Exercise attenuates PCB-induced changes in the mouse gut microbiome von Choi, Jeong June, Eum, Sung Yong, Rampersaud, Evadnie, Daunert, Sylvia, Abreu, Maria T, Toborek, Michal

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Mutations in UBQLN2 cause dominant X-linked juvenile and adult-onset ALS and ALS/dementia von Deng, Han-Xiang, Chen, Wenjie, Hong, Seong-Tshool, Boycott, Kym M., Gorrie, George H., Siddique, Nailah, Yang, Yi, Fecto, Faisal, Shi, Yong, Zhai, Hong, Jiang, Hujun, Hirano, Makito, Rampersaud, Evadnie, Jansen, Gerard H., Donkervoort, Sandra, Bigio, Eileen H., Brooks, Benjamin R., Ajroud, Kaouther, Sufit, Robert L., Haines, Jonathan L., Mugnaini, Enrico, Pericak-Vance, Margaret A., Siddique, Teepu

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Genome-wide Studies of Copy Number Variation and Exome Sequencing Identify Rare Variants in BAG3 as a Cause of Dilated Cardiomyopathy von Norton, Nadine, Li, Duanxiang, Rieder, Mark J., Siegfried, Jill D., Rampersaud, Evadnie, Züchner, Stephan, Mangos, Steve, Gonzalez-Quintana, Jorge, Wang, Libin, McGee, Sean, Reiser, Jochen, Martin, Eden, Nickerson, Deborah A., Hershberger, Ray E.

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Publisher Correction: The net electrostatic potential and hydration of ABCG2 affect substrate transport von Gose, Tomoka, Aitken, Heather M., Wang, Yao, Lynch, John, Rampersaud, Evadnie, Fukuda, Yu, Wills, Medb, Baril, Stefanie A., Ford, Robert C., Shelat, Anang, O’Mara, Megan L., Schuetz, John D.

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Children with sickle cell anemia and APOL1 genetic variants develop albuminuria early in life von Zahr, Rima S, Rampersaud, Evadnie, Kang, Guolian, Weiss, Mitchell J, Wu, Gang, Davis, Robert L, Hankins, Jane S, Estepp, Jeremie H, Lebensburger, Jeffrey

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The net electrostatic potential and hydration of ABCG2 affect substrate transport von Gose, Tomoka, Aitken, Heather M., Wang, Yao, Lynch, John, Rampersaud, Evadnie, Fukuda, Yu, Wills, Medb, Baril, Stefanie A., Ford, Robert C., Shelat, Anang, O’Mara, Megan L., Schuetz, John D.

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Whole-genome association study identifies STK39 as a hypertension susceptibility gene von Wang, Ying, O'Connell, Jeffrey R, McArdle, Patrick F, Wade, James B, Dorff, Sarah E, Shah, Sanjiv J, Shi, Xiaolian, Pan, Lin, Rampersaud, Evadnie, Shen, Haiqing, Kim, James D, Subramanya, Arohan R, Steinle, Nanette I, Parsa, Afshin, Ober, Carole C, Welling, Paul A, Chakravarti, Aravinda, Weder, Alan B, Cooper, Richard S, Mitchell, Braxton D, Shuldiner, Alan R, Chang, Yen-Pei C

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The severity of hereditary porphyria is modulated by the porphyrin exporter and Lan antigen ABCB6 von Fukuda, Yu, Cheong, Pak Leng, Lynch, John, Brighton, Cheryl, Frase, Sharon, Kargas, Vasileios, Rampersaud, Evadnie, Wang, Yao, Sankaran, Vijay G., Yu, Bing, Ney, Paul A., Weiss, Mitchell J., Vogel, Peter, Bond, Peter J., Ford, Robert C., Trent, Ronald J., Schuetz, John D.

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Evaluating Pathogenicity of Rare Variants From Dilated Cardiomyopathy in the Exome Era von Norton, Nadine, Robertson, Peggy D, Rieder, Mark J, Züchner, Stephan, Rampersaud, Evadnie, Martin, Eden, Li, Duanxiang, Nickerson, Deborah A, Hershberger, Ray E

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Temporal Relationship of Conduction System Disease and Ventricular Dysfunction in LMNA Cardiomyopathy von Brodt, Chad, MD, Siegfried, Jill D., MS, CGC, Hofmeyer, Mark, MD, Martel, Jose, MD, Rampersaud, Evadnie, PhD, Li, Duanxiang, MD, MS, Morales, Ana, MS, CGC, Hershberger, Ray E., MD

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Exome Sequencing and Genome-Wide Linkage Analysis in 17 Families Illustrate the Complex Contribution of TTN Truncating Variants to Dilated Cardiomyopathy von Norton, Nadine, Li, Duanxiang, Rampersaud, Evadnie, Morales, Ana, Martin, Eden R, Zuchner, Stephan, Guo, Shengru, Gonzalez, Michael, Hedges, Dale J, Robertson, Peggy D, Krumm, Niklas, Nickerson, Deborah A, Hershberger, Ray E

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Identification of Novel Candidate Genes for Type 2 Diabetes From a Genome-Wide Association Scan in the Old Order Amish von Rampersaud, Evadnie, Damcott, Coleen M., Fu, Mao, Shen, Haiqing, McArdle, Patrick, Shi, Xiaolian, Shelton, John, Yin, Jing, Chang, Yen-Pei C., Ott, Sandra H., Zhang, Li, Zhao, Yiju, Mitchell, Braxton D., O'Connell, Jeffery, Shuldiner, Alan R.

