Mark Daly
Impact in
- Genetics top 0.01%
- Genetic Associations and Epidemiology
- Inflammatory Bowel Disease
- Genomics and Rare Diseases
- Genetic Mapping and Diversity in Plants and Animals
- Genetic and phenotypic traits in livestock
- Genomic variations and chromosomal abnormalities
- Psychiatry and Mental health top 0.01%
- Schizophrenia research and treatment
Papers in
- Genetics 498
- Genetic Associations and Epidemiology 297
- Inflammatory Bowel Disease 95
- Genomics and Rare Diseases 75
- Genomic variations and chromosomal abnormalities 30
- Genetics and Neurodevelopmental Disorders 21
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- Schizophrenia research and treatment 46
- Co-authors
- Julian Maller (13 shared papers)Benjamin M. Neale (48 shared papers)Jeffrey C. Barrett (8 shared papers)Eric S. Lander (40 shared papers)Ben Fry (1 shared paper)Paul I. W. de Bakker (13 shared papers)Shaun Purcell (19 shared papers)David Altshuler (49 shared papers)
- Journals
- Nature Genetics (126 papers)The American Journal of Human Genetics (68 papers)Nature (53 papers)Nature Communications (45 papers)Gastroenterology (24 papers)
- Partner nations
- United StatesFinlandUnited Kingdom
In The Last Decade
Mark Daly
766 papers receiving 296.7k citations
Mark Daly's Hit Papers
Peers
Comparison fields: 5 of 227
- Genetics 142.6k
- Psychiatry and Mental health 30.8k
- Biological Psychiatry 1.4k
- Molecular Biology 47k
- Aging 1k
Countries citing papers authored by Mark Daly
This map shows the geographic impact of Mark 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 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 Daly more than expected).
Fields of papers citing papers by Mark Daly
This network shows the impact of papers produced by Mark 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 Daly. The network helps show where Mark Daly may publish in the future.
Co-authors
The 25 scholars most cited alongside Mark 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 787 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 | 26654 |
| 2 | Haploview: analysis and visualization of LD and haplotype maps Hit paper breakdown → | 2004 | 12928 |
| 3 | A global reference for human genetic variation Hit paper breakdown → | 2015 | 12887 |
| 4 | A framework for variation discovery and genotyping using next-generation DNA sequencing data Hit paper breakdown → | 2011 | 8867 |
| 5 | PGC-1α-responsive genes involved in oxidative phosphorylation are coordinately downregulated in human diabetes Hit paper breakdown → | 2003 | 8081 |
| 6 | Analysis of protein-coding genetic variation in 60,706 humans Hit paper breakdown → | 2016 | 7891 |
| 7 | The mutational constraint spectrum quantified from variation in 141,456 humans Hit paper breakdown → | 2020 | 6789 |
| 8 | Biological insights from 108 schizophrenia-associated genetic loci Hit paper breakdown → | 2014 | 6156 |
| 9 | MAPMAKER: An interactive computer package for constructing primary genetic linkage maps of experimental and natural populations Hit paper breakdown → | 1987 | 6125 |
| 10 | Initial sequencing and comparative analysis of the mouse genome Hit paper breakdown → | 2002 | 5353 |
| 11 | The International HapMap Project Hit paper breakdown → | 2003 | 4946 |
| 12 | The Structure of Haplotype Blocks in the Human Genome Hit paper breakdown → | 2002 | 4902 |
| 13 | Host–microbe interactions have shaped the genetic architecture of inflammatory bowel disease Hit paper breakdown → | 2012 | 3936 |
| 14 | Common polygenic variation contributes to risk of schizophrenia and bipolar disorder Hit paper breakdown → | 2009 | 3903 |
| 15 | LD Score regression distinguishes confounding from polygenicity in genome-wide association studies Hit paper breakdown → | 2015 | 3725 |
| 16 | A second generation human haplotype map of over 3.1 million SNPs Hit paper breakdown → | 2007 | 3536 |
| 17 | The landscape of somatic copy-number alteration across human cancers Hit paper breakdown → | 2010 | 3170 |
| 18 | An atlas of genetic correlations across human diseases and traits Hit paper breakdown → | 2015 | 2964 |
| 19 | A Genome-Wide Association Study Identifies IL23R as an Inflammatory Bowel Disease Gene Hit paper breakdown → | 2006 | 2560 |
| 20 | FinnGen provides genetic insights from a well-phenotyped isolated population Hit paper breakdown → | 2023 | 2526 |
About Mark Daly
Mark Daly is a scholar working on Genetics, Psychiatry and Mental health, Ophthalmology, Cognitive Neuroscience and Molecular Biology, having authored 787 papers that have together received 303.6k indexed citations. Recurring topics across this work include Genetic Associations and Epidemiology (297 papers), Inflammatory Bowel Disease (95 papers), Genomics and Rare Diseases (75 papers), Schizophrenia research and treatment (46 papers), Autism Spectrum Disorder Research (36 papers), Genomic variations and chromosomal abnormalities (30 papers), Retinal Diseases and Treatments (30 papers) and Genetics and Neurodevelopmental Disorders (21 papers). The work is most often cited by research in Genetics (142.6k citations), Psychiatry and Mental health (30.8k citations), Biological Psychiatry (1.4k citations), Molecular Biology (47k citations) and Aging (1k citations). Mark Daly has collaborated with scholars based in United States, Finland and United Kingdom. Frequent co-authors include Julian Maller, Benjamin M. Neale, Jeffrey C. Barrett, Eric S. Lander, Ben Fry, Paul I. W. de Bakker, Shaun Purcell, David Altshuler, Pamela B. Sklar and Pak Chung Sham. Their work appears in journals such as Nature Genetics, The American Journal of Human Genetics, Nature, Nature Communications and Gastroenterology.
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.