Alicia R. Martin

Genetics · 2015–2023

A researcher in the Science corpus: 19 papers; trusts 2 researchers and is trusted by 0 researchers here, as inferred from the citation graph.

Subfields

• Genetics — 693 citations into it

Whom Alicia R. Martin trusts overall

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

1. Jian Yang
2. John Novembre
3. David H. Alexander
4. D. Curtis
5. N. Jablonski
6. A. Khera
7. Po-Ru Loh
8. Naomi R. Wray
9. Bjarni J. Vilhjálmsson
10. Alkes L Price

Who trusts Alicia R. Martin overall

1. Konrad J. Karczewski
2. D. Curtis

Papers from Alicia R. Martin's perspective

Ordered by how strongly the researchers Alicia R. Martin trusts endorse each paper. Same corpus, a different order for every researcher.

1. MAGMA: Generalized Gene-Set Analysis of GWAS Data (PLoS Comput. Biol.)
2. FINEMAP: efficient variable selection using summary data from genome-wide association studies (bioRxiv)
3. Next-generation genotype imputation service and methods (Nature Genetics)
4. GCTA: a tool for genome-wide complex trait analysis. (American Journal of Human Genetics)
5. Fast and accurate long-range phasing in a UK Biobank cohort
6. Partitioning heritability by functional annotation using genome-wide association summary statistics (Nature Genetics)
7. PLINK: a tool set for whole-genome association and population-based linkage analyses.
8. Assessing the impact of population stratification on genetic association studies (Nature Genetics)
9. Integration of summary data from GWAS and eQTL studies predicts complex trait gene targets (Nature Genetics)
10. LD Score Regression Distinguishes Confounding from Polygenicity in Genome-Wide Association Studies (Nature Genetics)

Their papers

• A global reference for human genetic variation (2015) — 16,925 citations
• Large-Scale Exome Sequencing Study Implicates Both Developmental and Functional Changes in the Neurobiology of Autism (2019) — 2,000 citations
• Genome-wide association studies (2021) — 1,011 citations
• A genomic mutational constraint map using variation in 76,156 human genomes (2023) — 1,228 citations
• Mapping genomic loci implicates genes and synaptic biology in schizophrenia (2022) — 2,226 citations
• A genome-wide mutational constraint map quantified from variation in 76,156 human genomes (2022) — 258 citations
• Mapping the human genetic architecture of COVID-19 (2021) — 807 citations
• Clinical use of current polygenic risk scores may exacerbate health disparities (2019) — 2,286 citations
• Genome-wide association studies in ancestrally diverse populations: opportunities, methods, pitfalls, and recommendations. (2019) — 634 citations
• Identification of common genetic risk variants for autism spectrum disorder (2019) — 2,059 citations
• Hidden ‘risk’ in polygenic scores: clinical use today could exacerbate health disparities (2018) — 93 citations
• Discovery of the first genome-wide significant risk loci for attention-deficit/hyperactivity disorder (2018) — 1,821 citations
• Geographic variation and bias in polygenic scores of complex diseases and traits in Finland (2018) — 32 citations
• Comparative genetic architectures of schizophrenia in East Asian and European populations (2018) — 580 citations
• The critical needs and challenges for genetic architecture studies in Africa (2018) — 65 citations
• Signals of polygenic adaptation on height have been overestimated due to uncorrected population structure in genome-wide association studies (2018) — 30 citations
• Quantifying the impact of rare and ultra-rare coding variation across the phenotypic spectrum (2017) — 114 citations
• An Unexpectedly Complex Architecture for Skin Pigmentation in Africans (2017) — 167 citations
• Human demographic history impacts genetic risk prediction across diverse populations (2016) — 1,291 citations