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Jessica L. Jackson

Observed name: Jessica Jackson
OpenAlex ID: A5112299366
Physician interpretation of variants of uncertain significance
2018 · Sarah K. Macklin, Jessica L. Jackson, et al. · Familial Cancer · 78
Impact of integrated translational research on clinical exome sequencing
2020 · Eric W. Klee, Margot A. Cousin, et al. · Genetics in Medicine · 57
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De novo variants in FBXO11 cause a syndromic form of intellectual disability with behavioral problems and dysmorphisms
2019 · Sandra Jansen, Ilse M. van der Werf, et al. · European Journal of Human Genetics · 38
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Case report: 5 year follow-up of adult late-onset mitochondrial encephalomyopathy with lactic acid and stroke-like episodes (MELAS)
2016 · Kiri Sunde, Patrick R. Blackburn, et al. · Molecular Genetics and Metabolism Reports · 25
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Expanded phenotype in a patient with spastic paraplegia 7
2017 · Jennifer Gass, Patrick R. Blackburn, et al. · Clinical Case Reports · 13
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Integrative data fusion for comprehensive assessment of a novel CHEK2 variant using combined genomics, imaging, and functional–structural assessments via protein informatics
2018 · Stephanie L Hines, Ahmed N Mohammad, et al. · Molecular Omics · 10
Novel GFAP Variant in Adult-onset Alexander Disease With Progressive Ataxia and Palatal Tremor
2017 · Jennifer M. Gass, Anvir Cheema, et al. · The Neurologist · 9
Impact of integrated translational research on clinical exome sequencing
2023 · Eric W. Klee, Margot A. Cousin, et al. · Genetics in Medicine · 8
TANGO2 Mutation: A Genetic Cause of Multifocal Combined Dystonia
2021 · Jessica Frey, Matthew R. Burns, et al. · Movement Disorders Clinical Practice · 6
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Whole exome sequencing of a patient with suspected mitochondrial myopathy reveals novel compound heterozygous variants in RYR 1
2017 · Patrick R. Blackburn, Duygu Selcen, et al. · Molecular Genetics & Genomic Medicine · 6
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Early‐onset limb‐girdle muscular dystrophy‐2L in a female athlete
2016 · Patrick R. Blackburn, Duygu Selcen, et al. · Muscle & Nerve · 6
A case of contralateral breast cancer and skin cancer associated with NBN heterozygous pathogenic variant c.698_701delAACA
2017 · Jennifer Gass, Jessica Jackson, et al. · Familial Cancer · 5
Incidence of Pathogenic Variants in Those With a Family History of Pancreatic Cancer
2018 · Sarah K. Macklin, Pashtoon M. Kasi, et al. · Frontiers in Oncology · 4
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Whole Exome Sequencing Identifies Atypical Welander Distal Myopathy in Patient
2017 · Jennifer Gass, Patrick Blackburn, et al. · Journal of Clinical Neuromuscular Disease · 4
Personalized molecular modeling for pinpointing associations of protein dysfunction and variants associated with hereditary cancer syndromes
2018 · Sarah Macklin, Ahmed Mohammed, et al. · Molecular Genetics & Genomic Medicine · 3
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Late onset asymptomatic pancreatic neuroendocrine tumor – A case report on the phenotypic expansion for MEN1
2017 · Charu Kaiwar, Sarah K. Macklin, et al. · Hereditary Cancer in Clinical Practice · 2
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An infant with large fontanelles, aplasia cutis congenita, tessier facial cleft, polydactyly inversus, and toe syndactyly: A previously undescribed syndrome?
2015 · Jessica Jackson, Paula Delk, et al. · American Journal of Medical Genetics Part A · 1
Abstract 1769: Significant in vivo activity of an APE1/Ref-1 redox inhibitor, E3330, alone and in combination with Bevacizumab in a glioblastoma mouse model analyzed by a whole slide digital imaging system and quantitative immunohistochemistry
2012 · Krishan Kumar, Jessica L. Jackson, et al. · Cancer Research · 1
Abstract 5380: Detection of OvCa1 in human malignancies.
2013 · Jessica L. Jackson, Kristen A. Grothaus, et al. · Cancer Research
Works count: 19
Citation count: 276
H-index: 8
I10-index: 6
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