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Fingerprint Dive into the research topics where Tara Matise is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 20 Similar Profiles
Genomics Medicine & Life Sciences
Epidemiology Medicine & Life Sciences
Single Nucleotide Polymorphism Medicine & Life Sciences
Human Chromosomes Medicine & Life Sciences
Population Medicine & Life Sciences
Genes Medicine & Life Sciences
African Americans Medicine & Life Sciences
Chromosome Mapping Medicine & Life Sciences

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Projects 2007 2019

Genome
National Human Genome Research Institute (U.S.)
Genomics
Telecommunications
Information Dissemination
Genomics
Epidemiology
Population
National Human Genome Research Institute (U.S.)
Information Science
Genetic Association Studies
Information Science
National Human Genome Research Institute (U.S.)
Research Personnel
Population
Software
Radiation Hybrid Mapping
Chromosome Mapping
Maintenance
Human Genome Project
Menopause
Genes
Infertility
Single Nucleotide Polymorphism
Follicular Atresia

Research Output 1989 2019

16 Citations (Scopus)

Genetic analyses of diverse populations improves discovery for complex traits

Wojcik, G. L., Graff, M., Nishimura, K. K., Tao, R., Haessler, J., Gignoux, C. R., Highland, H. M., Patel, Y. M., Sorokin, E. P., Avery, C. L., Belbin, G. M., Bien, S. A., Cheng, I., Cullina, S., Hodonsky, C. J., Hu, Y., Huckins, L. M., Jeff, J., Justice, A. E., Kocarnik, J. M. & 66 others, Lim, U., Lin, B. M., Lu, Y., Nelson, S. C., Park, S. S. L., Poisner, H., Preuss, M. H., Richard, M. A., Schurmann, C., Setiawan, V. W., Sockell, A., Vahi, K., Verbanck, M., Vishnu, A., Walker, R. W., Young, K. L., Zubair, N., Acuña-Alonso, V., Ambite, J. L., Barnes, K. C., Boerwinkle, E., Bottinger, E. P., Bustamante, C. D., Caberto, C., Canizales-Quinteros, S., Conomos, M. P., Deelman, E., Do, R., Doheny, K., Fernández-Rhodes, L., Fornage, M., Hailu, B., Heiss, G., Henn, B. M., Hindorff, L. A., Jackson, R. D., Laurie, C. A., Laurie, C. C., Li, Y., Lin, D. Y., Moreno-Estrada, A., Nadkarni, G., Norman, P. J., Pooler, L. C., Reiner, A. P., Romm, J., Sabatti, C., Sandoval, K., Sheng, X., Stahl, E. A., Stram, D. O., Thornton, T. A., Wassel, C. L., Wilkens, L. R., Winkler, C. A., Yoneyama, S., Buyske, S., Haiman, C. A., Kooperberg, C., Le Marchand, L., Loos, R. J. F., Matise, T. C., North, K. E., Peters, U., Kenny, E. E. & Carlson, C. S., Jun 27 2019, In : Nature. 570, 7762, p. 514-518 5 p.

Rutgers, The State University

Research output: Contribution to journalLetter

Population
Genome-Wide Association Study
Healthcare Disparities
Genetic Research
Precision Medicine
1 Citation (Scopus)

Genetics of chronic kidney disease stages across ancestries: The PAGE study

Lin, B. M., Nadkarni, G. N., Tao, R., Graff, M., Fornage, M., Buyske, S., Matise, T. C., Highland, H. M., Wilkens, L. R., Carlson, C. S., Lani Park, S., Wendy Setiawan, V., Ambite, J. L., Heiss, G., Boerwinkle, E., Lin, D. Y., Morris, A. P., Loos, R. J. F., Kooperberg, C., North, K. E. & 2 others, Wassel, C. L. & Franceschini, N., Jan 1 2019, In : Frontiers in Genetics. 10, MAY, 494.

Rutgers, The State University

Research output: Contribution to journalArticle

Open Access
Genomics
Chronic Renal Insufficiency
Epidemiology
Population
Chronic Kidney Failure
12 Citations (Scopus)

Insights into genetics, human biology and disease gleaned from family based genomic studies

Centers for Mendelian Genomics, Apr 1 2019, In : Genetics in Medicine. 21, 4, p. 798-812 15 p.

Rutgers, The State University

Research output: Contribution to journalReview article

Medical Genetics
Genomics
Rare Diseases
Human Genome
Genes
1 Citation (Scopus)

The Future of Genomic Studies Must Be Globally Representative: Perspectives from PAGE

Bien, S. A., Wojcik, G. L., Hodonsky, C. J., Gignoux, C. R., Cheng, I., Matise, T., Peters, U., Kenny, E. E. & North, K. E., Aug 31 2019, In : Annual Review of Genomics and Human Genetics. 20, p. 181-200 20 p.

Rutgers, The State University

Research output: Contribution to journalReview article

Genomics
Epidemiology
Population
Molecular Epidemiology
Medical Genetics
6 Citations (Scopus)

Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects

Regier, A. A., Farjoun, Y., Larson, D. E., Krasheninina, O., Kang, H. M., Howrigan, D. P., Chen, B. J., Kher, M., Banks, E., Ames, D. C., English, A. C., Li, H., Xing, J., Zhang, Y., Matise, T., Abecasis, G. R., Salerno, W., Zody, M. C., Neale, B. M. & Hall, I. M., Dec 1 2018, In : Nature communications. 9, 1, 4038.

Rutgers, The State University

Research output: Contribution to journalArticle

sequencing
genome
Medical Genetics
equivalence
Pipelines