Effects of immunomodulatory drugs on depressive symptoms: A mega-analysis of randomized, placebo-controlled clinical trials in inflammatory disorders
Wittenberg, Gayle M., Stylianou, Annie, Zhang, Yun, Sun, Yu, Gupta, Ashutosh, Jagannatha, P. S., Wang, Dai, Hsu, Benjamin, Curran, Mark E., Khan, Shahid, Chen, Guang, Bullmore, Edward T., Drevets, Wayne C.
Published in Molecular psychiatry (01.06.2020)
Published in Molecular psychiatry (01.06.2020)
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Modular Analysis of Peripheral Blood Gene Expression in Rheumatoid Arthritis Captures Reproducible Gene Expression Changes in Tumor Necrosis Factor Responders
Oswald, Michaela, Curran, Mark E., Lamberth, Sarah L., Townsend, Robert M., Hamilton, Jennifer D., Chernoff, David N., Carulli, John, Townsend, Michael J., Weinblatt, Michael E., Kern, Marlena, Pond, Cassandra M., Lee, Annette, Gregersen, Peter K.
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.02.2015)
Published in Arthritis & rheumatology (Hoboken, N.J.) (01.02.2015)
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Ethnic Differences in Cardiac Potassium Channel Variants: Implications for Genetic Susceptibility to Sudden Cardiac Death and Genetic Testing for Congenital Long QT Syndrome
Ackerman, Michael J., Tester, David J., Jones, Gregg S., Will, Melissa L., Burrow, Christopher R., Curran, Mark E.
Published in Mayo Clinic proceedings (01.12.2003)
Published in Mayo Clinic proceedings (01.12.2003)
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Spectrum and prevalence of cardiac sodium channel variants among black, white, Asian, and Hispanic individuals: implications for arrhythmogenic susceptibility and Brugada/long QT syndrome genetic testing
Ackerman, Michael J, Splawski, Igor, Makielski, Jonathan C, Tester, David J, Will, Melissa L, Timothy, Katherine W, Keating, Mark T, Jones, Gregg, Chadha, Monica, Burrow, Christopher R, Stephens, J Claiborne, Xu, Chuanbo, Judson, Richard, Curran, Mark E
Published in Heart rhythm (01.11.2004)
Published in Heart rhythm (01.11.2004)
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Idiopathic congenital central hypoventilation syndrome: Analysis of genes pertinent to early autonomic nervous system embryologic development and identification of mutations in PHOX2b
Weese-Mayer, Debra E., Berry-Kravis, Elizabeth M., Zhou, Lili, Maher, Brion S., Silvestri, Jean M., Curran, Mark E., Marazita, Mary L.
Published in American journal of medical genetics. Part A (15.12.2003)
Published in American journal of medical genetics. Part A (15.12.2003)
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A mechanistic link between an inherited and an acquird cardiac arrthytmia: HERG encodes the IKr potassium channel
Sanguinetti, Michael C, Jiang, Changan, Curran, Mark E, Keating, Mark T
Published in Cell (01.04.1995)
Published in Cell (01.04.1995)
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A molecular basis for cardiac arrhythmia: HERG mutations cause long QT syndrome
Curran, Mark E, Splawski, Igor, Timothy, Katherine W, Vincen, G.Michael, Green, Eric D, Keating, Mark T
Published in Cell (10.03.1995)
Published in Cell (10.03.1995)
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Integrative genomic deconvolution of rheumatoid arthritis GWAS loci into gene and cell type associations
Walsh, Alice M, Whitaker, John W, Huang, C Chris, Cherkas, Yauheniya, Lamberth, Sarah L, Brodmerkel, Carrie, Curran, Mark E, Dobrin, Radu
Published in Genome Biology (30.04.2016)
Published in Genome Biology (30.04.2016)
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Sex stratification of an inflammatory bowel disease genome search shows male-specific linkage to the HLA region of chromosome 6
Fisher, Sheila A, Hampe, Jochen, Macpherson, Andrew J S, Forbes, Alastair, Lennard-Jones, John E, Schreiber, Stefan, Curran, Mark E, Mathew, Christopher G, Lewis, Cathryn M
Published in European journal of human genetics : EJHG (01.04.2002)
Published in European journal of human genetics : EJHG (01.04.2002)
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Group-based variant calling leveraging next-generation supercomputing for large-scale whole-genome sequencing studies
Standish, Kristopher A, Carland, Tristan M, Lockwood, Glenn K, Pfeiffer, Wayne, Tatineni, Mahidhar, Huang, C Chris, Lamberth, Sarah, Cherkas, Yauheniya, Brodmerkel, Carrie, Jaeger, Ed, Smith, Lance, Rajagopal, Gunaretnam, Curran, Mark E, Schork, Nicholas J
Published in BMC bioinformatics (22.09.2015)
Published in BMC bioinformatics (22.09.2015)
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Sudden infant death syndrome: Case-control frequency differences at genes pertinent to early autonomic nervous system embryologic development
WEESE-MAYER, Debra E, BERRY-KRAVIS, Elizabeth M, ZHOU, Lili, MAHER, Brion S, CURRAN, Mark E, SILVESTRI, Jean M, MARAZITA, Mary L
Published in Pediatric research (01.09.2004)
Published in Pediatric research (01.09.2004)
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Fast inactivation causes rectification of the IKr channel
Spector, P S, Curran, M E, Zou, A, Keating, M T, Sanguinetti, M C
Published in The Journal of general physiology (01.05.1996)
Published in The Journal of general physiology (01.05.1996)
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Sudden infant death syndrome: Association with a promoter polymorphism of the serotonin transporter gene
Weese-Mayer, Debra E., Berry-Kravis, Elizabeth M., Maher, Brion S., Silvestri, Jean M., Curran, Mark E., Marazita, Mary L.
Published in American journal of medical genetics. Part A (15.03.2003)
Published in American journal of medical genetics. Part A (15.03.2003)
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Linkage of Inflammatory Bowel Disease to Human Chromosome 6p
Hampe, Jochen, Shaw, Sarah H., Saiz, Robert, Leysens, Nancy, Lantermann, Annette, Mascheretti, Silvia, Lynch, Nicholas J., MacPherson, Andrew J.S., Bridger, Stephen, van Deventer, Sander, Stokkers, Pieter, Morin, Phil, Mirza, Mudassar M., Forbes, Alastair, Lennard-Jones, John E., Mathew, Christopher G., Curran, Mark E., Schreiber, Stefan
Published in American journal of human genetics (01.12.1999)
Published in American journal of human genetics (01.12.1999)
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Direct Activation of an Inwardly Rectifying Potassium Channel by Arachidonic Acid
Liu, Y, Liu, D, Heath, L, Meyers, D M, Krafte, D S, Wagoner, P K, Silvia, C P, Yu, W, Curran, M E
Published in Molecular pharmacology (01.05.2001)
Published in Molecular pharmacology (01.05.2001)
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