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89 PR articles • 141,232 PR citations • Sorted by year • Download PDF (PDF by citations)
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1Extremely sparse models of linkage disequilibrium in ancestrally diverse association studies
Nature Genetics, 2023, 55, 1494-1502
26.131Citations (PDF)
2Mapping transcriptomic vector fields of single cells
Cell, 2022, 185, 690-711.e45
34.1406Citations (PDF)
3Compatibility rules of human enhancer and promoter sequences
Nature, 2022, 607, 176-184
38.7140Citations (PDF)
4Gene Sequencing Identifies Perturbation in Nitric Oxide Signaling as a Nonlipid Molecular Subtype of Coronary Artery Disease
Circulation Genomic and Precision Medicine, 2022, 15,
3.39Citations (PDF)
5A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density
Cell Metabolism, 2021, 33, 615-628.e13
26.242Citations (PDF)
6Genome-wide enhancer maps link risk variants to disease genes
Nature, 2021, 593, 238-243
38.7600Citations (PDF)
7Inherited causes of clonal haematopoiesis in 97,691 whole genomes
Nature, 2020, 586, 763-768
38.7655Citations (PDF)
8Towards a treatment for genetic prion disease: trials and biomarkers
Lancet Neurology, The, 2020, 19, 361-368
18.482Citations (PDF)
9Prioritizing disease and trait causal variants at the TNFAIP3 locus using functional and genomic features
Nature Communications, 2020, 11,
13.952Citations (PDF)
10The SARS-CoV-2 RNA–protein interactome in infected human cells
Nature Microbiology, 2020, 6, 339-353
16.5312Citations (PDF)
11Identification of cancer driver genes based on nucleotide context
Nature Genetics, 2020, 52, 208-218
26.1226Citations (PDF)
12HyPR-seq: Single-cell quantification of chosen RNAs via hybridization and sequencing of DNA probes
Proceedings of the National Academy of Sciences of the United States of America, 2020, 117, 33404-33413
7.636Citations (PDF)
13Small Molecule Targets TMED9 and Promotes Lysosomal Degradation to Reverse Proteinopathy
Cell, 2019, 178, 521-535.e23
34.1185Citations (PDF)
14Rare Genetic Variants Associated With Sudden Cardiac Death in Adults
Journal of the American College of Cardiology, 2019, 74, 2623-2634
2.439Citations (PDF)
15Optimal-Transport Analysis of Single-Cell Gene Expression Identifies Developmental Trajectories in Reprogramming
Cell, 2019, 176, 928-943.e22
34.1684Citations (PDF)
16Polygenic Prediction of Weight and Obesity Trajectories from Birth to Adulthood
Cell, 2019, 177, 587-596.e9
34.1733Citations (PDF)
17Ribosome Levels Selectively Regulate Translation and Lineage Commitment in Human Hematopoiesis
Cell, 2018, 173, 90-103.e19
34.1371Citations (PDF)
18Strain-Level Analysis of Mother-to-Child Bacterial Transmission during the First Few Months of Life
Cell Host and Microbe, 2018, 24, 146-154.e4
15.3421Citations (PDF)
19Positional specificity of different transcription factor classes within enhancers
Proceedings of the National Academy of Sciences of the United States of America, 2018, 115,
7.687Citations (PDF)
20Deep-coverage whole genome sequences and blood lipids among 16,324 individuals
Nature Communications, 2018, 9,
13.9163Citations (PDF)
21Systematic dissection of genomic features determining transcription factor binding and enhancer function
Proceedings of the National Academy of Sciences of the United States of America, 2017, 114,
7.6172Citations (PDF)
22Gene Essentiality Profiling Reveals Gene Networks and Synthetic Lethal Interactions with Oncogenic Ras
Cell, 2017, 168, 890-903.e15
34.1617Citations (PDF)
23Response to the ANZFSS council statement on the President’s Council Of Advisors On Science And Technology Report
Australian Journal of Forensic Sciences, 2017, 49, 366-368
1.513Citations (PDF)
24Comprehensive population-based genome sequencing provides insight into hematopoietic regulatory mechanisms
Proceedings of the National Academy of Sciences of the United States of America, 2017, 114,
7.645Citations (PDF)
25Cohesin Loss Eliminates All Loop Domains
Cell, 2017, 171, 305-320.e24
34.11,904Citations (PDF)
26Efficient Generation of Transcriptomic Profiles by Random Composite Measurements
Cell, 2017, 171, 1424-1436.e18
34.1114Citations (PDF)
27Type 2 Diabetes Variants Disrupt Function of SLC16A11 through Two Distinct Mechanisms
Cell, 2017, 170, 199-212.e20
34.1151Citations (PDF)
28Perturb-Seq: Dissecting Molecular Circuits with Scalable Single-Cell RNA Profiling of Pooled Genetic Screens
Cell, 2016, 167, 1853-1866.e17
34.11,682Citations (PDF)
29Genomic Correlates of Immune-Cell Infiltrates in Colorectal Carcinoma
Cell Reports, 2016, 15, 857-865
6.4786Citations (PDF)
