, Leah and Travaglia, Jo and Robertson, Hamish and Wong, Ann and Jackson, Debra
Journal of clinical nursing, ISSN 0962-1067, 07/2020, Volume 29, Issue 13-14, pp. 2710 - 2722
type 2 diabetes | health literacy | qualitative study | aboriginal | diabetes | low socioeconomic | multicultural issues | fatalism | Life Sciences & Biomedicine | Nursing | Science & Technology
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