Amniotic membrane allografts: development and clinical utility in ophthalmology by Rizzuti A, Goldenberg A, Lazzaro DR

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Negativity spreads more than positivity on Twitter after both positive and negative political situations by Schöne, J, Parkinson, B, Goldenberg, A

Melanoma risk perception and prevention behavior among African-Americans: the minority melanoma paradox by Goldenberg A, Vujic I, Sanlorenzo M, Ortiz-Urda S

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Negative expressions are shared more on Twitter for public figures than for ordinary users by Schone, J, Garcia, D, Parkinson, B, Goldenberg, A

Use of marginal organs in kidney transplantation for marginal recipients: too close to the margins of safety? by Heuer M, Zeiger A, Kaiser GM, Mathé Z, Goldenberg A, Sauerland S, Paul A, Treckmann JW

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A multi-country test of brief reappraisal interventions on emotions during the COVID-19 pandemic by Wang, K, Goldenberg, A, Dorisson, CA, Pantazi, M, Vally, Z, Levy, N, Pit, IL, Misiak, M, Friedemann, M

Better Understanding of the Metamorphosis of Pregnancy (BUMP): protocol for a digital feasibility study in women from preconception to postpartum by Goodday, SM, Karlin, E, Brooks, A, Chapman, C, Karlin, DR, Foschini, L, Kipping, E, Wildman, M, Francis, M, Greenman, H, Li, Li, Schadt, E, Ghassemi, M, Goldenberg, A, Cormack, F, Taptiklis, N, Centen, C, Smith, S, Friend, S

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Large spectrum of lissencephaly and pachygyria phenotypes resulting from de novo missense mutations in tubulin alpha 1A (TUBA1A). by Poirier, K, Keays, D, Francis, F, Saillour, Y, Bahi, N, Manouvrier, S, Fallet-Bianco, C, Pasquier, L, Toutain, A, Tuy, F, Bienvenu, T, Joriot, S, Odent, S, Ville, D, Desguerre, I, Goldenberg, A, Moutard, M, Fryns, J, van Esch, H, Harvey, R, Siebold, C, Flint, J, Beldjord, C, Chelly, J

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome. by Koolen, D, Sharp, A, Hurst, J, Firth, H, Knight, S, Goldenberg, A, Saugier-Veber, P, Pfundt, R, Vissers, L, Destrée, A, Grisart, B, Rooms, L, Van der Aa, N, Field, M, Hackett, A, Bell, K, Nowaczyk, M, Mancini, G, Poddighe, P, Schwartz, C, Rossi, E, De Gregori, M, Antonacci-Fulton, L, McLellan, MD, Garrett, J

Clinical and molecular delineation of the 17q21.31 microdeletion syndrome by Koolen, D, Sharp, A, Hurst, J, Firth, H, Knight, S, Goldenberg, A, Saugier-Veber, P, Pfundt, R, Vissers, L, Destree, A, Grisart, B, Rooms, L, Van der Aa, N, Field, M, Hackett, A, Bell, K, Nowaczyk, M, Mancini, G, Poddighe, P, Schwartz, C, Rossi, E, De Gregori, M, Antonacci-Fulton, L, Ii, M, Garrett, J

Public involvement in the governance of population-level biomedical research: Unresolved questions and future directions by Erikainen, S, Friesen, P, Rand, L, Jongsma, K, Dunn, M, Sorbie, A, McCoy, M, Bell, J, Burgess, M, Chen, H, Chico, V, Cunningham-Burley, S, Darbyshire, J, Dawson, R, Evans, A, Fahy, N, Finlay, T, Frith, L, Goldenberg, A, Hinton, L, Hoppe, N, Hughes, N, Koenig, B, Lignou, S, McGowan, M, Parker, M, Prainsack, B, Shabani, M, Staunton, C, Thompson, R, Varnai, K, Vayena, E, Williams, O, Williamson, M, Chan, S, Sheehan, M

De novo heterozygous POLR2A variants cause a neurodevelopmental syndrome with profound infantile-onset hypotonia by Haijes, H, Koster, M, Rehmann, H, Li, D, Hakonarson, H, Cappuccio, G, Hancarova, M, Lehalle, D, Reardon, W, Schaefer, G, Lehman, A, Van De Laar, I, Tesselaar, C, Turner, C, Goldenberg, A, Patrier, S, Thevenon, J, Pinelli, M, Brunetti-Pierri, N, Prchalová, D, Havlovicová, M, Vlckova, M, Sedláček, Z, Lopez, E, Ragoussis, V, Pagnamenta, A, Kini, U, Vos, H, Van Es, R, Van Schaik, R, Van Essen, T, Kibaek, M, Taylor, J, Sullivan, J, Shashi, V, Petrovski, S, Fagerberg, C, Martin, D, Van Gassen, K, Pfundt, R, Falk, M, McCormick, E, Timmers, H, Van Hasselt, P