Author details

Full Name

Elin Grundberg

Affiliation

ORCID

Career Start Year

2003

Papers

H Index

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
37039021	DNA Methylation of Birthweight-Blood Pressure Genes and Changes of Blood Pressure in Response to Weight-Loss Diets in the POUNDS Lost Trial.		2023
37579195	Leveraging osteoclast genetic regulatory data to identify genes with a role in osteoarthritis.	Genetics	2023
37563143	Extravillous trophoblast cell lineage development is associated with active remodeling of the chromatin landscape.	Nat Commun	2023
36718845	Insurance denials and diagnostic rates in a pediatric genomic research cohort.		2023
36824040	Rare and Common Variants in GALNT3 May Affect Bone Mass Independently of Phosphate Metabolism.		2023
36800272	DNA Methylation Near CPT1A and Changes in Triglyceride-rich Lipoproteins in Response to Weight-loss Diet Interventions.		2023
36537711	Neonatal hyperoxia induces activated pulmonary cellular states and sex-dependent transcriptomic changes in a model of experimental bronchopulmonary dysplasia.		2023
35165382	Blood DNA methylation at TXNIP and glycemic changes in response to weight-loss diet interventions: the POUNDS lost trial.	International Journal of Obesity	2022
35843982	Adipose methylome integrative-omic analyses reveal genetic and dietary metabolic health drivers and insulin resistance classifiers.	Genome Med	2022
35444221	Cross-reactive antibodies elicited to conserved epitopes on SARS-CoV-2 spike protein after infection and vaccination.	Sci Rep	2022
35809202	Large-scale analysis of circulating glutamate and adipose gene expression in relation to abdominal obesity.	Amino Acids	2022
36259078	The Role of Dynamic DNA Methylation in Liver Transplant Rejection in Children.	Transplantation Direct	2022
34551091	The Impact of Prior Infection and Age on Antibody Persistence After Severe Acute Respiratory Syndrome Coronavirus 2 Messenger RNA Vaccine.	Clin Infect Dis	2022
34876522	Intersection of regulatory pathways controlling hemostasis and hemochorial placentation.	Proceedings of the National Academy of Sciences of the United States of America	2021
33675863	AKR1C2 and AKR1C3 expression in adipose tissue: Association with body fat distribution and regulatory variants.	Molecular and Cellular Endocrinology	2021
33758880	High-resolution epigenome analysis in nasal samples derived from children with respiratory viral infections reveals striking changes upon SARS-CoV-2 infection.	medRxiv	2021
34304742	Humoral immune responses during SARS-CoV-2 mRNA vaccine administration in seropositive and seronegative individuals.	BMC Med	2021
34354210	Immune cell residency in the nasal mucosa may partially explain respiratory disease severity across the age range.	Sci Rep	2021
33755375	Antibody Responses after a Single Dose of SARS-CoV-2 mRNA Vaccine.	N Engl J Med	2021
33649217	ASCL2 reciprocally controls key trophoblast lineage decisions during hemochorial placenta development.	Proceedings of the National Academy of Sciences of the United States of America	2021
32173762	Dominant gut Prevotella copri in gastrectomised non-obese diabetic Goto-Kakizaki rats improves glucose homeostasis through enhanced FXR signalling.	Diabetologia	2020
32199819	Capturing functional epigenomes for insight into metabolic diseases.	Molecular Metabolism	2020
32066997	Single-cell analysis of human adipose tissue identifies depot and disease specific cell types.	Nat Metab	2020
31393794	Customized MethylC-Capture Sequencing to Evaluate Variation in the Human Sperm DNA Methylome Representative of Altered Folate Metabolism.	Environ Health Perspect	2019
30320955	Identification of Novel Loci Associated With Hip Shape: A Meta-Analysis of Genomewide Association Studies.	J Bone Miner Res	2019
30872577	Dissecting features of epigenetic variants underlying cardiometabolic risk using full-resolution epigenome profiling in regulatory elements.	Nat Commun	2019
31170332	Mendelian Randomization Analysis Reveals a Causal Influence of Circulating Sclerostin Levels on Bone Mineral Density and Fractures.	J Bone Miner Res	2019
31064398	Correction to: Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.	Genome Biol	2019
30996144	UCP1 expression-associated gene signatures of human epicardial adipose tissue.	JCI insight	2019
28283040	Functional variation in allelic methylomes underscores a strong genetic contribution and reveals novel epigenetic alterations in the human epigenome.	Genome Biol	2017
28869591	Identification of 153 new loci associated with heel bone mineral density and functional involvement of GPC6 in osteoporosis.	Nat Genet	2017
27729386	Higher chylomicron remnants and LDL particle numbers associate with CD36 SNPs and DNA methylation sites that reduce CD36.	J Lipid Res	2016
26367794	Whole-genome sequencing identifies EN1 as a determinant of bone density and fracture.	Nature	2015
25707804	An epigenome-wide association study of total serum immunoglobulin E concentration.	Nature	2015
25743335	Whole-genome sequence-based analysis of thyroid function.	Nat Commun	2015
26219997	Erratum: Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.	Nat Commun	2015
26078267	Global miRNA expression and correlation with mRNA levels in primary human bone cells.	RNA	2015
25989729	Erratum: Whole-genome sequence-based analysis of thyroid function.	Nat Commun	2015
26025128	Genetic risk factors for decreased bone mineral accretion in children with asthma receiving multiple oral corticosteroid bursts.	Journal of Allergy and Clinical Immunology	2015
26021296	Characterization of functional methylomes by next-generation capture sequencing identifies novel disease-associated variants.	Nat Commun	2015
26699896	Population whole-genome bisulfite sequencing across two tissues highlights the environment as the principal source of human methylome variation.	Genome Biol	2015
24509480	Genome-wide trans-ancestry meta-analysis provides insight into the genetic architecture of type 2 diabetes susceptibility.	Nat Genet	2014
25424692	Cigarette smoking reduces DNA methylation levels at multiple genomic loci but the effect is partially reversible upon cessation.	Epigenetics	2014
24306210	Expression of phosphofructokinase in skeletal muscle is influenced by genetic variation and associated with insulin sensitivity.	Diabetes	2014
24816252	An atlas of genetic influences on human blood metabolites.	Nat Genet	2014
24678845	Interrogating causal pathways linking genetic variants, small molecule metabolites, and circulating lipids.	Genome Med	2014
24945404	Phenotypic dissection of bone mineral density reveals skeletal site specificity and facilitates the identification of novel loci in the genetic regulation of bone mass attainment.	PLoS Genet	2014
25102180	Meta-analysis of genome-wide association studies in African Americans provides insights into the genetic architecture of type 2 diabetes.	PLoS Genet	2014
23202125	Large-scale association analysis identifies new risk loci for coronary artery disease.	Nat Genet	2013
23889843	Gene expression changes with age in skin, adipose tissue, blood and brain.	Genome Biol	2013