Albert E. Chudley

10.1k total citations · 2 hit papers
173 papers, 4.9k citations indexed

About

Albert E. Chudley is a scholar working on Genetics, Pediatrics, Perinatology and Child Health and Molecular Biology. According to data from OpenAlex, Albert E. Chudley has authored 173 papers receiving a total of 4.9k indexed citations (citations by other indexed papers that have themselves been cited), including 79 papers in Genetics, 60 papers in Pediatrics, Perinatology and Child Health and 50 papers in Molecular Biology. Recurrent topics in Albert E. Chudley's work include Prenatal Substance Exposure Effects (33 papers), Genomic variations and chromosomal abnormalities (32 papers) and Genetics and Neurodevelopmental Disorders (21 papers). Albert E. Chudley is often cited by papers focused on Prenatal Substance Exposure Effects (33 papers), Genomic variations and chromosomal abnormalities (32 papers) and Genetics and Neurodevelopmental Disorders (21 papers). Albert E. Chudley collaborates with scholars based in Canada, United States and Germany. Albert E. Chudley's co-authors include Bernard N. Chodirker, Svetlana Popova, Jürgen Rehm, Shannon Lange, Randi J. Hagerman, Kevin D. Shield, Cheryl R. Greenberg, John M. Opitz, Alanna Mihic and Raja Mukherjee and has published in prestigious journals such as The Lancet, Circulation and Nature Genetics.

In The Last Decade

Albert E. Chudley

167 papers receiving 4.7k citations

Hit Papers

align trajectories

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.

Fetal alcohol spectrum disorder: a guideline for diagnosis across the lifespan

2015 385 citations Jocelynn L. Cook, Albert E. Chudley et al. Canadian Medical Association Journal profile →
Comorbidity of fetal alcohol spectrum disorder: a systematic review and meta-analysis

2016 326 citations Svetlana Popova, Shannon Lange et al. The Lancet profile →

Peers — A (Enhanced Table)

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

Name	h						Papers	Cites
Albert E. Chudley Canada	38	1.9k	1.8k	1.6k	564	563	173	4.9k
Eric Haan Australia	48	2.3k 1.2×	2.3k 1.3×	2.4k 1.5×	534 0.9×	122 0.2×	185	7.3k
Sterling K. Clarren United States	40	4.3k 2.2×	1.4k 0.8×	1.1k 0.7×	1.4k 2.4×	122 0.2×	96	6.7k
Ze’ev Hochberg Israel	49	1.1k 0.6×	1.6k 0.9×	2.2k 1.3×	258 0.5×	117 0.2×	242	7.4k
Miguel Del Campo United States	24	884 0.5×	1.3k 0.7×	1.2k 0.8×	209 0.4×	191 0.3×	78	3.4k
Markku Ryynänen Finland	38	1.0k 0.5×	953 0.5×	1.1k 0.6×	476 0.8×	399 0.7×	132	4.4k
H. Eugene Hoyme United States	52	6.4k 3.3×	1.6k 0.9×	1.6k 1.0×	2.5k 4.4×	270 0.5×	163	9.9k
Dian Donnai United Kingdom	48	1.2k 0.6×	3.0k 1.7×	3.1k 1.9×	125 0.2×	245 0.4×	177	7.8k
F. John Meaney United States	29	612 0.3×	865 0.5×	1.0k 0.6×	112 0.2×	585 1.0×	84	3.2k
Mårten Kyllerman Sweden	34	1.0k 0.5×	759 0.4×	1.2k 0.7×	154 0.3×	291 0.5×	88	3.1k
Kerstin Strömland Sweden	27	960 0.5×	579 0.3×	417 0.3×	223 0.4×	467 0.8×	62	2.3k

Countries citing papers authored by Albert E. Chudley

Since Specialization

Citations

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

Fields of papers citing papers by Albert E. Chudley

Since Specialization

Physical SciencesHealth SciencesLife SciencesSocial Sciences

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

Co-authorship network of co-authors of Albert E. Chudley

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

All Works

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20 of 20 papers shown

Neilson, Christine, Marni Brownell, Ana Hanlon‐Dearman, et al.. (2018). Effectiveness of evidence-based treatments of fetal alcohol spectrum disorders in children and adolescents: a systematic review protocol. BMJ Open. 8(3). e013775–e013775. 5 indexed citations

