Carrie L Blout Zawatsky, Nidhi Shah, Kalotina Machini, Emma Perez, Kurt D Christensen, Hana Zouk, Marcie Steeves, Christopher Koch, Melissa Uveges, Janelle Shea, Nina Gold, Joel Krier, Natalie Boutin, Lisa Mahanta, Heidi L Rehm, Scott T Weiss, Elizabeth W Karlson, Jordan W Smoller, Matthew S Lebo, Robert C Green. Am J Hum Genet 2021
Times Cited: 2
Times Cited: 2
List of co-cited articles
articles co-cited >1
Times Cited
Times Co-cited
Similarity
ACMG recommendations for reporting of incidental findings in clinical exome and genome sequencing.
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
Robert C Green, Jonathan S Berg, Wayne W Grody, Sarah S Kalia, Bruce R Korf, Christa L Martin, Amy L McGuire, Robert L Nussbaum, Julianne M O'Daniel, Kelly E Ormond,[...]. Genet Med 2013
50
An international policy on returning genomic research results.
Anna C F Lewis, Bartha Maria Knoppers, Robert C Green. Genome Med 2021
Anna C F Lewis, Bartha Maria Knoppers, Robert C Green. Genome Med 2021
50
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2016 update (ACMG SF v2.0): a policy statement of the American College of Medical Genetics and Genomics.
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
Sarah S Kalia, Kathy Adelman, Sherri J Bale, Wendy K Chung, Christine Eng, James P Evans, Gail E Herman, Sophia B Hufnagel, Teri E Klein, Bruce R Korf,[...]. Genet Med 2017
50
Exploring the motivations of research participants who chose not to learn medically actionable secondary genetic findings about themselves.
Will Schupmann, Skye A Miner, Haley K Sullivan, Jamie R Glover, Janet E Hall, Shepherd H Schurman, Benjamin E Berkman. Genet Med 2021
Will Schupmann, Skye A Miner, Haley K Sullivan, Jamie R Glover, Janet E Hall, Shepherd H Schurman, Benjamin E Berkman. Genet Med 2021
50
Why genomics researchers are sometimes morally required to hunt for secondary findings.
Julian J Koplin, Julian Savulescu, Danya F Vears. BMC Med Ethics 2020
Julian J Koplin, Julian Savulescu, Danya F Vears. BMC Med Ethics 2020
50
Recommendations for reporting of secondary findings in clinical exome and genome sequencing, 2021 update: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Adam S Gordon, Laura M Amendola, Kathy Adelman, Sherri J Bale, Wendy K Chung, Michael H Gollob, Steven M Harrison, Gail E Herman,[...]. Genet Med 2021
David T Miller, Kristy Lee, Adam S Gordon, Laura M Amendola, Kathy Adelman, Sherri J Bale, Wendy K Chung, Michael H Gollob, Steven M Harrison, Gail E Herman,[...]. Genet Med 2021
50
ACMG SF v3.0 list for reporting of secondary findings in clinical exome and genome sequencing: a policy statement of the American College of Medical Genetics and Genomics (ACMG).
David T Miller, Kristy Lee, Wendy K Chung, Adam S Gordon, Gail E Herman, Teri E Klein, Douglas R Stewart, Laura M Amendola, Kathy Adelman, Sherri J Bale,[...]. Genet Med 2021
David T Miller, Kristy Lee, Wendy K Chung, Adam S Gordon, Gail E Herman, Teri E Klein, Douglas R Stewart, Laura M Amendola, Kathy Adelman, Sherri J Bale,[...]. Genet Med 2021
50
The Ensembl Variant Effect Predictor.
William McLaren, Laurent Gil, Sarah E Hunt, Harpreet Singh Riat, Graham R S Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham. Genome Biol 2016
William McLaren, Laurent Gil, Sarah E Hunt, Harpreet Singh Riat, Graham R S Ritchie, Anja Thormann, Paul Flicek, Fiona Cunningham. Genome Biol 2016
50
The effect of communicating the genetic risk of cardiometabolic disorders on motivation and actual engagement in preventative lifestyle modification and clinical outcome: a systematic review and meta-analysis of randomised controlled trials.
Sherly X Li, Zheng Ye, Kevin Whelan, Helen Truby. Br J Nutr 2016
Sherly X Li, Zheng Ye, Kevin Whelan, Helen Truby. Br J Nutr 2016
50
The mutational constraint spectrum quantified from variation in 141,456 humans.
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
Konrad J Karczewski, Laurent C Francioli, Grace Tiao, Beryl B Cummings, Jessica Alföldi, Qingbo Wang, Ryan L Collins, Kristen M Laricchia, Andrea Ganna, Daniel P Birnbaum,[...]. Nature 2020
50
Clinical decision support for genetically guided personalized medicine: a systematic review.
