Publications by authors named "Greg Peters"

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Further delineation of dosage-sensitive K/L mediated Xq28 duplication syndrome includes incomplete penetrance.
Melanie Leffler, Louise Christie, Anna Hackett, Bruce Bennetts, Himanshu Goel, Greg B Peters

Clin Genet· June 2023

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ClinSV: clinical grade structural and copy number variant detection from whole genome sequencing data.
Andre E Minoche, Ben Lundie, Greg B Peters, Thomas Ohnesorg, Mark Pinese

Genome Med· February 2021

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Yield of comparative genomic hybridization microarray in pediatric neurology practice.
Shibalik Misra, Greg Peters, Elizabeth Barnes, Simone Ardern-Holmes, Richard Webster

Neurol Genet· December 2019

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Unintentionally retained vascular devices: improving recognition and removal.
Gilbert Whang, Ilya Lekht, Rita Krane, Greg Peters, Suzanne L Palmer

Diagn Interv Radiol· January 2018

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Assessing burden of disease as disability adjusted life years in life cycle assessment.
Yumi Kobayashi, Greg M Peters, Nicholas J Ashbolt, Sean Shiels, Stuart J Khan

Sci Total Environ· October 2015

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Deletion of protein tyrosine phosphatase, non-receptor type 4 (PTPN4) in twins with a Rett syndrome-like phenotype.
Sarah L Williamson, Carolyn J Ellaway, Greg B Peters, Gregory J Pelka, Patrick P L Tam

Eur J Hum Genet· September 2015

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Global and local health burden trade-off through the hybridisation of quantitative microbial risk assessment and life cycle assessment to aid water management.
Yumi Kobayashi, Greg M Peters, Nicholas J Ashbolt, Sara Heimersson, Magdalena Svanström

Water Res· August 2015

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Chromosome microarrays in diagnostic testing: interpreting the genomic data.
Greg B Peters, Mark D Pertile

Methods Mol Biol· January 2015

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High-pressure paint gun injury: clinical presentation and imaging findings.
Greg Peters, Thomas Learch, Eric White, Deborah Forrester

Emerg Radiol· December 2014

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The hippocampus, medial prefrontal cortex, and selective memory retrieval: evidence from a rodent model of the retrieval-induced forgetting effect.
Jade Q Wu, Greg J Peters, Pedro Rittner, Thomas A Cleland, David M Smith

Hippocampus· September 2014

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Method for technical, economic and environmental assessment of advanced sludge processing routes.
Magdalena Svanström, Giorgio Bertanza, David Bolzonella, Matteo Canato, Carlo Collivignarelli, Greg Peters

Water Sci Technol· September 2014

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pH-rate profiles support a general base mechanism for galactokinase (Lactococcus lactis).
Laurie A Reinhardt, James B Thoden, Greg S Peters, Hazel M Holden, W W Cleland

FEBS Lett· September 2013

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Microdeletions detected using chromosome microarray in children with suspected genetic movement disorders: a single-centre study.
Russell C Dale, Padraic Grattan-Smith, Michelle Nicholson, Greg B Peters

Dev Med Child Neurol· July 2012

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Chromosome microarray in Australia: a guide for paediatricians.
Elizabeth E Palmer, Greg B Peters, David Mowat

J Paediatr Child Health· February 2012

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Infantile convulsions and paroxysmal kinesigenic dyskinesia with 16p11.2 microdeletion.
Russell C Dale, Padraic Grattan-Smith, Victor S C Fung, Greg B Peters

Neurology· October 2011

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Familial 7q21.3 microdeletion involving epsilon-sarcoglycan causing myoclonus dystonia, cognitive impairment, and psychosis.
Russell C Dale, Julian J Nasti, Greg B Peters

Mov Disord· August 2011

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Fibrosarcomatous variant of dermatofibrosarcoma protuberans showing COL1A1-PDGFB gene fusion, detected using a novel and disease-specific RT-PCR protocol.
Hema Mahajan, Raghwa Sharma, Artur Darmanian, Greg B Peters

Pathology· October 2010

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Chromosomal rearrangements and novel genes in disorders of eye development, cataract and glaucoma.
Marija Mihelec, Luke St Heaps, Maree Flaherty, Frank Billson, Christina Rudduck, Greg B Peters

Twin Res Hum Genet· August 2008

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Resolution of trisomic mosaicism in prenatal diagnosis: estimated performance of a 50K SNP microarray.
Jillian Cross, Greg Peters, Zhanhe Wu, Jesper Brohede, Garry N Hannan

Prenat Diagn· December 2007

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An innocuous duplication of 11.2 Mb at 13q21 is gene poor: sub-bands of gene paucity and pervasive CNV characterize the chromosome anomalies.
Art Daniel, Artur Darmanian, Greg Peters, Linda Goodwin, Jason R Hort

Am J Med Genet A· October 2007

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Paternally inherited submicroscopic duplication at 11p15.5 implicates insulin-like growth factor II in overgrowth and Wilms' tumorigenesis.
Elizabeth M Algar, Luke St Heaps, Artur Darmanian, Vinod Dagar, Dirk Prawitt, Greg B Peters

Cancer Res· March 2007

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Similar chromosomal changes in cisplatin and oxaliplatin-resistant sublines of the H69 SCLC cell line are not associated with platinum resistance.
Britta Stordal, Greg Peters, Ross Davey

Genes Chromosomes Cancer· December 2006

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Deletion at 14q22-23 indicates a contiguous gene syndrome comprising anophthalmia, pituitary hypoplasia, and ear anomalies.
Leisha D Nolen, David Amor, Ashley Haywood, Luke St Heaps, Chris Willcock, Greg Peters

Am J Med Genet A· August 2006

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Chromosome microdissection identifies genomic amplifications associated with drug resistance in a leukemia cell line: an approach to understanding drug resistance in cancer.
Frouzandeh Mahjoubi, Ronald J Hill, Greg B Peters

Chromosome Res· July 2006

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Chromosome 7 aberrations in a young girl with myelodysplasia and hepatoblastoma: an unusual association.
Katherine Neas, Greg Peters, Julianne Jackson, Mrinal Tembe, Zhan He Wu

Clin Dysmorphol· January 2006

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