Researchclopedia

Research Researchers Institutions Topics Submit About

Command Palette

Search for a command to run...

Researchclopedia

Research Researchers Institutions About

© 2026 Researchclopedia. Powered by OpenAlex under CC0 license.

I Cross | Researchclopedia

Back to researchers

I Cross

20

Works

1,430

Citations

12

h-index

13

i10-index

Research Topics

Genomic variations and chromosomal abnormalities Congenital heart defects research Congenital Heart Disease Studies

Affiliations

Tethys Research Institute1999–1999

Salisbury District Hospital1996–1996

Royal Victoria Infirmary1999–2002

Freeman Hospital1998–1998

National Energy Action1986–1986

Top Works

Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.

John Burn,Atsuyoshi Takao,et al.

1993269 citations

Genomics and Chromatin Dynamics

Prenatal Screening and Diagnostics

A population study of chromosome 22q11 deletions in infancy

Judith Goodship,I Cross,et al.

1998250 citations

Confirmation that the velo‐cardio‐facial syndrome is associated with haplo‐insufficiency of genes at chromosome 22q11

David A. Kelly,Rosalie Goldberg,et al.

1993181 citations

Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease

Stephanle Halford,Roy Wadey,et al.

1993140 citations

Characterisation of interstitial duplications and triplications of chromosome 15q11–q13

Siân E. Roberts,Nicholas R. Dennis,et al.

2002134 citations

Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.

Judith Goodship,I Cross,et al.

1995134 citations

An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.

I Cross,JDA Delhanty,et al.

199280 citations

A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.

Mark Ireland,Carol English,et al.

199180 citations

VACTERL with hydrocephalus: One end of the Fanconi anemia spectrum of anomalies?

Mary Porteous,I Cross,et al.

199262 citations