Jessie C. Jacobsen

University of Auckland — New Zealand

Neuroscience · Life Sciences

15h-index1.5kcitations51works1.82yr avg
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Research Topics

Genetic Neurodegenerative Diseases(13), Mitochondrial Function and Pathology(12), Genomic variations and chromosomal abnormalities(10), Genetics and Neurodevelopmental Disorders(9), Genomics and Rare Diseases(8)

Publications50 total

Foundations of an Ovine Model of Fragile X Syndrome
Genes·2026Open Access
T60. DIAGNOSTIC UTILITY OF GENOME-WIDE SEQUENCING REANALYSIS FOR DEVELOPMENTAL CONDITIONS: EXAMPLE CASES
European Neuropsychopharmacology·2025
The genetics of motor neuron disease in New Zealand
Journal of the Neurological Sciences·2025· 2 citedOpen Access
Germline mosaicism in TCF20-associated neurodevelopmental disorders: a case study and literature review
Journal of Human Genetics·2025Open Access
Unraveling ADHD: genes, co-occurring traits, and developmental dynamics
Life Science Alliance·2025· 2 citedOpen Access
Early Detection and Intervention in Autism: Emerging Behavioral and Biological Markers
2025
Genetics of Motor Neuron Disease in New Zealand
2024Open Access
Genetic diagnostic outcomes from a 10‐year research programme in autism in Aotearoa New Zealand
Journal of the Royal Society of New Zealand·2024· 1 citedOpen Access
The genes tell a story: new research offers much-needed certainty for autistic New Zealanders
2024
Single nucleotide polymorphisms in the cannabinoid CB<sub>2</sub> receptor: Molecular pharmacology and disease associations
British Journal of Pharmacology·2024· 8 citedOpen Access
Single nuclei RNA-seq reveals a medium spiny neuron glutamate excitotoxicity signature prior to the onset of neuronal death in an ovine Huntington’s disease model
Human Molecular Genetics·2024· 7 citedOpen Access
A bioinformatic analysis of gene editing off‐target loci altered by common polymorphisms, using ‘PopOff’
Journal of the Royal Society of New Zealand·2024· 3 citedOpen Access
Somatic CAG Repeat Stability in a Transgenic Sheep Model of Huntington’s Disease
Journal of Huntington s Disease·2024· 2 citedOpen Access
Early Detection and Intervention in Autism: Emerging Behavioral and Biological Markers
2024
A novel 11 base pair deletion in <scp><i>KMT2C</i></scp> resulting in Kleefstra syndrome 2
Molecular Genetics & Genomic Medicine·2023· 4 citedOpen Access
De novo network analysis reveals autism causal genes and developmental links to co-occurring traits
Life Science Alliance·2023· 7 citedOpen Access
Evidence for glutamate excitotoxicity that occurs before the onset of striatal cell loss and motor symptoms in an ovine Huntington’s Disease model
2023· 1 citedOpen Access
Evidence for glutamate excitotoxicity that occurs before the onset of cell loss and motor symptoms in an ovine Huntington's Disease model.
Zenodo (CERN European Organization for Nuclear Research)·2023Open Access
An unbiased <i>de novo</i> network analysis uncovering causal genes and the developmental intersection between autism and co-occurring traits
2023· 2 citedOpen Access
Isolated nuclei from frozen tissue are the superior source for single cell RNA-seq compared with whole cells
2023· 4 citedOpen Access
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Frequent Co-authors

Russell G. Snell(37), Klaus Lehnert(26), Whitney Whitford(16), Suzanne J. Reid(12), Juliet Taylor(12), Skye R. Rudiger(10), Marcy E. MacDonald(10), Renée R. Handley(10), Richard L. M. Faull(9), James F. Gusella(9), R. Sean Hill(8), Clive J. McLaughlan(8), C. Simon Bawden(8), Donald R. Love(8), Henry J. Waldvogel(7), Victoria Hawkins(7), Stefano Patassini(6), Brendan Swan(6), Paul J. Verma(5), David A. Koolen(4)