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Publisher Correction: Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein von Farhan, Sali M. K., Howrigan, Daniel P., Abbott, Liam E., Klim, Joseph R., Topp, Simon D., Byrnes, Andrea E., Churchhouse, Claire, Phatnani, Hemali, Smith, Bradley N., Rampersaud, Evadnie, Wu, Gang, Wuu, Joanne, Shatunov, Aleksey, Iacoangeli, Alfredo, Khleifat, Ahmad Al, Mordes, Daniel A., Ghosh, Sulagna, Eggan, Kevin, Rademakers, Rosa, McCauley, Jacob L., Schüle, Rebecca, Züchner, Stephan, Benatar, Michael, Taylor, J. Paul, Nalls, Michael, Gotkine, Marc, Shaw, Pamela J., Morrison, Karen E., Al-Chalabi, Ammar, Traynor, Bryan, Shaw, Christopher E., Goldstein, David B., Harms, Matthew B., Daly, Mark J., Neale, Benjamin M.

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Repeats expansions in ATXN2, NOP56, NIPA1 and ATXN1 are not associated with ALS in Africans von Nel, Melissa, Mavundla, Thandeka, Gultig, Kayleigh, Botha, Gerrit, Mulder, Nicola, Benatar, Michael, Wuu, Joanne, Cooley, Anne, Myers, Jason, Rampersaud, Evadnie, Wu, Gang, Heckmann, Jeannine M.

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The genetic response to short-term interventions affecting cardiovascular function: Rationale and design of the Heredity and Phenotype Intervention (HAPI) Heart Study von Mitchell, Braxton D., PhD, McArdle, Patrick F., PhD, Shen, Haiqing, PhD, Rampersaud, Evadnie, PhD, Pollin, Toni I., PhD, Bielak, Lawrence F., DDS, MPH, Jaquish, Cashell, PhD, Douglas, Julie A., PhD, Roy-Gagnon, Marie-Hélène, PhD, Sack, Paul, MD, Naglieri, Rosalie, MD, Hines, Scott, MD, Horenstein, Richard B., MD, Chang, Yen-Pei C., PhD, Post, Wendy, MD, MS, Ryan, Kathleen A., MPH, Brereton, Nga Hong, MS, RD, Pakyz, Ruth E., BS, MT, ASCD, Sorkin, John, MD, PhD, Damcott, Coleen M., PhD, O'Connell, Jeffrey R., PhD, Mangano, Charles, BA, RDMS, Corretti, Mary, MD, Vogel, Robert, MD, Herzog, William, MD, Weir, Matthew R., MD, Peyser, Patricia A., PhD, Shuldiner, Alan R., MD

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Germline deletion of ETV6 in familial acute lymphoblastic leukemia von Rampersaud, Evadnie, Ziegler, David S., Iacobucci, Ilaria, Payne-Turner, Debbie, Churchman, Michelle L., Schrader, Kasmintan A., Joseph, Vijai, Offit, Kenneth, Tucker, Katherine, Sutton, Rosemary, Warby, Meera, Chenevix-Trench, Georgia, Huntsman, David G., Tsoli, Maria, Mead, R. Scott, Qu, Chunxu, Leventaki, Vasiliki, Wu, Gang, Mullighan, Charles G.

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Validation of serum neurofilaments as prognostic and potential pharmacodynamic biomarkers for ALS von Benatar, Michael, Zhang, Lanyu, Wang, Lily, Granit, Volkan, Statland, Jeffrey, Barohn, Richard, Swenson, Andrea, Ravits, John, Jackson, Carlayne, Burns, Ted M., Trivedi, Jaya, Pioro, Erik P., Caress, James, Katz, Jonathan, McCauley, Jacob L., Rademakers, Rosa, Malaspina, Andrea, Ostrow, Lyle W., Wuu, Joanne

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BIOM-61. EXPLORING HOMOLOGOUS RECOMBINATION DEFICIENCY IN PEDIATRIC HIGH-GRADE GLIOMAS von Xu, Ke, Savage, Evan, Myers, Jason, Rampersaud, Evadnie, Hui, Yawei, Chang, Ti-Cheng, Wu, Gang, Tinkle, Christopher, Shelat, Anang

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Genetic Associations With an Amyotrophic Lateral Sclerosis Reversal Phenotype von Crayle, Jesse I, Rampersaud, Evadnie, Myers, Jason R, Wuu, Joanne, Taylor, J Paul, Wu, Gang, Benatar, Michael, Bedlack, Richard S

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Exome sequencing in amyotrophic lateral sclerosis implicates a novel gene, DNAJC7, encoding a heat-shock protein von Farhan, Sali M. K., Howrigan, Daniel P., Abbott, Liam E., Klim, Joseph R., Topp, Simon D., Byrnes, Andrea E., Churchhouse, Claire, Phatnani, Hemali, Smith, Bradley N., Rampersaud, Evadnie, Wu, Gang, Wuu, Joanne, Shatunov, Aleksey, Iacoangeli, Alfredo, Al Khleifat, Ahmad, Mordes, Daniel A., Ghosh, Sulagna, Eggan, Kevin, Rademakers, Rosa, McCauley, Jacob L., Schüle, Rebecca, Züchner, Stephan, Benatar, Michael, Taylor, J. Paul, Nalls, Michael, Gotkine, Marc, Shaw, Pamela J., Morrison, Karen E., Al-Chalabi, Ammar, Traynor, Bryan, Shaw, Christopher E., Goldstein, David B., Harms, Matthew B., Daly, Mark J., Neale, Benjamin M.

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