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JAMA|September 29, 2018
Prevalence of Variant Reclassification Following Hereditary Cancer Genetic TestingJacqueline Mersch, Nichole Brown, Sara Pirzadeh-Miller, et al.
Cancer Genetics|May 7, 2019
Prevalence and characteristics of likely-somatic variants in cancer susceptibility genes among individuals who had hereditary pan-cancer panel testingThomas P Slavin, Bradford Coffee, Ryan Bernhisel, et al.
Gene|October 12, 2012
Investigation of lymphotoxin α genetic variants in migraineLotta E Oikari, Shani Stuart, Rachel K Okolicsanyi, et al.
Headache|June 19, 2013
Association of a GRIA3 gene polymorphism with migraine in an Australian case-control cohortBridget H Maher, Rod A Lea, Jordan Follett, et al.
Future Oncology (London, England)|August 17, 2018
Hereditary cancer testing challenges: assembling the analytical pieces to solve the patient clinical puzzleKarla R Bowles, Debora Mancini-DiNardo, Bradford Coffee, et al.
Gene|December 27, 2011
Heritability and genome-wide linkage analysis of migraine in the genetic isolate of Norfolk IslandHannah C Cox, Rod A Lea, Claire Bellis, et al.
Cancer Genetics|October 14, 2017
Identification of pathogenic retrotransposon insertions in cancer predisposition genesYaping Qian, Debora Mancini-DiNardo, Thaddeus Judkins, et al.
Neurogenetics|June 9, 2012
A genome-wide analysis of 'Bounty' descendants implicates several novel variants in migraine susceptibilityHannah C Cox, Rod A Lea, Claire Bellis, et al.
Human Molecular Genetics|May 21, 2013
Unique X-linked familial FSGS with co-segregating heart block disorder is associated with a mutation in the NXF5 geneTeresa Esposito, Rod A Lea, Bridget H Maher, et al.
Alzheimer'S & Dementia : the Journal of the Alzheimer'S Association|November 19, 2013
Origin of the PSEN1 E280A mutation causing early-onset Alzheimer's diseaseMatthew A Lalli, Hannah C Cox, Mary L Arcila, et al.
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