Author

Thomas S. Scerri

The University of MelbourneORCID 0000-0003-0992-4042Unclaimed ORCID profile · follow to get notified of new preprints

Biology Disciplines

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Genetics· 2 Genomics· 1

Signature Assays, Organisms & Methods

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Organism:human· 3 Research Focus:GWAS / association mapping· 2 Assay:GWAS summary statistics· 2 Approach:statistical model· 2 Approach:experimental assay· 1 Organism:zebrafish· 1

Frequent Co-Authors

Melanie BahloiD· 2 shared Alan C. BirdiD· 1 shared Alessandro GialluisiiD· 1 shared Alexander P.A. StegmanniD· 1 shared Andrew P. MorrisiD· 1 shared Anniek VaesseniD· 1 shared Anthony P. MonacoiD· 1 shared Arndt Wilcke· 1 shared

Activity by Year

2018-2021 · peak 1/yr

Co-Author Collaboration Network

10 top collaborators · 17 mutual co-author links

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2 shared papersGenetics

Melanie BahloORCID

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Author profile →

3 papers

Recent·Most cited

GeneticsGenome MedicinePeer-reviewedMar 9, 2021

Genetic Disruption of Serine Biosynthesis is a Key Driver of Macular Telangiectasia Type 2 Etiology and Progression

Roberto Bonelli, Brendan R. E. Ansell, Luca Andrea Lotta…·Melanie Bahlo

This study identifies serine biosynthesis as a key driver of MacTel etiology and progression using statistical genetics methods.

28 citations

humanGWAS summary statistics

𝕏 PostBluesky

GenomicsTranslational PsychiatryPeer-reviewedFeb 11, 2019

Genome Wide Association Scan identifies new variants associated with a cognitive predictor of dyslexia.

Alessandro Gialluisi, Till F. M. Andlauer, Nazanin Mirza‐Schreiber…·Gerd Schulte‐Körne

The paper conducts a GWAS to identify genetic variants associated with a cognitive predictor of dyslexia, finding significant associations with variants near MIR924HG and NKAIN3.

105 citationstop 1%

humanGWAS summary statistics

𝕏 PostBluesky

GeneticsHuman Molecular GeneticsPeer-reviewedMay 3, 2018

Functional analysis of a hypomorphic allele shows that MMP14 catalytic activity is the prime determinant of the Winchester syndrome phenotype

Ivo J. H. M. de Vos, Evelyn Yaqiong Tao, Sheena L. M. Ong…·Maurice A. M. Van Steensel

The paper identifies a hypomorphic MMP14 mutation in Winchester syndrome and shows its catalytic activity determines disease severity using in vitro and zebrafish models.

30 citations

𝕏 PostBluesky