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life sciences & biomedicine (16) 16
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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. Full Text The impact of whole-genome sequencing on the primary care and outcomes of healthy adult patients: A pilot randomized trial
by Vassy, Jason L and Christensen, Kurt D and Schonman, Erica F and Blout, Carrie L and Robinson, Jill O and Krier, Joel B and Diamond, Pamela M and Lebo, Matthew and Machini, Kalotina and Azzariti, Danielle R and Dukhovny, Dmitry and Bates, David W and MacRae, Calum A and Murray, Michael F and Rehm, Heidi L and McGuire, Amy L and Green, Robert C and Cirino, Allison L and Ho, Carolyn Y and Lane, William J and Lehmann, Lisa S and Morton, Cynthia C and Perry, Denise L and Seidman, Christine E and Sunyaev, Shamil R and Nguyen, Tiffany and Steffens, Eleanor and Betting, Wendi Nicole and Aronson, Samuel J and Ceyhan-Birsoy, Ozge and Lebo, Matthew S and McLaughlin, Heather M and Tsai, Ellen A and Blumenthal-Barby, Jennifer and Feuerman, Lindsay Z and Lee, Kaitlyn and Slashinski, Melody J and Davis, Kelly and Ubel, Peter A and Kraft, Peter and Roberts, J. Scott and Garber, Judy E and Hambuch, Tina and Kohane, Isaac and Kong, Sek Won and MedSeq Project and for the MedSeq Project
Annals of internal medicine, ISSN 0003-4819, 08/2017, Volume 167, Issue 3, pp. 159 - 169
Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Young adults | Primary health care | Analysis | Models | Nucleotide sequencing | Health aspects | DNA sequencing | Health care | Genomes | Disease | Primary care | Evidence-based medicine | Health behavior | Index Medicus | Abridged Index Medicus
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3. Full Text Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
by Hart, M. Ragan and Biesecker, Barbara B and Blout, Carrie L and Christensen, Kurt D and Amendola, Laura M and Bergstrom, Katie L and Biswas, Sawona and Bowling, Kevin M and Brothers, Kyle B and Conlin, Laura K and Cooper, Greg M and Dulik, Matthew C and East, Kelly M and Everett, Jessica N and Finnila, Candice R and Ghazani, Arezou A and Gilmore, Marian J and Goddard, Katrina A. B and Jarvik, Gail P and Johnston, Jennifer J and Kauffman, Tia L and Kelley, Whitley V and Krier, Joel B and Lewis, Katie L and McGuire, Amy L and McMullen, Carmit and Ou, Jeffrey and Plon, Sharon E and Rehm, Heidi L and Richards, C. Sue and Romasko, Edward J and Miren Sagardia, Ane and Spinner, Nancy B and Thompson, Michelle L and Turbitt, Erin and Vassy, Jason L and Wilfond, Benjamin S and Veenstra, David L and Berg, Jonathan S and Green, Robert C and Biesecker, Leslie G and Hindorff, Lucia A
Genetics in medicine, ISSN 1098-3600, 05/2019, Volume 21, Issue 5, pp. 1100 - 1110
genomic sequencing | health-care resource utilization | secondary findings | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Prevalence | Genetic Testing - standards | Humans | Incidental Findings | Male | Genetic Testing - ethics | Disclosure | Health Knowledge, Attitudes, Practice | Patients | High-Throughput Nucleotide Sequencing - ethics | Exome | Health Care Costs | Decision Making - ethics | Health Personnel | Adult | Female | Intention | Whole Genome Sequencing - economics | Genetic Testing - economics | Genomics - methods | Whole Genome Sequencing - ethics | Consortia | Index Medicus
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4. Full Text Correction: Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
by Hart, M Ragan and Biesecker, Barbara B and Blout, Carrie L and Christensen, Kurt D and Amendola, Laura M and Bergstrom, Katie L and Biswas, Sawona and Bowling, Kevin M and Brothers, Kyle B and Conlin, Laura K and Cooper, Greg M and Dulik, Matthew C and East, Kelly M and Everett, Jessica N and Finnila, Candice R and Ghazani, Arezou A and Gilmore, Marian J and Goddard, Katrina A B and Jarvik, Gail P and Johnston, Jennifer J and Kauffman, Tia L and Kelley, Whitley V and Krier, Joel B and Lewis, Katie L and McGuire, Amy L and McMullen, Carmit and Ou, Jeffrey and Plon, Sharon E and Rehm, Heidi L and Richards, C Sue and Romasko, Edward J and Sagardia, Ane Miren and Spinner, Nancy B and Thompson, Michelle L and Turbitt, Erin and Vassy, Jason L and Wilfond, Benjamin S and Veenstra, David L and Berg, Jonathan S and Green, Robert C and Biesecker, Leslie G and Hindorff, Lucia A
