QoRTs: a comprehensive toolset for quality control and data processing of RNA-Seq experiments von Hartley, Stephen W, Mullikin, James C

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Genetic signatures of exceptional longevity in humans von Sebastiani, Paola, Solovieff, Nadia, Dewan, Andrew T, Walsh, Kyle M, Puca, Annibale, Hartley, Stephen W, Melista, Efthymia, Andersen, Stacy, Dworkis, Daniel A, Wilk, Jemma B, Myers, Richard H, Steinberg, Martin H, Montano, Monty, Baldwin, Clinton T, Hoh, Josephine, Perls, Thomas T

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Inflated expectations: Rare-variant association analysis using public controls von Kim, Jung, Karyadi, Danielle M, Hartley, Stephen W, Zhu, Bin, Wang, Mingyi, Wu, Dongjing, Song, Lei, Armstrong, Gregory T, Bhatia, Smita, Robison, Leslie L, Yasui, Yutaka, Carter, Brian, Sampson, Joshua N, Freedman, Neal D, Goldstein, Alisa M, Mirabello, Lisa, Chanock, Stephen J, Morton, Lindsay M, Savage, Sharon A, Stewart, Douglas R

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Neurotranscriptomics: The Effects of Neonatal Stimulus Deprivation on the Rat Pineal Transcriptome von Hartley, Stephen W, Coon, Steven L, Savastano, Luis E, Mullikin, James C, Fu, Cong, Klein, David C

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Detection and visualization of differential splicing in RNA-Seq data with JunctionSeq von Hartley, Stephen W, Mullikin, James C

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Alternative Isoform Analysis of Ttc8 Expression in the Rat Pineal Gland Using a Multi-Platform Sequencing Approach Reveals Neural Regulation von Hartley, Stephen W, Mullikin, James C, Klein, David C, Park, Morgan, Coon, Steven L

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A genome-wide association study of total bilirubin and cholelithiasis risk in sickle cell anemia von Milton, Jacqueline N, Sebastiani, Paola, Solovieff, Nadia, Hartley, Stephen W, Bhatnagar, Pallav, Arking, Dan E, Dworkis, Daniel A, Casella, James F, Barron-Casella, Emily, Bean, Christopher J, Hooper, W Craig, DeBaun, Michael R, Garrett, Melanie E, Soldano, Karen, Telen, Marilyn J, Ashley-Koch, Allison, Gladwin, Mark T, Baldwin, Clinton T, Steinberg, Martin H, Klings, Elizabeth S

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Bayesian methods for multivariate modeling of pleiotropic SNP associations and genetic risk prediction von Hartley, Stephen W, Monti, Stefano, Liu, Ching-Ti, Steinberg, Martin H, Sebastiani, Paola

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Polygenic risk scores, radiation treatment exposures and subsequent cancer risk in childhood cancer survivors von Gibson, Todd M., Karyadi, Danielle M., Hartley, Stephen W., Arnold, Michael A., Berrington de Gonzalez, Amy, Conces, Miriam R., Howell, Rebecca M., Kapoor, Vidushi, Leisenring, Wendy M., Neglia, Joseph P., Sampson, Joshua N., Turcotte, Lucie M., Chanock, Stephen J., Armstrong, Gregory T., Morton, Lindsay M.

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Genomic characterization of cervical lymph node metastases in papillary thyroid carcinoma following the Chornobyl accident von Morton, Lindsay M., Lee, Olivia W., Karyadi, Danielle M., Bogdanova, Tetiana I., Stewart, Chip, Hartley, Stephen W., Breeze, Charles E., Schonfeld, Sara J., Cahoon, Elizabeth K., Drozdovitch, Vladimir, Masiuk, Sergii, Chepurny, Mykola, Zurnadzhy, Liudmyla Yu, Dai, Jieqiong, Krznaric, Marko, Yeager, Meredith, Hutchinson, Amy, Hicks, Belynda D., Dagnall, Casey L., Steinberg, Mia K., Jones, Kristine, Jain, Komal, Jordan, Ben, Machiela, Mitchell J., Dawson, Eric T., Vij, Vibha, Gastier-Foster, Julie M., Bowen, Jay, Mabuchi, Kiyohiko, Hatch, Maureen, Berrington de Gonzalez, Amy, Getz, Gad, Tronko, Mykola D., Thomas, Gerry A., Chanock, Stephen J.

