This is an HTML version of an attachment to the Freedom of Information request 'Migraine research applications for NHMRC or MRFF funding'.

Attachment A
FOI Request 2021/22-010 - Successful applications for NHMRC funding from 2016–2020 that include search terms relating to ‘migraine research’
Number Application  Application  Funding 
Funding 
Title 
CIA Name
Administering  State
Sector
Grant Budget Broad 
Field of 
Keywords 
Media Summary
ID
Year
Type
Subtype
Institution
Research  Research
Area
1
APP1122387
2016 Project 
Standard 
Identifying novel 
Prof Lyn Griffiths Queensland 
QLD
University
$640,966.25 Clinical 
Neurogenetics migraine | population  This proposal aims to identify novel FHM genes by undertaking an NGS 
Grants
Project 
gene mutations for 
University of 
Medicine 
genetics | pedigree 
screen of the whole exome of 209 FHM patient samples. We will test 
Grant
molecular diagnosis 
Technology
and 
analysis | molecular 
the pathological relevance of detected novel mutations by functional 
of Familial 
Science
genetics | sequencing
analysis in human cel  models and using patient-specific stem cel  
Hemiplegic Migraine
techniques.  Using whole genome NGS technology to identify novel 
mutations wil  assist in the design and development of a 
comprehensive NGS approach to diagnose and differentiate this severe 
neurological disorder.
2
APP1124011
2016 Project 
Standard 
Coupling the 
Prof Benjamin  University of 
QLD
University
$1,272,784.91 Basic 
Developmental  developmental genetics  Cerebral cavernous malformations (CCMs) are thin wal ed, vascular 
Grants
Project 
mechanical, 
Hogan
Queensland
Science
Genetics (incl.  | cel  signal ing | 
malformations in the brain found in 1/200-250 individuals. They can 
Grant
signal ing and 
Sex 
vascular development |  cause migraine, neurological deficits or stroke.  This disease can be 
transcriptional 
Determination) vascular pathologies |  inherited due to damaging mutations in any of three CCM genes.  The 
mechanisms that 
zebrafish
project wil  investigate the molecular control of CCM pathogenesis in 
initiate pathogenesis 
animal models. We aim to uncover the molecular cause of these 
of Cerebral 
vascular malformations and in doing so identify new therapeutic 
Cavernous 
strategies.
Malformation
3
APP1126976
2016 Project 
Standard 
Ictal Characteristics  A/Pr Miriam 
University of 
NSW
University
$288,787.66 Clinical 
Sensory 
vertigo | eye 
vertigo is a disabling symptom affecting 1 mil ion Australians at any 
Grants
Project 
of Common 
Welgampola
Sydney
Medicine  Systems
movements | migraine |  given time. Acute vertigo is associated with abnormal eye movements 
Grant
Vestibular Diseases
and 
meniere's disease | 
or nystagmus, the pattern of which points to its origin. In this project, 
Science
vestibular neuritis
we extract the unique characteristics of distinct vertigo syndromes to 
enable their separation
4
APP1143547
2017 Project 
Standard 
Brainstem and 
Prof Luke 
University of 
NSW
University
$674,937.74 Basic 
Central Nervous  migraine | brain imaging  Migraine is a disabling condition characterized by mostly unilateral 
Grants
Project 
hypothalamic 
Henderson
Sydney
Science
System
| functional magnetic 
throbbing head pain and a range of associated neurological symptoms. 
Grant
function and 
resonance imaging 
The underlying mechanisms responsible for the initiation of migraine 
anatomy in Migraine
(fmri) | brainstem | 
remains unknown. We aim to determine brain anatomy and activity 
hypothalamus
patterns in migraineurs throughout the migraine cycle. An 
understanding of the mechanisms responsible for migraine wil  aid in 
better treatment development.
5
APP1159006
2018 Project 
Standard 
A structural 
Dr Yi-Lynn Liang Monash 
VIC
University
$1,202,523.80 Basic 
Structural 
electron microscopy |  The calcitonin-family receptor are physiological y important receptors 
Grants
Project 
understanding of 
University
Science
Biology (incl. 
signal ing pathways | g  that have been implicated in treatment of osteoporosis, migraine and 
Grant
calcitonin gene-
Macromolecular protein-coupled 
cardiovascular diseases. Therapeutic development targeting at these 
related peptide and 
Model ing)
receptors | structure-
receptors remains chal enging due to lack of mechanistic understanding 
adrenomedullin 
function | calcitonin 
in how these GPCRs are activated.  This proposal wil  explore the 
function
receptor
structure and function of the calcitonin-family receptors at a molecular 
level, enabling improved discovery and development of novel 
therapeutics.
6
APP1161467
2018 Career 
Clinical CDF Revolutionising 
A/Pr Trudy 
University of 
NSW
University
$270,837.10 Health 
Primary Health  health services research  In this Career Development Fel owship, I am to discover new 
Developme
health service 
Rebbeck
Sydney
Services  Care
| musculoskeletal 
mechanisms that underlie why many people with musculoskeletal pain 
nt 
delivery for 
Research
disorders | headache |  progress to have long term pain and disability. With my team, we wil  
Fel owships
musculoskeletal 
primary care | 
investigate recovery pathways and know early on who is at risk of non-
disorders through 
implementation
recovery. This wil  enable us to direct health care services to those who 
discovery, simplifying 
need them, referring at-risk individuals to expert musculoskeletal 
prognosis and 
physiotherapists early after injury, thereby reducing the burden on the 
implementing novel 
medical system.
clinical pathways.

7
APP1164494
2018 Project 
Standard 
The spilt personality  Prof Renae Ryan University of 
NSW
University
$996,180.28 Basic 
Structural 
membrane transport |  Membrane proteins are pumps that control the movement of nutrients, 
Grants
Project 
of glutamate 
Sydney
Science
Biology (incl. 
glutamate | chloride 
waste products and chemical messengers in and out of cel s. These 
Grant
transporters: the 
Macromolecular channel | structural 
pumps  break down in a wide range of diseases including neurological 
structural basis and 
Model ing)
biology | drosophila 
disorders and cancer. This project is focused on a unique type of  
physiological role of 
melanogaster
transporter/channel hybrid protein that uses a ‘twisting elevator’ 
a dual function 
mechanism. We wil  uncover how they work and what goes wrong in 
transporter/channel
disease.  This information can then be used to develop new drugs to 
improve transporter function.
8
APP1181643
2019 Ideas Grants Ideas Grants The contribution of  Dr Ehsan 
Australian 
ACT
University
$445,902.66 Basic 
Central Nervous  sensory cortex | ion 
Our recent discovery that transient receptor potential Ankyrin 1 
cortical TRPA1 to 
Kheradpezhouh National 
Science
System
channels | calcium 
(TRPA1) is highly expressed in rodent cortical neurons has shed light on 
sensory perception 
University
signal ing | sensory 
its role in the mammalian cortex. Recent studies have proposed a role 
and behaviour of 
function | sensory 
for cortical TRPA1 in Alzheimer’s disease and migraine and further 
mammals
neurons
suggested that its activation can lead to neuronal damage. We will 
further investigate the physiological role of TRPA1, focusing on its 
potential involvement in multisensory detection and processing.

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