Ada Hamosh
Impact in
- Genetics top 0.1%
- Genomics and Rare Diseases
- Connective tissue disorders research
- Genomic variations and chromosomal abnormalities
- Clinical Biochemistry top 0.5%
- Metabolism and Genetic Disorders
Papers in
- Genetics 51
- Genomics and Rare Diseases 38
- Genomic variations and chromosomal abnormalities 18
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- Biomedical Text Mining and Ontologies 7
- Congenital heart defects research 5
- Co-authors
- Joanna Amberger (12 shared papers)Carol Bocchini (8 shared papers)Alan F. Scott (4 shared papers)François Schiettecatte (6 shared papers)David Valle (14 shared papers)David Valle‐García (2 shared papers)Harry C. Dietz (3 shared papers)Victor A. McKusick (1 shared paper)
- Journals
- Human Mutation (12 papers)Nucleic Acids Research (6 papers)Genetics in Medicine (5 papers)The Journal of Pediatrics (5 papers)Molecular Genetics and Metabolism (4 papers)
- Partner nations
- United StatesUnited KingdomCanada
In The Last Decade
Ada Hamosh
98 papers receiving 13.4k citations
Ada Hamosh's Hit Papers
Peers
Comparison fields: 5 of 165
- Genetics 4.3k
- Clinical Biochemistry 687
- Molecular Biology 6.2k
- Cancer Research 972
- Aging 118
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 101 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 | 2434 |
| 2 | OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders Hit paper breakdown → | 2014 | 1713 |
| 3 | Marfan syndrome caused by a recurrent de novo missense mutation in the fibrillin gene Hit paper breakdown → | 1991 | 1475 |
| 4 | Online Mendelian Inheritance In Man (OMIM) Hit paper breakdown → | 2000 | 825 |
| 5 | OMIM.org: leveraging knowledge across phenotype–gene relationships Hit paper breakdown → | 2018 | 617 |
| 6 | Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders Hit paper breakdown → | 2002 | 555 |
| 7 | McKusick's Online Mendelian Inheritance in Man (OMIM(R)) Hit paper breakdown → | 2008 | 525 |
| 8 | Searching Online Mendelian Inheritance in Man (OMIM): A Knowledgebase of Human Genes and Genetic Phenotypes Hit paper breakdown → | 2017 | 498 |
| 9 | GeneMatcher: A Matching Tool for Connecting Investigators with an Interest in the Same Gene Hit paper breakdown → | 2015 | 458 |
| 10 | 2002 | 377 | |
| 11 | Haploinsufficiency of t e lomerase reverse transcriptase leads to anticipation in autosomal dominant dyskeratosis congenita Hit paper breakdown → | 2005 | 325 |
| 12 | How many rare diseases are there? Hit paper breakdown → | 2019 | 293 |
| 13 | 2011 | 256 | |
| 14 | 2007 | 249 | |
| 15 | 2018 | 232 | |
| 16 | 1998 | 187 | |
| 17 | 2007 | 140 | |
| 18 | 1991 | 127 | |
| 19 | 2004 | 114 | |
| 20 | 1991 | 111 |
About Ada Hamosh
Ada Hamosh is a scholar working on Genetics, Molecular Biology, Pulmonary and Respiratory Medicine, Clinical Biochemistry and Pediatrics, Perinatology and Child Health, having authored 101 papers that have together received 13.8k indexed citations. Recurring topics across this work include Genomics and Rare Diseases (38 papers), Genomic variations and chromosomal abnormalities (18 papers), Cystic Fibrosis Research Advances (18 papers), Metabolism and Genetic Disorders (17 papers), Neonatal Respiratory Health Research (10 papers), Cancer Genomics and Diagnostics (8 papers), Biomedical Text Mining and Ontologies (7 papers) and Congenital heart defects research (5 papers). The work is most often cited by research in Genetics (4.3k citations), Clinical Biochemistry (687 citations), Molecular Biology (6.2k citations), Cancer Research (972 citations) and Aging (118 citations). Ada Hamosh has collaborated with scholars based in United States, United Kingdom and Canada. Frequent co-authors include Joanna Amberger, Carol Bocchini, Alan F. Scott, François Schiettecatte, David Valle, David Valle‐García, Harry C. Dietz, Victor A. McKusick, Nara Sobreira and Clair A. Francomano. Their work appears in journals such as Human Mutation, Nucleic Acids Research, Genetics in Medicine, The Journal of Pediatrics and Molecular Genetics and Metabolism.
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.