Jodie N Painter
Jodie N Painter
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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), 668-681, 2018
The genetic architecture of the human cerebral cortex
KL Grasby, N Jahanshad, JN Painter, L Colodro-Conde, J Bralten, ...
Science 367 (6484), eaay6690, 2020
Maternal and fetal genetic effects on birth weight and their relevance to cardio-metabolic risk factors
NM Warrington, RN Beaumont, M Horikoshi, FR Day, Ø Helgeland, ...
Nature genetics 51 (5), 804-814, 2019
Genome-wide association study identifies a locus at 7p15. 2 associated with endometriosis
JN Painter, CA Anderson, DR Nyholt, S Macgregor, J Lin, SH Lee, ...
Nature genetics 43 (1), 51-54, 2011
Genome-wide association meta-analysis identifies new endometriosis risk loci
DR Nyholt, SK Low, CA Anderson, JN Painter, S Uno, AP Morris, ...
Nature genetics 44 (12), 1355-1359, 2012
Common variants in the trichohyalin gene are associated with straight hair in Europeans
SE Medland, DR Nyholt, JN Painter, BP McEvoy, AF McRae, G Zhu, ...
The American Journal of Human Genetics 85 (5), 750-755, 2009
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
Contribution of genetic variation to transgenerational inheritance of DNA methylation
AF McRae, JE Powell, AK Henders, L Bowdler, G Hemani, S Shah, ...
Genome biology 15, 1-10, 2014
The search for genes contributing to endometriosis risk
GW Montgomery, DR Nyholt, ZZ Zhao, SA Treloar, JN Painter, ...
Human reproduction update 14 (5), 447-457, 2008
Genetic insights into biological mechanisms governing human ovarian ageing
KS Ruth, FR Day, J Hussain, A Martínez-Marchal, CE Aiken, A Azad, ...
Nature 596 (7872), 393-397, 2021
Identification of 55,000 replicated DNA methylation QTL
AF McRae, RE Marioni, S Shah, J Yang, JE Powell, SE Harris, J Gibson, ...
Scientific reports 8 (1), 17605, 2018
Genome-wide association study identifies a new melanoma susceptibility locus at 1q21. 3
S MacGregor, GW Montgomery, JZ Liu, ZZ Zhao, AK Henders, M Stark, ...
Nature genetics 43 (11), 1114-1118, 2011
Genome-wide association study of offspring birth weight in 86 577 women identifies five novel loci and highlights maternal genetic effects that are independent of fetal genetics
RN Beaumont, NM Warrington, A Cavadino, J Tyrrell, M Nodzenski, ...
Human molecular genetics 27 (4), 742-756, 2018
Factors affecting avian cross‐species microsatellite amplification
C R. Primmer, J N. Painter, M T. Koskinen, J U. Palo, J Merilä
Journal of Avian Biology 36 (4), 348-360, 2005
Evidence of a causal association between insulinemia and endometrial cancer: a Mendelian randomization analysis
KT Nead, SJ Sharp, DJ Thompson, JN Painter, DB Savage, RK Semple, ...
Journal of the National Cancer Institute 107 (9), djv178, 2015
A 4-bp deletion in the Birt-Hogg-Dube gene (FLCN) causes dominantly inherited spontaneous pneumothorax
JN Painter, H Tapanainen, M Somer, P Tukiainen, K Aittomäki
The American Journal of Human Genetics 76 (3), 522-527, 2005
The genetics of the mood disorder spectrum: genome-wide association analyses of more than 185,000 cases and 439,000 controls
JRI Coleman, HA Gaspar, J Bryois, EM Byrne, AJ Forstner, PA Holmans, ...
Biological psychiatry 88 (2), 169-184, 2020
Dissecting the shared genetic architecture of suicide attempt, psychiatric disorders, and known risk factors
N Mullins, JE Kang, AI Campos, JRI Coleman, AC Edwards, H Galfalvy, ...
Biological psychiatry 91 (3), 313-327, 2022
A comparison of ten polygenic score methods for psychiatric disorders applied across multiple cohorts
G Ni, J Zeng, JA Revez, Y Wang, Z Zheng, T Ge, R Restuadi, J Kiewa, ...
Biological psychiatry 90 (9), 611-620, 2021
Sequence variation in the ATP8B1 gene and intrahepatic cholestasis of pregnancy
JN Painter, M Savander, A Ropponen, N Nupponen, S Riikonen, ...
European journal of human genetics 13 (4), 435-439, 2005
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