Author

Brendan Crawford

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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Genetics· 1

Signature Assays, Organisms & Methods

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Research Focus:differential expression· 1 Organism:human· 1 Approach:statistical model· 1 Assay:whole-exome sequencing· 1

Frequent Co-Authors

Catherine C Robertson· 1 shared Christopher E Gillies· 1 shared Edgar A Otto· 1 shared Hyun Min KangiD· 1 shared Matthew Sampson· 1 shared Matthias KretzleriD· 1 shared Virginia Vega-WarneriD· 1 shared

Activity by Year

2016-2016 · peak 1/yr

Co-Author Collaboration Network

7 top collaborators · 21 mutual co-author links

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1 shared paperGenetics

Catherine C Robertson

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1 paper

Recent·Most cited

Evaluating Mendelian nephrotic syndrome genes for evidence of risk alleles or oligogenicity that explain heritability

Brendan Crawford, Christopher E Gillies, Catherine C Robertson, Matthias Kretzler, Edgar A Otto, Virginia Vega-Warner, Hyun Min Kang, Matthew Sampson

This study evaluates whether risk alleles or oligogenicity in 21 Mendelian nephrotic syndrome genes explain NS heritability, but finds no significant burden or unique combinations in NS patients compared to a reference population.

Pediatric Nephrology · Oct 20, 2016Peer-reviewedGenetics