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Anne Heidi Skogholt
Anne Heidi Skogholt
Researcher NTNU
在 ntnu.no 的电子邮件经过验证 - 首页
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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
15622019
Biobank-driven genomic discovery yields new insight into atrial fibrillation biology
JB Nielsen, RB Thorolfsdottir, LG Fritsche, W Zhou, MW Skov, SE Graham, ...
Nature genetics 50 (9), 1234-1239, 2018
6362018
A genome-wide association study with 1,126,563 individuals identifies new risk loci for Alzheimer’s disease
DP Wightman, IE Jansen, JE Savage, AA Shadrin, S Bahrami, D Holland, ...
Nature genetics 53 (9), 1276-1282, 2021
5732021
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
CG Boer, K Hatzikotoulas, L Southam, L Stefánsdóttir, Y Zhang, ...
Cell 184 (18), 4784-4818. e17, 2021
3192021
Genome-wide analysis of 102,084 migraine cases identifies 123 risk loci and subtype-specific risk alleles
H Hautakangas, BS Winsvold, SE Ruotsalainen, G Bjornsdottir, ...
Nature genetics 54 (2), 152-160, 2022
2042022
Genetic diversity fuels gene discovery for tobacco and alcohol use
GRB Saunders, X Wang, F Chen, SK Jang, M Liu, C Wang, S Gao, ...
Nature 612 (7941), 720-724, 2022
1682022
Genome-wide analysis of 53,400 people with irritable bowel syndrome highlights shared genetic pathways with mood and anxiety disorders
C Eijsbouts, T Zheng, NA Kennedy, F Bonfiglio, CA Anderson, ...
Nature genetics 53 (11), 1543-1552, 2021
1492021
Genome-wide study of atrial fibrillation identifies seven risk loci and highlights biological pathways and regulatory elements involved in cardiac development
JB Nielsen, LG Fritsche, W Zhou, TM Teslovich, OL Holmen, S Gustafsson, ...
The American Journal of Human Genetics 102 (1), 103-115, 2018
1082018
GWAS of thyroid stimulating hormone highlights pleiotropic effects and inverse association with thyroid cancer
W Zhou, B Brumpton, O Kabil, J Gudmundsson, G Thorleifsson, ...
Nature communications 11 (1), 3981, 2020
1072020
Genetic architecture of abdominal aortic aneurysm in the million veteran program
D Klarin, SS Verma, R Judy, O Dikilitas, BN Wolford, I Paranjpe, MG Levin, ...
Circulation 142 (17), 1633-1646, 2020
892020
Sex-specific and pleiotropic effects underlying kidney function identified from GWAS meta-analysis
SE Graham, JB Nielsen, M Zawistowski, W Zhou, LG Fritsche, ...
Nature communications 10 (1), 1847, 2019
702019
Genome-wide risk prediction of common diseases across ancestries in one million people
N Mars, S Kerminen, YCA Feng, M Kanai, K Läll, LF Thomas, AH Skogholt, ...
Cell Genomics 2 (4), 2022
582022
The HUNT Study: a population-based cohort for genetic research
BM Brumpton, S Graham, I Surakka, AH Skogholt, M Løset, LG Fritsche, ...
Cell Genomics 2 (10), 2022
522022
Loss-of-function genomic variants highlight potential therapeutic targets for cardiovascular disease
JB Nielsen, O Rom, I Surakka, SE Graham, W Zhou, T Roychowdhury, ...
Nature communications 11 (1), 6417, 2020
452020
Dissecting the shared genetic basis of migraine and mental disorders using novel statistical tools
S Bahrami, G Hindley, BS Winsvold, KS O’Connell, O Frei, A Shadrin, ...
Brain 145 (1), 142-153, 2022
422022
Cross-ancestry investigation of venous thromboembolism genomic predictors
F Thibord, D Klarin, JA Brody, MH Chen, MG Levin, DI Chasman, ...
Circulation 146 (16), 1225-1242, 2022
402022
Largest GWAS (N= 1,126,563) of Alzheimer’s disease implicates microglia and immune cells
DP Wightman, IE Jansen, JE Savage, AA Shadrin, S Bahrami, A Rongve, ...
MedRxiv, 2020.11. 20.20235275, 2020
372020
Genetic effects on the timing of parturition and links to fetal birth weight
P Solé-Navais, C Flatley, V Steinthorsdottir, M Vaudel, J Juodakis, J Chen, ...
Nature Genetics 55 (4), 559-567, 2023
332023
Genome-wide analysis of 944 133 individuals provides insights into the etiology of haemorrhoidal disease
T Zheng, D Ellinghaus, S Juzenas, F Cossais, G Burmeister, G Mayr, ...
Gut 70 (8), 1538-1549, 2021
332021
Genome-wide analysis identifies impaired axonogenesis in chronic overlapping pain conditions
S Khoury, M Parisien, SJ Thompson, E Vachon-Presseau, M Roy, ...
Brain 145 (3), 1111-1123, 2022
322022
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