JenniferAnnBraultMD

Child Neurology • Nashville, TN

Physician

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Office
3601 21st Ave S
Nashville, TN 37232
Phone+1 615-322-3000

Fax+1 615-936-0605
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Education & Training

Indiana University School of MedicineFellowship, Child Neurology, 2009
Indiana University School of MedicineResidency, Medical Genetics and Genomics, 2012 - 2014
Indiana University School of MedicineResidency, Child Neurology, 2009 - 2012
Indiana University School of MedicineResidency, Pediatrics, 2007 - 2009
Indiana University School of MedicineClass of 2006

Certifications & Licensure

IN State Medical License 2014 - 2025
TN State Medical License 2015 - 2025
WV State Medical License 2023 - 2024
AL State Medical License 2020 - 2020
American Board of Psychiatry and Neurology Neurology with Special Qualification in Child Neurology
American Board of Medical Genetics and Genomics Clinical Genetics and Genomics

Publications & Presentations

PubMed

1 citations
Correction to: An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.
Sacha Ferdinandusse, Kirsty McWalter, Heleen Te Brinke, Lodewijk IJlst, Petra M Mooijer, Jos P N Ruiter, Alida E M van Lint, Mia Pras-Raves, Eric Wever, Francisca Mill...> ;Genetics in Medicine. 2021 Dec 1
1 citations
Klinefelter's Syndrome with Maternal Uniparental Disomy X, Interstitial Xp22.31 Deletion, X-linked Ichthyosis, and Severe Central Nervous System Regression
Jennifer A. Brault, Laurence E. Walsh, Gail H. Vance, David D. Weaver> ;Journal of Pediatric Genetics. 2021 Sep 1
1 citations
Patients With Extreme Early Onset Juvenile Huntington Disease Can Have Delays in Diagnosis: A Case Report and Literature Review.
Ashley A. Moeller, Marcia V. Felker, Jennifer A. Brault, Laura Duncan, Rizwan Hamid, Meredith R. Golomb> ;Child Neurology Open. 2021 Aug 5
27 citations
An autosomal dominant neurological disorder caused by de novo variants in FAR1 resulting in uncontrolled synthesis of ether lipids.
Sacha Ferdinandusse, Kirsty McWalter, Heleen Te Brinke, Lodewijk IJlst, Petra M Mooijer, Jos P N Ruiter, Alida E M van Lint, Mia Pras-Raves, Eric Wever, Francisca Mill...> ;Genetics in Medicine. 2021 Apr 1
5 citations
Practical Approaches and Knowledge Gaps in the Care for Children With Leukodystrophies.
Stephanie Keller, Eric J. Mallack, Jennifer Rubin, Jennifer A. Accardo, Jennifer A. Brault, Camille Corre, Camila Elizondo, Jennifer Garafola, April C. Jackson-Garcia,...> ;Journal of Child Neurology. 2021 Jan 1
An apparent new syndrome of extreme short stature, microcephaly, dysmorphic faces, intellectual disability, and a bone dysplasia of unknown etiology.
Jennifer L. Stinson, Jennifer A. Brault, Paula Delk, Brett H. Graham, Boaz Karmazyn, Bryan D. Hall, David D. Weaver> ;American Journal of Medical Genetics. Part A. 2020 Jul 1
17 citations
Whole genome sequencing reveals novel IGHMBP2 variant leading to unique cryptic splice-site and Charcot-Marie-Tooth phenotype with early onset symptoms.
Thomas A. Cassini, Laura Duncan, Lynette Rives, John H. Newman, John A. Phillips, Mary Koziura, Jennifer A. Brault, Rizwan Hamid, Joy D. Cogan> ;Molecular Genetics & Genomic Medicine. 2019 Jun 1
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Press Mentions

An Autosomal Dominant Neurological Disorder Caused by De Novo Variants in FAR1 Resulting in Uncontrolled Synthesis of Ether LipidsNovember 26th, 2020
Vanderbilt Joins National Neurofibromatosis NetworkNovember 9th, 2017