Author details

Full Name

Cramer Christensen

Affiliation

ORCID

Career Start Year

2005

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
31586654	Oxidatively generated modifications to nucleic acids in vivo: Measurement in urine and plasma.	Free Radical Biology and Medicine	2019
30547231	A novel rare CUBN variant and three additional genes identified in Europeans with and without diabetes: results from an exome-wide association study of albuminuria.	Diabetologia	2019
31415576	Sequencing reveals protective and pathogenic effects on development of diabetes of rare GLIS3 variants.	PLoS ONE	2019
29273807	Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
30297969	Fine-mapping type 2 diabetes loci to single-variant resolution using high-density imputation and islet-specific epigenome maps.	Nat Genet	2018
29861389	Cardiolipin Synthesis in Brown and Beige Fat Mitochondria Is Essential for Systemic Energy Homeostasis.	Cell Metab	2018
29703844	A Genome-Wide Association Study of Diabetic Kidney Disease in Subjects With Type 2 Diabetes.	Diabetes	2018
29549330	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29549329	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2018
29632382	Refining the accuracy of validated target identification through coding variant fine-mapping in type 2 diabetes.	Nat Genet	2018
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
29849136	Publisher Correction: Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.	Nat Commun	2018
29358691	Re-analysis of public genetic data reveals a rare X-chromosomal variant associated with type 2 diabetes.	Nat Commun	2018
28146470	Rare and low-frequency coding variants alter human adult height.	Nature	2017
28390926	Rhodopsin in plasma from patients with diabetic retinopathy - development and validation of digital ELISA by Single Molecule Array (Simoa) technology.	Journal of Immunological Methods	2017
28341696	A Low-Frequency Inactivating <i>AKT2</i> Variant Enriched in the Finnish Population Is Associated With Fasting Insulin Levels and Type 2 Diabetes Risk.	Diabetes	2017
29030403	New Blood Pressure-Associated Loci Identified in Meta-Analyses of 475â¿¿000 Individuals.	Circ Cardiovasc Genet	2017
29257133	Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2017
29083408	Exome-wide association study of plasma lipids in >300,000 individuals.	Nat Genet	2017
29061564	Cardiovascular and All-Cause Mortality Risk Associated With Urinary Excretion of 8-oxoGuo, a Biomarker for RNA Oxidation, in Patients With Type 2 Diabetes: A Prospective Cohort Study.	Diabetes Care	2017
28287274	The effect of smoking on the urinary excretion of 8-oxodG and 8-oxoGuo in patients with type 2 diabetes.	Scandinavian Journal of Clinical and Laboratory Investigation	2017
27920155	<i>SOS2</i> and <i>ACP1</i> Loci Identified through Large-Scale Exome Chip Analysis Regulate Kidney Development and Function.	J Am Soc Nephrol	2017
27799821	Vejle Diabetes Biobank - a resource for studies of the etiologies of diabetes and its comorbidities.	Clinical Epidemiology	2016
27068006	Functional and genetic epidemiological characterisation of the FFAR4 (GPR120) p.R270H variant in the Danish population.	Journal of Medical Genetics	2016
26818947	Genome-wide association studies in the Japanese population identify seven novel loci for type 2 diabetes.	Nat Commun	2016
27398621	The genetic architecture of type 2 diabetes.	Nature	2016
27618447	Trans-ancestry meta-analyses identify rare and common variants associated with blood pressure and hypertension.	Nat Genet	2016
26336608	Reduced CD300LG mRNA tissue expression, increased intramyocellular lipid content and impaired glucose metabolism in healthy male carriers of Arg82Cys in CD300LG: a novel genometabolic cross-link between CD300LG and common metabolic phenotypes.	BMJ Open Diabetes Research and Care	2015
25927630	Impact of PTBP1 rs11085226 on glucose-stimulated insulin release in adult Danes.	BMC Medical Genetics	2015
25799151	The type 2 diabetes risk allele of TMEM154-rs6813195 associates with decreased beta cell function in a study of 6,486 Danes.	PLoS ONE	2015
25625282	Identification and functional characterization of G6PC2 coding variants influencing glycemic traits define an effector transcript at the G6PC2-ABCB11 locus.	PLoS Genet	2015
25599387	Discovery of coding genetic variants influencing diabetes-related serum biomarkers and their impact on risk of type 2 diabetes.	Journal of Clinical Endocrinology and Metabolism	2015
26383953	Greenlandic Inuit show genetic signatures of diet and climate adaptation.	Science	2015
24659606	Changing from glucose to HbA1c for diabetes diagnosis: predictive values of one test and importance of analytical bias and imprecision.	Clinical Chemistry and Laboratory Medicine	2014
25314291	Blood pressure levels in male carriers of Arg82Cys in CD300LG.	PLoS ONE	2014
24464100	Identification of low-frequency and rare sequence variants associated with elevated or reduced risk of type 2 diabetes.	Nat Genet	2014
24814742	Diabetes mortality differs between registers due to various disease definitions.	Danish Medical Journal	2014
24584071	Loss-of-function mutations in SLC30A8 protect against type 2 diabetes.	Nat Genet	2014
23160641	Exome sequencing-driven discovery of coding polymorphisms associated with common metabolic phenotypes.	Diabetologia	2013
24156295	Studies of association of AGPAT6 variants with type 2 diabetes and related metabolic phenotypes in 12,068 Danes.	BMC Medical Genetics	2013
21781351	Studies of a genetic variant in HK1 in relation to quantitative metabolic traits and to the prevalence of type 2 diabetes.	BMC Medical Genetics	2011
18405479	[Antiplatelet treatment after acute and chronic ischemic heart and brain events is insufficient according to recommendations].	Ugeskrift for Laeger	2008
18940158	[Antihypertensive treatment preceding cerebrovascular diseases is insufficient according to recommendations].	Ugeskrift for Laeger	2008
16375593	Improvement in glycemic control over 11 years in patients monitored for diabetes in one county.	Clinical Chemistry and Laboratory Medicine	2006
16309374	Glycemic control in diabetes in three Danish counties.	Clinical Chemistry and Laboratory Medicine	2005