I Cross

1.4k total citations
15 papers, 1.0k citations indexed

About

I Cross is a scholar working on Molecular Biology, Genetics and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, I Cross has authored 15 papers receiving a total of 1.0k indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Molecular Biology, 6 papers in Genetics and 3 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in I Cross's work include Congenital heart defects research (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Congenital Heart Disease Studies (3 papers). I Cross is often cited by papers focused on Congenital heart defects research (5 papers), Genomic variations and chromosomal abnormalities (5 papers) and Congenital Heart Disease Studies (3 papers). I Cross collaborates with scholars based in United Kingdom, Australia and United States. I Cross's co-authors include Judith Goodship, John Burn, Peter Scambler, Jesse Li‐Ling, Christopher Wren, David I. Wilson, Atsuyoshi Takao, Kazuo Momma, R Wadey and Elizabeth Lindsay and has published in prestigious journals such as Human Molecular Genetics, Archives of Disease in Childhood and Journal of Medical Genetics.

In The Last Decade

I Cross

15 papers receiving 985 citations

Peers — A (Enhanced Table)

Peers by citation overlap · career bar shows stage (early→late) cites · hero ref

Name	h						Papers	Cites
I Cross United Kingdom	12	783	462	322	266	164	15	1.0k
Judith Goodship United Kingdom	11	729 0.9×	517 1.1×	220 0.7×	112 0.4×	92 0.6×	13	978
I E Cross United Kingdom	8	591 0.8×	304 0.7×	297 0.9×	269 1.0×	121 0.7×	8	728
Kosuke Izumi United States	19	606 0.8×	635 1.4×	77 0.2×	145 0.5×	169 1.0×	77	1.1k
Rossella Capolino Italy	18	449 0.6×	369 0.8×	146 0.5×	84 0.3×	92 0.6×	56	825
Marie‐France Portnoï France	19	446 0.6×	574 1.2×	94 0.3×	57 0.2×	71 0.4×	29	908
Anita S. Kulharya United States	14	509 0.7×	452 1.0×	77 0.2×	59 0.2×	64 0.4×	31	843
Jacqueline Siegel‐Bartelt Canada	8	820 1.0×	477 1.0×	57 0.2×	53 0.2×	89 0.5×	10	1.1k
Ayala Aviram‐Goldring Israel	17	411 0.5×	429 0.9×	84 0.3×	94 0.4×	55 0.3×	31	872
Fady M. Mikhail United States	19	700 0.9×	551 1.2×	70 0.2×	107 0.4×	62 0.4×	61	1.5k
Maria Cristina Digilio Italy	6	559 0.7×	202 0.4×	303 0.9×	189 0.7×	101 0.6×	8	659

Countries citing papers authored by I Cross

Since Specialization

Citations

This map shows the geographic impact of I Cross's research. It shows the number of citations coming from papers published by authors working in each country. You can also color the map by specialization and compare the number of citations received by I Cross with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites I Cross more than expected).

Fields of papers citing papers by I Cross

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by I Cross. Nodes represent research fields, and links connect fields that are likely to share authors. Colored nodes show fields that tend to cite the papers produced by I Cross. The network helps show where I Cross may publish in the future.

Co-authorship network of co-authors of I Cross

This figure shows the co-authorship network connecting the top 25 collaborators of I Cross. A scholar is included among the top collaborators of I Cross based on the total number of citations received by their joint publications. Widths of edges represent the number of papers authors have co-authored together. Node borders signify the number of papers an author published with I Cross. I Cross is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

Sort: Min cites: Since: Top N: Style:

15 of 15 papers shown

Mitchell, Alex J., David Kingdon, & I Cross. (2005). Management of self-harm following hospital discharge: role for general practitioners in continuity of care. 10(4). 149–158. 6 indexed citations

Cross, I, et al.. (2002). Trisomy of the short stature homeobox‐containing gene (SHOX), resulting from a duplication‐deletion of the X chromosome. Clinical Endocrinology. 56(5). 671–675. 21 indexed citations

Roberts, Siân E., Nicholas R. Dennis, C.E. Browne, et al.. (2002). Characterisation of interstitial duplications and triplications of chromosome 15q11–q13. Human Genetics. 110(3). 227–234. 71 indexed citations

Goodship, Judith, I Cross, Jesse Li‐Ling, & Christopher Wren. (1998). A population study of chromosome 22q11 deletions in infancy. Archives of Disease in Childhood. 79(4). 348–351. 190 indexed citations

Crolla, John A., et al.. (1996). FISH studies in a patient with sporadic aniridia and t(7;11) (q31.2;p13).. Journal of Medical Genetics. 33(1). 66–68. 18 indexed citations

Goodship, Judith, I Cross, Peter Scambler, & John Burn. (1995). Monozygotic twins with chromosome 22q11 deletion and discordant phenotype.. Journal of Medical Genetics. 32(9). 746–748. 92 indexed citations

Kelly, David A., Rosalie Goldberg, David I. Wilson, et al.. (1993). Confirmation that the velo‐cardio‐facial syndrome is associated with haplo‐insufficiency of genes at chromosome 22q11. American Journal of Medical Genetics. 45(3). 308–312. 143 indexed citations

Wadey, Roy, Catherine Roberts, S. C. M. Daw, et al.. (1993). Isolation of a putative transcriptional regulator from the region of 22q11 deleted in DiGeorge syndrome, Shprintzen syndrome and familial congenital heart disease. Human Molecular Genetics. 2(12). 2099–2107. 116 indexed citations

Burn, John, Atsuyoshi Takao, David I. Wilson, et al.. (1993). Conotruncal anomaly face syndrome is associated with a deletion within chromosome 22q11.. Journal of Medical Genetics. 30(10). 822–824. 204 indexed citations

10.

Porteous, Mary, I Cross, & John Burn. (1992). VACTERL with hydrocephalus: One end of the Fanconi anemia spectrum of anomalies?. American Journal of Medical Genetics. 43(6). 1032–1034. 43 indexed citations

11.

Cross, I, JDA Delhanty, Peter Chapman, et al.. (1992). An intrachromosomal insertion causing 5q22 deletion and familial adenomatous polyposis coli in two generations.. Journal of Medical Genetics. 29(3). 175–179. 37 indexed citations

12.

Ireland, Mark, et al.. (1991). A de novo translocation t(3;17)(q26.3;q23.1) in a child with Cornelia de Lange syndrome.. Journal of Medical Genetics. 28(9). 639–640. 50 indexed citations

13.

Whitworth, James, et al.. (1987). Childhood feeding practices and their effects on nutrition in a rural area of The Gambia.. PubMed. 90(5). 227–31. 3 indexed citations

14.

Bown, N, I Cross, E. V. Davison, & John Burn. (1986). Partial trisomy 20p resulting from a recombination of a familial pericentric inversion. Human Genetics. 74(4). 417–419. 14 indexed citations

15.

Cross, I. (1982). Training primary health care workers in Upper Volta. Medical Education. 16(2). 102–104. 4 indexed citations

Rankless uses publication and citation data sourced from OpenAlex, an open and comprehensive bibliographic database. While OpenAlex provides broad and valuable coverage of the global research landscape, it—like all bibliographic datasets—has inherent limitations. These include incomplete records, variations in author disambiguation, differences in journal indexing, and delays in data updates. As a result, some metrics and network relationships displayed in Rankless may not fully capture the entirety of a scholar's output or impact.

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