Kurt D. Christensen

Also affiliated with Harvard Pilgrim Health Care

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 2%percentile

2.2Author DataRank

Indexed papers

2in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Why this DataRank?

An author's DataRank is the sum of the DataRanks of all 2 indexed papers attributed to them. A prolific author with many moderate-impact papers can outrank one with a single high-impact paper.

Author scores recompute whenever paper DataRanks are refreshed, so this number lags the underlying paper scores by at most one batch run.

Read the full methodology →

The highest-impact dataset this researcher has shared, ranked by DataRank — the single contribution doing the most to lift their data-sharing standing.

Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.10.005

Top 11%

1.9DataRank

Top 11%73 citations

Nidhi Shah, Kalotina Machini, Emma Perez, Kurt D. Christensen, Hana Zouk +15 more

Papers

Driven by 31 papers — median percentile 68. Top paper: “Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study”.

Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study

Frontiers in Genetics(2022)10.3389/fgene.2022.867371

N/A

2.6DataRank · unranked

70 citations

Kurt D. Christensen, Casie A. Genetti, Richard B. Parad, Jill O. Robinson, Carrie L. Blout Zawatsky +9 more

Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization

The American Journal of Human Genetics(2021)10.1016/j.ajhg.2021.10.005

Top 11%

1.9DataRank

Top 11%73 citations

Nidhi Shah, Kalotina Machini, Emma Perez, Kurt D. Christensen, Hana Zouk +15 more

The GenoVA study: Equitable implementation of a pragmatic randomized trial of polygenic-risk scoring in primary care

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.10.001

N/A

0.996DataRank · unranked

23 citations

Charles A. Brunette, Matthew S. Lebo, Katharine MacIsaac, Thomas Yi, Morgan E. Danowski +15 more

Precision Population Medicine in Primary Care: The Sanford Chip Experience

Frontiers in Genetics(2021)10.3389/fgene.2021.626845

N/A

0.604DataRank · unranked

55 citations

Megan Bell, Carrie L. Blout Zawatsky, Lauren N. Galbraith, Robert C. Green, Allison M. Hutchinson +16 more

Effects of participation in a U.S. trial of newborn genomic sequencing on parents at risk for depression

Journal of Genetic Counseling(2021)10.1002/jgc4.1475

N/A

0.542DataRank · unranked

10 citations

Kurt D. Christensen, Melissa Kurtz Uveges, Susan E. Waisbren, Amy L. McGuire, Stacey Pereira +8 more

Quantifying Downstream Healthcare Utilization in Studies of Genomic Testing

Value in Health(2020)10.1016/j.jval.2020.01.017

N/A

0.416DataRank · unranked

15 citations

Dmitry Dukhovny, Kathryn A. Phillips, Alan H. Beggs, Robert C. Green, Richard B. Parad +27 more

Estimated Cost-effectiveness of Genetic Testing in Siblings of Newborns With Cancer Susceptibility Gene Variants

JAMA Network Open(2021)10.1001/jamanetworkopen.2021.29742

N/A

0.416DataRank · unranked

15 citations

Kurt D. Christensen, Haley K. Sullivan, Natasha K. Stout, Lisa Diller, Jennifer M. Yeh +2 more

Workforce Considerations When Building a Precision Medicine Program

Journal of Personalized Medicine(2022)10.3390/jpm12111929

N/A

0.416DataRank · unranked

15 citations

Jennifer Leonhard, Megan Bell, Michelle Moore, Natasha Petry, Dylan Platt +4 more

BATF2 promotes HSC myeloid differentiation by amplifying IFN response mediators during chronic infection

iScience(2023)10.1016/j.isci.2023.106059

N/A

0.406DataRank · unranked

14 citations

Marcus A. Florez, Paweł Kuś, Brandon T. Tran, Bailee Kain, Yingmin Zhu +5 more

Awareness and utilization of genetic testing among Hispanic and Latino adults living in the US: The Hispanic Community Health Study/Study of Latinos

