Kathryn Nance North AC is a paediatric physician, neurologist, and clinical geneticist. In 2013, she was appointed Director of the Murdoch Childrens Research Institute [1] and was named the David Danks Professor of Child Health Research at the University of Melbourne. [2] In 2012, North was appointed Chair of the National Health and Medical Research Council Research Committee. [3] In 2014, she was appointed Vice Chair of the Global Alliance for Genomics and Health (GA4GH) and Co-Chair of its Clinical Working Group.
North received a doctorate in neurogenetics in 1994 from University of Sydney and later completed a postdoctoral fellowship in the Genetics Program at Harvard Medical School. North's laboratory research is focused on the molecular and genetic basis of inherited muscle disorders including muscular dystrophies and congenital myopathies, and of elite athletic performance. Her clinical research is focused on cognitive deficits in neurofibromatosis type 1 and intervention strategies for children with learning disabilities and inherited myopathies.
Anita Elizabeth Harding was an Irish-British neurologist, and Professor of Clinical Neurology at the Institute of Neurology of the University of London. She is known for the discovery with Ian Holt and John Morgan-Hughes of the "first identification of a mitochondrial DNA mutation in human disease and the concept of tissue heteroplasmy of mutant mitochondrial DNA", published in Nature in 1986. In 1985 she established the first neurogenetics research group in the United Kingdom at the UCL Institute of Neurology.
The Kolling Institute is located in the grounds of the Royal North Shore Hospital in St Leonards, Sydney Australia. The institute, founded in 1920, is the oldest medical research institute in New South Wales.
Sir Edward Byrne is a neuroscientist who served as Principal of King's College London from August 2014 until January 2021. He was previously Vice-Chancellor of Monash University.
David Owen Sillence is an academic and medical geneticist. He is an emeritus professor at the University of Sydney, where he was the foundation chair (Professor) of Medical Genetics. An honours graduate of the University of Sydney, he obtained his MD in Medical Genetics from the University of Melbourne 1978 in bone dysplasia.
Bruce William Stillman, AO, FAA, FRS is a biochemist and cancer researcher who has served as the Director of Cold Spring Harbor Laboratory (CSHL) since 1994 and President since 2003. He also served as the Director of its NCI-designated Cancer Center for 25 years from 1992 to 2016. During his leadership, CSHL has been ranked as the No. 1 institution in molecular biology and genetics research by Thomson Reuters. Stillman's research focuses on how chromosomes are duplicated in human cells and in yeast Saccharomyces cerevisiae; the mechanisms that ensure accurate inheritance of genetic material from one generation to the next; and how missteps in this process lead to cancer. For his accomplishments, Stillman has received numerous awards, including the Alfred P. Sloan, Jr. Prize in 2004 and the 2010 Louisa Gross Horwitz Prize, both of which he shared with Thomas J. Kelly of Memorial Sloan-Kettering Cancer Center, as well as the 2019 Canada Gairdner International Award for biomedical research, which he shared with John Diffley.
Professor Samuel Frank Berkovic is an Australian neurologist and Laureate Professor in the Department of Medicine, University of Melbourne and Director of the Epilepsy Research Centre at Austin Health.
Julie Bernhardt is an Australian physiotherapist and clinician scientist, a Principal Research Fellow and an NHMRC Senior Research Fellow and Clinical Head of the Stroke Division at the Florey Institute of Neuroscience and Mental Health, University of Melbourne. Bernhardt is Principal Investigator of the 'A Very Early Rehabilitation Trial' (AVERT) and a leader in the field of stroke recovery.
Mary Pauline Galea is an Australian physiotherapist and neuroscientist at University of Melbourne. She resides in Melbourne, Australia. Galea is a professorial fellow at the University of Melbourne's Department of Medicine at the Royal Melbourne Hospital and a Senior Principal Fellow in the Florey Institute of Neurosciences and Mental Health. She was foundation professor of clinical physiotherapy and director of the Rehabilitation Sciences Research Centre at the University of Melbourne and Austin Health. She is internationally recognised for her work in spinal cord injury and rehabilitative interventions.
