MUC1 ligand, NM23-H1, is a novel growth factor that maintains human stem cells in a more naïve state von Smagghe, Benoit J, Stewart, Andrew K, Carter, Mark G, Shelton, Laura M, Bernier, Kyle J, Hartman, Eric J, Calhoun, Amy K, Hatziioannou, Vasilios M, Lillacci, Gabriele, Kirk, Brian A, DiNardo, Brian A, Kosik, Kenneth S, Bamdad, Cynthia

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MUC1 Ligand, NM23-H1, Is a Novel Growth Factor That Maintains Human Stem Cells in a More Naive State. e58601 von Smagghe, Benoit J, Stewart, Andrew K, Carter, Mark G, Shelton, Laura M, Bernier, Kyle J, Hartman, Eric J, Calhoun, Amy K, Hatziioannou, Vasilios M, Lillacci, Gabriele, Kirk, Brian A

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Clinical phenotype of the recurrent 1q21.1 copy-number variant von Bernier, Raphael, Steinman, Kyle J., Reilly, Beau, Wallace, Arianne Stevens, Sherr, Elliott H., Pojman, Nicholas, Mefford, Heather C., Gerdts, Jennifer, Earl, Rachel, Hanson, Ellen, Goin-Kochel, Robin P., Berry, Leandra, Kanne, Stephen, Snyder, LeeAnne Green, Spence, Sarah, Ramocki, Melissa B., Evans, David W., Spiro, John E., Martin, Christa L., Ledbetter, David H., Chung, Wendy K.

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Language characterization in 16p11.2 deletion and duplication syndromes von Kim, So Hyun, Green‐Snyder, LeeAnne, Lord, Catherine, Bishop, Somer, Steinman, Kyle J., Bernier, Raphael, Hanson, Ellen, Goin‐Kochel, Robin P., Chung, Wendy K.

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Simons Variation in Individuals Project (Simons VIP): A Genetics-First Approach to Studying Autism Spectrum and Related Neurodevelopmental Disorders von The Simons VIP Consortium

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Longitudinal report of child with de novo 16p11.2 triplication von Wallace, Arianne S., Hudac, Caitlin M., Steinman, Kyle J., Peterson, Jessica L., DesChamps, Trent D., Duyzend, Michael H., Nuttle, Xander, Eichler, Evan E., Bernier, Raphael A.

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A 600kb deletion syndrome at 16p11.2 leads to energy imbalance and neuropsychiatric disorders von Zufferey, Flore, Sherr, Elliott H, Beckmann, Noam D, Hanson, Ellen, Maillard, Anne M, Hippolyte, Loyse, Mace, Aurelien, Ferrari, Carina, Kutalik, Zoltan, Andrieux, Joris, Aylward, Elizabeth, Barker, Mandy, Bernier, Raphael, Bouquillon, Sonia, Conus, Philippe, Delobel, Bruno, Faucett, W Andrew, Goin-Kochel, Robin P, Grant, Ellen, Harewood, Louise, Hunter, Jill V, Lebon, Sebastien, Ledbetter, David H, Martin, Christa Lese, Maennik, Katrin, Martinet, Danielle, Mukherjee, Pratik, Ramocki, Melissa B, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Spiro, John E, Reymond, Alexandre, Beckmann, Jacques S, Chung, Wendy K, Jacquemont, Sebastien

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A 600 kb Deletion Syndrome at 16p11.2 Leads to Energy Imbalance and Neuropsychiatric Disorders von Zufferey, Flore, Sherr, Elliott H, Beckmann, Noam D, Hanson, Ellen M, Maillard, Anne M, Hippolyte, Loyse, Macé, Aurélien, Ferrari, Carina, Kutalik, Zoltán, Andrieux, Joris, Aylward, Elizabeth, Barker, Mandy, Bernier, Raphael, Bouquillon, Sonia, Conus, Philippe, Delobel, Bruno, Faucett, W Andrew, Goin-Kochel, Robin P, Grant, Ellen, Harewood, Louise, Hunter, Jill V, Lebon, Sébastien, Ledbetter, David H, Martin, Christa Lese, Männik, Katrin, Martinet, Danielle, Mukherjee, Pratik, Ramocki, Melissa B, Spence, Sarah J, Steinman, Kyle J, Tjernagel, Jennifer, Spiro, John E, Reymond, Alexandre, Beckmann, Jacques S, Chung, Wendy K, Jacquemont, Sébastien

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Hormonal and metabolic responses of untrained, moderately trained, and highly trained men to three exercise intensities von Deuster, P.A., Chrousos, G.P., Luger, A., DeBolt, J.E., Bernier, L.L., Trostmann, U.H., Kyle, S.B., Montgomery, L.C., Loriaux, D.L.

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Longitudinal report of child with de novo 16p11.2 triplication von Wallace, Arianne S, Hudac, Caitlin M, Steinman, Kyle J, Peterson, Jessica L, DesChamps, Trent D, Duyzend, Michael H, Nuttle, Xander, Eichler, Evan E, Bernier, Raphael A

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Hormonal and metabolism responses of untrained, moderately traited, and highly trained men to three exercise intensities von DEUSTER, P. A, CHROUSOS, G. P, LUGER, A, DEBOLT, J. E, BERNIER, L. L, TROSTMANN, U. H, KYLE, S. B, MONTGOMERY, L. C, LORIAUX, D. L

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