A. H. Child

640 total citations
8 papers, 409 citations indexed

About

A. H. Child is a scholar working on Genetics, Surgery and Pulmonary and Respiratory Medicine. According to data from OpenAlex, A. H. Child has authored 8 papers receiving a total of 409 indexed citations (citations by other indexed papers that have themselves been cited), including 7 papers in Genetics, 3 papers in Surgery and 2 papers in Pulmonary and Respiratory Medicine. Recurrent topics in A. H. Child's work include Connective tissue disorders research (7 papers), Congenital limb and hand anomalies (2 papers) and Aortic Disease and Treatment Approaches (2 papers). A. H. Child is often cited by papers focused on Connective tissue disorders research (7 papers), Congenital limb and hand anomalies (2 papers) and Aortic Disease and Treatment Approaches (2 papers). A. H. Child collaborates with scholars based in United Kingdom, Finland and United States. A. H. Child's co-authors include B Steinmann, Petros Tsipouras, Maurice Godfrey, M. Sarfarazi, Richard B. Devereux, D. Hewett, Katariina Kainulainen, B Lee, Emilia Vitale and Leena Peltonen and has published in prestigious journals such as New England Journal of Medicine, Genomics and Journal of Medical Genetics.

In The Last Decade

A. H. Child

7 papers receiving 389 citations

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
A. H. Child United Kingdom	5	285	125	94	89	86	8	409
B Lee United States	5	279 1.0×	78 0.6×	61 0.6×	72 0.8×	124 1.4×	5	386
José Antonio Aragon-Martin United Kingdom	10	223 0.8×	84 0.7×	69 0.7×	45 0.5×	135 1.6×	17	370
Vishwanathan Hucthagowder United States	9	342 1.2×	141 1.1×	35 0.4×	63 0.7×	200 2.3×	12	521
Josephina Meester Belgium	10	264 0.9×	223 1.8×	112 1.2×	51 0.6×	122 1.4×	24	479
Mark Veugelers Belgium	8	224 0.8×	139 1.1×	129 1.4×	41 0.5×	325 3.8×	12	611
Markus S. Ladewig Germany	11	327 1.1×	62 0.5×	44 0.5×	42 0.5×	170 2.0×	19	547
Anthony Vandersteen United Kingdom	11	355 1.2×	40 0.3×	34 0.4×	27 0.3×	152 1.8×	21	448
Herbert Neuhaus Germany	10	78 0.3×	84 0.7×	90 1.0×	43 0.5×	406 4.7×	22	582
Pauline Arnaud France	13	363 1.3×	350 2.8×	175 1.9×	54 0.6×	148 1.7×	36	609
Loren E. Dupuis United States	9	64 0.2×	65 0.5×	105 1.1×	77 0.9×	135 1.6×	11	322

Countries citing papers authored by A. H. Child

Since Specialization

Citations

This map shows the geographic impact of A. H. Child'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 A. H. Child with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites A. H. Child more than expected).

Fields of papers citing papers by A. H. Child

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by A. H. Child. 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 A. H. Child. The network helps show where A. H. Child may publish in the future.

Co-authorship network of co-authors of A. H. Child

This figure shows the co-authorship network connecting the top 25 collaborators of A. H. Child. A scholar is included among the top collaborators of A. H. Child 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 A. H. Child. A. H. Child 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:

8 of 8 papers shown

1.

Østergaard, Pia, Michael A. Simpson, Glen Brice, et al.. (2011). Rapid identification of mutations in GJC2 in primary lymphoedema using whole exome sequencing combined with linkage analysis with delineation of the phenotype. Journal of Medical Genetics. 48(4). 251–255. 85 indexed citations

2.

Vasu, Vimal, A. H. Child, Neena Modi, Mary Rutherford, & Frances M. Cowan. (2011). Dilated neonatal cisterna magna and Marfan syndrome. BMJ Case Reports. 2011. bcr0620114328–bcr0620114328. 2 indexed citations

3.

Dündar, Munis, Kuddusi Erkılıç, Ahmet Okay Çağlayan, et al.. (2008). Scoliosis, blindness and arachnodactyly in a large Turkish family: Is it a new syndrome?. PubMed. 19(3). 319–30.

4.

Foguet, Pedro, et al.. (2005). Infantile scoliosis in Beals syndrome: the use of a non-fusion technique for surgical correction. European Spine Journal. 15(4). 433–439. 4 indexed citations

5.

Comeglio, Paolo, Alison Evans, Glen Brice, Britt‐Marie Anderlid, & A. H. Child. (2002). Gene symbol: FBN1. Disease: Marfan syndrome.. Human Genetics. 112(1). 104–104. 5 indexed citations

6.

Child, A. H., et al.. (1994). A Novel Mutation of the Fibrillin Gene Causing Ectopia Lentis. Genomics. 19(3). 573–576. 70 indexed citations

7.

Tsipouras, Petros, M. Sarfarazi, B Lee, et al.. (1992). Genetic Linkage of the Marfan Syndrome, Ectopia Lentis, and Congenital Contractural Arachnodactyly to the Fibrillin Genes on Chromosomes 15 and 5. New England Journal of Medicine. 326(14). 905–909. 205 indexed citations

8.

Kainulainen, Katariina, B Steinmann, Hal Dietz, et al.. (1991). Marfan syndrome: no evidence for heterogeneity in different populations, and more precise mapping of the gene.. PubMed. 49(3). 662–7. 38 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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