Human Genetics and Genomics Advances(2022)10.1016/j.xhgg.2022.100160

N/A

0.360DataRank · unranked

10 citations

Mengran Zhang, Lauren N. Galbraith, Einat Granot‐Hershkovitz, Sarah C. Nelson, Sara González +12 more

Clinical impact of preemptive pharmacogenomic testing on antiplatelet therapy in a real-world setting

European Journal of Human Genetics(2024)10.1038/s41431-024-01567-1

N/A

0.345DataRank · unranked

9 citations

Kurt D. Christensen, Joel Van Heukelom, April Schultz, Muhammad Hamza Saad Shaukat, Catherine Hajek +8 more

Neptune: an environment for the delivery of genomic medicine

Genetics in Medicine(2021)10.1038/s41436-021-01230-w

N/A

0.330DataRank · unranked

8 citations

Victoria Yi, David R. Murdock, Sara E. Kalla, Tsung-Jung Wu, Aniko Sabo +93 more

SLCO1B1 Gene-Based Clinical Decision Support Reduces Statin-Associated Muscle Symptoms Risk With Simvastatin

Pharmacogenomics(2023)10.2217/pgs-2023-0056

N/A

0.330DataRank · unranked

8 citations

Joel Van Heukelom, Robert C. Green, Catherine Hajek, Madison R. Hickingbotham, Eric Larson +6 more

Returning Actionable Genomic Results in a Research Biobank: Analytic Validity, Clinical Implementation and Resource Utilization

medRxiv(2021)10.1101/2021.08.03.21261489

Top 53%

0.319DataRank

Top 53%4 citations

Nidhi Shah, Kalotina Machini, Emma Perez, Kurt D. Christensen, Hana Zouk +15 more

Medical Evaluation of Unanticipated Monogenic Disease Risks Identified through Newborn Genomic Screening: Findings from the BabySeq Project

medRxiv(2022)10.1101/2022.03.18.22272284

N/A

0.241DataRank · unranked

4 citations

Nidhi Shah, Casie A. Genetti, Timothy W. Yu, Bethany Zettler, Talia S. Schwartz +13 more

Diverse Participant Recruitment for Infant Sequencing in the BabySeq Project

medRxiv(2024)10.1101/2024.10.01.24314717

N/A

0.165DataRank · unranked

2 citations

Sheyenne A. Walmsley, Barbara W. Harrison, Crystal T. Stephens, Bethany Zettler, Greysha Rivera-Cruz +17 more

A framework evaluating the utility of multi-gene, multi-disease population-based panel testing that accounts for uncertainty in penetrance estimates

bioRxiv (Cold Spring Harbor Laboratory)(2022)10.1101/2022.08.10.503415

N/A

0DataRank · unranked

0 citations

Kurt D. Christensen, Robert C. Green, Peter Kraft, Jane W. Liang

Actionability of unanticipated monogenic disease risks in newborn genomic screening: Findings from the BabySeq Project

The American Journal of Human Genetics(2023)10.1016/j.ajhg.2023.05.007

N/A

0DataRank · unranked

55 citations

Nidhi Shah, Casie A. Genetti, Timothy W. Yu, Bethany Zettler, Melissa Kurtz Uveges +12 more

Parents’ decision-making regarding whether to receive adult-onset only genetic findings for their children: Findings from the BabySeq Project

Genetics in Medicine(2022)10.1016/j.gim.2022.100002

N/A

0DataRank · unranked

24 citations

Amanda M. Gutierrez, Jill O. Robinson, Kurt D. Christensen, Casie A. Genetti, Carrie L. Blout Zawatsky +9 more

Behavioral and psychological impact of genome sequencing: a pilot randomized trial of primary care and cardiology patients

npj Genomic Medicine(2021)10.1038/s41525-021-00236-2

N/A

0DataRank · unranked

15 citations

Erica F. Schonman, Jill O. Robinson, J. Scott Roberts, Pamela M. Diamond, Kaitlyn B. Lee +3 more

