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D-Index & Metrics

Biology and Biochemistry

D-Index
50
Citations
13719
World Ranking
17456
National Ranking
1374

Overview

Janine A. Lamb is affiliated with the University of Manchester in the United Kingdom. Their research primarily spans the field of Medicine, with a focus on Epidemiology, Gastroenterology, Immunology, Pathology and Forensic Medicine, and Rheumatology.

The scientist's work addresses topics including:

  • Inflammatory Myopathies and Dermatomyositis
  • Celiac Disease Research and Management
  • Immunodeficiency and Autoimmune Disorders
  • Muscle Physiology and Disorders
  • Eosinophilic Disorders and Syndromes
  • Systemic Sclerosis and Related Diseases
  • Viral Infections and Immunology Research

Recent publications by Janine A. Lamb include:

  • "Antibodies against immunogenic epitopes with high sequence identity to SARS-CoV-2 in patients with autoimmune dermatomyositis" (2020), published in Annals of the Rheumatic Diseases
  • "Epidemiology of the idiopathic inflammatory myopathies" (2023), published in Nature Reviews Rheumatology
  • "47XXY and 47XXX in Scleroderma and Myositis" (2022), published in ACR Open Rheumatology
  • "Low copy numbers of complement C4 and C4A deficiency are risk factors for myositis, its subgroups and autoantibodies" (2022), published in Annals of the Rheumatic Diseases
  • "MicroRNA and mRNA profiling in the idiopathic inflammatory myopathies" (2020), published in BMC Rheumatology

Their frequent coauthors include:

  • Hector Chinoy
  • Ingrid E. Lundberg
  • Simon Rothwell
  • Jiří Vencovský
  • Leonid Padyukov

Janine A. Lamb's work has appeared repeatedly in several key publication venues such as:

  • Lara D. Veeken (11 publications)
  • Annals of the Rheumatic Diseases (8 publications)
  • Arthritis & Rheumatology (3 publications)
  • Nature Reviews Rheumatology (2 publications)
  • ACR Open Rheumatology (1 publication)

Best Publications

  • Functional impact of global rare copy number variation in autism spectrum disorders

    Dalila Pinto;Alistair T. Pagnamenta;Lambertus Klei;Richard Anney

  • Mapping autism risk loci using genetic linkage and chromosomal rearrangements

    Peter Szatmari;Andrew D. Paterson;Lonnie Zwaigenbaum;Wendy Roberts

  • A genome-wide linkage and association scan reveals novel loci for autism

    Lauren A. Weiss;Lauren A. Weiss;Dan E. Arking;Mark J. Daly;Mark J. Daly;Aravinda Chakravarti

  • A full genome screen for autism with evidence for linkage to a region on chromosome 7q International Molecular Genetic Study of Autism Consortium

    Anthony Bailey;Amaia Hervas;Nicola Matthews;Sarah Palferman

  • A genome-wide scan for common alleles affecting risk for autism

    Richard Anney;Lambertus Klei;Dalila Pinto;Regina Regan

  • Individual common variants exert weak effects on the risk for autism spectrum disorders.

    Richard Anney;Lambertus Klei;Dalila Pinto;Dalila Pinto;Joana Almeida

  • A genomewide screen for autism: strong evidence for linkage to chromosomes 2q, 7q and 16p

    Le, Couteur, A;TP Kelly;T Berney;HR McConachie

  • A quantitative-trait locus on chromosome 6p influences different aspects of developmental dyslexia.

    Simon E. Fisher;Angela J. Marlow;Janine Lamb;Elena Maestrini

  • FOXP2 is not a major susceptibility gene for autism or specific language impairment.

    D.F. Newbury;E. Bonora;J.A. Lamb;S.E. Fisher

  • A whole-genome scan and fine-mapping linkage study of auditory-visual synesthesia reveals evidence of linkage to chromosomes 2q24, 5q33, 6p12, and 12p12.

    Julian E. Asher;Janine A. Lamb;Denise Brocklebank;Jean Baptiste Cazier

  • Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q

    Sarah Palferman;Nicola Matthews;Martha Turner;Janette Moore

  • A novel approach of homozygous haplotype sharing identifies candidate genes in autism spectrum disorder

    Jillian P. Casey;Tiago R. Magalhães;Tiago R. Magalhães;Judith M. Conroy;Regina Regan

  • The EuroMyositis registry: an international collaborative tool to facilitate myositis research

    James B Lilleker;James B Lilleker;Jiri Vencovsky;Guochun Wang;Lucy R Wedderburn

  • Candidate-gene screening and association analysis at the autism-susceptibility locus on chromosome 16p: evidence of association at GRIN2A and ABAT.

    Gabrielle Barnby;Aaron Abbott;Nuala Sykes;Andrew Morris

  • Autism: recent molecular genetic advances

    Janine A. Lamb;Janette Moore;Anthony Bailey;Anthony P. Monaco

  • Risk for myasthenia gravis maps to a (151) Pro→Ala change in TNIP1 and to human leukocyte antigen-B*08.

    Peter K. Gregersen;Roman Kosoy;Annette T. Lee;Janine Lamb

  • High-density SNP association study and copy number variation analysis of the AUTS1 and AUTS5 loci implicate the IMMP2L-DOCK4 gene region in autism susceptibility.

    E Maestrini;A T Pagnamenta;J A Lamb;J A Lamb;E Bacchelli

  • Risk factors and disease mechanisms in myositis.

    Frederick W. Miller;Janine A. Lamb;Jens Schmidt;Kanneboyina Nagaraju

  • Molecular findings from 537 individuals with inherited retinal disease

    Jamie M Ellingford;Jamie M Ellingford;Stephanie Barton;Sanjeev Bhaskar;James O'Sullivan;James O'Sullivan

  • Further characterization of the autism susceptibility locus AUTS1 on chromosome 7q International Molecular Genetic Study of Autism Consortium (IMGSAC)

    Sarah Palferman;Nicola Matthews;Martha Turner;Janette Moore

Frequent Co-Authors

Anthony P. Monaco
Anthony P. Monaco Tufts University
William E R Ollier
William E R Ollier University of Manchester
Anthony J. Bailey
Anthony J. Bailey University of British Columbia
Neil McHugh
Neil McHugh University of Bath
Lucy R. Wedderburn
Lucy R. Wedderburn University College London
Elena Maestrini
Elena Maestrini University of Bologna
Ingrid E. Lundberg
Ingrid E. Lundberg Karolinska University Hospital
Peter K. Gregersen
Peter K. Gregersen Feinstein Institute for Medical Research
Annette T. Lee
Annette T. Lee Northwell Health
Geraldine Dawson
Geraldine Dawson Duke University

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