Brandon M Welch, Kensaku Kawamoto. J Am Med Inform Assoc 2013
Brandon M Welch, Kensaku Kawamoto. J Am Med Inform Assoc 2013
50
Comprehensive genetic testing for female and male infertility using next-generation sequencing.
Bonny Patel, Sasha Parets, Matthew Akana, Gregory Kellogg, Michael Jansen, Chihyu Chang, Ying Cai, Rebecca Fox, Mohammad Niknazar, Roman Shraga,[...]. J Assist Reprod Genet 2018
Bonny Patel, Sasha Parets, Matthew Akana, Gregory Kellogg, Michael Jansen, Chihyu Chang, Ying Cai, Rebecca Fox, Mohammad Niknazar, Roman Shraga,[...]. J Assist Reprod Genet 2018
50
Estimated nationwide impact of implementing a preemptive pharmacogenetic panel approach to guide drug prescribing in primary care in The Netherlands.
P C D Bank, J J Swen, H J Guchelaar. BMC Med 2019
P C D Bank, J J Swen, H J Guchelaar. BMC Med 2019
50
Effect of genetic testing for risk of type 2 diabetes mellitus on health behaviors and outcomes: study rationale, development and design.
Alex H Cho, Ley A Killeya-Jones, Julianne M O'Daniel, Kensaku Kawamoto, Patrick Gallagher, Susanne Haga, Joseph E Lucas, Gloria M Trujillo, Scott V Joy, Geoffrey S Ginsburg. BMC Health Serv Res 2012
Alex H Cho, Ley A Killeya-Jones, Julianne M O'Daniel, Kensaku Kawamoto, Patrick Gallagher, Susanne Haga, Joseph E Lucas, Gloria M Trujillo, Scott V Joy, Geoffrey S Ginsburg. BMC Health Serv Res 2012
50
High-Accuracy HLA Type Inference from Whole-Genome Sequencing Data Using Population Reference Graphs.
Alexander T Dilthey, Pierre-Antoine Gourraud, Alexander J Mentzer, Nezih Cereb, Zamin Iqbal, Gil McVean. PLoS Comput Biol 2016
Alexander T Dilthey, Pierre-Antoine Gourraud, Alexander J Mentzer, Nezih Cereb, Zamin Iqbal, Gil McVean. PLoS Comput Biol 2016
50
Public perceptions of disease severity but not actionability correlate with interest in receiving genomic results: nonalignment with current trends in practice.
Kristi D Graves, Pamela S Sinicrope, Jennifer B McCormick, Yingjun Zhou, Susan T Vadaparampil, Noralane M Lindor. Public Health Genomics 2015
Kristi D Graves, Pamela S Sinicrope, Jennifer B McCormick, Yingjun Zhou, Susan T Vadaparampil, Noralane M Lindor. Public Health Genomics 2015
50
Physician-directed genetic screening to evaluate personal risk for medically actionable disorders: a large multi-center cohort study.
Eden V Haverfield, Edward D Esplin, Sienna J Aguilar, Kathryn E Hatchell, Kelly E Ormond, Andrea Hanson-Kahn, Paldeep S Atwal, Sarah Macklin-Mantia, Stephanie Hines, Caron W-M Sak,[...]. BMC Med 2021
Eden V Haverfield, Edward D Esplin, Sienna J Aguilar, Kathryn E Hatchell, Kelly E Ormond, Andrea Hanson-Kahn, Paldeep S Atwal, Sarah Macklin-Mantia, Stephanie Hines, Caron W-M Sak,[...]. BMC Med 2021
50
DNA-based screening and population health: a points to consider statement for programs and sponsoring organizations from the American College of Medical Genetics and Genomics (ACMG).
Michael F Murray, Monica A Giovanni, Debra L Doyle, Steven M Harrison, Elaine Lyon, Kandamurugu Manickam, Kristin G Monaghan, Sonja A Rasmussen, Maren T Scheuner, Glenn E Palomaki,[...]. Genet Med 2021
Michael F Murray, Monica A Giovanni, Debra L Doyle, Steven M Harrison, Elaine Lyon, Kandamurugu Manickam, Kristin G Monaghan, Sonja A Rasmussen, Maren T Scheuner, Glenn E Palomaki,[...]. Genet Med 2021
50
Characterization of 107 genomic DNA reference materials for CYP2D6, CYP2C19, CYP2C9, VKORC1, and UGT1A1: a GeT-RM and Association for Molecular Pathology collaborative project.
