Penelope Lind
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Genome-wide association study identifies 74 loci associated with educational attainment
A Okbay, JP Beauchamp, MA Fontana, JJ Lee, TH Pers, CA Rietveld, ...
Nature 533 (7604), 539-542, 2016
7772016
Genome-wide association analyses identify 44 risk variants and refine the genetic architecture of major depression
NR Wray, S Ripke, M Mattheisen, M Trzaskowski, EM Byrne, A Abdellaoui, ...
Nature genetics 50 (5), 668, 2018
7342018
GWAS of 126,559 individuals identifies genetic variants associated with educational attainment
CA Rietveld, SE Medland, J Derringer, J Yang, T Esko, NW Martin, ...
science 340 (6139), 1467-1471, 2013
6822013
Genetic variants associated with subjective well-being, depressive symptoms, and neuroticism identified through genome-wide analyses
A Okbay, BML Baselmans, JE De Neve, P Turley, MG Nivard, MA Fontana, ...
Nature genetics 48 (6), 624-633, 2016
5432016
LRRTM1 on chromosome 2p12 is a maternally suppressed gene that is associated paternally with handedness and schizophrenia
C Francks, S Maegawa, J Laurén, BS Abrahams, A Velayos-Baeza, ...
Molecular psychiatry 12 (12), 1129-1139, 2007
4082007
Identification of heart rate–associated loci and their effects on cardiac conduction and rhythm disorders
M Den Hoed, M Eijgelsheim, T Esko, BJJM Brundel, DS Peal, DM Evans, ...
Nature genetics 45 (6), 621, 2013
2272013
Genomic analyses identify hundreds of variants associated with age at menarche and support a role for puberty timing in cancer risk
FR Day, DJ Thompson, H Helgason, DI Chasman, H Finucane, P Sulem, ...
Nature genetics 49 (6), 834-841, 2017
1872017
Associations of ADH and ALDH2 gene variation with self report alcohol reactions, consumption and dependence: an integrated analysis
S Macgregor, PA Lind, KK Bucholz, NK Hansell, PAF Madden, ...
Human molecular genetics 18 (3), 580-593, 2009
1862009
A quantitative-trait genome-wide association study of alcoholism risk in the community: findings and implications
AC Heath, JB Whitfield, NG Martin, ML Pergadia, AM Goate, PA Lind, ...
Biological psychiatry 70 (6), 513-518, 2011
1832011
Association studies of up to 1.2 million individuals yield new insights into the genetic etiology of tobacco and alcohol use
M Liu, Y Jiang, R Wedow, Y Li, DM Brazel, F Chen, G Datta, ...
Nature genetics 51 (2), 237-244, 2019
1542019
Genetic evidence for causal relationships between maternal obesity-related traits and birth weight
J Tyrrell, RC Richmond, TM Palmer, B Feenstra, J Rangarajan, ...
Jama 315 (11), 1129-1140, 2016
1452016
Genome-wide analysis identifies 12 loci influencing human reproductive behavior
N Barban, R Jansen, R De Vlaming, A Vaez, JJ Mandemakers, FC Tropf, ...
Nature genetics 48 (12), 1462-1472, 2016
1332016
The ongoing adaptive evolution of ASPM and Microcephalin is not explained by increased intelligence
N Mekel-Bobrov, D Posthuma, SL Gilbert, P Lind, MF Gosso, M Luciano, ...
Human molecular genetics 16 (6), 600-608, 2007
1282007
A meta-analysis of genome-wide association studies identifies novel variants associated with osteoarthritis of the hip
E Evangelou, HJ Kerkhof, U Styrkarsdottir, EE Ntzani, SD Bos, T Esko, ...
Annals of the rheumatic diseases 73 (12), 2130-2136, 2014
1252014
Transancestral GWAS of alcohol dependence reveals common genetic underpinnings with psychiatric disorders
RK Walters, R Polimanti, EC Johnson, JN McClintick, MJ Adams, ...
Nature neuroscience 21 (12), 1656-1669, 2018
1232018
Directional dominance on stature and cognition in diverse human populations
PK Joshi, T Esko, H Mattsson, N Eklund, I Gandin, T Nutile, AU Jackson, ...
Nature 523 (7561), 459-462, 2015
1122015
A haplotype spanning KIAA0319 and TTRAP is associated with normal variation in reading and spelling ability
M Luciano, PA Lind, DL Duffy, A Castles, MJ Wright, GW Montgomery, ...
Biological psychiatry 62 (7), 811-817, 2007
1092007
A genomewide association study of nicotine and alcohol dependence in Australian and Dutch populations
PA Lind, S Macgregor, JM Vink, ML Pergadia, NK Hansell, MHM De Moor, ...
Twin Research and Human Genetics 13 (1), 11-29, 2010
1022010
Dyslexia and DYX1C1: deficits in reading and spelling associated with a missense mutation
TC Bates, PA Lind, M Luciano, GW Montgomery, NG Martin, MJ Wright
Molecular psychiatry 15 (12), 1190-1196, 2010
942010
Dyslexia and DCDC2: normal variation in reading and spelling is associated with DCDC2 polymorphisms in an Australian population sample
PA Lind, M Luciano, MJ Wright, GW Montgomery, NG Martin, TC Bates
European Journal of Human Genetics 18 (6), 668-673, 2010
882010
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