Bridget H. Maher
60 Musk Avenue, Kelvin Grove
Brisbane, QLD 4059, Australia
Brisbane, QLD 4059, Australia
Last Updated: 09/26/2026
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Found 16 publications
Tiered analysis of whole-exome sequencing for epilepsy diagnosis.
Journal: Molecular genetics and genomics : MGG
Published: August 16, 2019
The NRP1 migraine risk variant shows evidence of association with menstrual migraine.
Journal: The journal of headache and pain
Published: February 01, 2018
Comparison of outcomes for cancer patients discussed and not discussed at a multidisciplinary meeting.
Journal: Public health
Published: September 07, 2016
De novo mutations of KIAA2022 in females cause intellectual disability and intractable epilepsy.
Journal: Journal of medical genetics
Published: March 17, 2016
Genetic and neurodevelopmental spectrum of SYNGAP1-associated intellectual disability and epilepsy.
Journal: Journal of medical genetics
Published: August 12, 2015
Genome-wide Polygenic Burden of Rare Deleterious Variants in Sudden Unexpected Death in Epilepsy.
Journal: EBioMedicine
Published: June 09, 2015
Case-control study of ADARB1 and ADARB2 gene variants in migraine.
Journal: The journal of headache and pain
Published: December 23, 2014
De novo loss- or gain-of-function mutations in KCNA2 cause epileptic encephalopathy.
Journal: Nature genetics
Published: July 09, 2014
Investigation of brain-derived neurotrophic factor (BDNF) gene variants in migraine.
Journal: Headache
Published: February 17, 2014
Genetic variation in cytokine-related genes and migraine susceptibility.
Journal: Twin research and human genetics : the official journal of the International Society for Twin Studies
Published: September 24, 2013
Association of oestrogen-receptor gene (ESR1) polymorphisms with migraine in the large Norfolk Island pedigree.
Journal: Cephalalgia : an international journal of headache
Published: May 16, 2013
Last Updated: 09/26/2026