CRISPR-Cas9 globin editing can induce megabase-scale copy-neutral losses of heterozygosity in hematopoietic cells von Boutin, J., Rosier, J., Cappellen, D., Prat, F., Toutain, J., Pennamen, P., Bouron, J., Rooryck, C., Merlio, J. P., Lamrissi-Garcia, I., Cullot, G., Amintas, S., Guyonnet-Duperat, V., Ged, C., Blouin, J. M., Richard, E., Dabernat, S., Moreau-Gaudry, F., Bedel, A.

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Xeroderma pigmentosum in South Africa: Evidence for a prevalent founder effect von Kgokolo, M., Morice‐Picard, F., Rezvani, H. R., Austerlitz, F., Cartault, F., Sarasin, A., Sathekge, M., Taieb, A., Ged, C.

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Syndrome of the trephined: When bone becomes the cure von Ged, C., Samson, E., Riffaud, L.

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Comprehensive functional annotation of 18 missense mutations found in suspected hemochromatosis type 4 patients von Callebaut, Isabelle, Joubrel, Rozenn, Pissard, Serge, Kannengiesser, Caroline, Gérolami, Victoria, Ged, Cécile, Cadet, Estelle, Cartault, François, Ka, Chandran, Gourlaouen, Isabelle, Gourhant, Lénaick, Oudin, Claire, Goossens, Michel, Grandchamp, Bernard, De Verneuil, Hubert, Rochette, Jacques, Férec, Claude, Le Gac, Gérald

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Compound heterozygosity for novel KRT85 variants associated with pure hair and nail ectodermal dysplasia von Amico, S., Ged, C., Taïeb, A., Morice‐Picard, F.

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Reversed actinic damage in two children with xeroderma pigmentosum treated with topical imiquimod von Latour, I., Hernández‐Martín, A., Ged, C., Knöpfel, N., Taïeb, A., Torrelo, A.

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A management algorithm for congenital erythropoietic porphyria derived from a study of 29 cases von Katugampola, R.P., Anstey, A.V., Finlay, A.Y., Whatley, S., Woolf, J., Mason, N., Deybach, J.C., Puy, H., Ged, C., de Verneuil, H., Hanneken, S., Minder, E., Schneider-Yin, X., Badminton, M.N.

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Recurrent posterior reversible encephalopathy syndrome in a patient with acute intermittent porphyria von Fourgeaud, M., Vidal, T., Schmitt, C., Blouin, J.-M., Ged, C., Richard, E.

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Effect of seawater intrusion on formation of bromine-containing trihalomethanes and haloacetic acids during chlorination von Ged, Evan C., Boyer, Treavor H.

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Analysis of SPINK 5, KLK 7 and FLG genotypes in a French atopic dermatitis cohort von HUBICHE, Thomas, GED, Cécile, BENARD, Antoine, LEAUTE-LABREZE, Christine, MCELREAVEY, Ken, DE VERNEUIL, Hubert, TAÏEB, Alain, BORALEVI, Franck

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Congenital erythropoietic porphyria: a single-observer clinical study of 29 cases von Katugampola, R.P., Badminton, M.N., Finlay, A.Y., Whatley, S., Woolf, J., Mason, N., Deybach, J.C., Puy, H., Ged, C., de Verneuil, H., Hanneken, S., Minder, E., Schneider-Yin, X., Anstey, A.V.

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ADAR1 splicing mutation leading to dyschromatosis hereditaria in a Caucasian patient von Petre, J., Lasseaux, E., Ged, C., Arveiler, B., Taïeb, A., Morice‐Picard, F.

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Identification of a novel alpha1-antitrypsin variant von de Seynes, Camille, Ged, C, de Verneuil, H, Chollet, N, Balduyck, M, Raherison, C

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Usefulness of a global clinical ichthyosis vulgaris scoring system for predicting common FLG null mutations in an adult caucasian population von Ezzedine, K., Droitcourt, C., Ged, C., Diallo, A., Hubiche, T., de Verneuil, H., Boralevi, F., Taïeb, A.

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Predictive capability of chlorination disinfection byproducts models von Ged, Evan C., Chadik, Paul A., Boyer, Treavor H.

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Molecular weight distribution of phosphorus fraction of aquatic dissolved organic matter von Ged, Evan C., Boyer, Treavor H.

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A Prospective Study of Filaggrin Null Mutations in Keratoconus Patients with or without Atopic Disorders von Droitcourt, C., Touboul, D., Ged, C., Ezzedine, K., Cario-André, M., de Verneuil, H., Colin, J., Taïeb, A.

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Porphyrie érythropoïétique congénitale traitée par allogreffe de cellules souches hématopoïétiques von Lebreuilly-Sohyer, I., Morice, A., Acher, A., Dompmartin, A., Clement, C., de Verneuil, H., Ged, C., Leroy, D., Verneuil, L.

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Protection of normal human reconstructed epidermis from UV by catalase overexpression von Rezvani, H R, Cario-André, M, Pain, C, Ged, C, deVerneuil, H, Taïeb, A

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Hyperhomocystéinémie sévère induite par le givosiran au cours d’une porphyrie aiguë intermittente : le traitement par vitamine B6 est efficace von Mercié, P., Redonnet, I., Ged, C., Bronnimann, D., Blouin, J.M., Mesli, S., Vial, G., Jourde, W., Ribeiro, E., Gensous, N., Duffau, P., Richard, E.

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