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I Cross

Observed names: CROSS, I, CROSS, IE, I. Cross, IAN CROSS, IE Cross, Ian Cross
OpenAlex ID: A5109840314
Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.
1993 · J Burn, A Takao, et al. · Journal of Medical Genetics · 270
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A population study of chromosome 22q11 deletions in infancy
1998 · J. Goodship, I. Cross, et al. · Archives of Disease in Childhood · 246
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Confirmation that the velo‐cardio‐facial syndrome is associated with haplo‐insufficiency of genes at chromosome 22q11
1993 · David Kelly, Rosalie Goldberg, et al. · American Journal of Medical Genetics · 181
Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease
1993 · Stephanle Halford, Roy Wadey, et al. · Human Molecular Genetics · 139
Characterisation of interstitial duplications and triplications of chromosome 15q11–q13
2002 · Siân E. Roberts, Nicholas R. Dennis, et al. · Human Genetics · 135
Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.
1995 · J Goodship, I Cross, et al. · Journal of Medical Genetics · 134
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Alagille syndrome and deletion of 20p.
1990 · F Anad, J Burn, et al. · Journal of Medical Genetics · 96
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A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.
1991 · M Ireland, C English, et al. · Journal of Medical Genetics · 81
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An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.
1992 · I Cross, J Delhanty, et al. · Journal of Medical Genetics · 79
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VACTERL with hydrocephalus: One end of the Fanconi anemia spectrum of anomalies?
1992 · M. E. M. Porteous, I. Cross, et al. · American Journal of Medical Genetics · 61
Partial trisomy 3q and the mild Cornelia de Lange syndrome phenotype.
1995 · M Ireland, C English, et al. · Journal of Medical Genetics · 50
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Trisomy of the short stature homeobox‐containing gene (SHOX), resulting from a duplication‐deletion of the X chromosome
2002 · K. A. Adamson, I. Cross, et al. · Clinical Endocrinology · 28
FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13).
1996 · J A Crolla, I Cross, et al. · Journal of Medical Genetics · 19
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Partial trisomy 20p resulting from a recombination of a familial pericentric inversion
1986 · N. Bown, I. Cross, et al. · Human Genetics · 19
Frequency and predictive value of 22q11 deletion
1999 · JESSE LILING, IAN CROSS, et al. · Journal of Medical Genetics · 12
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The Clinical Significance of 22q11 Deletion
1995 · BURN, J, WILSON, DI, et al. · UCL Discovery (University College London) · 12
An introduction to human chromosomes and their analysis
2001 · I Cross, J Wolstenholme · 6
Early confirmation of trisomy 18 in newborn babies
1992 · J. Wolstenholme, I. Cross, et al. · The Lancet · 2
Characterisation of interstitial duplications and triplications of chromosome 15q11-q13
2002 · SE Roberts, NR Dennis, et al. · Newcastle University ePrints (Newcastle Univesity)
Short stature, asymmetry and limitation of movement at the elbow in a patient with a mosaic marker karyotype resulting in partial trisomy 8q24-qter
2001 · Laura Yates, I Cross, et al. · Newcastle University ePrints (Newcastle Univesity)
A simple method for performing FISH on formaldehyde-fixed, paraffin-embedded tissue
2001 · C English, IE Cross, et al. · Newcastle University ePrints (Newcastle Univesity)
Isodicentric Y-chromosomal abnormality associated with cryptorchidism and severe hypogonadotrophic pubertal delay
2000 · A Basu, SG Ball, et al. · Newcastle University ePrints (Newcastle Univesity)
Familial predisposition to variant Turner's syndrome through inheritance of a balanced inversion of an X chromosome
1999 · Susan Ball, I Cross, et al.
Identification of Interstitial 22q11 Deletions in Contruncal Anomaly Face Syndrome
1994 · John Burn, David I. Wilson, et al. · UCL Discovery (University College London)
Noonans-syndrome and Digeorge Syndrome With Monosomy 22q11
1993 · WILSON, DI, BRITTON, SB, et al. · UCL Discovery (University College London)
Works count: 26
Citation count: 1,570
H-index: 14
I10-index: 16
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