Author

Cornelia Kornblum

University Hospital BonnORCID 0000-0002-0111-7281Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetic & Genomic Medicine· 1

Signature Assays, Organisms & Methods

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Research Focus:gene regulatory network inference· 1 Organism:human· 1 Approach:statistical model· 1

Frequent Co-Authors

Andrew M. SchaeferiD· 1 shared Andrew Tym HattersleyiD· 1 shared Annemarie ThaeleiD· 1 shared Boriana BüchneriD· 1 shared Catherine L FeeneyiD· 1 shared Cathy E. Woodward· 1 shared Charlotte L. AlstoniD· 1 shared Chiara PizzamiglioiD· 1 shared

Activity by Year

2022-2022 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 45 mutual co-author links

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1 shared paperGenetic & Genomic Medicine

Andrew M. SchaeferORCID

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1 paper

Recent·Most cited

Defining the nuclear genetic architecture of a common maternally inherited mitochondrial disorder

Róisín M. Boggan, Yi Shiau Ng, Imogen G. Franklin, Charlotte L. Alston, Emma L. Blakely, Boriana Büchner, Enrico Bugiardini, Kevin Colclough, Catherine L Feeney, Michael G. Hanna, Andrew Tym Hattersley, Thomas Klopstock, Cornelia Kornblum, Michelangelo Mancuso, Kashyap Amratlal Patel, , Sarah J. Pickett

This paper identifies nuclear genetic factors modifying the clinical phenotype of m.3243A>G mitochondrial disease using genetic linkage analysis across 76 pedigrees.

medRxiv · Nov 18, 2022 · PreprintGenetic & Genomic Medicine