Tom Walsh
Impact in
- Genetics top 0.1%
- BRCA gene mutations in cancer
- Genomic variations and chromosomal abnormalities
- Genomics and Rare Diseases
- Sensory Systems top 0.2%
- Hearing, Cochlea, Tinnitus, Genetics
Papers in
- Genetics 52
- BRCA gene mutations in cancer 35
- Genomic variations and chromosomal abnormalities 8
- Genomics and Rare Diseases 4
- Blood disorders and treatments 3
-
- Hearing, Cochlea, Tinnitus, Genetics 18
- Co-authors
- Mary‐Claire King (85 shared papers)Ming K. Lee (38 shared papers)Silvia Casadei (23 shared papers)Elizabeth M. Swisher (20 shared papers)Alex S. Nord (9 shared papers)Anne Thornton (9 shared papers)Barbara M. Norquist (13 shared papers)Sunday M. Stray (7 shared papers)
- Journals
- Proceedings of the National Academy of Sciences (14 papers)The American Journal of Human Genetics (12 papers)Gynecologic Oncology (10 papers)Journal of Medical Genetics (5 papers)European Journal of Human Genetics (5 papers)
- Partner nations
- United StatesIsraelPalestinian Territory
In The Last Decade
Tom Walsh
138 papers receiving 19.4k citations
Tom Walsh's Hit Papers
Peers
Comparison fields: 5 of 115
- Genetics 6.1k
- Sensory Systems 1.1k
- Psychiatry and Mental health 1.0k
- Reproductive Medicine 539
- Hematology 722
Countries citing papers authored by Tom Walsh
This map shows the geographic impact of Tom Walsh'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 Tom Walsh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Tom Walsh more than expected).
Fields of papers citing papers by Tom Walsh
This network shows the impact of papers produced by Tom Walsh. 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 Tom Walsh. The network helps show where Tom Walsh may publish in the future.
Co-authors
The 25 scholars most cited alongside Tom Walsh, 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 139 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Strong Association of De Novo Copy Number Mutations with Autism Hit paper breakdown → | 2007 | 2232 |
| 2 | Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia Hit paper breakdown → | 2008 | 1467 |
| 3 | Inherited DNA-Repair Gene Mutations in Men with Metastatic Prostate Cancer Hit paper breakdown → | 2016 | 1344 |
| 4 | Germline and Somatic Mutations in Homologous Recombination Genes Predict Platinum Response and Survival in Ovarian, Fallopian Tube, and Peritoneal Carcinomas Hit paper breakdown → | 2013 | 837 |
| 5 | Mutations in 12 genes for inherited ovarian, fallopian tube, and peritoneal carcinoma identified by massively parallel sequencing Hit paper breakdown → | 2011 | 771 |
| 6 | Recurrent Rearrangements of Chromosome 1q21.1 and Variable Pediatric Phenotypes Hit paper breakdown → | 2008 | 629 |
| 7 | Inherited Mutations in Women With Ovarian Carcinoma Hit paper breakdown → | 2015 | 608 |
| 8 | Microduplications of 16p11.2 are associated with schizophrenia Hit paper breakdown → | 2009 | 580 |
| 9 | 2006 | 530 | |
| 10 | A recurrent 16p12.1 microdeletion supports a two-hit model for severe developmental delay Hit paper breakdown → | 2010 | 523 |
| 11 | Mutant Adenosine Deaminase 2 in a Polyarteritis Nodosa Vasculopathy Hit paper breakdown → | 2014 | 516 |
| 12 | Spatial and Temporal Mapping of De Novo Mutations in Schizophrenia to a Fetal Prefrontal Cortical Network Hit paper breakdown → | 2013 | 432 |
| 13 | 2010 | 402 | |
| 14 | 2007 | 366 | |
| 15 | 2013 | 323 | |
| 16 | 2015 | 291 | |
| 17 | 2013 | 261 | |
| 18 | 2013 | 237 | |
| 19 | 2011 | 230 | |
| 20 | 2010 | 226 |
About Tom Walsh
Tom Walsh is a scholar working on Genetics, Sensory Systems, Pathology and Forensic Medicine, Hematology and Reproductive Medicine, having authored 139 papers that have together received 20.0k indexed citations. Recurring topics across this work include BRCA gene mutations in cancer (35 papers), Hearing, Cochlea, Tinnitus, Genetics (18 papers), Genetic factors in colorectal cancer (11 papers), Genomic variations and chromosomal abnormalities (8 papers), Genomics and Rare Diseases (4 papers), Blood disorders and treatments (3 papers), Immunodeficiency and Autoimmune Disorders (3 papers) and Ovarian cancer diagnosis and treatment (3 papers). The work is most often cited by research in Genetics (6.1k citations), Sensory Systems (1.1k citations), Psychiatry and Mental health (1.0k citations), Reproductive Medicine (539 citations) and Hematology (722 citations). Tom Walsh has collaborated with scholars based in United States, Israel and Palestinian Territory. Frequent co-authors include Mary‐Claire King, Ming K. Lee, Silvia Casadei, Elizabeth M. Swisher, Alex S. Nord, Anne Thornton, Barbara M. Norquist, Sunday M. Stray, Christopher C. Pennil and Jessica B. Mandell. Their work appears in journals such as Proceedings of the National Academy of Sciences, The American Journal of Human Genetics, Gynecologic Oncology, Journal of Medical Genetics and European Journal of Human Genetics.
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.