Author

Androo J. Markham

Oxford Nanopore Technologies (United Kingdom)

Listed by name: these papers carry no ORCID for this author, so different people with the same name may be mixed together.

Biology Disciplines

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Genetic & Genomic Medicine· 2 Genetics· 1

Signature Assays, Organisms & Methods

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Approach:experimental assay· 3 Organism:human· 3 Research Focus:variant calling· 3 Assay:whole-genome sequencing· 3 Research Focus:benchmarking· 1 Approach:statistical model· 1 Research Focus:variant effect prediction· 1

Frequent Co-Authors

Andrew SingletoniD· 2 shared Bradford H. CaseyiD· 2 shared Cornelis BlauwendraatiD· 2 shared Kimberley J. BillingsleyiD· 2 shared Mark CooksoniD· 2 shared Mike A. NallsiD· 2 shared Pilar Álvarez JereziD· 2 shared Abigail Miano‐BurkhardtiD· 1 shared

Activity by Year

2022-2025 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 43 mutual co-author links

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2 shared papersGenetic & Genomic Medicine

Andrew SingletonORCID

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Author profile →

3 papers

Recent·Most cited

Long-read sequencing identifies FGF14 repeat expansions in Parkinson's disease

Fulya Akçimen, Kensuke Daida, Lara Mariah Lange, Abraham G Moller, Abigail Miano‐Burkhardt, Laksh Malik, Kimberly Paquette, Pilar Álvarez Jerez, Jackson Mingle, Breeana Baker, Melissa Meredith, Cedric Kouam, Paige Jarreau, Androo J. Markham, Jessica Anderson, , Kimberley J Billingsley

The paper identifies FGF14 GAA repeat expansions in Parkinson's disease using long-read sequencing and finds they occur in both patients and controls.

Brain · Nov 29, 2025Peer-reviewedGenetic & Genomic Medicine

3-hour genome sequencing and targeted analysis to rapidly assess genetic risk

Miranda Pg Zalusky, Jonas A. Gustafson, Stephanie C. Bohaczuk, Benjamin J. Mallory, Paxton Reed, Tara Lynn Wenger, Erika Beckman, Irene J. Chang, Cate Randall Paschal, Jillian G. Buchan, Christina M. Lockwood, Mihai Puia‐Dumitrescu, Daniel R. Garalde, Joseph Guillory, Androo J. Markham, , Danny E. Miller

This study demonstrates rapid whole-genome sequencing and targeted analysis within three hours to assess genetic risk in a newborn, showing they are not affected or a carrier for a specific Mendelian condition.

Genetics in Medicine Open · Jan 1, 2024Peer-reviewedGenetic & Genomic Medicine

Genome-wide analysis of Structural Variants in Parkinson's Disease using Short-Read Sequencing data

Kimberley J. Billingsley, Jinhui Ding, Pilar Álvarez Jerez, Anastasia Illarionova, Francis P. Grenn, Mary B. Makarious, Anni K. Moore, Dan Vitale, Xylena Reed, Dena G. Hernandez, Ali Torkamani, Mina Ryten, John Hardy, Ruth Chia, Sonja W. Scholz, , Andrew Singleton

This study identifies 3,154 high-confidence structural variants in Parkinson's disease using short-read sequencing and validates some with long-read data, highlighting limitations of short-read methods.

bioRxiv · Aug 22, 2022 · PreprintGenetics