| Brain–immune interactions as the basis of Gulf War Illness: Clinical assessment and deployment profile of 1990–1991 Gulf War veterans in the Gulf War Illness consortium (GWIC … L Steele, N Klimas, M Krengel, E Quinn, R Toomey, D Little, M Abreu, ... Brain sciences 11 (9), 1132, 2021 | 19 | 2021 |
| Frontal versus dysexecutive syndromes: relevance of an interactionist approach in a case series of patients with prefrontal lobe damage J Besnard, P Allain, V Lerma, G Aubin, V Chauviré, F Etcharry-Bouyx, ... Neuropsychological rehabilitation 28 (6), 919-936, 2018 | 13 | 2018 |
| An Integrated Phenotypic and Genotypic Approach Reveals a High‐Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger Domain CA Deisseroth, VC Lerma, CL Magyar, JM Pfliger, A Nayak, ND Bliss, ... Annals of Neurology 92 (1), 138-153, 2022 | 7 | 2022 |
| A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3 MS Paul, SL Michener, H Pan, H Chan, JM Pfliger, JA Rosenfeld, ... The American Journal of Human Genetics 111 (1), 96-118, 2024 | 4 | 2024 |
| Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy MS Paul, SL Michener, H Pan, JM Pfliger, JA Rosenfeld, VC Lerma, ... medRxiv, 2023.03. 27.23287689, 2023 | 2 | 2023 |
| Integrated phenotypic and genotypic approach defines EBF3-related genotype-phenotype relationships CA Deisseroth, A Nayak, ND Bliss, V Lerma, AW LeMaire, V Narayanan, ... medRxiv, 2020.12. 07.20238691, 2020 | 2 | 2020 |
| PAK1 c.1409 T > a (p. Leu470Gln) de novo variant affects the protein kinase domain, leading to epilepsy, macrocephaly, spastic quadriplegia, and … ML Corriveau, SI Amaya, MC Koebel, VC Lerma, SL Michener, A Turner, ... American Journal of Medical Genetics Part A 191 (6), 1619-1625, 2023 | 1 | 2023 |
| Neurofunctional and neuroanatomical markers of EBF3-related neurodevelopmental disorder VC Lerma¹, B Serrallach, RJ Franzen, E Devara, C Deisseroth⁴, ... | | 2022 |
| Integrated deep phenotypic and mutational approach defines EBF3-related HADD syndrome genotype-phenotype relationships (2850) C Deisseroth, A Nayak, N Bliss, V Lerma, A Lemaire, V Narayanan, ... Neurology 96 (15 Supplement), 2021 | | 2021 |
