Gene patents in the US - focusing on what really matters

por Dobson, Allison W, Evans, James P
Publicado 2012

Plagiarism in submitted manuscripts: incidence, characteristics and optimization of screening—case study in a major specialty medical journal

por Higgins, Janet R., Lin, Feng-Chang, Evans, James P.
Publicado 2016

The next controversy in genetic testing: clinical data as trade secrets?

por Cook-Deegan, Robert, Conley, John M, Evans, James P, Vorhaus, Daniel
Publicado 2013

The Promise and Peril of Genomic Screening in the General Population

por Adams, Michael C., Evans, James P., Henderson, Gail E., Berg, Jonathan S.
Publicado 2015

From Genetics to Genomics: Facing the Liability Implications in Clinical Care

por Marchant, Gary, Barnes, Mark, Evans, James P., LeRoy, Bonnie, Wolf, Susan M.
Publicado 2020

Genomic Screening of the General Adult Population: Key Concepts for Assessing Net Benefit with Systematic Evidence Reviews

por Prince, Anya E.R., Berg, Jonathan S., Evans, James P., Jonas, Daniel E., Henderson, Gail
Publicado 2014

A New Framework and Prototype Solution for Clinical Decision Support and Research in Genomics and Other Data-intensive Fields of Medicine

por Evans, James P., Wilhelmsen, Kirk C., Berg, Jonathan, Schmitt, Charles P., Krishnamurthy, Ashok, Fecho, Karamarie, Ahalt, Stanley C.
Publicado 2016

Characterizing biobank organizations in the U.S.: results from a national survey

por Henderson, Gail E, Cadigan, R Jean, Edwards, Teresa P, Conlon, Ian, Nelson, Anders G, Evans, James P, Davis, Arlene M, Zimmer, Catherine, Weiner, Bryan J
Publicado 2013

“Possibly positive or certainly uncertain?”: Participants’ responses to uncertain diagnostic results from exome sequencing

por Skinner, Debra, Roche, Myra I., Weck, Karen E., Raspberry, Kelly A., Foreman, A. Katherine M., Strande, Natasha T., Berg, Jonathan S., Evans, James P., Henderson, Gail E.
Publicado 2017

Genomic Knowledge in the Context of Diagnostic Exome Sequencing: Changes over Time, Persistent Subgroup Differences, and Associations with Psychological Sequencing Outcomes

por Rini, Christine, Henderson, Gail E., Evans, James P., Berg, Jonathan S., Foreman, Ann Katherine M., Griesemer, Ida, Waltz, Margaret, O’Daniel, Julianne M., Roche, Myra I.
Publicado 2019

Professional Responsibilities Regarding the Provision, Publication and Dissemination of Patient Phenotypes in the Context of Clinical Genetic and Genomic Testing: Points to Conside...

por Bush, Lynn W., Beck, Anita E., Biesecker, Leslie G., Evans, James P., Hamosh, Ada, Holm, Ingrid A., Martin, Christa L., Richards, C. Sue, Rehm, Heidi L.
Publicado 2018

Combination of exome sequencing and immune testing confirms Aicardi–Goutières syndrome type 5 in a challenging pediatric neurology case

por Haskell, Gloria T., Mori, Mari, Powell, Cynthia, Amrhein, Timothy J., Rice, Gillian I., Bailey, Lauren, Strande, Natasha, Weck, Karen E., Evans, James P., Berg, Jonathan S., Kishnani, Priya
Publicado 2018

Returning negative results to individuals in a genomic screening program: Lessons learned

por Butterfield, Rita M., Evans, James P., Rini, Christine, Kuczynski, Kristine J., Waltz, Margaret, Cadigan, R. Jean, Goddard, Katrina A.B., Muessig, Kristin R., Henderson, Gail E.
Publicado 2018

Is there evidence that we should screen the general population for Lynch syndrome with genetic testing? A systematic review

por Prince, Anya E R, Cadigan, R Jean, Henderson, Gail E, Evans, James P, Adams, Michael, Coker-Schwimmer, Emmanuel, Penn, Dolly C, Van Riper, Marcia, Corbie-Smith, Giselle, Jonas, Daniel E
Publicado 2017

Increasing the diagnostic yield of exome sequencing by copy number variant analysis

por Marchuk, Daniel S., Crooks, Kristy, Strande, Natasha, Kaiser-Rogers, Kathleen, Milko, Laura V., Brandt, Alicia, Arreola, Alexandra, Tilley, Christian R., Bizon, Chris, Vora, Neeta L., Wilhelmsen, Kirk C., Evans, James P., Berg, Jonathan S.
Publicado 2018

The who, what and why of research participants’ intentions to request a broad range of secondary findings in a diagnostic genomic sequencing study

por Rini, Christine, Khan, Cynthia M., Moore, Elizabeth, Roche, Myra I., Evans, James P., Berg, Jonathan S., Powell, Bradford C., Corbie-Smith, Giselle, Foreman, Ann Katherine M., Griesemer, Ida, Lee, Kristy, O’Daniel, Julianne M., Henderson, Gail E.
Publicado 2017

Factors influencing NCGENES research participants’ requests for non-medically actionable secondary findings

por Roche, Myra I., Griesemer, Ida, Khan, Cynthia M., Moore, Elizabeth, Lin, Feng-Chang, O’Daniel, Julianne M., Foreman, Ann Katherine M., Lee, Kristy, Powell, Bradford C., Berg, Jonathan S., Evans, James P., Henderson, Gail E., Rini, Christine
Publicado 2018

Prenatal Exome Sequencing in Anomalous Fetuses: New Opportunities and Challenges

por Vora, Neeta L., Powell, Bradford, Brandt, Alicia, Strande, Natasha, Hardisty, Emily, Gilmore, Kelly, Foreman, Ann Katherine M., Wilhelmsen, Kirk, Bizon, Chris, Reilly, Jason, Owen, Phil, Powell, Cynthia M., Skinner, Debra, Rini, Christine, Lyerly, Anne D., Boggess, Kim A., Weck, Karen, Berg, Jonathan S., Evans, James P.
Publicado 2017

Diagnostic utility of exome sequencing in the evaluation of neuromuscular disorders

por Haskell, Gloria T., Adams, Michael C., Fan, Zheng, Amin, Krunal, Guzman Badillo, Roberto J., Zhou, Linran, Bizon, Christopher, Chahin, Nizar, Greenwood, Robert S., Milko, Laura V., Shiloh-Malawsky, Yael, Crooks, Kristy R., Strande, Natasha, Tennison, Michael, Tilley, Christian R., Brandt, Alicia, Wilhelmsen, Kirk C., Weck, Karen, Evans, James P., Berg, Jonathan S.
Publicado 2018

A semiquantitative metric for evaluating clinical actionability of incidental or secondary findings from genome-scale sequencing

por Berg, Jonathan S., Foreman, Ann Katherine M., O'Daniel, Julianne M., Booker, Jessica K., Boshe, Lacey, Carey, Timothy, Crooks, Kristy R., Jensen, Brian C., Juengst, Eric T., Lee, Kristy, Nelson, Daniel K., Powell, Bradford C., Powell, Cynthia M., Roche, Myra I., Skrzynia, Cecile, Strande, Natasha T., Weck, Karen E., Wilhelmsen, Kirk C., Evans, James P.
Publicado 2016