Gregory M. Cooper

Molecular Biology · 2004–2018

A researcher in the Science corpus: 20 papers; trusts 29 researchers and is trusted by 14 researchers here, as inferred from the citation graph.

Subfields

Molecular Biology — 365 citations into it; #3,081 of 17,773 by trust here, #367 by citations
Genetics — 286 citations into it; #1,523 of 6,854 by trust here, #116 by citations
Plant Science — 100 citations into it
Computational Biology & Bioinformatics — 22 citations into it; #623 of 660 by trust here, #170 by citations
Paleontology — 8 citations into it

Whom Gregory M. Cooper trusts overall

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

Who trusts Gregory M. Cooper overall

Papers from Gregory M. Cooper's perspective

Ordered by how strongly the researchers Gregory M. Cooper trusts endorse each paper. Same corpus, a different order for every researcher.

Distribution and intensity of constraint in mammalian genomic sequence. (Genome Research)
Scanning Human Gene Deserts for Long-Range Enhancers (Science)
Transcriptional regulatory elements in the human genome. (Annual review of genomics and human genetics (Print))
FAIRE (Formaldehyde-Assisted Isolation of Regulatory Elements) isolates active regulatory elements from human chromatin. (Genome Research)
Control of developmental regulators by Polycomb in human embryonic stem cells. (Cell)
Distinct and predictive chromatin signatures of transcriptional promoters and enhancers in the human genome (Nature Genetics)
Genome sequence of the Brown Norway rat yields insights into mammalian evolution (Nature)
Widespread occurrence of antisense transcription in the human genome (Nature Biotechnology)
Unbiased mapping of transcription factor binding sites along human chromosomes 21 and 22 points to widespread regulation of noncoding RNAs. (Cell)
Antisense Transcription in the Mammalian Transcriptome (Science)

Their papers

Distribution and intensity of constraint in mammalian genomic sequence. (2005) — 1,400 citations
Identification and analysis of functional elements in 1% of the human genome by the ENCODE pilot project (2007) — 5,374 citations
Genome sequence of the Brown Norway rat yields insights into mammalian evolution (2004) — 2,140 citations
A general framework for estimating the relative pathogenicity of human genetic variants (2014) — 5,961 citations
The ENCODE (ENCyclopedia Of DNA Elements) Project (2004) — 2,411 citations
Mapping and sequencing of structural variation from eight human genomes (2008) — 1,208 citations
Needles in stacks of needles: finding disease-causal variants in a wealth of genomic data (2011) — 610 citations
Identifying a High Fraction of the Human Genome to be under Selective Constraint Using GERP++ (2010) — 1,712 citations
CADD: predicting the deleteriousness of variants throughout the human genome (2018) — 3,218 citations
Massively parallel functional dissection of mammalian enhancers in vivo (2012) — 552 citations
A Copy Number Variation Morbidity Map of Developmental Delay (2011) — 1,344 citations
Single-nucleotide evolutionary constraint scores highlight disease-causing mutations (2010) — 208 citations
A recurrent 16p12.1 microdeletion suggests a two-hit model for severe developmental delay (2010) — 596 citations
Genomic diagnosis for children with intellectual disability and/or developmental delay (2016) — 268 citations
Exome sequencing in amyotrophic lateral sclerosis identifies risk genes and pathways (2015) — 948 citations
Guidelines for investigating causality of sequence variants in human disease (2014) — 1,235 citations
Exome sequencing identifies MLL2 mutations as a cause of Kabuki syndrome (2010) — 1,398 citations
Population analysis of large copy number variants and hotspots of human genetic disease. (2009) — 624 citations
Six new loci associated with blood low-density lipoprotein cholesterol, high-density lipoprotein cholesterol or triglycerides in humans (2008) — 1,459 citations
Rare Structural Variants Disrupt Multiple Genes in Neurodevelopmental Pathways in Schizophrenia (2008) — 1,770 citations