I E Cross

960 total citations
8 papers, 728 citations indexed

About

I E Cross is a scholar working on Molecular Biology, Epidemiology and Pulmonary and Respiratory Medicine. According to data from OpenAlex, I E Cross has authored 8 papers receiving a total of 728 indexed citations (citations by other indexed papers that have themselves been cited), including 8 papers in Molecular Biology, 4 papers in Epidemiology and 3 papers in Pulmonary and Respiratory Medicine. Recurrent topics in I E Cross's work include Congenital heart defects research (7 papers), Congenital Heart Disease Studies (4 papers) and Tracheal and airway disorders (2 papers). I E Cross is often cited by papers focused on Congenital heart defects research (7 papers), Congenital Heart Disease Studies (4 papers) and Tracheal and airway disorders (2 papers). I E Cross collaborates with scholars based in United Kingdom. I E Cross's co-authors include David I. Wilson, John Burn, Peter Scambler, Judith A. Goodship, David A. Kelly, Elizabeth Lindsay, Robert J. Shprintzen, Rosalie Goldberg, R. Williamson and H H Bain and has published in prestigious journals such as The Lancet, The American Journal of Human Genetics and Heart.

In The Last Decade

I E Cross

8 papers receiving 702 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
I E Cross United Kingdom	8	591	304	297	269	121	8	728
Milton D. Berkman United States	8	369 0.6×	365 1.2×	161 0.5×	232 0.9×	129 1.1×	12	622
Christine E. Seidman United States	5	877 1.5×	172 0.6×	349 1.2×	123 0.5×	123 1.0×	8	1.0k
Carole Brewer United Kingdom	8	191 0.3×	301 1.0×	75 0.3×	27 0.1×	50 0.4×	9	484
Makoto Nishibatake Japan	10	362 0.6×	69 0.2×	290 1.0×	285 1.1×	111 0.9×	26	614
Reema L. Habiby United States	13	569 1.0×	491 1.6×	72 0.2×	51 0.2×	48 0.4×	23	932
F Serville France	12	258 0.4×	292 1.0×	22 0.1×	49 0.2×	111 0.9×	45	547
Giorgio Filippi Italy	14	304 0.5×	281 0.9×	17 0.1×	61 0.2×	54 0.4×	27	581
Jan-Maarten Cobben Netherlands	10	193 0.3×	125 0.4×	68 0.2×	18 0.1×	87 0.7×	24	439
Sophie Julia France	12	163 0.3×	241 0.8×	42 0.1×	29 0.1×	26 0.2×	27	372
Leah W. Burke United States	13	182 0.3×	247 0.8×	51 0.2×	36 0.1×	53 0.4×	22	552

Countries citing papers authored by I E Cross

Since Specialization

Citations

This map shows the geographic impact of I E 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 E 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 E Cross more than expected).

Fields of papers citing papers by I E Cross

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by I E 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 E Cross. The network helps show where I E Cross may publish in the future.

Co-authorship network of co-authors of I E Cross

This figure shows the co-authorship network connecting the top 25 collaborators of I E Cross. A scholar is included among the top collaborators of I E 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 E Cross. I E Cross is excluded from the visualization to improve readability, since they are connected to all nodes in the network.

All Works

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8 of 8 papers shown

1.

Barber, John, et al.. (1998). Neurofibromatosis pseudogene amplification underlies euchromatic cytogenetic duplications and triplications of proximal 15q. Human Genetics. 103(5). 600–607. 25 indexed citations

2.

Goodship, Judith, Stephen C. Robson, Stephen N. Sturgiss, I E Cross, & C. Wright. (1997). Renal Abnormalities on Obstetric Ultrasound as a presentation of DiGeorge Syndrome. Prenatal Diagnosis. 17(9). 867–870. 16 indexed citations

3.

Wilson, David I., I E Cross, & John Burn. (1994). Minimum prevalence of chromosome 22q11 deletions.. The American Journal of Human Genetics. 55. 64 indexed citations

4.

Wilson, David I., et al.. (1993). Noonan's and DiGeorge syndromes with monosomy 22q11.. Archives of Disease in Childhood. 68(2). 187–189. 28 indexed citations

5.

Scambler, Peter, David A. Kelly, Elizabeth Lindsay, et al.. (1992). Velo-cardio-facial syndrome associated with chromosome 22 deletions encompassing the DiGeorge locus. The Lancet. 339(8802). 1138–1139. 333 indexed citations

6.

Wilson, David I., Judith A. Goodship, John Burn, I E Cross, & Peter Scambler. (1992). Deletions within chromosome 22q11 in familial congenital heart disease. The Lancet. 340(8819). 573–575. 120 indexed citations

7.

Wilson, David I., I E Cross, Judith A. Goodship, et al.. (1992). A prospective cytogenetic study of 36 cases of DiGeorge syndrome.. PubMed. 51(5). 957–63. 68 indexed citations

8.

Wilson, David I., I E Cross, Judith A. Goodship, et al.. (1991). DiGeorge syndrome with isolated aortic coarctation and isolated ventricular septal defect in three sibs with a 22q11 deletion of maternal origin.. Heart. 66(4). 308–312. 74 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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