Research output per year
Research output per year
Personal profile
Education
Molecular & Cellular Biology of Development, Ph.D., Sorbonne Université
2006
M.S., Institut Pasteur de Madagascar
2000
Fingerprint
Dive into the research topics where Bruno Reversade is active. These topic labels come from the works of this person. Together they form a unique fingerprint.
- 1 Similar Profiles
Network
Recent external collaboration on country/territory level. Dive into details by clicking on the dots or
-
Author Correction: Mutations in PYCR1 cause cutis laxa with progeroid features (Nature Genetics, (2009), 41, 9, (1016-1021), 10.1038/ng.413)
Reversade, B., Escande-Beillard, N., Dimopoulou, A., Fischer, B., Chng, S. C., Li, Y., Shboul, M., Tham, P. Y., Kayserili, H., Al-Gazali, L., Shahwan, M., Brancati, F., Lee, H., O’Connor, B. D., Kegler, M. S. V., Merriman, B., Nelson, S. F., Masri, A., Alkazaleh, F., Guerra, D., & 27 others, Feb 1 2022, In: Nature Genetics. 54, 2Research output: Contribution to journal › Article › peer-review
-
Biallelic ZNFX1 variants are associated with a spectrum of immuno-hematological abnormalities
Alawbathani, S., Westenberger, A., Ordonez-Herrera, N., Al-Hilali, M., Al Hebby, H., Alabbas, F., Alhashem, A. M., Elyamany, G., Megarbane, A., Kose, M., Alhashmi, N., Al Sukaiti, N., Al-Raqad, M., Al-Tawalbeh, S., Abu Adas Blanco, O., Alkhattabi, F., Sng, D., Al-Ali, R., Khan, S., Tawamie, H., & 7 others, Feb 1 2022, In: Clinical Genetics. 101, 2, p. 247-254 8 p.Research output: Contribution to journal › Article › peer-review
7 Scopus citations -
C10orf99/GPR15L Regulates Proinflammatory Response of Keratinocytes and Barrier Formation of the Skin
Dainichi, T., Nakano, Y., Doi, H., Nakamizo, S., Nakajima, S., Matsumoto, R., Farkas, T., Wong, P. M., Narang, V., Moreno Traspas, R., Kawakami, E., Guttman-Yassky, E., Dreesen, O., Litman, T., Reversade, B. & Kabashima, K., Feb 22 2022, In: Frontiers in Immunology. 13Research output: Contribution to journal › Article › peer-review
3 Scopus citations -
Corrigendum to: Heterozygous missense variant in EIF6 gene: A novel form of Shwachman–Diamond syndrome? (American Journal of Medical Genetics Part A, (2020), 182, 9, (2010-2020), 10.1002/ajmg.a.61758)
Koh, A. L., Bonnard, C., Binte Ali, N. A., Reversade, B. & Jamuar, S., Jan 1 2022, In: American Journal of Medical Genetics, Part A. 188, 1Research output: Contribution to journal › Article › peer-review
-
Direct identification of A-to-I editing sites with nanopore native RNA sequencing
Nguyen, T. A., Heng, J. W. J., Kaewsapsak, P., Kok, E. P. L., Stanojević, D., Liu, H., Cardilla, A., Praditya, A., Yi, Z., Lin, M., Aw, J. G. A., Ho, Y. Y., Peh, K. L. E., Wang, Y., Zhong, Q., Heraud-Farlow, J., Xue, S., Reversade, B., Walkley, C., Ho, Y. S., & 3 others, Jul 1 2022, In: Nature Methods. 19, 7, p. 833-844 12 p.Research output: Contribution to journal › Article › peer-review
8 Scopus citations -
Discovery of a genetic module essential for assigning left–right asymmetry in humans and ancestral vertebrates
Szenker-Ravi, E., Ott, T., Khatoo, M., de Bellaing, A. M., Goh, W. X., Chong, Y. L., Beckers, A., Kannesan, D., Louvel, G., Anujan, P., Ravi, V., Bonnard, C., Moutton, S., Schoen, P., Fradin, M., Colin, E., Megarbane, A., Daou, L., Chehab, G., Di Filippo, S., & 21 others, Jan 1 2022, In: Nature Genetics. 54, 1, p. 62-72 11 p.Research output: Contribution to journal › Article › peer-review
8 Scopus citations -
Ermin deficiency leads to compromised myelin, inflammatory milieu, and susceptibility to demyelinating insult
Ziaei, A., Garcia-Miralles, M., Radulescu, C. I., Sidik, H., Silvin, A., Bae, H. G., Bonnard, C., Yusof, N. A. B. M., Ferrari Bardile, C., Tan, L. J., Ng, A. Y. J., Tohari, S., Dehghani, L., Henry, L., Yeo, X. Y., Lee, S., Venkatesh, B., Langley, S. R., Shaygannejad, V., Reversade, B., & 3 others, Sep 1 2022, In: Brain Pathology. 32, 5Research output: Contribution to journal › Article › peer-review
-
Generation of three human induced pluripotent stem cell lines with IRX5 knockout and knockin genetic editions using CRISPR-Cas9 system
Canac, R., Caillaud, A., Cimarosti, B., Girardeau, A., Hamamy, H., Reversade, B., Bonnard, C., Al Sayed, Z. R., David, L., Poschmann, J., Lemarchand, P., Lamirault, G. & Gaborit, N., Jan 1 2022, In: Stem Cell Research. 58Research output: Contribution to journal › Article › peer-review
2 Scopus citations
Press/Media
-
Research finds mutations in novel gene responsible for severe liver disease in children
08/13/22 → 08/14/22
4 items of Media coverage
Press/Media: Press / Media
-
Nature, smells, and human wellbeing - Ambio
08/3/22
1 item of Media coverage
Press/Media: Press / Media
-
Loss of FOCAD, operating via the SKI messenger RNA surveillance pathway, causes a pediatric syndrome with liver cirrhosis - Nature Genetics
08/2/22
1 item of Media coverage
Press/Media: Press / Media
-
Mutations in novel gene found to be responsible for severe liver disease in children
08/1/22 → 08/2/22
4 items of Media coverage
Press/Media: Press / Media
-
-
Genetic roots of 3 mitochondrial diseases ID'd via new approach
05/25/22 → 05/27/22
2 items of Media coverage
Press/Media: Press / Media
-
Researchers identify the genetic causes of three mitochondrial diseases using new approach
05/26/22
2 items of Media coverage
Press/Media: Press / Media
-
Genetic roots of 3 mitochondrial diseases ID’d via new approach
05/25/22 → 05/26/22
6 items of Media coverage
Press/Media: Press / Media