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J. Backman · SciRah

Researcher profile · Semantic Scholar

J. Backman

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J. Backman — researcher profile on SciRah

h-index: 23
Works: 57
Citations: 4,820

Most-cited papers

Computationally efficient whole-genome regression for quantitative and binary traits
J. Mbatchou, Leland Barnard, J. Backman, A. Marcketta +13 more
2020Nature Genetics1,338 citations Open access
Semantic Scholar
Exome sequencing and analysis of 454,787 UK Biobank participants
J. Backman, Alexander Li, A. Marcketta, Dylan Sun +37 more
2021Nature831 citations Open access
Semantic Scholar
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
J. Nielsen, Rosa B. Thorolfsdottir, Lars G. Fritsche, Wei Zhou +45 more
2018Nature Genetics771 citations Open access
Semantic Scholar
Exome sequencing and characterization of 49,960 individuals in the UK Biobank
C. V. van Hout, I. Tachmazidou, J. Backman, Joshua D. Hoffman +47 more
2020Nature469 citations Open access
Semantic Scholar
Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease
J. Horowitz, J. Kosmicki, A. Damask, D. Sharma +55 more
2022Nature Genetics148 citations Open access
Semantic Scholar
Genome-wide association and multi-trait analyses characterize the common genetic architecture of heart failure
M. Levin, Noah L. Tsao, Pankhuri Singhal, Chang Liu +39 more
2022Nature Communications125 citations Open access
Semantic Scholar
Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank
C. V. van Hout, I. Tachmazidou, J. Backman, Joshua Hoffman +45 more
2019bioRxiv122 citations Open access
Semantic Scholar
A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Y. Sun, Xiao-Dong Bai, Si-Ying Chen, Su-Ying Bao +44 more
2024Nature94 citations Open access
Semantic Scholar
Genotyping, sequencing and analysis of 140,000 adults from Mexico City
A. Ziyatdinov, J. Torres, J. Alegre-Díaz, J. Backman +45 more
2023Nature91 citations Open access
Semantic Scholar
Pharmacogenomic Polygenic Response Score Predicts Ischemic Events and Cardiovascular Mortality in Clopidogrel-Treated Patients.
J. Lewis, J. Backman, J. Reny, T. Bergmeijer +42 more
2019European Heart Journal - Cardiovascular Pharmacotherapy88 citations Open access
Semantic Scholar
Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals
J. Kosmicki, J. Horowitz, N. Banerjee, R. Lanche +77 more
2021American Journal of Human Genetics85 citations Open access
Semantic Scholar
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Sonia H. Shah, Albert Henry, C. Roselli, Hong-Huang Lin +142 more
2020Nature Communications74 citations Open access
Semantic Scholar
Genome-wide association analysis provides insights into the molecular etiology of dilated cardiomyopathy
Sean L. Zheng, Albert Henry, D. Cannie, Michael Lee +102 more
2024Nature Genetics55 citations Open access
Semantic Scholar
Genome-wide association study meta-analysis provides insights into the etiology of heart failure and its subtypes
Albert Henry, Xiaodong Mo, C. Finan, M. Chaffin +177 more
2025Nature Genetics48 citations Open access
Semantic Scholar
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease
C. Tcheandjieu, K. Xiao, H. Tejeda, J. Lynch +99 more
2022Nature Genetics47 citations Open access
Semantic Scholar
Genome-wide association study of platelet reactivity and cardiovascular response in patients treated with clopidogrel: a study by the International Clopidogrel Pharmacogenomics Consortium (ICPC)
S. Verma, T. Bergmeijer, L. Gong, J. Reny +44 more
2020Clinical pharmacology and therapy44 citations Open access
Semantic Scholar
