AE Chudley

1.4k total citations · 1 hit paper
25 papers, 944 citations indexed

About

AE Chudley is a scholar working on Genetics, Molecular Biology and Pediatrics, Perinatology and Child Health. According to data from OpenAlex, AE Chudley has authored 25 papers receiving a total of 944 indexed citations (citations by other indexed papers that have themselves been cited), including 16 papers in Genetics, 10 papers in Molecular Biology and 5 papers in Pediatrics, Perinatology and Child Health. Recurrent topics in AE Chudley's work include Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetic Syndromes and Imprinting (3 papers). AE Chudley is often cited by papers focused on Genetics and Neurodevelopmental Disorders (8 papers), Genomic variations and chromosomal abnormalities (6 papers) and Genetic Syndromes and Imprinting (3 papers). AE Chudley collaborates with scholars based in Canada and United States. AE Chudley's co-authors include Joan H.M. Knoll, J. W. Gerrard, Julie Richer, J.L. Hamerton, Marc J. Kaufman, L. Pinsky, Cheryl R. Greenberg, C. Prasad, C. R. Greenberg and Jack C. Schultz and has published in prestigious journals such as Journal of Clinical Investigation, The American Journal of Human Genetics and British Journal of Ophthalmology.

In The Last Decade

AE Chudley

25 papers receiving 865 citations

Hit Papers

Fetal alcohol spectrum disorder: Canadian guidelines for ... 2005 2026 2012 2019 2005 200 400 600
What are hit papers?

Hit papers significantly outperform the citation benchmark for their cohort. A paper qualifies if it has ≥500 total citations, achieves ≥1.5× the top-1% citation threshold for papers in the same subfield and year (this is the minimum needed to enter the top 1%, not the average within it), or reaches the top citation threshold in at least one of its specific research topics.

  1. Fetal alcohol spectrum disorder: Canadian guidelines for diagnosis
    2005 719 citations AE Chudley Canadian Medical Association Journal profile →

Peers — A (Enhanced Table)

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

Name h Career Trend Papers Cites
AE Chudley Canada 9 719 301 270 162 142 25 944
John T. Martsolf United States 23 689 1.0× 268 0.9× 200 0.7× 158 1.0× 411 2.9× 38 1.2k
Nathaniel Khaole United States 11 1.5k 2.0× 571 1.9× 370 1.4× 384 2.4× 36 0.3× 14 1.6k
Anna-Susan Marais United States 17 1.6k 2.3× 815 2.7× 564 2.1× 394 2.4× 195 1.4× 19 2.0k
Alfredo S. Aragón United States 9 1.0k 1.4× 417 1.4× 280 1.0× 261 1.6× 17 0.1× 10 1.2k
Josephine L. Nanson Canada 8 361 0.5× 115 0.4× 101 0.4× 52 0.3× 50 0.4× 13 497
Suzy Davies United States 19 384 0.5× 120 0.4× 117 0.4× 22 0.1× 34 0.2× 45 906
Rudolf P. Talens Netherlands 5 686 1.0× 203 0.7× 18 0.1× 63 0.4× 379 2.7× 5 1.5k
Alexandre A. Lussier United States 14 332 0.5× 73 0.2× 36 0.1× 38 0.2× 66 0.5× 32 572
Maria S. Baker United States 12 413 0.6× 116 0.4× 14 0.1× 55 0.3× 187 1.3× 15 804
Arianne B. Dessens Netherlands 19 227 0.3× 76 0.3× 38 0.1× 44 0.3× 284 2.0× 42 1.0k

Countries citing papers authored by AE Chudley

Since Specialization
Citations

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

Fields of papers citing papers by AE Chudley

Since Specialization
Physical SciencesHealth SciencesLife SciencesSocial Sciences

This network shows the impact of papers produced by AE Chudley. 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 AE Chudley. The network helps show where AE Chudley may publish in the future.