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

UNC Libraries(2020)10.17615/8n4d-eh72

N/A

0DataRank · unranked

0 citations

Barbara A. Bernhardt, David L. Veenstra, Kurt D. Christensen, Stacy W. Gray, Yolanda Martins +5 more

Benefits, harms, and costs of newborn genetic screening for hypertrophic cardiomyopathy: Estimates from the PreEMPT model

Genetics in Medicine(2023)10.1016/j.gim.2023.100797

N/A

0DataRank · unranked

7 citations

Pamela M. McMahon, Lauren N. Galbraith, Jennifer M. Yeh, Natasha K. Stout, Christine Y. Lu +5 more

Returning personalized, genetic health test results to individuals of African descent or ancestry in precision medicine research

Health Affairs Scholar(2023)10.1093/haschl/qxad066

N/A

0DataRank · unranked

0 citations

Nora Emmott, Maryam Nafie, Lauren Edgar, Tracey Johnson-Glover, Kurt D. Christensen +3 more

Disclosing genetic risk for Alzheimer's dementia to individuals with mild cognitive impairment

Alzheimer s & Dementia Translational Research & Clinical Interventions(2020)10.1002/trc2.12002

N/A

0DataRank · unranked

33 citations

Jason Karlawish, J. Scott Roberts, Wendy R. Uhlmann, Kristin Harkins, Elisabeth McCarty Wood +13 more

Family genetic risk communication and reverse cascade testing in the BabySeq project

Genetics in Medicine(2024)10.1016/j.gim.2024.101350

N/A

0DataRank · unranked

3 citations

Hadley Stevens Smith, Stacey Pereira, Casie A. Genetti, Amy L. McGuire, Alan H. Beggs +38 more

Primary Care Providers’ Experiences With an Active Elective Genetic Testing Program

Health Education & Behavior(2024)10.1177/10901981241266849

N/A

0DataRank · unranked

2 citations

Carrie L. Blout Zawatsky, Kurt D. Christensen, Robert C. Green, Catherine Hajek, Madison R. Hickingbotham +5 more

Attitudes, knowledge, and risk perceptions of patients who received elective genomic testing as a clinical service

Genetics in Medicine(2024)10.1016/j.gim.2024.101200

N/A

0DataRank · unranked

3 citations

Megan Bell, Madison R. Hickingbotham, Ann Chen Wu, Lauren N. Galbraith, Jessica L LeBlanc +8 more

Modernizing Newborn Screening in the Genomic Era: Importance of Health-Related Quality of Life

PharmacoEconomics - Open(2024)10.1007/s41669-024-00528-0

N/A

0DataRank · unranked

2 citations

Ann Chen Wu, Kurt D. Christensen, Davene R. Wright, Jennifer M. Yeh, Hadley Stevens Smith +1 more

Evaluating the utility of multi-gene, multi-disease population-based panel testing accounting for uncertainty in penetrance estimates

npj Genomic Medicine(2024)10.1038/s41525-024-00414-y

N/A

0DataRank · unranked

0 citations

Kurt D. Christensen, Robert C. Green, Peter Kraft, Jane W. Liang

Population-Based Newborn Screening for Germline TP53 Variants: Clinical Benefits, Cost-Effectiveness, and Value of Further Research

JNCI Journal of the National Cancer Institute(2022)10.1093/jnci/djac013

N/A

0DataRank · unranked

10 citations

Natasha K. Stout, Grace O’Brien, Kurt D. Christensen, Pamela M. McMahon, Ann Chen Wu +3 more

450 Opportunities amid complexities in returning genetic results to black precision medicine research participants: Interview themes in context with open All of Us data

Journal of Clinical and Translational Science(2025)10.1017/cts.2025.67

N/A

0DataRank · unranked

0 citations

Nora Emmott, Maryam Nafie, Stephanie Argetsinger, Lauren Edgar, Tracey Johnson-Glover +2 more

Kurt D. Christensen

Indexed papers

Top data-sharing exemplar

Papers