J. Derry

发表

Integrative genomics and drug development.

E. Schadt, P. Lum, J. Derry, 2009, Pharmacogenomics.

Mapping the Genetic Architecture of Gene Expression in Human Liver

John D. Storey, K. Hao, A. Kasarskis, 2008, PLoS biology.

Identification of Genes and Networks Driving Cardiovascular and Metabolic Phenotypes in a Mouse F2 Intercross

A. Kasarskis, Bin Zhang, C. Molony, 2010, PloS one.

Developing predictive molecular maps of human disease through community-based modeling

S. Friend, C. Suver, B. Bot, 2011, Nature Genetics.

Gene Expression Elucidates Functional Impact of Polygenic Risk for Schizophrenia

Benjamin A. Logsdon, Kristen K. Dang, K. Roeder, 2016, Nature Neuroscience.

Molecular characterization of the human interleukin (IL)-17 receptor.

J. Derry, M. Spriggs, Z. Yao, 1997, Cytokine.

Cutting Edge: Interleukin 17 Signals through a Heteromeric Receptor Complex

J. Derry, M. Wolfson, J. Peschon, 2006, The Journal of Immunology.

Lung eQTLs to Help Reveal the Molecular Underpinnings of Asthma

David C. Nickle, Don D. Sin, Ke Hao, 2012, PLoS genetics.

Landscape of Conditional eQTL in Dorsolateral Prefrontal Cortex and Co-localization with Schizophrenia GWAS

Benjamin A. Logsdon, Kristen K. Dang, Benjamin S. Glicksberg, 2018, American journal of human genetics.

A transcript map of a 2-Mb BAC contig in the proximal portion of the mouse X chromosome and regional mapping of the scurfy mutation.

J. Derry, D. Toy, P R Baum, 2000, Genomics.

Transgenic rescue of the tattered phenotype by using a BAC encoding Ebp

J. Derry, Y. Boyd, G. Means, 2001, Mammalian Genome.

The mouse homolog of the Wiskott-Aldrich syndrome protein (WASP) gene is highly conserved and maps near the scurfy (sf) mutation on the X chromosome.

U. Francke, V. Godfrey, J. Derry, 1995, Genomics.

Mutations in a Δ8-Δ7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata

J. Derry, A. Meindl, G. Herman, 1999, Nature Genetics.

Sox5 regulates beta-cell phenotype and is reduced in type 2 diabetes

Ivan G. Costa, L. Eliasson, B. Mecham, 2017, Nature Communications.

Resolving candidate genes of mouse skeletal muscle QTL via RNA-Seq and expression network analyses

J. Derry, A. M. Carroll, D. Blizard, 2012, BMC Genomics.

Impaired dendritic-cell function in ectodermal dysplasia with immune deficiency is linked to defective NEMO ubiquitination.

J. Derry, Shuying Liu, Chi A. Ma, 2006, Blood.

Flow cytometric determination of intracytoplasmic Wiskott-Aldrich syndrome protein in peripheral blood lymphocyte subpopulations.

J. Derry, M. Minegishi, K. Horibe, 2002, Journal of immunological methods.

Tumor suppressor CYLD regulates acute lung injury in lethal Streptococcus pneumoniae infections.

J. Derry, R. Flavell, P. Bourne, 2007, Immunity.

Impaired regulation of NF-kappaB and increased susceptibility to colitis-associated tumorigenesis in CYLD-deficient mice.

J. Derry, Chi A. Ma, Ashish Jain, 2006, The Journal of clinical investigation.

A Systems Biology Framework Identifies Molecular Underpinnings of Coronary Heart Disease

Xia Yang, Peter J. Munson, Roby Joehanes, 2013, Arteriosclerosis, thrombosis, and vascular biology.

Differentially regulated functional gene clusters identified during ischemia and reperfusion in isolated cardiac myocytes using coverslip hypoxia.

J. Derry, K. Pitts, K. Kerkof, 2008, Journal of pharmacological and toxicological methods.

Expression of human Wiskott–Aldrich syndrome protein in patients’ cells leads to partial correction of a phenotypic abnormality of cell surface glycoproteins

S. Tsuboi, U. Francke, J. Derry, 2000, Gene Therapy.

Osteoclast Differentiation Is Impaired in the Absence of Inhibitor of κB Kinase α*

S. Akira, J. Derry, K. Takeda, 2004, Journal of Biological Chemistry.

Chromosomal localization of GABAA receptor subunit genes: relationship to human genetic disease

P. Seeburg, P. Schofield, J. Derry, 1989, Neuron.

RIP4 Is an Ankyrin Repeat-Containing Kinase Essential for Keratinocyte Differentiation

J. Derry, J. Peschon, S. Kanaly, 2002, Current Biology.

The Wiskott-Aldrich syndrome and X-linked congenital thrombocytopenia are caused by mutations of the same gene.

U. Francke, J. Derry, H. Ochs, 1995, Blood.

WASP gene mutations in Wiskott-Aldrich syndrome and X-linked thrombocytopenia.

