James Macpherson
Impact in
- Genetics top 5%
- Genetics and Neurodevelopmental Disorders
- Genomic variations and chromosomal abnormalities
- Cognitive Neuroscience top 5%
- Autism Spectrum Disorder Research
Papers in
- Genetics 15
- Genetics and Neurodevelopmental Disorders 14
- Genomic variations and chromosomal abnormalities 7
- Genomics and Rare Diseases 1
- Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities 1
-
- Autism Spectrum Disorder Research 6
- Co-authors
- Patricia A. Jacobs (5 shared papers)David L. Nelson (2 shared papers)Stephanie L. Sherman (2 shared papers)Sarah L. Nolin (2 shared papers)Evan E. Eichler (2 shared papers)Anne Glicksman (2 shared papers)Helle Hjalgrim (2 shared papers)Sheila Youings (2 shared papers)
- Journals
- Human Molecular Genetics (2 papers)European Journal of Human Genetics (1 paper)The American Journal of Human Genetics (1 paper)Genes (1 paper)BMC Genomics (1 paper)
- Partner nations
- United KingdomUnited StatesCanada
In The Last Decade
James Macpherson
17 papers receiving 706 citations
Peers
Comparison fields: 5 of 52
- Genetics 584
- Cognitive Neuroscience 278
- Molecular Biology 289
- Cellular and Molecular Neuroscience 74
- Reproductive Medicine 28
Countries citing papers authored by James Macpherson
This map shows the geographic impact of James Macpherson'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 James Macpherson with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites James Macpherson more than expected).
Fields of papers citing papers by James Macpherson
This network shows the impact of papers produced by James Macpherson. 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 James Macpherson. The network helps show where James Macpherson may publish in the future.
Co-authors
The 25 scholars most cited alongside James Macpherson, linked wherever they have co-authored with each other. Click a name or a connecting line to browse the papers they share.
All Works
| # | Work | ||
|---|---|---|---|
| 1 | 2003 | 311 | |
| 2 | 1994 | 70 | |
| 3 | 2013 | 69 | |
| 4 | 1995 | 64 | |
| 5 | Predisposition to the fragile X syndrome in Jews of Tunisian descent is due to the absence of AGG interruptions on a rare Mediterranean haplotype. | 1997 | 60 |
| 6 | 2019 | 48 | |
| 7 | 2010 | 27 | |
| 8 | 1992 | 21 | |
| 9 | 2000 | 21 | |
| 10 | 1992 | 15 | |
| 11 | 2016 | 12 | |
| 12 | 2017 | 10 | |
| 13 | 2000 | 4 | |
| 14 | Practice Guidelines for Molecular Diagnosis of Fragile X Syndrome | 2014 | 4 |
| 15 | 2022 | 1 | |
| 16 | 2004 | 1 | |
| 17 | 1999 | 1 |
About James Macpherson
James Macpherson is a scholar working on Genetics, Cognitive Neuroscience, Molecular Biology, Cell Biology and Infectious Diseases, having authored 17 papers that have together received 739 indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (14 papers), Genomic variations and chromosomal abnormalities (7 papers), Autism Spectrum Disorder Research (6 papers), Ubiquitin and proteasome pathways (2 papers), Endoplasmic Reticulum Stress and Disease (2 papers), Congenital heart defects research (2 papers), Genomics and Rare Diseases (1 paper) and Genetic and Clinical Aspects of Sex Determination and Chromosomal Abnormalities (1 paper). The work is most often cited by research in Genetics (584 citations), Cognitive Neuroscience (278 citations), Molecular Biology (289 citations), Cellular and Molecular Neuroscience (74 citations) and Reproductive Medicine (28 citations). James Macpherson has collaborated with scholars based in United Kingdom, United States and Canada. Frequent co-authors include Patricia A. Jacobs, David L. Nelson, Stephanie L. Sherman, Sarah L. Nolin, Evan E. Eichler, Anne Glicksman, Helle Hjalgrim, Sheila Youings, H. Bullman and François Rousseau. Their work appears in journals such as Human Molecular Genetics, European Journal of Human Genetics, The American Journal of Human Genetics, Genes and BMC Genomics.
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.