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D-Index & Metrics

Genetics

D-Index
105
Citations
59516
World Ranking
618
National Ranking
93

Medicine

D-Index
107
Citations
60837
World Ranking
6122
National Ranking
595

Overview

Jonathan Mill is affiliated with the University of Exeter in the United Kingdom. Their research spans multiple fields with a strong focus on Biochemistry, Genetics and Molecular Biology as well as Medicine. Within these domains, their work often intersects with key subfields such as Molecular Biology, Genetics, Neurology, Psychiatry and Mental Health, and Physiology.

The primary research topics covered by Jonathan Mill include:

  • Epigenetics and DNA Methylation
  • Amyotrophic Lateral Sclerosis Research
  • Dementia and Cognitive Impairment Research
  • Genetic Syndromes and Imprinting
  • Genetics and Neurodevelopmental Disorders
  • Genetic Associations and Epidemiology
  • Alzheimer's Disease Research and Treatments

Jonathan Mill has authored or co-authored numerous papers. Notable recent publications include:

  • Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS, 2022, New England Journal of Medicine
  • Phase 1-2 Trial of Antisense Oligonucleotide Tofersen for SOD1 ALS, 2020, New England Journal of Medicine
  • Non-neuronal expression of SARS-CoV-2 entry genes in the olfactory system suggests mechanisms underlying COVID-19-associated anosmia, 2020, Science Advances

Frequent co-authors in their research network include:

  • Eilís Hannon
  • Emma Dempster
  • Joe Burrage
  • Katie Lunnon
  • Gemma Shireby

The scientist's work is often published in venues that include:

  • bioRxiv (Cold Spring Harbor Laboratory)
  • Alzheimer's & Dementia
  • European Neuropsychopharmacology
  • Nature Communications
  • Molecular Psychiatry

Best Publications

  • Influence of Life Stress on Depression: Moderation by a Polymorphism in the 5-HTT Gene

    Avshalom Caspi;Karen Sugden;Terrie E. Moffitt;Alan Taylor

  • Role of Genotype in the Cycle of Violence in Maltreated Children

    Avshalom Caspi;Avshalom Caspi;Joseph McClay;Terrie E. Moffitt;Terrie E. Moffitt;Jonathan Mill

  • Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression

    Naomi R. Wray;Stephan Ripke;Stephan Ripke;Stephan Ripke;Manuel Mattheisen;MacIej Trzaskowski

  • Transcriptomic analysis of autistic brain reveals convergent molecular pathology

    Irina Voineagu;Xinchen Wang;Patrick G Johnston;Jennifer K Lowe

  • Common schizophrenia alleles are enriched in mutation-intolerant genes and in regions under strong background selection

    Antonio F. Pardiñas;Peter Holmans;Andrew J. Pocklington;Valentina Escott-Price

  • Non-neuronal expression of SARS-CoV-2 entry genes in the olfactory system suggests mechanisms underlying COVID-19-associated anosmia.

    David H. Brann;Tatsuya Tsukahara;Caleb Weinreb;Marcela Lipovsek

  • A data-driven approach to preprocessing Illumina 450K methylation array data

    Ruth Pidsley;Chloe C Y Wong;Manuela Volta;Katie Lunnon

  • Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci.

    Philip Lawrence De Jager;Gyan Srivastava;Katie Lunnon;Jeremy Burgess

  • Epigenomic Profiling Reveals DNA-Methylation Changes Associated with Major Psychosis

    Jonathan Mill;Thomas Tang;Zachary Kaminsky;Tarang Khare

  • Epigenome-Wide Scans Identify Differentially Methylated Regions for Age and Age-Related Phenotypes in a Healthy Ageing Population

    Jordana T. Bell;Pei-Chien Tsai;Tsun-Po Yang;Ruth Pidsley

  • Genome-wide Analyses Identify KIF5A as a Novel ALS Gene.

    Aude Nicolas;Kevin P. Kenna;Alan E. Renton;Alan E. Renton;Nicola Ticozzi

  • Functional annotation of the human brain methylome identifies tissue-specific epigenetic variation across brain and blood

    Matthew N Davies;Manuela Volta;Ruth Pidsley;Katie Lunnon

  • Methylomic profiling implicates cortical deregulation of ANK1 in Alzheimer's disease

    Katie Lunnon;Rebecca Smith;Eilis Hannon;Philip L De Jager

  • Exposure to violence during childhood is associated with telomere erosion from 5 to 10 years of age: a longitudinal study

    I. Shalev;Terrie Moffitt;Karen Sugden;Benjamin Williams

  • Disease-associated epigenetic changes in monozygotic twins discordant for schizophrenia and bipolar disorder

    Emma L. Dempster;Ruth Pidsley;Leonard C. Schalkwyk;Sheena Owens

  • Interindividual methylomic variation across blood, cortex, and cerebellum: implications for epigenetic studies of neurological and neuropsychiatric phenotypes.

    Eilis Hannon;Katie Lunnon;Leonard C Schalkwyk;Jonathan Mill

  • Expression of the dopamine transporter gene is regulated by the 3' UTR VNTR: Evidence from brain and lymphocytes using quantitative RT-PCR.

    Jonathan Mill;Philip Asherson;Clare Browes;Ursula D'Souza

  • A longitudinal study of epigenetic variation in twins

    Chloe Chung Yi Wong;Avshalom Caspi;Benjamin Williams;Ian W. Craig

  • A common haplotype of the dopamine transporter gene associated with attention-deficit/hyperactivity disorder and interacting with maternal use of alcohol during pregnancy.

    Keeley-Joanne Brookes;Jon Mill;Camilla Guindalini;Sarah Curran

  • Alzheimer's disease: early alterations in brain DNA methylation at ANK1, BIN1, RHBDF2 and other loci

    Gyan Srivastava;Katie Lunnon;Jeremy Burgess;Lei Yu

Frequent Co-Authors

Leonard C. Schalkwyk
Leonard C. Schalkwyk University of Essex
Terrie E. Moffitt
Terrie E. Moffitt Duke University
Philip Asherson
Philip Asherson King's College London
Avshalom Caspi
Avshalom Caspi Duke University
Louise Arseneault
Louise Arseneault King's College London
David A. Collier
David A. Collier Eli Lilly (United States)
Ian W. Craig
Ian W. Craig King's College London
Richie Poulton
Richie Poulton University of Otago
Gerome Breen
Gerome Breen King's College London
Michael Conlon O'Donovan
Michael Conlon O'Donovan Cardiff University

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