Author

Brian King

Congenica Ltd. (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· 1

Signature Assays, Organisms & Methods

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Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

A. Haworth· 1 shared Elaine J. Marchi· 1 shared Gholson J. LyoniD· 1 shared Karen Amble· 1 shared Maureen Gavin· 1 shared Milen T. VelinoviD· 1 shared Mohd ArifiD· 1 shared Naomi Horowitz· 1 shared

Activity by Year

2021-2021 · peak 1/yr

Co-Author Collaboration Network

9 top collaborators · 36 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

A. Haworth

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1 paper

Recent·Most cited

Autosomal recessive SLC30A9 Mutations in a Proband with a Cerebro-Renal Syndrome and No Parental Consanguinity

Robert S. Kleyner, Mohd Arif, Elaine J. Marchi, Naomi Horowitz, A. Haworth, Brian King, Karen Amble, Maureen Gavin, Milen T. Velinov, Gholson J. Lyon

This paper reports a non-consanguineous family with autosomal recessive SLC30A9 mutations associated with a cerebro-renal syndrome and conducts a limited population allele frequency analysis.

Molecular Case Studies · Oct 29, 2021Peer-reviewedGenetic & Genomic Medicine