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PleioGRiP: genetic risk prediction with pleiotropy von Hartley, Stephen W, Sebastiani, Paola

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In-utero exposure to zidovudine-containing antiretroviral therapy and clonal hematopoiesis in HIV-exposed uninfected newborns von Lin, Shu-Hong, Wang, Youjin, Hartley, Stephen W., Karyadi, Danielle M., Lee, Olivia W., Zhu, Bin, Zhou, Weiyin, Brown, Derek W., Beilstein-Wedel, Erin, Hazra, Rohan, Kacanek, Deborah, Chadwick, Ellen G., Marsit, Carmen J., Poirier, Miriam C., Brummel, Sean S., Chanock, Stephen J., Engels, Eric A., Machiela, Mitchell J.

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Fetal hemoglobin in sickle cell anemia: genome-wide association studies suggest a regulatory region in the 5′ olfactory receptor gene cluster von Solovieff, Nadia, Milton, Jacqueline N., Hartley, Stephen W., Sherva, Richard, Sebastiani, Paola, Dworkis, Daniel A., Klings, Elizabeth S., Farrer, Lindsay A., Garrett, Melanie E., Ashley-Koch, Allison, Telen, Marilyn J., Fucharoen, Supan, Ha, Shau Yin, Li, Chi-Kong, Chui, David H.K., Baldwin, Clinton T., Steinberg, Martin H.

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Genetic signatures of exceptional longevity in humans von Sebastiani, Paola, Solovieff, Nadia, Puca, Annibale, Hartley, Stephen W, Melista, Efthymia, Andersen, Stacy, Dworkis, Daniel A, Wilk, Jemma B, Myers, Richard H, Steinberg, Martin H, Montano, Monty, Baldwin, Clinton T, Perls, Thomas T

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A GCH1 haplotype confers sex‐specific susceptibility to pain crises and altered endothelial function in adults with sickle cell anemia von Belfer, Inna, Youngblood, Victoria, Darbari, Deepika S., Wang, Zhengyuan, Diaw, Lena, Freeman, Lita, Desai, Krupa, Dizon, Michael, Allen, Darlene, Cunnington, Colin, Channon, Keith M., Milton, Jacqueline, Hartley, Stephen W., Nolan, Vikki, Kato, Gregory J., Steinberg, Martin H., Goldman, David, Taylor, James G.

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Genetic modifiers of the severity of sickle cell anemia identified through a genome‐wide association study von Sebastiani, Paola, Solovieff, Nadia, Hartley, Stephen W., Milton, Jacqueline N., Riva, Alberto, Dworkis, Daniel A., Melista, Efthymia, Klings, Elizabeth S., Garrett, Melanie E., Telen, Marilyn J., Ashley‐Koch, Allison, Baldwin, Clinton T., Steinberg, Martin H.

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Hippocampal morphometry in population-based incident Alzheimer's disease and vascular dementia: the HAAS von Scher, Ann I, Xu, Yuan, Korf, Esther S C, Hartley, Stephen W, Witter, Menno P, Scheltens, Philip, White, Lon R, Thompson, Paul M, Toga, Arthur W, Valentino, Daniel J, Launer, Lenore J

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Severe sickle cell anemia is associated with increased plasma levels of TNF‐R1 and VCAM‐1 von Dworkis, Daniel A., Klings, Elizabeth S., Solovieff, Nadia, Li, Guihua, Milton, Jacqueline N., Hartley, Stephen W., Melista, Efthymia, Parente, Jason, Sebastiani, Paola, Steinberg, Martin H., Baldwin, Clinton T.

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Ancestry of African Americans with sickle cell disease von Solovieff, Nadia, Hartley, Stephen W., Baldwin, Clinton T., Klings, Elizabeth S., Gladwin, Mark T., Taylor, James G., Kato, Gregory J., Farrer, Lindsay A., Steinberg, Martin H., Sebastiani, Paola

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Clustering by genetic ancestry using genome-wide SNP data von Solovieff, Nadia, Hartley, Stephen W, Baldwin, Clinton T, Perls, Thomas T, Steinberg, Martin H, Sebastiani, Paola

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