Publications

Participant Satisfaction With a Preference-Setting Tool for the Return of Individual Research Results in Pediatric Genomic Research.

J Empir Res Hum Res Ethics
Holm IA, Iles BR, Ziniel SI, Bacon PL, Savage SK, Christensen KD, Weitzman ER, Green RC, Huntington NL

Are physicians prepared for whole genome sequencing? a qualitative analysis.

Clin. Genet.
Christensen KD, Vassy JL, Jamal L, Lehmann LS, Slashinski MJ, Perry DL, Robinson JO, Blumenthal-Barby J, Feuerman LZ, Murray MF, Green RC, McGuire AL,

Someday it will be the norm': physician perspectives on the utility of genome sequencing for patient care in the MedSeq Project.

Per Med
Vassy JL, Christensen KD, Slashinski MJ, Lautenbach DM, Raghavan S, Robinson JO, Blumenthal-Barby J, Feuerman LZ, Lehmann LS, Murray MF, Green RC, McGuire AL

Disclosing genetic risk for coronary heart disease: effects on perceived personal control and genetic counseling satisfaction.

Clin. Genet.
Robinson CL, Jouni H, Kruisselbrink TM, Austin EE, Christensen KD, Green RC, Kullo IJ

Associations between self-referral and health behavior responses to genetic risk information.

Genome Med
Christensen KD, Roberts JS, Zikmund-Fisher BJ, Kardia SL, McBride CM, Linnenbringer E, Green RC,

Factors affecting recall of different types of personal genetic information about Alzheimer's disease risk: the REVEAL study.

Public Health Genomics
Besser AG, Sanderson SC, Roberts JS, Chen CA, Christensen KD, Lautenbach DM, Cupples LA, Green RC

A systematic approach to the reporting of medically relevant findings from whole genome sequencing.

BMC Med. Genet.
McLaughlin HM, Ceyhan-Birsoy O, Christensen KD, Kohane IS, Krier J, Lane WJ, Lautenbach D, Lebo MS, Machini K, MacRae CA, Azzariti DR, Murray MF, Seidman CE, Vassy JL, Green RC, Rehm HL,

A randomized noninferiority trial of condensed protocols for genetic risk disclosure of Alzheimer's disease.

Alzheimers Dement
Green RC, Christensen KD, Cupples LA, Relkin NR, Whitehouse PJ, Royal CD, Obisesan TO, Cook-Deegan R, Linnenbringer E, Butson MB, Fasaye GA, Levinson E, Roberts JS,

How can psychological science inform research about genetic counseling for clinical genomic sequencing?

J Genet Couns
Khan CM, Rini C, Bernhardt BA, Roberts JS, Christensen KD, Evans JP, Brothers KB, Roche MI, Berg JS, Henderson GE

The MedSeq Project: a randomized trial of integrating whole genome sequencing into clinical medicine.

Trials
Vassy JL, Lautenbach DM, McLaughlin HM, Kong SW, Christensen KD, Krier J, Kohane IS, Feuerman LZ, Blumenthal-Barby J, Roberts JS, Lehmann LS, Ho CY, Ubel PA, MacRae CA, Seidman CE, Murray MF, McGuire AL, Rehm HL, Green RC,

Social and behavioral research in genomic sequencing: approaches from the Clinical Sequencing Exploratory Research Consortium Outcomes and Measures Working Group.

Genet. Med.
Gray SW, Martins Y, Feuerman LZ, Bernhardt BA, Biesecker BB, Christensen KD, Joffe S, Rini C, Veenstra D, McGuire AL,

Communicating genetic risk information for common disorders in the era of genomic medicine.

Annu Rev Genomics Hum Genet
Lautenbach DM, Christensen KD, Sparks JA, Green RC

How could disclosing incidental information from whole-genome sequencing affect patient behavior?

Per Med
Christensen KD, Green RC

Community engagement about genetic variation research.

Popul Health Manag
Terry SF, Christensen KD, Metosky S, Rudofsky G, Deignan KP, Martinez H, Johnson-Moore P, Citrin T

Using Alzheimer's disease as a model for genetic risk disclosure: implications for personal genomics.

Clin. Genet.
Roberts JS, Christensen KD, Green RC

Disclosing individual CDKN2A research results to melanoma survivors: interest, impact, and demands on researchers.

Cancer Epidemiol. Biomarkers Prev.
Christensen KD, Roberts JS, Shalowitz DI, Everett JN, Kim SY, Raskin L, Gruber SB

Changes to perceptions of the pros and cons of genetic susceptibility testing after APOE genotyping for Alzheimer disease risk.

Genet. Med.
Christensen KD, Roberts JS, Uhlmann WR, Green RC

Direct-to-consumer genetic testing: an assessment of genetic counselors' knowledge and beliefs.

Genet. Med.
Hock KT, Christensen KD, Yashar BM, Roberts JS, Gollust SE, Uhlmann WR

Understandings of basic genetics in the United States: results from a national survey of black and white men and women.

Public Health Genomics
Christensen KD, Jayaratne TE, Roberts JS, Kardia SL, Petty EM

Incorporating ethnicity into genetic risk assessment for Alzheimer disease: the REVEAL study experience.

Genet. Med.
Christensen KD, Roberts JS, Royal CD, Fasaye GA, Obisesan T, Cupples LA, Whitehouse PJ, Butson MB, Linnenbringer E, Relkin NR, Farrer L, Cook-Deegan R, Green RC