Line Skotte

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Coauteurs

Mads MelbyeProfessorAdresse e-mail validée de sund.ku.dk
Bjarke FeenstraSenior Scientist, Department of Epidemiology Research, Statens Serum Institut, Copenhagen, DenmarkAdresse e-mail validée de ssi.dk
Anders AlbrechtsenCopenhagen university, Bioinformatics CenterAdresse e-mail validée de binf.ku.dk
Thorfinn Sand KorneliussenPostdoc, Department of Zoology, University of CambridgeAdresse e-mail validée de binf.ku.dk
Ida MoltkeUniversity of CopenhagenAdresse e-mail validée de binf.ku.dk
Marit Eika JørgensenClinical Epidemiology, Steno Diabetes CenterAdresse e-mail validée de steno.dk
Torben HansenProfessor of Metabolic Genetics, University of Copenhagen, DenmarkAdresse e-mail validée de sund.ku.dk
Niels GrarupUniversity of CopenhagenAdresse e-mail validée de sund.ku.dk
Oluf PedersenProfessor of Metabolic Genetics, University of CopenhagenAdresse e-mail validée de sund.ku.dk
Robert TibshiraniProfessor of Biomedical Data Sciences, and of Statistics, Stanford UniversityAdresse e-mail validée de stanford.edu
Joao FadistaPrincipal Scientist, Novo Nordisk (Denmark)Adresse e-mail validée de ssi.dk
Rasmus NielsenUC Berkeley, University of CopenhagenAdresse e-mail validée de bio.ku.dk
Fernando RacimoUniversity of CopenhagenAdresse e-mail validée de sund.ku.dk
Emilia Huerta-SanchezBrown universityAdresse e-mail validée de brown.edu
Matteo FumagalliQueen Mary University of LondonAdresse e-mail validée de qmul.ac.uk
Thuy NgoAssistant Professor, Oregon Health and Science UniversityAdresse e-mail validée de ohsu.edu
David HougaardDirector Department for Congenital Disorders, Statens Serum InstitutAdresse e-mail validée de ssi.dk
Jonas Bybjerg-GrauholmStatens Serum insitutAdresse e-mail validée de ssi.dk
Anders KochProfessor, Ilisimatusarfik, University of Greenland; Statens Serum Institut; RigshospitaletAdresse e-mail validée de ssi.dk
Patrick A. DionMcGill UniversityAdresse e-mail validée de mcgill.ca

Suivre

Line Skotte

Postdoctoral Fellow, Statens Serum Institute, Copenhagen, Denmark

Adresse e-mail validée de ssi.dk

Statistical genetics Population genetics Statistics Evolutionary genomics


Titre Trier par citations Trier par année Trier par titre	Citée par Citée par	Année
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	837	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	517	2015
Estimating Individual Admixture Proportions from Next Generation Sequencing Data L Skotte, TS Korneliussen, A Albrechtsen Genetics 195 (3), 693-702, 2013	515	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	271	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	211	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	155	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	138	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	136	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	103	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	80	2019
Association Testing for Next‐Generation Sequencing Data Using Score Statistics L Skotte, TS Korneliussen, A Albrechtsen Genetic Epidemiology 36 (5), 430-437, 2012	58	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	52	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	37	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	35	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	32	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	32	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	28	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	28	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	23	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	23	2018

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