Genome-wide analysis in 756,646 individuals provides first genetic evidence that ACE2 expression influences COVID-19 risk and yields genetic risk scores predictive of severe disease
J. Horowitz, J. Kosmicki, A. Damask, D. Sharma +55 more
2020medRxiv33 citations Open access
Semantic Scholar
Agonist antibody to guanylate cyclase receptor NPR1 regulates vascular tone
Michael E. Dunn, A. Kithcart, Jee Hae Kim, A. Ho +188 more
2024Nature31 citations Open access
Semantic Scholar
Genetic Variation in the Platelet Endothelial Aggregation Receptor 1 Gene Results in Endothelial Dysfunction
Adam S. Fisch, L. Yerges-Armstrong, J. Backman, Hong Wang +10 more
2015PLoS ONE31 citations Open access
Semantic Scholar
MEPE loss-of-function variant associates with decreased bone mineral density and increased fracture risk
I. Surakka, Lars G. Fritsche, Wei Zhou, J. Backman +22 more
2020Nature Communications30 citations Open access
Semantic Scholar
A catalog of associations between rare coding variants and COVID-19 outcomes
J. Kosmicki, J. E. Horowitz, N. Banerjee, R. Lanche +76 more
2020medRxiv29 citations Open access
Semantic Scholar
Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank
Sheila M. Gaynor, Tyler Joseph, Xiao-Dong Bai, Yu-Xin Zou +16 more
2023Nature Genetics28 citations Open access
Semantic Scholar
Genome-Wide Analysis of Clopidogrel Active Metabolite Levels Identifies Novel Variants that Influence Antiplatelet Response
J. Backman, J. O'Connell, K. Tanner, C. Peer +7 more
2017Pharmacogenetics & Genomics24 citations Open access
Semantic Scholar
Genome‐wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals
Chuan Gao, A. Marcketta, J. Backman, C. O'Dushlaine +13 more
2021Genetic Epidemiology23 citations Open access
Semantic Scholar
The genomics of heart failure: design and rationale of the HERMES consortium
R. Lumbers, Sonia H. Shah, Hong-Huang Lin, T. Czuba +170 more
2021ESC Heart Failure21 citations Open access
Semantic Scholar
Exome-Chip Meta-Analysis Identifies Association between Variation in ANKRD26 and Platelet Aggregation
Ming-Huei Chen, L. Yanek, J. Backman, J. Eicher +12 more
2017Platelets17 citations Open access
Semantic Scholar
From Genotype to Phenotype: Nonsense Variants in SLC13A1 Are Associated with Decreased Serum Sulfate and Increased Serum Aminotransferases
Christina G. Tise, James A. Perry, Leslie E. Anforth, M. Pavlovich +6 more
2016G3: Genes, Genomes, Genetics17 citations Open access
Semantic Scholar
Genotyping, sequencing and analysis of 140,000 adults from the Mexico City Prospective Study
A. Ziyatdinov, J. Torres, J. Alegre-Díaz, J. Backman +40 more
2022bioRxiv14 citations Open access
Semantic Scholar
A deep catalog of protein-coding variation in 985,830 individuals
Kathie Y. Sun, Xiao-Dong Bai, Si-Ying Chen, S. Bao +42 more
2023bioRxiv13 citations Open access
Semantic Scholar
Genome-wide association study of 1 million people identifies 111 loci for atrial fibrillation
J. Nielsen, Rosa B. Thorolfsdottir, Lars G. Fritsche, Wei Zhou +44 more
2018bioRxiv13 citations Open access
Semantic Scholar
Familial aggregation of tobacco use behaviors among Amish men.
Katie L. Nugent, Amber Million-Mrkva, J. Backman, Sarah H. Stephens +6 more
2014Nicotine & Tobacco Research13 citations Open access
Semantic Scholar
Joint testing of rare variant burden scores using non-negative least squares
A. Ziyatdinov, J. Mbatchou, A. Marcketta, J. Backman +15 more
2023bioRxiv12 citations Open access
Semantic Scholar
Effect of Two Lipoprotein (a)-Associated Genetic Variants on Plasminogen Levels and Fibrinolysis
Hong Wang, C. Hong, J. Lewis, Yanbei Zhu +8 more
2016G3: Genes, Genomes, Genetics9 citations Open access
