Ada Hamosh
Genetics · 2000–2023
A researcher in the Science corpus: 15 papers; trusts 3 researchers and is trusted by 15 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 107 citations into it; #1,089 of 6,854 by trust here, #192 by citations
- Molecular Biology — 104 citations into it; #3,414 of 17,773 by trust here, #1,267 by citations
- Computational Biology & Bioinformatics — 18 citations into it
Whom Ada Hamosh trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Ada Hamosh overall
- Sebastian Köhler
- Peter N. Robinson
- Oded Magger
- Yaling Nie
- Pauline Crystal Ng
- Yongjin Li
- J. Chen
- Ferenc Jorda¤n
- Joanna S. Amberger
- Gang Su
Papers from Ada Hamosh's perspective
Ordered by how strongly the researchers Ada Hamosh trusts endorse each paper. Same corpus, a different order for every researcher.
- The Mammalian Phenotype Ontology as a tool for annotating, analyzing and comparing phenotypic information (Genome Biology)
- The Human Phenotype Ontology in 2017 (Nucleic Acids Res.)
- The Human Phenotype Ontology: a tool for annotating and analyzing human hereditary disease. (American Journal of Human Genetics)
- DECIPHER: Database of Chromosomal Imbalance and Phenotype in Humans Using Ensembl Resources. (American Journal of Human Genetics)
- Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders
- Improved exome prioritization of disease genes through cross-species phenotype comparison (Genome Research)
- Expansion of the Human Phenotype Ontology (HPO) knowledge base and resources (Nucleic Acids Res.)
- OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders
- ClinGen--the Clinical Genome Resource. (New England Journal of Medicine)
- Validation of a common data model for active safety surveillance research (J. Am. Medical Informatics Assoc.)
Their papers
- McKusick's Online Mendelian Inheritance in Man (OMIM®) (2008) — 740 citations
- OMIM.org: Online Mendelian Inheritance in Man (OMIM®), an online catalog of human genes and genetic disorders (2014) — 2,478 citations
- Online Mendelian Inheritance in Man (OMIM), a knowledgebase of human genes and genetic disorders (2004) — 3,380 citations
- Development of human protein reference database as an initial platform for approaching systems biology in humans. (2003) — 1,149 citations
- OMIM.org: leveraging knowledge across phenotype–gene relationships (2018) — 914 citations
- A new face and new challenges for Online Mendelian Inheritance in Man (OMIM®) (2011) — 335 citations
- The Human Phenotype Ontology in 2017 (2016) — 742 citations
- Consensus statement: chromosomal microarray is a first-tier clinical diagnostic test for individuals with developmental disabilities or congenital anomalies. (2010) — 2,697 citations
- Searching Online Mendelian Inheritance in Man (OMIM): A Knowledgebase of Human Genes and Genetic Phenotypes (2017) — 658 citations
- GeneMatcher: A Matching Tool for Connecting Investigators with an Interest in the Same Gene (2015) — 1,396 citations
- The Human Phenotype Ontology in 2024: phenotypes around the world (2023) — 333 citations
- Insights into genetics, human biology and disease gleaned from family based genomic studies (2019) — 179 citations
- The Matchmaker Exchange: A Platform for Rare Disease Gene Discovery (2015) — 453 citations
- The Genetic Basis of Mendelian Phenotypes: Discoveries, Challenges, and Opportunities. (2015) — 611 citations
- Online Mendelian Inheritance In Man (OMIM) (2000) — 1,419 citations