Christian Fuchsberger
Genetics · 2010–2021
A researcher in the Science corpus: 15 papers; trusts 12 researchers and is trusted by 3 researchers here, as inferred from the citation graph.
Subfields
- Genetics — 316 citations into it; #3,963 of 6,854 by trust here, #95 by citations
- Molecular Biology — 181 citations into it
Whom Christian Fuchsberger trusts overall
Their strongest outbound trust, strongest first, inferred from their citations.
- Jonathan Marchini
- Bryan N. Howie
- Brian L. Browning
- Sharon R. Browning
- Matthew Stephens
- Yun Li
- Paul Scheet
- Shaun Purcell
- Gonçalo R. Abecasis
- Cristen J. Willer
Who trusts Christian Fuchsberger overall
Papers from Christian Fuchsberger's perspective
Ordered by how strongly the researchers Christian Fuchsberger trusts endorse each paper. Same corpus, a different order for every researcher.
- Genotype Imputation with Thousands of Genomes (G3: Genes, Genomes, Genetics)
- A new statistical method for haplotype reconstruction from population data. (American Journal of Human Genetics)
- MaCH: Using Sequence and Genotype Data to Estimate Haplotypes and Unobserved Genotypes (Genetic Epidemiology)
- Accounting for decay of linkage disequilibrium in haplotype inference and missing-data imputation. (American Journal of Human Genetics)
- A new multipoint method for genome-wide association studies by imputation of genotypes (Nature Genetics)
- A fast and flexible statistical model for large-scale population genotype data: applications to inferring missing genotypes and haplotypic phase. (American Journal of Human Genetics)
- A comparison of bayesian methods for haplotype reconstruction from population genotype data. (American Journal of Human Genetics)
- Fast and accurate long-range phasing in a UK Biobank cohort
- A linear complexity phasing method for thousands of genomes (Nature Methods)
- Common SNPs explain a large proportion of heritability for human height (Nature Genetics)
Their papers
- A global reference for human genetic variation (2015) — 16,925 citations
- Next-generation genotype imputation service and methods (2016) — 3,622 citations
- Sequencing of 53,831 diverse genomes from the NHLBI TOPMed Program (2019) — 1,941 citations
- The genetic architecture of type 2 diabetes (2016) — 1,066 citations
- The Metabochip, a Custom Genotyping Array for Genetic Studies of Metabolic, Cardiovascular, and Anthropometric Traits (2012) — 551 citations
- Multiple New Loci Associated with Kidney Function and Chronic Kidney Disease: The CKDGen consortium (2010) — 799 citations
- The power of genetic diversity in genome-wide association studies of lipids (2021) — 765 citations
- Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
- Associations of autozygosity with a broad range of human phenotypes (2019) — 112 citations
- A catalog of genetic loci associated with kidney function from analyses of a million individuals (2019) — 744 citations
- An Expanded Genome-Wide Association Study of Type 2 Diabetes in Europeans (2017) — 677 citations
- Reference-based phasing using the Haplotype Reference Consortium panel (2016) — 1,643 citations
- Minimac2: Faster Genotype Imputation (2015) — 598 citations
- An integrated map of genetic variation from 1,092 human genomes (2012) — 8,008 citations
- Fast and accurate genotype imputation in genome-wide association studies through pre-phasing (2012) — 1,829 citations