A meta-analysis of genome-wide association studies identifies 17 new Parkinson's disease risk loci von Chang, Diana, Nalls, Mike A, Hallgrímsdóttir, Ingileif B, Hunkapiller, Julie, van der Brug, Marcel, Cai, Fang, Kerchner, Geoffrey A, Ayalon, Gai, Bingol, Baris, Sheng, Morgan, Hinds, David, Behrens, Timothy W, Singleton, Andrew B, Bhangale, Tushar R, Graham, Robert R

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Association of NCF2, IKZF1, IRF8, IFIH1, and TYK2 with systemic lupus erythematosus von Cunninghame Graham, Deborah S, Morris, David L, Bhangale, Tushar R, Criswell, Lindsey A, Syvänen, Ann-Christine, Rönnblom, Lars, Behrens, Timothy W, Graham, Robert R, Vyse, Timothy J

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Paired Immunoglobulin-like Type 2 Receptor Alpha G78R variant alters ligand binding and confers protection to Alzheimer's disease von Rathore, Nisha, Ramani, Sree Ranjani, Pantua, Homer, Payandeh, Jian, Bhangale, Tushar, Wuster, Arthur, Kapoor, Manav, Sun, Yonglian, Kapadia, Sharookh B, Gonzalez, Lino, Zarrin, Ali A, Goate, Alison, Hansen, David V, Behrens, Timothy W, Graham, Robert R

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LACC1 Regulates TNF and IL-17 in Mouse Models of Arthritis and Inflammation von Skon-Hegg, Cara, Zhang, Juan, Wu, Xiumin, Sagolla, Meredith, Ota, Naruhisa, Wuster, Arthur, Tom, Jennifer, Doran, Emma, Ramamoorthi, Nandhini, Caplazi, Patrick, Monroe, John, Lee, Wyne P, Behrens, Timothy W

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RAC2 loss-of-function mutation in 2 siblings with characteristics of common variable immunodeficiency von Alkhairy, Omar K., MD, Rezaei, Nima, MD, PhD, Graham, Robert R., PhD, Abolhassani, Hassan, MD, Borte, Stephan, MD, Hultenby, Kjell, PhD, Wu, Chenglin, PhD, Aghamohammadi, Asghar, MD, PhD, Williams, David A., MD, Behrens, Timothy W., MD, Hammarström, Lennart, MD, PhD, Pan-Hammarström, Qiang, MD, PhD

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Functional studies on the IBD susceptibility gene IL23R implicate reduced receptor function in the protective genetic variant R381Q von Pidasheva, Svetlana, Trifari, Sara, Phillips, Anne, Hackney, Jason A, Ma, Yan, Smith, Ashley, Sohn, Sue J, Spits, Hergen, Little, Randall D, Behrens, Timothy W, Honigberg, Lee, Ghilardi, Nico, Clark, Hilary F

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The genetics of type I interferon in systemic lupus erythematosus von Bronson, Paola G, Chaivorapol, Christina, Ortmann, Ward, Behrens, Timothy W, Graham, Robert R

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A rare mutation in UNC5C predisposes to late-onset Alzheimer's disease and increases neuronal cell death von Wetzel-Smith, Monica K, Hunkapiller, Julie, Bhangale, Tushar R, Srinivasan, Karpagam, Maloney, Janice A, Atwal, Jasvinder K, Sa, Susan M, B Yaylaoglu, Murat, Foreman, Oded, Ortmann, Ward, Rathore, Nisha, Hansen, David V, Tessier-Lavigne, Marc, Mayeux, Richard, Pericak-Vance, Margaret, Haines, Jonathan, Farrer, Lindsay A, Schellenberg, Gerard D, Goate, Alison, Behrens, Timothy W, Cruchaga, Carlos, Watts, Ryan J, Graham, Robert R

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Identifying and mitigating batch effects in whole genome sequencing data von Tom, Jennifer A, Reeder, Jens, Forrest, William F, Graham, Robert R, Hunkapiller, Julie, Behrens, Timothy W, Bhangale, Tushar R

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Interferon-Inducible Gene Expression Signature in Peripheral Blood Cells of Patients with Severe Lupus von Baechler, Emily C., Batliwalla, Franak M., Karypis, George, Gaffney, Patrick M., Ortmann, Ward A., Espe, Karl J., Shark, Katherine B., Grande, William J., Hughes, Karis M., Kapur, Vivek, Gregersen, Peter K., Behrens, Timothy W.

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Selective IgA deficiency in autoimmune diseases von Wang, Ning, Shen, Nan, Vyse, Timothy J, Anand, Vidya, Gunnarson, Iva, Sturfelt, Gunnar, Rantapää-Dahlqvist, Solbritt, Elvin, Kerstin, Truedsson, Lennart, Andersson, Bengt A, Dahle, Charlotte, Ortqvist, Eva, Gregersen, Peter K, Behrens, Timothy W, Hammarström, Lennart

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Genetics of autoimmune diseases - disorders of immune homeostasis von Gregersen, Peter K, Behrens, Timothy W

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Transmembrane activator and calcium-modulating cyclophilin ligand interactor mutations in common variable immunodeficiency: Clinical and immunologic outcomes in heterozygotes von Zhang, Li, Radigan, Lin, Salzer, Ulrich, MD, Behrens, Timothy W., MD, Grimbacher, Bodo, MD, Diaz, George, MD, PhD, Bussel, James, MD, Cunningham-Rundles, Charlotte, MD, PhD

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Elevated serum levels of interferon-regulated chemokines are biomarkers for active human systemic lupus erythematosus von Bauer, Jason W, Baechler, Emily C, Petri, Michelle, Batliwalla, Franak M, Crawford, Dianna, Ortmann, Ward A, Espe, Karl J, Li, Wentian, Patel, Dhavalkumar D, Gregersen, Peter K, Behrens, Timothy W

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The chemokine receptor CXCR7 functions to regulate cardiac valve remodeling von Yu, Sangho, Crawford, Dianna, Tsuchihashi, Takatoshi, Behrens, Timothy W., Srivastava, Deepak

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Polymorphism at the TNF superfamily gene TNFSF4 confers susceptibility to systemic lupus erythematosus von Vyse, Timothy J, Graham, Deborah S Cunninghame, Graham, Robert R, Manku, Harinder, Wong, Andrew K, Whittaker, John C, Gaffney, Patrick M, Moser, Kathy L, Rioux, John D, Altshuler, David, Behrens, Timothy W

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The emerging role of interferon in human systemic lupus erythematosus von Baechler, Emily C, Gregersen, Peter K, Behrens, Timothy W

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Delineating the Genetic Basis of Systemic Lupus Erythematosus von Wakeland, Edward K, Liu, Kui, Graham, Robert R, Behrens, Timothy W

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STXBP6 and B3GNT6 Genes are Associated With Selective IgA Deficiency von Lim, Che Kang, Bronson, Paola G, Varade, Jezabel, Behrens, Timothy W, Hammarström, Lennart

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Reexamining the role of TACI coding variants in common variable immunodeficiency and selective IgA deficiency von Pan-Hammarström, Qiang, Hammarström, Lennart, Salzer, Ulrich, Du, Likun, Björkander, Janne, Cunningham-Rundles, Charlotte, Nelson, David L, Bacchelli, Chiara, Gaspar, H Bobby, Offer, Steven, Behrens, Timothy W, Grimbacher, Bodo

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