• 18515 Citations
  • 70 Scopus h-Index
1991 …2019
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Fingerprint Dive into the research topics where Mariza De Andrade is active. These topic labels come from the works of this person. Together they form a unique fingerprint.

  • 6 Similar Profiles
Single Nucleotide Polymorphism Medicine & Life Sciences
Genome-Wide Association Study Medicine & Life Sciences
Genes Medicine & Life Sciences
Lung Neoplasms Medicine & Life Sciences
Pancreatic Neoplasms Medicine & Life Sciences
Electronic Health Records Medicine & Life Sciences
Genome Medicine & Life Sciences
Alleles Medicine & Life Sciences

Network Recent external collaboration on country level. Dive into details by clicking on the dots.

Projects 1998 2019

Mayo Clinic SPORE in Pancreatic Cancer

Cohen, P. A., Urrutia, R. A., De Andrade, M., Chari, S. T., Lingle, W. L., Billadeau, D. D., Petersen, G. M., Couch, F. J., Mukhopadhyay, D., Chini, E. N., Smyrk, T. C., Oberg, A. L., Gendler, S. J., Couch, F. J., Mukherjee, P., Mukherjee, P., Andrade, M., Fernandez-Zapico, M. E. & Billadeau, D. D.

National Institutes of Health

9/29/038/31/19

Project: Research project

Pancreatic Neoplasms
Research
Biostatistics
Glycogen Synthase Kinase 3
Neoplasms
Organized Financing
Blood Pressure
Hypertension
National Heart, Lung, and Blood Institute (U.S.)
Molecular Epidemiology
Alopecia Areata
Histocompatibility Antigens
Hair Follicle
Alopecia
Virus Diseases

Research Output 1991 2019

  • 18515 Citations
  • 70 Scopus h-Index
  • 308 Article
  • 3 Review article
  • 2 Comment/debate
  • 1 Chapter

A phenome-wide association study to discover pleiotropic effects of PCSK9, APOB, and LDLR

Safarova, M. S., Satterfield, B. A., Fan, X., Austin, E. E., Ye, Z., Bastarache, L., Zheng, N., Ritchie, M. D., Borthwick, K. M., Williams, M. S., Larson, E. B., Scrol, A., Jarvik, G. P., Crosslin, D. R., Leppig, K., Rasmussen-Torvik, L. J., Pendergrass, S. A., Sturm, A. C., Namjou, B., Shah, A. S. & 12 others, Carroll, R. J., Chung, W. K., Wei, W. Q., Feng, Q. P., Stein, C. M., Roden, D. M., Manolio, T. A., Schaid, D. J., Denny, J. C., Hebbring, S. J., De Andrade, M. & Kullo, I. J., Dec 1 2019, In : npj Genomic Medicine. 4, 1, 3.

Research output: Contribution to journalArticle

Open Access
Electronic Health Records
Precision Medicine
Genetic Models
Myopia
Linkage Disequilibrium
14 Citations (Scopus)

Association of the PHACTR1/EDN1 Genetic Locus With Spontaneous Coronary Artery Dissection

DISCO Consortium & CARDIoGRAMPlusC4D Study Group, Jan 8 2019, In : Journal of the American College of Cardiology. 73, 1, p. 58-66 9 p.

Research output: Contribution to journalArticle

Genetic Loci
Endothelin-1
Fibromuscular Dysplasia
Odds Ratio
Confidence Intervals
4 Citations (Scopus)

Associations of Mitochondrial and Nuclear Mitochondrial Variants and Genes with Seven Metabolic Traits

