Dianne F. Newbury

Also affiliated with Centre for Human Genetics, University of Oxford, Oxford BioMedica (United Kingdom)

Biochemistry, Genetics and Molecular BiologyPsychology

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 5 papers. Top paper: “A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures”.

A rare missense variant in the ATP2C2 gene is associated with language impairment and related measures

Human Molecular Genetics(2021)10.1093/hmg/ddab111

N/A

0DataRank · unranked

16 citations

Mabel L. Rice, Joel B. Talcott, Rebeca Diaz, Shelley D. Smith, Muhammad Hashim Raza +10 more

Genome-wide association analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.11.04.466897

N/A

0DataRank · unranked

14 citations

Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini +85 more

Analysis of expression Quantitative Trait Loci for NLGN4X in relation to language and neurodevelopmental function: an exploratory analysis using FUSION and GTEx workflows

bioRxiv (Cold Spring Harbor Laboratory)(2021)10.1101/2021.06.29.450314

N/A

0DataRank · unranked

0 citations

Dorothy Bishop, Dianne F. Newbury, Nuala H. Simpson

Genome-wide analyses of individual differences in quantitatively assessed reading- and language-related skills in up to 34,000 people

Proceedings of the National Academy of Sciences(2022)10.1073/pnas.2202764119

N/A

0DataRank · unranked

134 citations

Nazanin Mirza‐Schreiber, Eveline L. de Zeeuw, Carol A. Wang, Dongnhu T. Truong, Andrea G. Allegrini +90 more

Hypothesis-driven genome-wide association studies provide novel insights into genetics of reading disabilities

Translational Psychiatry(2022)10.1038/s41398-022-02250-z

N/A

0DataRank · unranked

14 citations

Karen Wigg, Else Eising, Yu Feng, Kirsten Blokland, Margaret Wilkinson +85 more