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Author Details

Julie Hunkapiller
Genentech Inc.
2010
19
11
Nevan J Krogan (CM4AI)
PMIDPaper TitleJournal TitlePublished Year
36829046Author Correction: FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
36653562FinnGen provides genetic insights from a well-phenotyped isolated population.Nature2023
35263013Allelic variation in HLA-DRB1 is associated with development of antidrug antibodies in cancer patients treated with atezolizumab that are neutralizing in vitro.Clin Transl Sci2022
35368043A whole genome sequencing study of moderate to severe asthma identifies a lung function locus associated with asthma risk.Sci Rep2022
32940337In silico tools for accurate HLA and KIR inference from clinical sequencing data empower immunogenetics on individual-patient and population scales.Brief Bioinform2021
32430334Polygenic risk for skin autoimmunity impacts immune checkpoint blockade in bladder cancer.Proc Natl Acad Sci U S A2020
29550837Previously reported placebo-response-associated variants do not predict patient outcomes in inflammatory disease Phase III trial placebo arms.Genes Immun2019
30997344Influence of genetic copy number variants of the human GLUT3 glucose transporter gene <i>SLC2A3</i> on protein expression, glycolysis and rheumatoid arthritis risk: A genetic replication study.Mol Genet Metab Rep2019
30366082Enabling genome-wide association testing with multiple diseases and no healthy controls.Gene2019
29725081Publisher Correction: Natural variation in the parameters of innate immune cells is preferentially driven by genetic factors.Nat Immunol2018
29891356Analysis of protein-altering variants in telomerase genes and their association with MUC5B common variant status in patients with idiopathic pulmonary fibrosis: a candidate gene sequencing study.Lancet Respir Med2018
29476184Natural variation in the parameters of innate immune cells is preferentially driven by genetic factors.Nat Immunol2018
28892059A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci.Nat Genet2017
28738841Identifying and mitigating batch effects in whole genome sequencing data.BMC Bioinformatics2017
25419706A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death.Nat Med2014
22438827Polycomb-like 3 promotes polycomb repressive complex 2 binding to CpG islands and embryonic stem cell self-renewal.PLoS Genet2012
20873986The ciliogenic protein Oral-Facial-Digital 1 regulates the neuronal differentiation of embryonic stem cells.Stem Cells Dev2011
19966808Floxin, a resource for genetically engineering mouse ESCs.Nat Methods2010
20144788Polycomb-like 2 associates with PRC2 and regulates transcriptional networks during mouse embryonic stem cell self-renewal and differentiation.Cell Stem Cell2010
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Collaborators

Genentech Inc.
Co-authored papers 8
Genentech Inc.
Co-authored papers 8
Genentech Inc.
Co-authored papers 7
Cardiovascular Research Institute
Co-authored papers 4
Genentech Inc.
Co-authored papers 4
Co-authored papers 3
Genentech Inc.
Co-authored papers 3
Co-authored papers 2
The University of Chicago
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Institute for Molecular Medicine Finland (FIMM), University of Helsinki
Co-authored papers 2
Massachusetts General Hospital
Co-authored papers 2
Institute of Biomedicine, University of Turku
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
University of California San Francisco
Co-authored papers 2
Co-authored papers 2
University of Minnesota School of Medicine
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Co-authored papers 2
Genentech Inc.
Co-authored papers 2