Kurt D. Christensen
机构: Assistant Professor in Population Medicine, Harvard Pilgrim Health Care Institute
主页: kdchrist.com
每年引用次数
引用次数
引用: 3,919
H-指数: 36
I10-指数 : 63
出版物: 136
Universal newborn genetic screening for pediatric cancer predisposition syndromes: model-based insights.
Jennifer M Yeh , Natasha K Stout , Aeysha Chaudhry , Kurt D Christensen
Genetics in Medicine 1 -6
2021
Patient understanding of, satisfaction with, and perceived utility of whole-genome sequencing: findings from the MedSeq Project.
J Scott Roberts , , Jill O Robinson , Pamela M Diamond
Genetics in Medicine 20 ( 9) 1069 -1076
51
2018
Anticipated responses of early adopter genetic specialists and nongenetic specialists to unsolicited genomic secondary findings.
Kurt D Christensen , Barbara A Bernhardt , Gail P Jarvik , Lucia A Hindorff
Genetics in Medicine 20 ( 10) 1186 -1195
8
2018
Short-term costs of integrating whole-genome sequencing into primary care and cardiology settings: a pilot randomized trial.
Kurt D Christensen , Jason L Vassy , Kathryn A Phillips , Carrie L Blout
Genetics in Medicine 20 ( 12) 1544 -1553
15
2018
The MedSeq Project: A randomized trial of integrating whole genome sequencing into clinical medicine
Jason L Vassy , Denise M Lautenbach , Heather M McLaughlin , Sek Won Kong
Trials 15 ( 1) 85 -85
143
2014
A systematic approach to the reporting of medically relevant findings from whole genome sequencing.
Heather M McLaughlin , Ozge Ceyhan-Birsoy , Kurt D Christensen , Isaac S Kohane
BMC Medical Genetics 15 ( 1) 134 -134
68
2014
A randomized controlled trial of disclosing genetic risk information for Alzheimer disease via telephone.
Kurt D Christensen , Wendy R Uhlmann , J Scott Roberts , Erin Linnenbringer
Genetics in Medicine 20 ( 1) 132 -141
19
2018
Associations between self-referral and health behavior responses to genetic risk information
Kurt D Christensen , J Scott Roberts , Brian J Zikmund-Fisher , Sharon LR Kardia
Genome Medicine 7 ( 1) 10 -10
17
2015
Providers' knowledge of genetics: A survey of 5915 individuals and families with genetic conditions
Erin K Harvey , Chana E Fogel , Mark Peyrot , Kurt D Christensen
Genetics in Medicine 9 ( 5) 259 -267
65
2007
Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experience.
Kurt D Christensen , J Scott Roberts , Charmaine D M Royal , Grace-Ann Fasaye
Genetics in Medicine 10 ( 3) 207 -214
37
2008
Direct-to-consumer genetic testing: An assessment of genetic counselors' knowledge and beliefs
Kathryn T Hock , Kurt D Christensen , Beverly M Yashar , J Scott Roberts
Genetics in Medicine 13 ( 4) 325 -332
46
2011
Changes to perceptions of the pros and cons of genetic susceptibility testing after APOE genotyping for Alzheimer disease risk
Kurt D Christensen , J Scott Roberts , Wendy R Uhlmann , Robert C Green
Genetics in Medicine 13 ( 5) 409 -414
33
2011
‘Someday it will be the norm’: physician perspectives on the utility of genome sequencing for patient care in the MedSeq Project
Jason L Vassy , Kurt D Christensen , Melody J Slashinski , Denise M Lautenbach
Personalized Medicine 12 ( 1) 23 -32
30
2015
How could disclosing incidental information from whole-genome sequencing affect patient behavior?
Kurt D Christensen , Robert C Green
Personalized Medicine 10 ( 4) 377 -386
11
2013
Patients’ perceived utility of whole-genome sequencing for their healthcare: findings from the MedSeq project
Philip J Lupo , Jill O Robinson , Pamela M Diamond , Leila Jamal
Personalized Medicine 13 ( 1) 13 -20
21
2016
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
M Ragan Hart , Barbara B Biesecker , Carrie L Blout , Kurt D Christensen
Genetics in Medicine 21 ( 5) 1100 -1110
120
2019
Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization
Carrie L Blout Zawatsky , Nidhi Shah , Kalotina Machini , Emma Perez
The American Journal of Human Genetics 108 ( 12) 2224 -2237
19
2021
Benefits, harms, and costs of newborn genetic screening for hypertrophic cardiomyopathy: Estimates from the PreEMPT model
Kurt D Christensen , Pamela M McMahon , Lauren N Galbraith , Jennifer M Yeh
Genetics in Medicine 25 ( 4) 100797
2023
Paving the path for implementation of clinical genomic sequencing globally: Are we ready?
Deborah A Marshall , Nicolle Hua , James Buchanan , Kurt D Christensen
Health Affairs Scholar 2 ( 5) qxae053 -qxae053
2024
A whole genome approach for discovering the genetic basis of blood group antigens: independent confirmation for P1 and Xga.
William J Lane , Maria Aguad , Robin Smeland‐Wagman , Sunitha Vege
Transfusion 59 ( 3) 908 -915
8
2019
J Scott Roberts Jason L. Vassy, MD, MPH, SM Heidi Rehm Michael F. Murray, MD Matthew Lebo Stacey Pereira Peter J Whitehouse Alan H. Beggs, PhD Richard Parad Erin Linnenbringer Kathryn A. Phillips Lisa Soleymani Lehmann Jennifer M. Yeh Leila Jamal Christine Rini Christine Y. Lu Pankaj Agrawal Robert Cook-Deegan Timothy W. Yu