Mark J. Daly
Impact in
- Genetics top 0.01%
- Genetic Associations and Epidemiology
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Genetic diversity and population structure
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Molecular Biology top 0.02%
- Genomics and Phylogenetic Studies
- Bioinformatics and Genomic Networks
Papers in
- Genetics 213
- Genetic Associations and Epidemiology 106
- Genomics and Rare Diseases 61
- Genetic Mapping and Diversity in Plants and Animals 44
- Inflammatory Bowel Disease 34
- Genomic variations and chromosomal abnormalities 32
- Genetic and phenotypic traits in livestock 29
- Genetics and Neurodevelopmental Disorders 23
- Co-authors
- David Altshuler (49 shared papers)Benjamin M. Neale (47 shared papers)Eric S. Lander (29 shared papers)Stacey Gabriel (9 shared papers)Paul I. W. de Bakker (10 shared papers)Julian Maller (12 shared papers)Shaun Purcell (17 shared papers)Pak C. Sham (4 shared papers)
- Journals
- Nature Genetics (39 papers)The American Journal of Human Genetics (37 papers)European Journal of Human Genetics (19 papers)Gastroenterology (14 papers)PLoS Genetics (13 papers)
- Partner nations
- United StatesFinlandUnited Kingdom
In The Last Decade
Mark J. Daly
357 papers receiving 107.3k citations
Mark J. Daly's Hit Papers
Peers
Comparison fields: 5 of 215
- Genetics 48.3k
- Molecular Biology 35.4k
- Cancer Research 6.5k
- Sensory Systems 2.0k
- Biological Psychiatry 948
Countries citing papers authored by Mark J. Daly
This map shows the geographic impact of Mark J. Daly'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 Mark J. Daly with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Mark J. Daly more than expected).
Fields of papers citing papers by Mark J. Daly
This network shows the impact of papers produced by Mark J. Daly. 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 Mark J. Daly. The network helps show where Mark J. Daly may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark J. Daly, 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 374 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | PLINK: A Tool Set for Whole-Genome Association and Population-Based Linkage Analyses Hit paper breakdown → | 2007 | 22617 |
| 2 | The Genome Analysis Toolkit: A MapReduce framework for analyzing next-generation DNA sequencing data Hit paper breakdown → | 2010 | 18056 |
| 3 | A framework for variation discovery and genotyping using next-generation DNA sequencing data Hit paper breakdown → | 2011 | 7482 |
| 4 | MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations Hit paper breakdown → | 1987 | 6151 |
| 5 | The Structure of Haplotype Blocks in the Human Genome Hit paper breakdown → | 2002 | 4681 |
| 6 | LD Score regression distinguishes confounding from polygenicity in genome-wide association studies Hit paper breakdown → | 2015 | 2647 |
| 7 | Parametric and nonparametric linkage analysis: a unified multipoint approach. Hit paper breakdown → | 1996 | 2338 |
| 8 | An atlas of genetic correlations across human diseases and traits Hit paper breakdown → | 2015 | 2318 |
| 9 | Genome-wide association studies for common diseases and complex traits Hit paper breakdown → | 2005 | 2091 |
| 10 | A mutation in Orai1 causes immune deficiency by abrogating CRAC channel function Hit paper breakdown → | 2006 | 1886 |
| 11 | Schizophrenia risk from complex variation of complement component 4 Hit paper breakdown → | 2016 | 1643 |
| 12 | Clinical use of current polygenic risk scores may exacerbate health disparities Hit paper breakdown → | 2019 | 1428 |
| 13 | Efficiency and power in genetic association studies Hit paper breakdown → | 2005 | 1418 |
| 14 | High-resolution haplotype structure in the human genome Hit paper breakdown → | 2001 | 1364 |
| 15 | Efficient Control of Population Structure in Model Organism Association Mapping Hit paper breakdown → | 2008 | 1325 |
| 16 | Genetic Mapping in Human Disease Hit paper breakdown → | 2008 | 1020 |
| 17 | Human Demographic History Impacts Genetic Risk Prediction across Diverse Populations Hit paper breakdown → | 2017 | 855 |
| 18 | Genetic architectures of psychiatric disorders: the emerging picture and its implications Hit paper breakdown → | 2012 | 831 |
| 19 | HLA-B*5701 genotype is a major determinant of drug-induced liver injury due to flucloxacillin Hit paper breakdown → | 2009 | 821 |
| 20 | The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping Hit paper breakdown → | 1994 | 628 |
About Mark J. Daly
Mark J. Daly is a scholar working on Genetics, Molecular Biology, Immunology, Surgery and Cancer Research, having authored 374 papers that have together received 109.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (106 papers), Genomics and Rare Diseases (61 papers), Genetic Mapping and Diversity in Plants and Animals (44 papers), Inflammatory Bowel Disease (34 papers), Genomic variations and chromosomal abnormalities (32 papers), Genetic and phenotypic traits in livestock (29 papers), Genetics and Neurodevelopmental Disorders (23 papers) and Immunodeficiency and Autoimmune Disorders (19 papers). The work is most often cited by research in Genetics (48.3k citations), Molecular Biology (35.4k citations), Cancer Research (6.5k citations), Sensory Systems (2.0k citations) and Biological Psychiatry (948 citations). Mark J. Daly has collaborated with scholars based in United States, Finland and United Kingdom. Frequent co-authors include David Altshuler, Benjamin M. Neale, Eric S. Lander, Stacey Gabriel, Paul I. W. de Bakker, Julian Maller, Shaun Purcell, Pak C. Sham, Pamela Sklar and Eric Banks. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, European Journal of Human Genetics, Gastroenterology and PLoS 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.