Elliott Rees

Biochemistry, Genetics and Molecular BiologyMedicine

Pilot corpus only

This score is computed over theSindex pilot corpus and does not cover the full scientific literature. Scores are relative to papers we have ingested — papers, authors, and institutions outside the pilot are not represented. Methodology.

Top 100%percentile

0Author DataRank

Indexed papers

0in pilot corpus

datarank_citation_only_1hop_v6· scope data_onlyMethodology

Papers

Driven by 9 papers. Top paper: “Rare coding variants in ten genes confer substantial risk for schizophrenia”.

Rare coding variants in ten genes confer substantial risk for schizophrenia

Nature(2022)10.1038/s41586-022-04556-w

N/A

7.2DataRank · unranked

900 citations

Timothy Poterba, David Curtis, Huda Akil, Mariam Al Eissa, Jack D. Barchas +95 more

Evidence that duplications of 22q11.2 protect against schizophrenia

Molecular Psychiatry(2013)10.1038/mp.2013.156

N/A

5.8DataRank · unranked

188 citations

James T.R. Walters, J T R Walters, K D Chambert, Dragan M. Švrakić, J Szatkiewicz +53 more

De novo CNV analysis implicates specific abnormalities of postsynaptic signalling complexes in the pathogenesis of schizophrenia

Molecular Psychiatry(2011)10.1038/mp.2011.154

N/A

1.0DataRank · unranked

874 citations

A J Pocklington, D Ivanov, Samuel A. Rose, Andrew McQuillin, Hywel Williams +46 more

The contribution of rare variants to risk of schizophrenia in individuals with and without intellectual disability

Nature Genetics(2017)10.1038/ng.3903

N/A

0.826DataRank · unranked

246 citations

David M. Hougaard, Mandy Johnstone, Nicholas Bass, Jaana Suvisaari, Minna Torniainen +21 more

Novel Findings from CNVs Implicate Inhibitory and Excitatory Signaling Complexes in Schizophrenia

Neuron(2015)10.1016/j.neuron.2015.04.022

N/A

0.799DataRank · unranked

205 citations

Elliott Rees, James T.R. Walters, Jun Han, David H. Kavanagh, Kimberly D. Chambert +9 more

DLG2 knockout reveals neurogenic transcriptional programs underlying neuropsychiatric disorders and cognition

bioRxiv (Cold Spring Harbor Laboratory)(2020)10.1101/2020.01.10.898676

N/A

0.165DataRank · unranked

2 citations

Daniel D’Andrea, Mark O. Collins, Elliott Rees, Tom G. J. Steward, Ying Zhu +13 more

FAN1 nuclease activity affects CAG expansion and age at onset of Huntington’s disease

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.04.13.439716

N/A

0DataRank · unranked

3 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more

Exome sequencing of individuals with Huntington’s disease implicates FAN1 nuclease activity in slowing CAG expansion and disease onset

Nature Neuroscience(2022)10.1038/s41593-022-01033-5

N/A

0DataRank · unranked

92 citations

Jasmine Donaldson, Caroline S. Binda, Sophie Powell, Uroosa Chughtai, Gareth Edwards +29 more

Rare loss-of-function variants in SETD1A are associated with schizophrenia and developmental disorders

UNC Libraries(2024)10.17615/4nb8-at41

N/A

0DataRank · unranked

0 citations

David Curtis, Jennifer Sambrook, Robin Murray, David St Clair, Trevor Cole +54 more