Semantic Scholar
Mapping the aetiological foundations of the heart failure spectrum using human genetics
A. Henry, X. Mo, C. Finan, M. Chaffin +41 more
2023medRxiv6 citations Open access
Semantic Scholar
NOTCH3 p.Arg1231Cys is markedly enriched in South Asians and associated with stroke
J. Rodriguez-Flores, S. Khalid, Neelroop N. Parikshak, A. Rasheed +44 more
2023Nature Communications6 citations Open access
Semantic Scholar
Genome-wide association study of liver fat, iron, and extracellular fluid fraction in the UK Biobank
C. O'Dushlaine, M. Germino, N. Verweij, J. Nielsen +11 more
2021medRxiv6 citations Open access
Semantic Scholar
Genome-wide association study provides new insights into the genetic architecture and pathogenesis of heart failure
Sonia H. Shah, Albert Henry, C. Roselli, Hong-Huang Lin +142 more
2019bioRxiv6 citations Open access
Semantic Scholar
Analysis of 173,303 exomes and genomes in the Pakistan Genome Resource
Christopher Koch, Shareef Khalid, M. Khan, Shruthi Bandyadka +247 more
2026Nature5 citations Open access
Semantic Scholar
Insights from the Biorepository and Integrative Genomics pediatric resource
S. Buonaiuto, Franco Marsico, A. Mohammed, L. Chinthala +190 more
2025Nature Communications5 citations Open access
Semantic Scholar
FNIP1 variants are associated with favourable metabolism in 1 million humans
G. Hindy, Rene C. Adam, O. Sosina, Dwaine Pryce +364 more
2026Nature3 citations Open access
Semantic Scholar
Genome-wide association analysis reveals insights into the molecular aetiology underlying dilated cardiomyopathy
S.-L. Zheng, A. Henry, D. Cannie, M. Lee +40 more
2023medRxiv3 citations Open access
Semantic Scholar
Common genetic variants identify targets for COVID-19 and individuals at 1 high risk of severe disease 2
J. Horowitz, J. Kosmicki, A. Damask, D. Sharma +57 more
20213 citations
Semantic Scholar
Polygenic scores for risk of pancreatic ductal adenocarcinoma: evaluation of novel and published models
S. Antwi, B. Coombes, Erin E. Carlson, Nicholas B. Larson +247 more
2026npj Precision Oncology1 citations Open access
Semantic Scholar
Metabolomics Ex/GWAS in the Amish reveals novel insights into cardiometabolic disease pathways
M. Jallow, G. Tzoneva, Bin Ye, J. Backman +16 more
2025bioRxiv1 citations Open access
Semantic Scholar
Tissue factor (F3) gene variants and thrombotic risk among middle-aged and older adults: a population-based cohort study
Eric Manderstedt, C. Lind-Halldén, C. Halldén, Johan Elf +181 more
2024Thrombosis Update1 citations Open access
Semantic Scholar
Author Correction: Genotyping, sequencing and analysis of 140,000 adults from Mexico City
A. Ziyatdinov, J. Torres, J. Alegre-Díaz, J. Backman +43 more
2024Nature1 citations Open access
Semantic Scholar
Familial aggregation of t obacco Use Behaviors in a mish Men
Katie L. Nugent, J. Backman, P. Kochunov, L. Hong
20141 citations
Semantic Scholar
Rare protein-coding variation and the genetic architecture of height in >1.4 million individuals
J. Kosmicki, L. Ganel, Kyoko Watanabe, Tyler A. Joseph +26 more
2026medRxiv0 citations Open access
Semantic Scholar
Author Correction: A deep catalogue of protein-coding variation in 983,578 individuals
Kathie Y. Sun, Xiao-Dong Bai, Si-Ying Chen, Su-Ying Bao +44 more
2025Nature0 citations Open access
Semantic Scholar
Genome-wide analysis in 756,646 individuals provides first genetic evidence 1 that ACE2 expression influences COVID-19 risk and yields genetic risk scores 2 predictive of severe disease 3
J. E. Horowitz, J. Kosmicki, A. Damask, D. Sharma +57 more
20210 citations
Semantic Scholar

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