Clonal genetic and hematopoietic heterogeneity among human-induced pluripotent stem cell lines von Mills, Jason A., Wang, Kai, Paluru, Prasuna, Ying, Lei, Lu, Lin, Galvão, Aline M., Xu, Dongbin, Yao, Yu, Sullivan, Spencer K., Sullivan, Lisa M., Mac, Helen, Omari, Amel, Jean, Jyh-Chang, Shen, Steve, Gower, Adam, Spira, Avi, Mostoslavsky, Gustavo, Kotton, Darrell N., French, Deborah L., Weiss, Mitchell J., Gadue, Paul

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Hematopoietic Differentiation of Pluripotent Stem Cells in Culture von Mills, Jason A., Paluru, Prasuna, Weiss, Mitchell J., Gadue, Paul, French, Deborah L.

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The phenotypic spectrum of ZIC3 mutations includes isolated d-transposition of the great arteries and double outlet right ventricle von D'Alessandro, Lisa C.A., Latney, Brande C., Paluru, Prasuna C., Goldmuntz, Elizabeth

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Identification of a Novel Locus on 2q for Autosomal Dominant High-Grade Myopia von Paluru, Prasuna C, Nallasamy, Sudha, Devoto, Marcella, Rappaport, Eric F, Young, Terri L

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Genetic linkage study of high-grade myopia in a Hutterite population from South Dakota von Nallasamy, Sudha, Paluru, Prasuna C, Devoto, Marcella, Wasserman, Nora F, Zhou, Jie, Young, Terri L

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The negative impact of Wnt signaling on megakaryocyte and primitive erythroid progenitors derived from human embryonic stem cells von Paluru, Prasuna, Hudock, Kristin M., Cheng, Xin, Mills, Jason A., Ying, Lei, Galvão, Aline M., Lu, Lin, Tiyaboonchai, Amita, Sim, Xiuli, Sullivan, Spencer K., French, Deborah L., Gadue, Paul

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Sequence variants in the transforming growth β-induced factor (TGIF) gene are not associated with high myopia von SCAVELLO, Genaro S, PALURU, Prasuna C, GANTER, William R, YOUNG, Terri L

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Exclusion of lumican and fibromodulin as candidate genes in MYP3 linked high grade myopia von Paluru, Prasuna C, Scavello, Genaro S, Ganter, William R, Young, Terri L

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Microarray analysis of gene expression in human donor sclera von Young, Terri L, Scavello, Genaro S, Paluru, Prasuna C, Choi, Jonathan D, Rappaport, Eric F, Rada, Jody A

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Patient-derived induced pluripotent stem cells recapitulate hematopoietic abnormalities of juvenile myelomonocytic leukemia von Gandre-Babbe, Shilpa, Paluru, Prasuna, Aribeana, Chiaka, Chou, Stella T., Bresolin, Silvia, Lu, Lin, Sullivan, Spencer K., Tasian, Sarah K., Weng, Julie, Favre, Helene, Choi, John K., French, Deborah L., Loh, Mignon L., Weiss, Mitchell J.

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Genomic structure and organization of the high grade Myopia-2 locus (MYP2) critical region: mutation screening of 9 positional candidate genes von Scavello, Jr, Genaro S, Paluru, Prasuna C, Zhou, Jie, White, Peter S, Rappaport, Eric F, Young, Terri L

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MicroRNA Screen of Human Embryonic Stem Cell Differentiation Reveals miR‐105 as an Enhancer of Megakaryopoiesis from Adult CD34+ Cells von Kamat, Viraj, Paluru, Prasuna, Myint, Melissa, French, Deborah L., Gadue, Paul, Diamond, Scott L.

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High-level transgene expression in induced pluripotent stem cell–derived megakaryocytes: correction of Glanzmann thrombasthenia von Sullivan, Spencer K., Mills, Jason A., Koukouritaki, Sevasti B., Vo, Karen K., Lyde, Randolph B., Paluru, Prasuna, Zhao, Guoha, Zhai, Li, Sullivan, Lisa M., Wang, Yuhuan, Kishore, Siddharth, Gharaibeh, Eyad Z., Lambert, Michele P., Wilcox, David A., French, Deborah L., Poncz, Mortimer, Gadue, Paul

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Mutations in NTRK3 Suggest a Novel Signaling Pathway in Human Congenital Heart Disease von Werner, Petra, Paluru, Prasuna, Simpson, Anisha M., Latney, Brande, Iyer, Radhika, Brodeur, Garrett M., Goldmuntz, Elizabeth

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Microdeletions and Microduplications in Patients with Congenital Heart Disease and Multiple Congenital Anomalies von Goldmuntz, Elizabeth, Paluru, Prasuna, Glessner, Joseph, Hakonarson, Hakon, Biegel, Jaclyn A., White, Peter S., Gai, Xiaowu, Shaikh, Tamim H.

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Insights Into Thrombopoiesis From Infused Human Megakaryocytes Into Mice von Wang, Yuhuan, Hayes, Vincent M., Paluru, Prasuna, Chou, Stella T., French, Deborah L., Poncz, Mortimer

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New Locus for Autosomal Dominant High Myopia Maps to the Long Arm of Chromosome 17 von Paluru, Prasuna, Ronan, Shawn M, Heon, Elise, Devoto, Marcella, Wildenberg, Scott C, Scavello, Genaro, Holleschau, Ann, Makitie, Outi, Cole, William G, King, Richard A, Young, Terri L

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Abstract 17979: A Subset of Patients with Isolated Transposition of the Great Arteries and Double Outlet Right Ventricle Fall Within the Spectrum of Heterotaxy Syndrome von D'Alessandro, Lisa C, Latney, Brande C, Paluru, Prasuna C, Goldmuntz, Elizabeth

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Refinement of the X-linked nonsyndromic high-grade myopia locus MYP1 on Xq28 and exclusion of 13 known positional candidate genes by direct sequencing von Ratnamala, Uppala, Lyle, Robert, Rawal, Rakesh, Singh, Raminder, Vishnupriya, Satti, Himabindu, Pamini, Rao, Vittal, Aggarwal, Somesh, Paluru, Prasuna, Bartoloni, Lucia, Young, Terri L, Paoloni-Giacobino, Ariane, Morris, Michael A, Nath, Swapan K, Antonarakis, Stylianos E, Radhakrishna, Uppala

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Variants of folate metabolism genes and risk of left-sided cardiac defects von Mitchell, Laura E., Long, Jin, Garbarini, Jennifer, Paluru, Prasuna, Goldmuntz, Elizabeth

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