Carrie L. Blout Zawatsky

Author

Also Known As

Argos, Maria, Biswas, Sawona, C.L. Blout Zawatsky, Carrie Blout, Carrie L Blout Zawatsky, Carrie L. B. Zawatsky, Carrie L. Blout, Carrie L. Blout Zawatsky, Carrie L. Blout Zawatsky, Carrie L.B. Zawatsky

Publications

1.9K

Citations

H-Index

Concepts

All Affiliations

Broad Institute Harvard University Brigham and Women's Hospital Harvard Pilgrim Health Care Mass General Brigham

About

Carrie L. Blout Zawatsky is an author at Broad Institute specializing in medicine, genetics, and genomics.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	13	15	1K
2	Public Health	6	6	306
3	Engineering	1	1	114
4	Natural Sciences	1	1	71
5	Biology	1	1	71

Carrie L. Blout Zawatsky

Publications

1.6K

Citations

H-Index

Page 1

	Year	Citations
The Impact of Whole-Genome Sequencing on the Primary Care and Outcomes of Healthy Adult Patients Jason L. Vassy, Kurt D. Christensen, Erica F. Schonman, Annals of Internal Medicine	2017	164
Clinical Sequencing Exploratory Research Consortium: Accelerating Evidence-Based Practice of Genomic Medicine Robert C. Green, Katrina A.B. Goddard, Gail P. Jarvik, The American Journal of Human Genetics EpidemiologySequencingMedicineNext-generation SequencingGenomics	2016	161
Secondary findings from clinical genomic sequencing: prevalence, patient perspectives, family history assessment, and health-care costs from a multisite study Ragan Hart, Barbara B. Biesecker, Carrie L. Blout Zawatsky, Genetics in Medicine Genetic TestingClinical Genomic SequencingNext-generation SequencingGenetic EpidemiologyGenomics	2018	154
Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network Hana Zouk, Eric Venner, Niall J. Lennon, The American Journal of Human Genetics BioinformaticsFunctional GenomicsEngineeringClinical SequencingTranslational Bioinformatics	2019	114
A Comparison of Whole Genome Sequencing to Multigene Panel Testing in Hypertrophic Cardiomyopathy Patients Allison L. Cirino, Neal K. Lakdawala, Barbara McDonough, Circulation Cardiovascular Genetics	2017	92
Automated typing of red blood cell and platelet antigens: a whole-genome sequencing study William J. Lane, Connie M. Westhoff, Nicholas Gleadall, The Lancet Haematology BioinformaticsDna SequencingRed Blood CellMedicineGenetics	2018	88
Psychosocial Effect of Newborn Genomic Sequencing on Families in the BabySeq Project Stacey Pereira, Hadley Stevens Smith, Leslie A. Frankel, JAMA Pediatrics	2021	76
Mutations in PCYT1A, Encoding a Key Regulator of Phosphatidylcholine Metabolism, Cause Spondylometaphyseal Dysplasia with Cone-Rod Dystrophy Julie Hoover‐Fong, Nara Sobreira, Julie A. Jurgens, The American Journal of Human Genetics BiologyDevelopmental BiologyMedicineGeneticsNatural Sciences	2014	71
Returning actionable genomic results in a research biobank: Analytic validity, clinical implementation, and resource utilization Carrie L. Blout Zawatsky, Nidhi Shah, Kalotina Machini, The American Journal of Human Genetics	2021	69
Parental Attitudes Toward Standard Newborn Screening and Newborn Genomic Sequencing: Findings From the BabySeq Study Brittan Armstrong, Kurt D. Christensen, Casie A. Genetti, Frontiers in Genetics	2022	62

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