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Hagit Baris-Feldman

Professor

20192025

Research activity per year

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  • A common form of dominant human IFNAR1 deficiency impairs IFN-α and -ω but not IFN-β-dependent immunity

    Al Qureshah, F., Le Pen, J., de Weerd, N. A., Moncada-Velez, M., Materna, M., Lin, D., Milisavljevic, B., Vianna, F., Bizien, L., Lorenzo, L., Lecuit, M., Pommier, J. D., Keles, S., Ozcelik, T., Pedraza-Sanchez, S., de Prost, N., El Zein, L., Hammoud, H., F P Ng, L. & Halwani, R. & 166 others, Sharif-Askari, N. S., Lau, Y. L., Tam, A. R., Singh, N., Bhattad, S., Berkun, Y., Chantratita, W., Aguilar-López, R., Shahrooei, M., Abel, L., Bastard, P., Jouanguy, E., Béziat, V., Zhang, P., M Rice, C., Cobat, A., Zhang, S. Y., Hertzog, P. J., Casanova, J. L., Zhang, Q., Aiuti, A., Al-Muhsen, S., Alcántara-Garduño, A. B., Andreakos, E., Arias, A. A., Feldman, H. B., Bolze, A., Borghesi, A., Bousfiha, A. A., Brodin, P., Christodoulou, J., Colobran, R., Condino-Neto, A., Duvlis, S., Duval, X., Dündar, M., Fakhreddine, S., Fellay, J., Flores, C., Franco, J. L., Gorochov, G., Gregersen, P. K., Hagin, D., Halwani, R., Herrera, M. T., Hung, I. F. N., Lau, Y. L., Leung, D., Le-Voyer, T., Mansouri, D., Mercado-García, J., Meyts, I., Mogensen, T. H., Ng, L. F. P., Novelli, A., Novelli, G., Okada, S., Ozcelik, F., de Diego, R. P., Perez-Tur, J., Pesole, G., Puel, A., Renia, L., Resnick, I., Rodríguez-Gallego, C., Sbeity, M., Sedighzadeh, S., Shahrooei, M., Soler-Palacín, P., Spaan, A. N., Tangye, S. G., Tayoun, A. A., Temel, Ş. G., Thorball, C., Torktaz, I., Trouillet-Assant, S., Turvey, S. E., Furkan Uddin, K. M., Luiz Vianna, F. S., Vinh, D. C., Zabaleta-Martínez, O., Eng, C., Bun, K., Mengheng Oum, M., Piola, P., Tarantola, A., Channa, M., Duong, V., Buchy, P., Gorman, C., Crabol, Y., Dussart, P., Bunleat, M., Panha, M., Kanarith Sim, M., Bunnakea, E., Laurent, D., Sothy, H., Santy, K., Douangnouvong, A., Chommanam, D., Phakhounthong, K., Vongsouvath, M., Seephone, M., Sibounheunang, B., Rattanavong, S., Davong, V., Vongsouvath, M., Mayxay, M., Dubot-Pérès, A., Newton, P. N., Phangmanixay, S., Phongsavath, K., Duc Anh, D., Do Quyen, M., Mai Hung, T. T., Thu Thuy, N. T., Minh Tan, M. L., Pham, A. T., Hien, N., Huong, D. T., Hai, L. T., Lam, N. V., An, P. N., Phuc, P. H., Thuy, P. B., Thu Huong, T. T., Hlaing, C. S., Min Aye, A. M., Thair, C., Linn, K., July, M., Thein, W., Kyaw, L. L., Tin, H. H., Tin, O. S., Oo, K. Y., Crabol, Y., Herrant, M., Lago, M., Seguy, M., Jouan, M., Hafner, L., Pérot, P., Eloit, M., Lecuit, M., Lortholary, O., Capelle, J., Rosset, B., Chevalier, V., Honnorat, J., Pinto, A. L., Dubot-Peres, A., de Lamballerie, X., Bleakley, K., Murgue, C. B., Ferrant, C., Devaux, C., Tissot-Dupont, H., Moatti, J. P., Mayxay, M., Bonnet, P., Fontenille, D., Delfraissy, J. F., Debré, P. & Durand, B., 3 Feb 2025, In: Journal of Experimental Medicine. 222, 2, e20241413.

    Research output: Contribution to journal › Article › peer-review

  • A plain language summary of a study looking at the effects of pozelimab in children with CHAPLE disease

    Ozen, A., Chongsrisawat, V., Sefer, A. P., Kolukisa, B., Jalbert, J. J., Meagher, K. A., Brackin, T., Feldman, H. B., Baris, S., Karakoc-Aydiner, E., Ergelen, R., Fuss, I. J., Moorman, H., Suratannon, N., Suphapeetiporn, K., Perlee, L., Harari, O. A. & Lenardo, M. J., 2025, In: Future Rare Diseases. 5, 1, 2498826.

    Research output: Contribution to journal › Article › peer-review

  • Changes in glycinergic neurotransmission alter mammalian retinal information processing

    Joachimsthaler, A., Hauf, K., Armbruster, A., Zayit-Soudry, S., Naaman, E., Perlman, I., Leibu, R., Kurolap, A., Baris Feldman, H., Kremers, J. & Eulenburg, V., 2025, In: Frontiers in Molecular Neuroscience. 18, 1564870.

    Research output: Contribution to journal › Article › peer-review

  • Deletion of RAI1 noncoding exons 1–2 causes Smith–Magenis syndrome

    Hamiel, U., Kurolap, A., Chai Gadot, C., Mory, A., Bar Shira, A., Baris Feldman, H. & Marom, D., Jun 2025, In: Journal of Genetics. 104, 1, 9.

    Research output: Contribution to journal › Article › peer-review

  • Evaluation of the digital genetic assistant in technology assisted genetic counseling for genetic carrier screening

    Yaron, Y., Ofen Glassner, V., Berkenstadt, M., Goldstein, N., Reznik Wolf, H., Ries Levavi, L., Abo Gutstein, L., Furman, Y., Anouchi, M., Delmar, G., Behar, D. M., Pras, E., Reches, A., Kurolap, A. & Baris Feldman, H., Dec 2025, In: npj Digital Medicine. 8, 1, 183.

    Research output: Contribution to journal › Article › peer-review

    Open Access
View all 92 Research outputs