W.J. Greenleaf

Molecular Biology · 2005–2021

A researcher in the Science corpus: 17 papers; trusts 11 researchers and is trusted by 16 researchers here, as inferred from the citation graph.

Subfields

• Molecular Biology — 297 citations into it; #3,250 of 17,773 by trust here, #1,229 by citations
• Cancer Research — 52 citations into it; #1,390 of 1,780 by trust here, #409 by citations
• Artificial Intelligence — 14 citations into it

Whom W.J. Greenleaf trusts overall

Their strongest outbound trust, strongest first, inferred from their citations.

1. Jason D. Buenrostro
2. R. Vale
3. Marcel Martin

Who trusts W.J. Greenleaf overall

1. Kishan Dholakia
2. Jason D. Buenrostro
3. M. Corces
4. Tomás Cizmár

Papers from W.J. Greenleaf's perspective

Ordered by how strongly the researchers W.J. Greenleaf trusts endorse each paper. Same corpus, a different order for every researcher.

1. Hematopoiesis: an evolving paradigm for stem cell biology. (Cell)
2. Massively parallel single cell RNA-Seq for marker-free decomposition of tissues into cell types (Science)
3. Forcing cells to change lineages (Nature)
4. Transposition of native chromatin for multimodal regulatory analysis and personal epigenomics
5. Transcriptional Heterogeneity and Lineage Commitment in Myeloid Progenitors. (Cell)
6. Tissue-Resident Macrophage Enhancer Landscapes Are Shaped by the Local Microenvironment (Cell)
7. Integrative analysis of 111 reference human epigenomes (Nature)
8. Induction of pluripotent stem cells from mouse embryonic and adult fibroblast cultures by defined factors.
9. Systematic mapping of functional enhancer-promoter connections with CRISPR interference (Science)
10. Epigenetics: A Landscape Takes Shape (Cell)

Their papers

• Single-cell chromatin accessibility reveals principles of regulatory variation (2015) — 2,079 citations
• Transposition of native chromatin for multimodal regulatory analysis and personal epigenomics (2013) — 5,662 citations
• Lineage-specific and single cell chromatin accessibility charts human hematopoiesis and leukemia evolution (2016) — 1,038 citations
• ATAC-seq: A Method for Assaying Chromatin Accessibility Genome-Wide (2015) — 3,080 citations
• HiChIP: Efficient and sensitive analysis of protein-directed genome architecture (2016) — 971 citations
• chromVAR: Inferring transcription factor-associated accessibility from single-cell epigenomic data (2017) — 1,401 citations
• An improved ATAC-seq protocol reduces background and enables interrogation of frozen tissues (2017) — 2,152 citations
• ArchR is a scalable software package for integrative single-cell chromatin accessibility analysis (2021) — 1,123 citations
• The chromatin accessibility landscape of primary human cancers (2018) — 1,069 citations
• Direct observation of base-pair stepping by RNA polymerase (2005) — 858 citations
• Chromatin accessibility and the regulatory epigenome (2019) — 1,455 citations
• Massively parallel single-cell chromatin landscapes of human immune cell development and intratumoral T cell exhaustion (2019) — 858 citations
• The human body at cellular resolution: the NIH Human Biomolecular Atlas Program (2019) — 537 citations
• Variable chromatin structure revealed by in situ spatially correlated DNA cleavage mapping (2016) — 154 citations
• Integrated single-cell analysis maps the continuous regulatory landscape of human hematopoietic differentiation (2018) — 609 citations
• The Human Tumor Atlas Network: Charting Tumor Transitions across Space and Time at Single-Cell Resolution (2020) — 482 citations
• Blind tests of RNA–protein binding affinity prediction (2019) — 26 citations