Nutritional Ketosis for Weight Management and Reversal of Metabolic Syndrome von Gershuni, Victoria M., Yan, Stephanie L., Medici, Valentina

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A complete reference genome improves analysis of human genetic variation von Aganezov, Sergey, Yan, Stephanie M, Soto, Daniela C, Kirsche, Melanie, Zarate, Samantha, Avdeyev, Pavel, Taylor, Dylan J, Shafin, Kishwar, Shumate, Alaina, Xiao, Chunlin, Wagner, Justin, McDaniel, Jennifer, Olson, Nathan D, Sauria, Michael E G, Vollger, Mitchell R, Rhie, Arang, Meredith, Melissa, Martin, Skylar, Lee, Joyce, Koren, Sergey, Rosenfeld, Jeffrey A, Paten, Benedict, Layer, Ryan, Chin, Chen-Shan, Sedlazeck, Fritz J, Hansen, Nancy F, Miller, Danny E, Phillippy, Adam M, Miga, Karen H, McCoy, Rajiv C, Dennis, Megan Y, Zook, Justin M, Schatz, Michael C

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Digital Close Reading for Lower Primary Students von Lo‐Philip, Stephanie Wing Yan

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Familial Clonal Hematopoiesis in a Long Telomere Syndrome von DeBoy, Emily A., Tassia, Michael G., Schratz, Kristen E., Yan, Stephanie M., Cosner, Zoe L., McNally, Emily J., Gable, Dustin L., Xiang, Zhimin, Lombard, David B., Antonarakis, Emmanuel S., Gocke, Christopher D., McCoy, Rajiv C., Armanios, Mary

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Archaic hominin genomics provides a window into gene expression evolution von Yan, Stephanie M, McCoy, Rajiv C

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"Clinicians Are From Mars and Pathologists Are From Venus" Revisited: Synoptic Reports Improve Clinician Comprehension of Pathology Reports in Inflammatory Bowel Disease von Yan, Stephanie L, Yang, Nuen Tsang, Schaberg, Kurt B, Mao, Eric J

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Local adaptation and archaic introgression shape global diversity at human structural variant loci von Yan, Stephanie M, Sherman, Rachel M, Taylor, Dylan J, Nair, Divya R, Bortvin, Andrew N, Schatz, Michael C, McCoy, Rajiv C

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Sources of gene expression variation in a globally diverse human cohort von Taylor, Dylan J., Chhetri, Surya B., Tassia, Michael G., Biddanda, Arjun, Yan, Stephanie M., Wojcik, Genevieve L., Battle, Alexis, McCoy, Rajiv C.

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Multiparametric Quantitative MRI of Peripheral Nerves in the Leg: A Reliability Study von Chen, Yongsheng, Baraz, Jacob, Xuan, Stephanie Yan, Yang, Xue, Castoro, Ryan, Xuan, Yang, Roth, Alison R., Dortch, Richard D., Li, Jun

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Haplotype-aware inference of human chromosome abnormalities von Ariad, Daniel, Yan, Stephanie M., Victor, Andrea R., Barnes, Frank L., Zouves, Christo G., Viotti, Manuel, McCoy, Rajiv C.