Popova, Svetlana, Shannon Lange, Kevin D. Shield, et al.. (2016). Comorbidity of fetal alcohol spectrum disorder: a systematic review and meta-analysis. The Lancet. 387(10022). 978–987. 326 indexed citations breakdown →

Brownell, Marni, et al.. (2013). Use of health, education, and social services by individuals with fetal alcohol spectrum disorder.. PubMed. 20(2). e95–e106. 12 indexed citations

Loucks, Catrina M., Jillian S. Parboosingh, Jessica X. Chong, et al.. (2012). A shared founder mutation underlies restrictive dermopathy in Old Colony (Dutch‐German) Mennonite and Hutterite patients in North America. American Journal of Medical Genetics Part A. 158A(5). 1229–1232. 8 indexed citations

Doherty, Dan, Albert E. Chudley, Gail Coghlan, et al.. (2012). GPSM2 Mutations Cause the Brain Malformations and Hearing Loss in Chudley-McCullough Syndrome. The American Journal of Human Genetics. 91(1). 209–209. 2 indexed citations

Liu, Xudong, Ying Qiao, Monica Hrynchak, et al.. (2011). Association of GTF2i in the Williams-Beuren Syndrome Critical Region with Autism Spectrum Disorders. Journal of Autism and Developmental Disorders. 42(7). 1459–1469. 49 indexed citations

Mhanni, Aziz, et al.. (2011). Variable expressivity of a novel mutation in the SCN1A gene leading to an autosomal dominant seizure disorder. Seizure. 20(9). 711–712. 3 indexed citations

Metcalfe, Kelly, Parviz Ghadirian, Barry P. Rosen, et al.. (2007). Variation in Rates of Uptake of Preventive Options in BRCA1 and BRCA2 Mutation Carriers Across Canada. 1(2). 92–98. 8 indexed citations

Chudley, Albert E., et al.. (2007). Challenges of diagnosis in fetal alcohol syndrome and fetal alcohol spectrum disorder in the adult. American Journal of Medical Genetics Part C Seminars in Medical Genetics. 145C(3). 261–272. 49 indexed citations

10.

Loock, Christine, et al.. (2005). Correction. Canadian Medical Association Journal. 173(9). 1071–1071. 2 indexed citations

11.

Glass, Hannah C., Kym M. Boycott, Coleen Adams, et al.. (2005). Autosomal recessive cerebellar hypoplasia in the Hutterite population. Developmental Medicine & Child Neurology. 47(10). 691–691. 28 indexed citations

12.

Elliott, Alison M., Jane Evans, Albert E. Chudley, & Martin H. Reed. (2004). The duplicated longitudinal epiphysis or ?kissing delta phalanx?: evolution and variation in three different disorders. Skeletal Radiology. 33(6). 345–351. 11 indexed citations

13.

Bigio, Marc R. Del, et al.. (2004). Late Infantile Onset Krabbe Disease in Siblings with Cortical Degeneration and Absence of Cerebral Globoid Cells. Neuropediatrics. 35(5). 297–301. 3 indexed citations

14.

Innes, A. Micheil, Molly Seshia, Chitra Prasad, et al.. (2002). Congenital rickets caused by maternal vitamin D deficiency. Paediatrics & Child Health. 7(7). 455–458. 32 indexed citations

15.

Mhanni, Aizeddin A. & Albert E. Chudley. (1999). Genetic landmarks through philately – Kabuki theater and Kabuki syndrome. Clinical Genetics. 56(2). 116–117. 6 indexed citations

16.

Evans, Jane & Albert E. Chudley. (1999). Tibial agenesis, femoral duplication, and caudal midline anomalies. American Journal of Medical Genetics. 85(1). 13–19. 22 indexed citations

17.

Chudley, Albert E.. (1998). Genetic landmarks through philately – Gregor Johann Mendel (1822–1884). Clinical Genetics. 54(2). 121–123. 1 indexed citations

18.

Schapira, David V. & Albert E. Chudley. (1984). Successful pregnancy following continuous treatment with combination chemotherapy before conception and throughout pregnancy. Cancer. 54(5). 800–803. 45 indexed citations

19.

Tervo, Raymond C. & Albert E. Chudley. (1981). Management of cleft lip and palate: a team approach.. Europe PMC (PubMed Central). 2 indexed citations

20.

Houston, C. Stuart, et al.. (1980). Hydrometrocolpos in Kaufman syndrome.. PubMed. 31(3). 193–5. 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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