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L. Lotta · SciRah

Researcher profile · Semantic Scholar

L. Lotta

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L. Lotta — researcher profile on SciRah

h-index: 55
Works: 191
Citations: 11K

Most-cited papers

Exome sequencing and analysis of 454,787 UK Biobank participants
J. Backman, Alexander Li, A. Marcketta, Dylan Sun +37 more
2021Nature831 citations Open access
Semantic Scholar
Discovery and systematic characterization of risk variants and genes for coronary artery disease in over a million participants
K. Aragam, T. Jiang, A. Goel, S. Kanoni +91 more
2021Nature Genetics639 citations Open access
Semantic Scholar
Deciphering osteoarthritis genetics across 826,690 individuals from 9 populations
C. Boer, K. Hatzikotoulas, L. Southam, L. Stefánsdóttir +151 more
2021Cell433 citations Open access
Semantic Scholar
Large-scale genome-wide association study of coronary artery disease in genetically diverse populations
C. Tcheandjieu, Xiang Zhu, A. Hilliard, S. Clarke +79 more
2022Nature Medicine317 citations Open access
Semantic Scholar
Common and rare variant associations with clonal haematopoiesis phenotypes
M. D. Kessler, A. Damask, S. O'Keeffe, N. Banerjee +39 more
2022Nature270 citations Open access
Semantic Scholar
Sequencing of 640,000 exomes identifies GPR75 variants associated with protection from obesity
P. Akbari, Ankit Gilani, O. Sosina, J. Kosmicki +56 more
2021Science262 citations Open access
Semantic Scholar
A multiancestry genome-wide association study of unexplained chronic ALT elevation as a proxy for nonalcoholic fatty liver disease with histological and radiological validation
Marijana Vujković, S. Ramdas, Kim M. Lorenz, Xiu-Qing Guo +86 more
2022Nature Genetics174 citations Open access
Semantic Scholar
Cross-platform genetic discovery of small molecule products of metabolism and application to clinical outcomes
L. Lotta, M. Pietzner, I. Stewart, L. Wittemans +31 more
2021Nature Genetics172 citations Open access
Semantic Scholar
Genome-wide Association Analysis in Humans Links Nucleotide Metabolism to Leukocyte Telomere Length
Chen Li, S. Stoma, L. Lotta, S. Warner +92 more
2020American Journal of Human Genetics155 citations Open access
Semantic Scholar
Analysis of rare genetic variation underlying cardiometabolic diseases and traits among 200,000 individuals in the UK Biobank
S. Jurgens, Seung-Ho-An Choi, Valerie N. Morrill, M. Chaffin +66 more
2022Nature Genetics146 citations Open access
Semantic Scholar
Discovery of rare variants associated with blood pressure regulation through meta-analysis of 1.3 million individuals
P. Surendran, E. Feofanova, N. Lahrouchi, I. Ntalla +278 more
2020Nature Genetics145 citations Open access
Semantic Scholar
Advancing human genetics research and drug discovery through exome sequencing of the UK Biobank
J. Szustakowski, S. Balasubramanian, E. Kvikstad, S. Khalid +107 more
2021Nature Genetics143 citations Open access
Semantic Scholar
Rare and common genetic determinants of metabolic individuality and their effects on human health
P. Surendran, I. Stewart, Victoria P W Au Yeung, M. Pietzner +32 more
2022Nature Medicine140 citations Open access
Semantic Scholar
Genome-wide association analyses highlight etiological differences underlying newly defined subtypes of diabetes
Dina Mansour Aly, O. Dwivedi, R. Prasad, A. Käräjämäki +48 more
2021Nature Genetics134 citations
Semantic Scholar
Plasma Vitamin C and Type 2 Diabetes: Genome-Wide Association Study and Mendelian Randomization Analysis in European Populations
Ju-Sheng Zheng, J. Luan, E. Sofianopoulou, F. Imamura +38 more
2020Diabetes Care123 citations Open access
Semantic Scholar
Germline Mutations in CIDEB and Protection against Liver Disease.
N. Verweij, M. Haas, J. Nielsen, O. Sosina +43 more
2022New England Journal of Medicine96 citations Open access
Semantic Scholar
Translational genomics of osteoarthritis in 1,962,069 individuals
K. Hatzikotoulas, L. Southam, L. Stefánsdóttir, C. Boer +169 more