30Juicebox Provides a Visualization System for Hi-C Contact Maps with Unlimited Zoom
Cell Systems, 2016, 3, 99-101
5.82,128Citations (PDF)
31Juicer Provides a One-Click System for Analyzing Loop-Resolution Hi-C Experiments
Cell Systems, 2016, 3, 95-98
5.83,533Citations (PDF)
32Deletion of <i>DXZ4</i> on the human inactive X chromosome alters higher-order genome architecture
Proceedings of the National Academy of Sciences of the United States of America, 2016, 113,
7.6269Citations (PDF)
33Natural history of the infant gut microbiome and impact of antibiotic treatment on bacterial strain diversity and stability
Science Translational Medicine, 2016, 8,
12.7961Citations (PDF)
34Direct Identification of Hundreds of Expression-Modulating Variants using a Multiplexed Reporter Assay
Cell, 2016, 165, 1519-1529
34.1479Citations (PDF)
35C2c2 is a single-component programmable RNA-guided RNA-targeting CRISPR effector
Science, 2016, 353,
36.42,154Citations (PDF)
36Single Guide RNA Library Design and Construction
Cold Spring Harbor Protocols, 2016, 2016, pdb.prot090803
0.338Citations (PDF)
37Viral Packaging and Cell Culture for CRISPR-Based Screens
Cold Spring Harbor Protocols, 2016, 2016, pdb.prot090811
0.334Citations (PDF)
38Large-Scale Single Guide RNA Library Construction and Use for CRISPR–Cas9-Based Genetic Screens
Cold Spring Harbor Protocols, 2016, 2016, pdb.top086892
0.325Citations (PDF)
39Integrative Analyses of Human Reprogramming Reveal Dynamic Nature of Induced Pluripotency
Cell, 2015, 162, 412-424
34.1234Citations (PDF)
40A global reference for human genetic variation
Nature, 2015, 526, 68-74
38.717,885Citations (PDF)
41Chromatin extrusion explains key features of loop and domain formation in wild-type and engineered genomes
Proceedings of the National Academy of Sciences of the United States of America, 2015, 112,
7.61,762Citations (PDF)
42Measuring missing heritability: Inferring the contribution of common variants
Proceedings of the National Academy of Sciences of the United States of America, 2014, 111,
7.6305Citations (PDF)
43Complementary genomic approaches highlight the PI3K/mTOR pathway as a common vulnerability in osteosarcoma
Proceedings of the National Academy of Sciences of the United States of America, 2014, 111,
7.6418Citations (PDF)
44A 3D Map of the Human Genome at Kilobase Resolution Reveals Principles of Chromatin Looping
Cell, 2014, 159, 1665-1680
34.18,887Citations (PDF)
45Searching for missing heritability: Designing rare variant association studies
Proceedings of the National Academy of Sciences of the United States of America, 2014, 111,
7.6622Citations (PDF)
46Discovery and saturation analysis of cancer genes across 21 tumour types
Nature, 2014, 505, 495-501
38.72,956Citations (PDF)
47RNF43 is frequently mutated in colorectal and endometrial cancers
Nature Genetics, 2014, 46, 1264-1266
26.1452Citations (PDF)
48Perturbation of m6A Writers Reveals Two Distinct Classes of mRNA Methylation at Internal and 5′ Sites
Cell Reports, 2014, 8, 284-296
6.41,162Citations (PDF)
49RNA-RNA Interactions Enable Specific Targeting of Noncoding RNAs to Nascent Pre-mRNAs and Chromatin Sites
Cell, 2014, 159, 188-199
34.1482Citations (PDF)
50Transcriptome-wide Mapping Reveals Widespread Dynamic-Regulated Pseudouridylation of ncRNA and mRNA
Cell, 2014, 159, 148-162
34.1947Citations (PDF)
51Development and Applications of CRISPR-Cas9 for Genome Engineering
Cell, 2014, 157, 1262-1278
34.15,308Citations (PDF)
52High-Resolution Mapping Reveals a Conserved, Widespread, Dynamic mRNA Methylation Program in Yeast Meiosis
Cell, 2013, 155, 1409-1421
34.1621Citations (PDF)
53Discovery and characterization of artifactual mutations in deep coverage targeted capture sequencing data due to oxidative DNA damage during sample preparation
Nucleic Acids Research, 2013, 41, e67-e67
15.7474Citations (PDF)
54Lessons from the Cancer Genome
Cell, 2013, 153, 17-37
34.11,257Citations (PDF)
55The Xist lncRNA Exploits Three-Dimensional Genome Architecture to Spread Across the X Chromosome
Science, 2013, 341,
36.4946Citations (PDF)
56The mystery of missing heritability: Genetic interactions create phantom heritability
Proceedings of the National Academy of Sciences of the United States of America, 2012, 109, 1193-1198
7.61,421Citations (PDF)
57Cyclin D3 coordinates the cell cycle during differentiation to regulate erythrocyte size and number
Genes and Development, 2012, 26, 2075-2087
4.7115Citations (PDF)
58Systematic dissection and optimization of inducible enhancers in human cells using a massively parallel reporter assay
Nature Biotechnology, 2012, 30, 271-277
