Relationship between Apgar scores and long-term cognitive outcomes in individuals with Down syndrome von del Hoyo Soriano, Laura, Rosser, Tracie C., Hamilton, Debra R., Harvey, Danielle J., Abbeduto, Leonard, Sherman, Stephanie L.

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Capturing cognitive and behavioral variability among individuals with Down syndrome: a latent profile analysis von Channell, Marie Moore, Mattie, Laura J., Hamilton, Debra R., Capone, George T., Mahone, E. Mark, Sherman, Stephanie L., Rosser, Tracie C., Reeves, Roger H., Kalb, Luther G.

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Contribution of copy-number variation to Down syndrome–associated atrioventricular septal defects von Ramachandran, Dhanya, Mulle, Jennifer G., Locke, Adam E., Bean, Lora J.H., Rosser, Tracie C., Bose, Promita, Dooley, Kenneth J., Cua, Clifford L., Capone, George T., Reeves, Roger H., Maslen, Cheryl L., Cutler, David J., Sherman, Stephanie L., Zwick, Michael E.

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Analysis of Copy Number Variants on Chromosome 21 in Down Syndrome-Associated Congenital Heart Defects von Rambo-Martin, Benjamin L, Mulle, Jennifer G, Cutler, David J, Bean, Lora J H, Rosser, Tracie C, Dooley, Kenneth J, Cua, Clifford, Capone, George, Maslen, Cheryl L, Reeves, Roger H, Sherman, Stephanie L, Zwick, Michael E

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Genome-Wide Association Study of Down Syndrome-Associated Atrioventricular Septal Defects von Ramachandran, Dhanya, Zeng, Zhen, Locke, Adam E, Mulle, Jennifer G, Bean, Lora J H, Rosser, Tracie C, Dooley, Kenneth J, Cua, Clifford L, Capone, George T, Reeves, Roger H, Maslen, Cheryl L, Cutler, David J, Feingold, Eleanor, Sherman, Stephanie L, Zwick, Michael E

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Pur α Binds to rCGG Repeats and Modulates Repeat-Mediated Neurodegeneration in a Drosophila Model of Fragile X Tremor/Ataxia Syndrome von Jin, Peng, Duan, Ranhui, Qurashi, Abrar, Qin, Yunlong, Tian, Donghua, Rosser, Tracie C., Liu, Huijie, Feng, Yue, Warren, Stephen T.

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Characteristics Associated with Autism Spectrum Disorder Risk in Individuals with Down Syndrome von Channell, Marie Moore, Hahn, Laura J., Rosser, Tracie C., Hamilton, Debra, Frank-Crawford, Michelle A., Capone, George T., Sherman, Stephanie L.

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Genomic landscape of Down syndrome–associated acute lymphoblastic leukemia von Li, Zhenhua, Chang, Ti-Cheng, Junco, Jacob J., Devidas, Meenakshi, Li, Yizhen, Yang, Wenjian, Huang, Xin, Hedges, Dale J., Cheng, Zhongshan, Shago, Mary, Carroll, Andrew J., Heerema, Nyla A., Gastier-Foster, Julie, Wood, Brent L., Borowitz, Michael J., Sanclemente, Lauren, Raetz, Elizabeth A., Hunger, Stephen P., Feingold, Eleanor, Rosser, Tracie C., Sherman, Stephanie L., Loh, Mignon L., Mullighan, Charles G., Yu, Jiyang, Wu, Gang, Lupo, Philip J., Rabin, Karen R., Yang, Jun J.

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Investigation of hypertension and type 2 diabetes as risk factors for dementia in the All of Us cohort von Nagar, Shashwat Deepali, Pemu, Priscilla, Qian, Jun, Boerwinkle, Eric, Cicek, Mine, Clark, Cheryl R., Cohn, Elizabeth, Gebo, Kelly, Loperena, Roxana, Mayo, Kelsey, Mockrin, Stephen, Ohno-Machado, Lucila, Ramirez, Andrea H., Schully, Sheri, Able, Ashley, Green, Ashley, Zuchner, Stephan, Jordan, I. King, Meller, Robert

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Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome von Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A.J., Goldmuntz, Elizabeth, Gruber, Peter J., O’Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.

