Mapping trends in the concept of nurse rounding: A bibliometric analysis and research agenda by Hutchinson, Marie, Higson, Mary, Jackson, Debra

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Nursing expertise: a course of ambiguity and evolution in a concept by Hutchinson, Marie, Higson, Mary, Cleary, Michelle, Jackson, Debra

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Ambiguous loss of home: Syrian refugees and the process of losing and remaking home by Bunn, Mary, Samuels, Gina, Higson-Smith, Craig

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Prevalence of pre-eclampsia and adverse pregnancy outcomes in women with pre-existing cardiomyopathy: a multi-centre retrospective cohort study by Ormesher, Laura, Vause, Sarah, Higson, Suzanne, Roberts, Anna, Clarke, Bernard, Curtis, Stephanie, Ordonez, Victoria, Ansari, Faiza, Everett, Thomas R., Hordern, Claire, Mackillop, Lucy, Stern, Victoria, Bonnett, Tessa, Reid, Alice, Wallace, Suzanne, Oyekan, Ebruba, Douglas, Hannah, Cauldwell, Matthew, Reddy, Maya, Palmer, Kirsten, Simpson, Maggie, Brennand, Janet, Minns, Laura, Freeman, Leisa, Murray, Sarah, Mary, Nirmala, Castleman, James, Morris, Katie R., Haslett, Elizabeth, Cassidy, Christopher, Johnstone, Edward D., Myers, Jenny E.

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In search of genetic factors predisposing to familial hairy cell leukemia (HCL): exome-sequencing of four multiplex HCL pedigrees by Pemov, Alexander, Pathak, Anand, Jones, Samantha J., Dewan, Ramita, Merberg, Jessica, Karra, Sirisha, Kim, Jung, Arons, Evgeny, Ravichandran, Sarangan, Luke, Brian T., Suman, Shalabh, Yeager, Meredith, Dyer, Martin J. S., Lynch, Henry T., Greene, Mark H., Caporaso, Neil E., Kreitman, Robert J., Goldin, Lynn R., Spinelli, John J., Brooks-Wilson, Angela, McMaster, Mary L., Stewart, Douglas R.

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Hoyeraal-Hreidarsson syndrome caused by a germline mutation in the TEL patch of the telomere protein TPP1 by Kocak, Hande, Ballew, Bari J, Bisht, Kamlesh, Eggebeen, Rebecca, Hicks, Belynda D, Suman, Shalabh, O'Neil, Adri, Giri, Neelam, Maillard, Ivan, Alter, Blanche P, Keegan, Catherine E, Nandakumar, Jayakrishnan, Savage, Sharon A

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Synthesis of Mixed Sequence Borane Phosphonate DNA by McCuen, Heather Brummel, Noé, Mary S, Sierzchala, Agnieszka B, Higson, Adrian P, Caruthers, Marvin H

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Whole exome sequencing reveals a C-terminal germline variant in CEBPA-associated acute myeloid leukemia: 45-year follow up of a large family by Pathak, Anand, Seipel, Katja, Pemov, Alexander, Dewan, Ramita, Brown, Christina, Ravichandran, Sarangan, Luke, Brian T, Malasky, Michael, Suman, Shalabh, Yeager, Meredith, Gatti, Richard A, Caporaso, Neil E, Mulvihill, John J, Goldin, Lynn R, Pabst, Thomas, McMaster, Mary L, Stewart, Douglas R

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Juvenile myelomonocytic leukemia due to a germline CBL Y371C mutation: 35-year follow-up of a large family by Pathak, Anand, Pemov, Alexander, McMaster, Mary L., Dewan, Ramita, Ravichandran, Sarangan, Pak, Evgenia, Dutra, Amalia, Lee, Hyo Jung, Vogt, Aurelie, Zhang, Xijun, Yeager, Meredith, Anderson, Stacie, Kirby, Martha, Caporaso, Neil, Greene, Mark H., Goldin, Lynn R., Stewart, Douglas R.

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Hoyeraal-Hreidarsson Syndrome due to PARN Mutations: Fourteen Years of Follow-Up by Burris, Ashley M., DO, Ballew, Bari J., PhD, Kentosh, Joshua B., DO, Turner, Clesson E., MD, Norton, Scott A., MD, MPH, Giri, Neelam, MD, Alter, Blanche P., MD, MPH, Nellan, Anandani, MD, Gamper, Christopher, MD, PhD, Hartman, Kip R., MD, Savage, Sharon A., MD

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Novel FANCI mutations in Fanconi anemia with VACTERL association by Savage, Sharon A., Ballew, Bari J., Giri, Neelam, Chandrasekharappa, Settara C., Ameziane, Najim, de Winter, Johan, Alter, Blanche P.

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Synthesis and Biochemical Activity of New Oligonucleotide Analogs by McCuen, Heather Brummel, Noe, Mary S., Olesiak, Magdalena, Sierzchala, Agnieszka B., Caruthers, Marvin H., Higson, Adrian P.

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