N. Banerjee

发表

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

Spiros C. Denaxas, Alexander E. Lopez, Andrew L Blumenfeld, 2020, Nature Communications.

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. Marchini, S. McCarthy, M. Cantor, 2020, medRxiv.

Metabolome and exposome profiling of the biospecimens from COVID-19 patients in India

Sanjeev Srivastava, S. Kumar, N. Banerjee, 2021, Journal of microbiology, epidemiology and immunobiology.

ANGPTL7, a therapeutic target for increased intraocular pressure and glaucoma

Alexander E. Lopez, Tanya M. Teslovich, Gaurang C. Patel, 2022, Communications Biology.

Exome sequencing and analysis of 454,787 UK Biobank participants

J. Marchini, G. Abecasis, H. Kang, 2021, Nature.

Exome sequencing and characterization of 49,960 individuals in the UK Biobank

Alexander E. Lopez, Alexander Hanbo Li, Andrew L Blumenfeld, 2020, Nature.

Common and rare variant associations with clonal haematopoiesis phenotypes

J. Marchini, G. Abecasis, H. Kang, 2022, Nature.

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

Spiros C. Denaxas, Alexander E. Lopez, Andrew L Blumenfeld, 2020, Nature Communications.

Whole exome sequencing and characterization of coding variation in 49,960 individuals in the UK Biobank

Gonçalo Abecasis, Alan R. Shuldiner, Jeffrey Staples, 2019, bioRxiv.

Genome-wide analysis provides genetic evidence that ACE2 influences COVID-19 risk and yields risk scores associated with severe disease

Alexander E. Lopez, Eurie L. Hong, G. D. Gatta, 2022, Nature Genetics.

Exome sequencing and characterization of 49,960 individuals in the UK Biobank

Alexander E. Lopez, Andrew L Blumenfeld, J. Marchini, 2020, Nature.

Pan-ancestry exome-wide association analyses of COVID-19 outcomes in 586,157 individuals

J. Marchini, G. Abecasis, H. Kang, 2021, The American Journal of Human Genetics.

A catalog of associations between rare coding variants and COVID-19 outcomes

Alexander Hanbo Li, J. Marchini, J. Szustakowski, 2020, medRxiv : the preprint server for health sciences.

A catalog of associations between rare coding variants and COVID-19 outcomes

Alexander Hanbo Li, J. Marchini, G. Abecasis, 2020, medRxiv.

Exome sequencing of 628,388 individuals identifies common and rare variant associations with clonal hematopoiesis phenotypes

J. Marchini, G. Atwal, Y. Houvras, 2022, medRxiv.

Advancing Human Genetics Research and Drug Discovery through Exome Sequencing of the UK Biobank

Alexander E. Lopez, Jason A. Grundstad, Sri V. V. Deevi, 2020, medRxiv.

High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease

Alexander E. Lopez, Manuel A. Rivas, Manuel A Rivas, 2022, Nature Genetics.

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

Alexander Hanbo Li, J. Marchini, S. Balasubramanian, 2020, medRxiv.

Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure

Spiros C. Denaxas, Alexander E. Lopez, Andrew L Blumenfeld, 2020, Nature Communications.

Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis

G. Abecasis, C. Greenwood, J. Richards, 2023, Nature Genetics.

Gamma-Aminobutyric Acid Type A Receptor Variants are Associated with Autism Spectrum Disorders

S. Sinha, N. Banerjee, A. Bandyopadhyay, 2023, Journal of Molecular Neuroscience.

A catalog of associations between rare coding variants and COVID-19 outcomes

Alexander Hanbo Li, J. Marchini, J. Szustakowski, 2020, medRxiv : the preprint server for health sciences.

Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank

Sri V. V. Deevi, J. Szustakowski, S. Balasubramanian, 2021, Nature Genetics.

Pharmacologic and Genetic Downregulation of Proprotein Convertase Subtilisin/Kexin Type 9 and Survival From Sepsis

L. Milani, B. Nordestgaard, K. Hveem, 2023, Critical care explorations.

Reviewers ' comments : Reviewer # 1 ( Remarks

Alexander E. Lopez, Andrew L Blumenfeld, J. Cook, 2019 .

NOTCH3 p.Arg1231Cys is Markedly Enriched in South Asians and Associated with Stroke

J. Danesh, D. Saleheen, F. Sepehrband, 2023, medRxiv.

Genotyping, sequencing and analysis of 140,000 adults from Mexico City

R. Collins, S. Balasubramanian, A. Hawes, 2023, Nature.