Author details

Full Name

Cecilia M Lindgren

Affiliation

ORCID

Career Start Year

1999

Papers

251

H Index

100

Expertise

CM4AI Collaborator

PMID	Paper Title	Journal Title	Published Year
36693378	Loci for insulin processing and secretion provide insight into type 2 diabetes risk.	Am J Hum Genet	2023
37736706	Genic constraint against nonsynonymous variation across the mouse genome.	BMC Genomics	2023
37034649	Multi-ancestry genome-wide study in >2.5 million individuals reveals heterogeneity in mechanistic pathways of type 2 diabetes and complications.	medRxiv	2023
36711652	The genetic architecture of changes in adiposity during adulthood.	medRxiv	2023
37461573	Exome-wide evidence of compound heterozygous effects across common phenotypes in the UK Biobank.	medRxiv	2023
37253881	A non-coding variant linked to metabolic obesity with normal weight affects actin remodelling in subcutaneous adipocytes.	Nat Metab	2023
35220425	Multi-ancestry genome-wide association study of gestational diabetes mellitus highlights genetic links with type 2 diabetes.	Hum Mol Genet	2022
35697829	Differential and shared genetic effects on kidney function between diabetic and non-diabetic individuals.	Commun Biol	2022
35490555	Transcriptome and fatty-acid signatures of adipocyte hypertrophy and its non-invasive MR-based characterization in human adipose tissue.	EBioMedicine	2022
35551307	Multi-ancestry genetic study of type 2 diabetes highlights the power of diverse populations for discovery and translation.	Nat Genet	2022
36054878	Correction: Obesity and risk of female reproductive conditions: A Mendelian randomisation study.	PLoS Medicine	2022
35317627	Modelling the genetic aetiology of complex disease: human-mouse conservation of noncoding features and disease-associated loci.	Biol Lett	2022
34969092	Evidence From Men for Ovary-independent Effects of Genetic Risk Factors for Polycystic Ovary Syndrome.	J Clin Endocrinol Metab	2022
35104295	Obesity and risk of female reproductive conditions: A Mendelian randomisation study.	PLoS Medicine	2022
35090532	Making sense of the linear genome, gene function and TADs.	Epigenetics Chromatin	2022
34480422	The genomics of heart failure: design and rationale of the HERMES consortium.	ESC Heart Fail	2021
34290091	Linking the <i>FTO</i> obesity rs1421085 variant circuitry to cellular, metabolic, and organismal phenotypes in vivo.	Sci Adv	2021
34172828	A distribution-centered approach for analyzing human adipocyte size estimates and their association with obesity-related traits and mitochondrial function.	Int J Obes (Lond)	2021
33521676	Genetic IL-6R variants and therapeutic inhibition of IL-6 receptor signalling in COVID-19 - Authors' reply.	Lancet Rheumatology, The	2021
33727701	Publisher Correction: Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2021
33664499	Colocalization analysis of polycystic ovary syndrome to identify potential disease-mediating genes and proteins.	European Journal of Human Genetics	2021
33513366	A regulatory variant at 3q21.1 confers an increased pleiotropic risk for hyperglycemia and altered bone mineral density.	Cell Metab	2021
33558525	Publisher Correction: Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
32989287	Genome-wide association study identifies 48 common genetic variants associated with handedness.	Nat Hum Behav	2021
33402679	Sex-dimorphic genetic effects and novel loci for fasting glucose and insulin variability.	Nat Commun	2021
34851696	Response to comment on "Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics".	Sci Transl Med	2021
33067605	Genomic and drug target evaluation of 90 cardiovascular proteins in 30,931 individuals.	Nat Metab	2020
32180562	Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort.	Mol Metab	2020
32097451	Commentary: Using human genetics to guide the repurposing of medicines.	International Journal of Epidemiology	2020
32439900	Multi-ancestry GWAS of the electrocardiographic PR interval identifies 202 loci underlying cardiac conduction.	Nat Commun	2020
31915397	A brief history of human disease genetics.	Nature	2020
32581134	Evaluating the cardiovascular safety of sclerostin inhibition using evidence from meta-analysis of clinical trials and human genetics.	Sci Transl Med	2020
33239672	The genetic architecture of sporadic and multiple consecutive miscarriage.	Nat Commun	2020
32916155	Corrigendum to "Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort" [Molecular Metabolism 34 (2020) 85-96].	Mol Metab	2020
32797044	Machine Learning based histology phenotyping to investigate the epidemiologic and genetic basis of adipocyte morphology and cardiometabolic traits.	PLoS Comput Biol	2020
33230300	Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals.	Nat Genet	2020
33015641	Genetic variants mimicking therapeutic inhibition of IL-6 receptor signaling and risk of COVID-19.	Lancet Rheumatology, The	2020
31151930	MicroRNA-196a links human body fat distribution to adipose tissue extracellular matrix composition.	EBioMedicine	2019
31647808	Causal relationships between obesity and the leading causes of death in women and men.	PLoS Genetics	2019
31805045	Correction:Â Large-scale genome-wide meta-analysis of polycystic ovary syndrome suggests shared genetic architecture for different diagnosis criteria.	PLoS Genet	2019
30604766	Trans-ethnic kidney function association study reveals putative causal genes and effects on kidney-specific disease aetiologies.	Nat Commun	2019
30583798	GWAS Identifies Risk Locus for Erectile Dysfunction and Implicates Hypothalamic Neurobiology and Diabetes in Etiology.	Am J Hum Genet	2019
30239722	Meta-analysis of genome-wide association studies for body fat distribution in 694Â 649 individuals of European ancestry.	Hum Mol Genet	2019
31491410	Exome-Derived Adiponectin-Associated Variants Implicate Obesity and Lipid Biology.	Am J Hum Genet	2019
31172050	Deep clinical and biological phenotyping of the preterm birth and small for gestational age syndromes: The INTERBIO-21 <sup>st</sup> Newborn Case-Control Study protocol.	Gates Open Res	2019
31160809	Publisher Correction: Protein-altering variants associated with body mass index implicate pathways that control energy intake and expenditure in obesity.	Nat Genet	2019
30779634	Common Genetic Variation in Relation to Brachial Vascular Dimensions and Flow-Mediated Vasodilation.	Circ Genom Precis Med	2019
31152163	A catalog of genetic loci associated with kidney function from analyses of a million individuals.	Nat Genet	2019
29360107	Erratum: Sequence data and association statistics from 12,940 type 2 diabetes cases and controls.	Sci Data	2018
29892015	Multi-ethnic genome-wide association study for atrial fibrillation.	Nat Genet	2018