Z. Onadim

发表

Single cell detection of inherited retinoblastoma predisposition

J. Delhanty, M. Sütterlin, P. Sleiman, 1999, Prenatal diagnosis.

The chemosensitivity profile of retinoblastoma.

I. Cree, F. Di Nicolantonio, Z. Onadim, 2003, Recent results in cancer research. Fortschritte der Krebsforschung. Progres dans les recherches sur le cancer.

Examinations under anaesthesia as a measure of disease burden in unilateral retinoblastoma: the London experience

Z. Onadim, C. Duncan, M. Reddy, 2019, British Journal of Ophthalmology.

A case of naevus sebaceous associated with familial retinoblastoma, multiple lipomata and meningioma.

Z. Onadim, S. D. Morris, R. Yu, 2000 .

Detection of heterozygous mutations in the RB1 gene in retinoblastoma patients using single-strand conformation polymorphism analysis and polymerase chain reaction sequencing.

A. Hogg, J. Cowell, Z. Onadim, 1992, Oncogene.

Primary intravenous chemotherapy for group D retinoblastoma: a 13-year retrospective analysis

Kenneth P. Johnson, Z. Onadim, A. Stacey, 2016, British Journal of Ophthalmology.

Oncogenic point mutations in exon 20 of the RB1 gene in families showing incomplete penetrance and mild expression of the retinoblastoma phenotype.

A. Hogg, J. Cowell, Z. Onadim, 1992, Proceedings of the National Academy of Sciences of the United States of America.

The RB1 gene mutation in a child with ectopic intracranial retinoblastoma.

Z. Onadim, A. Woolford, J. Hungerford, 1997, British Journal of Cancer.

Molecular mechanisms of oncogenic mutations in tumors from patients with bilateral and unilateral retinoblastoma.

A. Hogg, J. Cowell, Z. Onadim, 1993, Proceedings of the National Academy of Sciences of the United States of America.

MYCN amplification levels in primary retinoblastoma tumors analyzed by Multiple Ligation-dependent Probe Amplification

Z. Onadim, M. Reddy, M. Sagoo, 2021, Ophthalmic Genetics.

THE RECOGNITION OF CAVITARY RETINOBLASTOMA TUMORS: Implications for Management and Genetic Analysis

Z. Onadim, M. Reddy, M. Sagoo, 2017, Retina.

Extensive Variation in the Mutation Rate Between and Within Human Genes Associated with Mendelian Disease

A. Eyre-Walker, C. Houdayer, J. Christodoulou, 2016, Human mutation.

The management of retinoblastoma

Z. Onadim, C. Duncan, M. Reddy, 2018, Oncogene.

Mechanisms of oncogenesis in patients with familial retinoblastoma.

A. Hogg, J. Cowell, Z. Onadim, 1993, British Journal of Cancer.

Spectrum of RB1 mutations identified in 403 retinoblastoma patients

Z. Onadim, M. Reddy, J. Hungerford, 2013, Journal of Medical Genetics.

Genomic alterations in blastic natural killer/extranodal natural killer-like T cell lymphoma with cutaneous involvement.

S. Whittaker, Z. Onadim, B. Young, 2003, The Journal of investigative dermatology.

A novel real-time PCR assay for quantitative analysis of methylated alleles (QAMA): analysis of the retinoblastoma locus.

Stefan Böhringer, Michael Zeschnigk, S. Böhringer, 2004, Nucleic acids research.

Heritable retinoblastoma and accelerated aortic valve disease

Z. Onadim, S. Dubrey, J. Kingston, 2013, BMJ Case Reports.

High level amplification of N-MYC is not associated with adverse histology or outcome in primary retinoblastoma tumours

Z. Onadim, B. Young, D. Lillington, 2002, British Journal of Cancer.

Detection and reporting of RB1 promoter hypermethylation in diagnostic screening

Z. Onadim, M. Reddy, M. Sagoo, 2018, Ophthalmic genetics.

Comparative genomic hybridization of 49 primary retinoblastoma tumors identifies chromosomal regions associated with histopathology, progression, and patient outcome

Z. Onadim, B. Young, D. Lillington, 2003, Genes, chromosomes & cancer.

Application of PCR amplification of DNA from paraffin embedded tissue sections to linkage analysis in familial retinoblastoma.

J. Cowell, Z. Onadim, 1991, Journal of medical genetics.

Genetic counselling in retinoblastoma: importance of ocular fundus examination of first degree relatives and linkage analysis.

J. Cowell, Z. Onadim, J. Hungerford, 1991, The British journal of ophthalmology.

Retinoblastoma in Great Britain 1963–2002

G. Draper, C. Stiller, J. Birch, 2008, British Journal of Ophthalmology.

The Management of Retinoblastoma Running title : Management of Retinoblastoma

Z. Onadim, C. Duncan, M. Reddy, 2018 .

Whole-Genome Sequencing of Retinoblastoma Reveals the Diversity of Rearrangements Disrupting RB1 and Uncovers a Treatment-Related Mutational Signature

S. Nik-Zainal, H. Davies, K. Broad, 2021, Cancers.

Application of intragenic DNA probes in prenatal screening for retinoblastoma gene carriers in the United Kingdom.

M. Jay, J. Cowell, Z. Onadim, 1990, Archives of disease in childhood.

Follow-up of retinoblastoma patients having prenatal and perinatal predictions for mutant gene carrier status using intragenic polymorphic probes from the RB1 gene.

J. Cowell, Z. Onadim, J. Hungerford, 1992, British Journal of Cancer.

Dde I RFLP may falsify linkage analysis of hereditary retinoblastoma when using SSCP of p88PR0.6 region.

J. Delhanty, M. Sütterlin, P. Sleiman, 2000, Anticancer research.

Strabismus in retinoblastoma survivors with long-term follow-up.

Z. Onadim, A. Stacey, C. Duncan, 2018, Journal of AAPOS : the official publication of the American Association for Pediatric Ophthalmology and Strabismus.

Prognostic information for known genetic carriers of RB1 pathogenic variants (germline and mosaic).

Z. Onadim, C. Duncan, M. Reddy, 2020, Ophthalmology. Retina.

Patient understanding of genetic information influences reproductive decision making in retinoblastoma

L. Boyes, M. Parulekar, Z. Onadim, 2017, Clinical genetics.

An overview of RB1 transcript alterations detected during retinoblastoma genetic screening.

Z. Onadim, E. Price, Mandeep S. Sagoo, 2023, Ophthalmic genetics.

Carrier detection and prenatal screening of the retinoblastoma gene

J. Cowell, Z. Onadim, 1990, The Journal of pathology.