2025Nature95 citations Open access
Semantic Scholar
A Genome-wide Polygenic Score, Clinical Risk Factors, and Long-term Trajectories of Coronary Artery Disease
G. Hindy, K. Aragam, Kenney Ng, M. Chaffin +7 more
2020Arteriosclerosis, Thrombosis and Vascular Biology91 citations Open access
Semantic Scholar
Increased soluble urokinase plasminogen activator levels modulate monocyte function to promote atherosclerosis
G. Hindy, D. Tyrrell, A. Vasbinder, Changli Wei +38 more
2022Journal of Clinical Investigation77 citations Open access
Semantic Scholar
Genome-wide association and Mendelian randomisation analysis provide insights into the pathogenesis of heart failure
Sonia H. Shah, Albert Henry, C. Roselli, Hong-Huang Lin +142 more
2020Nature Communications74 citations Open access
Semantic Scholar
Kidney Multiome-based Genetic Scorecard Reveals Convergent Coding and Regulatory Variants
Hong-Bo Liu, A. Abedini, E. Ha, Ziyuan Ma +61 more
2025Science69 citations Open access
Semantic Scholar
Integrative common and rare variant analyses provide insights into the genetic architecture of liver cirrhosis
J. Ghouse, G. Sveinbjornsson, Marijana Vujković, A. Seidelin +47 more
2024Nature Genetics67 citations Open access
Semantic Scholar
The association between circulating 25-hydroxyvitamin D metabolites and type 2 diabetes in European populations: A meta-analysis and Mendelian randomisation analysis
Ju-Sheng Zheng, J. Luan, Eleni Sofianopoulou, S. Sharp +46 more
2020PLoS Medicine66 citations Open access
Semantic Scholar
GWAS of serum ALT and AST reveals an association of SLC30A10 Thr95Ile with hypermanganesemia symptoms
L. D. Ward, Ho-Chou Tu, Chelsea B. Quenneville, Shira Tsour +10 more
2021Nature Communications51 citations Open access
Semantic Scholar
Rare and Common Genetic Variation Underlying Atrial Fibrillation Risk
O. Vad, L. M. Monfort, C. Paludan-Müller, K. Kahnert +7 more
2024JAMA cardiology48 citations Open access
Semantic Scholar
Multiancestry exome sequencing reveals INHBE mutations associated with favorable fat distribution and protection from diabetes
P. Akbari, O. Sosina, J. Bovijn, K. Landheer +56 more
2022Nature Communications48 citations Open access
Semantic Scholar
High heritability of ascending aortic diameter and trans-ancestry prediction of thoracic aortic disease
C. Tcheandjieu, K. Xiao, H. Tejeda, J. Lynch +99 more
2022Nature Genetics47 citations Open access
Semantic Scholar
Gene-level analysis of rare variants in 379,066 whole exome sequences identifies an association of GIGYF1 loss of function with type 2 diabetes
A. Deaton, M. Parker, L. D. Ward, A. Flynn-Carroll +89 more
2021Scientific Reports43 citations Open access
Semantic Scholar
Polygenic risk of psychiatric disorders exhibits cross-trait associations in electronic health record data from European ancestry individuals
R. Kember, A. Merikangas, S. Verma, A. Verma +43 more
2020Biological Psychiatry41 citations Open access
Semantic Scholar
Activin E–ACVR1C cross talk controls energy storage via suppression of adipose lipolysis in mice
Rene C. Adam, Dwaine Pryce, Joseph S. Lee, Yuanqi Zhao +13 more
2023Proceedings of the National Academy of Sciences of the United States of America38 citations Open access
Semantic Scholar
Thrombomodulin (THBD) gene variants and thrombotic risk in a population‐based cohort study
Eric Manderstedt, C. Halldén, C. Lind-Halldén, Johan Elf +6 more
2021Journal of Thrombosis and Haemostasis33 citations Open access
Semantic Scholar
Agonist antibody to guanylate cyclase receptor NPR1 regulates vascular tone
Michael E. Dunn, A. Kithcart, Jee Hae Kim, A. Ho +188 more
2024Nature31 citations Open access
Semantic Scholar
Sequencing in over 50,000 cases identifies coding and structural variation underlying atrial fibrillation risk
S. Choi, S. Jurgens, Ling Xiao, M. Hill +496 more
2025Nature Genetics29 citations Open access
Semantic Scholar
Genetic and functional evidence links a missense variant in B4GALT1 to lower LDL and fibrinogen
