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Natali Gulbahce

Researcher at University of California, San Francisco

Publications -  52
Citations -  7599

Natali Gulbahce is an academic researcher from University of California, San Francisco. The author has contributed to research in topics: Genome & Genomics. The author has an hindex of 23, co-authored 49 publications receiving 6456 citations. Previous affiliations of Natali Gulbahce include Northeastern University & California Institute for Quantitative Biosciences.

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Network Medicine: A Network-Based Approach to Human Disease

TL;DR: Advances in this direction are essential for identifying new disease genes, for uncovering the biological significance of disease-associated mutations identified by genome-wide association studies and full-genome sequencing, and for identifying drug targets and biomarkers for complex diseases.
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Global landscape of HIV-human protein complexes

TL;DR: The use of affinity tagging and purification mass spectrometry is reported to determine systematically the physical interactions of all 18 HIV-1 proteins and polyproteins with host proteins in two different human cell lines (HEK293 and Jurkat).
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Extensive sequencing of seven human genomes to characterize benchmark reference materials

TL;DR: A large, diverse set of sequencing data for seven human genomes is described; five are current or candidate NIST Reference Materials and two Personal Genome Project trios, one of Ashkenazim Jewish ancestry and one of Chinese ancestry are described.
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Interpreting cancer genomes using systematic host network perturbations by tumour virus proteins

TL;DR: It is shown that systematic analyses of host targets of viral proteins can identify cancer genes with a success rate on a par with their identification through functional genomics and large-scale cataloguing of tumour mutations, to increase the specificity of cancer gene identification.
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MicroRNA-21 Integrates Pathogenic Signaling to Control Pulmonary Hypertension Results of a Network Bioinformatics Approach

TL;DR: In this article, microRNA-21 (miR-21) is predicted as a PH-modifying microRNA, regulating targets integral to bone morphogenetic protein (BMP) and Rho/Rho-kinase signaling as well as functional pathways associated with hypoxia, inflammation, and genetic haploinsufficiency of BMP receptor type 2.