Publications by authors named "Fabian Grubert"

24Publications

Patient-Specific iPSC-Derived Endothelial Cells Uncover Pathways that Protect against Pulmonary Hypertension in BMPR2 Mutation Carriers.

Cell Stem Cell 2017 04 22;20(4):490-504.e5. Epub 2016 Dec 22.

Vera Moulton Wall Center for Pulmonary Vascular Diseases, Stanford University School of Medicine, Stanford, CA 94305, USA; Stanford Cardiovascular Institute, Stanford University School of Medicine, Stanford, CA 94305, USA; Department of Pediatrics, Stanford University School of Medicine, Stanford, CA 94305, USA. Electronic address:

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http://www.cell.com/cell-stem-cell/pdf/S1934-5909(16)30266-1
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http://linkinghub.elsevier.com/retrieve/pii/S193459091630266
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http://dx.doi.org/10.1016/j.stem.2016.08.019DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5500296PMC
April 2017

Genome-wide map of regulatory interactions in the human genome.

Genome Res 2014 Dec 16;24(12):1905-17. Epub 2014 Sep 16.

Department of Genetics, Stanford University School of Medicine, Stanford, California 94305, USA;

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http://dx.doi.org/10.1101/gr.176586.114DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4248309PMC
December 2014

Defining a personal, allele-specific, and single-molecule long-read transcriptome.

Proc Natl Acad Sci U S A 2014 Jul 24;111(27):9869-74. Epub 2014 Jun 24.

Department of Genetics, Stanford University, Stanford, CA 94305-5120; and

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http://www.pnas.org/lookup/doi/10.1073/pnas.1400447111
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http://dx.doi.org/10.1073/pnas.1400447111DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4103364PMC
July 2014

A single-molecule long-read survey of the human transcriptome.

Nat Biotechnol 2013 Nov 13;31(11):1009-14. Epub 2013 Oct 13.

1] Department of Genetics, Stanford University, Stanford, California, USA. [2] Department of Molecular, Cellular and Developmental Biology, Yale University, New Haven, Connecticut, USA. [3].

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http://www.nature.com/articles/nbt.2705
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http://dx.doi.org/10.1038/nbt.2705DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4075632PMC
November 2013

A procedure for highly specific, sensitive, and unbiased whole-genome amplification.

Proc Natl Acad Sci U S A 2008 Oct 1;105(40):15499-504. Epub 2008 Oct 1.

Department of Genetics, Yale University School of Medicine, New Haven, CT 06520-8005, USA.

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http://dx.doi.org/10.1073/pnas.0808028105DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC2563063PMC
October 2008

Systematic prediction and validation of breakpoints associated with copy-number variants in the human genome.

Proc Natl Acad Sci U S A 2007 Jun 5;104(24):10110-5. Epub 2007 Jun 5.

Departments of Molecular Biophysics and Biochemistry, Yale University School of Medicine, New Haven, CT 06520, USA.

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http://dx.doi.org/10.1073/pnas.0703834104DOI Listing
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC1891248PMC
June 2007