Endosomal Toll-like receptors in clinically overt and silent autoimmunity von Clancy, Robert M., Markham, Androo J., Buyon, Jill P.

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3-hour genome sequencing and targeted analysis to rapidly assess genetic risk von Zalusky, Miranda P.G., Gustafson, Jonas A., Bohaczuk, Stephanie C., Mallory, Ben, Reed, Paxton, Wenger, Tara, Beckman, Erika, Chang, Irene J., Paschal, Cate R., Buchan, Jillian G., Lockwood, Christina M., Puia-Dumitrescu, Mihai, Garalde, Daniel R., Guillory, Joseph, Markham, Androo J., Bamshad, Michael J., Eichler, Evan E., Stergachis, Andrew B., Miller, Danny E.

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Cardiac fibroblast transcriptome analyses support a role for interferogenic, profibrotic, and inflammatory genes in anti-SSA/Ro-associated congenital heart block von Clancy, Robert M, Markham, Androo J, Jackson, Tanisha, Rasmussen, Sara E, Blumenberg, Miroslav, Buyon, Jill P

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Reactivity to the p305 Epitope of the α1G T‐Type Calcium Channel and Autoimmune‐Associated Congenital Heart Block von Markham, Androo J., Rasmussen, Sara E., Salmon, Jane E., Martinez‐Ortiz, Wilnelly, Cardozo, Timothy J., Clancy, Robert M., Buyon, Jill P.

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Targeting downstream transcription factors and epigenetic modifications following Toll-like receptor 7/8 ligation to forestall tissue injury in anti-Ro60 associated heart block von Clancy, Robert M, Markham, Androo J, Reed, Joanne H, Blumenberg, Miroslav, Halushka, Marc K, Buyon, Jill P

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Defining a kinetic mechanism for l-DOPA 2,3 dioxygenase, a single-domain type I extradiol dioxygenase from Streptomyces lincolnensis von Colabroy, Keri L., Smith, Ian R., Vlahos, Alexander H.S., Markham, Androo J., Jakubik, Matthew E.

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Reactivity to the p305 Epitope of the α 1G T‐Type Calcium Channel and Autoimmune‐Associated Congenital Heart Block von Markham, Androo J., Rasmussen, Sara E., Salmon, Jane E., Martinez‐Ortiz, Wilnelly, Cardozo, Timothy J., Clancy, Robert M., Buyon, Jill P.

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Genome‐Wide Analysis of Structural Variants in Parkinson Disease von Billingsley, Kimberley J., Ding, Jinhui, Jerez, Pilar Alvarez, Illarionova, Anastasia, Levine, Kristin, Grenn, Francis P., Makarious, Mary B., Moore, Anni, Vitale, Daniel, Reed, Xylena, Hernandez, Dena, Torkamani, Ali, Ryten, Mina, Hardy, John, Chia, Ruth, Scholz, Sonja W., Traynor, Bryan J., Dalgard, Clifton L., Ehrlich, Debra J., Tanaka, Toshiko, Ferrucci, Luigi, Beach, Thomas G., Serrano, Geidy E., Quinn, John P., Bubb, Vivien J., Collins, Ryan L, Zhao, Xuefang, Walker, Mark, Pierce‐Hoffman, Emma, Brand, Harrison, Talkowski, Michael E., Casey, Bradford, Cookson, Mark R, Markham, Androo, Nalls, Mike A., Mahmoud, Medhat, Sedlazeck, Fritz J, Blauwendraat, Cornelis, Gibbs, J. Raphael, Singleton, Andrew B.

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Profiling complex repeat expansions in RFC1 in Parkinson’s disease von Alvarez Jerez, Pilar, Daida, Kensuke, Miano-Burkhardt, Abigail, Iwaki, Hirotaka, Malik, Laksh, Cogan, Guillaume, Makarious, Mary B., Sullivan, Roisin, Vandrovcova, Jana, Ding, Jinhui, Gibbs, J. Raphael, Markham, Androo, Nalls, Mike A., Kesharwani, Rupesh K., Sedlazeck, Fritz J., Casey, Bradford, Hardy, John, Houlden, Henry, Blauwendraat, Cornelis, Singleton, Andrew B., Billingsley, Kimberley J.

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Genome-wide analysis of Structural Variants in Parkinson’s Disease von Billingsley, Kimberley J., Ding, Jinhui, Jerez, Pilar Alvarez, Illarionova, Anastasia, Levine, Kristin, Grenn, Francis P., Makarious, Mary B., Moore, Anni, Vitale, Daniel, Reed, Xylena, Hernandez, Dena, Torkamani, Ali, Ryten, Mina, Hardy, John, Chia, Ruth, Scholz, Sonja W., Traynor, Bryan J., Dalgard, Clifton L., Ehrlich, Debra J., Tanaka, Toshiko, Ferrucci, Luigi, Beach, Thomas.G., Serrano, Geidy E., Quinn, John P., Bubb, Vivien J., Collins, Ryan L, Zhao, Xuefang, Walker, Mark, Pierce-Hoffman, Emma, Brand, Harrison, Talkowski, Michael E., Casey, Bradford, Cookson, Mark R, Markham, Androo, Nalls, Mike A., Mahmoud, Medhat, Sedlazeck, Fritz J, Blauwendraat, Cornelis, Gibbs, J. Raphael, Singleton, Andrew B.

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