The Murdoch Children's Research Institute (MCRI) is an Australian paediatric medical research institute located in Melbourne, Victoria, affiliated with the Royal Children's Hospital and the University of Melbourne. The institute has six research themes: cellular biology, clinical sciences, genetics, infection and immunity, population health, and data science.
David Chaim Rubinsztein FRS FMedSci is the Deputy Director of the Cambridge Institute of Medical Research (CIMR), Professor of Molecular Neurogenetics at the University of Cambridge and a UK Dementia Research Institute Professor.
Melissa Helen Little is an Australian scientist and academic, currently Theme Director of Cell Biology, heading up the Kidney Regeneration laboratory at the Murdoch Children's Research Institute. She is also a Professor in the Faculty of Medicine, Dentistry and Health Sciences, University of Melbourne, and Program Leader of Stem Cells Australia. In January 2022, she became CEO of the Novo Nordisk Foundation Center for Stem Cell Medicine reNEW, an international stem cell research center based at University of Copenhagen, and a collaboration between the University of Copenhagen, Denmark, Murdoch Children’s Research Institute, Australia, and Leiden University Medical Center, The Netherlands.
Judith Ann Whitworth is an Australian medical researcher in the areas of kidney function and blood pressure. Now an Emeritus Professor, she is the former Director of the John Curtin School of Medical Research and Howard Florey Professor of Medical Research at the Australian National University (ANU).
Robert Williamson is a retired British-Australian molecular biologist who specialised in the mapping, gene identification, and diagnosis of human genetic disorders.
Michel Fardeau, born on 24 October 1929 in Paris 12th arrondissement, is a medical researcher in medical pathology, pioneering founder in France of myology, a medical discipline treating diseases of the neuromuscular system. He was also a full professor at the Conservatoire National des Arts et Métiers in a chair dedicated to the social integration of disabled people.
Mustafa Abdalla Mohamed Salih, , is a Sudanese academic professor, scientist and pediatric neurologist. He established the first pediatric neurology specialty in Sudan and is also one of the founders of the pediatric neurology specialty in Saudi Arabia. He identified inherited neurologic diseases which were subsequently named after him. Salih Myopathy, Salih ataxia, and Bosley-Salih-Alorainy syndrome resulting from mutations in HOXA1 gene. He is also known to have led a team of scientists who proved that the extract from broad beans also known as hoarse beans had the ability to cure epilepsy spasms. Mustafa is also credited for having discovered a novel form of hereditary spastic paraplegia.
Olga Margaret Garson, better known as Margaret Garson, was an Australian physician and cytogenetics researcher.
Professor Patrick Francis Chinnery, FRCP, FRCPath, FMedSci, is a neurologist, clinician scientist, and Wellcome Trust Principal Research Fellow based in the Medical Research Council Mitochondrial Biology Unit and the University of Cambridge, where he is also Professor of Neurology and Head of the Department of Clinical Neurosciences.
Grant Robert Sutherland is a retired Australian human geneticist and celebrated cytogeneticist. He was the Director, Department of Cytogenetics and Molecular Genetics, Adelaide Women's and Children's Hospital for 27 years (1975-2002), then became the Foundation Research Fellow there until 2007. He is an Emeritus Professor in the Departments of Paediatrics and Genetics at the University of Adelaide.
John Christodoulou is an Australian medical geneticist, genetic pathologist and clinical scientist. He is director of the Genetics Theme and Group Co-Leader of the Brain and Mitochondrial Research Group at Murdoch Children's Research Institute. Additionally, he holds the Chair in Genomic Medicine, Department of Paediatrics, The University of Melbourne.
David Miles Danks was a celebrated paediatrician, medical researcher and is considered the founder of medical genetics in Australia. He identified the cause of Menkes disease in 1972. Danks was appointed Professor of Paediatrics at the Royal Children's Hospital, Melbourne in 1974. The David Danks Professorship of Child Health Research at the University of Melbourne is named in his honour.