Author

Vanesa C. Lerma

Observed names: Lerma, Vanesa C., Vanesa Lerma

Institutions: Baylor College of Medicine, Texas Children's Hospital, University of Houston

Observed institutions: Baylor College of Medicine, Texas Children's Hospital, Weill Cornell Medicine, University of Houston, St. Edward's University

OpenAlex ID: A5112903708

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) Multisite Case-Control Study

2021 · Lea Steele, Nancy Klimas, et al. · Brain Sciences · 27

An Integrated Phenotypic and Genotypic Approach Reveals a High‐Risk Subtype Association for EBF3 Missense Variants Affecting the Zinc Finger Domain

2022 · Cole A. Deisseroth, Vanesa C. Lerma, et al. · Annals of Neurology · 17

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

2024 · Maimuna S. Paul, Sydney L. Michener, et al. · The American Journal of Human Genetics · 15

Frontal versus dysexecutive syndromes: relevance of an interactionist approach in a case series of patients with prefrontal lobe damage

2016 · Jérémy Besnard, Philippe Allain, et al. · Neuropsychological Rehabilitation · 12

PAK1 c. 1409 T > a (p. Leu470Gln ) de novo variant affects the protein kinase domain, leading to epilepsy, macrocephaly, spastic quadriplegia, and hydrocephalus: Case report and review of the literature

2023 · Melina L. Corriveau, Sabrina I. Amaya, et al. · American Journal of Medical Genetics Part A · 8

Rare variants in PPFIA3 cause delayed development, intellectual disability, autism, and epilepsy

2023 · Maimuna S. Paul, Sydney L. Michener, et al. · medRxiv · 3

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

2024 · Maimuna S. Paul, Sydney L. Michener, et al. · The American Journal of Human Genetics · 2

Mnemonic Techniques

2018 · Amanda L. Sacks-Zimmerman, Vanesa C. Lerma · Springer eBooks · 2

Integrated phenotypic and mutational approach defines EBF3-related HADD syndrome genotype-phenotype relationships

2020 · Cole A. Deisseroth, Aarushi Nayak, et al. · medRxiv · 1

Mnemonic Techniques

2017 · Amanda L. Sacks-Zimmerman, Vanesa C. Lerma · Springer eBooks · 1

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

2024 · Maimuna S. Paul, Sydney L. Michener, et al. · The American Journal of Human Genetics

A syndromic neurodevelopmental disorder caused by rare variants in PPFIA3

2024 · Paul, Maimuna S., Michener, Sydney L., et al. · RWTH Publications (RWTH Aachen)

Integrated deep phenotypic and mutational approach defines EBF3-related HADD syndrome genotype-phenotype relationships (2850)

2021 · Cole Deisseroth, Aarushi Nayak, et al. · Neurology

Works count: 13

Citation count: 88

H-index: 5

I10-index: 4