M
Meena Kumari
Researcher at University of Essex
Publications - 434
Citations - 57017
Meena Kumari is an academic researcher from University of Essex. The author has contributed to research in topics: Population & Genome-wide association study. The author has an hindex of 97, co-authored 407 publications receiving 49488 citations. Previous affiliations of Meena Kumari include Kansas State University & University of Copenhagen.
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Journal ArticleDOI
Corrigendum: Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses (vol 48, pg 624, 2016)
Aysu Okbay,Bart M. L. Baselmans,Jan-Emmanuel De Neve,Patrick Turley,Michel G. Nivard,Mark Alan Fontana,S. Fleur W. Meddens,Richard Karlsson Linnér,Cornelius A. Rietveld,Jaime Derringer,Jacob Gratten,James J. Lee,Jimmy Z. Liu,Ronald de Vlaming,Tarunveer S. Ahluwalia,Jadwiga Buchwald,Alana Cavadino,Alexis C. Frazier-Wood,Nicholas A. Furlotte,Victoria Garfield,Marie Henrike Geisel,Juan R. González,Saskia Haitjema,Robert Karlsson,Sander W. van der Laan,Karl-Heinz Ladwig,Jari Lahti,Sven J. van der Lee,Penelope A. Lind,Tian Liu,Lindsay K. Matteson,Evelin Mihailov,Michael B. Miller,Camelia C. Minică,Ilja M. Nolte,Dennis O. Mook-Kanamori,Peter J. van der Most,Christopher Oldmeadow,Yong Qian,Olli T. Raitakari,Rajesh Rawal,Anu Realo,Harm-Jan Westra,Meena Kumari,Lude Franke,Harold Snieder,Ute Bültmann,Melinda Mills,Albertine J. Oldehinkel,Behrooz Z. Alizadeh +49 more
TL;DR: In the version of this article initially published, one of the affiliations listed for author Maciej Trzaskowski, to the Department of Public Health, Faculty of Medicine, University of Split, Split, Croatia, was included in error.
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IRS1 gene variants, dysglycaemic metabolic changes and type-2 diabetes risk
Nikos Yiannakouris,J.A. Cooper,Sonia Shah,Fotios Drenos,Helen Ireland,Jeffrey W. Stephens,KaWah Li,Robert S. Elkeles,Ian F. Godsland,Mika Kivimäki,Aroon D. Hingorani,Meena Kumari,P.J. Talmud,Steve E. Humphries +13 more
TL;DR: The association of rs2943641T with T2D protection is confirmed and there is a possible independent effect on risk of a putative IRS1 promoter variant.
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Translating genomics into improved healthcare.
TL;DR: The recent discoveries in genetic research are summarised and the implications of newly acquired knowledge for medical practice and public health are reviewed.
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Use of allele-specific FAIRE to determine functional regulatory polymorphism using large-scale genotyping arrays.
Andrew J. Smith,Philip N. Howard,Sonia Shah,Per Eriksson,Stefan Stender,Claudia Giambartolomei,Lasse Folkersen,Anne Tybjærg-Hansen,Meena Kumari,Jutta Palmen,Aroon D. Hingorani,Philippa J. Talmud,Steve E. Humphries +12 more
TL;DR: The technique of allele-specific FAIRE, utilising large-scale genotyping technology (FAIRE-gen) to determine allelic effects on chromatin accessibility and regulatory potential is described, which has the potential to aid the identification of many causal SNPs associated with disease from GWAS.
Journal ArticleDOI
Negative Aspects of Close Relationships as Risk Factors for Cognitive Aging
Jing Liao,Jenny Head,Meena Kumari,Stephen Stansfeld,Mika Kivimäki,Archana Singh-Manoux,Eric J. Brunner +6 more
TL;DR: Negative aspects of close relationships, but not positive aspects, were associated with accelerated cognitive aging and the importance of differentiating aspects of social relationships to evaluate their unique associations with cognitive aging is highlighted.