Christian Theil Have
Christian Theil Have
Bekræftet mail på sund.ku.dk
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An expanded genome-wide association study of type 2 diabetes in Europeans
RA Scott, LJ Scott, R Mägi, L Marullo, KJ Gaulton, M Kaakinen, ...
Diabetes 66 (11), 2888-2902, 2017
3402017
Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
KJ Gaulton, T Ferreira, Y Lee, A Raimondo, R Mägi, ME Reschen, ...
Nature genetics 47 (12), 1415-1425, 2015
2622015
Genome-wide associations for birth weight and correlations with adult disease
M Horikoshi, RN Beaumont, FR Day, NM Warrington, MN Kooijman, ...
Nature 538 (7624), 248-252, 2016
2472016
Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity
V Turcot, Y Lu, HM Highland, C Schurmann, AE Justice, RS Fine, ...
Nature genetics 50 (1), 26-41, 2018
1292018
Are graph databases ready for bioinformatics?
CT Have, LJ Jensen
Bioinformatics 29 (24), 3107, 2013
792013
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
752019
Sequencing and de novo assembly of 150 genomes from Denmark as a population reference
L Maretty, JM Jensen, B Petersen, JA Sibbesen, S Liu, P Villesen, L Skov, ...
Nature 548 (7665), 87-91, 2017
712017
Genetic evidence of a causal effect of insulin resistance on branched-chain amino acid levels
Y Mahendran, A Jonsson, CT Have, KH Allin, DR Witte, ME Jørgensen, ...
Diabetologia 60 (5), 873-878, 2017
632017
DIAbetes Genetics Replication And Meta-analysis (DIAGRAM) Consortium. Genetic fine mapping and genomic annotation defines causal mechanisms at type 2 diabetes susceptibility loci
KJ Gaulton, T Ferreira, Y Lee, A Raimondo, R Mägi, ME Reschen, ...
Nat Genet 47 (12), 1415-1425, 2015
452015
Rare genetic variants previously associated with congenital forms of long QT syndrome have little or no effect on the QT interval
J Ghouse, CT Have, P Weeke, J Bille Nielsen, G Ahlberg, ...
European heart journal 36 (37), 2523-2529, 2015
382015
A glycogene mutation map for discovery of diseases of glycosylation
L Hansen, A Lind-Thomsen, HJ Joshi, NB Pedersen, CT Have, Y Kong, ...
Glycobiology 25 (2), 211-224, 2015
312015
New Blood Pressure–Associated Loci Identified in Meta-Analyses of 475 000 Individuals
AT Kraja, JP Cook, HR Warren, P Surendran, C Liu, E Evangelou, ...
Circulation: Cardiovascular Genetics 10 (5), e001778, 2017
302017
From use cases to UML class diagrams using logic grammars and constraints
H Christiansen, CT Have, K Tveitane
Recent Advances in Natural Language Processing 2007 7, 128–132, 2007
292007
Efficient tabling of structured data with enhanced hash-consing
NF Zhou, CT Have
arXiv preprint arXiv:1210.1611, 2012
272012
High prevalence of diabetes-predisposing variants in MODY genes among Danish women with gestational diabetes mellitus
AP Gjesing, G Rui, J Lauenborg, CT Have, M Hollensted, E Andersson, ...
Journal of the Endocrine Society 1 (6), 681-690, 2017
242017
Associations of mitochondrial and nuclear mitochondrial variants and genes with seven metabolic traits
AT Kraja, C Liu, JL Fetterman, M Graff, CT Have, C Gu, LR Yanek, ...
The American Journal of Human Genetics 104 (1), 112-138, 2019
232019
Genetic variations in the human G protein-coupled receptor class C, group 6, member A (GPRC6A) control cell surface expression and function
S Jørgensen, CT Have, CR Underwood, LD Johansen, P Wellendorph, ...
Journal of Biological Chemistry 292 (4), 1524-1534, 2017
182017
Numerous Brugada syndrome–associated genetic variants have no effect on J-point elevation, syncope susceptibility, malignant cardiac arrhythmia, and all-cause mortality
J Ghouse, CT Have, MW Skov, L Andreasen, G Ahlberg, JB Nielsen, ...
Genetics in Medicine 19 (5), 521-528, 2017
172017
Reasoning about use cases using logic grammars and constraints
H Christiansen, CT Have, K Tveitane
Proceedings of the 4th International Workshop on Constraints and Language …, 2007
152007
Common variants in LEPR, IL6, AMD1, and NAMPT do not associate with risk of juvenile and childhood obesity in Danes: a case–control study
M Hollensted, TS Ahluwalia, CT Have, N Grarup, CE Fonvig, TRH Nielsen, ...
BMC medical genetics 16 (1), 105, 2015
142015
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Artikler 1–20