32.2716Citations (PDF)
59lincRNAs act in the circuitry controlling pluripotency and differentiation
Nature, 2011, 477, 295-300
38.71,811Citations (PDF)
60Initial impact of the sequencing of the human genome
Nature, 2011, 470, 187-197
38.7961Citations (PDF)
61Initial genome sequencing and analysis of multiple myeloma
Nature, 2011, 471, 467-472
38.71,350Citations (PDF)
62High-quality draft assemblies of mammalian genomes from massively parallel sequence data
Proceedings of the National Academy of Sciences of the United States of America, 2011, 108, 1513-1518
7.61,527Citations (PDF)
63Systematic investigation of genetic vulnerabilities across cancer cell lines reveals lineage-specific dependencies in ovarian cancer
Proceedings of the National Academy of Sciences of the United States of America, 2011, 108, 12372-12377
7.6407Citations (PDF)
64A Draft Sequence of the Neandertal Genome
Science, 2010, 328, 710-722
36.44,055Citations (PDF)
65The landscape of somatic copy-number alteration across human cancers
Nature, 2010, 463, 899-905
38.73,772Citations (PDF)
66Ab initio reconstruction of cell type–specific transcriptomes in mouse reveals the conserved multi-exonic structure of lincRNAs
Nature Biotechnology, 2010, 28, 503-510
32.21,277Citations (PDF)
67Comparative Epigenomic Analysis of Murine and Human Adipogenesis
Cell, 2010, 143, 156-169
34.1500Citations (PDF)
68Comprehensive Mapping of Long-Range Interactions Reveals Folding Principles of the Human Genome
Science, 2009, 326, 289-293
36.48,581Citations (PDF)
69Identification of Selective Inhibitors of Cancer Stem Cells by High-Throughput Screening
Cell, 2009, 138, 645-659
34.12,314Citations (PDF)
70Dissecting direct reprogramming through integrative genomic analysis
Nature, 2008, 454, 49-55
38.71,384Citations (PDF)
71Genetic Mapping in Human Disease
Science, 2008, 322, 881-888
36.41,334Citations (PDF)
72Highly parallel identification of essential genes in cancer cells
Proceedings of the National Academy of Sciences of the United States of America, 2008, 105, 20380-20385
7.6518Citations (PDF)
73Systematic discovery of regulatory motifs in conserved regions of the human genome, including thousands of CTCF insulator sites
Proceedings of the National Academy of Sciences of the United States of America, 2007, 104, 7145-7150
7.6284Citations (PDF)
74Distinguishing protein-coding and noncoding genes in the human genome
Proceedings of the National Academy of Sciences of the United States of America, 2007, 104, 19428-19433
7.6539Citations (PDF)
75Integrative Genomic Approaches Identify IKBKE as a Breast Cancer Oncogene
Cell, 2007, 129, 1065-1079
34.1568Citations (PDF)
76Genome of the marsupial Monodelphis domestica reveals innovation in non-coding sequences
Nature, 2007, 447, 167-177
38.7689Citations (PDF)
77Genome-wide maps of chromatin state in pluripotent and lineage-committed cells
Nature, 2007, 448, 553-560
38.73,913Citations (PDF)
78A Bivalent Chromatin Structure Marks Key Developmental Genes in Embryonic Stem Cells
Cell, 2006, 125, 315-326
34.15,107Citations (PDF)
79Gene set enrichment analysis: A knowledge-based approach for interpreting genome-wide expression profiles
Proceedings of the National Academy of Sciences of the United States of America, 2005, 102, 15545-15550
7.649,638Citations (PDF)
80Genome sequence, comparative analysis and haplotype structure of the domestic dog
Nature, 2005, 438, 803-819
38.72,353Citations (PDF)
81Assembly of polymorphic genomes: Algorithms and application to Ciona savignyi
Genome Research, 2005, 15, 1127-1135
4.6174Citations (PDF)
82Genomic Maps and Comparative Analysis of Histone Modifications in Human and Mouse
Cell, 2005, 120, 169-181
34.11,401Citations (PDF)
83Whole-Genome Sequence Assembly for Mammalian Genomes: Arachne 2
Genome Research, 2003, 13, 91-96
4.6268Citations (PDF)
84Initial sequencing and comparative analysis of the mouse genome
Nature, 2002, 420, 520-562
38.76,666Citations (PDF)
85Initial sequencing and analysis of the human genome
Nature, 2001, 409, 860-921
38.722,433Citations (PDF)
86Recognition of related proteins by iterative template refinement (ITR)
Protein Science, 1994, 3, 1315-1328
6.049Citations (PDF)
87Direct isolation of polymorphic markers linked to a trait by genetically directed representational difference analysis
Nature Genetics, 1994, 6, 57-63
26.1119Citations (PDF)
88The diastrophic dysplasia gene encodes a novel sulfate transporter: Positional cloning by fine-structure linkage disequilibrium mapping
Cell, 1994, 78, 1073-1087
34.1760Citations (PDF)
89The Human Cell Atlas
ELife, 0, 6,
1.62,143Citations (PDF)