John A. Crolla
Impact in
- Genetics top 0.5%
- Genomic variations and chromosomal abnormalities
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities
- Genetics and Neurodevelopmental Disorders
- Genetic Syndromes and Imprinting
-
- Prenatal Screening and Diagnostics
Papers in
- Genetics 90
- Genomic variations and chromosomal abnormalities 58
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 14
- Genetic Syndromes and Imprinting 12
-
- Genomics and Chromatin Dynamics 16
- Renal and related cancers 10
- Congenital heart defects research 9
- Co-authors
- Veronica van Heyningen (4 shared papers)M. R. Creasy (4 shared papers)P. A. Jacobs (8 shared papers)Annette E. Cockwell (10 shared papers)Patricia A. Jacobs (8 shared papers)Eva Alberman (1 shared paper)David Robinson (9 shared papers)N. Simon Thomas (8 shared papers)
- Journals
- Journal of Medical Genetics (18 papers)Human Genetics (12 papers)European Journal of Human Genetics (11 papers)The American Journal of Human Genetics (7 papers)Prenatal Diagnosis (4 papers)
- Partner nations
- United KingdomUnited StatesFrance
In The Last Decade
John A. Crolla
123 papers receiving 4.1k citations
Peers
Comparison fields: 5 of 100
- Genetics 2.9k
- Pediatrics, Perinatology and Child Health 1.2k
- Genetics 371
- Molecular Biology 1.9k
- Plant Science 943
Countries citing papers authored by John A. Crolla
This map shows the geographic impact of John A. Crolla'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 John A. Crolla with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John A. Crolla more than expected).
Fields of papers citing papers by John A. Crolla
This network shows the impact of papers produced by John A. Crolla. 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 John A. Crolla. The network helps show where John A. Crolla may publish in the future.
Co-authors
The 25 scholars most cited alongside John A. Crolla, 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 126 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 1976 | 223 | |
| 2 | 2002 | 150 | |
| 3 | 2008 | 148 | |
| 4 | 2008 | 134 | |
| 5 | 2001 | 134 | |
| 6 | 2013 | 128 | |
| 7 | 2002 | 127 | |
| 8 | 1998 | 126 | |
| 9 | 2005 | 107 | |
| 10 | 2008 | 102 | |
| 11 | 1990 | 95 | |
| 12 | 2005 | 95 | |
| 13 | 1996 | 87 | |
| 14 | 2007 | 85 | |
| 15 | 1996 | 84 | |
| 16 | 2008 | 84 | |
| 17 | 2011 | 81 | |
| 18 | 1992 | 81 | |
| 19 | 1989 | 80 | |
| 20 | 2004 | 79 |
About John A. Crolla
John A. Crolla is a scholar working on Genetics, Molecular Biology, Pediatrics, Perinatology and Child Health, Plant Science and Surgery, having authored 126 papers that have together received 4.7k indexed citations. Recurring topics across this work include Genomic variations and chromosomal abnormalities (58 papers), Prenatal Screening and Diagnostics (34 papers), Chromosomal and Genetic Variations (32 papers), Genomics and Chromatin Dynamics (16 papers), Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (14 papers), Genetic Syndromes and Imprinting (12 papers), Renal and related cancers (10 papers) and Congenital heart defects research (9 papers). The work is most often cited by research in Genetics (2.9k citations), Pediatrics, Perinatology and Child Health (1.2k citations), Genetics (371 citations), Molecular Biology (1.9k citations) and Plant Science (943 citations). John A. Crolla has collaborated with scholars based in United Kingdom, United States and France. Frequent co-authors include Veronica van Heyningen, M. R. Creasy, P. A. Jacobs, Annette E. Cockwell, Patricia A. Jacobs, Eva Alberman, David Robinson, N. Simon Thomas, N R Dennis and Nicholas R. Dennis. Their work appears in journals such as Journal of Medical Genetics, Human Genetics, European Journal of Human Genetics, The American Journal of Human Genetics and Prenatal Diagnosis.
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.