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Kurt D. Christensen
Kurt D. Christensen
Assistant Professor in Population Medicine, Harvard Pilgrim Health Care Institute
Verified email at hphci.harvard.edu - Homepage
Title
Cited by
Cited by
Year
Interpretation of genomic sequencing results in healthy and ill newborns: results from the BabySeq Project
O Ceyhan-Birsoy, JB Murry, K Machini, MS Lebo, WY Timothy, S Fayer, ...
The American Journal of Human Genetics 104 (1), 76-93, 2019
2332019
The impact of whole-genome sequencing on the primary care and outcomes of healthy adult patients: a pilot randomized trial
JL Vassy, KD Christensen, EF Schonman, CL Blout, JO Robinson, ...
Annals of internal medicine 167 (3), 159-169, 2017
1962017
Clinical sequencing exploratory research consortium: accelerating evidence-based practice of genomic medicine
RC Green, KAB Goddard, GP Jarvik, LM Amendola, PS Appelbaum, ...
The American Journal of Human Genetics 98 (6), 1051-1066, 2016
1722016
Communicating genetic risk information for common disorders in the era of genomic medicine
DM Lautenbach, KD Christensen, JA Sparks, RC Green
Annual review of genomics and human genetics 14 (1), 491-513, 2013
1632013
The BabySeq project: implementing genomic sequencing in newborns
IA Holm, PB Agrawal, O Ceyhan-Birsoy, KD Christensen, S Fayer, ...
BMC pediatrics 18, 1-10, 2018
1572018
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study
MR Hart, BB Biesecker, CL Blout, KD Christensen, LM Amendola, ...
Genetics in Medicine 21 (5), 1100-1110, 2019
1532019
The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine
JL Vassy, DM Lautenbach, HM McLaughlin, SW Kong, KD Christensen, ...
Trials 15, 1-12, 2014
1512014
Are physicians prepared for whole genome sequencing? A qualitative analysis
KD Christensen, JL Vassy, L Jamal, LS Lehmann, MJ Slashinski, ...
Clinical genetics 89 (2), 228-234, 2016
1372016
Assessing the costs and cost-effectiveness of genomic sequencing
KD Christensen, D Dukhovny, U Siebert, RC Green
Journal of personalized medicine 5 (4), 470-486, 2015
1312015
Understandings of basic genetics in the United States: results from a national survey of black and white men and women
KD Christensen, TE Jayaratne, JS Roberts, SLR Kardia, EM Petty
Public health genomics 13 (7-8), 467-476, 2010
1272010
A systematic approach to the reporting of medically relevant findings from whole genome sequencing
HM McLaughlin, O Ceyhan-Birsoy, KD Christensen, IS Kohane, J Krier, ...
BMC Medical Genetics 15, 1-12, 2014
1012014
Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study
WJ Lane, CM Westhoff, NS Gleadall, M Aguad, R Smeland-Wagman, ...
The Lancet Haematology 5 (6), e241-e251, 2018
992018
Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomics
JS Roberts, KD Christensen, RC Green
Clinical genetics 80 (5), 407-414, 2011
992011
Providers' knowledge of genetics: a survey of 5915 individuals and families with genetic conditions
EK Harvey, CE Fogel, M Peyrot, KD Christensen, SF Terry, JD McInerney
Genetics in Medicine 9 (5), 259-267, 2007
992007
Harmonizing clinical sequencing and interpretation for the eMERGE III network
H Zouk, E Venner, NJ Lennon, DM Muzny, D Abrams, S Adunyah, ...
The American Journal of Human Genetics 105 (3), 588-605, 2019
952019
Parental interest in genomic sequencing of newborns: enrollment experience from the BabySeq Project
CA Genetti, TS Schwartz, JO Robinson, GE VanNoy, D Petersen, ...
Genetics in Medicine 21 (3), 622-630, 2019
902019
Direct-to-consumer genetic testing: an assessment of genetic counselors' knowledge and beliefs
KT Hock, KD Christensen, BM Yashar, JS Roberts, SE Gollust, ...
Genetics in Medicine 13 (4), 325-332, 2011
882011
Psychological outcomes related to exome and genome sequencing result disclosure: a meta-analysis of seven Clinical Sequencing Exploratory Research (CSER) Consortium studies
JO Robinson, J Wynn, B Biesecker, LG Biesecker, B Bernhardt, ...
Genetics in Medicine 21 (12), 2781-2790, 2019
712019
Methodological issues in assessing the economic value of next-generation sequencing tests: many challenges and not enough solutions
KA Phillips, PA Deverka, DA Marshall, S Wordsworth, DA Regier, ...
Value in Health 21 (9), 1033-1042, 2018
692018
Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group
SW Gray, Y Martins, LZ Feuerman, BA Bernhardt, BB Biesecker, ...
Genetics in Medicine 16 (10), 727-735, 2014
662014
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