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Author

Ashanté Lakey

Observed names: A. Lakey, Ashante Lakey
ORCID: 0000-0002-9714-6019
Observed ORCID: 0000-0002-9714-6019
OpenAlex ID: A5033721426
Origins and impact of extrachromosomal DNA
2024 · Chris Bailey, Oriol Pich, et al. · Nature · 197
An intermediate-effect size variant in UMOD confers risk for chronic kidney disease
2022 · Eric Olinger, Céline Schaeffer, et al. · Proceedings of the National Academy of Sciences · 48
The genomic landscape of familial glioma
2023 · Dong-Joo Choi, Georgina Armstrong, et al. · Science Advances · 47
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Specialist multidisciplinary input maximises rare disease diagnoses from whole genome sequencing
2022 · William L. Macken, Micol Falabella, et al. · Nature Communications · 32
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Mutation-Attention (MuAt): deep representation learning of somatic mutations for tumour typing and subtyping
2023 · Prima Sanjaya, Katri Maljanen, et al. · Genome Medicine · 31
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Gain and loss of function variants in EZH1 disrupt neurogenesis and cause dominant and recessive neurodevelopmental disorders
2023 · Carolina Gracia-Diaz, Yijing Zhou, et al. · Nature Communications · 27
Biallelic variants in coenzyme Q10 biosynthesis pathway genes cause a retinitis pigmentosa phenotype
2022 · Neringa Jurkute, Francesca Cancellieri, et al. · npj Genomic Medicine · 26
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HNRNPC haploinsufficiency affects alternative splicing of intellectual disability-associated genes and causes a neurodevelopmental disorder
2023 · Eva Niggl, Arjan Bouman, et al. · The American Journal of Human Genetics · 24
The relationship between the gastric cancer microbiome and clinicopathological factors: a metagenomic investigation from the 100,000 genomes project and The Cancer Genome Atlas
2025 · Mary E. Booth, Henry M. Wood, et al. · Gastric Cancer · 12
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Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14
2023 · Adam Jackson, Sheng-Jia Lin, et al. · Human Genetics and Genomics Advances · 12
A gene pathogenicity tool “GenePy” identifies missed biallelic diagnoses in the 100,000 Genomes Project
2024 · Eleanor G. Seaby, Gary Leggatt, et al. · Genetics in Medicine · 8
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A genotype-to-phenotype approach suggests under-reporting of single nucleotide variants in nephrocystin-1 (NPHP1) related disease (UK 100,000 Genomes Project)
2023 · Gary Leggatt, Guo Cheng, et al. · Scientific Reports · 8
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Framework for artificial intelligence implementation research in healthcare: synthesizing current evidence on barriers and facilitators
2026 · Melanie Powis, Aly M. Ladak, et al. · npj Digital Medicine · 7
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What we can afford is what kills us”: An Intersectional Analysis of Food Insecurity Among Black Households in Toronto, Canada
2026 · Emmanuel Kyeremeh, Jonathan Amoyaw, et al. · SSRN Electronic Journal
Supportive Care Needs of Patients with Breast Cancer Who Self-Identify as Black: An Integrative Review
2025 · Etienne Oshinowo, Emily Peterson, et al. · Current Oncology
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Works count: 15
Citation count: 479
H-index: 10
I10-index: 10
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