Iuliana Ionita-Laza
Molecular Biology · 2014–2021
A researcher in the Science corpus: 4 papers; trusts 2 researchers and is trusted by 2 researchers here, as inferred from the citation graph.
Subfields
- Molecular Biology — 77 citations into it; #14,188 of 17,773 by trust here, #9,727 by citations
Whom Iuliana Ionita-Laza trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- ENCODEConsortium
- Martin Kircher
- Eugene Davydov
- Ivan A. Adzhubei
- Martin Renqiang Min
- Michael L. Metzker
- Elaine R. Mardis
- Joseph K. Pickrell
Who trusts Iuliana Ionita-Laza overall
Papers from Iuliana Ionita-Laza's perspective
Ordered by how strongly the researchers Iuliana Ionita-Laza trusts endorse each paper. Same corpus, a different order for every researcher.
- A method and server for predicting damaging missense mutations
- Functional Impact of Global Rare Copy Number Variation in Autism Spectrum Disorder (Nature)
- De novo mutations revealed by whole-exome sequencing are strongly associated with autism (Nature)
- A general framework for estimating the relative pathogenicity of human genetic variants
- Exome sequencing as a tool for Mendelian disease gene discovery
- A Copy Number Variation Morbidity Map of Developmental Delay (Nature Genetics)
- Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome (Nature Genetics)
- Sequencing technologies — the next generation (Nature reviews genetics)
- Partitioning heritability of regulatory and cell-type-specific variants across 11 common diseases. (American Journal of Human Genetics)
- Joint analysis of functional genomic data and genome-wide association studies of 18 human traits (bioRxiv)
Their papers
- A SPECTRAL APPROACH INTEGRATING FUNCTIONAL GENOMIC ANNOTATIONS FOR CODING AND NONCODING VARIANTS (2016) — 572 citations
- Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- Synaptic, transcriptional, and chromatin genes disrupted in autism (2014) — 816 citations