Ann-Christine Syvänen

Molecular Biology · 2001–2016

A researcher in the Science corpus: 14 papers; trusts 3 researchers and is trusted by 17 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 104 citations into it; #3,486 of 17,773 by trust here, #2,170 by citations

Whom Ann-Christine Syvänen trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Xiaohu Gao
2. Benoit Dubertret
3. Mark J. Daly
4. Shuming Nie

Who trusts Ann-Christine Syvänen overall

1. A. Lorenz
2. B. Collard
3. V. V. van Ginneken
4. Jacqueline Batley
5. Tingjian Chen
6. S. Chao
7. Chengsong Zhu
8. Franco G. Asoro
9. Chitra Raghavan

Papers from Ann-Christine Syvänen's perspective

Ordered by how strongly the researchers Ann-Christine Syvänen trusts endorse each paper. Same corpus, a different order for every researcher.

1. Quantum-dot-tagged microbeads for multiplexed optical coding of biomolecules (Nature Biotechnology)
2. Gene Ontology: tool for the unification of biology
3. A genome-wide association study of global gene expression (Nature Genetics)
4. A new multipoint method for genome-wide association studies by imputation of genotypes (Nature Genetics)
5. Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
6. Meta-analysis of genome-wide association data and large-scale replication identifies additional susceptibility loci for type 2 diabetes (Nature Genetics)
7. High-resolution haplotype structure in the human genome (Nature Genetics)
8. Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility
9. The Sequence of the Human Genome (Science)
10. Principal components analysis corrects for stratification in genome-wide association studies

Their papers

• Transcriptome and genome sequencing uncovers functional variation in humans (2013) — 2,017 citations
• Large-scale association analysis provides insights into the genetic architecture and pathophysiology of type 2 diabetes (2012) — 1,982 citations
• The genetic architecture of type 2 diabetes (2016) — 1,066 citations
• Large-scale association analysis identifies new risk loci for coronary artery disease (2012) — 1,642 citations
• Accessing genetic variation: genotyping single nucleotide polymorphisms (2001) — 1,095 citations
• Genetic association analyses implicate aberrant regulation of innate and adaptive immunity genes in the pathogenesis of systemic lupus erythematosus (2015) — 941 citations
• Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility (2014) — 1,017 citations
• Defining the role of common variation in the genomic and biological architecture of adult human height (2014)
• Genetic risk and a primary role for cell-mediated immune mechanisms in multiple sclerosis (2011) — 2,780 citations
• A large-scale replication study identifies TNIP1, PRDM1, JAZF1, UHRF1BP1 and IL10 as risk loci for systemic lupus erythematosus (2009) — 832 citations
• Faculty Opinions recommendation of Genome-wide association study identifies eight loci associated with blood pressure. (2009) — 1,206 citations
• Genome Sequence, Comparative Analysis, and Population Genetics of the Domestic Horse (2009) — 808 citations
• Association of systemic lupus erythematosus with C8orf13-BLK and ITGAM-ITGAX. (2008) — 966 citations
• Polymorphisms in the tyrosine kinase 2 and interferon regulatory factor 5 genes are associated with systemic lupus erythematosus. (2005) — 644 citations