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Jake Allen

De novo coding variants in the AGO1 gene cause a neurodevelopmental disorder with intellectual disability
2021 · Audrey Schalk, Margot A. Cousin, et al. · Journal of Medical Genetics · 32
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De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures
2021 · Beryl Royer-Bertrand, Marine Jequier Gygax, et al. · Molecular Autism · 20
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Phenotype and genetic analysis of data collected within the first year of NeuroDev
2023 · Patricia Kipkemoi, Heesu Ally Kim, et al. · Neuron · 18
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Participant Reactions to a Literacy-Focused, Web-Based Informed Consent Approach for a Genomic Implementation Study
2020 · Stephanie A. Kraft, Kathryn M. Porter, et al. · AJOB Empirical Bioethics · 18
Most people share genetic test results with relatives even if the findings are normal: Family communication in a diverse population
2023 · Jessica Ezzell Hunter, Leslie Riddle, et al. · Genetics in Medicine · 16
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Adaptation and early implementation of the PREdiction model for gene mutations (PREMM5™) for lynch syndrome risk assessment in a diverse population
2021 · Kathleen F. Mittendorf, Chinedu Ukaegbu, et al. · Familial Cancer · 13
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Laboratory-related outcomes from integrating an accessible delivery model for hereditary cancer risk assessment and genetic testing in populations with barriers to access
2022 · Laura M. Amendola, Elizabeth Shuster, et al. · Genetics in Medicine · 12
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Abstract 2339 The Role of an Intermediate Conformation of SHP2 in the MEK Pathway of KRAS-Driven Cancers
2024 · Daniel Shannon, Gavin Poetker, et al. · Journal of Biological Chemistry
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P523: The NeuroDev Study: Genetic characterization of neurodevelopmental disorders in African populations
2023 · Emily O'Heir, Patricia Kipkemoi, et al. · Genetics in Medicine Open
Genetic Characterization of Neurodevelopmental Disorders in African Populations: the Neurodev Trio Pilot
2021 · Patricia Kipkemoi, Björn Christ, et al. · European Neuropsychopharmacology
Additional file 1 of De novo variants in CACNA1E found in patients with intellectual disability, developmental regression and social cognition deficit but no seizures
2021 · Royer-Bertrand, Beryl, Jequier Gygax, Marine, et al. · Figshare
Abstract PR02: Using web-based tools to assess familial cancer risk in diverse populations
2020 · Heather Spencer Feigelson, Kathleen F. Mittendorf, et al. · Cancer Epidemiology Biomarkers & Prevention
Works count: 14
Citation count: 129
H-index: 7
I10-index: 7
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