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Associations between Medical History, Cognition, and Behavior in Youth with Down Syndrome: A Report from the Down Syndrome Cognition Project von Rosser, Tracie C, Edgin, Jamie O, Capone, George T, Hamilton, Debra R, Allen, Emily G, Dooley, Kenneth J, Anand, Payal, Strang, John F, Armour, A. Chelsea, Frank-Crawford, Michelle A, Moore Channell, Marie, Pierpont, Elizabeth I, Feingold, Eleanor, Maslen, Cheryl L, Reeves, Roger H, Sherman, Stephanie L

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Cross-Sectional Exploration of Plasma Biomarkers of Alzheimer's Disease in Down Syndrome: Early Data from the Longitudinal Investigation for Enhancing Down Syndrome Research (LIFE-... von Hendrix, James A., Airey, David C., Britton, Angela, Burke, Anna D., Capone, George T., Chavez, Ronelyn, Chen, Jacqueline, Chicoine, Brian, Costa, Alberto C. S., Dage, Jeffrey L., Doran, Eric, Esbensen, Anna, Evans, Casey L., Faber, Kelley M., Foroud, Tatiana M., Hart, Sarah, Haugen, Kelsey, Head, Elizabeth, Hendrix, Suzanne, Hillerstrom, Hampus, Kishnani, Priya S., Krell, Kavita, Ledesma, Duvia Lara, Lai, Florence, Lott, Ira, Ochoa-Lubinoff, Cesar, Mason, Jennifer, Nicodemus-Johnson, Jessie, Proctor, Nicholas Kyle, Pulsifer, Margaret B., Revta, Carolyn, Rosas, H. Diana, Rosser, Tracie C., Santoro, Stephanie, Schafer, Kim, Scheidemantel, Thomas, Schmitt, Frederick, Skotko, Brian G., Stasko, Melissa R., Talboy, Amy, Torres, Amy, Wilmes, Kristi, Woodward, Jason, Zimmer, Jennifer A., Feldman, Howard H., Mobley, William

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Heritable Variation in Lymphocyte-Related Traits and Risk of Down Syndrome Acute Lymphoblastic Leukemia: A Mendelian Randomization Study von Li, Yunqi, Richard, Melissa A., Kachuri, Linda, Yu, Yao, Hsu, Ching-Ju Ruu, Rosser, Tracie C., Leslie, Elizabeth J., Devidas, Meenakshi, Raetz, Elizabeth A., Loh, Mignon L., Hunger, Stephen P., Paul Eduthan, Neetha, Galbraith, Matthew D., Espinosa, Joaquin, Yang, Jun J., Sherman, Stephanie L., Huff, Chad D., Rabin, Karen R., Lupo, Philip J., de Smith, Adam J.

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Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome (vol 10, 18051, 2020) von Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A. J., Goldmuntz, Elizabeth, Gruber, Peter J., O'Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.

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Author Correction: Identifying genetic factors that contribute to the increased risk of congenital heart defects in infants with Down syndrome von Trevino, Cristina E., Holleman, Aaron M., Corbitt, Holly, Maslen, Cheryl L., Rosser, Tracie C., Cutler, David J., Johnston, H. Richard, Rambo-Martin, Benjamin L., Oberoi, Jai, Dooley, Kenneth J., Capone, George T., Reeves, Roger H., Cordell, Heather J., Keavney, Bernard D., Agopian, A. J., Goldmuntz, Elizabeth, Gruber, Peter J., O’Brien, James E., Bittel, Douglas C., Wadhwa, Lalita, Cua, Clifford L., Moskowitz, Ivan P., Mulle, Jennifer G., Epstein, Michael P., Sherman, Stephanie L., Zwick, Michael E.

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Pur [alpha] Binds to rCGG Repeats and Modulates Repeat-Mediated Neurodegeneration in a Drosophila Model of Fragile X Tremor/Ataxia Syndrome von Jin, Peng, Duan, Ranhui, Qurashi, Abrar, Qin, Yunlong, Tian, Donghua, Rosser, Tracie C, Liu, Huijie, Feng, Yue, Warren, Stephen T

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Article: Pur Binds to rCGG Repeats and Modulates Repeat-Mediated Neurodegeneration in a Drosophila Model of Fragile X Tremor/Ataxia Syndrome von Jin, Peng, Duan, Ranhui, Qurashi, Abrar, Qin, Yunlong, Tian, Donghua, Rosser, Tracie C, Liu, Huijie, Feng, Yue, Warren, Stephen T

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