Changing nursing culture to welcome second-degree students: herding and corralling sacred cows by Hegge, Margaret J, Hallman, Patricia A

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Blood myo-inositol concentrations in preterm and term infants by Brion, Luc P., Phelps, Dale L., Ward, Robert M., Nolen, Tracy L., Hallman, N. Mikko K., Das, Abhik, Zaccaro, Daniel J., Ball, M. Bethany, Watterberg, Kristi L., Frantz, Ivan D., Cotten, C. Michael, Poindexter, Brenda B., Oh, William, Lugo, Ralph A., Van Meurs, Krisa P., O’Shea, T. Michael, Zaterka-Baxter, Kristin M., Higgins, Rosemary D.

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Nurse and patient characteristics predict communication about complementary and alternative medicine by Spencer, Christine N., Lopez, Gabriel, Cohen, Lorenzo, Urbauer, Diana L., Hallman, D. Michael, Fisch, Michael J., Parker, Patricia A.

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Association between Intermittent Hypoxemia and Severe Bronchopulmonary Dysplasia in Preterm Infants by Jensen, Erik A, Whyte, Robin K, Schmidt, Barbara, Bassler, Dirk, Vain, Nestor E, Roberts, Robin S

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Clinical, epidemiologic, histopathologic and molecular features of an unexplained dermopathy by Pearson, Michele L, Selby, Joseph V, Katz, Kenneth A, Cantrell, Virginia, Braden, Christopher R, Parise, Monica E, Paddock, Christopher D, Lewin-Smith, Michael R, Kalasinsky, Victor F, Goldstein, Felicia C, Hightower, Allen W, Papier, Arthur, Lewis, Brian, Motipara, Sarita, Eberhard, Mark L

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A Subset-Based Approach Improves Power and Interpretation for the Combined Analysis of Genetic Association Studies of Heterogeneous Traits by Bhattacharjee, Samsiddhi, Rajaraman, Preetha, Jacobs, Kevin B., Wheeler, William A., Melin, Beatrice S., Hartge, Patricia, Yeager, Meredith, Chung, Charles C., Chanock, Stephen J., Chatterjee, Nilanjan

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Candidate Gene Analysis: Severe Intraventricular Hemorrhage in Inborn Preterm Neonates by Ådén, Ulrika, MD, PhD, Lin, Aiping, MD, Carlo, Waldemar, MD, Leviton, Alan, MD, Murray, Jeffrey C., MD, Hallman, Mikko, MD, PhD, Lifton, Richard P., MD, PhD, Zhang, Heping, PhD, Ment, Laura R., MD

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Evaluation of association of HNF1B variants with diverse cancers: collaborative analysis of data from 19 genome-wide association studies by Elliott, Katherine S, Zeggini, Eleftheria, McCarthy, Mark I, Gudmundsson, Julius, Sulem, Patrick, Stacey, Simon N, Thorlacius, Steinunn, Amundadottir, Laufey, Grönberg, Henrik, Xu, Jianfeng, Gaborieau, Valerie, Eeles, Rosalind A, Neal, David E, Donovan, Jenny L, Hamdy, Freddie C, Muir, Kenneth, Hwang, Shih-Jen, Spitz, Margaret R, Zanke, Brent, Carvajal-Carmona, Luis, Brown, Kevin M, Hayward, Nicholas K, Macgregor, Stuart, Tomlinson, Ian P M, Lemire, Mathieu, Amos, Christopher I, Murabito, Joanne M, Isaacs, William B, Easton, Douglas F, Brennan, Paul, Barkardottir, Rosa B, Gudbjartsson, Daniel F, Rafnar, Thorunn, Hunter, David J, Chanock, Stephen J, Stefansson, Kari, Ioannidis, John P A

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