Ada Hamosh
Impact in
- Genetics top 0.1%
- Genomics and Rare Diseases
- Genomic variations and chromosomal abnormalities
- Genetics and Neurodevelopmental Disorders
- Connective tissue disorders research
- Clinical Biochemistry top 0.2%
Papers in
- Genetics 88
- Genomics and Rare Diseases 62
- Genomic variations and chromosomal abnormalities 31
- Genetics and Neurodevelopmental Disorders 12
-
- Metabolism and Genetic Disorders 23
- Co-authors
- Joanna S. Amberger (12 shared papers)Carol A. Bocchini (8 shared papers)Alan F. Scott (4 shared papers)François Schiettecatte (6 shared papers)David Valle (14 shared papers)Nara Lygia de Macena Sobreira (10 shared papers)Harry C. Dietz (5 shared papers)David Valle‐García (1 shared paper)
- Journals
- Human Mutation (15 papers)Genetics in Medicine (12 papers)The American Journal of Human Genetics (9 papers)Nucleic Acids Research (9 papers)The Journal of Pediatrics (5 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Ada Hamosh
145 papers receiving 21.3k citations
Ada Hamosh's Hit Papers
Peers
Comparison fields: 5 of 182
- Genetics 8.8k
- Clinical Biochemistry 932
- Molecular Biology 9.6k
- Cancer Research 1.6k
- Aging 163
Countries citing papers authored by Ada Hamosh
This map shows the geographic impact of Ada Hamosh'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 Ada Hamosh with the expected number of citations based on a country's size and research output (numbers larger than one mean the country cites Ada Hamosh more than expected).
Fields of papers citing papers by Ada Hamosh
This network shows the impact of papers produced by Ada Hamosh. 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 Ada Hamosh. The network helps show where Ada Hamosh may publish in the future.
Co-authors
The 25 scholars most cited alongside Ada Hamosh, 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 151 papers — load more, or switch the sort, to bring in the rest.
| # | Work | ||
|---|---|---|---|
| 1 | Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders Hit paper breakdown → | 2004 | 2651 |
| 2 | Consensus Statement: Chromosomal Microarray Is a First-Tier Clinical Diagnostic Test for Individuals with Developmental Disabilities or Congenital Anomalies Hit paper breakdown → | 2010 | 2162 |
| 3 | OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders Hit paper breakdown → | 2014 | 1920 |
| 4 | Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene Hit paper breakdown → | 1991 | 1662 |
| 5 | GeneMatcher: A Matching Tool for Connecting Investigators with an Interest in the Same Gene Hit paper breakdown → | 2015 | 1216 |
| 6 | Online Mendelian Inheritance In Man (OMIM) Hit paper breakdown → | 2000 | 913 |
| 7 | OMIM.org: leveraging knowledge across phenotype–gene relationships Hit paper breakdown → | 2018 | 710 |
| 8 | 2002 | 589 | |
| 9 | 2008 | 588 | |
| 10 | The Human Phenotype Ontology in 2017 Hit paper breakdown → | 2016 | 580 |
| 11 | Searching Online Mendelian Inheritance in Man (OMIM): A Knowledgebase of Human Genes and Genetic Phenotypes Hit paper breakdown → | 2017 | 548 |
| 12 | The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities Hit paper breakdown → | 2015 | 484 |
| 13 | 2002 | 425 | |
| 14 | 2015 | 378 | |
| 15 | 2005 | 371 | |
| 16 | How many rare diseases are there? Hit paper breakdown → | 2019 | 338 |
| 17 | International Cooperation to Enable the Diagnosis of All Rare Genetic Diseases Hit paper breakdown → | 2017 | 314 |
| 18 | 2007 | 292 | |
| 19 | 2011 | 285 | |
| 20 | 2018 | 276 |
About Ada Hamosh
Ada Hamosh is a scholar working on Genetics, Clinical Biochemistry, Pediatrics, Perinatology and Child Health, Cancer Research and Molecular Biology, having authored 151 papers that have together received 22.1k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (62 papers), Genomic variations and chromosomal abnormalities (31 papers), Metabolism and Genetic Disorders (23 papers), Cystic Fibrosis Research Advances (21 papers), Cancer Genomics and Diagnostics (14 papers), Biomedical Text Mining and Ontologies (12 papers), Genetics and Neurodevelopmental Disorders (12 papers) and Neonatal Respiratory Health Research (11 papers). The work is most often cited by research in Genetics (8.8k citations), Clinical Biochemistry (932 citations), Molecular Biology (9.6k citations), Cancer Research (1.6k citations) and Aging (163 citations). Ada Hamosh has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Joanna S. Amberger, Carol A. Bocchini, Alan F. Scott, François Schiettecatte, David Valle, Nara Lygia de Macena Sobreira, Harry C. Dietz, David Valle‐García, Victor A. McKusick and Clair A. Francomano. Their work appears in journals such as Human Mutation, Genetics in Medicine, The American Journal of Human Genetics, Nucleic Acids Research and The Journal of Pediatrics.
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.