Predicting Marine In Situ Heat Flow Using a Geospatial Machine Learning Conformal Prediction von Graw, J. H., Wood, W. T., Phrampus, B. J.

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Lower versus higher hemoglobin threshold for transfusion in ARDS patients with and without ECMO von Hunsicker, O., Materne, L., Buenger, Krannich, A., Balzer, F., Spies, C., Francis, R. C., Weber-Carstens, S., Menk, M., Graw, J. A.

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Radiation Cataractogenesis: A Review of Recent Studies von Ainsbury, E. A., Bouffler, S. D., Dörr, W., Graw, J., Muirhead, C. R., Edwards, A. A., Cooper, J.

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Promotional ballpens offered to orthopaedic surgeons and anaesthetists by medical device and pharmaceutical companies von Graw, J. A., Schuster, M.

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Safety in Female Genital Plastic Surgery von Furnas, Heather J., Graw, Grace J., Cho, Min-Jeong, Othman, Sammy, Graw, Bradley, Percec, Ivona

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Revisiting the impact of red cell storage duration on adverse outcomes after transfusion von Graw, J. A., Melzer‐Gartzke, C., Francis, R. C. E.

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Deficiency in the expression of Vps13C is associated with altered retinal and lens development in mice von Amarie, O., Rathkolb, B., Fuchs, H., Gailus‐Durner, V., Hrabě de Angelis, M., Graw, J.

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Mutation in the Crybb1 gene encoding beta‐B1‐crystallin leads to recessive cataracts in the mouse von Graw, J., Amarie, O., Kumar, D., Scheideler, A., Hrabé de Angelis, M., Przemeck, G., Sabrautzki, S.

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Neurotransmitter receptor density changes in Pitx3ak mice – A model relevant to Parkinson’s disease von Cremer, J.N, Amunts, K, Graw, J, Piel, M, Rösch, F, Zilles, K

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Novel mouse phenotypes identified in the eye screen of the German Mouse Clinic von Amarie, O.V., Fuchs, H., Gailus‐Durner, V., Hrabě de Angelis, M., Graw, J.

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The genetic and molecular basis of congenital eye defects von Graw, Jochen

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Lifetime Study in mice: radiation‐induced cataract von Dalke, C., Kunze, S., Rößler, U., Neff, F., Greiter, M., Gomolka, M., Hornhardt, S., Garrett, L., Unger, K., Rosemann, M., Azimzadeh, O., Wurst, W., Zitzelsberger, H., Hölter, S.M., Tapio, S., Kulka, U., Atkinson, M., Graw, J.

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Congenital hereditary cataracts von Graw, Jochen

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Mutation in the Ercc2 gene of the mouse causes cataracts von Graw, J., Kunze, S., Dalke, C., Fuchs, H., Klaften, M., Sabrautzki, S., Hrabe de Angelis, M.

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Splice‐site mutation in the Bmpr1b gene of the mouse causes optic nerve head dysgenesis and retinal gliosis von Graw, J., Yan, X., Amarie, O.V., Puk, O., Sabrautzki, S., Klaften, M., Thiele, F., Fuchs, H., Hrabe de Angelis, M.

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Lifetime Study in mice: 24 months follow up after low doses of ionizing radiation with Scheimpflug imaging and OCT von Dalke, C., Rößler, U., Neff, F., Greiter, M., Gomolka, M., Hornhardt, S., Garrett, L., Kunze, S., Unger, K., Rosemann, M., Kempf, S.J., Azimzadeh, O., Wurst, W., Aubele, M., Zitzelsberger, H., Hölter, S.M., Tapio, S., Hoeschen, C., Kulka, U., Atkinson, M., Graw, J.

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Novel mutations in the γ-crystallin genes cause autosomal dominant congenital cataracts von Santhiya, S T, Shyam Manohar, M, Rawlley, D, Vijayalakshmi, P, Namperumalsamy, P, Gopinath, P M, Löster, J, Graw, J

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Lifetime study in mice for radiation‐induced cataracts von Dalke, C., Rößler, U., Neff, F., Greiter, M., Gomolka, M., Hornhardt, S., Unger, K., Garrett, L., Rosemann, M., Kempf, S., Azimzadeh, O., Wurst, W., Aubele, M., Zitzelsberger, H., Hölter, S., Tapio, S., Hoeschen, C., Kulka, U., Atkinson, M., Graw, J.

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Predicting Global Marine Sediment Density Using the Random Forest Regressor Machine Learning Algorithm von Graw, J. H., Wood, W. T., Phrampus, B. J.

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Analysis of mRNA in hemophilia A patients with undetectable mutations reveals normal splicing in the factor VIII gene von EL‐MAARRI, O., HERBINIAUX, U., GRAW, J., SCHRÖDER, J., TERZIC, A., WATZKA, M., BRACKMANN, H. H., SCHRAMM, W., HANFLAND, P., SCHWAAB, R., MÜLLER, C. R., OLDENBURG, J.

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