Victoria M Pratt, Barbara Zehnbauer, Jean Amos Wilson, Ruth Baak, Nikolina Babic, Maria Bettinotti, Arlene Buller, Ken Butz, Matthew Campbell, Chris Civalier,[...]. J Mol Diagn 2010
Victoria M Pratt, Barbara Zehnbauer, Jean Amos Wilson, Ruth Baak, Nikolina Babic, Maria Bettinotti, Arlene Buller, Ken Butz, Matthew Campbell, Chris Civalier,[...]. J Mol Diagn 2010
50
A program for annotating and predicting the effects of single nucleotide polymorphisms, SnpEff: SNPs in the genome of Drosophila melanogaster strain w1118; iso-2; iso-3.
Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
Pablo Cingolani, Adrian Platts, Le Lily Wang, Melissa Coon, Tung Nguyen, Luan Wang, Susan J Land, Xiangyi Lu, Douglas M Ruden. Fly (Austin) 2012
50
Genetic Testing for Inherited Cardiovascular Diseases: A Scientific Statement From the American Heart Association.
Kiran Musunuru, Ray E Hershberger, Sharlene M Day, N Jennifer Klinedinst, Andrew P Landstrom, Victoria N Parikh, Siddharth Prakash, Christopher Semsarian, Amy C Sturm. Circ Genom Precis Med 2020
Kiran Musunuru, Ray E Hershberger, Sharlene M Day, N Jennifer Klinedinst, Andrew P Landstrom, Victoria N Parikh, Siddharth Prakash, Christopher Semsarian, Amy C Sturm. Circ Genom Precis Med 2020
50
Identification of Neuropsychiatric Copy Number Variants in a Health Care System Population.
Christa Lese Martin, Karen E Wain, Matthew T Oetjens, Kasia Tolwinski, Emily Palen, Abby Hare-Harris, Lukas Habegger, Evan K Maxwell, Jeffrey G Reid, Lauren Kasparson Walsh,[...]. JAMA Psychiatry 2020
Christa Lese Martin, Karen E Wain, Matthew T Oetjens, Kasia Tolwinski, Emily Palen, Abby Hare-Harris, Lukas Habegger, Evan K Maxwell, Jeffrey G Reid, Lauren Kasparson Walsh,[...]. JAMA Psychiatry 2020
50
A Systematic Review of Genetic Testing and Lifestyle Behaviour Change: Are We Using High-Quality Genetic Interventions and Considering Behaviour Change Theory?
Justine Horne, Janet Madill, Colleen O'Connor, Jacob Shelley, Jason Gilliland. Lifestyle Genom 2018
Justine Horne, Janet Madill, Colleen O'Connor, Jacob Shelley, Jason Gilliland. Lifestyle Genom 2018
50
HLA*LA-HLA typing from linearly projected graph alignments.
Alexander T Dilthey, Alexander J Mentzer, Raphael Carapito, Clare Cutland, Nezih Cereb, Shabir A Madhi, Arang Rhie, Sergey Koren, Seiamak Bahram, Gil McVean,[...]. Bioinformatics 2019
Alexander T Dilthey, Alexander J Mentzer, Raphael Carapito, Clare Cutland, Nezih Cereb, Shabir A Madhi, Arang Rhie, Sergey Koren, Seiamak Bahram, Gil McVean,[...]. Bioinformatics 2019
50
Flexible and Scalable Full-Length CYP2D6 Long Amplicon PacBio Sequencing.
Henk P J Buermans, Rolf H A M Vossen, Seyed Yahya Anvar, William G Allard, Henk-Jan Guchelaar, Stefan J White, Johan T den Dunnen, Jesse J Swen, Tahar van der Straaten. Hum Mutat 2017
Henk P J Buermans, Rolf H A M Vossen, Seyed Yahya Anvar, William G Allard, Henk-Jan Guchelaar, Stefan J White, Johan T den Dunnen, Jesse J Swen, Tahar van der Straaten. Hum Mutat 2017
50
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients: A Pilot Randomized Trial.
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
Jason L Vassy, Kurt D Christensen, Erica F Schonman, Carrie L Blout, Jill O Robinson, Joel B Krier, Pamela M Diamond, Matthew Lebo, Kalotina Machini, Danielle R Azzariti,[...]. Ann Intern Med 2017
50
Characterization of 137 Genomic DNA Reference Materials for 28 Pharmacogenetic Genes: A GeT-RM Collaborative Project.
Victoria M Pratt, Robin E Everts, Praful Aggarwal, Brittany N Beyer, Ulrich Broeckel, Ruth Epstein-Baak, Paul Hujsak, Ruth Kornreich, Jun Liao, Rachel Lorier,[...]. J Mol Diagn 2016
Victoria M Pratt, Robin E Everts, Praful Aggarwal, Brittany N Beyer, Ulrich Broeckel, Ruth Epstein-Baak, Paul Hujsak, Ruth Kornreich, Jun Liao, Rachel Lorier,[...]. J Mol Diagn 2016
50
[Principles and practice of mass screening for disease].