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The complete sequence of a human genome von Nurk, Sergey, Koren, Sergey, Rhie, Arang, Rautiainen, Mikko, Bzikadze, Andrey V, Mikheenko, Alla, Vollger, Mitchell R, Altemose, Nicolas, Uralsky, Lev, Gershman, Ariel, Aganezov, Sergey, Hoyt, Savannah J, Diekhans, Mark, Logsdon, Glennis A, Alonge, Michael, Antonarakis, Stylianos E, Borchers, Matthew, Bouffard, Gerard G, Brooks, Shelise Y, Caldas, Gina V, Chen, Nae-Chyun, Cheng, Haoyu, Chin, Chen-Shan, Chow, William, de Lima, Leonardo G, Dishuck, Philip C, Durbin, Richard, Dvorkina, Tatiana, Fiddes, Ian T, Formenti, Giulio, Fulton, Robert S, Fungtammasan, Arkarachai, Garrison, Erik, Grady, Patrick G S, Graves-Lindsay, Tina A, Hall, Ira M, Hansen, Nancy F, Hartley, Gabrielle A, Haukness, Marina, Howe, Kerstin, Hunkapiller, Michael W, Jain, Chirag, Jain, Miten, Jarvis, Erich D, Kerpedjiev, Peter, Kirsche, Melanie, Kolmogorov, Mikhail, Korlach, Jonas, Kremitzki, Milinn, Li, Heng, Maduro, Valerie V, Marschall, Tobias, McCartney, Ann M, McDaniel, Jennifer, Miller, Danny E, Mullikin, James C, Myers, Eugene W, Olson, Nathan D, Paten, Benedict, Peluso, Paul, Pevzner, Pavel A, Porubsky, David, Potapova, Tamara, Rogaev, Evgeny I, Rosenfeld, Jeffrey A, Salzberg, Steven L, Schneider, Valerie A, Sedlazeck, Fritz J, Shafin, Kishwar, Shew, Colin J, Shumate, Alaina, Sims, Ying, Smit, Arian F A, Soto, Daniela C, Sović, Ivan, Storer, Jessica M, Streets, Aaron, Sullivan, Beth A, Thibaud-Nissen, Françoise, Torrance, James, Wagner, Justin, Walenz, Brian P, Wenger, Aaron, Wood, Jonathan M D, Xiao, Chunlin, Yan, Stephanie M, Young, Alice C, Zarate, Samantha, Surti, Urvashi, McCoy, Rajiv C, Dennis, Megan Y, Alexandrov, Ivan A, Gerton, Jennifer L, O'Neill, Rachel J, Timp, Winston, Zook, Justin M, Schatz, Michael C, Eichler, Evan E, Miga, Karen H, Phillippy, Adam M

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Destabilizing mutations encode nongenetic variation that drives evolutionary innovation von Petrie, Katherine L, Palmer, Nathan D, Johnson, Daniel T, Medina, Sarah J, Yan, Stephanie J, Li, Victor, Burmeister, Alita R, Meyer, Justin R

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Impact of EMR Automated Results Routing Tool Implementation on Notification of Inpatient Endoscopy Biopsy Results von Spiewak, Ted A., Yan, Stephanie L., Tejaswi, Sooraj

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Clinical impact of digital cholangioscopy in management of indeterminate biliary strictures and complex biliary stones: a single-center study von Yan, Stephanie, Tejaswi, Sooraj

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Repression of glucocorticoid-stimulated angiopoietin-like 4 gene transcription by insulin von Kuo, Taiyi, Chen, Tzu-Chieh, Yan, Stephanie, Foo, Fritz, Ching, Cecilia, McQueen, Allison, Wang, Jen-Chywan

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Functional divergence among hominins von Yan, Stephanie M., McCoy, Rajiv C.

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Comparison of colon adenoma detection rates using cap-assisted and Endocuff-assisted colonoscopy: a randomized controlled trial von Marsano, Joseph, Johnson, Sheeva, Yan, Stephanie, Alli-Akintade, Latifat, Wilson, Machelle, Al-Juburi, Amar, Stondell, Jesse, Tejaswi, Sooraj

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Dickkopf-1: As a Diagnostic and Prognostic Serum Marker for Early Hepatocellular Carcinoma von Yang, Hao, Chen, Guo-Dong, Fang, Feng, Liu, Zhen, Hiu Yan Lau, Stephanie, Zhang, Jin-Fan, Lau, Wan Yee, Yang, Lian-Yue

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A broader view of the diversity of human gene expression

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Finding le mot juste: Differences between bilingual and monolingual children's lexical access in comprehension and production von YAN, STEPHANIE, NICOLADIS, ELENA

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