Genetics in medicine, ISSN 1098-3600, 05/2019, Volume 21, Issue 5, pp. 1261 - 1262
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5. Full Text A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xga
by Lane, William J and Aguad, Maria and Smeland‐Wagman, Robin and Vege, Sunitha and Mah, Helen H and Joseph, Abigail and Blout, Carrie L and Nguyen, Tiffany T and Lebo, Matthew S and Sidhu, Manpreet and Lomas‐Francis, Christine and Kaufman, Richard M and Green, Robert C and Westhoff, Connie M and Bates, David W and Blout, Carrie and Christensen, Kurt D and Cirino, Allison L and Green, Robert C and Ho, Carolyn Y and Krier, Joel B and Lane, William J and Lehmann, Lisa S and MacRae, Calum A and Morton, Cynthia C and Perry, Denise L and Seidman, Christine E and Sunyaev, Shamil R and Vassy, Jason L and Schonman, Erica and Nguyen, Tiffany and Steffens, Eleanor and Betting, Wendi Nicole and Aronson, Samuel J and Ceyhan‐Birsoy, Ozge and Lebo, Matthew S and Machini, Kalotina and McLaughlin, Heather M and Azzariti, Danielle R and Rehm, Heidi L and Tsai, Ellen A and Blumenthal‐Barby, Jennifer and Feuerman, Lindsay Z and McGuire, Amy L and Lee, Kaitlyn and Robinson, Jill O and Slashinski, Melody J and Diamond, Pamela M and Davis, Kelly and Ubel, Peter A and Kraft, Peter and Scott Roberts, J and Garber, Judy E and Hambuch, Tina and Murray, Michael F and Kohane, Isaac and Kong, Sek Won
Transfusion (Philadelphia, Pa.), ISSN 0041-1132, 03/2019, Volume 59, Issue 3, pp. 908 - 915
Antigens | Genomics | Genetic research | Genetic aspects | Genomes | Genetic transcription | Nucleotide sequencing | DNA sequencing | Phenotypes | Typing | Data processing | Gene expression | Males | Gene sequencing | Design factors | Disruption | Y Chromosomes | Bioinformatics | Blood groups | Index Medicus | red blood cell antigen | whole genome sequencing | WGS | Xga | next generation sequencing | blood group | GATA-1 | genomics | transfusion medicine | NGS | RUNX1 | personalized medicine
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6. Full Text Airmen and health-care providers’ attitudes toward the use of genomic sequencing in the US Air Force: findings from the MilSeq Project
by Pereira, Stacey and Hsu, Rebecca L and Islam, Rubaiya and Robinson, Jill Oliver and Ramapriyan, Rishab and Sirotich, Emily and Maxwell, Megan D and Majumder, Mary and Blout, Carrie L and Christensen, Kurt D and Mehlman, Maxwell and Parasidis, Efthimios and Gardner, Cubby L and Killian, Jacqueline M and De Castro, Mauricio and Green, Robert C and Blout, Carrie L and Christensen, Kurt D and De Castro, Mauricio and Gardner, Cubby L and Green, Robert C and Hsu, Rebecca and Killian, Jacqueline and Krier, Joel B and Lane, William and Lebo, Matthew S and Majumder, Mary and Maxwell, Megan D and McGuire, Amy L and Mehlman, Maxwell J and Parasidis, Efthimios and Pereira, Stacey and Robinson, Jill O and Vassy, Jason L and Voss, Jameson and Zettler, Bethany and McGuire, Amy L and MilSeq Project and The MilSeq Project
Genetics in medicine, ISSN 1098-3600, 12/2020, Volume 22, Issue 12, pp. 2003 - 2010
genomics | exome sequencing | military | healthy populations | ELSI | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Index Medicus
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7. Full Text Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial
by Christensen, Kurt D and Vassy, Jason L and Phillips, Kathryn A and Blout, Carrie L and Azzariti, Danielle R and Lu, Christine Y and Robinson, Jill O and Lee, Kaitlyn and Douglas, Michael P and Yeh, Jennifer M and Machini, Kalotina and Stout, Natasha K and Rehm, Heidi L and McGuire, Amy L and Green, Robert C and Dukhovny, Dmitry and MedSeq Project and for the MedSeq Project