Co-authorship network of co-authors of AE Chudley

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

All Works

20 of 20 papers shown
1.
Kozenko, Mariya & AE Chudley. (2010). Genetic implications and health consequences following the Chernobyl nuclear accident. Clinical Genetics. 77(3). 221–226. 1 indexed citations
2.
Innes, A. Micheil, Erik G. Puffenberger, Ian M. MacDonald, et al.. (2010). A founder mutation in BBS2 is responsible for Bardet‐Biedl syndrome in the Hutterite population: utility of SNP arrays in genetically heterogeneous disorders. Clinical Genetics. 78(5). 424–431. 16 indexed citations
3.
Chudley, AE, et al.. (2006). Stem cell research: cloning, therapy and scientific fraud. Clinical Genetics. 70(4). 302–305. 6 indexed citations
4.
Richer, Julie & AE Chudley. (2005). The hemoglobinopathies and malaria. Clinical Genetics. 68(4). 332–336. 14 indexed citations
5.
Chudley, AE. (2005). Fetal alcohol spectrum disorder: Canadian guidelines for diagnosis. Canadian Medical Association Journal. 172(5_suppl). S1–S21. 719 indexed citations breakdown →
6.
Chudley, AE. (2004). Genetic landmarks through philately – autism spectrum disorders: a genetic update. Clinical Genetics. 65(5). 352–357. 6 indexed citations
7.
Chudley, AE. (2003). Genetic landmarks through philately: Georges Marinesco (1863–1938). Clinical Genetics. 64(4). 297–299. 2 indexed citations
8.
Chudley, AE, et al.. (2003). Landmarks in genetics through philately: Down syndrome. Clinical Genetics. 63(4). 268–272. 4 indexed citations
9.
Chudley, AE, et al.. (2002). Genetic landmarks through philately: Luís Morquio 1867–1935. Clinical Genetics. 62(6). 438–439. 5 indexed citations
10.
Schultz, Jack C., et al.. (2002). Cryptic chromosome rearrangements detected by subtelomere assay in patients with mental retardation and dysmorphic features. Clinical Genetics. 62(6). 488–494. 30 indexed citations
11.
Brown, Jill M., et al.. (2002). Identification of a dup(5)(p15.3) by multicolor banding. Clinical Genetics. 61(4). 277–282. 4 indexed citations
12.
Prasad, C. & AE Chudley. (2002). History of genetics through philately: Sir William Osler (1849–1919) and the Osler–Weber–Rendu syndrome. Clinical Genetics. 61(6). 404–407. 2 indexed citations
13.
Chudley, AE. (2001). Genetic landmarks through philately – Charles Robert Darwin. Clinical Genetics. 60(4). 270–272. 1 indexed citations
14.
Chudley, AE, et al.. (2001). Dwarfs in art. Clinical Genetics. 59(2). 84–87. 10 indexed citations
15.
Chudley, AE, et al.. (1998). Functional mosaic trisomy of 1q12 1q21 resulting from X‐autosome insertion translocation with random inactivation. Clinical Genetics. 54(1). 70–73. 1 indexed citations
16.
Nelson, David L., et al.. (1994). Absence of FMR1 protein in two mentally retarded fragile X males without CGG repeat expansion. The American Journal of Human Genetics. 55. 2 indexed citations
17.
Chudley, AE, et al.. (1992). Transmission of the fra(X) haplotype from three nonpenetrant brothers to their affected grandsons. American Journal of Medical Genetics. 43(3). 588–591. 3 indexed citations
18.
Greenberg, Cheryl R., et al.. (1990). Detection of molecular rearrangements in Prader‐Willi syndrome patients by using genomic probes recognizing four loci within thePWCR. American Journal of Medical Genetics. 35(4). 536–545. 24 indexed citations
19.
Knoll, Joan H.M., AE Chudley, & J. W. Gerrard. (1984). Fragile (X) X-linked mental retardation. II. Frequency and replication pattern of fragile (X)(q28) in heterozygotes.. PubMed. 36(3). 640–5. 30 indexed citations
20.
Chudley, AE, et al.. (1983). Autosomal dominant iridogoniodysgenesis with associated somatic anomalies: four-generation family with Rieger's syndrome.. British Journal of Ophthalmology. 67(8). 529–534. 41 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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