Christian Theil Have
Christian Theil Have
Verified email at sund.ku.dk
TitleCited byYear
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
2452017
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, 2015
2322015
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, 2016
2072016
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, 2018
1002018
Are graph databases ready for bioinformatics?
CT Have, LJ Jensen
Bioinformatics 29 (24), 3107, 2013
722013
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, 2017
562017
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
502017
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
432015
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
372015
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, 2014
272014
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
262017
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
252007
Efficient tabling of structured data with enhanced hash-consing
NF Zhou, CT Have
Theory and Practice of Logic Programming 12 (4-5), 547-563, 2012
242012
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, 1, 2019
162019
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
162017
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, 2017
152017
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
142007
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
132017
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
122015
Assembly and analysis of 100 full MHC haplotypes from the Danish population
JM Jensen, P Villesen, RM Friborg, T Mailund, S Besenbacher, ...
Genome research 27 (9), 1597-1607, 2017
102017
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