Genetics in medicine, ISSN 1098-3600, 12/2018, Volume 20, Issue 12, pp. 1544 - 1553
costs | primary care | economics | whole-genome sequencing | cardiology | Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology | Confidence intervals | Costs | Genomes | Cardiology | Primary care | Patients | Index Medicus | whole genome sequencing
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8. Full Text Returning Results in the Genomic Era: Initial Experiences of the eMERGE Network
by Wiesner, Georgia L and Rahm, Alanna Kulchak and Appelbaum, Paul and Aufox, Sharon and Bland, Sarah T and Blout, Carrie L and Christensen, Kurt D and Chung, Wendy K and Clayton, Ellen Wright and Green, Robert C and Harr, Margaret H and Henrikson, Nora and Hoell, Christin and Holm, Ingrid A and Jarvik, Gail P and Kullo, Iftikhar J and Lammers, Philip E and Larson, Eric B and Lindor, Noralane M and Marasa, Maddalena and Myers, Melanie F and Peterson, Josh F and Prows, Cynthia A and Ralston, James D and Rasouly, Hila Milo and Sharp, Richard R and Smith, Maureen E and Van Driest, Sara L and Williams, Janet L and Williams, Marc S and Wynn, Julia and Leppig, Kathleen A
Journal of personalized medicine, ISSN 2075-4426, 06/2020, Volume 10, Issue 2, p. 30
Health Care Sciences & Services | Medicine, General & Internal | Life Sciences & Biomedicine | General & Internal Medicine | Science & Technology | Medicine | Studies | Clinics | Medical laboratories | Genomics | Health care policy | Medical records | Population | Genomes | Clinical medicine | Patients | Electronic medical records | genomic medicine | return of results | electronic health record | genetic testing
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9. Full Text A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xg a
by Lane, William J and Aguad, Maria and Smeland-Wagman, Robin and Vege, Sunitha and Mah, Helen H and Joseph, Abigail and Blout, Carrie L and Nguyen, Tiffany T and Lebo, Matthew S and Sidhu, Manpreet and Lomas-Francis, Christine and Kaufman, Richard M and Green, Robert C and Westhoff, Connie M and Bates, David W and Blout, Carrie and Christensen, Kurt D and Cirino, Allison L and Green, Robert C and Ho, Carolyn Y and Krier, Joel B and Lane, William J and Lehmann, Lisa S and MacRae, Calum A and Morton, Cynthia C and Perry, Denise L and Seidman, Christine E and Sunyaev, Shamil R and Vassy, Jason L and Schonman, Erica and Nguyen, Tiffany and Steffens, Eleanor and Betting, Wendi Nicole and Aronson, Samuel J and Ceyhan-Birsoy, Ozge and Lebo, Matthew S and Machini, Kalotina and McLaughlin, Heather M and Azzariti, Danielle R and Rehm, Heidi L and Tsai, Ellen A and Blumenthal-Barby, Jennifer and Feuerman, Lindsay Z and McGuire, Amy L and Lee, Kaitlyn and Robinson, Jill O and Slashinski, Melody J and Diamond, Pamela M and Davis, Kelly and Ubel, Peter A and Kraft, Peter and Scott Roberts, J and Garber, Judy E and Hambuch, Tina and Murray, Michael F and Kohane, Isaac and Kong, Sek Won and MedSeq Project
Transfusion (Philadelphia, Pa.), ISSN 0041-1132, 03/2019, Volume 59, Issue 3, pp. 908 - 915
Life Sciences & Biomedicine | Hematology | Science & Technology | Computational Biology - methods | Phenotype | Humans | Alleles | Polymorphism, Single Nucleotide - genetics | Genotype | Blood Group Antigens - genetics | Galactosyltransferases - genetics | Whole Genome Sequencing - methods
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10. Full Text Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine (vol 98, pg 1051, 2016)
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 CSER Consortium
American journal of human genetics, ISSN 0002-9297, 07/2016, Volume 99, Issue 1, pp. 246 - 246
Life Sciences & Biomedicine | Genetics & Heredity | Science & Technology
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