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Author Details

Eric Banks
Broad Institute of MIT and Harvard
1999
44
27
PMIDPaper TitleJournal TitlePublished Year
37291427High-throughput RNA isoform sequencing using programmed cDNA concatenation.Nat Biotechnol2024
38057664A genomic mutational constraint map using variation in 76,156 human genomes.Nature2024
37291427High-throughput RNA isoform sequencing using programmed cDNA concatenation.Nat Biotechnol2024
38057664A genomic mutational constraint map using variation in 76,156 human genomes.Nature2024
37604963GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data.Nat Genet2023
37604963GATK-gCNV enables the discovery of rare copy number variants from exome sequencing data.Nat Genet2023
37561600The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research.Annu Rev Biomed Data Sci2023
37550580Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender.Nat Methods2023
37561600The <i>All of Us</i> Data and Research Center: Creating a Secure, Scalable, and Sustainable Ecosystem for Biomedical Research.Annu Rev Biomed Data Sci2023
37550580Unsupervised removal of systematic background noise from droplet-based single-cell experiments using CellBender.Nat Methods2023
35074858Mitochondrial DNA variation across 56,434 individuals in gnomAD.Genome Res2022
35982160Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.Nat Genet2022
35074858Mitochondrial DNA variation across 56,434 individuals in gnomAD.Genome Res2022
35982160Rare coding variation provides insight into the genetic architecture and phenotypic context of autism.Nat Genet2022
34373650Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2021
33536627Author Correction: A structural variation reference for medical and population genetics.Nature2021
33536625Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2021
34373650Addendum: The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2021
33536627Author Correction: A structural variation reference for medical and population genetics.Nature2021
33536625Author Correction: The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2021
32461654The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2020
31830260Lean and deep models for more accurate filtering of SNP and INDEL variant calls.Bioinformatics2020
32461654The mutational constraint spectrum quantified from variation in 141,456 humans.Nature2020
33293579A validated lineage-derived somatic truth data set enables benchmarking in cancer genome analysis.Commun Biol2020
31830260Lean and deep models for more accurate filtering of SNP and INDEL variant calls.Bioinformatics2020
33293579A validated lineage-derived somatic truth data set enables benchmarking in cancer genome analysis.Commun Biol2020
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
30279509Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.Nat Commun2018
29360107Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2018
30279509Functional equivalence of genome sequencing analysis pipelines enables harmonized variant calling across human genetics projects.Nat Commun2018
27876817A framework for the detection of de novo mutations in family-based sequencing data.Eur J Hum Genet2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
27876817A framework for the detection of de novo mutations in family-based sequencing data.Eur J Hum Genet2017
28341696A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.Diabetes2017
29257133Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.Sci Data2017
27398621The genetic architecture of type 2 diabetes.Nature2016
27398621The genetic architecture of type 2 diabetes.Nature2016
27535533Analysis of protein-coding genetic variation in 60,706 humans.Nature2016
27535533Analysis of protein-coding genetic variation in 60,706 humans.Nature2016
25765891The distribution and mutagenesis of short coding INDELs from 1,128 whole exomes.BMC Genomics2015
25765891The distribution and mutagenesis of short coding INDELs from 1,128 whole exomes.BMC Genomics2015
25954003Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.Science2015
26381377Tools and best practices for data processing in allelic expression analysis.Genome Biol2015
26196440Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.Transl Psychiatry2015
26381377Tools and best practices for data processing in allelic expression analysis.Genome Biol2015
26196440Analysis of exome sequence in 604 trios for recessive genotypes in schizophrenia.Transl Psychiatry2015
25954003Human genomics. Effect of predicted protein-truncating genetic variants on the human transcriptome.Science2015
24463507De novo mutations in schizophrenia implicate synaptic networks.Nature2014
24463508A polygenic burden of rare disruptive mutations in schizophrenia.Nature2014
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Collaborators

Mark A DePristo
Co-authored papers 19
Mark J Daly
Massachusetts General Hospital
Co-authored papers 19
Stacey Gabriel
Broad Institute of MIT and Harvard
Co-authored papers 18
Benjamin M Neale
Massachusetts General Hospital
Co-authored papers 14
Ryan Poplin
Co-authored papers 11
David Altshuler
Broad Institute of Harvard and Massachusetts Institute of Technology (MIT)
Co-authored papers 11
Yossi Farjoun
Co-authored papers 11
Kiran Garimella
Co-authored papers 10
Laura Gauthier
Co-authored papers 10
Tim Fennell
Co-authored papers 10
Shaun Purcell
Brigham and Women's Hospital
Co-authored papers 10
Menachem Fromer
Co-authored papers 9
Khalid Shakir
Co-authored papers 9
Daniel G MacArthur
Broad Institute of MIT and Harvard
Co-authored papers 9
Jason Flannick
Co-authored papers 8
Jared Maguire
Co-authored papers 8
Konrad J Karczewski
Broad Institute of MIT and Harvard
Co-authored papers 8
Kristian Cibulskis
Co-authored papers 7
Kaitlin E Samocha
Co-authored papers 7
Manuel A Rivas
Stanford University School of Medicine
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Grace Tiao
Co-authored papers 7
Nicholas A Watts
Co-authored papers 6
Mark I McCarthy
Co-authored papers 6
Steven A McCarroll
Co-authored papers 6
Eric S Lander
Vanderbilt-Ingram Cancer Center, Vanderbilt University
Co-authored papers 6
Gon??alo R Abecasis
Regeneron Pharmaceuticals Inc.
Co-authored papers 6
Douglas M Ruderfer
Vanderbilt University Medical Center
Co-authored papers 6
Anthony A Philippakis
Broad Institute of Harvard and the Massachusetts Institute of Technology
Co-authored papers 6
Monkol Lek
Co-authored papers 6
Anne O'Donnell-Luria
Broad Institute of MIT and Harvard
Co-authored papers 6
Release 1.2