Albert E. Chudley
Impact in
-
- Prenatal Substance Exposure Effects
- Birth, Development, and Health
- Genetics top 0.5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
Papers in
- Genetics 76
- Genomic variations and chromosomal abnormalities 30
- Genetics and Neurodevelopmental Disorders 21
- Genomics and Rare Diseases 13
-
- Prenatal Substance Exposure Effects 33
- Co-authors
- Bernard N. Chodirker (18 shared papers)Svetlana Popova (5 shared papers)Jürgen Rehm (5 shared papers)Shannon Lange (5 shared papers)Randi J. Hagerman (2 shared papers)Kevin D. Shield (2 shared papers)Cheryl R. Greenberg (13 shared papers)John M. Opitz (11 shared papers)
- Journals
- Clinical Genetics (15 papers)Journal of Medical Genetics (6 papers)The American Journal of Human Genetics (4 papers)American Journal of Medical Genetics (32 papers)Journal of Obstetrics and Gynaecology Canada (3 papers)
- Partner nations
- CanadaUnited StatesGermany
In The Last Decade
Albert E. Chudley
168 papers receiving 4.8k citations
Albert E. Chudley's Hit Papers
Peers
Comparison fields: 5 of 124
- Pediatrics, Perinatology and Child Health 1.8k
- Genetics 1.7k
- Obstetrics and Gynecology 301
- Developmental Biology 85
- Clinical Biochemistry 197
Countries citing papers authored by Albert E. Chudley
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
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-authors
The 25 scholars most cited alongside Albert E. Chudley, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
Showing the 20 most-cited of 174 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Fetal alcohol spectrum disorder: a guideline for diagnosis across the lifespan Hit paper breakdown → | 2015 | 391 |
| 2 | Comorbidity of fetal alcohol spectrum disorder: a systematic review and meta-analysis Hit paper breakdown → | 2016 | 329 |
| 3 | 2004 | 219 | |
| 4 | 2007 | 174 | |
| 5 | 2005 | 151 | |
| 6 | 2018 | 136 | |
| 7 | 2016 | 108 | |
| 8 | 1987 | 106 | |
| 9 | 1991 | 100 | |
| 10 | 2008 | 90 | |
| 11 | 2005 | 88 | |
| 12 | 2012 | 81 | |
| 13 | 2019 | 80 | |
| 14 | 1974 | 78 | |
| 15 | 2008 | 71 | |
| 16 | 2018 | 70 | |
| 17 | 1983 | 69 | |
| 18 | 2000 | 69 | |
| 19 | 2015 | 65 | |
| 20 | 2012 | 58 |
About Albert E. Chudley
Albert E. Chudley is a scholar working on Genetics, Pediatrics, Perinatology and Child Health, Molecular Biology, Cognitive Neuroscience and Rheumatology, having authored 174 papers that have together received 5.0k indexed citations. Recurring topics across this work include Prenatal Substance Exposure Effects (33 papers), Genomic variations and chromosomal abnormalities (30 papers), Genetics and Neurodevelopmental Disorders (21 papers), Autism Spectrum Disorder Research (19 papers), Genomics and Rare Diseases (13 papers), Folate and B Vitamins Research (12 papers), Congenital limb and hand anomalies (11 papers) and Congenital heart defects research (10 papers). The work is most often cited by research in Pediatrics, Perinatology and Child Health (1.8k citations), Genetics (1.7k citations), Obstetrics and Gynecology (301 citations), Developmental Biology (85 citations) and Clinical Biochemistry (197 citations). Albert E. Chudley has collaborated with scholars based in Canada, United States and Germany. Frequent co-authors include Bernard N. Chodirker, Svetlana Popova, Jürgen Rehm, Shannon Lange, Randi J. Hagerman, Kevin D. Shield, Cheryl R. Greenberg, John M. Opitz, Raja Mukherjee and Alanna Mihic. Their work appears in journals such as Clinical Genetics, Journal of Medical Genetics, The American Journal of Human Genetics, American Journal of Medical Genetics and Journal of Obstetrics and Gynaecology Canada.
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.