Päivi Pajukanta - Concepedia

Author

Päivi Pajukanta

University of California, Los Angeles ORCID

Also Known As

Cruz-Bautista, Ivette, Damrauer, Scott M., Kar, Asha, Ko, Arthur, Kuusisto, Johanna, Oravilahti, Anniina, P E Pajukanta, P Pajukanta, P. PAJUKANTA, P. Pajukanta

252

Publications

13.8K

Citations

H-Index

129

Concepts

All Affiliations

University of California, Los Angeles University of Eastern Finland University of Helsinki Kuopio University Hospital Helsinki University Hospital

About

Päivi Pajukanta is an author at University of California, Los Angeles specializing in medicine, genetics, and genetic epidemiology.

Top Concepts

#	Concept	H-Index	Publications	Citations
1	Medicine	36	53	6.8K
2	Health Sciences	13	13	1.1K
3	Engineering	4	4	245
4	Natural Sciences	2	2	453
5	Management	1	1	21

Päivi Pajukanta

114

Publications

10.8K

Citations

H-Index

Page 1

	Year	Citations
Integrative approaches for large-scale transcriptome-wide association studies Alexander Gusev, Arthur Ko, Huwenbo Shi, Nature Genetics Functional GenomicsGeneticsMultiomicsTranscriptomics TechnologyOmics	2016	2.6K
A saturated map of common genetic variants associated with human height Loïc Yengo, Sailaja Vedantam, Eirini Marouli, Nature	2022	827
Accurate estimation of cell composition in bulk expression through robust integration of single-cell information Brandon Jew, Marcus Alvarez, Elior Rahmani, Nature Communications	2020	424
Familial combined hyperlipidemia is associated with upstream transcription factor 1 (USF1) Päivi Pajukanta, Heidi E. Lilja, Janet S. Sinsheimer, Nature Genetics Transcriptional RegulationGenetic DisorderMedicineGeneticsNatural Sciences	2004	345
Hyperglycemia and a Common Variant of<i>GCKR</i>Are Associated With the Levels of Eight Amino Acids in 9,369 Finnish Men Alena Stančáková, Mete Civelek, Niyas K. Saleem, Diabetes Eight Amino AcidsMetabolic DisorderGenetic EpidemiologyInsulin SignalingObesity	2012	273
Linkage of familial combined hyperlipidaemia to chromosome 1q21–q23 Päivi Pajukanta, Ilpo Nuotio, Joseph D. Terwilliger, Nature Genetics CytogeneticsGenetic DisorderGeneticsInherited Metabolic DiseaseGenetic Epidemiology	1998	266
Mutations in LMF1 cause combined lipase deficiency and severe hypertriglyceridemia Miklós Péterfy, Osnat Ben-Zeev, Hui Mao, Nature Genetics Metabolic SyndromeMetabolic DisorderBiochemistryGeneticsPathology	2007	222
The Metabolic Syndrome in Men study: a resource for studies of metabolic and cardiovascular diseases Markku Laakso, Johanna Kuusisto, Alena Stančáková, Journal of Lipid Research	2017	214
Genetic Regulation of Adipose Gene Expression and Cardio-Metabolic Traits Mete Civelek, Ying Wu, Calvin Pan, The American Journal of Human Genetics ObesityMetabolic SyndromeBody CompositionGeneticsPhysiology	2017	198
Two Loci on Chromosomes 2 and X for Premature Coronary Heart Disease Identified in Early- and Late-Settlement Populations of Finland Päivi Pajukanta, Michele Cargill, Laura Viitanen, The American Journal of Human Genetics CytogeneticsMedicineGeneticsGenetic DisorderGenetic Epidemiology	2000	176

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