X. Estivill, U. Francke, J. Derry, 1995, Human molecular genetics.

Inflammation and Inflammatory Bowel Disease

J. Derry, T. Born, S. Kanaly, 2022 .

Heteromeric Receptor Complex Cutting Edge : Interleukin 17 Signals through Peschon

J. Derry, M. Wolfson, J. Peschon, 2006 .

Dystroglycan: brain localisation and chromosome mapping in the mouse.

J. Derry, E. Barnard, D. Górecki, 1994, Human molecular genetics.

Crowdsourcing genetic prediction of clinical utility in the Rheumatoid Arthritis Responder Challenge

Gustavo Stolovitzky, Henk-Jan Guchelaar, Larry W. Moreland, 2013, Nature Genetics.

Osteoclast differentiation is impaired in the absence of inhibitor of kappa B kinase alpha.

S. Akira, J. Derry, K. Takeda, 2004, The Journal of biological chemistry.

Altered gene expression in slc4a11−/− mouse cornea highlights SLC4A11 roles

J. Derry, B. Alvarez, J. Casey, 2021, Scientific Reports.

Sulforaphane reduces hepatic glucose production and improves glucose control in patients with type 2 diabetes

S. Friend, B. Mecham, J. Derry, 2017, Science Translational Medicine.

Wiskott–Aldrich Syndrome Protein, a Novel Effector for the GTPase CDC42Hs, Is Implicated in Actin Polymerization

U. Francke, J. Derry, Brian Karlak, 1996, Cell.

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome

U. Francke, J. Derry, H. Ochs, 1994, Cell.

Specific NEMO mutations impair CD40-mediated c-Rel activation and B cell terminal differentiation.

J. Orange, J. Derry, E. López-Granados, 2004, The Journal of clinical investigation.

Expression and Study of Ligand‐Gated Ion Channels in Xenopus laevis Oocytes

R. Hansen, J. Derry, A. Kapur, 2007 .

Isolation of a novel gene mutated in Wiskott-Aldrich syndrome.

U. Francke, J. Derry, H. Ochs, 1994, Cell.

Mapping of the glycine receptor α2-subunit gene and the GABAA α3-subunit gene on the mouse X chromosome

J. Derry, P. J. Barnard, 1991 .

Modeling RAS Phenotype in Colorectal Cancer Uncovers Novel Molecular Traits of RAS Dependency and Improves Prediction of Response to Targeted Agents in Patients

Justin Guinney, Claus Bendtsen, Charles Ferté, 2013, Clinical Cancer Research.

Mutations in a delta 8-delta 7 sterol isomerase in the tattered mouse and X-linked dominant chondrodysplasia punctata. jderry@immunex.com.

J. Derry, A. Meindl, G. Herman, 1999, Nature genetics.

Expression of four alternative dystrophin transcripts in brain regions regulated by different promoters.

A. Monaco, J. Derry, E. Barnard, 1992, Human molecular genetics.

Predictive Genes in Adjacent Normal Tissue Are Preferentially Altered by sCNV during Tumorigenesis in Liver Cancer and May Rate Limiting

Justin Guinney, Hongyue Dai, Eric E. Schadt, 2011, PloS one.

Cloning and characterization of a novel zinc finger gene in Xp11.2.

U. Francke, J. Derry, U. Jess, 1995, Genomics.

Nectin-like Protein 2 Defines a Subset of T-cell Zone Dendritic Cells and Is a Ligand for Class-I-restricted T-cell-associated Molecule*♦

J. Derry, D. Branstetter, M. Wolfson, 2005, Journal of Biological Chemistry.

RBM3, a novel human gene in Xp11.23 with a putative RNA-binding domain.

U. Francke, J. Derry, J. Kerns, 1995, Human molecular genetics.

Correction: Lung eQTLs to Help Reveal the Molecular Underpinnings of Asthma

Y. Bossé, K. Hao, D. Postma, 2012, PLoS Genetics.

Secreted frizzled-related protein 4 reduces insulin secretion and is overexpressed in type 2 diabetes.

L. Groop, L. Eliasson, V. Lyssenko, 2012, Cell metabolism.

Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy.

Bin Zhang, T. Gillis, M. MacDonald, 2013, Human molecular genetics.

Physical linkage of the A-raf-1, properdin, synapsin I, and TIMP genes on the human and mouse X chromosomes.

J. Derry, P. J. Barnard, 1992, Genomics.

Mapping of the phosphorylase kinase alpha subunit gene on the mouse X chromosome.

J. Derry, A. S. Ryder-Cook, P. J. Barnard, 1990, Cytogenetics and cell genetics.

Localization of monoamine oxidase A and B genes on the mouse X chromosome.

J. Derry, E. Barnard, N. Lan, 1989, Nucleic acids research.

Dominant effects of the Huntington's disease HTT CAG repeat length are captured in gene-expression data sets by a continuous analysis mathematical modeling strategy.

Bin Zhang, T. Gillis, M. MacDonald, 2013, Human molecular genetics.

Inflammation and Inflammatory Bowel Disease

J. Derry, T. Born, K. Garka, 2022 .