Endosomal Toll-like receptors in clinically overt and silent autoimmunity by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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 by 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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