Kraja, A. T., Liu, C., Fetterman, J. L., Graff, M., Have, C. T., Gu, C., Yanek, L. R., Feitosa, M. F., Arking, D. E., Chasman, D. I., Young, K., Ligthart, S., Hill, W. D., Weiss, S., Luan, J., Giulianini, F., Li-Gao, R., Hartwig, F. P., Lin, S. J., Wang, L. & 132 others, Richardson, T. G., Yao, J., Fernandez, E. P., Ghanbari, M., Wojczynski, M. K., Lee, W. J., Argos, M., Armasu, S. M., Barve, R. A., Ryan, K. A., An, P., Baranski, T. J., Bielinski, S. J., Bowden, D. W., Broeckel, U., Christensen, K., Chu, A. Y., Corley, J., Cox, S. R., Uitterlinden, A. G., Rivadeneira, F., Cropp, C. D., Daw, E. W., van Heemst, D., de las Fuentes, L., Gao, H., Tzoulaki, I., Ahluwalia, T. S., de Mutsert, R., Emery, L. S., Erzurumluoglu, A. M., Perry, J. A., Fu, M., Forouhi, N. G., Gu, Z., Hai, Y., Harris, S. E., Hemani, G., Hunt, S. C., Irvin, M. R., Jonsson, A. E., Justice, A. E., Kerrison, N. D., Larson, N., Lin, K. H., Love-Gregory, L. D., Mathias, R. A., Lee, J. H., Nauck, M., Noordam, R., Ong, K. K., Pankow, J., Patki, A., Pattie, A., Petersmann, A., Qi, Q., Ribel-Madsen, R., Rohde, R., Sandow, K., Schnurr, T. M., Sofer, T., Starr, J. M., Taylor, A. M., Teumer, A., Timpson, N. J., de Haan, H. G., Wang, Y., Weeke, P. E., Williams, C., Wu, H., Yang, W., Zeng, D., Witte, D. R., Weir, B. S., Wareham, N. J., Vestergaard, H., Turner, S. T., Torp-Pedersen, C., Stergiakouli, E., Sheu, W. H. H., Rosendaal, F. R., Ikram, M. A., Franco, O. H., Ridker, P. M., Perls, T. T., Pedersen, O., Nohr, E. A., Newman, A. B., Linneberg, A., Langenberg, C., Kilpeläinen, T. O., Kardia, S. L. R., Jørgensen, M. E., Jørgensen, T., Sørensen, T. I. A., Homuth, G., Hansen, T., Goodarzi, M. O., Deary, I. J., Christensen, C., Chen, Y. D. I., Chakravarti, A., Brandslund, I., Bonnelykke, K., Taylor, K. D., Wilson, J. G., Rodriguez, S., Davies, G., Horta, B. L., Thyagarajan, B., Rao, D. C., Grarup, N., Davila-Roman, V. G., Hudson, G., Guo, X., Arnett, D. K., Hayward, C., Vaidya, D., Mook-Kanamori, D. O., Tiwari, H. K., Levy, D., Loos, R. J. F., Dehghan, A., Elliott, P., Malik, A. N., Scott, R. A., Becker, D. M., De Andrade, M., Province, M. A., Meigs, J. B., Rotter, J. I. & North, K. E., Jan 3 2019, In : American Journal of Human Genetics. 104, 1, p. 112-138 27 p.

Research output: Contribution to journalArticle

Mitochondrial Genes
Mitochondria
Mitochondrial DNA
Genes
Waist-Hip Ratio
1 Citation (Scopus)

Atlas-CNV: a validated approach to call single-exon CNVs in the eMERGESeq gene panel

Chiang, T., Liu, X., Wu, T. J., Hu, J., Sedlazeck, F. J., White, S., Schaid, D., Andrade, M. D., Jarvik, G. P., Crosslin, D., Stanaway, I., Carrell, D. S., Connolly, J. J., Hakonarson, H., Groopman, E. E., Gharavi, A. G., Fedotov, A., Bi, W., Leduc, M. S., Murdock, D. R. & 10 others, Jiang, Y., Meng, L., Eng, C. M., Wen, S., Yang, Y., Muzny, D. M., Boerwinkle, E., Salerno, W., Venner, E. & Gibbs, R. A., Jan 1 2019, In : Genetics in Medicine.

Research output: Contribution to journalArticle

Open Access
Atlases
Exons
Genes
Ligation
Software
1 Citation (Scopus)

Harmonizing Clinical Sequencing and Interpretation for the eMERGE III Network

the eMERGE Consortium, Sep 5 2019, In : American journal of human genetics. 105, 3, p. 588-605 18 p.

Research output: Contribution to journalArticle

Genetic Testing
Clinical Decision Support Systems
Precision Medicine
Gene Targeting
Information Dissemination