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Wrong Michael Buckley?

Michael R. Buckley

Vice President

The Human Genetics Society of Australasia

HQ Phone:  +61 2 9669 6602

Email: m***@***.au

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I agree to the Terms of Service and Privacy Policy. I understand that I will receive a subscription to ZoomInfo Community Edition at no charge in exchange for downloading and installing the ZoomInfo Contact Contributor utility which, among other features, involves sharing my business contacts as well as headers and signature blocks from emails that I receive.

The Human Genetics Society of Australasia

P.O. Box 6012

Alexandria, New South Wales,2015

Australia

Company Description

The Human Genetics Society of Australasia was formed in 1977 to provide a forum for the various disciplines collected under the title of Human Genetics. The HGSA is a full member of the International Federation of Human Genetics Societies and domestically we... more

Find other employees at this company (21)

Background Information

Employment History

Vice President

South Eastern Area Laboratory Services


Clinical Director, SEALS Genetics

NSW Inc


JCPenney Company Chair of Leadership Studies

University of Oklahoma


Genetic Pathologist

Sydney Children's Hospital


Affiliations

RCPA/RACP JSAC

Member


Royal College of Pathologists of Australasia

Registrar of the Board of Censors, RCPA Chief Examiner In Genetics, HGSA Chief Examiner In Molecular Genetics


Education

PhD


Web References(23 Total References)


SEALS Pathology - Genetics

www.seals.health.nsw.gov.au [cached]

Dr Michael Buckley MBChB, BHB, PhD, MHGSA (Cytogenetics), FHGSA (Molecular Genetics), FRCPA (Genetics), FRCPath (UK) (Genetics), FFSc
Clinical Director and Senior Staff Specialist Genetic Pathologist Vice-President, Human Genetics Society of Australasia


SEALS Pathology - Genetics

seals.health.nsw.gov.au [cached]

Dr Michael Buckley
Phone: (+612) 9382 9125 Email: michael.buckley@health.nsw.gov.au Dr Michael Buckley is a Genetic Pathologist with Fellowships in Genetics from the Human Genetics Society of Australia, the Royal College of Pathologists of Australasia and the Royal College of Pathologists in the United Kingdom. He is the supervising pathologist of Genome.One Pty Ltd at the Kinghorn Centre for Clinical Genomics. Dr Buckley's research interest is principally in disease gene identification in paediatric congenital anomalies; with major publications concerning the identification of the SP110 gene as the cause of a form of severe combined immunodeficiency, the SCL29A3 gene in pigmented hypertrichosis with insulin dependent diabetes mellitus, and the FREM1 gene in metopic craniosynostosis. Between 2008 and 2011 he was the recipient of a Marie Curie International Incoming Fellowship for a project directed at the implementation of massively parallel sequencing for disease gene identification in diagnostics and in research, a project which is ongoing with the development of a Centre for Medical Genomics within the SEALS Genetic Laboratory. Current research funding includes support for Centre of Research Excellence for Neurocognitive Disorders. Dr Buckley is actively involved in specialist training having held positions as Registrar of the RCPA Board of Censors, RCPA Chief Examiner in Genetics, HGSA Chief Examiner in Molecular Genetics, and is currently the vice-president of the Human Genetics Society of Australasia.


HGSA Council - Human Genetics Society of Australasia

www.hgsa.org.au [cached]

Dr Michael Buckley
Vice President


SEALS Pathology - Genetics

www.seals.health.nsw.gov.au [cached]

Dr Michael Buckley
Phone: (+612) 9382 9125 Email: michael.buckley@sesiahs.health.nsw.gov.au Dr Michael Buckley is a Genetic Pathologist with Fellowships in Genetics from the Human Genetics Society of Australia, the Royal College of Pathologists of Australasia and the Royal College of Pathologists. Michael holds a conjoint appointment in the School of Medical Sciences at the University of New South Wales. He is also a consultant genetic pathologist of the Kinghorn Centre for Clinical Genomics at the Garvan Institute of Medical Research. Dr Buckley's research interest is principally in disease gene identification in paediatric congenital anomalies; with major publications concerning the identification of the SP110 gene as the cause of a form of severe combined immunodeficiency, the SCL29A3 gene in pigmented hypertrichosis with insulin dependent diabetes mellitus, and the FREM1 gene in metopic craniosynostosis. Between 2008 and 2011 he was the recipient of a Marie Curie International Incoming Fellowship for a project directed at the implementation of massively parallel sequencing for disease gene identification in diagnostics and in research, a project which is ongoing with the development of a Centre for Medical Genomics within the SEALS Genetic Laboratory. Current research funding includes support for Centre of Research Excellence for neuromuscular disease and an NHMRC project grant for neuromuscular diseases (PI Prof Kathryn North). Dr Buckley is actively involved in specialist training having held positions as Registrar of the RCPA Board of Censors, RCPA Chief Examiner in Genetics, HGSA Chief Examiner in Molecular Genetics, and is currently a member of the RCPA/RACP JSAC in Clinical Genetics/Genetic Pathology.


www.tcrn.unsw.edu.au

Michael Buckley
South Eastern Area Laboratory Services


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