Benjamin Michael Neale, Ph.D.
Co-Author
This page shows the publications co-authored by Benjamin Neale and Andrea Ganna.
Connection Strength
3.357
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Quantifying the Impact of Rare and Ultra-rare Coding Variation across the Phenotypic Spectrum. Am J Hum Genet. 2018 06 07; 102(6):1204-1211.
Score: 0.784
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Ultra-rare disruptive and damaging mutations influence educational attainment in the general population. Nat Neurosci. 2016 12; 19(12):1563-1565.
Score: 0.699
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Clinical Conditions and Their Impact on Utility of Genetic Scores for Prediction of Acute Coronary Syndrome. Circ Genom Precis Med. 2021 08; 14(4):e003283.
Score: 0.243
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Genetic analyses identify widespread sex-differential participation bias. Nat Genet. 2021 05; 53(5):663-671.
Score: 0.239
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Response to Comment on "Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior". Science. 2021 03 26; 371(6536).
Score: 0.238
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Genome studies must account for history-Response. Science. 2019 12 20; 366(6472):1461-1462.
Score: 0.218
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Large-scale GWAS reveals insights into the genetic architecture of same-sex sexual behavior. Science. 2019 08 30; 365(6456).
Score: 0.214
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Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans. Nature. 2021 Sep; 597(7874):E3-E4.
Score: 0.061
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Hematopoietic mosaic chromosomal alterations increase the risk for diverse types of infection. Nat Med. 2021 06; 27(6):1012-1024.
Score: 0.060
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Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans. Nature. 2021 Feb; 590(7846):E53.
Score: 0.059
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Hematopoietic mosaic chromosomal alterations and risk for infection among 767,891 individuals without blood cancer. medRxiv. 2020 Nov 16.
Score: 0.058
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The mutational constraint spectrum quantified from variation in 141,456 humans. Nature. 2020 05; 581(7809):434-443.
Score: 0.056
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Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries. Nat Commun. 2020 Apr 01; 11(1):1715.
Score: 0.056
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Correction: Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. PLoS Genet. 2019 May; 15(5):e1008190.
Score: 0.052
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Polygenic adaptation on height is overestimated due to uncorrected stratification in genome-wide association studies. Elife. 2019 03 21; 8.
Score: 0.052
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Deep-coverage whole genome sequences and blood lipids among 16,324 individuals. Nat Commun. 2018 08 23; 9(1):3391.
Score: 0.050
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Publisher Correction: Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries. Nat Commun. 2018 08 23; 9(1):3493.
Score: 0.050
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Deep coverage whole genome sequences and plasma lipoprotein(a) in individuals of European and African ancestries. Nat Commun. 2018 07 04; 9(1):2606.
Score: 0.049
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Insights into the genetic epidemiology of Crohn's and rare diseases in the Ashkenazi Jewish population. PLoS Genet. 2018 05; 14(5):e1007329.
Score: 0.049
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Common variants associated with plasma triglycerides and risk for coronary artery disease. Nat Genet. 2013 Nov; 45(11):1345-52.
Score: 0.035
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Genome-wide meta-analysis identifies 11 new loci for anthropometric traits and provides insights into genetic architecture. Nat Genet. 2013 May; 45(5):501-12.
Score: 0.034
Connection Strength
The connection strength for co-authors is the sum of the scores for each of their shared publications.
Publication scores are based on many factors, including how long ago they were written and whether the person is a first or senior author.