Simon Lovell

Simon Lovell

Manchester University

H-index: 40

North America-United States

About Simon Lovell

Simon Lovell, With an exceptional h-index of 40 and a recent h-index of 23 (since 2020), a distinguished researcher at Manchester University,

His recent articles reflect a diverse array of research interests and contributions to the field:

Essentiality, protein–protein interactions and evolutionary properties are key predictors for identifying cancer-associated genes using machine learning

Clinical, genetic, epidemiologic and functional delineation of TSPEAR-related Autosomal Recessive Ectodermal Dysplasia 14

Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

Assessing the pathogenicity of in-frame CACNA1F indel variants using structural modeling

Shared Runs of Heterozygosity Mapping using whole genome sequencing reveals a complex structural variant in GSN causing novel cutaneous-visceral organ …

Improving the clinical interpretation of missense variants in X linked genes using structural analysis

Recurrent KCNT2 missense variants affecting p.Arg190 result in a recognizable phenotype

Essentiality, Protein-Protein Interactions and Evolutionary Properties are Key Predictors for Identifying Cancer Genes Using Machine Learning

Simon Lovell Information

University

Position

Professor of Molecular Biology

Citations(all)

17357

Citations(since 2020)

7117

Cited By

13315

hIndex(all)

40

hIndex(since 2020)

23

i10Index(all)

72

i10Index(since 2020)

44

Email

University Profile Page

Manchester University

Google Scholar

View Google Scholar Profile

Top articles of Simon Lovell

Title

Journal

Author(s)

Publication Date

Essentiality, protein–protein interactions and evolutionary properties are key predictors for identifying cancer-associated genes using machine learning

Scientific Reports

Amro Safadi

Simon C Lovell

Andrew J Doig

2024/4/22

Clinical, genetic, epidemiologic and functional delineation of TSPEAR-related Autosomal Recessive Ectodermal Dysplasia 14

European Journal of Human Genetics

EA Jones

Z Haider

H Stewart

D Donnelly

S Lovell

...

2023/5/11

Clinical, genetic, epidemiologic, evolutionary, and functional delineation of TSPEAR-related autosomal recessive ectodermal dysplasia 14

Human Genetics and Genomics Advances

Adam Jackson

Sheng-Jia Lin

Elizabeth A Jones

Kate E Chandler

David Orr

...

2023/4/13

Assessing the pathogenicity of in-frame CACNA1F indel variants using structural modeling

The Journal of Molecular Diagnostics

Shalaw R Sallah

Panagiotis I Sergouniotis

Claire Hardcastle

Simon Ramsden

Andrew J Lotery

...

2022/12/1

Shared Runs of Heterozygosity Mapping using whole genome sequencing reveals a complex structural variant in GSN causing novel cutaneous-visceral organ …

European Journal of Human Genetics

Genomics England Res Consortium

2022/4

Improving the clinical interpretation of missense variants in X linked genes using structural analysis

Journal of Medical Genetics

Shalaw Rassul Sallah

Jamie M Ellingford

Panagiotis I Sergouniotis

Simon C Ramsden

Nicholas Lench

...

2022/4/1

Recurrent KCNT2 missense variants affecting p.Arg190 result in a recognizable phenotype

American Journal of Medical Genetics Part A

Adam Jackson

Siddharth Banka

Helen Stewart

Genomics England Research Consortium

Hannah Robinson

...

2021/10

Essentiality, Protein-Protein Interactions and Evolutionary Properties are Key Predictors for Identifying Cancer Genes Using Machine Learning

Scientific Reports

Amro Safadi

Simon C Lovell

Andrew J Doig

2024/4/22

EVI1 phosphorylation at S436 regulates interactions with CtBP1 and DNMT3A and promotes self-renewal

Cell death & disease

Roberto Paredes

James R Kelly

Bethany Geary

Batool Almarzouq

Marion Schneider

...

2020/10/20

Using an integrative machine learning approach utilising homology modelling to clinically interpret genetic variants: CACNA1F as an exemplar

European Journal of Human Genetics

Shalaw R Sallah

Panagiotis I Sergouniotis

Stephanie Barton

Simon Ramsden

Rachel L Taylor

...

2020/9

Variability in gene expression is associated with incomplete penetrance in inherited eye disorders

Genes

David J Green

Shalaw R Sallah

Jamie M Ellingford

Simon C Lovell

Panagiotis I Sergouniotis

2020/2/9

See List of Professors in Simon Lovell University(Manchester University)