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Physical Review Letters|September 28, 2010
Supersolid phases in a realistic three-dimensional spin modelLuis Seabra, Nic ShannonIEEE Transactions on Pattern Analysis and Machine Intelligence|July 9, 2019
Local-LDA: Open-Ended Learning of Latent Topics for 3D Object RecognitionS Hamidreza Kasaei, Luis Seabra Lopes, Ana Maria TomeIndian Journal of Ophthalmology|December 22, 2018
Familial Blau syndrome:First molecularly confirmed report from IndiaMahesh Janarthanan, Chanchal Poddar, S Sudharshan, et al.International Journal of Molecular Sciences|March 13, 2024
NOTCH1-Related Leukoencephalopathy: A Novel Variant and Literature ReviewStefania Della Vecchia, Alessandra Tessa, Rosa Pasquariello, et al.Journal of Human Immunity|March 30, 2026
Familial lupus associated with a <i>P2RY8</i> variant: Navigating the boundary between monogenic disease and genetic susceptibility to lupusClémence David, Anne Welfringer-Morin, Luis Seabra, et al.American Journal of Medical Genetics. Part A|January 3, 2025
Baricitinib Treatment in RNU7-1-Associated Aicardi-Goutières Syndrome in a South African Child: A Case ReportTimothy F Spracklen, Shehnaaz Akhalwaya, Sally Ackermann, et al.Neuropediatrics|May 29, 2020
A Novel Hypomorphic CSF1R Gene Mutation in the Biallelic State Leading to Fatal Childhood NeurodegenerationParag Mohan Tamhankar, Bin Zhu, Vasundhara Parag Tamhankar, et al.Molecular Genetics & Genomic Medicine|June 10, 2021
Novel compound heterozygous STN1 variants are associated with Coats Plus syndromeTanvi Acharya, Helen V Firth, Shilpa Dugar, et al.Stem Cell Research|December 6, 2025
Generation of two iPSC lines from patients with Aicardi-Goutières syndrome carrying either biallelic ADAR1 mutations (PC138) or a heterozygous IFIH1 mutation (PC139)Lisa Zerad, Blaise Didry-Barca, Céline Banal, et al.Journal of Medical Genetics|November 28, 2019
Cardiac valve involvement in <i>ADAR</i>-related type I interferonopathyYanick Crow, Nandaki Keshavan, Jacques Patrick Barbet, et al.Pageof 4