J M Wilson, Y G Jungner. Bol Oficina Sanit Panam 1968
J M Wilson, Y G Jungner. Bol Oficina Sanit Panam 1968
50
Applying Next-Generation Sequencing Platforms for Pharmacogenomic Testing in Clinical Practice.
Alireza Tafazoli, Henk-Jan Guchelaar, Wojciech Miltyk, Adam J Kretowski, Jesse J Swen. Front Pharmacol 2021
Alireza Tafazoli, Henk-Jan Guchelaar, Wojciech Miltyk, Adam J Kretowski, Jesse J Swen. Front Pharmacol 2021
50
A collaborative translational research framework for evaluating and implementing the appropriate use of human genome sequencing to improve health.
Muin J Khoury, W Gregory Feero, David A Chambers, Lawrence C Brody, Nazneen Aziz, Robert C Green, A Cecile J W Janssens, Michael F Murray, Laura Lyman Rodriguez, Joni L Rutter,[...]. PLoS Med 2018
Muin J Khoury, W Gregory Feero, David A Chambers, Lawrence C Brody, Nazneen Aziz, Robert C Green, A Cecile J W Janssens, Michael F Murray, Laura Lyman Rodriguez, Joni L Rutter,[...]. PLoS Med 2018
50
Public health genomics and genetic test evaluation: the challenge of conducting behavioural research on the utility of lifestyle-genetic tests.
Saskia C Sanderson, Jane Wardle, Steve E Humphries. J Nutrigenet Nutrigenomics 2008
Saskia C Sanderson, Jane Wardle, Steve E Humphries. J Nutrigenet Nutrigenomics 2008
50
Characterization of 108 Genomic DNA Reference Materials for 11 Human Leukocyte Antigen Loci: A GeT-RM Collaborative Project.
Maria P Bettinotti, Deborah Ferriola, Jamie L Duke, Timothy L Mosbruger, Nikolaos Tairis, Lawrence Jennings, Lisa V Kalman, Dimitri Monos. J Mol Diagn 2018
Maria P Bettinotti, Deborah Ferriola, Jamie L Duke, Timothy L Mosbruger, Nikolaos Tairis, Lawrence Jennings, Lisa V Kalman, Dimitri Monos. J Mol Diagn 2018
50
OptiType: precision HLA typing from next-generation sequencing data.
András Szolek, Benjamin Schubert, Christopher Mohr, Marc Sturm, Magdalena Feldhahn, Oliver Kohlbacher. Bioinformatics 2014
András Szolek, Benjamin Schubert, Christopher Mohr, Marc Sturm, Magdalena Feldhahn, Oliver Kohlbacher. Bioinformatics 2014
50
Allelic decomposition and exact genotyping of highly polymorphic and structurally variant genes.
Ibrahim Numanagić, Salem Malikić, Michael Ford, Xiang Qin, Lorraine Toji, Milan Radovich, Todd C Skaar, Victoria M Pratt, Bonnie Berger, Steve Scherer,[...]. Nat Commun 2018
Ibrahim Numanagić, Salem Malikić, Michael Ford, Xiang Qin, Lorraine Toji, Milan Radovich, Todd C Skaar, Victoria M Pratt, Bonnie Berger, Steve Scherer,[...]. Nat Commun 2018
50
Population genetic screening efficiently identifies carriers of autosomal dominant diseases.
J J Grzymski, G Elhanan, J A Morales Rosado, E Smith, K A Schlauch, R Read, C Rowan, N Slotnick, S Dabe, W J Metcalf,[...]. Nat Med 2020
J J Grzymski, G Elhanan, J A Morales Rosado, E Smith, K A Schlauch, R Read, C Rowan, N Slotnick, S Dabe, W J Metcalf,[...]. Nat Med 2020
50
A global reference for human genetic variation.
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
Adam Auton, Lisa D Brooks, Richard M Durbin, Erik P Garrison, Hyun Min Kang, Jan O Korbel, Jonathan L Marchini, Shane McCarthy, Gil A McVean, Gonçalo R Abecasis. Nature 2015
50
The -589C>T polymorphism in the interleukin-4 gene (IL-4) is associated with a reduced risk of myocardial infarction in young individuals.
E Paffen, P Medina, M C H de Visser, A van Wijngaarden, E Zorio, A Estellés, F R Rosendaal, F España, R M Bertina, C J M Doggen. J Thromb Haemost 2008
E Paffen, P Medina, M C H de Visser, A van Wijngaarden, E Zorio, A Estellés, F R Rosendaal, F España, R M Bertina, C J M Doggen. J Thromb Haemost 2008
50
Co-cited is the co-citation frequency, indicating how many articles cite the article together with the query article. Similarity is the co-citation as percentage of the times cited of the query article or the article in the search results, whichever is the lowest. These numbers are calculated for the last 100 citations when articles are cited more than 100 times.