John Longshore
Impact in
Papers in
- Genetics 13
- Genetics and Neurodevelopmental Disorders 9
- Genomic variations and chromosomal abnormalities 3
- Animal Genetics and Reproduction 2
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- Ubiquitin and proteasome pathways 2
- Co-authors
- Reinhard Büttner (2 shared papers)Fernando López‐Ríos (3 shared papers)Nicola Normanno (1 shared paper)Sabine Merkelbach‐Bruse (1 shared paper)Frédérique Penault‐Llorca (1 shared paper)Etienne Rouleau (1 shared paper)Charles E. Schwartz (2 shared papers)James Amos‐Landgraf (1 shared paper)
- Journals
- The American Journal of Human Genetics (3 papers)Human Genetics (2 papers)Clinical Genetics (2 papers)Journal of Clinical Oncology (1 paper)ESMO Open (1 paper)
- Partner nations
- United StatesFranceGermany
In The Last Decade
John Longshore
22 papers receiving 1.5k citations
John Longshore's Hit Papers
Peers
Comparison fields: 5 of 104
- Genetics 581
- Oncology 392
- Cancer Research 176
- Cognitive Neuroscience 159
- Pulmonary and Respiratory Medicine 213
Countries citing papers authored by John Longshore
This map shows the geographic impact of John Longshore'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 Longshore with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites John Longshore more than expected).
Fields of papers citing papers by John Longshore
This network shows the impact of papers produced by John Longshore. 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 Longshore. The network helps show where John Longshore may publish in the future.
Co-authors
The 25 scholars most cited alongside John Longshore, 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 26 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | 2017 | 302 | |
| 2 | 2003 | 278 | |
| 3 | Implementing TMB measurement in clinical practice: considerations on assay requirements Hit paper breakdown → | 2019 | 251 |
| 4 | 2006 | 231 | |
| 5 | 2001 | 82 | |
| 6 | 2002 | 68 | |
| 7 | 2001 | 53 | |
| 8 | 2001 | 46 | |
| 9 | 2014 | 39 | |
| 10 | 1994 | 29 | |
| 11 | 1996 | 26 | |
| 12 | 2015 | 25 | |
| 13 | 2022 | 24 | |
| 14 | 1999 | 16 | |
| 15 | 1997 | 13 | |
| 16 | 1996 | 12 | |
| 17 | 2000 | 11 | |
| 18 | 2000 | 9 | |
| 19 | 1996 | 6 | |
| 20 | FMR1 CGG expansion to full mutation: What is the lower limit in premutation females? | 2000 | 2 |
About John Longshore
John Longshore is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Cancer Research and Oncology, having authored 26 papers that have together received 1.5k indexed citations. Recurring topics across this work include Genetics and Neurodevelopmental Disorders (9 papers), Cancer Genomics and Diagnostics (5 papers), Genomic variations and chromosomal abnormalities (3 papers), Autism Spectrum Disorder Research (3 papers), Lung Cancer Treatments and Mutations (3 papers), Ubiquitin and proteasome pathways (2 papers), Animal Genetics and Reproduction (2 papers) and Genetic Neurodegenerative Diseases (2 papers). The work is most often cited by research in Genetics (581 citations), Oncology (392 citations), Cancer Research (176 citations), Cognitive Neuroscience (159 citations) and Pulmonary and Respiratory Medicine (213 citations). John Longshore has collaborated with scholars based in United States, France and Germany. Frequent co-authors include Reinhard Büttner, Fernando López‐Ríos, Nicola Normanno, Sabine Merkelbach‐Bruse, Frédérique Penault‐Llorca, Etienne Rouleau, Charles E. Schwartz, James Amos‐Landgraf, Huntington F. Willard and Robert M. Plenge. Their work appears in journals such as The American Journal of Human Genetics, Human Genetics, Clinical Genetics, Journal of Clinical Oncology and ESMO Open.
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.