M. Montasser, C. V. van Hout, Lawrence Miloscio, Alicia D. Howard +34 more
2021Science29 citations
Semantic Scholar
Yield of genetic association signals from genomes, exomes and imputation in the UK Biobank
Sheila M. Gaynor, Tyler Joseph, Xiao-Dong Bai, Yu-Xin Zou +16 more
2023Nature Genetics28 citations Open access
Semantic Scholar
Converging evidence from exome sequencing and common variants implicates target genes for osteoporosis
Si-Rui Zhou, O. Sosina, J. Bovijn, Laetitia Laurent +26 more
2023Nature Genetics28 citations Open access
Semantic Scholar
Translating polygenic risk scores for clinical use by estimating the confidence bounds of risk prediction
Jiang-Ming Sun, Yun-Peng Wang, L. Folkersen, Y. Borné +12 more
2021Nature Communications28 citations Open access
Semantic Scholar
Identification of Rare Loss-of-Function Genetic Variation Regulating Body Fat Distribution
M. Koprulu, Ya-Jie Zhao, E. Wheeler, Liang Dong +26 more
2021Journal of Clinical Endocrinology and Metabolism27 citations Open access
Semantic Scholar
Genetic disruption of serine biosynthesis is a key driver of macular telangiectasia type 2 aetiology and progression
R. Bonelli, B. Ansell, L. Lotta, T. Scerri +7 more
2020bioRxiv26 citations Open access
Semantic Scholar
Genome‐wide association analysis of serum alanine and aspartate aminotransferase, and the modifying effects of BMI in 388k European individuals
Chuan Gao, A. Marcketta, J. Backman, C. O'Dushlaine +13 more
2021Genetic Epidemiology23 citations Open access
Semantic Scholar
Classic Thrombophilias and Thrombotic Risk Among Middle‐Aged and Older Adults: A Population‐Based Cohort Study
Eric Manderstedt, C. Lind-Halldén, C. Halldén, Johan Elf +7 more
2022Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease21 citations Open access
Semantic Scholar
The genomics of heart failure: design and rationale of the HERMES consortium
R. Lumbers, Sonia H. Shah, Hong-Huang Lin, T. Czuba +170 more
2021ESC Heart Failure21 citations Open access
Semantic Scholar
The impact of common and rare genetic variants on bradyarrhythmia development
Lu-Chen Weng, Joel T. Rämö, S. Jurgens, S. Khurshid +103 more
2025Nature Genetics20 citations Open access
Semantic Scholar
Exome sequencing of 628,388 individuals identifies common and rare variant associations with clonal hematopoiesis phenotypes
Michael D. Kessler, A. Damask, S. O'Keeffe, Michael Michael Van Meter +30 more
2022medRxiv20 citations Open access
Semantic Scholar
Cross-platform genetic discovery of small molecule products of metabolism and application to clinical outcomes
L. Lotta, M. Pietzner, I. Stewart, L. Wittemans +30 more
2020bioRxiv17 citations Open access
Semantic Scholar
Clinical Evaluation of the Polygenetic Background of Blood Pressure in the Population-Based Setting
A. Giontella, Marketa Sjögren, L. Lotta, J. Overton +4 more
2020HYPERTENSION16 citations Open access
Semantic Scholar
Divergent role of Mitochondrial Amidoxime Reducing Component 1 (MARC1) in human and mouse
E. Smagris, Lisa M. Shihanian, Ivory J. Mintah, Parnian Bigdelou +15 more
2024PLoS Genetics14 citations Open access
Semantic Scholar
Genome-wide association study of adipocyte lipolysis in the GENetics of adipocyte lipolysis (GENiAL) cohort
A. Kulyté, Veroniqa Lundbäck, C. Lindgren, J. Luan +5 more
2020Molecular Metabolism14 citations Open access
Semantic Scholar
Causal Effect of Adiposity Measures on Blood Pressure Traits in 2 Urban Swedish Cohorts: A Mendelian Randomization Study
A. Giontella, L. Lotta, J. Overton, A. Baras +4 more
2021Journal of the American Heart Association : Cardiovascular and Cerebrovascular Disease13 citations Open access
Semantic Scholar
A genome-wide association study for nonalcoholic fatty liver disease identifies novel genetic loci and trait-relevant candidate genes in the Million Veteran Program.
M. Vujkovic, S. Ramdas, Kim M. Lorenz, Xiu-Qing Guo +86 more
2021medRxiv11 citations Open access
Semantic Scholar

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