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Line Skotte
Line Skotte
Postdoctoral Fellow, Statens Serum Institute, Copenhagen, Denmark
Verified email at ssi.dk
Title
Cited by
Cited by
Year
An Aboriginal Australian genome reveals separate human dispersals into Asia
M Rasmussen, X Guo, Y Wang, KE Lohmueller, S Rasmussen, ...
Science 334 (6052), 94-98, 2011
8642011
Estimating Individual Admixture Proportions from Next Generation Sequencing Data
L Skotte, TS Korneliussen, A Albrechtsen
Genetics 195 (3), 693-702, 2013
5712013
Greenlandic Inuit show genetic signatures of diet and climate adaptation
M Fumagalli, I Moltke, N Grarup, F Racimo, P Bjerregaard, ME Jørgensen, ...
Science 349 (6254), 1343-1347, 2015
5462015
The role of miRNAs in human papilloma virus (HPV)-associated cancers: bridging between HPV-related head and neck cancer and cervical cancer
CB Lajer, E Garnæs, L Friis-Hansen, B Norrild, MH Therkildsen, M Glud, ...
British Journal of Cancer, 2012
2812012
Noninvasive blood tests for fetal development predict gestational age and preterm delivery
TTM Ngo, MN Moufarrej, MLH Rasmussen, J Camunas-Soler, W Pan, ...
Science 360 (6393), 1133-1136, 2018
2332018
Metabolic Dynamics and Prediction of Gestational Age and Time to Delivery in Pregnant Women
L Liang, MLH Rasmussen, B Piening, X Shen, S Chen, H Röst, JK Snyder, ...
Cell 181 (7), 1680-1692. e15, 2020
1732020
Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes
A Albrechtsen, N Grarup, Y Li, T Sparsø, G Tian, H Cao, T Jiang, SY Kim, ...
Diabetologia 56 (2), 298-310, 2013
1622013
Genetic predisposition to hypertension is associated with preeclampsia in European and Central Asian women
V Steinthorsdottir, R McGinnis, NO Williams, L Stefansdottir, ...
Nature communications 11 (1), 1-14, 2020
1412020
Familial aggregation and heritability of pyloric stenosis
C Krogh, TK Fischer, L Skotte, RJ Biggar, N Øyen, A Skytthe, S Goertz, ...
JAMA 303 (23), 2393-2399, 2010
1352010
Associations of autozygosity with a broad range of human phenotypes
DW Clark, Y Okada, KHS Moore, D Mason, N Pirastu, I Gandin, ...
Nature communications 10 (1), 1-17, 2019
902019
Variants in the fetal genome near pro-inflammatory cytokine genes on 2q13 associate with gestational duration
X Liu, D Helenius, L Skotte, RN Beaumont, M Wielscher, F Geller, ...
Nature communications 10 (1), 1-13, 2019
632019
Association Testing for Next‐Generation Sequencing Data Using Score Statistics
L Skotte, TS Korneliussen, A Albrechtsen
Genetic Epidemiology 36 (5), 430-437, 2012
632012
Genome-wide study identifies association between HLA-B∗ 55: 01 and Self-Reported Penicillin Allergy
K Krebs, J Bovijn, N Zheng, M Lepamets, JC Censin, T Jürgenson, D Särg, ...
The American Journal of Human Genetics 107 (4), 612-621, 2020
422020
Maternal and fetal genetic contribution to gestational weight gain
NM Warrington, R Richmond, B Fenstra, R Myhre, R Gaillard, ...
International journal of obesity 42 (4), 775-784, 2018
402018
Strabismus Incidence in a Danish Population-Based Cohort of Children
T Torp-Pedersen, HA Boyd, L Skotte, B Haargaard, J Wohlfahrt, ...
Jama Ophthalmology 135 (10), 1047-1053, 2017
382017
The Early Growth Genetics (EGG) and EArly Genetics and Lifecourse Epidemiology (EAGLE) consortia: design, results and future prospects
CM Middeldorp, JF Felix, A Mahajan, MI McCarthy
European journal of epidemiology 34 (3), 279-300, 2019
352019
Genome-wide association study of febrile seizures implicates fever response and neuronal excitability genes
L Skotte, J Fadista, J Bybjerg-Grauholm, V Appadurai, MS Hildebrand, ...
Brain 145 (2), 555-568, 2022
312022
Ancestry‐specific association mapping in admixed populations
L Skotte, E Jørsboe, TS Korneliussen, I Moltke, A Albrechtsen
Genetic epidemiology 43 (5), 506-521, 2019
302019
CPT1A Missense Mutation Associated With Fatty Acid Metabolism and Reduced Height in Greenlanders
L Skotte, A Koch, V Yakimov, S Zhou, B Søborg, M Andersson, ...
Circulation: Cardiovascular Genetics 10 (3), e001618, 2017
292017
Genome-wide association study of Hirschsprung disease detects a novel low-frequency variant at the RET locus
J Fadista, M Lund, L Skotte, F Geller, P Nandakumar, S Chatterjee, ...
European Journal of Human Genetics, 1, 2018
252018
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