Line Skotte
Line Skotte
Postdoctoral Fellow, Statens Serum Institute, Copenhagen, Denmark
Adresse e-mail validée de
Citée par
Citée par
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
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
Estimating Individual Admixture Proportions from Next Generation Sequencing Data
L Skotte, TS Korneliussen, A Albrechtsen
Genetics 195 (3), 693-702, 2013
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
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
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
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
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
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
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
Association Testing for Next‐Generation Sequencing Data Using Score Statistics
L Skotte, TS Korneliussen, A Albrechtsen
Genetic Epidemiology 36 (5), 430-437, 2012
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
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
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
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
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
Ancestry‐specific association mapping in admixed populations
L Skotte, E Jørsboe, TS Korneliussen, I Moltke, A Albrechtsen
Genetic epidemiology 43 (5), 506-521, 2019
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
Genome-wide meta-analysis identifies BARX1 and EML4-MTA3 as new loci associated with infantile hypertrophic pyloric stenosis
J Fadista, L Skotte, F Geller, J Bybjerg-Grauholm, S Gørtz, PA Romitti, ...
Human molecular genetics 28 (2), 332-340, 2019
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
Le système ne peut pas réaliser cette opération maintenant. Veuillez réessayer plus tard.
Articles 1–20