David E Godler

Scopus Author ID Loop profile ORCID

Publication Activity (10 Years)

Years Active: 2018-2023
Publications (10 Years): 15

Top Venues

Genes

International journal of molecular sciences

American journal of medical genetics. Part A

Developmental medicine and child neurology

University of Melbourne

Alfred Health Alfred Medical Research and Education Precinct (PHD)

This page only lists publications with an associated author ORCID identifier.

Affiliation History

University of Melbourne Jan 15 2018

Australia

Associate Professor / Principal Fellow :: Paediatrics

Murdoch Childrens Research Institute Feb 02 2016

Australia

Laboratory Head :: Nucleic Acids Processing Facility, MCRI-Biobank

Murdoch Childrens Research Institute Feb 02 2016

Australia

Group Leader / Senior Research fellow :: Cyto-molecular Diagnotics Laboratory, Genetics

Bellberry Ltd Nov 01 2016 - Jan 01 2017

Australia

Clinical Trials Consultant (expert opinion)

Murdoch Childrens Research Institute Jan 01 2011 - Feb 02 2016

Australia

Senior Research Officer (post-doc) :: Cyto-molecular Diagnotics Laboratory and the Victorian Clinical Genetics Services

Murdoch Childrens Research Institute Jan 01 2009 - Feb 01 2012

Australia

Research Officer (post-doc) :: Laboratory and Community Genetics

Victoria University Jan 01 2005 - Dec 31 2006

Australia

Junior Lecturer :: Forensic Science

Monash University Department of Medicine at Alfred Medical Research and Education Precinct Jan 01 2005 - Jan 01 2006

Australia

Research Assistant :: Medicine

Education History

Alfred Health Alfred Medical Research and Education Precinct Feb 01 2001 - Feb 20 2017

Australia

PHD :: Medicine

Monash University Jan 01 1998 - Dec 01 2001

Australia

BSC :: Genetics

Publications

David E Godler, William T Brown
Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023. Genes 14 (6) (2023)
David E Godler, William T Brown
Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023. Genes 14 (6) (2023)
David E Godler, William T Brown
Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023. Genes 14 (6) (2023)
David E Godler, William T Brown
Editorial for the Fragile X Syndrome Genetics Special Issue: May 2023. Genes 14 (6) (2023)
David E Godler, Yoshimi Inaba, Minh Q Bui, David Francis, Cindy D Skinner, Charles E Schwartz, David J Amor
Defining the 3'Epigenetic Boundary of the FMR1 Promoter and Its Loss in Individuals with Fragile X Syndrome. International journal of molecular sciences 24 (13) (2023)
Emma K Baker, Marta Arpone, Minh Q Bui, Claudine M Kraan, Ling Ling, David Francis, Matthew Frank Hunter, Carolyn Rogers, Michael J Field, Lorena Santa María, Víctor Faundes, Bianca Curotto, Paulina Morales, Cesar Trigo, Isabel Salas, Angelica M Alliende, David J Amor, David E Godler
Tissue mosaicism, FMR1 expression and intellectual functioning in males with fragile X syndrome. American journal of medical genetics. Part A (2022)
Essra Bartlett, Alison D Archibald, David Francis, Ling Ling, Rob Thomas, Gabrielle Chandler, Lisa Ward, Gemma O'Farrell, Alison Pandelache, Martin B Delatycki, Bruce H Bennetts, Gladys Ho, Katrina Fisk, Emma K Baker, David J Amor, David E Godler
Paternal retraction of a fragile X allele to normal size, showing normal function over two generations. American journal of medical genetics. Part A (2021)
David E Godler, Merlin G Butler
Special Issue: Genetics of Prader-Willi Syndrome. Genes 12 (9) (2021)
Ellenore M Martin, Ying Zhu, Claudine M Kraan, Kishore Raj Kumar, David E Godler, Michael Field
Men with FMR1 premutation alleles of less than 71 CGG repeats have low risk of being affected with fragile X-associated tremor/ataxia syndrome (FXTAS). Journal of medical genetics (2021)
Alison Pandelache, David Francis, Ralph Oertel, Rebecca Dickson, Rani Sachdev, Ling Ling, Dinusha Gamage, David E Godler
Detection of Cryptic Fragile X Full Mutation Alleles by Southern Blot in a Female and Her Foetal DNA via Chorionic Villus Sampling, Complicated by Mosaicism for 45,X0/46,XX/47,XXX. Genes 12 (6) (2021)
Claudine M Kraan, Emma K Baker, Marta Arpone, Minh Q Bui, Ling Ling, Dinusha Gamage, Lesley Bretherton, Carolyn Rogers, Michael J Field, Tiffany L Wotton, David Francis, Matthew Frank Hunter, Jonathan Cohen, David J Amor, David E Godler
DNA Methylation at Birth Predicts Intellectual Functioning and Autism Features in Children with Fragile X Syndrome. International journal of molecular sciences 21 (20) (2020)
Emma K Baker, Merlin G Butler, Samantha N Hartin, Ling Ling, Minh Bui, David Francis, Carolyn Rogers, Michael J Field, Jennie Slee, Dinusha Gamage, David J Amor, David E Godler
Relationships between UBE3A and SNORD116 expression and features of autism in chromosome 15 imprinting disorders. Translational psychiatry 10 (1) (2020)
Daisy A Shepherd, Niels Vos, Susan M Reid, David E Godler, Angela Guzys, Margarita Moreno-Betancur, David J Amor
Growth Trajectories in Genetic Subtypes of Prader-Willi Syndrome. Genes 11 (7) (2020)
Michael Field, Tracy Dudding-Byth, Marta Arpone, Emma K Baker, Solange M Aliaga, Carolyn Rogers, Chriselle Hickerton, David Francis, Dean G Phelan, Elizabeth E Palmer, David J Amor, Howard Slater, Lesley Bretherton, Ling Ling, David E Godler
Significantly Elevated FMR1 mRNA and Mosaicism for Methylated Premutation and Full Mutation Alleles in Two Brothers with Autism Features Referred for Fragile X Testing. International journal of molecular sciences 20 (16) (2019)
Claudine M Kraan, David E Godler, David J Amor
Epigenetics of fragile X syndrome and fragile X-related disorders. Developmental medicine and child neurology 61 (2) (2018)

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Publication Activity (10 Years)

Top Topics

Top Venues

David E Godler