Bjarni V. Halldórsson
Genetics · 2003–2021
A researcher in the Science corpus: 12 papers; trusts 7 researchers and is trusted by 11 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 164 citations into it
- Molecular Biology — 153 citations into it
Whom Bjarni V. Halldórsson trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
Who trusts Bjarni V. Halldórsson overall
- Shushang Zhu
- Reha H. Tütüncü
- Dimitris J. Bertsimas
- Laurent El Ghaoui
- Mark Koenig
- David B. Brown
- Duan Li
- Maksim Oks
- Hamed Rahimian
- Constantine Caramanis
Papers from Bjarni V. Halldórsson's perspective
Ordered by how strongly the researchers Bjarni V. Halldórsson trusts endorse each paper. Same corpus, a different order for every researcher.
- Fitting a Mixture Model By Expectation Maximization To Discover Motifs In Biopolymer
- Convex analysis and minimization algorithms
- Gene Ontology: tool for the unification of biology
- T-Coffee: A novel method for fast and accurate multiple sequence alignment.
- Robust Portfolio Selection Problems (Mathematics of Operations Research)
- dbSNP: the NCBI database of genetic variation
- Association between microdeletion and microduplication at 16p11.2 and autism. (New England Journal of Medicine)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
- The PANTHER database of protein families, subfamilies, functions and pathways (Nucleic Acids Res.)
- Prediction of individual genetic risk to disease from genome-wide association studies.
Their papers
- An Interior-Point Method for a Class of Saddle-Point Problems (2003) — 96 citations
- Large recurrent microdeletions associated with schizophrenia (2008) — 1,814 citations
- Large-scale whole-genome sequencing of the Icelandic population (2015) — 776 citations
- The nature of nurture: Effects of parental genotypes (2017) — 849 citations
- Many sequence variants affecting diversity of adult human height (2008) — 709 citations
- Large-scale integration of the plasma proteome with genetics and disease (2021) — 1,317 citations
- Genome-wide association analyses of risk tolerance and risky behaviors in over 1 million individuals identify hundreds of loci and shared genetic influences (2019) — 629 citations
- Gene discovery and polygenic prediction from a 1.1-million-person GWAS of educational attainment (2018) — 2,165 citations
- Parental influence on human germline de novo mutations in 1,548 trios from Iceland (2017) — 505 citations
- Genome-wide association study identifies 74 loci associated with educational attainment (2016) — 1,288 citations
- Multiple genetic loci for bone mineral density and fractures. (2008) — 651 citations
- A Hybrid Micro–Macroevolutionary Approach to Gene Tree Reconstruction (2005) — 313 citations