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Allison A Dilliott

Showing results (1-10 of 48) with videos related to

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Neurobiology of Aging|May 5, 2022
Lack of association of TP73 with amyotrophic lateral sclerosis in a large cohort of casesAllison A Dilliott, Guy A Rouleau, Sali M K Farhan
Frontiers in Neurology|January 9, 2023
Sex-stratified RNA-seq analysis reveals traumatic brain injury-induced transcriptional changes in the female hippocampus conducive to dementiaMichael R Fiorini, Allison A Dilliott, Sali M K Farhan
Human Mutation|April 14, 2025
Evaluating the Utility of REVEL and CADD for Interpreting Variants in Amyotrophic Lateral Sclerosis GenesMichael R Fiorini, Allison A Dilliott, Sali M K Farhan
Journal of Investigative Medicine High Impact Case Reports|July 20, 2018
A De Novo <i>POLD1</i> Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner SyndromeLinda R Wang, Aleksandar Radonjic, Allison A Dilliott, et al.
Molecular Neurobiology|April 5, 2024
Transcriptomics of Human Brain Tissue in Parkinson's Disease: a Comparison of Bulk and Single-cell RNA SequencingMichael R Fiorini, Allison A Dilliott, Rhalena A Thomas, et al.
Brain : a Journal of Neurology|July 3, 2023
Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genesAllison A Dilliott, Seulki Kwon, Guy A Rouleau, et al.
International Journal of Molecular Sciences|April 23, 2022
DnaJC7 in Amyotrophic Lateral SclerosisAllison A Dilliott, Catherine M Andary, Meaghan Stoltz, et al.
American Journal of Medical Genetics. Part A|December 20, 2016
KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connectionLauren Badalato, Sali M K Farhan, Allison A Dilliott, et al.
Journal of Community Genetics|November 26, 2022
Cost-effectiveness of a gene sequencing test for Alzheimer's disease in OntarioNicolas Iragorri, Danielle Toccalino, Sujata Mishra, et al.
American Journal of Medical Genetics. Part A|October 12, 2020
A novel homozygous variant in REN in a family presenting with classic features of disorders involving the renin-angiotensin pathway, without renal tubular dysgenesisAllison A Dilliott, Jian Wang, Emma Brown, et al.
Pageof 5

Showing results (1-10 of 48) with videos related to

Sort By:
Pageof 5
Neurobiology of Aging|May 5, 2022
Lack of association of TP73 with amyotrophic lateral sclerosis in a large cohort of casesAllison A Dilliott, Guy A Rouleau, Sali M K Farhan
Frontiers in Neurology|January 9, 2023
Sex-stratified RNA-seq analysis reveals traumatic brain injury-induced transcriptional changes in the female hippocampus conducive to dementiaMichael R Fiorini, Allison A Dilliott, Sali M K Farhan
Human Mutation|April 14, 2025
Evaluating the Utility of REVEL and CADD for Interpreting Variants in Amyotrophic Lateral Sclerosis GenesMichael R Fiorini, Allison A Dilliott, Sali M K Farhan
Journal of Investigative Medicine High Impact Case Reports|July 20, 2018
A De Novo <i>POLD1</i> Mutation Associated With Mandibular Hypoplasia, Deafness, Progeroid Features, and Lipodystrophy Syndrome in a Family With Werner SyndromeLinda R Wang, Aleksandar Radonjic, Allison A Dilliott, et al.
Molecular Neurobiology|April 5, 2024
Transcriptomics of Human Brain Tissue in Parkinson's Disease: a Comparison of Bulk and Single-cell RNA SequencingMichael R Fiorini, Allison A Dilliott, Rhalena A Thomas, et al.
Brain : a Journal of Neurology|July 3, 2023
Characterizing proteomic and transcriptomic features of missense variants in amyotrophic lateral sclerosis genesAllison A Dilliott, Seulki Kwon, Guy A Rouleau, et al.
International Journal of Molecular Sciences|April 23, 2022
DnaJC7 in Amyotrophic Lateral SclerosisAllison A Dilliott, Catherine M Andary, Meaghan Stoltz, et al.
American Journal of Medical Genetics. Part A|December 20, 2016
KMT2D p.Gln3575His segregating in a family with autosomal dominant choanal atresia strengthens the Kabuki/CHARGE connectionLauren Badalato, Sali M K Farhan, Allison A Dilliott, et al.
Journal of Community Genetics|November 26, 2022
Cost-effectiveness of a gene sequencing test for Alzheimer's disease in OntarioNicolas Iragorri, Danielle Toccalino, Sujata Mishra, et al.
American Journal of Medical Genetics. Part A|October 12, 2020
A novel homozygous variant in REN in a family presenting with classic features of disorders involving the renin-angiotensin pathway, without renal tubular dysgenesisAllison A Dilliott, Jian Wang, Emma Brown, et al.
Pageof 5